data_SASDEB4_MAIN # _sas_result.id 1098 _sas_result.SASBDB_code SASDEB4 _sas_result.experimental_MW 24.500 _sas_result.experimental_MW_error . _sas_result.MW_standard . _sas_result.MW_standard_error . _sas_result.MW_Porod 24.500 _sas_result.MW_Porod_error . _sas_result.I0_from_PR 13.9400000000 _sas_result.I0_from_PR_error . _sas_result.I0_from_Guinier 13.9000000000 _sas_result.I0_from_Guinier_error 0.0190000000 _sas_result.Rg_from_PR 2.051 _sas_result.Rg_from_PR_error . _sas_result.Rg_from_Guinier 2.020 _sas_result.Rg_from_Guinier_error 0.010 _sas_result.D_max 6.70 _sas_result.Porod_volume 41.50 _sas_result.Porod_volume_error . _sas_result.estimated_volume . _sas_result.estimated_volume_error . _sas_result.estimated_volume_method . _sas_result.Guinier_point_min 22 _sas_result.Guinier_point_max 126 _sas_result.type_of_curve sec _sas_result.standard . _sas_result.Dmax_error . _sas_result.comments ;SEC column type: GE Healthcare S75 3.2/300; Sample Injection Concentration = 10 mg/mL; Column flow-rate = 0.1 mL/min. ; # _sas_scan.title "Tryparedoxin I109A, in the presence of CFT" _sas_scan.detc_id 16 _sas_scan.id 1098 _sas_scan.measurement_date 2018-05-31 _sas_scan.storage_temperature 20.0 _sas_scan.cell_temperature 20.0 _sas_scan.exposure_time 1.000 _sas_scan.number_of_frames . _sas_scan.unit 1/nm _sas_scan.qmin 0.0373 _sas_scan.qmax 4.9279 _sas_scan.sample_id 1058 _sas_scan.result_id 1098 _sas_scan.beam_id 10 # _sas_beam.id 10 _sas_beam.instrument_name "ESRF BM29" _sas_beam.instrument_city Grenoble _sas_beam.instrument_country France _sas_beam.shape . _sas_beam.type_of_source "X-ray synchrotron" _sas_beam.radiation_wavelength 0.099000 _sas_beam.dist_spec_to_detc 2.86900 # _sas_detc.id 16 _sas_detc.name "Pilatus 1M" _sas_detc.type Dectris _sas_detc.pixsize_x 172.000 # _sas_sample.id 1058 _sas_sample.name "Tryparedoxin I109A, in the presence of inhibitor CFT (2-(chloromethyl)-5-(4-fluorophenyl)thieno[2,3-d]pyrimidin-4(3H)-one)" _sas_sample.ext_coefficient . _sas_sample.contrast . _sas_sample.specific_vol . _sas_sample.purity_method . _sas_sample.dry_vol . _sas_sample.sample_MW . _sas_sample.specimen_concentration . _sas_sample.concentration_method . _sas_sample.entity_id 1275 # _sas_buffer.id 676 _sas_buffer.name "10 mM HEPES pH 7.5, 50 mM NaCl" _sas_buffer.concentration . _sas_buffer.unit . _sas_buffer.pK . _sas_buffer.pH 7.500 _sas_buffer.comment . _sas_buffer.composition . _sas_buffer.sample_id 1058 # _entity.id 1275 _entity.type protein _entity.pdbx_description "Tryparedoxin I109A" _entity.formula_weight 15.775 _entity.pdbx_number_of_molecules . # _entity_name_com.entity_id 1275 _entity_name_com.name . # _entity_poly.entity_id 1275 _entity_poly.pdbx_seq_one_letter_code ;GSGLAKYLPGATNLLSKSGEVSLGSLVGKTVFLYFSASWCPPCRG FTPVLAEFYEKHHVAKNFEVVLISWDENESDFHDYYGKMPWLALPFDQRSTVSELGKTFG VESAPTLITINADTGAIIGTQARTRVIEDPDGANFPWPN ; # _entity_src_gen.entity_id 1275 _entity_src_gen.gene_src_common_name "Trypanosoma brucei brucei" # _struct_ref.id 1 _struct_ref.entity_id 1275 _struct_ref.db_name UniProt _struct_ref.db_code O77404 _struct_ref.details http://www.uniprot.org/uniprot/O77404 # _citation.id 419 _citation.title "Inhibitor-induced dimerization of an essential oxidoreductase from African Trypanosomes." _citation.year "2019 Jan 3" _citation.pdbx_database_id_DOI 10.1002/anie.201810470 _citation.pdbx_database_id_PubMed 30605929 # loop_ _citation_author.citation_id _citation_author.ordinal _citation_author.name 419 1 "Wagner A" 419 2 "Le TA" 419 3 "Brennich M" 419 4 "Klein P" 419 5 "Bader N" 419 6 "Diehl E" 419 7 "Paszek D" 419 8 "Weickhmann AK" 419 9 "Dirdjaja N" 419 10 "Krauth-Siegel RL" 419 11 "Engels B" 419 12 "Opatz T" 419 13 "Schindelin H" # _pdbx_contact_author.id 68 _pdbx_contact_author.name_first Martha _pdbx_contact_author.name_last Brennich _pdbx_contact_author.role . _pdbx_contact_author.address_1 EMBL _pdbx_contact_author.address_2 "European Molecular Biology Laboratory (EMBL) - Grenoble Outstation" _pdbx_contact_author.address_3 "Grenoble, France" # loop_ _sas_scan_intensity.id _sas_scan_intensity.momentum_transfer _sas_scan_intensity.intensity _sas_scan_intensity.intensity_su_counting _sas_scan_intensity.scan_id 1 3.725576E-02 2.456100E+01 3.346146E+00 1098 2 4.194927E-02 3.645300E+01 1.792217E+00 1098 3 4.664278E-02 3.374100E+01 1.504549E+00 1098 4 5.133629E-02 3.116720E+01 1.220840E+00 1098 5 5.602979E-02 2.545690E+01 1.022102E+00 1098 6 6.072330E-02 2.466070E+01 7.825781E-01 1098 7 6.541680E-02 2.004550E+01 6.969888E-01 1098 8 7.011031E-02 1.984350E+01 5.994870E-01 1098 9 7.480382E-02 1.875810E+01 5.610927E-01 1098 10 7.949733E-02 1.656140E+01 4.646643E-01 1098 11 8.419084E-02 1.575820E+01 4.096912E-01 1098 12 8.888435E-02 1.537500E+01 4.059226E-01 1098 13 9.357785E-02 1.473270E+01 3.678346E-01 1098 14 9.827136E-02 1.507630E+01 3.325351E-01 1098 15 1.029649E-01 1.520990E+01 2.881656E-01 1098 16 1.076584E-01 1.458003E+01 2.974768E-01 1098 17 1.123519E-01 1.422105E+01 2.736981E-01 1098 18 1.170454E-01 1.390477E+01 2.495606E-01 1098 19 1.217389E-01 1.425601E+01 2.341458E-01 1098 20 1.264324E-01 1.383710E+01 2.310175E-01 1098 21 1.311259E-01 1.436205E+01 2.187870E-01 1098 22 1.358194E-01 1.368374E+01 2.120255E-01 1098 23 1.405129E-01 1.392083E+01 1.971657E-01 1098 24 1.452064E-01 1.345508E+01 1.935964E-01 1098 25 1.498999E-01 1.342978E+01 1.845947E-01 1098 26 1.545934E-01 1.348599E+01 1.813275E-01 1098 27 1.592870E-01 1.344013E+01 1.739606E-01 1098 28 1.639805E-01 1.364276E+01 1.623731E-01 1098 29 1.686740E-01 1.356285E+01 1.643413E-01 1098 30 1.733675E-01 1.343239E+01 1.618372E-01 1098 31 1.780610E-01 1.319544E+01 1.529277E-01 1098 32 1.827545E-01 1.327381E+01 1.483970E-01 1098 33 1.874480E-01 1.313368E+01 1.464101E-01 1098 34 1.921415E-01 1.347109E+01 1.467947E-01 1098 35 1.968350E-01 1.334090E+01 1.438431E-01 1098 36 2.015285E-01 1.304132E+01 1.378682E-01 1098 37 2.062220E-01 1.317756E+01 1.307158E-01 1098 38 2.109155E-01 1.305135E+01 1.333996E-01 1098 39 2.156090E-01 1.317225E+01 1.336367E-01 1098 40 2.203026E-01 1.291225E+01 1.274287E-01 1098 41 2.249961E-01 1.303447E+01 1.231922E-01 1098 42 2.296896E-01 1.295461E+01 1.245553E-01 1098 43 2.343831E-01 1.267806E+01 1.247778E-01 1098 44 2.390766E-01 1.273230E+01 1.208654E-01 1098 45 2.437701E-01 1.282710E+01 1.180734E-01 1098 46 2.484636E-01 1.280813E+01 1.184026E-01 1098 47 2.531571E-01 1.265412E+01 1.175742E-01 1098 48 2.578506E-01 1.262562E+01 1.119077E-01 1098 49 2.625441E-01 1.281388E+01 1.110642E-01 1098 50 2.672376E-01 1.232934E+01 1.116379E-01 1098 51 2.719311E-01 1.267215E+01 1.116559E-01 1098 52 2.766247E-01 1.250811E+01 1.091009E-01 1098 53 2.813182E-01 1.264288E+01 1.056777E-01 1098 54 2.860117E-01 1.239657E+01 1.036598E-01 1098 55 2.907052E-01 1.243249E+01 1.077601E-01 1098 56 2.953987E-01 1.220136E+01 1.060671E-01 1098 57 3.000922E-01 1.221777E+01 1.004149E-01 1098 58 3.047857E-01 1.228045E+01 1.007919E-01 1098 59 3.094792E-01 1.206767E+01 1.003715E-01 1098 60 3.141727E-01 1.199595E+01 1.033497E-01 1098 61 3.188662E-01 1.208684E+01 9.607295E-02 1098 62 3.235597E-01 1.205506E+01 9.746832E-02 1098 63 3.282532E-01 1.209297E+01 9.742106E-02 1098 64 3.329468E-01 1.192597E+01 9.917389E-02 1098 65 3.376403E-01 1.200342E+01 9.346757E-02 1098 66 3.423338E-01 1.169892E+01 9.513168E-02 1098 67 3.470272E-01 1.177747E+01 9.628096E-02 1098 68 3.517208E-01 1.177482E+01 1.003470E-01 1098 69 3.564143E-01 1.175507E+01 9.632230E-02 1098 70 3.611078E-01 1.178582E+01 9.829404E-02 1098 71 3.658013E-01 1.165388E+01 1.009564E-01 1098 72 3.704948E-01 1.138755E+01 1.025896E-01 1098 73 3.751883E-01 1.136134E+01 1.053933E-01 1098 74 3.798818E-01 1.127250E+01 9.973359E-02 1098 75 3.845753E-01 1.140413E+01 1.045694E-01 1098 76 3.892688E-01 1.121184E+01 1.049371E-01 1098 77 3.939623E-01 1.126881E+01 1.062432E-01 1098 78 3.986558E-01 1.118696E+01 1.044610E-01 1098 79 4.033493E-01 1.114824E+01 1.103541E-01 1098 80 4.080429E-01 1.095829E+01 1.122546E-01 1098 81 4.127364E-01 1.108451E+01 1.130710E-01 1098 82 4.174299E-01 1.097043E+01 1.166513E-01 1098 83 4.221234E-01 1.100707E+01 1.184115E-01 1098 84 4.268169E-01 1.094652E+01 1.224613E-01 1098 85 4.315104E-01 1.089094E+01 1.240542E-01 1098 86 4.362039E-01 1.082917E+01 1.243697E-01 1098 87 4.408974E-01 1.058431E+01 1.246779E-01 1098 88 4.455909E-01 1.062426E+01 1.303573E-01 1098 89 4.502844E-01 1.042471E+01 1.284942E-01 1098 90 4.549779E-01 1.048293E+01 1.301410E-01 1098 91 4.596714E-01 1.032509E+01 1.300888E-01 1098 92 4.643650E-01 1.034260E+01 1.295817E-01 1098 93 4.690585E-01 1.058199E+01 1.250098E-01 1098 94 4.737520E-01 1.010727E+01 1.216031E-01 1098 95 4.784455E-01 1.014941E+01 1.206372E-01 1098 96 4.831390E-01 1.010799E+01 1.206293E-01 1098 97 4.878325E-01 1.003974E+01 1.180519E-01 1098 98 4.925260E-01 9.966600E+00 1.193762E-01 1098 99 4.972195E-01 9.999560E+00 1.170554E-01 1098 100 5.019130E-01 1.009639E+01 1.146239E-01 1098 101 5.066065E-01 9.802600E+00 1.144763E-01 1098 102 5.113000E-01 9.663220E+00 1.167814E-01 1098 103 5.159935E-01 9.652070E+00 1.162870E-01 1098 104 5.206870E-01 9.682320E+00 1.099863E-01 1098 105 5.253805E-01 9.466580E+00 1.125923E-01 1098 106 5.300741E-01 9.445890E+00 1.145090E-01 1098 107 5.347676E-01 9.410250E+00 1.130409E-01 1098 108 5.394611E-01 9.491210E+00 1.094603E-01 1098 109 5.441546E-01 9.484150E+00 1.103395E-01 1098 110 5.488481E-01 9.284470E+00 1.102909E-01 1098 111 5.535416E-01 9.111740E+00 1.103955E-01 1098 112 5.582351E-01 9.069760E+00 1.051658E-01 1098 113 5.629286E-01 9.024060E+00 1.063649E-01 1098 114 5.676221E-01 8.975850E+00 1.064155E-01 1098 115 5.723156E-01 8.857680E+00 1.074414E-01 1098 116 5.770091E-01 8.832940E+00 1.042940E-01 1098 117 5.817026E-01 8.775230E+00 1.025773E-01 1098 118 5.863962E-01 8.652370E+00 1.036971E-01 1098 119 5.910897E-01 8.692240E+00 1.063239E-01 1098 120 5.957832E-01 8.463150E+00 1.032302E-01 1098 121 6.004767E-01 8.406810E+00 1.011760E-01 1098 122 6.051702E-01 8.461680E+00 1.011036E-01 1098 123 6.098637E-01 8.287890E+00 1.050246E-01 1098 124 6.145572E-01 8.400220E+00 1.004935E-01 1098 125 6.192507E-01 8.277910E+00 1.000084E-01 1098 126 6.239442E-01 8.265010E+00 1.011816E-01 1098 127 6.286377E-01 8.160190E+00 1.010779E-01 1098 128 6.333312E-01 8.150160E+00 1.025494E-01 1098 129 6.380248E-01 8.143430E+00 9.760594E-02 1098 130 6.427183E-01 7.984270E+00 1.009672E-01 1098 131 6.474118E-01 7.907640E+00 1.003636E-01 1098 132 6.521052E-01 8.000130E+00 1.010266E-01 1098 133 6.567987E-01 7.843280E+00 9.686968E-02 1098 134 6.614922E-01 7.687440E+00 9.797153E-02 1098 135 6.661857E-01 7.664400E+00 9.827863E-02 1098 136 6.708792E-01 7.501800E+00 9.971689E-02 1098 137 6.755728E-01 7.567040E+00 9.675096E-02 1098 138 6.802663E-01 7.512210E+00 9.619355E-02 1098 139 6.849598E-01 7.438520E+00 9.823742E-02 1098 140 6.896533E-01 7.382870E+00 9.819598E-02 1098 141 6.943468E-01 7.418350E+00 9.703239E-02 1098 142 6.990403E-01 7.203380E+00 9.398253E-02 1098 143 7.037338E-01 7.135810E+00 9.698980E-02 1098 144 7.084273E-01 6.892410E+00 9.506056E-02 1098 145 7.131208E-01 7.116310E+00 9.693315E-02 1098 146 7.178143E-01 6.968130E+00 9.373137E-02 1098 147 7.225078E-01 6.808630E+00 9.386838E-02 1098 148 7.272013E-01 6.824630E+00 9.508176E-02 1098 149 7.318948E-01 6.661220E+00 9.557483E-02 1098 150 7.365884E-01 6.565720E+00 9.214322E-02 1098 151 7.412819E-01 6.554850E+00 9.401499E-02 1098 152 7.459754E-01 6.577400E+00 9.374510E-02 1098 153 7.506689E-01 6.424580E+00 9.385964E-02 1098 154 7.553624E-01 6.562540E+00 9.271662E-02 1098 155 7.600559E-01 6.428360E+00 9.211894E-02 1098 156 7.647494E-01 6.411850E+00 9.260047E-02 1098 157 7.694429E-01 6.176030E+00 9.316194E-02 1098 158 7.741364E-01 6.347560E+00 9.226893E-02 1098 159 7.788299E-01 6.203220E+00 9.039689E-02 1098 160 7.835234E-01 6.150490E+00 9.081319E-02 1098 161 7.882170E-01 6.127330E+00 9.206658E-02 1098 162 7.929105E-01 6.071200E+00 9.227479E-02 1098 163 7.976040E-01 5.853300E+00 8.923308E-02 1098 164 8.022975E-01 6.017450E+00 8.978762E-02 1098 165 8.069910E-01 5.637850E+00 9.091537E-02 1098 166 8.116845E-01 5.838300E+00 9.090360E-02 1098 167 8.163780E-01 5.663380E+00 8.845334E-02 1098 168 8.210715E-01 5.704470E+00 8.836717E-02 1098 169 8.257650E-01 5.638390E+00 9.049078E-02 1098 170 8.304585E-01 5.480590E+00 8.876928E-02 1098 171 8.351520E-01 5.542590E+00 8.892183E-02 1098 172 8.398455E-01 5.765580E+00 8.813526E-02 1098 173 8.445390E-01 5.304930E+00 8.826651E-02 1098 174 8.492325E-01 5.333970E+00 8.896878E-02 1098 175 8.539261E-01 5.283550E+00 8.816329E-02 1098 176 8.586196E-01 5.311640E+00 8.569969E-02 1098 177 8.633131E-01 5.407450E+00 8.669842E-02 1098 178 8.680066E-01 5.165600E+00 8.845173E-02 1098 179 8.727001E-01 5.194450E+00 8.781377E-02 1098 180 8.773936E-01 5.060410E+00 8.507692E-02 1098 181 8.820871E-01 4.934790E+00 8.590985E-02 1098 182 8.867806E-01 5.179350E+00 8.701080E-02 1098 183 8.914741E-01 5.003930E+00 8.696608E-02 1098 184 8.961676E-01 4.812720E+00 8.497057E-02 1098 185 9.008611E-01 4.756760E+00 8.478496E-02 1098 186 9.055547E-01 4.832230E+00 8.555112E-02 1098 187 9.102482E-01 4.724220E+00 8.617142E-02 1098 188 9.149417E-01 4.823950E+00 8.396549E-02 1098 189 9.196352E-01 4.733280E+00 8.531029E-02 1098 190 9.243287E-01 4.472750E+00 8.395564E-02 1098 191 9.290222E-01 4.453350E+00 8.544252E-02 1098 192 9.337157E-01 4.391980E+00 8.414544E-02 1098 193 9.384092E-01 4.513240E+00 8.195064E-02 1098 194 9.431027E-01 4.314750E+00 8.421326E-02 1098 195 9.477962E-01 4.290390E+00 8.407798E-02 1098 196 9.524897E-01 4.377800E+00 8.388800E-02 1098 197 9.571832E-01 4.241680E+00 8.097380E-02 1098 198 9.618767E-01 4.128540E+00 8.314713E-02 1098 199 9.665703E-01 4.139020E+00 8.338347E-02 1098 200 9.712638E-01 4.166660E+00 8.286632E-02 1098 201 9.759573E-01 4.173610E+00 8.113594E-02 1098 202 9.806508E-01 4.008710E+00 8.167799E-02 1098 203 9.853443E-01 4.041400E+00 8.219590E-02 1098 204 9.900378E-01 3.968130E+00 8.247019E-02 1098 205 9.947313E-01 3.954570E+00 8.061726E-02 1098 206 9.994248E-01 3.663940E+00 8.011457E-02 1098 207 1.004118E+00 3.694520E+00 8.143521E-02 1098 208 1.008812E+00 3.752350E+00 8.166295E-02 1098 209 1.013505E+00 3.511870E+00 8.068941E-02 1098 210 1.018199E+00 3.731670E+00 7.927900E-02 1098 211 1.022892E+00 3.706620E+00 8.111285E-02 1098 212 1.027586E+00 3.579440E+00 8.052659E-02 1098 213 1.032279E+00 3.643290E+00 8.058371E-02 1098 214 1.036973E+00 3.617930E+00 7.782807E-02 1098 215 1.041666E+00 3.469970E+00 7.996803E-02 1098 216 1.046360E+00 3.375890E+00 7.962471E-02 1098 217 1.051053E+00 3.319650E+00 7.936987E-02 1098 218 1.055747E+00 3.289740E+00 7.830165E-02 1098 219 1.060440E+00 3.438400E+00 7.904601E-02 1098 220 1.065134E+00 3.330710E+00 7.882269E-02 1098 221 1.069827E+00 3.252070E+00 7.950664E-02 1098 222 1.074521E+00 3.208640E+00 7.755315E-02 1098 223 1.079215E+00 3.133330E+00 7.767855E-02 1098 224 1.083908E+00 3.142080E+00 7.825958E-02 1098 225 1.088602E+00 3.157100E+00 7.828740E-02 1098 226 1.093295E+00 3.149580E+00 7.781391E-02 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2.650900E-01 3.392380E-01 1098 1033 4.880956E+00 3.160500E-01 3.479166E-01 1098 1034 4.885649E+00 7.458000E-02 3.527838E-01 1098 1035 4.890343E+00 -1.177800E-01 3.828092E-01 1098 1036 4.895036E+00 7.808000E-02 4.087010E-01 1098 1037 4.899730E+00 4.809600E-01 4.265149E-01 1098 1038 4.904423E+00 -2.753200E-01 4.643921E-01 1098 1039 4.909117E+00 3.487300E-01 5.445913E-01 1098 1040 4.913810E+00 -1.217700E-01 5.919472E-01 1098 1041 4.918504E+00 2.575000E-01 6.200834E-01 1098 1042 4.923197E+00 3.827100E-01 7.648385E-01 1098 1043 4.927891E+00 2.982610E-01 4.730371E-01 1098 # _sas_p_of_R_details.id 1098 _sas_p_of_R_details.intensity_id 1098 _sas_p_of_R_details.software_p_of_R "GNOM 5.0" _sas_p_of_R_details.number_of_points 814 _sas_p_of_R_details.qmin 0.145206 _sas_p_of_R_details.qmax 3.96103 _sas_p_of_R_details.p_of_R_point_min 1 _sas_p_of_R_details.p_of_R_point_max 814 _sas_p_of_R_details.Rmin 0.0 _sas_p_of_R_details.Rmax 6.7 # loop_ _sas_p_of_R.id _sas_p_of_R.ordinal _sas_p_of_R.r _sas_p_of_R.P _sas_p_of_R.P_error 1098 1 0.000000E+00 0.000000E+00 0.000000E+00 1098 2 2.952000E-02 1.466000E-03 1.676000E-04 1098 3 5.903000E-02 3.217000E-03 3.127000E-04 1098 4 8.855000E-02 5.254000E-03 4.356000E-04 1098 5 1.181000E-01 7.576000E-03 5.368000E-04 1098 6 1.476000E-01 1.018000E-02 6.168000E-04 1098 7 1.771000E-01 1.306000E-02 6.764000E-04 1098 8 2.066000E-01 1.623000E-02 7.167000E-04 1098 9 2.361000E-01 1.966000E-02 7.387000E-04 1098 10 2.656000E-01 2.337000E-02 7.436000E-04 1098 11 2.952000E-01 2.735000E-02 7.331000E-04 1098 12 3.247000E-01 3.158000E-02 7.087000E-04 1098 13 3.542000E-01 3.608000E-02 6.726000E-04 1098 14 3.837000E-01 4.083000E-02 6.269000E-04 1098 15 4.132000E-01 4.582000E-02 5.747000E-04 1098 16 4.427000E-01 5.106000E-02 5.196000E-04 1098 17 4.722000E-01 5.652000E-02 4.666000E-04 1098 18 5.018000E-01 6.222000E-02 4.224000E-04 1098 19 5.313000E-01 6.813000E-02 3.950000E-04 1098 20 5.608000E-01 7.425000E-02 3.918000E-04 1098 21 5.903000E-01 8.057000E-02 4.152000E-04 1098 22 6.198000E-01 8.709000E-02 4.618000E-04 1098 23 6.493000E-01 9.378000E-02 5.247000E-04 1098 24 6.789000E-01 1.007000E-01 5.971000E-04 1098 25 7.084000E-01 1.077000E-01 6.739000E-04 1098 26 7.379000E-01 1.149000E-01 7.513000E-04 1098 27 7.674000E-01 1.222000E-01 8.265000E-04 1098 28 7.969000E-01 1.297000E-01 8.974000E-04 1098 29 8.264000E-01 1.372000E-01 9.625000E-04 1098 30 8.559000E-01 1.449000E-01 1.021000E-03 1098 31 8.855000E-01 1.527000E-01 1.071000E-03 1098 32 9.150000E-01 1.606000E-01 1.113000E-03 1098 33 9.445000E-01 1.685000E-01 1.145000E-03 1098 34 9.740000E-01 1.765000E-01 1.169000E-03 1098 35 1.004000E+00 1.845000E-01 1.183000E-03 1098 36 1.033000E+00 1.925000E-01 1.189000E-03 1098 37 1.063000E+00 2.006000E-01 1.185000E-03 1098 38 1.092000E+00 2.087000E-01 1.174000E-03 1098 39 1.122000E+00 2.167000E-01 1.155000E-03 1098 40 1.151000E+00 2.247000E-01 1.130000E-03 1098 41 1.181000E+00 2.327000E-01 1.100000E-03 1098 42 1.210000E+00 2.407000E-01 1.066000E-03 1098 43 1.240000E+00 2.485000E-01 1.030000E-03 1098 44 1.269000E+00 2.563000E-01 9.927000E-04 1098 45 1.299000E+00 2.640000E-01 9.575000E-04 1098 46 1.328000E+00 2.716000E-01 9.259000E-04 1098 47 1.358000E+00 2.790000E-01 9.000000E-04 1098 48 1.387000E+00 2.863000E-01 8.816000E-04 1098 49 1.417000E+00 2.935000E-01 8.722000E-04 1098 50 1.446000E+00 3.005000E-01 8.727000E-04 1098 51 1.476000E+00 3.073000E-01 8.830000E-04 1098 52 1.505000E+00 3.140000E-01 9.024000E-04 1098 53 1.535000E+00 3.204000E-01 9.298000E-04 1098 54 1.564000E+00 3.266000E-01 9.633000E-04 1098 55 1.594000E+00 3.326000E-01 1.001000E-03 1098 56 1.623000E+00 3.384000E-01 1.041000E-03 1098 57 1.653000E+00 3.439000E-01 1.082000E-03 1098 58 1.682000E+00 3.492000E-01 1.122000E-03 1098 59 1.712000E+00 3.542000E-01 1.160000E-03 1098 60 1.741000E+00 3.589000E-01 1.195000E-03 1098 61 1.771000E+00 3.634000E-01 1.226000E-03 1098 62 1.800000E+00 3.676000E-01 1.252000E-03 1098 63 1.830000E+00 3.715000E-01 1.272000E-03 1098 64 1.859000E+00 3.750000E-01 1.288000E-03 1098 65 1.889000E+00 3.783000E-01 1.298000E-03 1098 66 1.919000E+00 3.813000E-01 1.302000E-03 1098 67 1.948000E+00 3.839000E-01 1.302000E-03 1098 68 1.978000E+00 3.863000E-01 1.296000E-03 1098 69 2.007000E+00 3.883000E-01 1.287000E-03 1098 70 2.037000E+00 3.900000E-01 1.274000E-03 1098 71 2.066000E+00 3.913000E-01 1.259000E-03 1098 72 2.096000E+00 3.924000E-01 1.242000E-03 1098 73 2.125000E+00 3.931000E-01 1.224000E-03 1098 74 2.155000E+00 3.935000E-01 1.206000E-03 1098 75 2.184000E+00 3.936000E-01 1.190000E-03 1098 76 2.214000E+00 3.934000E-01 1.175000E-03 1098 77 2.243000E+00 3.928000E-01 1.164000E-03 1098 78 2.273000E+00 3.920000E-01 1.156000E-03 1098 79 2.302000E+00 3.908000E-01 1.153000E-03 1098 80 2.332000E+00 3.893000E-01 1.154000E-03 1098 81 2.361000E+00 3.876000E-01 1.160000E-03 1098 82 2.391000E+00 3.855000E-01 1.170000E-03 1098 83 2.420000E+00 3.832000E-01 1.184000E-03 1098 84 2.450000E+00 3.806000E-01 1.201000E-03 1098 85 2.479000E+00 3.777000E-01 1.221000E-03 1098 86 2.509000E+00 3.746000E-01 1.243000E-03 1098 87 2.538000E+00 3.712000E-01 1.267000E-03 1098 88 2.568000E+00 3.676000E-01 1.291000E-03 1098 89 2.597000E+00 3.638000E-01 1.315000E-03 1098 90 2.627000E+00 3.598000E-01 1.338000E-03 1098 91 2.656000E+00 3.555000E-01 1.361000E-03 1098 92 2.686000E+00 3.511000E-01 1.382000E-03 1098 93 2.715000E+00 3.465000E-01 1.402000E-03 1098 94 2.745000E+00 3.417000E-01 1.421000E-03 1098 95 2.774000E+00 3.367000E-01 1.438000E-03 1098 96 2.804000E+00 3.317000E-01 1.453000E-03 1098 97 2.833000E+00 3.264000E-01 1.467000E-03 1098 98 2.863000E+00 3.211000E-01 1.480000E-03 1098 99 2.893000E+00 3.157000E-01 1.492000E-03 1098 100 2.922000E+00 3.101000E-01 1.503000E-03 1098 101 2.952000E+00 3.045000E-01 1.515000E-03 1098 102 2.981000E+00 2.989000E-01 1.526000E-03 1098 103 3.011000E+00 2.931000E-01 1.537000E-03 1098 104 3.040000E+00 2.874000E-01 1.548000E-03 1098 105 3.070000E+00 2.816000E-01 1.561000E-03 1098 106 3.099000E+00 2.758000E-01 1.573000E-03 1098 107 3.129000E+00 2.700000E-01 1.586000E-03 1098 108 3.158000E+00 2.642000E-01 1.600000E-03 1098 109 3.188000E+00 2.584000E-01 1.614000E-03 1098 110 3.217000E+00 2.527000E-01 1.629000E-03 1098 111 3.247000E+00 2.470000E-01 1.643000E-03 1098 112 3.276000E+00 2.414000E-01 1.657000E-03 1098 113 3.306000E+00 2.358000E-01 1.671000E-03 1098 114 3.335000E+00 2.303000E-01 1.684000E-03 1098 115 3.365000E+00 2.249000E-01 1.696000E-03 1098 116 3.394000E+00 2.195000E-01 1.706000E-03 1098 117 3.424000E+00 2.143000E-01 1.716000E-03 1098 118 3.453000E+00 2.092000E-01 1.723000E-03 1098 119 3.483000E+00 2.042000E-01 1.729000E-03 1098 120 3.512000E+00 1.993000E-01 1.733000E-03 1098 121 3.542000E+00 1.945000E-01 1.735000E-03 1098 122 3.571000E+00 1.899000E-01 1.736000E-03 1098 123 3.601000E+00 1.854000E-01 1.735000E-03 1098 124 3.630000E+00 1.810000E-01 1.733000E-03 1098 125 3.660000E+00 1.767000E-01 1.729000E-03 1098 126 3.689000E+00 1.727000E-01 1.724000E-03 1098 127 3.719000E+00 1.687000E-01 1.719000E-03 1098 128 3.748000E+00 1.649000E-01 1.714000E-03 1098 129 3.778000E+00 1.612000E-01 1.709000E-03 1098 130 3.807000E+00 1.577000E-01 1.703000E-03 1098 131 3.837000E+00 1.543000E-01 1.699000E-03 1098 132 3.867000E+00 1.511000E-01 1.696000E-03 1098 133 3.896000E+00 1.480000E-01 1.693000E-03 1098 134 3.926000E+00 1.450000E-01 1.692000E-03 1098 135 3.955000E+00 1.422000E-01 1.693000E-03 1098 136 3.985000E+00 1.395000E-01 1.695000E-03 1098 137 4.014000E+00 1.369000E-01 1.699000E-03 1098 138 4.044000E+00 1.344000E-01 1.704000E-03 1098 139 4.073000E+00 1.321000E-01 1.711000E-03 1098 140 4.103000E+00 1.298000E-01 1.719000E-03 1098 141 4.132000E+00 1.277000E-01 1.729000E-03 1098 142 4.162000E+00 1.256000E-01 1.739000E-03 1098 143 4.191000E+00 1.237000E-01 1.750000E-03 1098 144 4.221000E+00 1.218000E-01 1.762000E-03 1098 145 4.250000E+00 1.200000E-01 1.775000E-03 1098 146 4.280000E+00 1.183000E-01 1.787000E-03 1098 147 4.309000E+00 1.167000E-01 1.800000E-03 1098 148 4.339000E+00 1.151000E-01 1.812000E-03 1098 149 4.368000E+00 1.135000E-01 1.824000E-03 1098 150 4.398000E+00 1.120000E-01 1.836000E-03 1098 151 4.427000E+00 1.106000E-01 1.847000E-03 1098 152 4.457000E+00 1.091000E-01 1.858000E-03 1098 153 4.486000E+00 1.077000E-01 1.868000E-03 1098 154 4.516000E+00 1.063000E-01 1.878000E-03 1098 155 4.545000E+00 1.049000E-01 1.886000E-03 1098 156 4.575000E+00 1.036000E-01 1.895000E-03 1098 157 4.604000E+00 1.022000E-01 1.902000E-03 1098 158 4.634000E+00 1.008000E-01 1.909000E-03 1098 159 4.663000E+00 9.943000E-02 1.915000E-03 1098 160 4.693000E+00 9.802000E-02 1.920000E-03 1098 161 4.722000E+00 9.660000E-02 1.925000E-03 1098 162 4.752000E+00 9.516000E-02 1.928000E-03 1098 163 4.781000E+00 9.369000E-02 1.931000E-03 1098 164 4.811000E+00 9.220000E-02 1.933000E-03 1098 165 4.841000E+00 9.067000E-02 1.934000E-03 1098 166 4.870000E+00 8.911000E-02 1.933000E-03 1098 167 4.900000E+00 8.752000E-02 1.932000E-03 1098 168 4.929000E+00 8.590000E-02 1.929000E-03 1098 169 4.959000E+00 8.423000E-02 1.925000E-03 1098 170 4.988000E+00 8.254000E-02 1.920000E-03 1098 171 5.018000E+00 8.081000E-02 1.914000E-03 1098 172 5.047000E+00 7.904000E-02 1.906000E-03 1098 173 5.077000E+00 7.724000E-02 1.898000E-03 1098 174 5.106000E+00 7.540000E-02 1.888000E-03 1098 175 5.136000E+00 7.354000E-02 1.878000E-03 1098 176 5.165000E+00 7.164000E-02 1.867000E-03 1098 177 5.195000E+00 6.972000E-02 1.855000E-03 1098 178 5.224000E+00 6.778000E-02 1.844000E-03 1098 179 5.254000E+00 6.581000E-02 1.832000E-03 1098 180 5.283000E+00 6.383000E-02 1.821000E-03 1098 181 5.313000E+00 6.183000E-02 1.811000E-03 1098 182 5.342000E+00 5.982000E-02 1.802000E-03 1098 183 5.372000E+00 5.780000E-02 1.794000E-03 1098 184 5.401000E+00 5.578000E-02 1.788000E-03 1098 185 5.431000E+00 5.376000E-02 1.784000E-03 1098 186 5.460000E+00 5.174000E-02 1.783000E-03 1098 187 5.490000E+00 4.972000E-02 1.784000E-03 1098 188 5.519000E+00 4.772000E-02 1.787000E-03 1098 189 5.549000E+00 4.574000E-02 1.794000E-03 1098 190 5.578000E+00 4.377000E-02 1.803000E-03 1098 191 5.608000E+00 4.182000E-02 1.815000E-03 1098 192 5.637000E+00 3.990000E-02 1.830000E-03 1098 193 5.667000E+00 3.801000E-02 1.847000E-03 1098 194 5.696000E+00 3.615000E-02 1.867000E-03 1098 195 5.726000E+00 3.432000E-02 1.888000E-03 1098 196 5.756000E+00 3.254000E-02 1.911000E-03 1098 197 5.785000E+00 3.079000E-02 1.935000E-03 1098 198 5.815000E+00 2.909000E-02 1.960000E-03 1098 199 5.844000E+00 2.743000E-02 1.986000E-03 1098 200 5.874000E+00 2.581000E-02 2.011000E-03 1098 201 5.903000E+00 2.425000E-02 2.035000E-03 1098 202 5.933000E+00 2.274000E-02 2.058000E-03 1098 203 5.962000E+00 2.127000E-02 2.079000E-03 1098 204 5.992000E+00 1.986000E-02 2.097000E-03 1098 205 6.021000E+00 1.850000E-02 2.113000E-03 1098 206 6.051000E+00 1.720000E-02 2.125000E-03 1098 207 6.080000E+00 1.594000E-02 2.133000E-03 1098 208 6.110000E+00 1.474000E-02 2.136000E-03 1098 209 6.139000E+00 1.359000E-02 2.133000E-03 1098 210 6.169000E+00 1.250000E-02 2.124000E-03 1098 211 6.198000E+00 1.145000E-02 2.108000E-03 1098 212 6.228000E+00 1.045000E-02 2.085000E-03 1098 213 6.257000E+00 9.507000E-03 2.052000E-03 1098 214 6.287000E+00 8.607000E-03 2.011000E-03 1098 215 6.316000E+00 7.753000E-03 1.959000E-03 1098 216 6.346000E+00 6.944000E-03 1.897000E-03 1098 217 6.375000E+00 6.177000E-03 1.823000E-03 1098 218 6.405000E+00 5.450000E-03 1.736000E-03 1098 219 6.434000E+00 4.763000E-03 1.637000E-03 1098 220 6.464000E+00 4.112000E-03 1.522000E-03 1098 221 6.493000E+00 3.496000E-03 1.393000E-03 1098 222 6.523000E+00 2.914000E-03 1.248000E-03 1098 223 6.552000E+00 2.362000E-03 1.087000E-03 1098 224 6.582000E+00 1.839000E-03 9.073000E-04 1098 225 6.611000E+00 1.344000E-03 7.098000E-04 1098 226 6.641000E+00 8.730000E-04 4.933000E-04 1098 227 6.670000E+00 4.257000E-04 2.569000E-04 1098 228 6.700000E+00 0.000000E+00 0.000000E+00 # loop_ _sas_p_of_R_extrapolated_intensity.id _sas_p_of_R_extrapolated_intensity.ordinal _sas_p_of_R_extrapolated_intensity.momentum_transfer _sas_p_of_R_extrapolated_intensity.intensity_reg 1098 1 0.000000E+00 1.393990E+01 1098 2 5.185940E-03 1.393940E+01 1098 3 1.037190E-02 1.393780E+01 1098 4 1.555780E-02 1.393520E+01 1098 5 2.074380E-02 1.393150E+01 1098 6 2.592970E-02 1.392680E+01 1098 7 3.111570E-02 1.392100E+01 1098 8 3.630160E-02 1.391420E+01 1098 9 4.148750E-02 1.390630E+01 1098 10 4.667350E-02 1.389740E+01 1098 11 5.185940E-02 1.388750E+01 1098 12 5.704540E-02 1.387650E+01 1098 13 6.223130E-02 1.386450E+01 1098 14 6.741730E-02 1.385140E+01 1098 15 7.260320E-02 1.383730E+01 1098 16 7.778910E-02 1.382220E+01 1098 17 8.297510E-02 1.380610E+01 1098 18 8.816100E-02 1.378890E+01 1098 19 9.334700E-02 1.377080E+01 1098 20 9.853290E-02 1.375160E+01 1098 21 1.037190E-01 1.373140E+01 1098 22 1.089050E-01 1.371020E+01 1098 23 1.140910E-01 1.368800E+01 1098 24 1.192770E-01 1.366490E+01 1098 25 1.244630E-01 1.364070E+01 1098 26 1.296490E-01 1.361560E+01 1098 27 1.348350E-01 1.358950E+01 1098 28 1.400200E-01 1.356240E+01 1098 29 1.452060E-01 1.353440E+01 1098 30 1.499000E-01 1.350820E+01 1098 31 1.545930E-01 1.348120E+01 1098 32 1.592870E-01 1.345350E+01 1098 33 1.639810E-01 1.342500E+01 1098 34 1.686740E-01 1.339570E+01 1098 35 1.733680E-01 1.336570E+01 1098 36 1.780610E-01 1.333490E+01 1098 37 1.827540E-01 1.330340E+01 1098 38 1.874480E-01 1.327120E+01 1098 39 1.921410E-01 1.323820E+01 1098 40 1.968350E-01 1.320450E+01 1098 41 2.015280E-01 1.317010E+01 1098 42 2.062220E-01 1.313500E+01 1098 43 2.109160E-01 1.309910E+01 1098 44 2.156090E-01 1.306260E+01 1098 45 2.203030E-01 1.302540E+01 1098 46 2.249960E-01 1.298750E+01 1098 47 2.296900E-01 1.294900E+01 1098 48 2.343830E-01 1.290970E+01 1098 49 2.390770E-01 1.286980E+01 1098 50 2.437700E-01 1.282930E+01 1098 51 2.484640E-01 1.278810E+01 1098 52 2.531570E-01 1.274630E+01 1098 53 2.578510E-01 1.270380E+01 1098 54 2.625440E-01 1.266070E+01 1098 55 2.672380E-01 1.261700E+01 1098 56 2.719310E-01 1.257270E+01 1098 57 2.766250E-01 1.252780E+01 1098 58 2.813180E-01 1.248230E+01 1098 59 2.860120E-01 1.243630E+01 1098 60 2.907050E-01 1.238960E+01 1098 61 2.953990E-01 1.234240E+01 1098 62 3.000920E-01 1.229470E+01 1098 63 3.047860E-01 1.224640E+01 1098 64 3.094790E-01 1.219750E+01 1098 65 3.141730E-01 1.214820E+01 1098 66 3.188660E-01 1.209830E+01 1098 67 3.235600E-01 1.204790E+01 1098 68 3.282530E-01 1.199700E+01 1098 69 3.329470E-01 1.194560E+01 1098 70 3.376400E-01 1.189370E+01 1098 71 3.423340E-01 1.184140E+01 1098 72 3.470270E-01 1.178860E+01 1098 73 3.517210E-01 1.173530E+01 1098 74 3.564140E-01 1.168160E+01 1098 75 3.611080E-01 1.162740E+01 1098 76 3.658010E-01 1.157290E+01 1098 77 3.704950E-01 1.151790E+01 1098 78 3.751880E-01 1.146250E+01 1098 79 3.798820E-01 1.140670E+01 1098 80 3.845750E-01 1.135050E+01 1098 81 3.892690E-01 1.129390E+01 1098 82 3.939620E-01 1.123690E+01 1098 83 3.986560E-01 1.117960E+01 1098 84 4.033490E-01 1.112200E+01 1098 85 4.080430E-01 1.106400E+01 1098 86 4.127360E-01 1.100570E+01 1098 87 4.174300E-01 1.094700E+01 1098 88 4.221230E-01 1.088810E+01 1098 89 4.268170E-01 1.082880E+01 1098 90 4.315100E-01 1.076930E+01 1098 91 4.362040E-01 1.070940E+01 1098 92 4.408970E-01 1.064930E+01 1098 93 4.455910E-01 1.058900E+01 1098 94 4.502840E-01 1.052830E+01 1098 95 4.549780E-01 1.046750E+01 1098 96 4.596710E-01 1.040640E+01 1098 97 4.643650E-01 1.034500E+01 1098 98 4.690580E-01 1.028350E+01 1098 99 4.737520E-01 1.022170E+01 1098 100 4.784460E-01 1.015980E+01 1098 101 4.831390E-01 1.009770E+01 1098 102 4.878330E-01 1.003540E+01 1098 103 4.925260E-01 9.972890E+00 1098 104 4.972190E-01 9.910260E+00 1098 105 5.019130E-01 9.847480E+00 1098 106 5.066060E-01 9.784560E+00 1098 107 5.113000E-01 9.721510E+00 1098 108 5.159930E-01 9.658340E+00 1098 109 5.206870E-01 9.595060E+00 1098 110 5.253810E-01 9.531670E+00 1098 111 5.300740E-01 9.468190E+00 1098 112 5.347680E-01 9.404630E+00 1098 113 5.394610E-01 9.341000E+00 1098 114 5.441550E-01 9.277290E+00 1098 115 5.488480E-01 9.213530E+00 1098 116 5.535420E-01 9.149720E+00 1098 117 5.582350E-01 9.085880E+00 1098 118 5.629290E-01 9.022000E+00 1098 119 5.676220E-01 8.958100E+00 1098 120 5.723160E-01 8.894180E+00 1098 121 5.770090E-01 8.830260E+00 1098 122 5.817030E-01 8.766350E+00 1098 123 5.863960E-01 8.702440E+00 1098 124 5.910900E-01 8.638550E+00 1098 125 5.957830E-01 8.574700E+00 1098 126 6.004770E-01 8.510880E+00 1098 127 6.051700E-01 8.447100E+00 1098 128 6.098640E-01 8.383370E+00 1098 129 6.145570E-01 8.319710E+00 1098 130 6.192510E-01 8.256110E+00 1098 131 6.239440E-01 8.192590E+00 1098 132 6.286380E-01 8.129150E+00 1098 133 6.333310E-01 8.065800E+00 1098 134 6.380250E-01 8.002550E+00 1098 135 6.427180E-01 7.939410E+00 1098 136 6.474120E-01 7.876370E+00 1098 137 6.521050E-01 7.813460E+00 1098 138 6.567990E-01 7.750680E+00 1098 139 6.614920E-01 7.688020E+00 1098 140 6.661860E-01 7.625510E+00 1098 141 6.708790E-01 7.563150E+00 1098 142 6.755730E-01 7.500930E+00 1098 143 6.802660E-01 7.438880E+00 1098 144 6.849600E-01 7.377000E+00 1098 145 6.896530E-01 7.315280E+00 1098 146 6.943470E-01 7.253750E+00 1098 147 6.990400E-01 7.192400E+00 1098 148 7.037340E-01 7.131250E+00 1098 149 7.084270E-01 7.070290E+00 1098 150 7.131210E-01 7.009530E+00 1098 151 7.178140E-01 6.948980E+00 1098 152 7.225080E-01 6.888650E+00 1098 153 7.272010E-01 6.828540E+00 1098 154 7.318950E-01 6.768650E+00 1098 155 7.365880E-01 6.708990E+00 1098 156 7.412820E-01 6.649560E+00 1098 157 7.459750E-01 6.590380E+00 1098 158 7.506690E-01 6.531440E+00 1098 159 7.553620E-01 6.472760E+00 1098 160 7.600560E-01 6.414320E+00 1098 161 7.647490E-01 6.356150E+00 1098 162 7.694430E-01 6.298240E+00 1098 163 7.741360E-01 6.240590E+00 1098 164 7.788300E-01 6.183220E+00 1098 165 7.835230E-01 6.126130E+00 1098 166 7.882170E-01 6.069320E+00 1098 167 7.929100E-01 6.012790E+00 1098 168 7.976040E-01 5.956550E+00 1098 169 8.022970E-01 5.900600E+00 1098 170 8.069910E-01 5.844940E+00 1098 171 8.116850E-01 5.789590E+00 1098 172 8.163780E-01 5.734530E+00 1098 173 8.210710E-01 5.679780E+00 1098 174 8.257650E-01 5.625340E+00 1098 175 8.304580E-01 5.571210E+00 1098 176 8.351520E-01 5.517400E+00 1098 177 8.398460E-01 5.463900E+00 1098 178 8.445390E-01 5.410720E+00 1098 179 8.492320E-01 5.357870E+00 1098 180 8.539260E-01 5.305330E+00 1098 181 8.586200E-01 5.253130E+00 1098 182 8.633130E-01 5.201250E+00 1098 183 8.680070E-01 5.149710E+00 1098 184 8.727000E-01 5.098500E+00 1098 185 8.773940E-01 5.047620E+00 1098 186 8.820870E-01 4.997090E+00 1098 187 8.867810E-01 4.946890E+00 1098 188 8.914740E-01 4.897030E+00 1098 189 8.961680E-01 4.847510E+00 1098 190 9.008610E-01 4.798340E+00 1098 191 9.055550E-01 4.749510E+00 1098 192 9.102480E-01 4.701020E+00 1098 193 9.149420E-01 4.652890E+00 1098 194 9.196350E-01 4.605100E+00 1098 195 9.243290E-01 4.557660E+00 1098 196 9.290220E-01 4.510570E+00 1098 197 9.337160E-01 4.463830E+00 1098 198 9.384090E-01 4.417450E+00 1098 199 9.431030E-01 4.371410E+00 1098 200 9.477960E-01 4.325730E+00 1098 201 9.524900E-01 4.280400E+00 1098 202 9.571830E-01 4.235420E+00 1098 203 9.618770E-01 4.190800E+00 1098 204 9.665700E-01 4.146520E+00 1098 205 9.712640E-01 4.102610E+00 1098 206 9.759570E-01 4.059040E+00 1098 207 9.806510E-01 4.015830E+00 1098 208 9.853440E-01 3.972970E+00 1098 209 9.900380E-01 3.930470E+00 1098 210 9.947310E-01 3.888310E+00 1098 211 9.994250E-01 3.846510E+00 1098 212 1.004120E+00 3.805060E+00 1098 213 1.008810E+00 3.763960E+00 1098 214 1.013510E+00 3.723220E+00 1098 215 1.018200E+00 3.682810E+00 1098 216 1.022890E+00 3.642760E+00 1098 217 1.027590E+00 3.603060E+00 1098 218 1.032280E+00 3.563710E+00 1098 219 1.036970E+00 3.524690E+00 1098 220 1.041670E+00 3.486030E+00 1098 221 1.046360E+00 3.447700E+00 1098 222 1.051050E+00 3.409730E+00 1098 223 1.055750E+00 3.372090E+00 1098 224 1.060440E+00 3.334790E+00 1098 225 1.065130E+00 3.297830E+00 1098 226 1.069830E+00 3.261210E+00 1098 227 1.074520E+00 3.224920E+00 1098 228 1.079220E+00 3.188970E+00 1098 229 1.083910E+00 3.153350E+00 1098 230 1.088600E+00 3.118060E+00 1098 231 1.093290E+00 3.083110E+00 1098 232 1.097990E+00 3.048480E+00 1098 233 1.102680E+00 3.014180E+00 1098 234 1.107380E+00 2.980200E+00 1098 235 1.112070E+00 2.946540E+00 1098 236 1.116760E+00 2.913210E+00 1098 237 1.121460E+00 2.880190E+00 1098 238 1.126150E+00 2.847500E+00 1098 239 1.130840E+00 2.815110E+00 1098 240 1.135540E+00 2.783040E+00 1098 241 1.140230E+00 2.751280E+00 1098 242 1.144920E+00 2.719820E+00 1098 243 1.149620E+00 2.688680E+00 1098 244 1.154310E+00 2.657840E+00 1098 245 1.159000E+00 2.627310E+00 1098 246 1.163700E+00 2.597070E+00 1098 247 1.168390E+00 2.567130E+00 1098 248 1.173080E+00 2.537490E+00 1098 249 1.177780E+00 2.508140E+00 1098 250 1.182470E+00 2.479080E+00 1098 251 1.187170E+00 2.450320E+00 1098 252 1.191860E+00 2.421830E+00 1098 253 1.196550E+00 2.393640E+00 1098 254 1.201250E+00 2.365720E+00 1098 255 1.205940E+00 2.338090E+00 1098 256 1.210630E+00 2.310730E+00 1098 257 1.215330E+00 2.283650E+00 1098 258 1.220020E+00 2.256840E+00 1098 259 1.224710E+00 2.230310E+00 1098 260 1.229410E+00 2.204030E+00 1098 261 1.234100E+00 2.178030E+00 1098 262 1.238790E+00 2.152290E+00 1098 263 1.243490E+00 2.126810E+00 1098 264 1.248180E+00 2.101590E+00 1098 265 1.252870E+00 2.076630E+00 1098 266 1.257570E+00 2.051910E+00 1098 267 1.262260E+00 2.027460E+00 1098 268 1.266960E+00 2.003240E+00 1098 269 1.271650E+00 1.979280E+00 1098 270 1.276340E+00 1.955560E+00 1098 271 1.281030E+00 1.932080E+00 1098 272 1.285730E+00 1.908840E+00 1098 273 1.290420E+00 1.885840E+00 1098 274 1.295120E+00 1.863070E+00 1098 275 1.299810E+00 1.840540E+00 1098 276 1.304500E+00 1.818230E+00 1098 277 1.309200E+00 1.796150E+00 1098 278 1.313890E+00 1.774300E+00 1098 279 1.318580E+00 1.752670E+00 1098 280 1.323280E+00 1.731260E+00 1098 281 1.327970E+00 1.710070E+00 1098 282 1.332660E+00 1.689090E+00 1098 283 1.337360E+00 1.668330E+00 1098 284 1.342050E+00 1.647780E+00 1098 285 1.346740E+00 1.627440E+00 1098 286 1.351440E+00 1.607300E+00 1098 287 1.356130E+00 1.587370E+00 1098 288 1.360820E+00 1.567640E+00 1098 289 1.365520E+00 1.548110E+00 1098 290 1.370210E+00 1.528780E+00 1098 291 1.374910E+00 1.509650E+00 1098 292 1.379600E+00 1.490710E+00 1098 293 1.384290E+00 1.471960E+00 1098 294 1.388990E+00 1.453400E+00 1098 295 1.393680E+00 1.435030E+00 1098 296 1.398370E+00 1.416840E+00 1098 297 1.403070E+00 1.398840E+00 1098 298 1.407760E+00 1.381020E+00 1098 299 1.412450E+00 1.363380E+00 1098 300 1.417150E+00 1.345910E+00 1098 301 1.421840E+00 1.328630E+00 1098 302 1.426530E+00 1.311510E+00 1098 303 1.431230E+00 1.294570E+00 1098 304 1.435920E+00 1.277790E+00 1098 305 1.440610E+00 1.261190E+00 1098 306 1.445310E+00 1.244750E+00 1098 307 1.450000E+00 1.228480E+00 1098 308 1.454700E+00 1.212370E+00 1098 309 1.459390E+00 1.196420E+00 1098 310 1.464080E+00 1.180630E+00 1098 311 1.468780E+00 1.164990E+00 1098 312 1.473470E+00 1.149520E+00 1098 313 1.478160E+00 1.134190E+00 1098 314 1.482860E+00 1.119030E+00 1098 315 1.487550E+00 1.104010E+00 1098 316 1.492240E+00 1.089140E+00 1098 317 1.496940E+00 1.074420E+00 1098 318 1.501630E+00 1.059850E+00 1098 319 1.506320E+00 1.045420E+00 1098 320 1.511020E+00 1.031130E+00 1098 321 1.515710E+00 1.016990E+00 1098 322 1.520400E+00 1.002990E+00 1098 323 1.525100E+00 9.891230E-01 1098 324 1.529790E+00 9.753990E-01 1098 325 1.534490E+00 9.618100E-01 1098 326 1.539180E+00 9.483600E-01 1098 327 1.543870E+00 9.350400E-01 1098 328 1.548560E+00 9.218560E-01 1098 329 1.553260E+00 9.088020E-01 1098 330 1.557950E+00 8.958800E-01 1098 331 1.562650E+00 8.830850E-01 1098 332 1.567340E+00 8.704210E-01 1098 333 1.572030E+00 8.578810E-01 1098 334 1.576730E+00 8.454700E-01 1098 335 1.581420E+00 8.331810E-01 1098 336 1.586110E+00 8.210190E-01 1098 337 1.590810E+00 8.089760E-01 1098 338 1.595500E+00 7.970580E-01 1098 339 1.600190E+00 7.852580E-01 1098 340 1.604890E+00 7.735800E-01 1098 341 1.609580E+00 7.620180E-01 1098 342 1.614270E+00 7.505770E-01 1098 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4.182090E-02 1098 771 3.627790E+00 4.171390E-02 1098 772 3.632480E+00 4.160760E-02 1098 773 3.637180E+00 4.150200E-02 1098 774 3.641870E+00 4.139720E-02 1098 775 3.646560E+00 4.129300E-02 1098 776 3.651260E+00 4.118960E-02 1098 777 3.655950E+00 4.108670E-02 1098 778 3.660640E+00 4.098460E-02 1098 779 3.665340E+00 4.088310E-02 1098 780 3.670030E+00 4.078220E-02 1098 781 3.674720E+00 4.068190E-02 1098 782 3.679420E+00 4.058220E-02 1098 783 3.684110E+00 4.048310E-02 1098 784 3.688800E+00 4.038470E-02 1098 785 3.693500E+00 4.028660E-02 1098 786 3.698190E+00 4.018920E-02 1098 787 3.702890E+00 4.009230E-02 1098 788 3.707580E+00 3.999590E-02 1098 789 3.712270E+00 3.990010E-02 1098 790 3.716970E+00 3.980470E-02 1098 791 3.721660E+00 3.970990E-02 1098 792 3.726350E+00 3.961550E-02 1098 793 3.731050E+00 3.952160E-02 1098 794 3.735740E+00 3.942820E-02 1098 795 3.740430E+00 3.933520E-02 1098 796 3.745130E+00 3.924260E-02 1098 797 3.749820E+00 3.915050E-02 1098 798 3.754510E+00 3.905880E-02 1098 799 3.759210E+00 3.896760E-02 1098 800 3.763900E+00 3.887680E-02 1098 801 3.768590E+00 3.878630E-02 1098 802 3.773290E+00 3.869570E-02 1098 803 3.777980E+00 3.860650E-02 1098 804 3.782670E+00 3.851740E-02 1098 805 3.787370E+00 3.842860E-02 1098 806 3.792060E+00 3.834010E-02 1098 807 3.796760E+00 3.825200E-02 1098 808 3.801450E+00 3.816420E-02 1098 809 3.806140E+00 3.807680E-02 1098 810 3.810840E+00 3.798980E-02 1098 811 3.815530E+00 3.790310E-02 1098 812 3.820220E+00 3.781680E-02 1098 813 3.824920E+00 3.773080E-02 1098 814 3.829610E+00 3.764510E-02 1098 815 3.834300E+00 3.755990E-02 1098 816 3.839000E+00 3.747490E-02 1098 817 3.843690E+00 3.739020E-02 1098 818 3.848380E+00 3.730590E-02 1098 819 3.853080E+00 3.722200E-02 1098 820 3.857770E+00 3.713830E-02 1098 821 3.862460E+00 3.705500E-02 1098 822 3.867160E+00 3.697180E-02 1098 823 3.871850E+00 3.688920E-02 1098 824 3.876550E+00 3.680690E-02 1098 825 3.881240E+00 3.672480E-02 1098 826 3.885930E+00 3.664300E-02 1098 827 3.890630E+00 3.656160E-02 1098 828 3.895320E+00 3.648050E-02 1098 829 3.900010E+00 3.639970E-02 1098 830 3.904710E+00 3.631920E-02 1098 831 3.909400E+00 3.623890E-02 1098 832 3.914090E+00 3.615910E-02 1098 833 3.918790E+00 3.607950E-02 1098 834 3.923480E+00 3.600020E-02 1098 835 3.928170E+00 3.592120E-02 1098 836 3.932870E+00 3.584250E-02 1098 837 3.937560E+00 3.576420E-02 1098 838 3.942250E+00 3.568610E-02 1098 839 3.946950E+00 3.560830E-02 1098 840 3.951640E+00 3.553090E-02 1098 841 3.956340E+00 3.545360E-02 1098 842 3.961030E+00 3.537620E-02 # data_SASDEB4_FIT_1706 # _sas_model_fitting_details.id 1706 _sas_model_fitting_details.unit 1/A _sas_model_fitting_details.chi_square 1.23 _sas_model_fitting_details.p_value 0.000060 _sas_model_fitting_details.result_id 1098 # loop_ _sas_model_fitting.id _sas_model_fitting.ordinal _sas_model_fitting.momentum_transfer _sas_model_fitting.intensity _sas_model_fitting.fit 1706 1 1.358000E-02 1.368000E+01 1.363000E+01 1706 2 1.405000E-02 1.392000E+01 1.360000E+01 1706 3 1.452000E-02 1.346000E+01 1.358000E+01 1706 4 1.499000E-02 1.343000E+01 1.355000E+01 1706 5 1.546000E-02 1.349000E+01 1.352000E+01 1706 6 1.593000E-02 1.344000E+01 1.349000E+01 1706 7 1.640000E-02 1.364000E+01 1.346000E+01 1706 8 1.687000E-02 1.356000E+01 1.343000E+01 1706 9 1.734000E-02 1.343000E+01 1.341000E+01 1706 10 1.781000E-02 1.320000E+01 1.337000E+01 1706 11 1.828000E-02 1.327000E+01 1.334000E+01 1706 12 1.874000E-02 1.313000E+01 1.331000E+01 1706 13 1.921000E-02 1.347000E+01 1.327000E+01 1706 14 1.968000E-02 1.334000E+01 1.324000E+01 1706 15 2.015000E-02 1.304000E+01 1.321000E+01 1706 16 2.062000E-02 1.318000E+01 1.317000E+01 1706 17 2.109000E-02 1.305000E+01 1.313000E+01 1706 18 2.156000E-02 1.317000E+01 1.309000E+01 1706 19 2.203000E-02 1.291000E+01 1.306000E+01 1706 20 2.250000E-02 1.303000E+01 1.302000E+01 1706 21 2.297000E-02 1.295000E+01 1.298000E+01 1706 22 2.344000E-02 1.268000E+01 1.294000E+01 1706 23 2.391000E-02 1.273000E+01 1.290000E+01 1706 24 2.438000E-02 1.283000E+01 1.286000E+01 1706 25 2.485000E-02 1.281000E+01 1.282000E+01 1706 26 2.532000E-02 1.265000E+01 1.277000E+01 1706 27 2.579000E-02 1.263000E+01 1.273000E+01 1706 28 2.625000E-02 1.281000E+01 1.268000E+01 1706 29 2.672000E-02 1.233000E+01 1.264000E+01 1706 30 2.719000E-02 1.267000E+01 1.260000E+01 1706 31 2.766000E-02 1.251000E+01 1.255000E+01 1706 32 2.813000E-02 1.264000E+01 1.250000E+01 1706 33 2.860000E-02 1.240000E+01 1.246000E+01 1706 34 2.907000E-02 1.243000E+01 1.241000E+01 1706 35 2.954000E-02 1.220000E+01 1.236000E+01 1706 36 3.001000E-02 1.222000E+01 1.231000E+01 1706 37 3.048000E-02 1.228000E+01 1.226000E+01 1706 38 3.095000E-02 1.207000E+01 1.221000E+01 1706 39 3.142000E-02 1.200000E+01 1.216000E+01 1706 40 3.189000E-02 1.209000E+01 1.211000E+01 1706 41 3.236000E-02 1.206000E+01 1.206000E+01 1706 42 3.283000E-02 1.209000E+01 1.201000E+01 1706 43 3.329000E-02 1.193000E+01 1.196000E+01 1706 44 3.376000E-02 1.200000E+01 1.191000E+01 1706 45 3.423000E-02 1.170000E+01 1.185000E+01 1706 46 3.470000E-02 1.178000E+01 1.180000E+01 1706 47 3.517000E-02 1.177000E+01 1.175000E+01 1706 48 3.564000E-02 1.176000E+01 1.169000E+01 1706 49 3.611000E-02 1.179000E+01 1.163000E+01 1706 50 3.658000E-02 1.165000E+01 1.158000E+01 1706 51 3.705000E-02 1.139000E+01 1.152000E+01 1706 52 3.752000E-02 1.136000E+01 1.147000E+01 1706 53 3.799000E-02 1.127000E+01 1.141000E+01 1706 54 3.846000E-02 1.140000E+01 1.135000E+01 1706 55 3.893000E-02 1.121000E+01 1.130000E+01 1706 56 3.940000E-02 1.127000E+01 1.124000E+01 1706 57 3.987000E-02 1.119000E+01 1.118000E+01 1706 58 4.033000E-02 1.115000E+01 1.112000E+01 1706 59 4.080000E-02 1.096000E+01 1.106000E+01 1706 60 4.127000E-02 1.108000E+01 1.100000E+01 1706 61 4.174000E-02 1.097000E+01 1.095000E+01 1706 62 4.221000E-02 1.101000E+01 1.089000E+01 1706 63 4.268000E-02 1.095000E+01 1.083000E+01 1706 64 4.315000E-02 1.089000E+01 1.077000E+01 1706 65 4.362000E-02 1.083000E+01 1.071000E+01 1706 66 4.409000E-02 1.058000E+01 1.064000E+01 1706 67 4.456000E-02 1.062000E+01 1.058000E+01 1706 68 4.503000E-02 1.042000E+01 1.052000E+01 1706 69 4.550000E-02 1.048000E+01 1.046000E+01 1706 70 4.597000E-02 1.033000E+01 1.040000E+01 1706 71 4.644000E-02 1.034000E+01 1.034000E+01 1706 72 4.691000E-02 1.058000E+01 1.028000E+01 1706 73 4.738000E-02 1.011000E+01 1.021000E+01 1706 74 4.784000E-02 1.015000E+01 1.015000E+01 1706 75 4.831000E-02 1.011000E+01 1.009000E+01 1706 76 4.878000E-02 1.004000E+01 1.002000E+01 1706 77 4.925000E-02 9.967000E+00 9.962000E+00 1706 78 4.972000E-02 1.000000E+01 9.899000E+00 1706 79 5.019000E-02 1.010000E+01 9.836000E+00 1706 80 5.066000E-02 9.803000E+00 9.772000E+00 1706 81 5.113000E-02 9.663000E+00 9.709000E+00 1706 82 5.160000E-02 9.652000E+00 9.645000E+00 1706 83 5.207000E-02 9.682000E+00 9.582000E+00 1706 84 5.254000E-02 9.467000E+00 9.518000E+00 1706 85 5.301000E-02 9.446000E+00 9.454000E+00 1706 86 5.348000E-02 9.410000E+00 9.390000E+00 1706 87 5.395000E-02 9.491000E+00 9.326000E+00 1706 88 5.442000E-02 9.484000E+00 9.262000E+00 1706 89 5.488000E-02 9.284000E+00 9.198000E+00 1706 90 5.535000E-02 9.112000E+00 9.134000E+00 1706 91 5.582000E-02 9.070000E+00 9.070000E+00 1706 92 5.629000E-02 9.024000E+00 9.006000E+00 1706 93 5.676000E-02 8.976000E+00 8.941000E+00 1706 94 5.723000E-02 8.858000E+00 8.877000E+00 1706 95 5.770000E-02 8.833000E+00 8.813000E+00 1706 96 5.817000E-02 8.775000E+00 8.749000E+00 1706 97 5.864000E-02 8.652000E+00 8.685000E+00 1706 98 5.911000E-02 8.692000E+00 8.621000E+00 1706 99 5.958000E-02 8.463000E+00 8.557000E+00 1706 100 6.005000E-02 8.407000E+00 8.493000E+00 1706 101 6.052000E-02 8.462000E+00 8.429000E+00 1706 102 6.099000E-02 8.288000E+00 8.365000E+00 1706 103 6.146000E-02 8.400000E+00 8.302000E+00 1706 104 6.193000E-02 8.278000E+00 8.238000E+00 1706 105 6.239000E-02 8.265000E+00 8.174000E+00 1706 106 6.286000E-02 8.160000E+00 8.111000E+00 1706 107 6.333000E-02 8.150000E+00 8.048000E+00 1706 108 6.380000E-02 8.143000E+00 7.984000E+00 1706 109 6.427000E-02 7.984000E+00 7.921000E+00 1706 110 6.474000E-02 7.908000E+00 7.858000E+00 1706 111 6.521000E-02 8.000000E+00 7.795000E+00 1706 112 6.568000E-02 7.843000E+00 7.733000E+00 1706 113 6.615000E-02 7.687000E+00 7.670000E+00 1706 114 6.662000E-02 7.664000E+00 7.608000E+00 1706 115 6.709000E-02 7.502000E+00 7.545000E+00 1706 116 6.756000E-02 7.567000E+00 7.483000E+00 1706 117 6.803000E-02 7.512000E+00 7.421000E+00 1706 118 6.850000E-02 7.439000E+00 7.360000E+00 1706 119 6.897000E-02 7.383000E+00 7.298000E+00 1706 120 6.943000E-02 7.418000E+00 7.237000E+00 1706 121 6.990000E-02 7.203000E+00 7.175000E+00 1706 122 7.037000E-02 7.136000E+00 7.115000E+00 1706 123 7.084000E-02 6.892000E+00 7.054000E+00 1706 124 7.131000E-02 7.116000E+00 6.994000E+00 1706 125 7.178000E-02 6.968000E+00 6.933000E+00 1706 126 7.225000E-02 6.809000E+00 6.873000E+00 1706 127 7.272000E-02 6.825000E+00 6.813000E+00 1706 128 7.319000E-02 6.661000E+00 6.754000E+00 1706 129 7.366000E-02 6.566000E+00 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7.463000E-02 1706 999 4.820000E-01 7.127000E-02 7.469000E-02 1706 1000 4.825000E-01 1.476000E-01 7.474000E-02 1706 1001 4.829000E-01 3.180000E-03 7.480000E-02 1706 1002 4.834000E-01 5.303000E-01 7.485000E-02 1706 1003 4.839000E-01 4.807000E-01 7.490000E-02 1706 1004 4.843000E-01 -2.844000E-01 7.495000E-02 1706 1005 4.848000E-01 1.514000E-01 7.500000E-02 1706 1006 4.853000E-01 1.465000E-01 7.504000E-02 1706 1007 4.857000E-01 7.835000E-02 7.509000E-02 1706 1008 4.862000E-01 4.093000E-01 7.513000E-02 1706 1009 4.867000E-01 2.100000E-03 7.518000E-02 1706 1010 4.872000E-01 2.434000E-01 7.522000E-02 1706 1011 4.876000E-01 2.651000E-01 7.527000E-02 1706 1012 4.881000E-01 3.160000E-01 7.531000E-02 1706 1013 4.886000E-01 7.458000E-02 7.534000E-02 1706 1014 4.890000E-01 -1.178000E-01 7.538000E-02 1706 1015 4.895000E-01 7.808000E-02 7.542000E-02 1706 1016 4.900000E-01 4.810000E-01 7.546000E-02 1706 1017 4.904000E-01 -2.753000E-01 7.550000E-02 1706 1018 4.909000E-01 3.487000E-01 7.553000E-02 1706 1019 4.914000E-01 -1.218000E-01 7.556000E-02 1706 1020 4.919000E-01 2.575000E-01 7.560000E-02 1706 1021 4.923000E-01 3.827000E-01 7.563000E-02 # data_SASDEB4_MODEL_2350 # _sas_model.id 2350 _sas_model.type_of_model atomic _sas_model.version . _sas_model.symmetry . _sas_model.comment . _sas_model.fitting_id 1706 _sas_model.radius . # loop_ _atom_site.group_PDB _atom_site.id _atom_site.type_symbol _atom_site.label_atom_id _atom_site.label_alt_id _atom_site.label_comp_id _atom_site.label_asym_id _atom_site.label_entity_id _atom_site.label_seq_id _atom_site.pdbx_PDB_ins_code _atom_site.Cartn_x _atom_site.Cartn_y _atom_site.Cartn_z _atom_site.occupancy _atom_site.B_iso_or_equiv _atom_site.Cartn_x_esd _atom_site.Cartn_y_esd _atom_site.Cartn_z_esd _atom_site.occupancy_esd _atom_site.B_iso_or_equiv_esd _atom_site.pdbx_formal_charge _atom_site.auth_seq_id _atom_site.auth_comp_id _atom_site.auth_asym_id _atom_site.auth_atom_id _atom_site.pdbx_PDB_model_num ATOM 1 N N . MET A 2350 1 . 1.498 -29.784 9.466 1.00 42.34 ? ? ? ? ? . 1 MET A N 2350 ATOM 2 C CA . MET A 2350 1 . 1.362 -28.330 9.713 1.00 38.79 ? ? ? ? ? . 1 MET A CA 2350 ATOM 3 C C . MET A 2350 1 . 2.451 -27.795 10.648 1.00 34.46 ? ? ? ? ? . 1 MET A C 2350 ATOM 4 O O . MET A 2350 1 . 3.019 -28.519 11.476 1.00 28.07 ? ? ? ? ? . 1 MET A O 2350 ATOM 5 C CB . MET A 2350 1 . -0.032 -28.003 10.280 1.00 43.44 ? ? ? ? ? . 1 MET A CB 2350 ATOM 6 C CG . MET A 2350 1 . -1.163 -28.074 9.261 1.00 48.34 ? ? ? ? ? . 1 MET A CG 2350 ATOM 7 S SD . MET A 2350 1 . -1.096 -26.763 8.019 1.00 56.59 ? ? ? ? ? . 1 MET A SD 2350 ATOM 8 C CE . MET A 2350 1 . -1.944 -27.553 6.650 1.00 53.77 ? ? ? ? ? . 1 MET A CE 2350 ATOM 9 N N . SER A 2350 2 . 2.702 -26.498 10.518 1.00 31.58 ? ? ? ? ? . 2 SER A N 2350 ATOM 10 C CA . SER A 2350 2 . 3.686 -25.813 11.340 1.00 29.58 ? ? ? ? ? . 2 SER A CA 2350 ATOM 11 C C . SER A 2350 2 . 3.179 -25.647 12.742 1.00 28.87 ? ? ? ? ? . 2 SER A C 2350 ATOM 12 O O . SER A 2350 2 . 1.976 -25.688 12.985 1.00 24.92 ? ? ? ? ? . 2 SER A O 2350 ATOM 13 C CB . SER A 2350 2 . 3.985 -24.427 10.800 1.00 31.81 ? ? ? ? ? . 2 SER A CB 2350 ATOM 14 O OG . SER A 2350 2 . 2.955 -23.494 11.097 1.00 29.45 ? ? ? ? ? . 2 SER A OG 2350 ATOM 15 N N . GLY A 2350 3 . 4.105 -25.396 13.653 1.00 26.92 ? ? ? ? ? . 3 GLY A N 2350 ATOM 16 C CA . GLY A 2350 3 . 3.752 -25.062 15.022 1.00 27.19 ? ? ? ? ? . 3 GLY A CA 2350 ATOM 17 C C . GLY A 2350 3 . 3.057 -23.717 15.142 1.00 26.26 ? ? ? ? ? . 3 GLY A C 2350 ATOM 18 O O . GLY A 2350 3 . 2.392 -23.466 16.134 1.00 31.06 ? ? ? ? ? . 3 GLY A O 2350 ATOM 19 N N . LEU A 2350 4 . 3.204 -22.842 14.148 1.00 27.31 ? ? ? ? ? . 4 LEU A N 2350 ATOM 20 C CA . LEU A 2350 4 . 2.393 -21.618 14.096 1.00 28.14 ? ? ? ? ? . 4 LEU A CA 2350 ATOM 21 C C . LEU A 2350 4 . 0.907 -21.935 13.926 1.00 26.94 ? ? ? ? ? . 4 LEU A C 2350 ATOM 22 O O . LEU A 2350 4 . 0.070 -21.235 14.495 1.00 25.83 ? ? ? ? ? . 4 LEU A O 2350 ATOM 23 C CB . LEU A 2350 4 . 2.859 -20.661 12.988 1.00 31.30 ? ? ? ? ? . 4 LEU A CB 2350 ATOM 24 C CG . LEU A 2350 4 . 4.018 -19.719 13.288 1.00 32.68 ? ? ? ? ? . 4 LEU A CG 2350 ATOM 25 C CD1 . LEU A 2350 4 . 4.270 -18.858 12.063 1.00 34.49 ? ? ? ? ? . 4 LEU A CD1 2350 ATOM 26 C CD2 . LEU A 2350 4 . 3.718 -18.844 14.497 1.00 34.30 ? ? ? ? ? . 4 LEU A CD2 2350 ATOM 27 N N . ALA A 2350 5 . 0.579 -22.994 13.176 1.00 26.99 ? ? ? ? ? . 5 ALA A N 2350 ATOM 28 C CA . ALA A 2350 5 . -0.817 -23.451 13.048 1.00 29.14 ? ? ? ? ? . 5 ALA A CA 2350 ATOM 29 C C . ALA A 2350 5 . -1.502 -23.807 14.377 1.00 31.57 ? ? ? ? ? . 5 ALA A C 2350 ATOM 30 O O . ALA A 2350 5 . -2.722 -23.642 14.499 1.00 38.23 ? ? ? ? ? . 5 ALA A O 2350 ATOM 31 C CB . ALA A 2350 5 . -0.923 -24.626 12.077 1.00 32.07 ? ? ? ? ? . 5 ALA A CB 2350 ATOM 32 N N . LYS A 2350 6 . -0.746 -24.274 15.372 1.00 28.88 ? ? ? ? ? . 6 LYS A N 2350 ATOM 33 C CA . LYS A 2350 6 . -1.337 -24.554 16.690 1.00 28.76 ? ? ? ? ? . 6 LYS A CA 2350 ATOM 34 C C . LYS A 2350 6 . -1.895 -23.293 17.343 1.00 24.63 ? ? ? ? ? . 6 LYS A C 2350 ATOM 35 O O . LYS A 2350 6 . -2.853 -23.372 18.095 1.00 25.15 ? ? ? ? ? . 6 LYS A O 2350 ATOM 36 C CB . LYS A 2350 6 . -0.356 -25.256 17.646 1.00 32.13 ? ? ? ? ? . 6 LYS A CB 2350 ATOM 37 C CG . LYS A 2350 6 . 0.511 -24.341 18.526 1.00 31.95 ? ? ? ? ? . 6 LYS A CG 2350 ATOM 38 C CD . LYS A 2350 6 . 1.607 -25.092 19.277 1.00 33.12 ? ? ? ? ? . 6 LYS A CD 2350 ATOM 39 C CE . LYS A 2350 6 . 2.655 -25.712 18.350 1.00 32.32 ? ? ? ? ? . 6 LYS A CE 2350 ATOM 40 N NZ . LYS A 2350 6 . 3.554 -26.649 19.060 1.00 28.93 ? ? ? ? ? 1+ 6 LYS A NZ 2350 ATOM 41 N N . TYR A 2350 7 . -1.273 -22.149 17.060 1.00 23.51 ? ? ? ? ? . 7 TYR A N 2350 ATOM 42 C CA . TYR A 2350 7 . -1.713 -20.858 17.597 1.00 24.18 ? ? ? ? ? . 7 TYR A CA 2350 ATOM 43 C C . TYR A 2350 7 . -2.735 -20.147 16.721 1.00 25.86 ? ? ? ? ? . 7 TYR A C 2350 ATOM 44 O O . TYR A 2350 7 . -3.549 -19.381 17.235 1.00 25.45 ? ? ? ? ? . 7 TYR A O 2350 ATOM 45 C CB . TYR A 2350 7 . -0.526 -19.931 17.799 1.00 22.86 ? ? ? ? ? . 7 TYR A CB 2350 ATOM 46 C CG . TYR A 2350 7 . 0.519 -20.473 18.741 1.00 20.79 ? ? ? ? ? . 7 TYR A CG 2350 ATOM 47 C CD1 . TYR A 2350 7 . 0.199 -20.788 20.060 1.00 19.65 ? ? ? ? ? . 7 TYR A CD1 2350 ATOM 48 C CD2 . TYR A 2350 7 . 1.841 -20.635 18.325 1.00 19.30 ? ? ? ? ? . 7 TYR A CD2 2350 ATOM 49 C CE1 . TYR A 2350 7 . 1.162 -21.270 20.934 1.00 19.28 ? ? ? ? ? . 7 TYR A CE1 2350 ATOM 50 C CE2 . TYR A 2350 7 . 2.805 -21.114 19.186 1.00 19.91 ? ? ? ? ? . 7 TYR A CE2 2350 ATOM 51 C CZ . TYR A 2350 7 . 2.462 -21.430 20.493 1.00 19.68 ? ? ? ? ? . 7 TYR A CZ 2350 ATOM 52 O OH . TYR A 2350 7 . 3.427 -21.901 21.354 1.00 19.23 ? ? ? ? ? . 7 TYR A OH 2350 ATOM 53 N N . LEU A 2350 8 . -2.711 -20.410 15.413 1.00 25.61 ? ? ? ? ? . 8 LEU A N 2350 ATOM 54 C CA . LEU A 2350 8 . -3.604 -19.742 14.468 1.00 27.57 ? ? ? ? ? . 8 LEU A CA 2350 ATOM 55 C C . LEU A 2350 8 . -4.522 -20.703 13.671 1.00 30.41 ? ? ? ? ? . 8 LEU A C 2350 ATOM 56 O O . LEU A 2350 8 . -4.503 -20.676 12.444 1.00 31.20 ? ? ? ? ? . 8 LEU A O 2350 ATOM 57 C CB . LEU A 2350 8 . -2.750 -18.882 13.517 1.00 26.23 ? ? ? ? ? . 8 LEU A CB 2350 ATOM 58 C CG . LEU A 2350 8 . -1.810 -17.852 14.164 1.00 24.95 ? ? ? ? ? . 8 LEU A CG 2350 ATOM 59 C CD1 . LEU A 2350 8 . -0.828 -17.290 13.142 1.00 26.14 ? ? ? ? ? . 8 LEU A CD1 2350 ATOM 60 C CD2 . LEU A 2350 8 . -2.602 -16.730 14.822 1.00 25.27 ? ? ? ? ? . 8 LEU A CD2 2350 ATOM 61 N N A PRO A 2350 9 . -5.300 -21.558 14.376 0.49 34.84 ? ? ? ? ? . 9 PRO A N 2350 ATOM 62 N N B PRO A 2350 9 . -5.359 -21.503 14.365 0.51 33.67 ? ? ? ? ? . 9 PRO A N 2350 ATOM 63 C CA A PRO A 2350 9 . -6.293 -22.381 13.700 0.49 37.05 ? ? ? ? ? . 9 PRO A CA 2350 ATOM 64 C CA B PRO A 2350 9 . -6.175 -22.534 13.697 0.51 35.34 ? ? ? ? ? . 9 PRO A CA 2350 ATOM 65 C C A PRO A 2350 9 . -7.506 -21.519 13.432 0.49 38.35 ? ? ? ? ? . 9 PRO A C 2350 ATOM 66 C C B PRO A 2350 9 . -7.186 -22.013 12.660 0.51 36.39 ? ? ? ? ? . 9 PRO A C 2350 ATOM 67 O O A PRO A 2350 9 . -8.118 -21.001 14.366 0.49 39.55 ? ? ? ? ? . 9 PRO A O 2350 ATOM 68 O O B PRO A 2350 9 . -7.420 -22.691 11.657 0.51 37.00 ? ? ? ? ? . 9 PRO A O 2350 ATOM 69 C CB A PRO A 2350 9 . -6.624 -23.442 14.742 0.49 36.54 ? ? ? ? ? . 9 PRO A CB 2350 ATOM 70 C CB B PRO A 2350 9 . -6.909 -23.210 14.865 0.51 34.76 ? ? ? ? ? . 9 PRO A CB 2350 ATOM 71 C CG A PRO A 2350 9 . -6.535 -22.693 16.022 0.49 36.43 ? ? ? ? ? . 9 PRO A CG 2350 ATOM 72 C CG B PRO A 2350 9 . -6.953 -22.172 15.932 0.51 34.10 ? ? ? ? ? . 9 PRO A CG 2350 ATOM 73 C CD A PRO A 2350 9 . -5.375 -21.751 15.840 0.49 36.25 ? ? ? ? ? . 9 PRO A CD 2350 ATOM 74 C CD B PRO A 2350 9 . -5.641 -21.459 15.815 0.51 34.53 ? ? ? ? ? . 9 PRO A CD 2350 ATOM 75 N N A GLY A 2350 10 . -7.850 -21.363 12.165 0.49 38.66 ? ? ? ? ? . 10 GLY A N 2350 ATOM 76 N N B GLY A 2350 10 . -7.776 -20.841 12.911 0.51 35.97 ? ? ? ? ? . 10 GLY A N 2350 ATOM 77 C CA A GLY A 2350 10 . -8.786 -20.329 11.768 0.49 37.94 ? ? ? ? ? . 10 GLY A CA 2350 ATOM 78 C CA B GLY A 2350 10 . -8.733 -20.217 11.981 0.51 36.27 ? ? ? ? ? . 10 GLY A CA 2350 ATOM 79 C C A GLY A 2350 10 . -8.121 -19.416 10.757 0.49 37.83 ? ? ? ? ? . 10 GLY A C 2350 ATOM 80 C C B GLY A 2350 10 . -8.107 -19.480 10.800 0.51 37.15 ? ? ? ? ? . 10 GLY A C 2350 ATOM 81 O O A GLY A 2350 10 . -8.796 -18.870 9.876 0.49 37.03 ? ? ? ? ? . 10 GLY A O 2350 ATOM 82 O O B GLY A 2350 10 . -8.798 -19.134 9.836 0.51 37.06 ? ? ? ? ? . 10 GLY A O 2350 ATOM 83 N N . ALA A 2350 11 . -6.803 -19.231 10.888 1.00 36.15 ? ? ? ? ? . 11 ALA A N 2350 ATOM 84 C CA . ALA A 2350 11 . -6.026 -18.586 9.835 1.00 35.46 ? ? ? ? ? . 11 ALA A CA 2350 ATOM 85 C C . ALA A 2350 11 . -5.687 -19.603 8.758 1.00 36.66 ? ? ? ? ? . 11 ALA A C 2350 ATOM 86 O O . ALA A 2350 11 . -5.713 -20.816 8.988 1.00 35.61 ? ? ? ? ? . 11 ALA A O 2350 ATOM 87 C CB . ALA A 2350 11 . -4.743 -17.992 10.401 1.00 34.28 ? ? ? ? ? . 11 ALA A CB 2350 ATOM 88 N N . THR A 2350 12 . -5.403 -19.089 7.571 1.00 35.16 ? ? ? ? ? . 12 THR A N 2350 ATOM 89 C CA . THR A 2350 12 . -4.620 -19.821 6.582 1.00 34.41 ? ? ? ? ? . 12 THR A CA 2350 ATOM 90 C C . THR A 2350 12 . -3.465 -18.927 6.157 1.00 30.55 ? ? ? ? ? . 12 THR A C 2350 ATOM 91 O O . THR A 2350 12 . -2.309 -19.284 6.369 1.00 33.15 ? ? ? ? ? . 12 THR A O 2350 ATOM 92 C CB . THR A 2350 12 . -5.447 -20.322 5.371 1.00 37.60 ? ? ? ? ? . 12 THR A CB 2350 ATOM 93 C CG2 . THR A 2350 12 . -5.624 -21.844 5.441 1.00 41.25 ? ? ? ? ? . 12 THR A CG2 2350 ATOM 94 O OG1 . THR A 2350 12 . -6.745 -19.707 5.356 1.00 40.05 ? ? ? ? ? . 12 THR A OG1 2350 ATOM 95 N N . ASN A 2350 13 . -3.761 -17.760 5.589 1.00 24.01 ? ? ? ? ? . 13 ASN A N 2350 ATOM 96 C CA . ASN A 2350 13 . -2.702 -16.909 5.058 1.00 21.19 ? ? ? ? ? . 13 ASN A CA 2350 ATOM 97 C C . ASN A 2350 13 . -2.485 -15.671 5.897 1.00 19.45 ? ? ? ? ? . 13 ASN A C 2350 ATOM 98 O O . ASN A 2350 13 . -3.378 -15.222 6.620 1.00 21.50 ? ? ? ? ? . 13 ASN A O 2350 ATOM 99 C CB . ASN A 2350 13 . -2.997 -16.518 3.609 1.00 23.60 ? ? ? ? ? . 13 ASN A CB 2350 ATOM 100 C CG . ASN A 2350 13 . -3.062 -17.718 2.683 1.00 25.11 ? ? ? ? ? . 13 ASN A CG 2350 ATOM 101 N ND2 . ASN A 2350 13 . -4.029 -17.717 1.771 1.00 24.16 ? ? ? ? ? . 13 ASN A ND2 2350 ATOM 102 O OD1 . ASN A 2350 13 . -2.256 -18.644 2.795 1.00 28.41 ? ? ? ? ? . 13 ASN A OD1 2350 ATOM 103 N N . LEU A 2350 14 . -1.277 -15.134 5.781 1.00 16.54 ? ? ? ? ? . 14 LEU A N 2350 ATOM 104 C CA . LEU A 2350 14 . -0.881 -13.881 6.390 1.00 15.38 ? ? ? ? ? . 14 LEU A CA 2350 ATOM 105 C C . LEU A 2350 14 . -0.723 -12.879 5.271 1.00 15.70 ? ? ? ? ? . 14 LEU A C 2350 ATOM 106 O O . LEU A 2350 14 . -0.384 -13.251 4.152 1.00 16.70 ? ? ? ? ? . 14 LEU A O 2350 ATOM 107 C CB . LEU A 2350 14 . 0.455 -14.057 7.118 1.00 15.56 ? ? ? ? ? . 14 LEU A CB 2350 ATOM 108 C CG . LEU A 2350 14 . 0.466 -15.081 8.254 1.00 15.33 ? ? ? ? ? . 14 LEU A CG 2350 ATOM 109 C CD1 . LEU A 2350 14 . 1.865 -15.199 8.824 1.00 16.03 ? ? ? ? ? . 14 LEU A CD1 2350 ATOM 110 C CD2 . LEU A 2350 14 . -0.512 -14.706 9.360 1.00 14.84 ? ? ? ? ? . 14 LEU A CD2 2350 ATOM 111 N N . LEU A 2350 15 . -0.963 -11.610 5.571 1.00 15.63 ? ? ? ? ? . 15 LEU A N 2350 ATOM 112 C CA . LEU A 2350 15 . -0.692 -10.536 4.620 1.00 16.16 ? ? ? ? ? . 15 LEU A CA 2350 ATOM 113 C C . LEU A 2350 15 . 0.817 -10.328 4.485 1.00 16.48 ? ? ? ? ? . 15 LEU A C 2350 ATOM 114 O O . LEU A 2350 15 . 1.537 -10.488 5.458 1.00 15.72 ? ? ? ? ? . 15 LEU A O 2350 ATOM 115 C CB . LEU A 2350 15 . -1.302 -9.224 5.088 1.00 15.78 ? ? ? ? ? . 15 LEU A CB 2350 ATOM 116 C CG . LEU A 2350 15 . -2.774 -9.203 5.473 1.00 16.53 ? ? ? ? ? . 15 LEU A CG 2350 ATOM 117 C CD1 . LEU A 2350 15 . -3.169 -7.778 5.854 1.00 17.40 ? ? ? ? ? . 15 LEU A CD1 2350 ATOM 118 C CD2 . LEU A 2350 15 . -3.657 -9.742 4.356 1.00 15.86 ? ? ? ? ? . 15 LEU A CD2 2350 ATOM 119 N N . SER A 2350 16 . 1.274 -9.967 3.289 1.00 16.81 ? ? ? ? ? . 16 SER A N 2350 ATOM 120 C CA . SER A 2350 16 . 2.659 -9.490 3.089 1.00 18.19 ? ? ? ? ? . 16 SER A CA 2350 ATOM 121 C C . SER A 2350 16 . 2.617 -8.199 2.266 1.00 19.91 ? ? ? ? ? . 16 SER A C 2350 ATOM 122 O O . SER A 2350 16 . 1.553 -7.749 1.839 1.00 18.64 ? ? ? ? ? . 16 SER A O 2350 ATOM 123 C CB . SER A 2350 16 . 3.525 -10.544 2.378 1.00 19.00 ? ? ? ? ? . 16 SER A CB 2350 ATOM 124 O OG . SER A 2350 16 . 3.353 -10.503 0.969 1.00 19.59 ? ? ? ? ? . 16 SER A OG 2350 ATOM 125 N N . LYS A 2350 17 . 3.780 -7.614 2.027 1.00 21.51 ? ? ? ? ? . 17 LYS A N 2350 ATOM 126 C CA . LYS A 2350 17 . 3.855 -6.435 1.165 1.00 24.73 ? ? ? ? ? . 17 LYS A CA 2350 ATOM 127 C C . LYS A 2350 17 . 3.444 -6.732 -0.283 1.00 25.66 ? ? ? ? ? . 17 LYS A C 2350 ATOM 128 O O . LYS A 2350 17 . 3.019 -5.819 -0.983 1.00 27.03 ? ? ? ? ? . 17 LYS A O 2350 ATOM 129 C CB . LYS A 2350 17 . 5.262 -5.832 1.197 1.00 25.50 ? ? ? ? ? . 17 LYS A CB 2350 ATOM 130 C CG . LYS A 2350 17 . 5.682 -5.273 2.551 1.00 25.81 ? ? ? ? ? . 17 LYS A CG 2350 ATOM 131 C CD . LYS A 2350 17 . 4.736 -4.187 3.056 1.00 28.95 ? ? ? ? ? . 17 LYS A CD 2350 ATOM 132 C CE . LYS A 2350 17 . 3.753 -4.693 4.113 1.00 28.57 ? ? ? ? ? . 17 LYS A CE 2350 ATOM 133 N NZ . LYS A 2350 17 . 2.971 -3.562 4.702 1.00 25.15 ? ? ? ? ? 1+ 17 LYS A NZ 2350 ATOM 134 N N . SER A 2350 18 . 3.555 -7.992 -0.712 1.00 25.74 ? ? ? ? ? . 18 SER A N 2350 ATOM 135 C CA . SER A 2350 18 . 3.177 -8.416 -2.070 1.00 30.18 ? ? ? ? ? . 18 SER A CA 2350 ATOM 136 C C . SER A 2350 18 . 2.143 -9.546 -2.074 1.00 32.37 ? ? ? ? ? . 18 SER A C 2350 ATOM 137 O O . SER A 2350 18 . 2.384 -10.619 -2.635 1.00 35.88 ? ? ? ? ? . 18 SER A O 2350 ATOM 138 C CB . SER A 2350 18 . 4.431 -8.893 -2.797 1.00 31.94 ? ? ? ? ? . 18 SER A CB 2350 ATOM 139 O OG . SER A 2350 18 . 4.959 -10.040 -2.149 1.00 33.68 ? ? ? ? ? . 18 SER A OG 2350 ATOM 140 N N . GLY A 2350 19 . 0.995 -9.323 -1.452 1.00 31.20 ? ? ? ? ? . 19 GLY A N 2350 ATOM 141 C CA . GLY A 2350 19 . -0.034 -10.370 -1.395 1.00 32.15 ? ? ? ? ? . 19 GLY A CA 2350 ATOM 142 C C . GLY A 2350 19 . 0.276 -11.471 -0.382 1.00 31.51 ? ? ? ? ? . 19 GLY A C 2350 ATOM 143 O O . GLY A 2350 19 . 1.310 -11.458 0.288 1.00 33.38 ? ? ? ? ? . 19 GLY A O 2350 ATOM 144 N N . GLU A 2350 20 . -0.629 -12.434 -0.282 1.00 26.41 ? ? ? ? ? . 20 GLU A N 2350 ATOM 145 C CA . GLU A 2350 20 . -0.691 -13.290 0.884 1.00 24.83 ? ? ? ? ? . 20 GLU A CA 2350 ATOM 146 C C . GLU A 2350 20 . 0.330 -14.411 0.824 1.00 21.95 ? ? ? ? ? . 20 GLU A C 2350 ATOM 147 O O . GLU A 2350 20 . 0.679 -14.879 -0.254 1.00 20.93 ? ? ? ? ? . 20 GLU A O 2350 ATOM 148 C CB . GLU A 2350 20 . -2.102 -13.854 1.040 1.00 28.97 ? ? ? ? ? . 20 GLU A CB 2350 ATOM 149 C CG . GLU A 2350 20 . -3.156 -12.772 1.249 1.00 29.83 ? ? ? ? ? . 20 GLU A CG 2350 ATOM 150 C CD . GLU A 2350 20 . -4.539 -13.321 1.561 1.00 31.70 ? ? ? ? ? . 20 GLU A CD 2350 ATOM 151 O OE1 . GLU A 2350 20 . -4.814 -14.491 1.202 1.00 33.49 ? ? ? ? ? . 20 GLU A OE1 2350 ATOM 152 O OE2 . GLU A 2350 20 . -5.349 -12.565 2.154 1.00 34.19 ? ? ? ? ? 1- 20 GLU A OE2 2350 ATOM 153 N N . VAL A 2350 21 . 0.799 -14.822 1.996 1.00 18.14 ? ? ? ? ? . 21 VAL A N 2350 ATOM 154 C CA . VAL A 2350 21 . 1.739 -15.940 2.130 1.00 18.05 ? ? ? ? ? . 21 VAL A CA 2350 ATOM 155 C C . VAL A 2350 21 . 1.210 -16.964 3.137 1.00 16.57 ? ? ? ? ? . 21 VAL A C 2350 ATOM 156 O O . VAL A 2350 21 . 0.519 -16.610 4.089 1.00 15.65 ? ? ? ? ? . 21 VAL A O 2350 ATOM 157 C CB . VAL A 2350 21 . 3.150 -15.466 2.542 1.00 18.57 ? ? ? ? ? . 21 VAL A CB 2350 ATOM 158 C CG1 . VAL A 2350 21 . 3.672 -14.437 1.540 1.00 19.84 ? ? ? ? ? . 21 VAL A CG1 2350 ATOM 159 C CG2 . VAL A 2350 21 . 3.176 -14.922 3.970 1.00 17.16 ? ? ? ? ? . 21 VAL A CG2 2350 ATOM 160 N N . SER A 2350 22 . 1.533 -18.230 2.906 1.00 15.34 ? ? ? ? ? . 22 SER A N 2350 ATOM 161 C CA . SER A 2350 22 . 1.073 -19.315 3.767 1.00 16.37 ? ? ? ? ? . 22 SER A CA 2350 ATOM 162 C C . SER A 2350 22 . 1.872 -19.345 5.061 1.00 16.62 ? ? ? ? ? . 22 SER A C 2350 ATOM 163 O O . SER A 2350 22 . 3.000 -18.826 5.142 1.00 15.98 ? ? ? ? ? . 22 SER A O 2350 ATOM 164 C CB . SER A 2350 22 . 1.237 -20.655 3.056 1.00 17.61 ? ? ? ? ? . 22 SER A CB 2350 ATOM 165 O OG . SER A 2350 22 . 2.618 -20.887 2.815 1.00 17.06 ? ? ? ? ? . 22 SER A OG 2350 ATOM 166 N N . LEU A 2350 23 . 1.305 -19.988 6.072 1.00 17.27 ? ? ? ? ? . 23 LEU A N 2350 ATOM 167 C CA . LEU A 2350 23 . 2.058 -20.286 7.290 1.00 17.54 ? ? ? ? ? . 23 LEU A CA 2350 ATOM 168 C C . LEU A 2350 23 . 3.271 -21.187 6.998 1.00 15.71 ? ? ? ? ? . 23 LEU A C 2350 ATOM 169 O O . LEU A 2350 23 . 4.357 -20.961 7.555 1.00 15.68 ? ? ? ? ? . 23 LEU A O 2350 ATOM 170 C CB . LEU A 2350 23 . 1.158 -20.925 8.354 1.00 19.09 ? ? ? ? ? . 23 LEU A CB 2350 ATOM 171 C CG . LEU A 2350 23 . 0.047 -20.044 8.926 1.00 19.85 ? ? ? ? ? . 23 LEU A CG 2350 ATOM 172 C CD1 . LEU A 2350 23 . -0.781 -20.855 9.912 1.00 20.80 ? ? ? ? ? . 23 LEU A CD1 2350 ATOM 173 C CD2 . LEU A 2350 23 . 0.588 -18.800 9.598 1.00 20.11 ? ? ? ? ? . 23 LEU A CD2 2350 ATOM 174 N N . GLY A 2350 24 . 3.092 -22.170 6.110 1.00 14.87 ? ? ? ? ? . 24 GLY A N 2350 ATOM 175 C CA . GLY A 2350 24 . 4.183 -23.039 5.652 1.00 14.51 ? ? ? ? ? . 24 GLY A CA 2350 ATOM 176 C C . GLY A 2350 24 . 5.381 -22.325 5.024 1.00 14.47 ? ? ? ? ? . 24 GLY A C 2350 ATOM 177 O O . GLY A 2350 24 . 6.505 -22.845 5.067 1.00 12.91 ? ? ? ? ? . 24 GLY A O 2350 ATOM 178 N N . SER A 2350 25 . 5.160 -21.133 4.454 1.00 14.24 ? ? ? ? ? . 25 SER A N 2350 ATOM 179 C CA . SER A 2350 25 . 6.248 -20.339 3.852 1.00 14.58 ? ? ? ? ? . 25 SER A CA 2350 ATOM 180 C C . SER A 2350 25 . 7.295 -19.881 4.877 1.00 15.23 ? ? ? ? ? . 25 SER A C 2350 ATOM 181 O O . SER A 2350 25 . 8.425 -19.538 4.510 1.00 15.85 ? ? ? ? ? . 25 SER A O 2350 ATOM 182 C CB . SER A 2350 25 . 5.691 -19.131 3.076 1.00 14.16 ? ? ? ? ? . 25 SER A CB 2350 ATOM 183 O OG . SER A 2350 25 . 5.236 -18.112 3.943 1.00 13.91 ? ? ? ? ? . 25 SER A OG 2350 ATOM 184 N N . LEU A 2350 26 . 6.900 -19.862 6.153 1.00 15.28 ? ? ? ? ? . 26 LEU A N 2350 ATOM 185 C CA . LEU A 2350 26 . 7.770 -19.517 7.262 1.00 15.71 ? ? ? ? ? . 26 LEU A CA 2350 ATOM 186 C C . LEU A 2350 26 . 8.551 -20.698 7.831 1.00 13.64 ? ? ? ? ? . 26 LEU A C 2350 ATOM 187 O O . LEU A 2350 26 . 9.162 -20.554 8.882 1.00 12.80 ? ? ? ? ? . 26 LEU A O 2350 ATOM 188 C CB . LEU A 2350 26 . 6.938 -18.882 8.384 1.00 17.44 ? ? ? ? ? . 26 LEU A CB 2350 ATOM 189 C CG . LEU A 2350 26 . 6.047 -17.702 7.946 1.00 20.26 ? ? ? ? ? . 26 LEU A CG 2350 ATOM 190 C CD1 . LEU A 2350 26 . 5.260 -17.143 9.118 1.00 22.13 ? ? ? ? ? . 26 LEU A CD1 2350 ATOM 191 C CD2 . LEU A 2350 26 . 6.881 -16.637 7.276 1.00 23.52 ? ? ? ? ? . 26 LEU A CD2 2350 ATOM 192 N N . VAL A 2350 27 . 8.555 -21.833 7.132 1.00 13.12 ? ? ? ? ? . 27 VAL A N 2350 ATOM 193 C CA . VAL A 2350 27 . 9.321 -23.014 7.537 1.00 13.59 ? ? ? ? ? . 27 VAL A CA 2350 ATOM 194 C C . VAL A 2350 27 . 10.754 -22.634 7.923 1.00 13.89 ? ? ? ? ? . 27 VAL A C 2350 ATOM 195 O O . VAL A 2350 27 . 11.416 -21.850 7.236 1.00 13.58 ? ? ? ? ? . 27 VAL A O 2350 ATOM 196 C CB . VAL A 2350 27 . 9.281 -24.133 6.469 1.00 12.77 ? ? ? ? ? . 27 VAL A CB 2350 ATOM 197 C CG1 . VAL A 2350 27 . 9.896 -23.694 5.145 1.00 12.72 ? ? ? ? ? . 27 VAL A CG1 2350 ATOM 198 C CG2 . VAL A 2350 27 . 9.933 -25.428 6.964 1.00 13.09 ? ? ? ? ? . 27 VAL A CG2 2350 ATOM 199 N N . GLY A 2350 28 . 11.165 -23.100 9.095 1.00 14.31 ? ? ? ? ? . 28 GLY A N 2350 ATOM 200 C CA . GLY A 2350 28 . 12.540 -22.930 9.573 1.00 14.56 ? ? ? ? ? . 28 GLY A CA 2350 ATOM 201 C C . GLY A 2350 28 . 12.871 -21.574 10.159 1.00 13.61 ? ? ? ? ? . 28 GLY A C 2350 ATOM 202 O O . GLY A 2350 28 . 14.008 -21.365 10.620 1.00 13.45 ? ? ? ? ? . 28 GLY A O 2350 ATOM 203 N N . LYS A 2350 29 . 11.900 -20.657 10.167 1.00 14.17 ? ? ? ? ? . 29 LYS A N 2350 ATOM 204 C CA . LYS A 2350 29 . 12.110 -19.302 10.657 1.00 14.57 ? ? ? ? ? . 29 LYS A CA 2350 ATOM 205 C C . LYS A 2350 29 . 11.932 -19.163 12.159 1.00 14.89 ? ? ? ? ? . 29 LYS A C 2350 ATOM 206 O O . LYS A 2350 29 . 11.235 -19.949 12.797 1.00 14.69 ? ? ? ? ? . 29 LYS A O 2350 ATOM 207 C CB . LYS A 2350 29 . 11.153 -18.306 9.975 1.00 15.81 ? ? ? ? ? . 29 LYS A CB 2350 ATOM 208 C CG . LYS A 2350 29 . 11.404 -18.134 8.484 1.00 16.45 ? ? ? ? ? . 29 LYS A CG 2350 ATOM 209 C CD . LYS A 2350 29 . 12.316 -16.947 8.202 1.00 17.42 ? ? ? ? ? . 29 LYS A CD 2350 ATOM 210 C CE . LYS A 2350 29 . 12.498 -16.708 6.715 1.00 17.30 ? ? ? ? ? . 29 LYS A CE 2350 ATOM 211 N NZ . LYS A 2350 29 . 13.044 -17.885 5.999 1.00 19.11 ? ? ? ? ? 1+ 29 LYS A NZ 2350 ATOM 212 N N . THR A 2350 30 . 12.603 -18.156 12.701 1.00 14.18 ? ? ? ? ? . 30 THR A N 2350 ATOM 213 C CA . THR A 2350 30 . 12.220 -17.550 13.977 1.00 14.27 ? ? ? ? ? . 30 THR A CA 2350 ATOM 214 C C . THR A 2350 30 . 11.144 -16.525 13.641 1.00 15.54 ? ? ? ? ? . 30 THR A C 2350 ATOM 215 O O . THR A 2350 30 . 11.293 -15.738 12.701 1.00 15.21 ? ? ? ? ? . 30 THR A O 2350 ATOM 216 C CB . THR A 2350 30 . 13.423 -16.869 14.660 1.00 15.36 ? ? ? ? ? . 30 THR A CB 2350 ATOM 217 C CG2 . THR A 2350 30 . 12.991 -16.093 15.905 1.00 17.24 ? ? ? ? ? . 30 THR A CG2 2350 ATOM 218 O OG1 . THR A 2350 30 . 14.393 -17.861 15.017 1.00 15.76 ? ? ? ? ? . 30 THR A OG1 2350 ATOM 219 N N . VAL A 2350 31 . 10.046 -16.537 14.380 1.00 14.34 ? ? ? ? ? . 31 VAL A N 2350 ATOM 220 C CA . VAL A 2350 31 . 8.934 -15.639 14.093 1.00 15.79 ? ? ? ? ? . 31 VAL A CA 2350 ATOM 221 C C . VAL A 2350 31 . 8.663 -14.816 15.342 1.00 16.49 ? ? ? ? ? . 31 VAL A C 2350 ATOM 222 O O . VAL A 2350 31 . 8.590 -15.357 16.455 1.00 15.72 ? ? ? ? ? . 31 VAL A O 2350 ATOM 223 C CB . VAL A 2350 31 . 7.675 -16.424 13.645 1.00 17.31 ? ? ? ? ? . 31 VAL A CB 2350 ATOM 224 C CG1 . VAL A 2350 31 . 6.467 -15.506 13.473 1.00 19.83 ? ? ? ? ? . 31 VAL A CG1 2350 ATOM 225 C CG2 . VAL A 2350 31 . 7.959 -17.190 12.356 1.00 16.54 ? ? ? ? ? . 31 VAL A CG2 2350 ATOM 226 N N . PHE A 2350 32 . 8.564 -13.502 15.158 1.00 16.30 ? ? ? ? ? . 32 PHE A N 2350 ATOM 227 C CA . PHE A 2350 32 . 8.143 -12.616 16.214 1.00 16.84 ? ? ? ? ? . 32 PHE A CA 2350 ATOM 228 C C . PHE A 2350 32 . 6.687 -12.259 15.980 1.00 16.42 ? ? ? ? ? . 32 PHE A C 2350 ATOM 229 O O . PHE A 2350 32 . 6.341 -11.721 14.924 1.00 18.32 ? ? ? ? ? . 32 PHE A O 2350 ATOM 230 C CB . PHE A 2350 32 . 8.955 -11.336 16.217 1.00 19.26 ? ? ? ? ? . 32 PHE A CB 2350 ATOM 231 C CG . PHE A 2350 32 . 10.415 -11.530 16.494 1.00 19.00 ? ? ? ? ? . 32 PHE A CG 2350 ATOM 232 C CD1 . PHE A 2350 32 . 10.870 -11.695 17.797 1.00 19.12 ? ? ? ? ? . 32 PHE A CD1 2350 ATOM 233 C CD2 . PHE A 2350 32 . 11.344 -11.506 15.462 1.00 20.74 ? ? ? ? ? . 32 PHE A CD2 2350 ATOM 234 C CE1 . PHE A 2350 32 . 12.222 -11.839 18.070 1.00 19.85 ? ? ? ? ? . 32 PHE A CE1 2350 ATOM 235 C CE2 . PHE A 2350 32 . 12.707 -11.659 15.734 1.00 21.50 ? ? ? ? ? . 32 PHE A CE2 2350 ATOM 236 C CZ . PHE A 2350 32 . 13.134 -11.818 17.049 1.00 20.68 ? ? ? ? ? . 32 PHE A CZ 2350 ATOM 237 N N . LEU A 2350 33 . 5.849 -12.554 16.959 1.00 14.24 ? ? ? ? ? . 33 LEU A N 2350 ATOM 238 C CA . LEU A 2350 33 . 4.475 -12.091 16.982 1.00 14.81 ? ? ? ? ? . 33 LEU A CA 2350 ATOM 239 C C . LEU A 2350 33 . 4.477 -10.717 17.622 1.00 15.85 ? ? ? ? ? . 33 LEU A C 2350 ATOM 240 O O . LEU A 2350 33 . 4.880 -10.578 18.777 1.00 15.41 ? ? ? ? ? . 33 LEU A O 2350 ATOM 241 C CB . LEU A 2350 33 . 3.592 -13.056 17.779 1.00 15.00 ? ? ? ? ? . 33 LEU A CB 2350 ATOM 242 C CG . LEU A 2350 33 . 3.603 -14.485 17.239 1.00 16.27 ? ? ? ? ? . 33 LEU A CG 2350 ATOM 243 C CD1 . LEU A 2350 33 . 2.632 -15.324 18.051 1.00 17.02 ? ? ? ? ? . 33 LEU A CD1 2350 ATOM 244 C CD2 . LEU A 2350 33 . 3.259 -14.541 15.757 1.00 17.70 ? ? ? ? ? . 33 LEU A CD2 2350 ATOM 245 N N . TYR A 2350 34 . 4.035 -9.718 16.859 1.00 16.06 ? ? ? ? ? . 34 TYR A N 2350 ATOM 246 C CA . TYR A 2350 34 . 4.112 -8.329 17.268 1.00 15.69 ? ? ? ? ? . 34 TYR A CA 2350 ATOM 247 C C . TYR A 2350 34 . 2.721 -7.828 17.608 1.00 15.39 ? ? ? ? ? . 34 TYR A C 2350 ATOM 248 O O . TYR A 2350 34 . 1.965 -7.440 16.735 1.00 14.35 ? ? ? ? ? . 34 TYR A O 2350 ATOM 249 C CB . TYR A 2350 34 . 4.773 -7.466 16.198 1.00 16.16 ? ? ? ? ? . 34 TYR A CB 2350 ATOM 250 C CG . TYR A 2350 34 . 4.825 -5.977 16.516 1.00 16.03 ? ? ? ? ? . 34 TYR A CG 2350 ATOM 251 C CD1 . TYR A 2350 34 . 4.977 -5.516 17.821 1.00 16.83 ? ? ? ? ? . 34 TYR A CD1 2350 ATOM 252 C CD2 . TYR A 2350 34 . 4.769 -5.031 15.488 1.00 17.63 ? ? ? ? ? . 34 TYR A CD2 2350 ATOM 253 C CE1 . TYR A 2350 34 . 5.030 -4.159 18.098 1.00 17.21 ? ? ? ? ? . 34 TYR A CE1 2350 ATOM 254 C CE2 . TYR A 2350 34 . 4.829 -3.670 15.759 1.00 17.31 ? ? ? ? ? . 34 TYR A CE2 2350 ATOM 255 C CZ . TYR A 2350 34 . 4.965 -3.243 17.069 1.00 16.44 ? ? ? ? ? . 34 TYR A CZ 2350 ATOM 256 O OH . TYR A 2350 34 . 5.016 -1.898 17.366 1.00 17.87 ? ? ? ? ? . 34 TYR A OH 2350 ATOM 257 N N . PHE A 2350 35 . 2.438 -7.854 18.898 1.00 15.23 ? ? ? ? ? . 35 PHE A N 2350 ATOM 258 C CA . PHE A 2350 35 . 1.192 -7.354 19.477 1.00 16.74 ? ? ? ? ? . 35 PHE A CA 2350 ATOM 259 C C . PHE A 2350 35 . 1.248 -5.831 19.553 1.00 16.39 ? ? ? ? ? . 35 PHE A C 2350 ATOM 260 O O . PHE A 2350 35 . 2.115 -5.268 20.223 1.00 17.11 ? ? ? ? ? . 35 PHE A O 2350 ATOM 261 C CB . PHE A 2350 35 . 0.966 -7.980 20.843 1.00 17.16 ? ? ? ? ? . 35 PHE A CB 2350 ATOM 262 C CG . PHE A 2350 35 . 0.735 -9.454 20.782 1.00 18.26 ? ? ? ? ? . 35 PHE A CG 2350 ATOM 263 C CD1 . PHE A 2350 35 . 1.802 -10.330 20.795 1.00 18.94 ? ? ? ? ? . 35 PHE A CD1 2350 ATOM 264 C CD2 . PHE A 2350 35 . -0.552 -9.974 20.684 1.00 19.43 ? ? ? ? ? . 35 PHE A CD2 2350 ATOM 265 C CE1 . PHE A 2350 35 . 1.605 -11.695 20.708 1.00 19.02 ? ? ? ? ? . 35 PHE A CE1 2350 ATOM 266 C CE2 . PHE A 2350 35 . -0.759 -11.344 20.614 1.00 19.14 ? ? ? ? ? . 35 PHE A CE2 2350 ATOM 267 C CZ . PHE A 2350 35 . 0.321 -12.205 20.626 1.00 19.19 ? ? ? ? ? . 35 PHE A CZ 2350 ATOM 268 N N . SER A 2350 36 . 0.344 -5.181 18.822 1.00 17.49 ? ? ? ? ? . 36 SER A N 2350 ATOM 269 C CA . SER A 2350 36 . 0.415 -3.732 18.583 1.00 18.12 ? ? ? ? ? . 36 SER A CA 2350 ATOM 270 C C . SER A 2350 36 . -0.954 -3.153 18.254 1.00 17.25 ? ? ? ? ? . 36 SER A C 2350 ATOM 271 O O . SER A 2350 36 . -1.942 -3.878 18.155 1.00 16.75 ? ? ? ? ? . 36 SER A O 2350 ATOM 272 C CB . SER A 2350 36 . 1.391 -3.425 17.436 1.00 19.11 ? ? ? ? ? . 36 SER A CB 2350 ATOM 273 O OG . SER A 2350 36 . 1.744 -2.041 17.380 1.00 20.12 ? ? ? ? ? . 36 SER A OG 2350 ATOM 274 N N . ALA A 2350 37 . -0.999 -1.835 18.129 1.00 16.02 ? ? ? ? ? . 37 ALA A N 2350 ATOM 275 C CA . ALA A 2350 37 . -2.210 -1.132 17.705 1.00 17.21 ? ? ? ? ? . 37 ALA A CA 2350 ATOM 276 C C . ALA A 2350 37 . -1.822 0.227 17.163 1.00 16.58 ? ? ? ? ? . 37 ALA A C 2350 ATOM 277 O O . ALA A 2350 37 . -0.894 0.865 17.681 1.00 16.07 ? ? ? ? ? . 37 ALA A O 2350 ATOM 278 C CB . ALA A 2350 37 . -3.176 -0.987 18.865 1.00 16.09 ? ? ? ? ? . 37 ALA A CB 2350 ATOM 279 N N . SER A 2350 38 . -2.538 0.673 16.134 1.00 16.09 ? ? ? ? ? . 38 SER A N 2350 ATOM 280 C CA . SER A 2350 38 . -2.180 1.894 15.393 1.00 15.94 ? ? ? ? ? . 38 SER A CA 2350 ATOM 281 C C . SER A 2350 38 . -2.215 3.154 16.234 1.00 16.06 ? ? ? ? ? . 38 SER A C 2350 ATOM 282 O O . SER A 2350 38 . -1.492 4.108 15.933 1.00 15.57 ? ? ? ? ? . 38 SER A O 2350 ATOM 283 C CB . SER A 2350 38 . -3.111 2.110 14.198 1.00 15.53 ? ? ? ? ? . 38 SER A CB 2350 ATOM 284 O OG . SER A 2350 38 . -4.417 2.483 14.611 1.00 13.61 ? ? ? ? ? . 38 SER A OG 2350 ATOM 285 N N . TRP A 2350 39 . -3.083 3.153 17.250 1.00 14.29 ? ? ? ? ? . 39 TRP A N 2350 ATOM 286 C CA . TRP A 2350 39 . -3.327 4.323 18.102 1.00 15.81 ? ? ? ? ? . 39 TRP A CA 2350 ATOM 287 C C . TRP A 2350 39 . -2.576 4.292 19.439 1.00 15.54 ? ? ? ? ? . 39 TRP A C 2350 ATOM 288 O O . TRP A 2350 39 . -2.677 5.230 20.197 1.00 14.28 ? ? ? ? ? . 39 TRP A O 2350 ATOM 289 C CB . TRP A 2350 39 . -4.835 4.560 18.336 1.00 16.03 ? ? ? ? ? . 39 TRP A CB 2350 ATOM 290 C CG . TRP A 2350 39 . -5.696 3.342 18.284 1.00 17.02 ? ? ? ? ? . 39 TRP A CG 2350 ATOM 291 C CD1 . TRP A 2350 39 . -6.597 3.017 17.301 1.00 16.62 ? ? ? ? ? . 39 TRP A CD1 2350 ATOM 292 C CD2 . TRP A 2350 39 . -5.734 2.265 19.233 1.00 17.48 ? ? ? ? ? . 39 TRP A CD2 2350 ATOM 293 C CE2 . TRP A 2350 39 . -6.689 1.329 18.758 1.00 16.65 ? ? ? ? ? . 39 TRP A CE2 2350 ATOM 294 C CE3 . TRP A 2350 39 . -5.061 2.002 20.438 1.00 17.08 ? ? ? ? ? . 39 TRP A CE3 2350 ATOM 295 N NE1 . TRP A 2350 39 . -7.186 1.815 17.579 1.00 16.89 ? ? ? ? ? . 39 TRP A NE1 2350 ATOM 296 C CZ2 . TRP A 2350 39 . -6.978 0.143 19.435 1.00 17.13 ? ? ? ? ? . 39 TRP A CZ2 2350 ATOM 297 C CZ3 . TRP A 2350 39 . -5.351 0.824 21.116 1.00 17.20 ? ? ? ? ? . 39 TRP A CZ3 2350 ATOM 298 C CH2 . TRP A 2350 39 . -6.305 -0.098 20.607 1.00 17.58 ? ? ? ? ? . 39 TRP A CH2 2350 ATOM 299 N N A CYS A 2350 40 . -1.820 3.233 19.710 0.50 15.53 ? ? ? ? ? . 40 CYS A N 2350 ATOM 300 N N B CYS A 2350 40 . -1.828 3.220 19.708 0.50 15.76 ? ? ? ? ? . 40 CYS A N 2350 ATOM 301 C CA A CYS A 2350 40 . -1.099 3.113 20.973 0.50 15.94 ? ? ? ? ? . 40 CYS A CA 2350 ATOM 302 C CA B CYS A 2350 40 . -1.048 3.086 20.945 0.50 16.31 ? ? ? ? ? . 40 CYS A CA 2350 ATOM 303 C C A CYS A 2350 40 . 0.252 3.841 20.875 0.50 15.63 ? ? ? ? ? . 40 CYS A C 2350 ATOM 304 C C B CYS A 2350 40 . 0.259 3.881 20.821 0.50 15.84 ? ? ? ? ? . 40 CYS A C 2350 ATOM 305 O O A CYS A 2350 40 . 1.104 3.413 20.104 0.50 15.01 ? ? ? ? ? . 40 CYS A O 2350 ATOM 306 O O B CYS A 2350 40 . 1.084 3.541 19.979 0.50 15.24 ? ? ? ? ? . 40 CYS A O 2350 ATOM 307 C CB A CYS A 2350 40 . -0.881 1.639 21.293 0.50 17.19 ? ? ? ? ? . 40 CYS A CB 2350 ATOM 308 C CB B CYS A 2350 40 . -0.732 1.603 21.194 0.50 17.85 ? ? ? ? ? . 40 CYS A CB 2350 ATOM 309 S SG A CYS A 2350 40 . -0.070 1.366 22.877 0.50 18.83 ? ? ? ? ? . 40 CYS A SG 2350 ATOM 310 S SG B CYS A 2350 40 . 0.692 1.280 22.270 0.50 20.15 ? ? ? ? ? . 40 CYS A SG 2350 ATOM 311 N N . PRO A 2350 41 . 0.452 4.940 21.641 1.00 15.67 ? ? ? ? ? . 41 PRO A N 2350 ATOM 312 C CA . PRO A 2350 41 . 1.703 5.735 21.475 1.00 16.29 ? ? ? ? ? . 41 PRO A CA 2350 ATOM 313 C C . PRO A 2350 41 . 3.027 4.964 21.556 1.00 17.16 ? ? ? ? ? . 41 PRO A C 2350 ATOM 314 O O . PRO A 2350 41 . 3.835 5.088 20.625 1.00 16.58 ? ? ? ? ? . 41 PRO A O 2350 ATOM 315 C CB . PRO A 2350 41 . 1.589 6.838 22.534 1.00 16.29 ? ? ? ? ? . 41 PRO A CB 2350 ATOM 316 C CG . PRO A 2350 41 . 0.113 6.972 22.756 1.00 17.02 ? ? ? ? ? . 41 PRO A CG 2350 ATOM 317 C CD . PRO A 2350 41 . -0.466 5.598 22.594 1.00 16.25 ? ? ? ? ? . 41 PRO A CD 2350 ATOM 318 N N . PRO A 2350 42 . 3.238 4.137 22.603 1.00 16.73 ? ? ? ? ? . 42 PRO A N 2350 ATOM 319 C CA . PRO A 2350 42 . 4.509 3.413 22.587 1.00 16.97 ? ? ? ? ? . 42 PRO A CA 2350 ATOM 320 C C . PRO A 2350 42 . 4.682 2.470 21.399 1.00 17.31 ? ? ? ? ? . 42 PRO A C 2350 ATOM 321 O O . PRO A 2350 42 . 5.815 2.236 21.007 1.00 18.01 ? ? ? ? ? . 42 PRO A O 2350 ATOM 322 C CB . PRO A 2350 42 . 4.524 2.635 23.913 1.00 18.24 ? ? ? ? ? . 42 PRO A CB 2350 ATOM 323 C CG . PRO A 2350 42 . 3.144 2.716 24.442 1.00 20.34 ? ? ? ? ? . 42 PRO A CG 2350 ATOM 324 C CD . PRO A 2350 42 . 2.500 3.930 23.859 1.00 17.99 ? ? ? ? ? . 42 PRO A CD 2350 ATOM 325 N N . CYS A 2350 43 . 3.583 1.953 20.830 1.00 17.08 ? ? ? ? ? . 43 CYS A N 2350 ATOM 326 C CA . CYS A 2350 43 . 3.654 1.131 19.615 1.00 17.71 ? ? ? ? ? . 43 CYS A CA 2350 ATOM 327 C C . CYS A 2350 43 . 4.071 1.965 18.412 1.00 18.28 ? ? ? ? ? . 43 CYS A C 2350 ATOM 328 O O . CYS A 2350 43 . 4.896 1.539 17.592 1.00 17.92 ? ? ? ? ? . 43 CYS A O 2350 ATOM 329 C CB . CYS A 2350 43 . 2.302 0.486 19.283 1.00 16.62 ? ? ? ? ? . 43 CYS A CB 2350 ATOM 330 S SG . CYS A 2350 43 . 1.804 -0.806 20.436 1.00 17.97 ? ? ? ? ? . 43 CYS A SG 2350 ATOM 331 N N . ARG A 2350 44 . 3.472 3.148 18.300 1.00 18.14 ? ? ? ? ? . 44 ARG A N 2350 ATOM 332 C CA . ARG A 2350 44 . 3.794 4.048 17.197 1.00 19.48 ? ? ? ? ? . 44 ARG A CA 2350 ATOM 333 C C . ARG A 2350 44 . 5.273 4.436 17.232 1.00 18.72 ? ? ? ? ? . 44 ARG A C 2350 ATOM 334 O O . ARG A 2350 44 . 5.871 4.609 16.184 1.00 18.31 ? ? ? ? ? . 44 ARG A O 2350 ATOM 335 C CB . ARG A 2350 44 . 2.889 5.272 17.211 1.00 19.31 ? ? ? ? ? . 44 ARG A CB 2350 ATOM 336 C CG . ARG A 2350 44 . 1.429 4.933 16.938 1.00 20.47 ? ? ? ? ? . 44 ARG A CG 2350 ATOM 337 C CD . ARG A 2350 44 . 0.501 5.909 17.620 1.00 25.71 ? ? ? ? ? . 44 ARG A CD 2350 ATOM 338 N NE . ARG A 2350 44 . 0.489 7.222 16.986 1.00 27.26 ? ? ? ? ? . 44 ARG A NE 2350 ATOM 339 C CZ . ARG A 2350 44 . -0.417 7.656 16.109 1.00 32.49 ? ? ? ? ? . 44 ARG A CZ 2350 ATOM 340 N NH1 . ARG A 2350 44 . -1.424 6.879 15.692 1.00 36.29 ? ? ? ? ? 1+ 44 ARG A NH1 2350 ATOM 341 N NH2 . ARG A 2350 44 . -0.309 8.895 15.634 1.00 31.30 ? ? ? ? ? . 44 ARG A NH2 2350 ATOM 342 N N . GLY A 2350 45 . 5.852 4.549 18.432 1.00 16.87 ? ? ? ? ? . 45 GLY A N 2350 ATOM 343 C CA . GLY A 2350 45 . 7.291 4.825 18.587 1.00 16.30 ? ? ? ? ? . 45 GLY A CA 2350 ATOM 344 C C . GLY A 2350 45 . 8.197 3.625 18.399 1.00 17.31 ? ? ? ? ? . 45 GLY A C 2350 ATOM 345 O O . GLY A 2350 45 . 9.343 3.761 17.968 1.00 16.80 ? ? ? ? ? . 45 GLY A O 2350 ATOM 346 N N . PHE A 2350 46 . 7.690 2.440 18.711 1.00 17.16 ? ? ? ? ? . 46 PHE A N 2350 ATOM 347 C CA . PHE A 2350 46 . 8.479 1.220 18.586 1.00 16.13 ? ? ? ? ? . 46 PHE A CA 2350 ATOM 348 C C . PHE A 2350 46 . 8.512 0.651 17.162 1.00 16.60 ? ? ? ? ? . 46 PHE A C 2350 ATOM 349 O O . PHE A 2350 46 . 9.535 0.198 16.710 1.00 16.70 ? ? ? ? ? . 46 PHE A O 2350 ATOM 350 C CB . PHE A 2350 46 . 7.967 0.150 19.541 1.00 15.86 ? ? ? ? ? . 46 PHE A CB 2350 ATOM 351 C CG . PHE A 2350 46 . 8.771 -1.108 19.489 1.00 16.05 ? ? ? ? ? . 46 PHE A CG 2350 ATOM 352 C CD1 . PHE A 2350 46 . 10.130 -1.082 19.799 1.00 17.33 ? ? ? ? ? . 46 PHE A CD1 2350 ATOM 353 C CD2 . PHE A 2350 46 . 8.199 -2.300 19.084 1.00 17.49 ? ? ? ? ? . 46 PHE A CD2 2350 ATOM 354 C CE1 . PHE A 2350 46 . 10.889 -2.235 19.714 1.00 18.28 ? ? ? ? ? . 46 PHE A CE1 2350 ATOM 355 C CE2 . PHE A 2350 46 . 8.954 -3.462 19.011 1.00 17.09 ? ? ? ? ? . 46 PHE A CE2 2350 ATOM 356 C CZ . PHE A 2350 46 . 10.300 -3.424 19.324 1.00 17.72 ? ? ? ? ? . 46 PHE A CZ 2350 ATOM 357 N N . THR A 2350 47 . 7.376 0.671 16.476 1.00 16.70 ? ? ? ? ? . 47 THR A N 2350 ATOM 358 C CA . THR A 2350 47 . 7.269 0.187 15.102 1.00 15.83 ? ? ? ? ? . 47 THR A CA 2350 ATOM 359 C C . THR A 2350 47 . 8.421 0.636 14.151 1.00 16.94 ? ? ? ? ? . 47 THR A C 2350 ATOM 360 O O . THR A 2350 47 . 9.011 -0.218 13.479 1.00 16.96 ? ? ? ? ? . 47 THR A O 2350 ATOM 361 C CB . THR A 2350 47 . 5.867 0.510 14.547 1.00 16.66 ? ? ? ? ? . 47 THR A CB 2350 ATOM 362 C CG2 . THR A 2350 47 . 5.752 0.297 13.034 1.00 16.80 ? ? ? ? ? . 47 THR A CG2 2350 ATOM 363 O OG1 . THR A 2350 47 . 4.915 -0.318 15.229 1.00 18.14 ? ? ? ? ? . 47 THR A OG1 2350 ATOM 364 N N . PRO A 2350 48 . 8.758 1.947 14.112 1.00 16.14 ? ? ? ? ? . 48 PRO A N 2350 ATOM 365 C CA . PRO A 2350 48 . 9.871 2.352 13.228 1.00 15.16 ? ? ? ? ? . 48 PRO A CA 2350 ATOM 366 C C . PRO A 2350 48 . 11.242 1.798 13.654 1.00 15.43 ? ? ? ? ? . 48 PRO A C 2350 ATOM 367 O O . PRO A 2350 48 . 12.110 1.557 12.800 1.00 15.62 ? ? ? ? ? . 48 PRO A O 2350 ATOM 368 C CB . PRO A 2350 48 . 9.825 3.888 13.265 1.00 15.95 ? ? ? ? ? . 48 PRO A CB 2350 ATOM 369 C CG . PRO A 2350 48 . 9.028 4.237 14.475 1.00 16.18 ? ? ? ? ? . 48 PRO A CG 2350 ATOM 370 C CD . PRO A 2350 48 . 8.057 3.109 14.670 1.00 16.84 ? ? ? ? ? . 48 PRO A CD 2350 ATOM 371 N N . VAL A 2350 49 . 11.421 1.568 14.952 1.00 15.24 ? ? ? ? ? . 49 VAL A N 2350 ATOM 372 C CA . VAL A 2350 49 . 12.653 0.979 15.497 1.00 15.00 ? ? ? ? ? . 49 VAL A CA 2350 ATOM 373 C C . VAL A 2350 49 . 12.738 -0.490 15.080 1.00 16.44 ? ? ? ? ? . 49 VAL A C 2350 ATOM 374 O O . VAL A 2350 49 . 13.785 -0.970 14.589 1.00 17.54 ? ? ? ? ? . 49 VAL A O 2350 ATOM 375 C CB . VAL A 2350 49 . 12.683 1.119 17.046 1.00 14.01 ? ? ? ? ? . 49 VAL A CB 2350 ATOM 376 C CG1 . VAL A 2350 49 . 13.850 0.377 17.659 1.00 13.62 ? ? ? ? ? . 49 VAL A CG1 2350 ATOM 377 C CG2 . VAL A 2350 49 . 12.703 2.591 17.436 1.00 13.12 ? ? ? ? ? . 49 VAL A CG2 2350 ATOM 378 N N . LEU A 2350 50 . 11.629 -1.205 15.264 1.00 16.04 ? ? ? ? ? . 50 LEU A N 2350 ATOM 379 C CA . LEU A 2350 50 . 11.549 -2.607 14.859 1.00 16.65 ? ? ? ? ? . 50 LEU A CA 2350 ATOM 380 C C . LEU A 2350 50 . 11.728 -2.754 13.346 1.00 16.14 ? ? ? ? ? . 50 LEU A C 2350 ATOM 381 O O . LEU A 2350 50 . 12.392 -3.689 12.896 1.00 17.52 ? ? ? ? ? . 50 LEU A O 2350 ATOM 382 C CB . LEU A 2350 50 . 10.228 -3.235 15.291 1.00 17.24 ? ? ? ? ? . 50 LEU A CB 2350 ATOM 383 C CG . LEU A 2350 50 . 10.134 -4.760 15.088 1.00 18.60 ? ? ? ? ? . 50 LEU A CG 2350 ATOM 384 C CD1 . LEU A 2350 50 . 11.292 -5.525 15.736 1.00 18.52 ? ? ? ? ? . 50 LEU A CD1 2350 ATOM 385 C CD2 . LEU A 2350 50 . 8.808 -5.265 15.625 1.00 20.67 ? ? ? ? ? . 50 LEU A CD2 2350 ATOM 386 N N . ALA A 2350 51 . 11.158 -1.827 12.578 1.00 15.16 ? ? ? ? ? . 51 ALA A N 2350 ATOM 387 C CA . ALA A 2350 51 . 11.350 -1.791 11.114 1.00 16.39 ? ? ? ? ? . 51 ALA A CA 2350 ATOM 388 C C . ALA A 2350 51 . 12.807 -1.689 10.702 1.00 16.39 ? ? ? ? ? . 51 ALA A C 2350 ATOM 389 O O . ALA A 2350 51 . 13.234 -2.388 9.789 1.00 16.12 ? ? ? ? ? . 51 ALA A O 2350 ATOM 390 C CB . ALA A 2350 51 . 10.558 -0.659 10.489 1.00 16.94 ? ? ? ? ? . 51 ALA A CB 2350 ATOM 391 N N . GLU A 2350 52 . 13.571 -0.833 11.380 1.00 15.83 ? ? ? ? ? . 52 GLU A N 2350 ATOM 392 C CA . GLU A 2350 52 . 15.018 -0.741 11.136 1.00 17.29 ? ? ? ? ? . 52 GLU A CA 2350 ATOM 393 C C . GLU A 2350 52 . 15.738 -2.056 11.452 1.00 16.77 ? ? ? ? ? . 52 GLU A C 2350 ATOM 394 O O . GLU A 2350 52 . 16.547 -2.538 10.644 1.00 17.83 ? ? ? ? ? . 52 GLU A O 2350 ATOM 395 C CB . GLU A 2350 52 . 15.655 0.398 11.929 1.00 19.04 ? ? ? ? ? . 52 GLU A CB 2350 ATOM 396 C CG . GLU A 2350 52 . 15.197 1.779 11.502 1.00 23.10 ? ? ? ? ? . 52 GLU A CG 2350 ATOM 397 C CD . GLU A 2350 52 . 15.652 2.158 10.111 1.00 27.07 ? ? ? ? ? . 52 GLU A CD 2350 ATOM 398 O OE1 . GLU A 2350 52 . 16.805 1.871 9.753 1.00 26.53 ? ? ? ? ? . 52 GLU A OE1 2350 ATOM 399 O OE2 . GLU A 2350 52 . 14.838 2.741 9.372 1.00 35.08 ? ? ? ? ? 1- 52 GLU A OE2 2350 ATOM 400 N N . PHE A 2350 53 . 15.440 -2.626 12.617 1.00 17.09 ? ? ? ? ? . 53 PHE A N 2350 ATOM 401 C CA . PHE A 2350 53 . 15.961 -3.927 13.008 1.00 17.72 ? ? ? ? ? . 53 PHE A CA 2350 ATOM 402 C C . PHE A 2350 53 . 15.659 -5.004 11.960 1.00 18.04 ? ? ? ? ? . 53 PHE A C 2350 ATOM 403 O O . PHE A 2350 53 . 16.544 -5.765 11.559 1.00 17.15 ? ? ? ? ? . 53 PHE A O 2350 ATOM 404 C CB . PHE A 2350 53 . 15.394 -4.344 14.367 1.00 17.66 ? ? ? ? ? . 53 PHE A CB 2350 ATOM 405 C CG . PHE A 2350 53 . 16.073 -5.523 14.955 1.00 17.72 ? ? ? ? ? . 53 PHE A CG 2350 ATOM 406 C CD1 . PHE A 2350 53 . 17.204 -5.365 15.759 1.00 19.84 ? ? ? ? ? . 53 PHE A CD1 2350 ATOM 407 C CD2 . PHE A 2350 53 . 15.613 -6.800 14.692 1.00 18.67 ? ? ? ? ? . 53 PHE A CD2 2350 ATOM 408 C CE1 . PHE A 2350 53 . 17.855 -6.470 16.294 1.00 18.69 ? ? ? ? ? . 53 PHE A CE1 2350 ATOM 409 C CE2 . PHE A 2350 53 . 16.250 -7.909 15.237 1.00 19.49 ? ? ? ? ? . 53 PHE A CE2 2350 ATOM 410 C CZ . PHE A 2350 53 . 17.381 -7.740 16.022 1.00 19.50 ? ? ? ? ? . 53 PHE A CZ 2350 ATOM 411 N N . TYR A 2350 54 . 14.402 -5.066 11.538 1.00 18.62 ? ? ? ? ? . 54 TYR A N 2350 ATOM 412 C CA . TYR A 2350 54 . 13.957 -5.985 10.484 1.00 16.78 ? ? ? ? ? . 54 TYR A CA 2350 ATOM 413 C C . TYR A 2350 54 . 14.740 -5.808 9.197 1.00 17.12 ? ? ? ? ? . 54 TYR A C 2350 ATOM 414 O O . TYR A 2350 54 . 15.274 -6.777 8.637 1.00 16.38 ? ? ? ? ? . 54 TYR A O 2350 ATOM 415 C CB . TYR A 2350 54 . 12.465 -5.744 10.204 1.00 17.54 ? ? ? ? ? . 54 TYR A CB 2350 ATOM 416 C CG . TYR A 2350 54 . 11.834 -6.704 9.220 1.00 17.88 ? ? ? ? ? . 54 TYR A CG 2350 ATOM 417 C CD1 . TYR A 2350 54 . 11.284 -7.902 9.655 1.00 17.99 ? ? ? ? ? . 54 TYR A CD1 2350 ATOM 418 C CD2 . TYR A 2350 54 . 11.783 -6.414 7.859 1.00 18.12 ? ? ? ? ? . 54 TYR A CD2 2350 ATOM 419 C CE1 . TYR A 2350 54 . 10.703 -8.787 8.776 1.00 17.40 ? ? ? ? ? . 54 TYR A CE1 2350 ATOM 420 C CE2 . TYR A 2350 54 . 11.201 -7.294 6.965 1.00 18.18 ? ? ? ? ? . 54 TYR A CE2 2350 ATOM 421 C CZ . TYR A 2350 54 . 10.656 -8.477 7.430 1.00 18.40 ? ? ? ? ? . 54 TYR A CZ 2350 ATOM 422 O OH . TYR A 2350 54 . 10.066 -9.352 6.548 1.00 18.64 ? ? ? ? ? . 54 TYR A OH 2350 ATOM 423 N N . GLU A 2350 55 . 14.825 -4.567 8.729 1.00 18.35 ? ? ? ? ? . 55 GLU A N 2350 ATOM 424 C CA . GLU A 2350 55 . 15.479 -4.298 7.450 1.00 19.54 ? ? ? ? ? . 55 GLU A CA 2350 ATOM 425 C C . GLU A 2350 55 . 16.941 -4.728 7.457 1.00 17.47 ? ? ? ? ? . 55 GLU A C 2350 ATOM 426 O O . GLU A 2350 55 . 17.426 -5.225 6.444 1.00 16.00 ? ? ? ? ? . 55 GLU A O 2350 ATOM 427 C CB . GLU A 2350 55 . 15.344 -2.832 7.037 1.00 23.35 ? ? ? ? ? . 55 GLU A CB 2350 ATOM 428 C CG . GLU A 2350 55 . 13.904 -2.394 6.757 1.00 27.78 ? ? ? ? ? . 55 GLU A CG 2350 ATOM 429 C CD . GLU A 2350 55 . 13.379 -2.755 5.374 1.00 33.34 ? ? ? ? ? . 55 GLU A CD 2350 ATOM 430 O OE1 . GLU A 2350 55 . 13.957 -3.640 4.695 1.00 38.81 ? ? ? ? ? . 55 GLU A OE1 2350 ATOM 431 O OE2 . GLU A 2350 55 . 12.365 -2.144 4.970 1.00 33.79 ? ? ? ? ? 1- 55 GLU A OE2 2350 ATOM 432 N N . LYS A 2350 56 . 17.630 -4.527 8.582 1.00 17.29 ? ? ? ? ? . 56 LYS A N 2350 ATOM 433 C CA . LYS A 2350 56 . 19.040 -4.884 8.705 1.00 17.51 ? ? ? ? ? . 56 LYS A CA 2350 ATOM 434 C C . LYS A 2350 56 . 19.255 -6.396 8.816 1.00 15.74 ? ? ? ? ? . 56 LYS A C 2350 ATOM 435 O O . LYS A 2350 56 . 20.181 -6.935 8.183 1.00 16.74 ? ? ? ? ? . 56 LYS A O 2350 ATOM 436 C CB . LYS A 2350 56 . 19.699 -4.158 9.902 1.00 20.10 ? ? ? ? ? . 56 LYS A CB 2350 ATOM 437 C CG . LYS A 2350 56 . 21.202 -4.417 10.024 1.00 22.06 ? ? ? ? ? . 56 LYS A CG 2350 ATOM 438 C CD . LYS A 2350 56 . 21.921 -3.570 11.086 1.00 24.35 ? ? ? ? ? . 56 LYS A CD 2350 ATOM 439 C CE . LYS A 2350 56 . 23.451 -3.707 10.942 1.00 26.58 ? ? ? ? ? . 56 LYS A CE 2350 ATOM 440 N NZ . LYS A 2350 56 . 24.320 -2.988 11.937 1.00 24.67 ? ? ? ? ? 1+ 56 LYS A NZ 2350 ATOM 441 N N . HIS A 2350 57 . 18.415 -7.076 9.599 1.00 14.57 ? ? ? ? ? . 57 HIS A N 2350 ATOM 442 C CA . HIS A 2350 57 . 18.718 -8.424 10.085 1.00 15.29 ? ? ? ? ? . 57 HIS A CA 2350 ATOM 443 C C . HIS A 2350 57 . 17.814 -9.569 9.624 1.00 15.31 ? ? ? ? ? . 57 HIS A C 2350 ATOM 444 O O . HIS A 2350 57 . 18.170 -10.726 9.880 1.00 16.33 ? ? ? ? ? . 57 HIS A O 2350 ATOM 445 C CB . HIS A 2350 57 . 18.690 -8.468 11.612 1.00 15.83 ? ? ? ? ? . 57 HIS A CB 2350 ATOM 446 C CG . HIS A 2350 57 . 19.586 -7.481 12.281 1.00 16.66 ? ? ? ? ? . 57 HIS A CG 2350 ATOM 447 C CD2 . HIS A 2350 57 . 19.312 -6.513 13.190 1.00 18.19 ? ? ? ? ? . 57 HIS A CD2 2350 ATOM 448 N ND1 . HIS A 2350 57 . 20.944 -7.457 12.094 1.00 16.54 ? ? ? ? ? . 57 HIS A ND1 2350 ATOM 449 C CE1 . HIS A 2350 57 . 21.471 -6.502 12.836 1.00 18.76 ? ? ? ? ? . 57 HIS A CE1 2350 ATOM 450 N NE2 . HIS A 2350 57 . 20.502 -5.918 13.519 1.00 17.63 ? ? ? ? ? . 57 HIS A NE2 2350 ATOM 451 N N . HIS A 2350 58 . 16.668 -9.294 8.996 1.00 15.07 ? ? ? ? ? . 58 HIS A N 2350 ATOM 452 C CA . HIS A 2350 58 . 15.663 -10.363 8.809 1.00 15.32 ? ? ? ? ? . 58 HIS A CA 2350 ATOM 453 C C . HIS A 2350 58 . 16.142 -11.508 7.916 1.00 15.60 ? ? ? ? ? . 58 HIS A C 2350 ATOM 454 O O . HIS A 2350 58 . 15.814 -12.666 8.172 1.00 16.71 ? ? ? ? ? . 58 HIS A O 2350 ATOM 455 C CB . HIS A 2350 58 . 14.270 -9.838 8.384 1.00 16.50 ? ? ? ? ? . 58 HIS A CB 2350 ATOM 456 C CG . HIS A 2350 58 . 14.110 -9.576 6.917 1.00 16.28 ? ? ? ? ? . 58 HIS A CG 2350 ATOM 457 C CD2 . HIS A 2350 58 . 13.530 -10.314 5.939 1.00 17.28 ? ? ? ? ? . 58 HIS A CD2 2350 ATOM 458 N ND1 . HIS A 2350 58 . 14.514 -8.401 6.318 1.00 18.08 ? ? ? ? ? . 58 HIS A ND1 2350 ATOM 459 C CE1 . HIS A 2350 58 . 14.236 -8.449 5.025 1.00 19.03 ? ? ? ? ? . 58 HIS A CE1 2350 ATOM 460 N NE2 . HIS A 2350 58 . 13.622 -9.592 4.773 1.00 19.90 ? ? ? ? ? . 58 HIS A NE2 2350 ATOM 461 N N . VAL A 2350 59 . 16.953 -11.183 6.909 1.00 14.27 ? ? ? ? ? . 59 VAL A N 2350 ATOM 462 C CA . VAL A 2350 59 . 17.521 -12.205 6.060 1.00 14.71 ? ? ? ? ? . 59 VAL A CA 2350 ATOM 463 C C . VAL A 2350 59 . 18.661 -12.908 6.783 1.00 14.94 ? ? ? ? ? . 59 VAL A C 2350 ATOM 464 O O . VAL A 2350 59 . 18.645 -14.134 6.937 1.00 14.29 ? ? ? ? ? . 59 VAL A O 2350 ATOM 465 C CB . VAL A 2350 59 . 17.994 -11.612 4.722 1.00 14.66 ? ? ? ? ? . 59 VAL A CB 2350 ATOM 466 C CG1 . VAL A 2350 59 . 18.666 -12.682 3.873 1.00 14.25 ? ? ? ? ? . 59 VAL A CG1 2350 ATOM 467 C CG2 . VAL A 2350 59 . 16.805 -10.993 3.980 1.00 14.94 ? ? ? ? ? . 59 VAL A CG2 2350 ATOM 468 N N . ALA A 2350 60 . 19.645 -12.144 7.246 1.00 15.73 ? ? ? ? ? . 60 ALA A N 2350 ATOM 469 C CA . ALA A 2350 60 . 20.864 -12.747 7.823 1.00 17.51 ? ? ? ? ? . 60 ALA A CA 2350 ATOM 470 C C . ALA A 2350 60 . 20.557 -13.591 9.054 1.00 16.03 ? ? ? ? ? . 60 ALA A C 2350 ATOM 471 O O . ALA A 2350 60 . 21.143 -14.653 9.242 1.00 15.29 ? ? ? ? ? . 60 ALA A O 2350 ATOM 472 C CB . ALA A 2350 60 . 21.898 -11.674 8.149 1.00 18.78 ? ? ? ? ? . 60 ALA A CB 2350 ATOM 473 N N . LYS A 2350 61 . 19.598 -13.149 9.864 1.00 14.83 ? ? ? ? ? . 61 LYS A N 2350 ATOM 474 C CA . LYS A 2350 61 . 19.226 -13.871 11.088 1.00 15.73 ? ? ? ? ? . 61 LYS A CA 2350 ATOM 475 C C . LYS A 2350 61 . 17.927 -14.693 10.936 1.00 17.18 ? ? ? ? ? . 61 LYS A C 2350 ATOM 476 O O . LYS A 2350 61 . 17.409 -15.236 11.923 1.00 18.10 ? ? ? ? ? . 61 LYS A O 2350 ATOM 477 C CB . LYS A 2350 61 . 19.132 -12.891 12.265 1.00 15.99 ? ? ? ? ? . 61 LYS A CB 2350 ATOM 478 C CG . LYS A 2350 61 . 20.452 -12.166 12.504 1.00 18.28 ? ? ? ? ? . 61 LYS A CG 2350 ATOM 479 C CD . LYS A 2350 61 . 20.439 -11.283 13.741 1.00 20.10 ? ? ? ? ? . 61 LYS A CD 2350 ATOM 480 C CE . LYS A 2350 61 . 21.754 -10.505 13.895 1.00 20.17 ? ? ? ? ? . 61 LYS A CE 2350 ATOM 481 N NZ . LYS A 2350 61 . 22.893 -11.355 14.328 1.00 19.55 ? ? ? ? ? 1+ 61 LYS A NZ 2350 ATOM 482 N N . ASN A 2350 62 . 17.428 -14.784 9.701 1.00 16.86 ? ? ? ? ? . 62 ASN A N 2350 ATOM 483 C CA . ASN A 2350 62 . 16.360 -15.705 9.305 1.00 16.87 ? ? ? ? ? . 62 ASN A CA 2350 ATOM 484 C C . ASN A 2350 62 . 15.135 -15.622 10.221 1.00 16.20 ? ? ? ? ? . 62 ASN A C 2350 ATOM 485 O O . ASN A 2350 62 . 14.743 -16.606 10.871 1.00 15.82 ? ? ? ? ? . 62 ASN A O 2350 ATOM 486 C CB . ASN A 2350 62 . 16.895 -17.137 9.242 1.00 17.98 ? ? ? ? ? . 62 ASN A CB 2350 ATOM 487 C CG . ASN A 2350 62 . 15.989 -18.059 8.453 1.00 17.03 ? ? ? ? ? . 62 ASN A CG 2350 ATOM 488 N ND2 . ASN A 2350 62 . 15.720 -19.247 8.994 1.00 15.43 ? ? ? ? ? . 62 ASN A ND2 2350 ATOM 489 O OD1 . ASN A 2350 62 . 15.544 -17.708 7.365 1.00 16.98 ? ? ? ? ? . 62 ASN A OD1 2350 ATOM 490 N N . PHE A 2350 63 . 14.555 -14.436 10.284 1.00 15.83 ? ? ? ? ? . 63 PHE A N 2350 ATOM 491 C CA . PHE A 2350 63 . 13.315 -14.245 11.005 1.00 15.98 ? ? ? ? ? . 63 PHE A CA 2350 ATOM 492 C C . PHE A 2350 63 . 12.272 -13.479 10.209 1.00 16.65 ? ? ? ? ? . 63 PHE A C 2350 ATOM 493 O O . PHE A 2350 63 . 12.540 -12.876 9.147 1.00 14.62 ? ? ? ? ? . 63 PHE A O 2350 ATOM 494 C CB . PHE A 2350 63 . 13.555 -13.608 12.392 1.00 15.93 ? ? ? ? ? . 63 PHE A CB 2350 ATOM 495 C CG . PHE A 2350 63 . 14.065 -12.191 12.351 1.00 16.47 ? ? ? ? ? . 63 PHE A CG 2350 ATOM 496 C CD1 . PHE A 2350 63 . 13.192 -11.131 12.154 1.00 17.02 ? ? ? ? ? . 63 PHE A CD1 2350 ATOM 497 C CD2 . PHE A 2350 63 . 15.419 -11.914 12.539 1.00 17.98 ? ? ? ? ? . 63 PHE A CD2 2350 ATOM 498 C CE1 . PHE A 2350 63 . 13.646 -9.823 12.123 1.00 16.99 ? ? ? ? ? . 63 PHE A CE1 2350 ATOM 499 C CE2 . PHE A 2350 63 . 15.874 -10.605 12.516 1.00 17.17 ? ? ? ? ? . 63 PHE A CE2 2350 ATOM 500 C CZ . PHE A 2350 63 . 14.992 -9.562 12.310 1.00 17.23 ? ? ? ? ? . 63 PHE A CZ 2350 ATOM 501 N N . GLU A 2350 64 . 11.065 -13.521 10.753 1.00 16.63 ? ? ? ? ? . 64 GLU A N 2350 ATOM 502 C CA . GLU A 2350 64 . 9.931 -12.790 10.211 1.00 16.06 ? ? ? ? ? . 64 GLU A CA 2350 ATOM 503 C C . GLU A 2350 64 . 9.161 -12.165 11.375 1.00 16.89 ? ? ? ? ? . 64 GLU A C 2350 ATOM 504 O O . GLU A 2350 64 . 9.251 -12.634 12.498 1.00 16.07 ? ? ? ? ? . 64 GLU A O 2350 ATOM 505 C CB . GLU A 2350 64 . 9.043 -13.756 9.433 1.00 17.67 ? ? ? ? ? . 64 GLU A CB 2350 ATOM 506 C CG . GLU A 2350 64 . 7.934 -13.109 8.651 1.00 20.12 ? ? ? ? ? . 64 GLU A CG 2350 ATOM 507 C CD . GLU A 2350 64 . 8.458 -12.085 7.676 1.00 20.42 ? ? ? ? ? . 64 GLU A CD 2350 ATOM 508 O OE1 . GLU A 2350 64 . 8.489 -10.901 8.045 1.00 19.99 ? ? ? ? ? . 64 GLU A OE1 2350 ATOM 509 O OE2 . GLU A 2350 64 . 8.839 -12.477 6.559 1.00 20.73 ? ? ? ? ? 1- 64 GLU A OE2 2350 ATOM 510 N N . VAL A 2350 65 . 8.413 -11.107 11.097 1.00 16.69 ? ? ? ? ? . 65 VAL A N 2350 ATOM 511 C CA . VAL A 2350 65 . 7.578 -10.458 12.100 1.00 15.86 ? ? ? ? ? . 65 VAL A CA 2350 ATOM 512 C C . VAL A 2350 65 . 6.140 -10.529 11.600 1.00 14.98 ? ? ? ? ? . 65 VAL A C 2350 ATOM 513 O O . VAL A 2350 65 . 5.879 -10.397 10.391 1.00 14.44 ? ? ? ? ? . 65 VAL A O 2350 ATOM 514 C CB . VAL A 2350 65 . 8.066 -9.013 12.345 1.00 17.34 ? ? ? ? ? . 65 VAL A CB 2350 ATOM 515 C CG1 . VAL A 2350 65 . 7.112 -8.225 13.239 1.00 18.32 ? ? ? ? ? . 65 VAL A CG1 2350 ATOM 516 C CG2 . VAL A 2350 65 . 9.464 -9.038 12.945 1.00 18.63 ? ? ? ? ? . 65 VAL A CG2 2350 ATOM 517 N N . VAL A 2350 66 . 5.212 -10.798 12.517 1.00 14.94 ? ? ? ? ? . 66 VAL A N 2350 ATOM 518 C CA . VAL A 2350 66 . 3.791 -10.901 12.186 1.00 15.77 ? ? ? ? ? . 66 VAL A CA 2350 ATOM 519 C C . VAL A 2350 66 . 3.013 -9.926 13.068 1.00 16.12 ? ? ? ? ? . 66 VAL A C 2350 ATOM 520 O O . VAL A 2350 66 . 2.954 -10.091 14.287 1.00 18.95 ? ? ? ? ? . 66 VAL A O 2350 ATOM 521 C CB . VAL A 2350 66 . 3.248 -12.327 12.365 1.00 15.17 ? ? ? ? ? . 66 VAL A CB 2350 ATOM 522 C CG1 . VAL A 2350 66 . 1.807 -12.407 11.883 1.00 14.64 ? ? ? ? ? . 66 VAL A CG1 2350 ATOM 523 C CG2 . VAL A 2350 66 . 4.127 -13.332 11.615 1.00 15.43 ? ? ? ? ? . 66 VAL A CG2 2350 ATOM 524 N N . LEU A 2350 67 . 2.413 -8.925 12.441 1.00 14.97 ? ? ? ? ? . 67 LEU A N 2350 ATOM 525 C CA . LEU A 2350 67 . 1.558 -7.976 13.155 1.00 15.42 ? ? ? ? ? . 67 LEU A CA 2350 ATOM 526 C C . LEU A 2350 67 . 0.311 -8.673 13.669 1.00 14.43 ? ? ? ? ? . 67 LEU A C 2350 ATOM 527 O O . LEU A 2350 67 . -0.406 -9.315 12.914 1.00 15.61 ? ? ? ? ? . 67 LEU A O 2350 ATOM 528 C CB . LEU A 2350 67 . 1.134 -6.830 12.239 1.00 16.16 ? ? ? ? ? . 67 LEU A CB 2350 ATOM 529 C CG . LEU A 2350 67 . 0.138 -5.813 12.822 1.00 16.89 ? ? ? ? ? . 67 LEU A CG 2350 ATOM 530 C CD1 . LEU A 2350 67 . 0.748 -5.117 14.038 1.00 18.06 ? ? ? ? ? . 67 LEU A CD1 2350 ATOM 531 C CD2 . LEU A 2350 67 . -0.302 -4.804 11.764 1.00 16.86 ? ? ? ? ? . 67 LEU A CD2 2350 ATOM 532 N N . ILE A 2350 68 . 0.069 -8.515 14.959 1.00 16.21 ? ? ? ? ? . 68 ILE A N 2350 ATOM 533 C CA . ILE A 2350 68 . -1.140 -8.969 15.618 1.00 16.24 ? ? ? ? ? . 68 ILE A CA 2350 ATOM 534 C C . ILE A 2350 68 . -1.759 -7.692 16.195 1.00 16.84 ? ? ? ? ? . 68 ILE A C 2350 ATOM 535 O O . ILE A 2350 68 . -1.309 -7.202 17.220 1.00 16.78 ? ? ? ? ? . 68 ILE A O 2350 ATOM 536 C CB . ILE A 2350 68 . -0.842 -9.969 16.752 1.00 15.81 ? ? ? ? ? . 68 ILE A CB 2350 ATOM 537 C CG1 . ILE A 2350 68 . 0.100 -11.106 16.287 1.00 15.85 ? ? ? ? ? . 68 ILE A CG1 2350 ATOM 538 C CG2 . ILE A 2350 68 . -2.143 -10.534 17.291 1.00 16.11 ? ? ? ? ? . 68 ILE A CG2 2350 ATOM 539 C CD1 . ILE A 2350 68 . -0.444 -11.963 15.172 1.00 15.85 ? ? ? ? ? . 68 ILE A CD1 2350 ATOM 540 N N . SER A 2350 69 . -2.769 -7.158 15.519 1.00 18.12 ? ? ? ? ? . 69 SER A N 2350 ATOM 541 C CA . SER A 2350 69 . -3.262 -5.825 15.839 1.00 18.34 ? ? ? ? ? . 69 SER A CA 2350 ATOM 542 C C . SER A 2350 69 . -4.568 -5.818 16.640 1.00 17.36 ? ? ? ? ? . 69 SER A C 2350 ATOM 543 O O . SER A 2350 69 . -5.517 -6.553 16.339 1.00 15.89 ? ? ? ? ? . 69 SER A O 2350 ATOM 544 C CB . SER A 2350 69 . -3.454 -5.013 14.563 1.00 20.93 ? ? ? ? ? . 69 SER A CB 2350 ATOM 545 O OG . SER A 2350 69 . -3.970 -3.726 14.871 1.00 22.79 ? ? ? ? ? . 69 SER A OG 2350 ATOM 546 N N . TRP A 2350 70 . -4.612 -4.932 17.630 1.00 17.71 ? ? ? ? ? . 70 TRP A N 2350 ATOM 547 C CA . TRP A 2350 70 . -5.849 -4.612 18.370 1.00 17.54 ? ? ? ? ? . 70 TRP A CA 2350 ATOM 548 C C . TRP A 2350 70 . -6.788 -3.654 17.619 1.00 16.23 ? ? ? ? ? . 70 TRP A C 2350 ATOM 549 O O . TRP A 2350 70 . -7.870 -3.325 18.129 1.00 15.84 ? ? ? ? ? . 70 TRP A O 2350 ATOM 550 C CB . TRP A 2350 70 . -5.522 -4.043 19.773 1.00 18.64 ? ? ? ? ? . 70 TRP A CB 2350 ATOM 551 C CG . TRP A 2350 70 . -5.764 -5.026 20.876 1.00 18.49 ? ? ? ? ? . 70 TRP A CG 2350 ATOM 552 C CD1 . TRP A 2350 70 . -6.897 -5.175 21.635 1.00 20.30 ? ? ? ? ? . 70 TRP A CD1 2350 ATOM 553 C CD2 . TRP A 2350 70 . -4.846 -6.010 21.326 1.00 19.25 ? ? ? ? ? . 70 TRP A CD2 2350 ATOM 554 C CE2 . TRP A 2350 70 . -5.481 -6.736 22.357 1.00 20.72 ? ? ? ? ? . 70 TRP A CE2 2350 ATOM 555 C CE3 . TRP A 2350 70 . -3.546 -6.347 20.958 1.00 20.16 ? ? ? ? ? . 70 TRP A CE3 2350 ATOM 556 N NE1 . TRP A 2350 70 . -6.733 -6.207 22.522 1.00 19.85 ? ? ? ? ? . 70 TRP A NE1 2350 ATOM 557 C CZ2 . TRP A 2350 70 . -4.852 -7.783 23.021 1.00 20.72 ? ? ? ? ? . 70 TRP A CZ2 2350 ATOM 558 C CZ3 . TRP A 2350 70 . -2.918 -7.378 21.619 1.00 21.27 ? ? ? ? ? . 70 TRP A CZ3 2350 ATOM 559 C CH2 . TRP A 2350 70 . -3.570 -8.090 22.638 1.00 22.10 ? ? ? ? ? . 70 TRP A CH2 2350 ATOM 560 N N . ASP A 2350 71 . -6.400 -3.183 16.430 1.00 14.95 ? ? ? ? ? . 71 ASP A N 2350 ATOM 561 C CA . ASP A 2350 71 . -7.261 -2.280 15.672 1.00 15.71 ? ? ? ? ? . 71 ASP A CA 2350 ATOM 562 C C . ASP A 2350 71 . -8.605 -2.930 15.328 1.00 14.08 ? ? ? ? ? . 71 ASP A C 2350 ATOM 563 O O . ASP A 2350 71 . -8.633 -4.074 14.887 1.00 13.83 ? ? ? ? ? . 71 ASP A O 2350 ATOM 564 C CB . ASP A 2350 71 . -6.575 -1.838 14.377 1.00 16.40 ? ? ? ? ? . 71 ASP A CB 2350 ATOM 565 C CG . ASP A 2350 71 . -5.488 -0.813 14.617 1.00 16.78 ? ? ? ? ? . 71 ASP A CG 2350 ATOM 566 O OD1 . ASP A 2350 71 . -5.861 0.357 14.863 1.00 16.06 ? ? ? ? ? . 71 ASP A OD1 2350 ATOM 567 O OD2 . ASP A 2350 71 . -4.277 -1.173 14.553 1.00 18.80 ? ? ? ? ? 1- 71 ASP A OD2 2350 ATOM 568 N N . GLU A 2350 72 . -9.689 -2.197 15.550 1.00 13.55 ? ? ? ? ? . 72 GLU A N 2350 ATOM 569 C CA A GLU A 2350 72 . -11.051 -2.601 15.169 0.66 14.70 ? ? ? ? ? . 72 GLU A CA 2350 ATOM 570 C CA B GLU A 2350 72 . -11.003 -2.662 15.116 0.34 14.17 ? ? ? ? ? . 72 GLU A CA 2350 ATOM 571 C C . GLU A 2350 72 . -11.544 -1.845 13.940 1.00 14.43 ? ? ? ? ? . 72 GLU A C 2350 ATOM 572 O O . GLU A 2350 72 . -12.612 -2.162 13.403 1.00 15.02 ? ? ? ? ? . 72 GLU A O 2350 ATOM 573 C CB A GLU A 2350 72 . -12.032 -2.365 16.325 0.66 15.58 ? ? ? ? ? . 72 GLU A CB 2350 ATOM 574 C CB B GLU A 2350 72 . -11.951 -2.732 16.315 0.34 14.14 ? ? ? ? ? . 72 GLU A CB 2350 ATOM 575 C CG A GLU A 2350 72 . -11.825 -3.284 17.523 0.66 17.74 ? ? ? ? ? . 72 GLU A CG 2350 ATOM 576 C CG B GLU A 2350 72 . -11.456 -3.763 17.335 0.34 14.63 ? ? ? ? ? . 72 GLU A CG 2350 ATOM 577 C CD A GLU A 2350 72 . -12.840 -3.071 18.643 0.66 18.62 ? ? ? ? ? . 72 GLU A CD 2350 ATOM 578 C CD B GLU A 2350 72 . -12.487 -4.156 18.381 0.34 15.00 ? ? ? ? ? . 72 GLU A CD 2350 ATOM 579 O OE1 A GLU A 2350 72 . -13.397 -1.946 18.785 0.66 20.42 ? ? ? ? ? . 72 GLU A OE1 2350 ATOM 580 O OE2 A GLU A 2350 72 . -13.078 -4.039 19.399 0.66 18.80 ? ? ? ? ? 1- 72 GLU A OE2 2350 ATOM 581 O OE1 B GLU A 2350 72 . -13.558 -3.519 18.446 0.34 15.59 ? ? ? ? ? . 72 GLU A OE1 2350 ATOM 582 O OE2 B GLU A 2350 72 . -12.220 -5.118 19.141 0.34 14.77 ? ? ? ? ? 1- 72 GLU A OE2 2350 ATOM 583 N N . ASN A 2350 73 . -10.789 -0.830 13.505 1.00 14.08 ? ? ? ? ? . 73 ASN A N 2350 ATOM 584 C CA . ASN A 2350 73 . -11.154 -0.041 12.336 1.00 14.22 ? ? ? ? ? . 73 ASN A CA 2350 ATOM 585 C C . ASN A 2350 73 . -10.271 -0.425 11.153 1.00 13.82 ? ? ? ? ? . 73 ASN A C 2350 ATOM 586 O O . ASN A 2350 73 . -9.048 -0.290 11.203 1.00 13.41 ? ? ? ? ? . 73 ASN A O 2350 ATOM 587 C CB . ASN A 2350 73 . -11.065 1.455 12.613 1.00 15.75 ? ? ? ? ? . 73 ASN A CB 2350 ATOM 588 C CG . ASN A 2350 73 . -11.382 2.282 11.378 1.00 16.44 ? ? ? ? ? . 73 ASN A CG 2350 ATOM 589 N ND2 . ASN A 2350 73 . -12.576 2.835 11.326 1.00 16.80 ? ? ? ? ? . 73 ASN A ND2 2350 ATOM 590 O OD1 . ASN A 2350 73 . -10.571 2.366 10.456 1.00 17.63 ? ? ? ? ? . 73 ASN A OD1 2350 ATOM 591 N N . GLU A 2350 74 . -10.908 -0.880 10.082 1.00 12.83 ? ? ? ? ? . 74 GLU A N 2350 ATOM 592 C CA . GLU A 2350 74 . -10.164 -1.428 8.942 1.00 13.34 ? ? ? ? ? . 74 GLU A CA 2350 ATOM 593 C C . GLU A 2350 74 . -9.264 -0.399 8.251 1.00 12.42 ? ? ? ? ? . 74 GLU A C 2350 ATOM 594 O O . GLU A 2350 74 . -8.163 -0.752 7.810 1.00 12.27 ? ? ? ? ? . 74 GLU A O 2350 ATOM 595 C CB . GLU A 2350 74 . -11.098 -2.104 7.937 1.00 13.28 ? ? ? ? ? . 74 GLU A CB 2350 ATOM 596 C CG . GLU A 2350 74 . -10.322 -2.877 6.864 1.00 14.42 ? ? ? ? ? . 74 GLU A CG 2350 ATOM 597 C CD . GLU A 2350 74 . -11.098 -3.992 6.185 1.00 15.31 ? ? ? ? ? . 74 GLU A CD 2350 ATOM 598 O OE1 . GLU A 2350 74 . -12.342 -4.043 6.291 1.00 16.61 ? ? ? ? ? . 74 GLU A OE1 2350 ATOM 599 O OE2 . GLU A 2350 74 . -10.428 -4.814 5.521 1.00 16.63 ? ? ? ? ? 1- 74 GLU A OE2 2350 ATOM 600 N N A SER A 2350 75 . -9.716 0.852 8.158 0.50 12.08 ? ? ? ? ? . 75 SER A N 2350 ATOM 601 N N B SER A 2350 75 . -9.720 0.852 8.162 0.50 12.17 ? ? ? ? ? . 75 SER A N 2350 ATOM 602 C CA A SER A 2350 75 . -8.889 1.908 7.555 0.50 12.63 ? ? ? ? ? . 75 SER A CA 2350 ATOM 603 C CA B SER A 2350 75 . -8.902 1.929 7.582 0.50 12.79 ? ? ? ? ? . 75 SER A CA 2350 ATOM 604 C C A SER A 2350 75 . -7.615 2.172 8.375 0.50 12.99 ? ? ? ? ? . 75 SER A C 2350 ATOM 605 C C B SER A 2350 75 . -7.614 2.148 8.378 0.50 13.06 ? ? ? ? ? . 75 SER A C 2350 ATOM 606 O O A SER A 2350 75 . -6.534 2.346 7.802 0.50 12.87 ? ? ? ? ? . 75 SER A O 2350 ATOM 607 O O B SER A 2350 75 . -6.530 2.275 7.797 0.50 12.91 ? ? ? ? ? . 75 SER A O 2350 ATOM 608 C CB A SER A 2350 75 . -9.691 3.193 7.344 0.50 12.19 ? ? ? ? ? . 75 SER A CB 2350 ATOM 609 C CB B SER A 2350 75 . -9.687 3.235 7.505 0.50 12.53 ? ? ? ? ? . 75 SER A CB 2350 ATOM 610 O OG A SER A 2350 75 . -9.929 3.865 8.562 0.50 12.51 ? ? ? ? ? . 75 SER A OG 2350 ATOM 611 O OG B SER A 2350 75 . -11.042 2.992 7.190 0.50 12.90 ? ? ? ? ? . 75 SER A OG 2350 ATOM 612 N N . ASP A 2350 76 . -7.737 2.174 9.705 1.00 13.63 ? ? ? ? ? . 76 ASP A N 2350 ATOM 613 C CA . ASP A 2350 76 . -6.574 2.273 10.604 1.00 14.12 ? ? ? ? ? . 76 ASP A CA 2350 ATOM 614 C C . ASP A 2350 76 . -5.635 1.088 10.406 1.00 14.27 ? ? ? ? ? . 76 ASP A C 2350 ATOM 615 O O . ASP A 2350 76 . -4.413 1.264 10.305 1.00 15.60 ? ? ? ? ? . 76 ASP A O 2350 ATOM 616 C CB . ASP A 2350 76 . -6.999 2.328 12.092 1.00 15.22 ? ? ? ? ? . 76 ASP A CB 2350 ATOM 617 C CG . ASP A 2350 76 . -7.739 3.609 12.471 1.00 17.74 ? ? ? ? ? . 76 ASP A CG 2350 ATOM 618 O OD1 . ASP A 2350 76 . -7.583 4.650 11.792 1.00 18.03 ? ? ? ? ? . 76 ASP A OD1 2350 ATOM 619 O OD2 . ASP A 2350 76 . -8.511 3.555 13.461 1.00 18.66 ? ? ? ? ? 1- 76 ASP A OD2 2350 ATOM 620 N N . PHE A 2350 77 . -6.198 -0.116 10.328 1.00 13.52 ? ? ? ? ? . 77 PHE A N 2350 ATOM 621 C CA . PHE A 2350 77 . -5.377 -1.318 10.207 1.00 14.12 ? ? ? ? ? . 77 PHE A CA 2350 ATOM 622 C C . PHE A 2350 77 . -4.500 -1.258 8.952 1.00 13.79 ? ? ? ? ? . 77 PHE A C 2350 ATOM 623 O O . PHE A 2350 77 . -3.297 -1.442 9.049 1.00 14.65 ? ? ? ? ? . 77 PHE A O 2350 ATOM 624 C CB . PHE A 2350 77 . -6.250 -2.570 10.169 1.00 14.39 ? ? ? ? ? . 77 PHE A CB 2350 ATOM 625 C CG . PHE A 2350 77 . -5.489 -3.825 9.863 1.00 14.28 ? ? ? ? ? . 77 PHE A CG 2350 ATOM 626 C CD1 . PHE A 2350 77 . -4.882 -4.561 10.885 1.00 14.15 ? ? ? ? ? . 77 PHE A CD1 2350 ATOM 627 C CD2 . PHE A 2350 77 . -5.389 -4.282 8.545 1.00 13.66 ? ? ? ? ? . 77 PHE A CD2 2350 ATOM 628 C CE1 . PHE A 2350 77 . -4.198 -5.736 10.592 1.00 14.66 ? ? ? ? ? . 77 PHE A CE1 2350 ATOM 629 C CE2 . PHE A 2350 77 . -4.715 -5.450 8.263 1.00 14.31 ? ? ? ? ? . 77 PHE A CE2 2350 ATOM 630 C CZ . PHE A 2350 77 . -4.106 -6.167 9.277 1.00 13.75 ? ? ? ? ? . 77 PHE A CZ 2350 ATOM 631 N N . HIS A 2350 78 . -5.105 -0.968 7.800 1.00 13.17 ? ? ? ? ? . 78 HIS A N 2350 ATOM 632 C CA . HIS A 2350 78 . -4.363 -1.017 6.526 1.00 15.15 ? ? ? ? ? . 78 HIS A CA 2350 ATOM 633 C C . HIS A 2350 78 . -3.291 0.066 6.463 1.00 16.44 ? ? ? ? ? . 78 HIS A C 2350 ATOM 634 O O . HIS A 2350 78 . -2.177 -0.197 6.034 1.00 18.01 ? ? ? ? ? . 78 HIS A O 2350 ATOM 635 C CB . HIS A 2350 78 . -5.293 -0.947 5.327 1.00 15.24 ? ? ? ? ? . 78 HIS A CB 2350 ATOM 636 C CG . HIS A 2350 78 . -6.138 -2.171 5.161 1.00 16.20 ? ? ? ? ? . 78 HIS A CG 2350 ATOM 637 C CD2 . HIS A 2350 78 . -7.474 -2.321 5.042 1.00 16.05 ? ? ? ? ? . 78 HIS A CD2 2350 ATOM 638 N ND1 . HIS A 2350 78 . -5.603 -3.438 5.092 1.00 16.80 ? ? ? ? ? . 78 HIS A ND1 2350 ATOM 639 C CE1 . HIS A 2350 78 . -6.577 -4.317 4.956 1.00 16.55 ? ? ? ? ? . 78 HIS A CE1 2350 ATOM 640 N NE2 . HIS A 2350 78 . -7.722 -3.664 4.911 1.00 16.79 ? ? ? ? ? . 78 HIS A NE2 2350 ATOM 641 N N . ASP A 2350 79 . -3.634 1.265 6.931 1.00 16.68 ? ? ? ? ? . 79 ASP A N 2350 ATOM 642 C CA . ASP A 2350 79 . -2.676 2.375 7.024 1.00 16.83 ? ? ? ? ? . 79 ASP A CA 2350 ATOM 643 C C . ASP A 2350 79 . -1.470 2.068 7.917 1.00 15.94 ? ? ? ? ? . 79 ASP A C 2350 ATOM 644 O O . ASP A 2350 79 . -0.336 2.356 7.523 1.00 17.28 ? ? ? ? ? . 79 ASP A O 2350 ATOM 645 C CB . ASP A 2350 79 . -3.376 3.617 7.558 1.00 17.23 ? ? ? ? ? . 79 ASP A CB 2350 ATOM 646 C CG . ASP A 2350 79 . -2.424 4.781 7.759 1.00 20.48 ? ? ? ? ? . 79 ASP A CG 2350 ATOM 647 O OD1 . ASP A 2350 79 . -2.084 5.421 6.759 1.00 20.77 ? ? ? ? ? . 79 ASP A OD1 2350 ATOM 648 O OD2 . ASP A 2350 79 . -2.011 5.037 8.914 1.00 25.19 ? ? ? ? ? 1- 79 ASP A OD2 2350 ATOM 649 N N . TYR A 2350 80 . -1.730 1.494 9.099 1.00 14.61 ? ? ? ? ? . 80 TYR A N 2350 ATOM 650 C CA . TYR A 2350 80 . -0.697 1.179 10.096 1.00 17.20 ? ? ? ? ? . 80 TYR A CA 2350 ATOM 651 C C . TYR A 2350 80 . 0.221 0.072 9.590 1.00 17.19 ? ? ? ? ? . 80 TYR A C 2350 ATOM 652 O O . TYR A 2350 80 . 1.447 0.196 9.633 1.00 16.67 ? ? ? ? ? . 80 TYR A O 2350 ATOM 653 C CB . TYR A 2350 80 . -1.340 0.758 11.427 1.00 18.55 ? ? ? ? ? . 80 TYR A CB 2350 ATOM 654 C CG . TYR A 2350 80 . -0.396 0.484 12.583 1.00 18.63 ? ? ? ? ? . 80 TYR A CG 2350 ATOM 655 C CD1 . TYR A 2350 80 . 0.683 1.323 12.833 1.00 23.04 ? ? ? ? ? . 80 TYR A CD1 2350 ATOM 656 C CD2 . TYR A 2350 80 . -0.627 -0.565 13.480 1.00 20.76 ? ? ? ? ? . 80 TYR A CD2 2350 ATOM 657 C CE1 . TYR A 2350 80 . 1.538 1.105 13.894 1.00 22.93 ? ? ? ? ? . 80 TYR A CE1 2350 ATOM 658 C CE2 . TYR A 2350 80 . 0.226 -0.795 14.558 1.00 21.46 ? ? ? ? ? . 80 TYR A CE2 2350 ATOM 659 C CZ . TYR A 2350 80 . 1.316 0.057 14.752 1.00 22.68 ? ? ? ? ? . 80 TYR A CZ 2350 ATOM 660 O OH . TYR A 2350 80 . 2.212 -0.095 15.781 1.00 22.57 ? ? ? ? ? . 80 TYR A OH 2350 ATOM 661 N N . TYR A 2350 81 . -0.381 -1.002 9.092 1.00 17.50 ? ? ? ? ? . 81 TYR A N 2350 ATOM 662 C CA . TYR A 2350 81 . 0.379 -2.102 8.498 1.00 16.24 ? ? ? ? ? . 81 TYR A CA 2350 ATOM 663 C C . TYR A 2350 81 . 1.140 -1.652 7.227 1.00 18.13 ? ? ? ? ? . 81 TYR A C 2350 ATOM 664 O O . TYR A 2350 81 . 2.207 -2.185 6.913 1.00 15.85 ? ? ? ? ? . 81 TYR A O 2350 ATOM 665 C CB . TYR A 2350 81 . -0.539 -3.302 8.214 1.00 16.74 ? ? ? ? ? . 81 TYR A CB 2350 ATOM 666 C CG . TYR A 2350 81 . 0.157 -4.417 7.487 1.00 15.44 ? ? ? ? ? . 81 TYR A CG 2350 ATOM 667 C CD1 . TYR A 2350 81 . 1.326 -4.962 7.996 1.00 15.29 ? ? ? ? ? . 81 TYR A CD1 2350 ATOM 668 C CD2 . TYR A 2350 81 . -0.327 -4.903 6.270 1.00 16.27 ? ? ? ? ? . 81 TYR A CD2 2350 ATOM 669 C CE1 . TYR A 2350 81 . 1.991 -5.974 7.330 1.00 16.12 ? ? ? ? ? . 81 TYR A CE1 2350 ATOM 670 C CE2 . TYR A 2350 81 . 0.337 -5.915 5.598 1.00 16.03 ? ? ? ? ? . 81 TYR A CE2 2350 ATOM 671 C CZ . TYR A 2350 81 . 1.494 -6.446 6.138 1.00 15.55 ? ? ? ? ? . 81 TYR A CZ 2350 ATOM 672 O OH . TYR A 2350 81 . 2.175 -7.436 5.481 1.00 15.91 ? ? ? ? ? . 81 TYR A OH 2350 ATOM 673 N N . GLY A 2350 82 . 0.590 -0.673 6.520 1.00 17.41 ? ? ? ? ? . 82 GLY A N 2350 ATOM 674 C CA . GLY A 2350 82 . 1.289 0.024 5.435 1.00 18.28 ? ? ? ? ? . 82 GLY A CA 2350 ATOM 675 C C . GLY A 2350 82 . 2.637 0.633 5.811 1.00 20.09 ? ? ? ? ? . 82 GLY A C 2350 ATOM 676 O O . GLY A 2350 82 . 3.493 0.785 4.952 1.00 24.29 ? ? ? ? ? . 82 GLY A O 2350 ATOM 677 N N . LYS A 2350 83 . 2.831 0.980 7.081 1.00 22.68 ? ? ? ? ? . 83 LYS A N 2350 ATOM 678 C CA . LYS A 2350 83 . 4.127 1.471 7.568 1.00 25.21 ? ? ? ? ? . 83 LYS A CA 2350 ATOM 679 C C . LYS A 2350 83 . 5.180 0.368 7.755 1.00 24.73 ? ? ? ? ? . 83 LYS A C 2350 ATOM 680 O O . LYS A 2350 83 . 6.347 0.694 7.939 1.00 27.09 ? ? ? ? ? . 83 LYS A O 2350 ATOM 681 C CB . LYS A 2350 83 . 3.966 2.226 8.900 1.00 27.32 ? ? ? ? ? . 83 LYS A CB 2350 ATOM 682 C CG . LYS A 2350 83 . 3.068 3.460 8.822 1.00 28.44 ? ? ? ? ? . 83 LYS A CG 2350 ATOM 683 C CD . LYS A 2350 83 . 2.696 3.960 10.213 1.00 29.59 ? ? ? ? ? . 83 LYS A CD 2350 ATOM 684 C CE . LYS A 2350 83 . 1.544 4.950 10.191 1.00 32.72 ? ? ? ? ? . 83 LYS A CE 2350 ATOM 685 N NZ . LYS A 2350 83 . 2.009 6.314 9.830 1.00 33.48 ? ? ? ? ? 1+ 83 LYS A NZ 2350 ATOM 686 N N . MET A 2350 84 . 4.781 -0.911 7.691 1.00 19.28 ? ? ? ? ? . 84 MET A N 2350 ATOM 687 C CA . MET A 2350 84 . 5.594 -2.020 8.159 1.00 17.95 ? ? ? ? ? . 84 MET A CA 2350 ATOM 688 C C . MET A 2350 84 . 6.094 -2.867 6.992 1.00 17.98 ? ? ? ? ? . 84 MET A C 2350 ATOM 689 O O . MET A 2350 84 . 5.361 -3.039 6.022 1.00 18.70 ? ? ? ? ? . 84 MET A O 2350 ATOM 690 C CB . MET A 2350 84 . 4.741 -2.887 9.073 1.00 18.33 ? ? ? ? ? . 84 MET A CB 2350 ATOM 691 C CG . MET A 2350 84 . 4.178 -2.120 10.259 1.00 17.16 ? ? ? ? ? . 84 MET A CG 2350 ATOM 692 S SD . MET A 2350 84 . 3.073 -3.159 11.216 1.00 18.23 ? ? ? ? ? . 84 MET A SD 2350 ATOM 693 C CE . MET A 2350 84 . 2.572 -2.030 12.508 1.00 19.33 ? ? ? ? ? . 84 MET A CE 2350 ATOM 694 N N . PRO A 2350 85 . 7.327 -3.413 7.084 1.00 15.09 ? ? ? ? ? . 85 PRO A N 2350 ATOM 695 C CA . PRO A 2350 85 . 7.898 -4.245 6.004 1.00 14.89 ? ? ? ? ? . 85 PRO A CA 2350 ATOM 696 C C . PRO A 2350 85 . 7.578 -5.746 6.060 1.00 14.31 ? ? ? ? ? . 85 PRO A C 2350 ATOM 697 O O . PRO A 2350 85 . 7.878 -6.490 5.111 1.00 16.07 ? ? ? ? ? . 85 PRO A O 2350 ATOM 698 C CB . PRO A 2350 85 . 9.418 -4.058 6.204 1.00 13.50 ? ? ? ? ? . 85 PRO A CB 2350 ATOM 699 C CG . PRO A 2350 85 . 9.557 -3.858 7.671 1.00 14.27 ? ? ? ? ? . 85 PRO A CG 2350 ATOM 700 C CD . PRO A 2350 85 . 8.354 -3.051 8.079 1.00 14.84 ? ? ? ? ? . 85 PRO A CD 2350 ATOM 701 N N . TRP A 2350 86 . 7.021 -6.177 7.179 1.00 14.39 ? ? ? ? ? . 86 TRP A N 2350 ATOM 702 C CA . TRP A 2350 86 . 6.848 -7.584 7.527 1.00 15.05 ? ? ? ? ? . 86 TRP A CA 2350 ATOM 703 C C . TRP A 2350 86 . 5.414 -8.087 7.212 1.00 14.93 ? ? ? ? ? . 86 TRP A C 2350 ATOM 704 O O . TRP A 2350 86 . 4.763 -7.552 6.308 1.00 15.89 ? ? ? ? ? . 86 TRP A O 2350 ATOM 705 C CB . TRP A 2350 86 . 7.249 -7.774 8.986 1.00 16.09 ? ? ? ? ? . 86 TRP A CB 2350 ATOM 706 C CG . TRP A 2350 86 . 6.594 -6.805 9.948 1.00 16.38 ? ? ? ? ? . 86 TRP A CG 2350 ATOM 707 C CD1 . TRP A 2350 86 . 5.277 -6.720 10.275 1.00 16.39 ? ? ? ? ? . 86 TRP A CD1 2350 ATOM 708 C CD2 . TRP A 2350 86 . 7.254 -5.759 10.661 1.00 16.60 ? ? ? ? ? . 86 TRP A CD2 2350 ATOM 709 C CE2 . TRP A 2350 86 . 6.275 -5.092 11.428 1.00 16.59 ? ? ? ? ? . 86 TRP A CE2 2350 ATOM 710 C CE3 . TRP A 2350 86 . 8.580 -5.340 10.752 1.00 17.11 ? ? ? ? ? . 86 TRP A CE3 2350 ATOM 711 N NE1 . TRP A 2350 86 . 5.074 -5.703 11.176 1.00 17.10 ? ? ? ? ? . 86 TRP A NE1 2350 ATOM 712 C CZ2 . TRP A 2350 86 . 6.576 -4.003 12.239 1.00 16.34 ? ? ? ? ? . 86 TRP A CZ2 2350 ATOM 713 C CZ3 . TRP A 2350 86 . 8.880 -4.259 11.571 1.00 16.26 ? ? ? ? ? . 86 TRP A CZ3 2350 ATOM 714 C CH2 . TRP A 2350 86 . 7.883 -3.601 12.300 1.00 16.70 ? ? ? ? ? . 86 TRP A CH2 2350 ATOM 715 N N . LEU A 2350 87 . 4.947 -9.122 7.918 1.00 14.24 ? ? ? ? ? . 87 LEU A N 2350 ATOM 716 C CA . LEU A 2350 87 . 3.666 -9.781 7.638 1.00 14.03 ? ? ? ? ? . 87 LEU A CA 2350 ATOM 717 C C . LEU A 2350 87 . 2.585 -9.335 8.606 1.00 13.87 ? ? ? ? ? . 87 LEU A C 2350 ATOM 718 O O . LEU A 2350 87 . 2.870 -8.625 9.570 1.00 15.16 ? ? ? ? ? . 87 LEU A O 2350 ATOM 719 C CB . LEU A 2350 87 . 3.834 -11.298 7.738 1.00 14.67 ? ? ? ? ? . 87 LEU A CB 2350 ATOM 720 C CG . LEU A 2350 87 . 4.941 -11.933 6.902 1.00 15.26 ? ? ? ? ? . 87 LEU A CG 2350 ATOM 721 C CD1 . LEU A 2350 87 . 4.898 -13.451 7.044 1.00 17.71 ? ? ? ? ? . 87 LEU A CD1 2350 ATOM 722 C CD2 . LEU A 2350 87 . 4.848 -11.552 5.423 1.00 15.24 ? ? ? ? ? . 87 LEU A CD2 2350 ATOM 723 N N . ALA A 2350 88 . 1.338 -9.735 8.355 1.00 14.07 ? ? ? ? ? . 88 ALA A N 2350 ATOM 724 C CA . ALA A 2350 88 . 0.243 -9.403 9.270 1.00 13.95 ? ? ? ? ? . 88 ALA A CA 2350 ATOM 725 C C . ALA A 2350 88 . -0.837 -10.476 9.311 1.00 14.05 ? ? ? ? ? . 88 ALA A C 2350 ATOM 726 O O . ALA A 2350 88 . -1.203 -11.084 8.292 1.00 13.51 ? ? ? ? ? . 88 ALA A O 2350 ATOM 727 C CB . ALA A 2350 88 . -0.376 -8.068 8.919 1.00 14.60 ? ? ? ? ? . 88 ALA A CB 2350 ATOM 728 N N . LEU A 2350 89 . -1.325 -10.720 10.521 1.00 14.21 ? ? ? ? ? . 89 LEU A N 2350 ATOM 729 C CA . LEU A 2350 89 . -2.521 -11.514 10.693 1.00 14.62 ? ? ? ? ? . 89 LEU A CA 2350 ATOM 730 C C . LEU A 2350 89 . -3.619 -10.667 10.045 1.00 15.33 ? ? ? ? ? . 89 LEU A C 2350 ATOM 731 O O . LEU A 2350 89 . -3.754 -9.482 10.397 1.00 16.78 ? ? ? ? ? . 89 LEU A O 2350 ATOM 732 C CB . LEU A 2350 89 . -2.799 -11.754 12.179 1.00 15.84 ? ? ? ? ? . 89 LEU A CB 2350 ATOM 733 C CG . LEU A 2350 89 . -4.017 -12.623 12.472 1.00 17.67 ? ? ? ? ? . 89 LEU A CG 2350 ATOM 734 C CD1 . LEU A 2350 89 . -3.789 -14.077 12.038 1.00 17.19 ? ? ? ? ? . 89 LEU A CD1 2350 ATOM 735 C CD2 . LEU A 2350 89 . -4.381 -12.542 13.948 1.00 18.01 ? ? ? ? ? . 89 LEU A CD2 2350 ATOM 736 N N . PRO A 2350 90 . -4.369 -11.236 9.079 1.00 15.61 ? ? ? ? ? . 90 PRO A N 2350 ATOM 737 C CA . PRO A 2350 90 . -5.337 -10.408 8.338 1.00 15.39 ? ? ? ? ? . 90 PRO A CA 2350 ATOM 738 C C . PRO A 2350 90 . -6.419 -9.804 9.235 1.00 16.09 ? ? ? ? ? . 90 PRO A C 2350 ATOM 739 O O . PRO A 2350 90 . -6.743 -10.365 10.289 1.00 17.53 ? ? ? ? ? . 90 PRO A O 2350 ATOM 740 C CB . PRO A 2350 90 . -5.942 -11.382 7.316 1.00 15.62 ? ? ? ? ? . 90 PRO A CB 2350 ATOM 741 C CG . PRO A 2350 90 . -5.047 -12.581 7.294 1.00 15.55 ? ? ? ? ? . 90 PRO A CG 2350 ATOM 742 C CD . PRO A 2350 90 . -4.440 -12.653 8.660 1.00 15.71 ? ? ? ? ? . 90 PRO A CD 2350 ATOM 743 N N . PHE A 2350 91 . -6.969 -8.674 8.808 1.00 15.01 ? ? ? ? ? . 91 PHE A N 2350 ATOM 744 C CA . PHE A 2350 91 . -8.012 -7.972 9.554 1.00 15.12 ? ? ? ? ? . 91 PHE A CA 2350 ATOM 745 C C . PHE A 2350 91 . -9.234 -8.855 9.838 1.00 14.96 ? ? ? ? ? . 91 PHE A C 2350 ATOM 746 O O . PHE A 2350 91 . -9.821 -8.765 10.919 1.00 14.30 ? ? ? ? ? . 91 PHE A O 2350 ATOM 747 C CB . PHE A 2350 91 . -8.419 -6.696 8.808 1.00 14.17 ? ? ? ? ? . 91 PHE A CB 2350 ATOM 748 C CG . PHE A 2350 91 . -9.368 -5.827 9.575 1.00 14.33 ? ? ? ? ? . 91 PHE A CG 2350 ATOM 749 C CD1 . PHE A 2350 91 . -8.907 -5.015 10.596 1.00 14.03 ? ? ? ? ? . 91 PHE A CD1 2350 ATOM 750 C CD2 . PHE A 2350 91 . -10.718 -5.837 9.293 1.00 14.08 ? ? ? ? ? . 91 PHE A CD2 2350 ATOM 751 C CE1 . PHE A 2350 91 . -9.778 -4.214 11.312 1.00 14.13 ? ? ? ? ? . 91 PHE A CE1 2350 ATOM 752 C CE2 . PHE A 2350 91 . -11.593 -5.031 10.000 1.00 14.14 ? ? ? ? ? . 91 PHE A CE2 2350 ATOM 753 C CZ . PHE A 2350 91 . -11.125 -4.227 11.017 1.00 13.32 ? ? ? ? ? . 91 PHE A CZ 2350 ATOM 754 N N . ASP A 2350 92 . -9.589 -9.745 8.906 1.00 15.56 ? ? ? ? ? . 92 ASP A N 2350 ATOM 755 C CA . ASP A 2350 92 . -10.703 -10.677 9.134 1.00 17.16 ? ? ? ? ? . 92 ASP A CA 2350 ATOM 756 C C . ASP A 2350 92 . -10.492 -11.723 10.253 1.00 16.55 ? ? ? ? ? . 92 ASP A C 2350 ATOM 757 O O . ASP A 2350 92 . -11.442 -12.405 10.630 1.00 15.77 ? ? ? ? ? . 92 ASP A O 2350 ATOM 758 C CB . ASP A 2350 92 . -11.183 -11.323 7.817 1.00 19.89 ? ? ? ? ? . 92 ASP A CB 2350 ATOM 759 C CG . ASP A 2350 92 . -10.238 -12.389 7.264 1.00 22.49 ? ? ? ? ? . 92 ASP A CG 2350 ATOM 760 O OD1 . ASP A 2350 92 . -9.083 -12.505 7.702 1.00 25.02 ? ? ? ? ? . 92 ASP A OD1 2350 ATOM 761 O OD2 . ASP A 2350 92 . -10.682 -13.123 6.358 1.00 28.11 ? ? ? ? ? 1- 92 ASP A OD2 2350 ATOM 762 N N . GLN A 2350 93 . -9.265 -11.838 10.772 1.00 18.68 ? ? ? ? ? . 93 GLN A N 2350 ATOM 763 C CA . GLN A 2350 93 . -8.950 -12.682 11.938 1.00 19.24 ? ? ? ? ? . 93 GLN A CA 2350 ATOM 764 C C . GLN A 2350 93 . -8.865 -11.918 13.267 1.00 19.92 ? ? ? ? ? . 93 GLN A C 2350 ATOM 765 O O . GLN A 2350 93 . -8.488 -12.498 14.294 1.00 19.87 ? ? ? ? ? . 93 GLN A O 2350 ATOM 766 C CB . GLN A 2350 93 . -7.613 -13.387 11.705 1.00 21.09 ? ? ? ? ? . 93 GLN A CB 2350 ATOM 767 C CG . GLN A 2350 93 . -7.585 -14.287 10.491 1.00 22.02 ? ? ? ? ? . 93 GLN A CG 2350 ATOM 768 C CD . GLN A 2350 93 . -8.625 -15.367 10.592 1.00 22.70 ? ? ? ? ? . 93 GLN A CD 2350 ATOM 769 N NE2 . GLN A 2350 93 . -9.587 -15.348 9.687 1.00 24.75 ? ? ? ? ? . 93 GLN A NE2 2350 ATOM 770 O OE1 . GLN A 2350 93 . -8.582 -16.194 11.502 1.00 26.33 ? ? ? ? ? . 93 GLN A OE1 2350 ATOM 771 N N . ARG A 2350 94 . -9.195 -10.629 13.268 1.00 18.83 ? ? ? ? ? . 94 ARG A N 2350 ATOM 772 C CA . ARG A 2350 94 . -9.008 -9.798 14.473 1.00 18.44 ? ? ? ? ? . 94 ARG A CA 2350 ATOM 773 C C . ARG A 2350 94 . -9.787 -10.249 15.731 1.00 20.01 ? ? ? ? ? . 94 ARG A C 2350 ATOM 774 O O . ARG A 2350 94 . -9.382 -9.946 16.856 1.00 21.06 ? ? ? ? ? . 94 ARG A O 2350 ATOM 775 C CB . ARG A 2350 94 . -9.362 -8.352 14.163 1.00 18.84 ? ? ? ? ? . 94 ARG A CB 2350 ATOM 776 C CG . ARG A 2350 94 . -10.833 -8.137 13.869 1.00 17.70 ? ? ? ? ? . 94 ARG A CG 2350 ATOM 777 C CD . ARG A 2350 94 . -11.074 -6.817 13.167 1.00 17.62 ? ? ? ? ? . 94 ARG A CD 2350 ATOM 778 N NE . ARG A 2350 94 . -12.479 -6.584 12.868 1.00 16.14 ? ? ? ? ? . 94 ARG A NE 2350 ATOM 779 C CZ . ARG A 2350 94 . -13.172 -7.168 11.890 1.00 15.93 ? ? ? ? ? . 94 ARG A CZ 2350 ATOM 780 N NH1 . ARG A 2350 94 . -12.618 -8.075 11.077 1.00 15.88 ? ? ? ? ? 1+ 94 ARG A NH1 2350 ATOM 781 N NH2 . ARG A 2350 94 . -14.447 -6.844 11.720 1.00 15.41 ? ? ? ? ? . 94 ARG A NH2 2350 ATOM 782 N N . SER A 2350 95 . -10.894 -10.966 15.554 1.00 18.52 ? ? ? ? ? . 95 SER A N 2350 ATOM 783 C CA . SER A 2350 95 . -11.631 -11.517 16.704 1.00 19.63 ? ? ? ? ? . 95 SER A CA 2350 ATOM 784 C C . SER A 2350 95 . -10.806 -12.529 17.529 1.00 20.04 ? ? ? ? ? . 95 SER A C 2350 ATOM 785 O O . SER A 2350 95 . -11.153 -12.802 18.675 1.00 23.68 ? ? ? ? ? . 95 SER A O 2350 ATOM 786 C CB . SER A 2350 95 . -12.957 -12.140 16.257 1.00 19.52 ? ? ? ? ? . 95 SER A CB 2350 ATOM 787 O OG . SER A 2350 95 . -12.750 -13.290 15.451 1.00 19.99 ? ? ? ? ? . 95 SER A OG 2350 ATOM 788 N N . THR A 2350 96 . -9.726 -13.065 16.955 1.00 18.79 ? ? ? ? ? . 96 THR A N 2350 ATOM 789 C CA . THR A 2350 96 . -8.848 -14.022 17.638 1.00 19.20 ? ? ? ? ? . 96 THR A CA 2350 ATOM 790 C C . THR A 2350 96 . -7.699 -13.365 18.408 1.00 18.18 ? ? ? ? ? . 96 THR A C 2350 ATOM 791 O O . THR A 2350 96 . -7.004 -14.049 19.141 1.00 18.92 ? ? ? ? ? . 96 THR A O 2350 ATOM 792 C CB . THR A 2350 96 . -8.234 -15.045 16.647 1.00 18.50 ? ? ? ? ? . 96 THR A CB 2350 ATOM 793 C CG2 . THR A 2350 96 . -9.306 -15.722 15.827 1.00 19.51 ? ? ? ? ? . 96 THR A CG2 2350 ATOM 794 O OG1 . THR A 2350 96 . -7.308 -14.396 15.773 1.00 17.89 ? ? ? ? ? . 96 THR A OG1 2350 ATOM 795 N N . VAL A 2350 97 . -7.509 -12.050 18.253 1.00 17.87 ? ? ? ? ? . 97 VAL A N 2350 ATOM 796 C CA . VAL A 2350 97 . -6.369 -11.333 18.837 1.00 17.37 ? ? ? ? ? . 97 VAL A CA 2350 ATOM 797 C C . VAL A 2350 97 . -6.320 -11.387 20.366 1.00 17.80 ? ? ? ? ? . 97 VAL A C 2350 ATOM 798 O O . VAL A 2350 97 . -5.255 -11.611 20.940 1.00 20.08 ? ? ? ? ? . 97 VAL A O 2350 ATOM 799 C CB . VAL A 2350 97 . -6.303 -9.861 18.321 1.00 17.84 ? ? ? ? ? . 97 VAL A CB 2350 ATOM 800 C CG1 . VAL A 2350 97 . -5.371 -8.987 19.152 1.00 19.58 ? ? ? ? ? . 97 VAL A CG1 2350 ATOM 801 C CG2 . VAL A 2350 97 . -5.879 -9.848 16.855 1.00 18.67 ? ? ? ? ? . 97 VAL A CG2 2350 ATOM 802 N N . SER A 2350 98 . -7.446 -11.187 21.024 1.00 18.78 ? ? ? ? ? . 98 SER A N 2350 ATOM 803 C CA . SER A 2350 98 . -7.464 -11.238 22.490 1.00 21.28 ? ? ? ? ? . 98 SER A CA 2350 ATOM 804 C C . SER A 2350 98 . -7.035 -12.609 23.030 1.00 18.77 ? ? ? ? ? . 98 SER A C 2350 ATOM 805 O O . SER A 2350 98 . -6.158 -12.685 23.897 1.00 18.08 ? ? ? ? ? . 98 SER A O 2350 ATOM 806 C CB . SER A 2350 98 . -8.832 -10.833 23.032 1.00 25.06 ? ? ? ? ? . 98 SER A CB 2350 ATOM 807 O OG . SER A 2350 98 . -9.007 -9.449 22.802 1.00 31.85 ? ? ? ? ? . 98 SER A OG 2350 ATOM 808 N N . GLU A 2350 99 . -7.616 -13.681 22.496 1.00 19.69 ? ? ? ? ? . 99 GLU A N 2350 ATOM 809 C CA . GLU A 2350 99 . -7.262 -15.038 22.954 1.00 21.24 ? ? ? ? ? . 99 GLU A CA 2350 ATOM 810 C C . GLU A 2350 99 . -5.793 -15.374 22.682 1.00 17.41 ? ? ? ? ? . 99 GLU A C 2350 ATOM 811 O O . GLU A 2350 99 . -5.151 -16.025 23.503 1.00 15.18 ? ? ? ? ? . 99 GLU A O 2350 ATOM 812 C CB . GLU A 2350 99 . -8.204 -16.125 22.399 1.00 26.09 ? ? ? ? ? . 99 GLU A CB 2350 ATOM 813 C CG . GLU A 2350 99 . -9.552 -16.237 23.134 1.00 32.76 ? ? ? ? ? . 99 GLU A CG 2350 ATOM 814 C CD . GLU A 2350 99 . -9.435 -16.520 24.639 1.00 38.23 ? ? ? ? ? . 99 GLU A CD 2350 ATOM 815 O OE1 . GLU A 2350 99 . -10.112 -15.830 25.435 1.00 38.21 ? ? ? ? ? . 99 GLU A OE1 2350 ATOM 816 O OE2 . GLU A 2350 99 . -8.659 -17.420 25.035 1.00 43.04 ? ? ? ? ? 1- 99 GLU A OE2 2350 ATOM 817 N N A LEU A 2350 100 . -5.267 -14.922 21.547 0.62 17.52 ? ? ? ? ? . 100 LEU A N 2350 ATOM 818 N N B LEU A 2350 100 . -5.274 -14.931 21.535 0.38 17.54 ? ? ? ? ? . 100 LEU A N 2350 ATOM 819 C CA A LEU A 2350 100 . -3.843 -15.073 21.262 0.62 17.97 ? ? ? ? ? . 100 LEU A CA 2350 ATOM 820 C CA B LEU A 2350 100 . -3.842 -15.024 21.233 0.38 17.83 ? ? ? ? ? . 100 LEU A CA 2350 ATOM 821 C C A LEU A 2350 100 . -2.991 -14.334 22.306 0.62 17.34 ? ? ? ? ? . 100 LEU A C 2350 ATOM 822 C C B LEU A 2350 100 . -2.996 -14.330 22.297 0.38 17.23 ? ? ? ? ? . 100 LEU A C 2350 ATOM 823 O O A LEU A 2350 100 . -2.009 -14.887 22.811 0.62 17.52 ? ? ? ? ? . 100 LEU A O 2350 ATOM 824 O O B LEU A 2350 100 . -2.015 -14.895 22.788 0.38 17.39 ? ? ? ? ? . 100 LEU A O 2350 ATOM 825 C CB A LEU A 2350 100 . -3.512 -14.591 19.845 0.62 17.99 ? ? ? ? ? . 100 LEU A CB 2350 ATOM 826 C CB B LEU A 2350 100 . -3.539 -14.408 19.866 0.38 17.92 ? ? ? ? ? . 100 LEU A CB 2350 ATOM 827 C CG A LEU A 2350 100 . -2.154 -15.017 19.286 0.62 18.53 ? ? ? ? ? . 100 LEU A CG 2350 ATOM 828 C CG B LEU A 2350 100 . -3.832 -15.294 18.660 0.38 18.30 ? ? ? ? ? . 100 LEU A CG 2350 ATOM 829 C CD1 A LEU A 2350 100 . -2.036 -16.528 19.154 0.62 18.85 ? ? ? ? ? . 100 LEU A CD1 2350 ATOM 830 C CD2 A LEU A 2350 100 . -1.922 -14.346 17.940 0.62 18.72 ? ? ? ? ? . 100 LEU A CD2 2350 ATOM 831 C CD1 B LEU A 2350 100 . -3.529 -14.555 17.366 0.38 18.21 ? ? ? ? ? . 100 LEU A CD1 2350 ATOM 832 C CD2 B LEU A 2350 100 . -3.032 -16.584 18.760 0.38 18.99 ? ? ? ? ? . 100 LEU A CD2 2350 ATOM 833 N N . GLY A 2350 101 . -3.394 -13.112 22.652 1.00 16.30 ? ? ? ? ? . 101 GLY A N 2350 ATOM 834 C CA . GLY A 2350 101 . -2.751 -12.353 23.730 1.00 17.07 ? ? ? ? ? . 101 GLY A CA 2350 ATOM 835 C C . GLY A 2350 101 . -2.761 -13.100 25.058 1.00 16.31 ? ? ? ? ? . 101 GLY A C 2350 ATOM 836 O O . GLY A 2350 101 . -1.743 -13.175 25.749 1.00 16.49 ? ? ? ? ? . 101 GLY A O 2350 ATOM 837 N N . LYS A 2350 102 . -3.894 -13.712 25.373 1.00 16.43 ? ? ? ? ? . 102 LYS A N 2350 ATOM 838 C CA . LYS A 2350 102 . -4.015 -14.519 26.581 1.00 18.92 ? ? ? ? ? . 102 LYS A CA 2350 ATOM 839 C C . LYS A 2350 102 . -3.185 -15.794 26.544 1.00 17.88 ? ? ? ? ? . 102 LYS A C 2350 ATOM 840 O O . LYS A 2350 102 . -2.693 -16.236 27.592 1.00 17.27 ? ? ? ? ? . 102 LYS A O 2350 ATOM 841 C CB . LYS A 2350 102 . -5.471 -14.864 26.852 1.00 20.65 ? ? ? ? ? . 102 LYS A CB 2350 ATOM 842 C CG . LYS A 2350 102 . -6.288 -13.651 27.240 1.00 23.12 ? ? ? ? ? . 102 LYS A CG 2350 ATOM 843 C CD . LYS A 2350 102 . -7.765 -13.982 27.284 1.00 26.40 ? ? ? ? ? . 102 LYS A CD 2350 ATOM 844 C CE . LYS A 2350 102 . -8.599 -12.716 27.350 1.00 30.33 ? ? ? ? ? . 102 LYS A CE 2350 ATOM 845 N NZ . LYS A 2350 102 . -10.031 -13.013 27.641 1.00 32.61 ? ? ? ? ? 1+ 102 LYS A NZ 2350 ATOM 846 N N . THR A 2350 103 . -3.048 -16.401 25.367 1.00 16.42 ? ? ? ? ? . 103 THR A N 2350 ATOM 847 C CA . THR A 2350 103 . -2.195 -17.586 25.218 1.00 17.78 ? ? ? ? ? . 103 THR A CA 2350 ATOM 848 C C . THR A 2350 103 . -0.744 -17.326 25.664 1.00 17.24 ? ? ? ? ? . 103 THR A C 2350 ATOM 849 O O . THR A 2350 103 . -0.141 -18.175 26.318 1.00 18.04 ? ? ? ? ? . 103 THR A O 2350 ATOM 850 C CB . THR A 2350 103 . -2.246 -18.126 23.775 1.00 18.81 ? ? ? ? ? . 103 THR A CB 2350 ATOM 851 C CG2 . THR A 2350 103 . -1.316 -19.326 23.587 1.00 20.17 ? ? ? ? ? . 103 THR A CG2 2350 ATOM 852 O OG1 . THR A 2350 103 . -3.593 -18.515 23.477 1.00 20.80 ? ? ? ? ? . 103 THR A OG1 2350 ATOM 853 N N . PHE A 2350 104 . -0.216 -16.152 25.328 1.00 19.05 ? ? ? ? ? . 104 PHE A N 2350 ATOM 854 C CA . PHE A 2350 104 . 1.181 -15.790 25.614 1.00 19.38 ? ? ? ? ? . 104 PHE A CA 2350 ATOM 855 C C . PHE A 2350 104 . 1.370 -14.884 26.835 1.00 20.42 ? ? ? ? ? . 104 PHE A C 2350 ATOM 856 O O . PHE A 2350 104 . 2.509 -14.490 27.138 1.00 21.98 ? ? ? ? ? . 104 PHE A O 2350 ATOM 857 C CB . PHE A 2350 104 . 1.800 -15.141 24.379 1.00 19.21 ? ? ? ? ? . 104 PHE A CB 2350 ATOM 858 C CG . PHE A 2350 104 . 1.787 -16.032 23.169 1.00 18.31 ? ? ? ? ? . 104 PHE A CG 2350 ATOM 859 C CD1 . PHE A 2350 104 . 2.515 -17.212 23.163 1.00 18.08 ? ? ? ? ? . 104 PHE A CD1 2350 ATOM 860 C CD2 . PHE A 2350 104 . 1.042 -15.701 22.042 1.00 18.77 ? ? ? ? ? . 104 PHE A CD2 2350 ATOM 861 C CE1 . PHE A 2350 104 . 2.515 -18.044 22.052 1.00 19.62 ? ? ? ? ? . 104 PHE A CE1 2350 ATOM 862 C CE2 . PHE A 2350 104 . 1.023 -16.536 20.933 1.00 19.73 ? ? ? ? ? . 104 PHE A CE2 2350 ATOM 863 C CZ . PHE A 2350 104 . 1.766 -17.706 20.933 1.00 19.63 ? ? ? ? ? . 104 PHE A CZ 2350 ATOM 864 N N . GLY A 2350 105 . 0.278 -14.584 27.535 1.00 17.32 ? ? ? ? ? . 105 GLY A N 2350 ATOM 865 C CA . GLY A 2350 105 . 0.314 -13.721 28.702 1.00 17.53 ? ? ? ? ? . 105 GLY A CA 2350 ATOM 866 C C . GLY A 2350 105 . 0.695 -12.289 28.385 1.00 18.09 ? ? ? ? ? . 105 GLY A C 2350 ATOM 867 O O . GLY A 2350 105 . 1.374 -11.625 29.192 1.00 18.88 ? ? ? ? ? . 105 GLY A O 2350 ATOM 868 N N . VAL A 2350 106 . 0.237 -11.800 27.229 1.00 16.90 ? ? ? ? ? . 106 VAL A N 2350 ATOM 869 C CA . VAL A 2350 106 . 0.450 -10.401 26.824 1.00 17.15 ? ? ? ? ? . 106 VAL A CA 2350 ATOM 870 C C . VAL A 2350 106 . -0.420 -9.510 27.720 1.00 17.09 ? ? ? ? ? . 106 VAL A C 2350 ATOM 871 O O . VAL A 2350 106 . -1.656 -9.601 27.679 1.00 17.42 ? ? ? ? ? . 106 VAL A O 2350 ATOM 872 C CB . VAL A 2350 106 . 0.113 -10.177 25.338 1.00 16.91 ? ? ? ? ? . 106 VAL A CB 2350 ATOM 873 C CG1 . VAL A 2350 106 . 0.239 -8.706 24.946 1.00 17.76 ? ? ? ? ? . 106 VAL A CG1 2350 ATOM 874 C CG2 . VAL A 2350 106 . 1.032 -11.025 24.467 1.00 16.80 ? ? ? ? ? . 106 VAL A CG2 2350 ATOM 875 N N A GLU A 2350 107 . 0.231 -8.684 28.544 0.48 16.42 ? ? ? ? ? . 107 GLU A N 2350 ATOM 876 N N B GLU A 2350 107 . 0.226 -8.667 28.525 0.52 16.18 ? ? ? ? ? . 107 GLU A N 2350 ATOM 877 C CA A GLU A 2350 107 . -0.457 -7.789 29.486 0.48 17.61 ? ? ? ? ? . 107 GLU A CA 2350 ATOM 878 C CA B GLU A 2350 107 . -0.482 -7.782 29.455 0.52 17.47 ? ? ? ? ? . 107 GLU A CA 2350 ATOM 879 C C A GLU A 2350 107 . -0.440 -6.314 29.071 0.48 16.30 ? ? ? ? ? . 107 GLU A C 2350 ATOM 880 C C B GLU A 2350 107 . -0.383 -6.294 29.118 0.52 16.22 ? ? ? ? ? . 107 GLU A C 2350 ATOM 881 O O A GLU A 2350 107 . -1.159 -5.512 29.658 0.48 15.00 ? ? ? ? ? . 107 GLU A O 2350 ATOM 882 O O B GLU A 2350 107 . -0.983 -5.467 29.799 0.52 14.91 ? ? ? ? ? . 107 GLU A O 2350 ATOM 883 C CB A GLU A 2350 107 . 0.136 -7.934 30.885 0.48 18.90 ? ? ? ? ? . 107 GLU A CB 2350 ATOM 884 C CB B GLU A 2350 107 . -0.026 -8.061 30.878 0.52 18.53 ? ? ? ? ? . 107 GLU A CB 2350 ATOM 885 C CG A GLU A 2350 107 . -0.152 -9.282 31.527 0.48 20.28 ? ? ? ? ? . 107 GLU A CG 2350 ATOM 886 C CG B GLU A 2350 107 . -0.457 -9.445 31.335 0.52 19.46 ? ? ? ? ? . 107 GLU A CG 2350 ATOM 887 C CD A GLU A 2350 107 . -1.634 -9.612 31.585 0.48 20.99 ? ? ? ? ? . 107 GLU A CD 2350 ATOM 888 C CD B GLU A 2350 107 . -0.230 -9.688 32.809 0.52 20.69 ? ? ? ? ? . 107 GLU A CD 2350 ATOM 889 O OE1 A GLU A 2350 107 . -1.964 -10.810 31.716 0.48 22.80 ? ? ? ? ? . 107 GLU A OE1 2350 ATOM 890 O OE2 A GLU A 2350 107 . -2.475 -8.685 31.501 0.48 20.81 ? ? ? ? ? 1- 107 GLU A OE2 2350 ATOM 891 O OE1 B GLU A 2350 107 . 0.552 -8.941 33.435 0.52 21.77 ? ? ? ? ? . 107 GLU A OE1 2350 ATOM 892 O OE2 B GLU A 2350 107 . -0.834 -10.641 33.338 0.52 20.72 ? ? ? ? ? 1- 107 GLU A OE2 2350 ATOM 893 N N . SER A 2350 108 . 0.380 -5.969 28.081 1.00 15.68 ? ? ? ? ? . 108 SER A N 2350 ATOM 894 C CA . SER A 2350 108 . 0.383 -4.638 27.500 1.00 17.08 ? ? ? ? ? . 108 SER A CA 2350 ATOM 895 C C . SER A 2350 108 . 0.985 -4.755 26.112 1.00 16.89 ? ? ? ? ? . 108 SER A C 2350 ATOM 896 O O . SER A 2350 108 . 1.450 -5.829 25.729 1.00 17.73 ? ? ? ? ? . 108 SER A O 2350 ATOM 897 C CB . SER A 2350 108 . 1.213 -3.668 28.353 1.00 18.24 ? ? ? ? ? . 108 SER A CB 2350 ATOM 898 O OG . SER A 2350 108 . 2.566 -4.088 28.395 1.00 19.50 ? ? ? ? ? . 108 SER A OG 2350 ATOM 899 N N . ILE A 2350 109 . 0.943 -3.654 25.361 1.00 16.59 ? ? ? ? ? . 109 ILE A N 2350 ATOM 900 C CA . ILE A 2350 109 . 1.631 -3.552 24.077 1.00 16.95 ? ? ? ? ? . 109 ILE A CA 2350 ATOM 901 C C . ILE A 2350 109 . 2.424 -2.244 24.042 1.00 17.07 ? ? ? ? ? . 109 ILE A C 2350 ATOM 902 O O . ILE A 2350 109 . 2.119 -1.314 24.806 1.00 15.40 ? ? ? ? ? . 109 ILE A O 2350 ATOM 903 C CB . ILE A 2350 109 . 0.661 -3.621 22.878 1.00 16.61 ? ? ? ? ? . 109 ILE A CB 2350 ATOM 904 C CG1 . ILE A 2350 109 . -0.342 -2.464 22.916 1.00 16.67 ? ? ? ? ? . 109 ILE A CG1 2350 ATOM 905 C CG2 . ILE A 2350 109 . -0.070 -4.947 22.864 1.00 17.96 ? ? ? ? ? . 109 ILE A CG2 2350 ATOM 906 C CD1 . ILE A 2350 109 . -1.334 -2.459 21.764 1.00 17.14 ? ? ? ? ? . 109 ILE A CD1 2350 ATOM 907 N N . PRO A 2350 110 . 3.455 -2.163 23.184 1.00 17.10 ? ? ? ? ? . 110 PRO A N 2350 ATOM 908 C CA . PRO A 2350 110 . 3.969 -3.163 22.255 1.00 16.27 ? ? ? ? ? . 110 PRO A CA 2350 ATOM 909 C C . PRO A 2350 110 . 4.615 -4.367 22.957 1.00 16.00 ? ? ? ? ? . 110 PRO A C 2350 ATOM 910 O O . PRO A 2350 110 . 5.305 -4.213 23.960 1.00 15.22 ? ? ? ? ? . 110 PRO A O 2350 ATOM 911 C CB . PRO A 2350 110 . 5.004 -2.363 21.462 1.00 16.63 ? ? ? ? ? . 110 PRO A CB 2350 ATOM 912 C CG . PRO A 2350 110 . 5.544 -1.416 22.461 1.00 14.86 ? ? ? ? ? . 110 PRO A CG 2350 ATOM 913 C CD . PRO A 2350 110 . 4.334 -0.974 23.215 1.00 16.56 ? ? ? ? ? . 110 PRO A CD 2350 ATOM 914 N N . THR A 2350 111 . 4.358 -5.563 22.450 1.00 16.65 ? ? ? ? ? . 111 THR A N 2350 ATOM 915 C CA . THR A 2350 111 . 5.020 -6.757 22.952 1.00 16.87 ? ? ? ? ? . 111 THR A CA 2350 ATOM 916 C C . THR A 2350 111 . 5.390 -7.633 21.753 1.00 16.48 ? ? ? ? ? . 111 THR A C 2350 ATOM 917 O O . THR A 2350 111 . 4.610 -7.759 20.799 1.00 16.90 ? ? ? ? ? . 111 THR A O 2350 ATOM 918 C CB . THR A 2350 111 . 4.107 -7.527 23.939 1.00 17.53 ? ? ? ? ? . 111 THR A CB 2350 ATOM 919 C CG2 . THR A 2350 111 . 4.684 -8.888 24.316 1.00 18.56 ? ? ? ? ? . 111 THR A CG2 2350 ATOM 920 O OG1 . THR A 2350 111 . 3.924 -6.761 25.132 1.00 18.31 ? ? ? ? ? . 111 THR A OG1 2350 ATOM 921 N N . LEU A 2350 112 . 6.592 -8.200 21.806 1.00 15.48 ? ? ? ? ? . 112 LEU A N 2350 ATOM 922 C CA . LEU A 2350 112 . 7.032 -9.243 20.872 1.00 16.77 ? ? ? ? ? . 112 LEU A CA 2350 ATOM 923 C C . LEU A 2350 112 . 7.096 -10.595 21.590 1.00 17.72 ? ? ? ? ? . 112 LEU A C 2350 ATOM 924 O O . LEU A 2350 112 . 7.684 -10.706 22.669 1.00 18.56 ? ? ? ? ? . 112 LEU A O 2350 ATOM 925 C CB . LEU A 2350 112 . 8.420 -8.917 20.311 1.00 16.88 ? ? ? ? ? . 112 LEU A CB 2350 ATOM 926 C CG . LEU A 2350 112 . 8.521 -7.687 19.408 1.00 17.77 ? ? ? ? ? . 112 LEU A CG 2350 ATOM 927 C CD1 . LEU A 2350 112 . 9.973 -7.390 19.033 1.00 16.92 ? ? ? ? ? . 112 LEU A CD1 2350 ATOM 928 C CD2 . LEU A 2350 112 . 7.689 -7.898 18.153 1.00 19.55 ? ? ? ? ? . 112 LEU A CD2 2350 ATOM 929 N N . ILE A 2350 113 . 6.496 -11.617 20.990 1.00 15.87 ? ? ? ? ? . 113 ILE A N 2350 ATOM 930 C CA . ILE A 2350 113 . 6.651 -12.997 21.460 1.00 15.67 ? ? ? ? ? . 113 ILE A CA 2350 ATOM 931 C C . ILE A 2350 113 . 7.452 -13.761 20.404 1.00 16.43 ? ? ? ? ? . 113 ILE A C 2350 ATOM 932 O O . ILE A 2350 113 . 7.100 -13.752 19.241 1.00 17.53 ? ? ? ? ? . 113 ILE A O 2350 ATOM 933 C CB . ILE A 2350 113 . 5.284 -13.665 21.671 1.00 16.79 ? ? ? ? ? . 113 ILE A CB 2350 ATOM 934 C CG1 . ILE A 2350 113 . 4.438 -12.866 22.669 1.00 16.77 ? ? ? ? ? . 113 ILE A CG1 2350 ATOM 935 C CG2 . ILE A 2350 113 . 5.450 -15.106 22.132 1.00 16.45 ? ? ? ? ? . 113 ILE A CG2 2350 ATOM 936 C CD1 . ILE A 2350 113 . 5.059 -12.691 24.033 1.00 17.44 ? ? ? ? ? . 113 ILE A CD1 2350 ATOM 937 N N . THR A 2350 114 . 8.548 -14.395 20.806 1.00 15.64 ? ? ? ? ? . 114 THR A N 2350 ATOM 938 C CA . THR A 2350 114 . 9.432 -15.065 19.851 1.00 15.54 ? ? ? ? ? . 114 THR A CA 2350 ATOM 939 C C . THR A 2350 114 . 9.105 -16.535 19.804 1.00 16.03 ? ? ? ? ? . 114 THR A C 2350 ATOM 940 O O . THR A 2350 114 . 9.069 -17.201 20.843 1.00 15.89 ? ? ? ? ? . 114 THR A O 2350 ATOM 941 C CB . THR A 2350 114 . 10.899 -14.877 20.248 1.00 16.17 ? ? ? ? ? . 114 THR A CB 2350 ATOM 942 C CG2 . THR A 2350 114 . 11.843 -15.242 19.082 1.00 17.31 ? ? ? ? ? . 114 THR A CG2 2350 ATOM 943 O OG1 . THR A 2350 114 . 11.091 -13.522 20.641 1.00 16.08 ? ? ? ? ? . 114 THR A OG1 2350 ATOM 944 N N A ILE A 2350 115 . 8.888 -17.070 18.605 0.55 16.54 ? ? ? ? ? . 115 ILE A N 2350 ATOM 945 N N B ILE A 2350 115 . 8.876 -17.020 18.585 0.45 15.81 ? ? ? ? ? . 115 ILE A N 2350 ATOM 946 C CA A ILE A 2350 115 . 8.499 -18.473 18.450 0.55 16.27 ? ? ? ? ? . 115 ILE A CA 2350 ATOM 947 C CA B ILE A 2350 115 . 8.382 -18.358 18.324 0.45 15.23 ? ? ? ? ? . 115 ILE A CA 2350 ATOM 948 C C A ILE A 2350 115 . 9.340 -19.134 17.352 0.55 15.48 ? ? ? ? ? . 115 ILE A C 2350 ATOM 949 C C B ILE A 2350 115 . 9.324 -19.049 17.348 0.45 14.86 ? ? ? ? ? . 115 ILE A C 2350 ATOM 950 O O A ILE A 2350 115 . 9.682 -18.500 16.351 0.55 15.76 ? ? ? ? ? . 115 ILE A O 2350 ATOM 951 O O B ILE A 2350 115 . 9.872 -18.421 16.445 0.45 14.85 ? ? ? ? ? . 115 ILE A O 2350 ATOM 952 C CB A ILE A 2350 115 . 6.978 -18.584 18.143 0.55 16.88 ? ? ? ? ? . 115 ILE A CB 2350 ATOM 953 C CB B ILE A 2350 115 . 6.970 -18.282 17.698 0.45 14.58 ? ? ? ? ? . 115 ILE A CB 2350 ATOM 954 C CG1 A ILE A 2350 115 . 6.158 -18.040 19.325 0.55 17.01 ? ? ? ? ? . 115 ILE A CG1 2350 ATOM 955 C CG2 A ILE A 2350 115 . 6.558 -20.022 17.847 0.55 17.77 ? ? ? ? ? . 115 ILE A CG2 2350 ATOM 956 C CG1 B ILE A 2350 115 . 6.030 -17.511 18.630 0.45 13.86 ? ? ? ? ? . 115 ILE A CG1 2350 ATOM 957 C CG2 B ILE A 2350 115 . 6.416 -19.669 17.440 0.45 15.79 ? ? ? ? ? . 115 ILE A CG2 2350 ATOM 958 C CD1 A ILE A 2350 115 . 4.718 -17.741 18.993 0.55 18.59 ? ? ? ? ? . 115 ILE A CD1 2350 ATOM 959 C CD1 B ILE A 2350 115 . 5.831 -18.198 19.961 0.45 13.69 ? ? ? ? ? . 115 ILE A CD1 2350 ATOM 960 N N A ASN A 2350 116 . 9.696 -20.393 17.578 0.55 14.26 ? ? ? ? ? . 116 ASN A N 2350 ATOM 961 N N B ASN A 2350 116 . 9.528 -20.339 17.550 0.45 14.15 ? ? ? ? ? . 116 ASN A N 2350 ATOM 962 C CA A ASN A 2350 116 . 10.195 -21.272 16.531 0.55 14.49 ? ? ? ? ? . 116 ASN A CA 2350 ATOM 963 C CA B ASN A 2350 116 . 10.161 -21.166 16.547 0.45 14.57 ? ? ? ? ? . 116 ASN A CA 2350 ATOM 964 C C A ASN A 2350 116 . 8.994 -21.667 15.677 0.55 14.67 ? ? ? ? ? . 116 ASN A C 2350 ATOM 965 C C B ASN A 2350 116 . 9.036 -21.700 15.669 0.45 14.67 ? ? ? ? ? . 116 ASN A C 2350 ATOM 966 O O A ASN A 2350 116 . 8.060 -22.285 16.182 0.55 14.82 ? ? ? ? ? . 116 ASN A O 2350 ATOM 967 O O B ASN A 2350 116 . 8.204 -22.467 16.147 0.45 14.81 ? ? ? ? ? . 116 ASN A O 2350 ATOM 968 C CB A ASN A 2350 116 . 10.852 -22.511 17.146 0.55 14.78 ? ? ? ? ? . 116 ASN A CB 2350 ATOM 969 C CB B ASN A 2350 116 . 10.920 -22.308 17.211 0.45 15.08 ? ? ? ? ? . 116 ASN A CB 2350 ATOM 970 C CG A ASN A 2350 116 . 11.479 -23.433 16.108 0.55 14.39 ? ? ? ? ? . 116 ASN A CG 2350 ATOM 971 C CG B ASN A 2350 116 . 11.701 -23.154 16.220 0.45 15.35 ? ? ? ? ? . 116 ASN A CG 2350 ATOM 972 N ND2 A ASN A 2350 116 . 12.807 -23.467 16.077 0.55 15.51 ? ? ? ? ? . 116 ASN A ND2 2350 ATOM 973 O OD1 A ASN A 2350 116 . 10.785 -24.115 15.358 0.55 13.66 ? ? ? ? ? . 116 ASN A OD1 2350 ATOM 974 N ND2 B ASN A 2350 116 . 11.743 -24.447 16.470 0.45 15.08 ? ? ? ? ? . 116 ASN A ND2 2350 ATOM 975 O OD1 B ASN A 2350 116 . 12.279 -22.646 15.258 0.45 15.65 ? ? ? ? ? . 116 ASN A OD1 2350 ATOM 976 N N . ALA A 2350 117 . 9.000 -21.278 14.401 1.00 14.43 ? ? ? ? ? . 117 ALA A N 2350 ATOM 977 C CA . ALA A 2350 117 . 7.853 -21.558 13.494 1.00 15.56 ? ? ? ? ? . 117 ALA A CA 2350 ATOM 978 C C . ALA A 2350 117 . 7.501 -23.034 13.368 1.00 16.26 ? ? ? ? ? . 117 ALA A C 2350 ATOM 979 O O . ALA A 2350 117 . 6.317 -23.404 13.362 1.00 19.27 ? ? ? ? ? . 117 ALA A O 2350 ATOM 980 C CB . ALA A 2350 117 . 8.106 -20.984 12.098 1.00 15.32 ? ? ? ? ? . 117 ALA A CB 2350 ATOM 981 N N . ASP A 2350 118 . 8.530 -23.869 13.280 1.00 13.71 ? ? ? ? ? . 118 ASP A N 2350 ATOM 982 C CA . ASP A 2350 118 . 8.340 -25.280 12.997 1.00 13.63 ? ? ? ? ? . 118 ASP A CA 2350 ATOM 983 C C . ASP A 2350 118 . 7.697 -26.025 14.164 1.00 13.30 ? ? ? ? ? . 118 ASP A C 2350 ATOM 984 O O . ASP A 2350 118 . 6.772 -26.787 13.955 1.00 12.97 ? ? ? ? ? . 118 ASP A O 2350 ATOM 985 C CB . ASP A 2350 118 . 9.665 -25.950 12.628 1.00 13.67 ? ? ? ? ? . 118 ASP A CB 2350 ATOM 986 C CG . ASP A 2350 118 . 10.195 -25.494 11.295 1.00 14.35 ? ? ? ? ? . 118 ASP A CG 2350 ATOM 987 O OD1 . ASP A 2350 118 . 9.479 -24.785 10.536 1.00 13.29 ? ? ? ? ? . 118 ASP A OD1 2350 ATOM 988 O OD2 . ASP A 2350 118 . 11.353 -25.828 11.017 1.00 16.07 ? ? ? ? ? 1- 118 ASP A OD2 2350 ATOM 989 N N . THR A 2350 119 . 8.191 -25.774 15.372 1.00 13.59 ? ? ? ? ? . 119 THR A N 2350 ATOM 990 C CA . THR A 2350 119 . 7.739 -26.479 16.573 1.00 13.80 ? ? ? ? ? . 119 THR A CA 2350 ATOM 991 C C . THR A 2350 119 . 6.693 -25.695 17.356 1.00 13.84 ? ? ? ? ? . 119 THR A C 2350 ATOM 992 O O . THR A 2350 119 . 6.050 -26.256 18.241 1.00 15.00 ? ? ? ? ? . 119 THR A O 2350 ATOM 993 C CB . THR A 2350 119 . 8.912 -26.737 17.531 1.00 14.43 ? ? ? ? ? . 119 THR A CB 2350 ATOM 994 C CG2 . THR A 2350 119 . 10.039 -27.489 16.838 1.00 16.16 ? ? ? ? ? . 119 THR A CG2 2350 ATOM 995 O OG1 . THR A 2350 119 . 9.392 -25.493 18.029 1.00 14.78 ? ? ? ? ? . 119 THR A OG1 2350 ATOM 996 N N . GLY A 2350 120 . 6.550 -24.410 17.051 1.00 13.31 ? ? ? ? ? . 120 GLY A N 2350 ATOM 997 C CA . GLY A 2350 120 . 5.745 -23.482 17.845 1.00 15.55 ? ? ? ? ? . 120 GLY A CA 2350 ATOM 998 C C . GLY A 2350 120 . 6.291 -23.172 19.227 1.00 15.73 ? ? ? ? ? . 120 GLY A C 2350 ATOM 999 O O . GLY A 2350 120 . 5.607 -22.535 20.029 1.00 18.55 ? ? ? ? ? . 120 GLY A O 2350 ATOM 1000 N N . ALA A 2350 121 . 7.522 -23.581 19.519 1.00 15.46 ? ? ? ? ? . 121 ALA A N 2350 ATOM 1001 C CA . ALA A 2350 121 . 8.064 -23.394 20.865 1.00 15.87 ? ? ? ? ? . 121 ALA A CA 2350 ATOM 1002 C C . ALA A 2350 121 . 8.213 -21.904 21.136 1.00 15.57 ? ? ? ? ? . 121 ALA A C 2350 ATOM 1003 O O . ALA A 2350 121 . 8.585 -21.138 20.241 1.00 13.38 ? ? ? ? ? . 121 ALA A O 2350 ATOM 1004 C CB . ALA A 2350 121 . 9.389 -24.104 21.016 1.00 16.46 ? ? ? ? ? . 121 ALA A CB 2350 ATOM 1005 N N . ILE A 2350 122 . 7.880 -21.483 22.353 1.00 15.28 ? ? ? ? ? . 122 ILE A N 2350 ATOM 1006 C CA . ILE A 2350 122 . 8.156 -20.104 22.776 1.00 14.91 ? ? ? ? ? . 122 ILE A CA 2350 ATOM 1007 C C . ILE A 2350 122 . 9.641 -20.062 23.119 1.00 15.51 ? ? ? ? ? . 122 ILE A C 2350 ATOM 1008 O O . ILE A 2350 122 . 10.119 -20.875 23.900 1.00 16.67 ? ? ? ? ? . 122 ILE A O 2350 ATOM 1009 C CB . ILE A 2350 122 . 7.290 -19.669 23.961 1.00 15.79 ? ? ? ? ? . 122 ILE A CB 2350 ATOM 1010 C CG1 . ILE A 2350 122 . 5.823 -19.696 23.552 1.00 17.18 ? ? ? ? ? . 122 ILE A CG1 2350 ATOM 1011 C CG2 . ILE A 2350 122 . 7.689 -18.266 24.434 1.00 17.48 ? ? ? ? ? . 122 ILE A CG2 2350 ATOM 1012 C CD1 . ILE A 2350 122 . 4.864 -19.526 24.708 1.00 17.88 ? ? ? ? ? . 122 ILE A CD1 2350 ATOM 1013 N N A ILE A 2350 123 . 10.392 -19.155 22.503 0.47 13.95 ? ? ? ? ? . 123 ILE A N 2350 ATOM 1014 N N B ILE A 2350 123 . 10.323 -19.113 22.485 0.53 15.23 ? ? ? ? ? . 123 ILE A N 2350 ATOM 1015 C CA A ILE A 2350 123 . 11.809 -18.977 22.850 0.47 14.95 ? ? ? ? ? . 123 ILE A CA 2350 ATOM 1016 C CA B ILE A 2350 123 . 11.762 -18.894 22.572 0.53 17.28 ? ? ? ? ? . 123 ILE A CA 2350 ATOM 1017 C C A ILE A 2350 123 . 12.170 -17.581 23.356 0.47 15.02 ? ? ? ? ? . 123 ILE A C 2350 ATOM 1018 C C B ILE A 2350 123 . 12.096 -17.681 23.473 0.53 16.15 ? ? ? ? ? . 123 ILE A C 2350 ATOM 1019 O O A ILE A 2350 123 . 13.349 -17.281 23.543 0.47 15.33 ? ? ? ? ? . 123 ILE A O 2350 ATOM 1020 O O B ILE A 2350 123 . 13.152 -17.646 24.107 0.53 15.98 ? ? ? ? ? . 123 ILE A O 2350 ATOM 1021 C CB A ILE A 2350 123 . 12.723 -19.369 21.683 0.47 14.78 ? ? ? ? ? . 123 ILE A CB 2350 ATOM 1022 C CB B ILE A 2350 123 . 12.330 -18.807 21.116 0.53 19.50 ? ? ? ? ? . 123 ILE A CB 2350 ATOM 1023 C CG1 A ILE A 2350 123 . 12.353 -18.591 20.417 0.47 14.37 ? ? ? ? ? . 123 ILE A CG1 2350 ATOM 1024 C CG2 A ILE A 2350 123 . 12.618 -20.868 21.444 0.47 15.29 ? ? ? ? ? . 123 ILE A CG2 2350 ATOM 1025 C CG1 B ILE A 2350 123 . 13.033 -20.116 20.737 0.53 21.28 ? ? ? ? ? . 123 ILE A CG1 2350 ATOM 1026 C CG2 B ILE A 2350 123 . 13.317 -17.675 20.906 0.53 20.71 ? ? ? ? ? . 123 ILE A CG2 2350 ATOM 1027 C CD1 A ILE A 2350 123 . 13.153 -19.012 19.200 0.47 14.19 ? ? ? ? ? . 123 ILE A CD1 2350 ATOM 1028 C CD1 B ILE A 2350 123 . 12.135 -21.339 20.747 0.53 22.34 ? ? ? ? ? . 123 ILE A CD1 2350 ATOM 1029 N N . GLY A 2350 124 . 11.173 -16.729 23.568 1.00 15.77 ? ? ? ? ? . 124 GLY A N 2350 ATOM 1030 C CA . GLY A 2350 124 . 11.373 -15.508 24.323 1.00 15.97 ? ? ? ? ? . 124 GLY A CA 2350 ATOM 1031 C C . GLY A 2350 124 . 10.096 -14.707 24.394 1.00 15.46 ? ? ? ? ? . 124 GLY A C 2350 ATOM 1032 O O . GLY A 2350 124 . 9.193 -14.882 23.581 1.00 15.31 ? ? ? ? ? . 124 GLY A O 2350 ATOM 1033 N N . THR A 2350 125 . 10.008 -13.856 25.405 1.00 14.42 ? ? ? ? ? . 125 THR A N 2350 ATOM 1034 C CA . THR A 2350 125 . 8.920 -12.890 25.529 1.00 14.27 ? ? ? ? ? . 125 THR A CA 2350 ATOM 1035 C C . THR A 2350 125 . 9.371 -11.431 25.677 1.00 14.34 ? ? ? ? ? . 125 THR A C 2350 ATOM 1036 O O . THR A 2350 125 . 8.520 -10.535 25.770 1.00 13.54 ? ? ? ? ? . 125 THR A O 2350 ATOM 1037 C CB . THR A 2350 125 . 8.063 -13.230 26.766 1.00 15.10 ? ? ? ? ? . 125 THR A CB 2350 ATOM 1038 C CG2 . THR A 2350 125 . 7.560 -14.673 26.687 1.00 15.56 ? ? ? ? ? . 125 THR A CG2 2350 ATOM 1039 O OG1 . THR A 2350 125 . 8.859 -13.073 27.951 1.00 15.70 ? ? ? ? ? . 125 THR A OG1 2350 ATOM 1040 N N A GLN A 2350 126 . 10.689 -11.200 25.676 0.65 15.74 ? ? ? ? ? . 126 GLN A N 2350 ATOM 1041 N N B GLN A 2350 126 . 10.683 -11.184 25.692 0.35 15.08 ? ? ? ? ? . 126 GLN A N 2350 ATOM 1042 C CA A GLN A 2350 126 . 11.267 -9.893 25.996 0.65 16.74 ? ? ? ? ? . 126 GLN A CA 2350 ATOM 1043 C CA B GLN A 2350 126 . 11.214 -9.851 25.975 0.35 15.65 ? ? ? ? ? . 126 GLN A CA 2350 ATOM 1044 C C A GLN A 2350 126 . 11.938 -9.209 24.799 0.65 16.96 ? ? ? ? ? . 126 GLN A C 2350 ATOM 1045 C C B GLN A 2350 126 . 11.948 -9.214 24.801 0.35 16.17 ? ? ? ? ? . 126 GLN A C 2350 ATOM 1046 O O A GLN A 2350 126 . 12.672 -8.231 24.982 0.65 18.20 ? ? ? ? ? . 126 GLN A O 2350 ATOM 1047 O O B GLN A 2350 126 . 12.738 -8.285 25.009 0.35 17.02 ? ? ? ? ? . 126 GLN A O 2350 ATOM 1048 C CB A GLN A 2350 126 . 12.281 -10.056 27.137 0.65 17.82 ? ? ? ? ? . 126 GLN A CB 2350 ATOM 1049 C CB B GLN A 2350 126 . 12.138 -9.924 27.186 0.35 15.92 ? ? ? ? ? . 126 GLN A CB 2350 ATOM 1050 C CG A GLN A 2350 126 . 11.700 -10.649 28.418 0.65 19.05 ? ? ? ? ? . 126 GLN A CG 2350 ATOM 1051 C CG B GLN A 2350 126 . 11.370 -10.101 28.485 0.35 16.11 ? ? ? ? ? . 126 GLN A CG 2350 ATOM 1052 C CD A GLN A 2350 126 . 10.613 -9.780 29.040 0.65 21.28 ? ? ? ? ? . 126 GLN A CD 2350 ATOM 1053 C CD B GLN A 2350 126 . 12.269 -10.217 29.694 0.35 16.65 ? ? ? ? ? . 126 GLN A CD 2350 ATOM 1054 N NE2 A GLN A 2350 126 . 9.365 -10.244 28.979 0.65 21.64 ? ? ? ? ? . 126 GLN A NE2 2350 ATOM 1055 O OE1 A GLN A 2350 126 . 10.896 -8.711 29.578 0.65 24.99 ? ? ? ? ? . 126 GLN A OE1 2350 ATOM 1056 N NE2 B GLN A 2350 126 . 12.111 -9.296 30.636 0.35 16.48 ? ? ? ? ? . 126 GLN A NE2 2350 ATOM 1057 O OE1 B GLN A 2350 126 . 13.085 -11.133 29.790 0.35 16.80 ? ? ? ? ? . 126 GLN A OE1 2350 ATOM 1058 N N . ALA A 2350 127 . 11.681 -9.681 23.580 1.00 16.07 ? ? ? ? ? . 127 ALA A N 2350 ATOM 1059 C CA . ALA A 2350 127 . 12.365 -9.138 22.395 1.00 15.77 ? ? ? ? ? . 127 ALA A CA 2350 ATOM 1060 C C . ALA A 2350 127 . 12.118 -7.629 22.136 1.00 16.92 ? ? ? ? ? . 127 ALA A C 2350 ATOM 1061 O O . ALA A 2350 127 . 12.988 -6.961 21.574 1.00 16.61 ? ? ? ? ? . 127 ALA A O 2350 ATOM 1062 C CB . ALA A 2350 127 . 12.088 -9.962 21.152 1.00 15.60 ? ? ? ? ? . 127 ALA A CB 2350 ATOM 1063 N N A ARG A 2350 128 . 10.956 -7.112 22.537 0.56 17.01 ? ? ? ? ? . 128 ARG A N 2350 ATOM 1064 N N B ARG A 2350 128 . 10.970 -7.103 22.563 0.44 16.65 ? ? ? ? ? . 128 ARG A N 2350 ATOM 1065 C CA A ARG A 2350 128 . 10.675 -5.662 22.452 0.56 17.35 ? ? ? ? ? . 128 ARG A CA 2350 ATOM 1066 C CA B ARG A 2350 128 . 10.711 -5.658 22.477 0.44 16.75 ? ? ? ? ? . 128 ARG A CA 2350 ATOM 1067 C C A ARG A 2350 128 . 11.742 -4.852 23.213 0.56 17.98 ? ? ? ? ? . 128 ARG A C 2350 ATOM 1068 C C B ARG A 2350 128 . 11.832 -4.909 23.210 0.44 17.06 ? ? ? ? ? . 128 ARG A C 2350 ATOM 1069 O O A ARG A 2350 128 . 12.117 -3.754 22.795 0.56 19.74 ? ? ? ? ? . 128 ARG A O 2350 ATOM 1070 O O B ARG A 2350 128 . 12.397 -3.949 22.691 0.44 18.15 ? ? ? ? ? . 128 ARG A O 2350 ATOM 1071 C CB A ARG A 2350 128 . 9.263 -5.347 22.979 0.56 17.73 ? ? ? ? ? . 128 ARG A CB 2350 ATOM 1072 C CB B ARG A 2350 128 . 9.339 -5.312 23.066 0.44 16.87 ? ? ? ? ? . 128 ARG A CB 2350 ATOM 1073 C CG A ARG A 2350 128 . 8.870 -3.865 23.016 0.56 18.71 ? ? ? ? ? . 128 ARG A CG 2350 ATOM 1074 C CG B ARG A 2350 128 . 8.901 -3.861 22.874 0.44 17.49 ? ? ? ? ? . 128 ARG A CG 2350 ATOM 1075 C CD A ARG A 2350 128 . 9.128 -3.215 24.373 0.56 20.16 ? ? ? ? ? . 128 ARG A CD 2350 ATOM 1076 C CD B ARG A 2350 128 . 9.642 -2.916 23.804 0.44 18.39 ? ? ? ? ? . 128 ARG A CD 2350 ATOM 1077 N NE A ARG A 2350 128 . 8.614 -1.848 24.461 0.56 21.19 ? ? ? ? ? . 128 ARG A NE 2350 ATOM 1078 N NE B ARG A 2350 128 . 9.174 -1.532 23.713 0.44 18.67 ? ? ? ? ? . 128 ARG A NE 2350 ATOM 1079 C CZ A ARG A 2350 128 . 9.152 -0.774 23.876 0.56 22.12 ? ? ? ? ? . 128 ARG A CZ 2350 ATOM 1080 C CZ B ARG A 2350 128 . 8.307 -0.973 24.557 0.44 18.88 ? ? ? ? ? . 128 ARG A CZ 2350 ATOM 1081 N NH1 A ARG A 2350 128 . 10.245 -0.862 23.118 0.56 21.19 ? ? ? ? ? 1+ 128 ARG A NH1 2350 ATOM 1082 N NH2 A ARG A 2350 128 . 8.582 0.419 24.051 0.56 22.67 ? ? ? ? ? . 128 ARG A NH2 2350 ATOM 1083 N NH1 B ARG A 2350 128 . 7.788 -1.677 25.551 0.44 18.59 ? ? ? ? ? 1+ 128 ARG A NH1 2350 ATOM 1084 N NH2 B ARG A 2350 128 . 7.951 0.296 24.402 0.44 19.51 ? ? ? ? ? . 128 ARG A NH2 2350 ATOM 1085 N N A THR A 2350 129 . 12.197 -5.402 24.338 0.56 16.60 ? ? ? ? ? . 129 THR A N 2350 ATOM 1086 N N B THR A 2350 129 . 12.172 -5.391 24.401 0.44 16.19 ? ? ? ? ? . 129 THR A N 2350 ATOM 1087 C CA A THR A 2350 129 . 13.260 -4.819 25.151 0.56 15.90 ? ? ? ? ? . 129 THR A CA 2350 ATOM 1088 C CA B THR A 2350 129 . 13.262 -4.829 25.190 0.44 15.82 ? ? ? ? ? . 129 THR A CA 2350 ATOM 1089 C C A THR A 2350 129 . 14.648 -5.072 24.556 0.56 15.75 ? ? ? ? ? . 129 THR A C 2350 ATOM 1090 C C B THR A 2350 129 . 14.652 -5.082 24.590 0.44 15.77 ? ? ? ? ? . 129 THR A C 2350 ATOM 1091 O O A THR A 2350 129 . 15.501 -4.173 24.523 0.56 14.19 ? ? ? ? ? . 129 THR A O 2350 ATOM 1092 O O B THR A 2350 129 . 15.508 -4.188 24.583 0.44 14.57 ? ? ? ? ? . 129 THR A O 2350 ATOM 1093 C CB A THR A 2350 129 . 13.199 -5.413 26.563 0.56 16.22 ? ? ? ? ? . 129 THR A CB 2350 ATOM 1094 C CB B THR A 2350 129 . 13.239 -5.411 26.607 0.44 16.28 ? ? ? ? ? . 129 THR A CB 2350 ATOM 1095 C CG2 A THR A 2350 129 . 14.194 -4.750 27.499 0.56 16.27 ? ? ? ? ? . 129 THR A CG2 2350 ATOM 1096 O OG1 A THR A 2350 129 . 11.866 -5.240 27.067 0.56 15.54 ? ? ? ? ? . 129 THR A OG1 2350 ATOM 1097 C CG2 B THR A 2350 129 . 14.425 -4.927 27.397 0.44 16.31 ? ? ? ? ? . 129 THR A CG2 2350 ATOM 1098 O OG1 B THR A 2350 129 . 12.025 -5.011 27.257 0.44 16.08 ? ? ? ? ? . 129 THR A OG1 2350 ATOM 1099 N N . ARG A 2350 130 . 14.877 -6.301 24.106 1.00 15.66 ? ? ? ? ? . 130 ARG A N 2350 ATOM 1100 C CA . ARG A 2350 130 . 16.188 -6.692 23.577 1.00 16.35 ? ? ? ? ? . 130 ARG A CA 2350 ATOM 1101 C C . ARG A 2350 130 . 16.559 -5.897 22.320 1.00 15.65 ? ? ? ? ? . 130 ARG A C 2350 ATOM 1102 O O . ARG A 2350 130 . 17.720 -5.558 22.136 1.00 15.70 ? ? ? ? ? . 130 ARG A O 2350 ATOM 1103 C CB . ARG A 2350 130 . 16.246 -8.188 23.306 1.00 18.25 ? ? ? ? ? . 130 ARG A CB 2350 ATOM 1104 C CG . ARG A 2350 130 . 16.058 -9.052 24.544 1.00 20.23 ? ? ? ? ? . 130 ARG A CG 2350 ATOM 1105 C CD . ARG A 2350 130 . 17.267 -9.045 25.461 1.00 24.15 ? ? ? ? ? . 130 ARG A CD 2350 ATOM 1106 N NE . ARG A 2350 130 . 16.962 -9.671 26.747 1.00 26.08 ? ? ? ? ? . 130 ARG A NE 2350 ATOM 1107 C CZ . ARG A 2350 130 . 16.384 -9.059 27.784 1.00 29.65 ? ? ? ? ? . 130 ARG A CZ 2350 ATOM 1108 N NH1 . ARG A 2350 130 . 15.999 -7.782 27.725 1.00 30.49 ? ? ? ? ? 1+ 130 ARG A NH1 2350 ATOM 1109 N NH2 . ARG A 2350 130 . 16.171 -9.748 28.906 1.00 33.51 ? ? ? ? ? . 130 ARG A NH2 2350 ATOM 1110 N N . VAL A 2350 131 . 15.561 -5.570 21.501 1.00 15.55 ? ? ? ? ? . 131 VAL A N 2350 ATOM 1111 C CA . VAL A 2350 131 . 15.755 -4.735 20.300 1.00 16.06 ? ? ? ? ? . 131 VAL A CA 2350 ATOM 1112 C C . VAL A 2350 131 . 16.319 -3.355 20.678 1.00 15.16 ? ? ? ? ? . 131 VAL A C 2350 ATOM 1113 O O . VAL A 2350 131 . 17.149 -2.806 19.958 1.00 14.17 ? ? ? ? ? . 131 VAL A O 2350 ATOM 1114 C CB . VAL A 2350 131 . 14.431 -4.608 19.503 1.00 18.89 ? ? ? ? ? . 131 VAL A CB 2350 ATOM 1115 C CG1 . VAL A 2350 131 . 14.491 -3.492 18.465 1.00 19.08 ? ? ? ? ? . 131 VAL A CG1 2350 ATOM 1116 C CG2 . VAL A 2350 131 . 14.079 -5.950 18.859 1.00 21.65 ? ? ? ? ? . 131 VAL A CG2 2350 ATOM 1117 N N A ILE A 2350 132 . 15.856 -2.817 21.806 0.19 15.13 ? ? ? ? ? . 132 ILE A N 2350 ATOM 1118 N N B ILE A 2350 132 . 15.884 -2.809 21.816 0.81 15.27 ? ? ? ? ? . 132 ILE A N 2350 ATOM 1119 C CA A ILE A 2350 132 . 16.341 -1.547 22.332 0.19 15.00 ? ? ? ? ? . 132 ILE A CA 2350 ATOM 1120 C CA B ILE A 2350 132 . 16.395 -1.520 22.293 0.81 14.70 ? ? ? ? ? . 132 ILE A CA 2350 ATOM 1121 C C A ILE A 2350 132 . 17.808 -1.612 22.736 0.19 14.96 ? ? ? ? ? . 132 ILE A C 2350 ATOM 1122 C C B ILE A 2350 132 . 17.849 -1.630 22.707 0.81 14.54 ? ? ? ? ? . 132 ILE A C 2350 ATOM 1123 O O A ILE A 2350 132 . 18.613 -0.783 22.313 0.19 14.79 ? ? ? ? ? . 132 ILE A O 2350 ATOM 1124 O O B ILE A 2350 132 . 18.686 -0.831 22.296 0.81 13.48 ? ? ? ? ? . 132 ILE A O 2350 ATOM 1125 C CB A ILE A 2350 132 . 15.520 -1.130 23.564 0.19 14.92 ? ? ? ? ? . 132 ILE A CB 2350 ATOM 1126 C CB B ILE A 2350 132 . 15.575 -0.974 23.489 0.81 14.72 ? ? ? ? ? . 132 ILE A CB 2350 ATOM 1127 C CG1 A ILE A 2350 132 . 14.034 -1.319 23.280 0.19 15.02 ? ? ? ? ? . 132 ILE A CG1 2350 ATOM 1128 C CG2 A ILE A 2350 132 . 15.824 0.307 23.942 0.19 14.66 ? ? ? ? ? . 132 ILE A CG2 2350 ATOM 1129 C CG1 B ILE A 2350 132 . 14.149 -0.656 23.059 0.81 15.47 ? ? ? ? ? . 132 ILE A CG1 2350 ATOM 1130 C CG2 B ILE A 2350 132 . 16.235 0.255 24.089 0.81 13.99 ? ? ? ? ? . 132 ILE A CG2 2350 ATOM 1131 C CD1 A ILE A 2350 132 . 13.567 -0.581 22.051 0.19 15.23 ? ? ? ? ? . 132 ILE A CD1 2350 ATOM 1132 C CD1 B ILE A 2350 132 . 13.182 -0.605 24.230 0.81 16.62 ? ? ? ? ? . 132 ILE A CD1 2350 ATOM 1133 N N . GLU A 2350 133 . 18.144 -2.599 23.559 1.00 14.85 ? ? ? ? ? . 133 GLU A N 2350 ATOM 1134 C CA . GLU A 2350 133 . 19.500 -2.725 24.095 1.00 15.86 ? ? ? ? ? . 133 GLU A CA 2350 ATOM 1135 C C . GLU A 2350 133 . 20.510 -3.300 23.114 1.00 15.18 ? ? ? ? ? . 133 GLU A C 2350 ATOM 1136 O O . GLU A 2350 133 . 21.694 -3.025 23.243 1.00 14.71 ? ? ? ? ? . 133 GLU A O 2350 ATOM 1137 C CB . GLU A 2350 133 . 19.516 -3.523 25.385 1.00 18.34 ? ? ? ? ? . 133 GLU A CB 2350 ATOM 1138 C CG . GLU A 2350 133 . 19.099 -4.959 25.269 1.00 21.00 ? ? ? ? ? . 133 GLU A CG 2350 ATOM 1139 C CD . GLU A 2350 133 . 19.009 -5.600 26.628 1.00 24.62 ? ? ? ? ? . 133 GLU A CD 2350 ATOM 1140 O OE1 . GLU A 2350 133 . 17.888 -5.653 27.182 1.00 24.54 ? ? ? ? ? . 133 GLU A OE1 2350 ATOM 1141 O OE2 . GLU A 2350 133 . 20.070 -6.015 27.133 1.00 24.87 ? ? ? ? ? 1- 133 GLU A OE2 2350 ATOM 1142 N N . ASP A 2350 134 . 20.031 -4.102 22.163 1.00 15.80 ? ? ? ? ? . 134 ASP A N 2350 ATOM 1143 C CA . ASP A 2350 134 . 20.885 -4.847 21.228 1.00 16.53 ? ? ? ? ? . 134 ASP A CA 2350 ATOM 1144 C C . ASP A 2350 134 . 20.373 -4.627 19.798 1.00 16.35 ? ? ? ? ? . 134 ASP A C 2350 ATOM 1145 O O . ASP A 2350 134 . 19.922 -5.562 19.131 1.00 16.33 ? ? ? ? ? . 134 ASP A O 2350 ATOM 1146 C CB . ASP A 2350 134 . 20.881 -6.341 21.606 1.00 16.03 ? ? ? ? ? . 134 ASP A CB 2350 ATOM 1147 C CG . ASP A 2350 134 . 21.859 -7.184 20.769 1.00 16.81 ? ? ? ? ? . 134 ASP A CG 2350 ATOM 1148 O OD1 . ASP A 2350 134 . 22.869 -6.642 20.264 1.00 16.39 ? ? ? ? ? . 134 ASP A OD1 2350 ATOM 1149 O OD2 . ASP A 2350 134 . 21.614 -8.404 20.635 1.00 16.25 ? ? ? ? ? 1- 134 ASP A OD2 2350 ATOM 1150 N N . PRO A 2350 135 . 20.451 -3.379 19.309 1.00 15.65 ? ? ? ? ? . 135 PRO A N 2350 ATOM 1151 C CA . PRO A 2350 135 . 19.917 -3.103 17.962 1.00 16.45 ? ? ? ? ? . 135 PRO A CA 2350 ATOM 1152 C C . PRO A 2350 135 . 20.699 -3.798 16.828 1.00 17.49 ? ? ? ? ? . 135 PRO A C 2350 ATOM 1153 O O . PRO A 2350 135 . 20.164 -3.961 15.727 1.00 19.27 ? ? ? ? ? . 135 PRO A O 2350 ATOM 1154 C CB . PRO A 2350 135 . 20.036 -1.580 17.849 1.00 16.15 ? ? ? ? ? . 135 PRO A CB 2350 ATOM 1155 C CG . PRO A 2350 135 . 21.147 -1.228 18.767 1.00 15.72 ? ? ? ? ? . 135 PRO A CG 2350 ATOM 1156 C CD . PRO A 2350 135 . 21.003 -2.165 19.931 1.00 16.34 ? ? ? ? ? . 135 PRO A CD 2350 ATOM 1157 N N . ASP A 2350 136 . 21.943 -4.192 17.089 1.00 18.50 ? ? ? ? ? . 136 ASP A N 2350 ATOM 1158 C CA . ASP A 2350 136 . 22.709 -4.962 16.102 1.00 18.72 ? ? ? ? ? . 136 ASP A CA 2350 ATOM 1159 C C . ASP A 2350 136 . 22.475 -6.472 16.207 1.00 19.15 ? ? ? ? ? . 136 ASP A C 2350 ATOM 1160 O O . ASP A 2350 136 . 23.067 -7.249 15.446 1.00 18.36 ? ? ? ? ? . 136 ASP A O 2350 ATOM 1161 C CB . ASP A 2350 136 . 24.208 -4.659 16.203 1.00 19.68 ? ? ? ? ? . 136 ASP A CB 2350 ATOM 1162 C CG . ASP A 2350 136 . 24.951 -5.002 14.926 1.00 20.65 ? ? ? ? ? . 136 ASP A CG 2350 ATOM 1163 O OD1 . ASP A 2350 136 . 24.302 -4.958 13.849 1.00 19.34 ? ? ? ? ? . 136 ASP A OD1 2350 ATOM 1164 O OD2 . ASP A 2350 136 . 26.167 -5.316 14.990 1.00 18.99 ? ? ? ? ? 1- 136 ASP A OD2 2350 ATOM 1165 N N . GLY A 2350 137 . 21.644 -6.897 17.152 1.00 19.37 ? ? ? ? ? . 137 GLY A N 2350 ATOM 1166 C CA . GLY A 2350 137 . 21.276 -8.295 17.269 1.00 18.65 ? ? ? ? ? . 137 GLY A CA 2350 ATOM 1167 C C . GLY A 2350 137 . 22.434 -9.246 17.520 1.00 18.62 ? ? ? ? ? . 137 GLY A C 2350 ATOM 1168 O O . GLY A 2350 137 . 22.362 -10.405 17.126 1.00 17.20 ? ? ? ? ? . 137 GLY A O 2350 ATOM 1169 N N . ALA A 2350 138 . 23.489 -8.772 18.186 1.00 18.23 ? ? ? ? ? . 138 ALA A N 2350 ATOM 1170 C CA . ALA A 2350 138 . 24.618 -9.638 18.572 1.00 18.91 ? ? ? ? ? . 138 ALA A CA 2350 ATOM 1171 C C . ALA A 2350 138 . 24.172 -10.873 19.359 1.00 18.87 ? ? ? ? ? . 138 ALA A C 2350 ATOM 1172 O O . ALA A 2350 138 . 24.763 -11.937 19.209 1.00 18.45 ? ? ? ? ? . 138 ALA A O 2350 ATOM 1173 C CB . ALA A 2350 138 . 25.646 -8.865 19.388 1.00 19.07 ? ? ? ? ? . 138 ALA A CB 2350 ATOM 1174 N N . ASN A 2350 139 . 23.150 -10.721 20.207 1.00 17.91 ? ? ? ? ? . 139 ASN A N 2350 ATOM 1175 C CA . ASN A 2350 139 . 22.657 -11.826 21.042 1.00 18.78 ? ? ? ? ? . 139 ASN A CA 2350 ATOM 1176 C C . ASN A 2350 139 . 21.320 -12.415 20.575 1.00 18.34 ? ? ? ? ? . 139 ASN A C 2350 ATOM 1177 O O . ASN A 2350 139 . 20.716 -13.222 21.284 1.00 16.63 ? ? ? ? ? . 139 ASN A O 2350 ATOM 1178 C CB . ASN A 2350 139 . 22.558 -11.357 22.493 1.00 20.43 ? ? ? ? ? . 139 ASN A CB 2350 ATOM 1179 C CG . ASN A 2350 139 . 23.907 -11.007 23.077 1.00 22.54 ? ? ? ? ? . 139 ASN A CG 2350 ATOM 1180 N ND2 . ASN A 2350 139 . 24.033 -9.800 23.604 1.00 24.70 ? ? ? ? ? . 139 ASN A ND2 2350 ATOM 1181 O OD1 . ASN A 2350 139 . 24.826 -11.813 23.049 1.00 25.00 ? ? ? ? ? . 139 ASN A OD1 2350 ATOM 1182 N N . PHE A 2350 140 . 20.862 -12.019 19.387 1.00 19.01 ? ? ? ? ? . 140 PHE A N 2350 ATOM 1183 C CA . PHE A 2350 140 . 19.669 -12.603 18.768 1.00 20.41 ? ? ? ? ? . 140 PHE A CA 2350 ATOM 1184 C C . PHE A 2350 140 . 19.812 -14.133 18.747 1.00 20.42 ? ? ? ? ? . 140 PHE A C 2350 ATOM 1185 O O . PHE A 2350 140 . 20.913 -14.633 18.513 1.00 17.90 ? ? ? ? ? . 140 PHE A O 2350 ATOM 1186 C CB . PHE A 2350 140 . 19.522 -12.084 17.327 1.00 21.52 ? ? ? ? ? . 140 PHE A CB 2350 ATOM 1187 C CG . PHE A 2350 140 . 18.452 -12.782 16.532 1.00 22.24 ? ? ? ? ? . 140 PHE A CG 2350 ATOM 1188 C CD1 . PHE A 2350 140 . 18.719 -13.998 15.901 1.00 21.67 ? ? ? ? ? . 140 PHE A CD1 2350 ATOM 1189 C CD2 . PHE A 2350 140 . 17.181 -12.252 16.440 1.00 21.18 ? ? ? ? ? . 140 PHE A CD2 2350 ATOM 1190 C CE1 . PHE A 2350 140 . 17.745 -14.662 15.185 1.00 20.84 ? ? ? ? ? . 140 PHE A CE1 2350 ATOM 1191 C CE2 . PHE A 2350 140 . 16.205 -12.923 15.721 1.00 21.80 ? ? ? ? ? . 140 PHE A CE2 2350 ATOM 1192 C CZ . PHE A 2350 140 . 16.490 -14.121 15.089 1.00 20.62 ? ? ? ? ? . 140 PHE A CZ 2350 ATOM 1193 N N . PRO A 2350 141 . 18.713 -14.878 18.978 1.00 19.68 ? ? ? ? ? . 141 PRO A N 2350 ATOM 1194 C CA . PRO A 2350 141 . 17.322 -14.496 19.270 1.00 20.19 ? ? ? ? ? . 141 PRO A CA 2350 ATOM 1195 C C . PRO A 2350 141 . 17.031 -14.317 20.773 1.00 20.52 ? ? ? ? ? . 141 PRO A C 2350 ATOM 1196 O O . PRO A 2350 141 . 15.896 -14.485 21.219 1.00 20.28 ? ? ? ? ? . 141 PRO A O 2350 ATOM 1197 C CB . PRO A 2350 141 . 16.531 -15.649 18.667 1.00 20.58 ? ? ? ? ? . 141 PRO A CB 2350 ATOM 1198 C CG . PRO A 2350 141 . 17.408 -16.822 18.883 1.00 22.19 ? ? ? ? ? . 141 PRO A CG 2350 ATOM 1199 C CD . PRO A 2350 141 . 18.835 -16.342 18.841 1.00 21.97 ? ? ? ? ? . 141 PRO A CD 2350 ATOM 1200 N N . TRP A 2350 142 . 18.070 -13.962 21.521 1.00 19.76 ? ? ? ? ? . 142 TRP A N 2350 ATOM 1201 C CA . TRP A 2350 142 . 17.983 -13.534 22.901 1.00 21.33 ? ? ? ? ? . 142 TRP A CA 2350 ATOM 1202 C C . TRP A 2350 142 . 17.420 -14.620 23.822 1.00 25.77 ? ? ? ? ? . 142 TRP A C 2350 ATOM 1203 O O . TRP A 2350 142 . 16.345 -14.426 24.421 1.00 25.77 ? ? ? ? ? . 142 TRP A O 2350 ATOM 1204 C CB . TRP A 2350 142 . 17.210 -12.224 23.014 1.00 19.99 ? ? ? ? ? . 142 TRP A CB 2350 ATOM 1205 C CG . TRP A 2350 142 . 17.778 -11.119 22.165 1.00 18.70 ? ? ? ? ? . 142 TRP A CG 2350 ATOM 1206 C CD1 . TRP A 2350 142 . 18.994 -10.522 22.306 1.00 18.19 ? ? ? ? ? . 142 TRP A CD1 2350 ATOM 1207 C CD2 . TRP A 2350 142 . 17.132 -10.461 21.076 1.00 17.96 ? ? ? ? ? . 142 TRP A CD2 2350 ATOM 1208 C CE2 . TRP A 2350 142 . 18.022 -9.480 20.595 1.00 18.04 ? ? ? ? ? . 142 TRP A CE2 2350 ATOM 1209 C CE3 . TRP A 2350 142 . 15.890 -10.610 20.454 1.00 18.59 ? ? ? ? ? . 142 TRP A CE3 2350 ATOM 1210 N NE1 . TRP A 2350 142 . 19.156 -9.555 21.357 1.00 17.87 ? ? ? ? ? . 142 TRP A NE1 2350 ATOM 1211 C CZ2 . TRP A 2350 142 . 17.711 -8.645 19.516 1.00 17.55 ? ? ? ? ? . 142 TRP A CZ2 2350 ATOM 1212 C CZ3 . TRP A 2350 142 . 15.574 -9.787 19.397 1.00 19.05 ? ? ? ? ? . 142 TRP A CZ3 2350 ATOM 1213 C CH2 . TRP A 2350 142 . 16.486 -8.803 18.938 1.00 18.51 ? ? ? ? ? . 142 TRP A CH2 2350 ATOM 1214 N N A PRO A 2350 143 . 18.105 -15.758 23.889 0.43 25.91 ? ? ? ? ? . 143 PRO A N 2350 ATOM 1215 N N B PRO A 2350 143 . 18.145 -15.709 23.950 0.57 28.56 ? ? ? ? ? . 143 PRO A N 2350 ATOM 1216 C CA A PRO A 2350 143 . 17.728 -16.750 24.895 0.43 26.55 ? ? ? ? ? . 143 PRO A CA 2350 ATOM 1217 C CA B PRO A 2350 143 . 17.683 -16.682 24.925 0.57 30.66 ? ? ? ? ? . 143 PRO A CA 2350 ATOM 1218 C C A PRO A 2350 143 . 18.114 -16.109 26.241 0.43 27.90 ? ? ? ? ? . 143 PRO A C 2350 ATOM 1219 C C B PRO A 2350 143 . 18.148 -16.217 26.307 0.57 33.98 ? ? ? ? ? . 143 PRO A C 2350 ATOM 1220 O O A PRO A 2350 143 . 19.033 -15.280 26.295 0.43 29.57 ? ? ? ? ? . 143 PRO A O 2350 ATOM 1221 O O B PRO A 2350 143 . 17.516 -16.577 27.281 0.57 40.90 ? ? ? ? ? . 143 PRO A O 2350 ATOM 1222 C CB A PRO A 2350 143 . 18.662 -17.907 24.589 0.43 26.47 ? ? ? ? ? . 143 PRO A CB 2350 ATOM 1223 C CB B PRO A 2350 143 . 18.464 -17.930 24.540 0.57 31.72 ? ? ? ? ? . 143 PRO A CB 2350 ATOM 1224 C CG A PRO A 2350 143 . 19.869 -17.262 24.025 0.43 27.23 ? ? ? ? ? . 143 PRO A CG 2350 ATOM 1225 C CG B PRO A 2350 143 . 19.714 -17.418 23.925 0.57 32.06 ? ? ? ? ? . 143 PRO A CG 2350 ATOM 1226 C CD A PRO A 2350 143 . 19.399 -16.061 23.265 0.43 26.55 ? ? ? ? ? . 143 PRO A CD 2350 ATOM 1227 C CD B PRO A 2350 143 . 19.334 -16.157 23.214 0.57 30.24 ? ? ? ? ? . 143 PRO A CD 2350 ATOM 1228 N N A ASN A 2350 144 . 17.447 -16.445 27.332 0.43 29.72 ? ? ? ? ? . 144 ASN A N 2350 ATOM 1229 N N B ASN A 2350 144 . 19.154 -15.333 26.349 0.57 43.48 ? ? ? ? ? . 144 ASN A N 2350 ATOM 1230 C CA A ASN A 2350 144 . 17.845 -15.794 28.584 0.43 31.67 ? ? ? ? ? . 144 ASN A CA 2350 ATOM 1231 C CA B ASN A 2350 144 . 19.879 -14.941 27.567 0.57 41.21 ? ? ? ? ? . 144 ASN A CA 2350 ATOM 1232 C C A ASN A 2350 144 . 19.155 -16.376 29.126 0.43 34.18 ? ? ? ? ? . 144 ASN A C 2350 ATOM 1233 C C B ASN A 2350 144 . 19.928 -16.021 28.652 0.57 46.68 ? ? ? ? ? . 144 ASN A C 2350 ATOM 1234 O O A ASN A 2350 144 . 19.292 -16.688 30.295 0.43 37.95 ? ? ? ? ? . 144 ASN A O 2350 ATOM 1235 O O B ASN A 2350 144 . 20.998 -16.385 29.101 0.57 44.85 ? ? ? ? ? . 144 ASN A O 2350 ATOM 1236 C CB A ASN A 2350 144 . 16.725 -15.785 29.643 0.43 31.33 ? ? ? ? ? . 144 ASN A CB 2350 ATOM 1237 C CB B ASN A 2350 144 . 19.766 -13.486 28.103 0.57 37.67 ? ? ? ? ? . 144 ASN A CB 2350 ATOM 1238 C CG A ASN A 2350 144 . 16.683 -14.482 30.437 0.43 30.34 ? ? ? ? ? . 144 ASN A CG 2350 ATOM 1239 C CG B ASN A 2350 144 . 18.456 -12.779 27.779 0.57 32.86 ? ? ? ? ? . 144 ASN A CG 2350 ATOM 1240 N ND2 A ASN A 2350 144 . 15.880 -14.449 31.481 0.43 29.27 ? ? ? ? ? . 144 ASN A ND2 2350 ATOM 1241 O OD1 A ASN A 2350 144 . 17.350 -13.516 30.096 0.43 30.43 ? ? ? ? ? . 144 ASN A OD1 2350 ATOM 1242 N ND2 B ASN A 2350 144 . 18.201 -12.534 26.509 0.57 28.80 ? ? ? ? ? . 144 ASN A ND2 2350 ATOM 1243 O OD1 B ASN A 2350 144 . 17.731 -12.384 28.685 0.57 29.27 ? ? ? ? ? . 144 ASN A OD1 2350 ATOM 1244 O OXT A ASN A 2350 144 . 20.133 -16.520 28.420 0.43 34.42 ? ? ? ? ? 1- 144 ASN A OXT 2350 ATOM 1245 O OXT B ASN A 2350 144 . 18.927 -16.583 29.037 0.57 53.68 ? ? ? ? ? 1- 144 ASN A OXT 2350 ATOM 1247 N N A MET B 2350 1 . -11.706 5.017 56.656 0.43 22.18 ? ? ? ? ? . 1 MET B N 2350 ATOM 1248 N N B MET B 2350 1 . -10.263 6.625 55.038 0.57 23.08 ? ? ? ? ? . 1 MET B N 2350 ATOM 1249 C CA A MET B 2350 1 . -12.271 6.276 56.125 0.43 21.05 ? ? ? ? ? . 1 MET B CA 2350 ATOM 1250 C CA B MET B 2350 1 . -11.550 6.284 55.722 0.57 21.74 ? ? ? ? ? . 1 MET B CA 2350 ATOM 1251 C C A MET B 2350 1 . -12.880 6.055 54.737 0.43 18.63 ? ? ? ? ? . 1 MET B C 2350 ATOM 1252 C C B MET B 2350 1 . -12.611 6.015 54.645 0.57 18.84 ? ? ? ? ? . 1 MET B C 2350 ATOM 1253 O O A MET B 2350 1 . -13.635 6.891 54.262 0.43 17.39 ? ? ? ? ? . 1 MET B O 2350 ATOM 1254 O O B MET B 2350 1 . -13.609 6.729 54.541 0.57 17.32 ? ? ? ? ? . 1 MET B O 2350 ATOM 1255 C CB A MET B 2350 1 . -11.191 7.364 56.082 0.43 23.26 ? ? ? ? ? . 1 MET B CB 2350 ATOM 1256 C CB B MET B 2350 1 . -11.956 7.421 56.682 0.57 22.75 ? ? ? ? ? . 1 MET B CB 2350 ATOM 1257 C CG A MET B 2350 1 . -11.725 8.759 55.817 0.43 24.37 ? ? ? ? ? . 1 MET B CG 2350 ATOM 1258 C CG B MET B 2350 1 . -11.759 8.816 56.094 0.57 25.92 ? ? ? ? ? . 1 MET B CG 2350 ATOM 1259 S SD A MET B 2350 1 . -12.403 9.556 57.288 0.43 28.56 ? ? ? ? ? . 1 MET B SD 2350 ATOM 1260 S SD B MET B 2350 1 . -12.629 10.143 56.953 0.57 32.83 ? ? ? ? ? . 1 MET B SD 2350 ATOM 1261 C CE A MET B 2350 1 . -10.917 10.251 58.005 0.43 26.64 ? ? ? ? ? . 1 MET B CE 2350 ATOM 1262 C CE B MET B 2350 1 . -11.453 10.487 58.263 0.57 31.42 ? ? ? ? ? . 1 MET B CE 2350 ATOM 1263 N N A SER B 2350 2 . -12.566 4.937 54.084 0.43 16.60 ? ? ? ? ? . 2 SER B N 2350 ATOM 1264 N N B SER B 2350 2 . -12.362 4.985 53.835 0.57 16.28 ? ? ? ? ? . 2 SER B N 2350 ATOM 1265 C CA A SER B 2350 2 . -13.172 4.646 52.781 0.43 15.75 ? ? ? ? ? . 2 SER B CA 2350 ATOM 1266 C CA B SER B 2350 2 . -13.169 4.686 52.653 0.57 15.59 ? ? ? ? ? . 2 SER B CA 2350 ATOM 1267 C C A SER B 2350 2 . -13.107 3.179 52.350 0.43 15.40 ? ? ? ? ? . 2 SER B C 2350 ATOM 1268 C C B SER B 2350 2 . -13.096 3.213 52.265 0.57 15.32 ? ? ? ? ? . 2 SER B C 2350 ATOM 1269 O O A SER B 2350 2 . -12.045 2.561 52.401 0.43 14.21 ? ? ? ? ? . 2 SER B O 2350 ATOM 1270 O O B SER B 2350 2 . -12.017 2.623 52.257 0.57 13.61 ? ? ? ? ? . 2 SER B O 2350 ATOM 1271 C CB A SER B 2350 2 . -12.523 5.490 51.687 0.43 15.63 ? ? ? ? ? . 2 SER B CB 2350 ATOM 1272 C CB B SER B 2350 2 . -12.692 5.524 51.467 0.57 15.50 ? ? ? ? ? . 2 SER B CB 2350 ATOM 1273 O OG A SER B 2350 2 . -13.065 5.154 50.418 0.43 15.21 ? ? ? ? ? . 2 SER B OG 2350 ATOM 1274 O OG B SER B 2350 2 . -13.386 5.187 50.274 0.57 14.86 ? ? ? ? ? . 2 SER B OG 2350 ATOM 1275 N N . GLY B 2350 3 . -14.245 2.642 51.902 1.00 14.47 ? ? ? ? ? . 3 GLY B N 2350 ATOM 1276 C CA . GLY B 2350 3 . -14.298 1.314 51.277 1.00 14.80 ? ? ? ? ? . 3 GLY B CA 2350 ATOM 1277 C C . GLY B 2350 3 . -13.580 1.196 49.938 1.00 15.16 ? ? ? ? ? . 3 GLY B C 2350 ATOM 1278 O O . GLY B 2350 3 . -13.220 0.087 49.533 1.00 15.61 ? ? ? ? ? . 3 GLY B O 2350 ATOM 1279 N N . LEU B 2350 4 . -13.361 2.324 49.247 1.00 14.58 ? ? ? ? ? . 4 LEU B N 2350 ATOM 1280 C CA . LEU B 2350 4 . -12.556 2.342 48.006 1.00 15.55 ? ? ? ? ? . 4 LEU B CA 2350 ATOM 1281 C C . LEU B 2350 4 . -11.104 1.921 48.248 1.00 14.48 ? ? ? ? ? . 4 LEU B C 2350 ATOM 1282 O O . LEU B 2350 4 . -10.423 1.450 47.326 1.00 15.12 ? ? ? ? ? . 4 LEU B O 2350 ATOM 1283 C CB . LEU B 2350 4 . -12.567 3.735 47.363 1.00 15.28 ? ? ? ? ? . 4 LEU B CB 2350 ATOM 1284 C CG . LEU B 2350 4 . -13.938 4.254 46.926 1.00 16.58 ? ? ? ? ? . 4 LEU B CG 2350 ATOM 1285 C CD1 . LEU B 2350 4 . -13.856 5.731 46.587 1.00 17.96 ? ? ? ? ? . 4 LEU B CD1 2350 ATOM 1286 C CD2 . LEU B 2350 4 . -14.485 3.440 45.759 1.00 18.60 ? ? ? ? ? . 4 LEU B CD2 2350 ATOM 1287 N N . ALA B 2350 5 . -10.626 2.111 49.479 1.00 14.44 ? ? ? ? ? . 5 ALA B N 2350 ATOM 1288 C CA . ALA B 2350 5 . -9.297 1.636 49.884 1.00 14.79 ? ? ? ? ? . 5 ALA B CA 2350 ATOM 1289 C C . ALA B 2350 5 . -9.128 0.108 49.844 1.00 14.46 ? ? ? ? ? . 5 ALA B C 2350 ATOM 1290 O O . ALA B 2350 5 . -8.012 -0.380 49.926 1.00 14.88 ? ? ? ? ? . 5 ALA B O 2350 ATOM 1291 C CB . ALA B 2350 5 . -8.953 2.150 51.264 1.00 15.63 ? ? ? ? ? . 5 ALA B CB 2350 ATOM 1292 N N . LYS B 2350 6 . -10.227 -0.637 49.760 1.00 14.86 ? ? ? ? ? . 6 LYS B N 2350 ATOM 1293 C CA . LYS B 2350 6 . -10.178 -2.076 49.494 1.00 16.27 ? ? ? ? ? . 6 LYS B CA 2350 ATOM 1294 C C . LYS B 2350 6 . -9.396 -2.367 48.203 1.00 16.76 ? ? ? ? ? . 6 LYS B C 2350 ATOM 1295 O O . LYS B 2350 6 . -8.616 -3.325 48.141 1.00 16.83 ? ? ? ? ? . 6 LYS B O 2350 ATOM 1296 C CB . LYS B 2350 6 . -11.604 -2.645 49.393 1.00 16.82 ? ? ? ? ? . 6 LYS B CB 2350 ATOM 1297 C CG . LYS B 2350 6 . -11.681 -4.156 49.223 1.00 17.15 ? ? ? ? ? . 6 LYS B CG 2350 ATOM 1298 C CD . LYS B 2350 6 . -13.116 -4.635 49.318 1.00 17.25 ? ? ? ? ? . 6 LYS B CD 2350 ATOM 1299 C CE . LYS B 2350 6 . -13.189 -6.150 49.305 1.00 17.66 ? ? ? ? ? . 6 LYS B CE 2350 ATOM 1300 N NZ . LYS B 2350 6 . -14.571 -6.571 49.617 1.00 17.19 ? ? ? ? ? 1+ 6 LYS B NZ 2350 ATOM 1301 N N . TYR B 2350 7 . -9.617 -1.529 47.190 1.00 19.75 ? ? ? ? ? . 7 TYR B N 2350 ATOM 1302 C CA . TYR B 2350 7 . -9.014 -1.687 45.856 1.00 21.36 ? ? ? ? ? . 7 TYR B CA 2350 ATOM 1303 C C . TYR B 2350 7 . -7.965 -0.642 45.491 1.00 21.83 ? ? ? ? ? . 7 TYR B C 2350 ATOM 1304 O O . TYR B 2350 7 . -7.142 -0.868 44.582 1.00 23.46 ? ? ? ? ? . 7 TYR B O 2350 ATOM 1305 C CB . TYR B 2350 7 . -10.127 -1.690 44.823 1.00 23.09 ? ? ? ? ? . 7 TYR B CB 2350 ATOM 1306 C CG . TYR B 2350 7 . -11.029 -2.868 45.004 1.00 24.75 ? ? ? ? ? . 7 TYR B CG 2350 ATOM 1307 C CD1 . TYR B 2350 7 . -10.552 -4.151 44.794 1.00 24.42 ? ? ? ? ? . 7 TYR B CD1 2350 ATOM 1308 C CD2 . TYR B 2350 7 . -12.353 -2.714 45.400 1.00 27.18 ? ? ? ? ? . 7 TYR B CD2 2350 ATOM 1309 C CE1 . TYR B 2350 7 . -11.363 -5.257 44.967 1.00 27.58 ? ? ? ? ? . 7 TYR B CE1 2350 ATOM 1310 C CE2 . TYR B 2350 7 . -13.172 -3.816 45.574 1.00 27.12 ? ? ? ? ? . 7 TYR B CE2 2350 ATOM 1311 C CZ . TYR B 2350 7 . -12.674 -5.083 45.353 1.00 29.00 ? ? ? ? ? . 7 TYR B CZ 2350 ATOM 1312 O OH . TYR B 2350 7 . -13.474 -6.184 45.532 1.00 31.06 ? ? ? ? ? . 7 TYR B OH 2350 ATOM 1313 N N . LEU B 2350 8 . -7.988 0.490 46.190 1.00 20.58 ? ? ? ? ? . 8 LEU B N 2350 ATOM 1314 C CA . LEU B 2350 8 . -6.995 1.534 46.034 1.00 22.55 ? ? ? ? ? . 8 LEU B CA 2350 ATOM 1315 C C . LEU B 2350 8 . -6.258 1.733 47.379 1.00 24.85 ? ? ? ? ? . 8 LEU B C 2350 ATOM 1316 O O . LEU B 2350 8 . -6.306 2.818 47.947 1.00 23.30 ? ? ? ? ? . 8 LEU B O 2350 ATOM 1317 C CB . LEU B 2350 8 . -7.674 2.820 45.535 1.00 21.81 ? ? ? ? ? . 8 LEU B CB 2350 ATOM 1318 C CG . LEU B 2350 8 . -8.652 2.723 44.351 1.00 22.20 ? ? ? ? ? . 8 LEU B CG 2350 ATOM 1319 C CD1 . LEU B 2350 8 . -9.436 4.019 44.145 1.00 21.75 ? ? ? ? ? . 8 LEU B CD1 2350 ATOM 1320 C CD2 . LEU B 2350 8 . -7.923 2.341 43.078 1.00 23.03 ? ? ? ? ? . 8 LEU B CD2 2350 ATOM 1321 N N . PRO B 2350 9 . -5.585 0.670 47.908 1.00 30.34 ? ? ? ? ? . 9 PRO B N 2350 ATOM 1322 C CA . PRO B 2350 9 . -4.840 0.839 49.177 1.00 32.73 ? ? ? ? ? . 9 PRO B CA 2350 ATOM 1323 C C . PRO B 2350 9 . -3.645 1.806 49.120 1.00 36.29 ? ? ? ? ? . 9 PRO B C 2350 ATOM 1324 O O . PRO B 2350 9 . -3.262 2.365 50.164 1.00 40.31 ? ? ? ? ? . 9 PRO B O 2350 ATOM 1325 C CB . PRO B 2350 9 . -4.339 -0.580 49.490 1.00 31.95 ? ? ? ? ? . 9 PRO B CB 2350 ATOM 1326 C CG . PRO B 2350 9 . -4.271 -1.254 48.169 1.00 31.95 ? ? ? ? ? . 9 PRO B CG 2350 ATOM 1327 C CD . PRO B 2350 9 . -5.444 -0.710 47.397 1.00 29.49 ? ? ? ? ? . 9 PRO B CD 2350 ATOM 1328 N N A GLY B 2350 10 . -3.058 1.957 47.930 0.77 38.24 ? ? ? ? ? . 10 GLY B N 2350 ATOM 1329 N N B GLY B 2350 10 . -3.067 1.997 47.933 0.23 34.42 ? ? ? ? ? . 10 GLY B N 2350 ATOM 1330 C CA A GLY B 2350 10 . -1.979 2.917 47.683 0.77 39.23 ? ? ? ? ? . 10 GLY B CA 2350 ATOM 1331 C CA B GLY B 2350 10 . -1.975 2.950 47.737 0.23 32.92 ? ? ? ? ? . 10 GLY B CA 2350 ATOM 1332 C C A GLY B 2350 10 . -2.440 4.297 47.238 0.77 39.23 ? ? ? ? ? . 10 GLY B C 2350 ATOM 1333 C C B GLY B 2350 10 . -2.466 4.376 47.572 0.23 31.25 ? ? ? ? ? . 10 GLY B C 2350 ATOM 1334 O O A GLY B 2350 10 . -1.600 5.153 46.952 0.77 39.50 ? ? ? ? ? . 10 GLY B O 2350 ATOM 1335 O O B GLY B 2350 10 . -1.769 5.323 47.932 0.23 30.40 ? ? ? ? ? . 10 GLY B O 2350 ATOM 1336 N N A ALA B 2350 11 . -3.757 4.512 47.157 0.77 38.23 ? ? ? ? ? . 11 ALA B N 2350 ATOM 1337 N N B ALA B 2350 11 . -3.671 4.530 47.029 0.23 30.15 ? ? ? ? ? . 11 ALA B N 2350 ATOM 1338 C CA A ALA B 2350 11 . -4.326 5.822 46.813 0.77 40.95 ? ? ? ? ? . 11 ALA B CA 2350 ATOM 1339 C CA B ALA B 2350 11 . -4.203 5.852 46.697 0.23 29.99 ? ? ? ? ? . 11 ALA B CA 2350 ATOM 1340 C C A ALA B 2350 11 . -4.804 6.550 48.057 0.77 42.60 ? ? ? ? ? . 11 ALA B C 2350 ATOM 1341 C C B ALA B 2350 11 . -4.673 6.627 47.920 0.23 29.56 ? ? ? ? ? . 11 ALA B C 2350 ATOM 1342 O O A ALA B 2350 11 . -5.473 5.956 48.913 0.77 38.62 ? ? ? ? ? . 11 ALA B O 2350 ATOM 1343 O O B ALA B 2350 11 . -4.896 6.055 48.992 0.23 29.66 ? ? ? ? ? . 11 ALA B O 2350 ATOM 1344 C CB A ALA B 2350 11 . -5.484 5.674 45.843 0.77 39.60 ? ? ? ? ? . 11 ALA B CB 2350 ATOM 1345 C CB B ALA B 2350 11 . -5.346 5.725 45.701 0.23 29.66 ? ? ? ? ? . 11 ALA B CB 2350 ATOM 1346 N N A THR B 2350 12 . -4.465 7.837 48.124 0.77 39.49 ? ? ? ? ? . 12 THR B N 2350 ATOM 1347 N N B THR B 2350 12 . -4.834 7.935 47.739 0.23 27.19 ? ? ? ? ? . 12 THR B N 2350 ATOM 1348 C CA A THR B 2350 12 . -4.919 8.740 49.169 0.77 38.81 ? ? ? ? ? . 12 THR B CA 2350 ATOM 1349 C CA B THR B 2350 12 . -5.309 8.803 48.802 0.23 25.87 ? ? ? ? ? . 12 THR B CA 2350 ATOM 1350 C C A THR B 2350 12 . -5.822 9.788 48.516 0.77 36.92 ? ? ? ? ? . 12 THR B C 2350 ATOM 1351 C C B THR B 2350 12 . -6.085 9.992 48.240 0.23 24.45 ? ? ? ? ? . 12 THR B C 2350 ATOM 1352 O O A THR B 2350 12 . -7.019 9.833 48.805 0.77 38.96 ? ? ? ? ? . 12 THR B O 2350 ATOM 1353 O O B THR B 2350 12 . -7.280 10.134 48.496 0.23 24.79 ? ? ? ? ? . 12 THR B O 2350 ATOM 1354 C CB A THR B 2350 12 . -3.715 9.350 49.932 0.77 43.31 ? ? ? ? ? . 12 THR B CB 2350 ATOM 1355 C CB B THR B 2350 12 . -4.146 9.331 49.661 0.23 25.76 ? ? ? ? ? . 12 THR B CB 2350 ATOM 1356 C CG2 A THR B 2350 12 . -4.034 10.710 50.580 0.77 44.76 ? ? ? ? ? . 12 THR B CG2 2350 ATOM 1357 O OG1 A THR B 2350 12 . -3.305 8.441 50.966 0.77 48.33 ? ? ? ? ? . 12 THR B OG1 2350 ATOM 1358 C CG2 B THR B 2350 12 . -3.507 8.198 50.450 0.23 26.96 ? ? ? ? ? . 12 THR B CG2 2350 ATOM 1359 O OG1 B THR B 2350 12 . -3.157 9.935 48.817 0.23 25.88 ? ? ? ? ? . 12 THR B OG1 2350 ATOM 1360 N N A ASN B 2350 13 . -5.262 10.611 47.633 0.77 31.56 ? ? ? ? ? . 13 ASN B N 2350 ATOM 1361 N N B ASN B 2350 13 . -5.412 10.841 47.470 0.23 22.85 ? ? ? ? ? . 13 ASN B N 2350 ATOM 1362 C CA A ASN B 2350 13 . -6.027 11.685 46.991 0.77 30.90 ? ? ? ? ? . 13 ASN B CA 2350 ATOM 1363 C CA B ASN B 2350 13 . -6.025 12.088 47.015 0.23 22.03 ? ? ? ? ? . 13 ASN B CA 2350 ATOM 1364 C C A ASN B 2350 13 . -6.517 11.306 45.593 0.77 26.89 ? ? ? ? ? . 13 ASN B C 2350 ATOM 1365 C C B ASN B 2350 13 . -6.297 12.126 45.512 0.23 20.53 ? ? ? ? ? . 13 ASN B C 2350 ATOM 1366 O O A ASN B 2350 13 . -5.977 10.403 44.946 0.77 27.86 ? ? ? ? ? . 13 ASN B O 2350 ATOM 1367 O O B ASN B 2350 13 . -5.403 12.391 44.707 0.23 18.91 ? ? ? ? ? . 13 ASN B O 2350 ATOM 1368 C CB A ASN B 2350 13 . -5.201 12.975 46.924 0.77 32.33 ? ? ? ? ? . 13 ASN B CB 2350 ATOM 1369 C CB B ASN B 2350 13 . -5.158 13.276 47.425 0.23 22.65 ? ? ? ? ? . 13 ASN B CB 2350 ATOM 1370 C CG A ASN B 2350 13 . -5.018 13.624 48.287 0.77 33.72 ? ? ? ? ? . 13 ASN B CG 2350 ATOM 1371 C CG B ASN B 2350 13 . -5.104 13.456 48.927 0.23 22.73 ? ? ? ? ? . 13 ASN B CG 2350 ATOM 1372 N ND2 A ASN B 2350 13 . -3.789 14.040 48.583 0.77 32.95 ? ? ? ? ? . 13 ASN B ND2 2350 ATOM 1373 O OD1 A ASN B 2350 13 . -5.972 13.755 49.064 0.77 36.48 ? ? ? ? ? . 13 ASN B OD1 2350 ATOM 1374 N ND2 B ASN B 2350 13 . -3.898 13.564 49.467 0.23 22.84 ? ? ? ? ? . 13 ASN B ND2 2350 ATOM 1375 O OD1 B ASN B 2350 13 . -6.139 13.488 49.597 0.23 23.02 ? ? ? ? ? . 13 ASN B OD1 2350 ATOM 1376 N N A LEU B 2350 14 . -7.561 12.004 45.156 0.77 22.05 ? ? ? ? ? . 14 LEU B N 2350 ATOM 1377 N N B LEU B 2350 14 . -7.552 11.874 45.153 0.23 19.29 ? ? ? ? ? . 14 LEU B N 2350 ATOM 1378 C CA A LEU B 2350 14 . -8.025 11.956 43.783 0.77 19.30 ? ? ? ? ? . 14 LEU B CA 2350 ATOM 1379 C CA B LEU B 2350 14 . -7.976 11.910 43.764 0.23 18.51 ? ? ? ? ? . 14 LEU B CA 2350 ATOM 1380 C C A LEU B 2350 14 . -7.920 13.356 43.196 0.77 18.33 ? ? ? ? ? . 14 LEU B C 2350 ATOM 1381 C C B LEU B 2350 14 . -7.877 13.327 43.209 0.23 18.03 ? ? ? ? ? . 14 LEU B C 2350 ATOM 1382 O O A LEU B 2350 14 . -8.134 14.353 43.895 0.77 18.60 ? ? ? ? ? . 14 LEU B O 2350 ATOM 1383 O O B LEU B 2350 14 . -8.049 14.300 43.943 0.23 18.30 ? ? ? ? ? . 14 LEU B O 2350 ATOM 1384 C CB A LEU B 2350 14 . -9.469 11.484 43.723 0.77 19.92 ? ? ? ? ? . 14 LEU B CB 2350 ATOM 1385 C CB B LEU B 2350 14 . -9.417 11.422 43.639 0.23 18.83 ? ? ? ? ? . 14 LEU B CB 2350 ATOM 1386 C CG A LEU B 2350 14 . -9.749 10.069 44.232 0.77 19.69 ? ? ? ? ? . 14 LEU B CG 2350 ATOM 1387 C CG B LEU B 2350 14 . -9.712 10.028 44.194 0.23 18.81 ? ? ? ? ? . 14 LEU B CG 2350 ATOM 1388 C CD1 A LEU B 2350 14 . -11.252 9.842 44.242 0.77 21.45 ? ? ? ? ? . 14 LEU B CD1 2350 ATOM 1389 C CD2 A LEU B 2350 14 . -9.054 9.028 43.375 0.77 17.90 ? ? ? ? ? . 14 LEU B CD2 2350 ATOM 1390 C CD1 B LEU B 2350 14 . -11.209 9.763 44.163 0.23 19.36 ? ? ? ? ? . 14 LEU B CD1 2350 ATOM 1391 C CD2 B LEU B 2350 14 . -8.959 8.967 43.412 0.23 18.31 ? ? ? ? ? . 14 LEU B CD2 2350 ATOM 1392 N N . LEU B 2350 15 . -7.599 13.428 41.911 1.00 17.26 ? ? ? ? ? . 15 LEU B N 2350 ATOM 1393 C CA . LEU B 2350 15 . -7.617 14.696 41.206 1.00 17.59 ? ? ? ? ? . 15 LEU B CA 2350 ATOM 1394 C C . LEU B 2350 15 . -9.072 15.103 41.062 1.00 16.76 ? ? ? ? ? . 15 LEU B C 2350 ATOM 1395 O O . LEU B 2350 15 . -9.936 14.262 40.835 1.00 16.90 ? ? ? ? ? . 15 LEU B O 2350 ATOM 1396 C CB . LEU B 2350 15 . -7.025 14.573 39.813 1.00 19.34 ? ? ? ? ? . 15 LEU B CB 2350 ATOM 1397 C CG . LEU B 2350 15 . -5.610 14.033 39.700 1.00 21.37 ? ? ? ? ? . 15 LEU B CG 2350 ATOM 1398 C CD1 . LEU B 2350 15 . -5.159 14.206 38.257 1.00 21.66 ? ? ? ? ? . 15 LEU B CD1 2350 ATOM 1399 C CD2 . LEU B 2350 15 . -4.668 14.726 40.666 1.00 24.43 ? ? ? ? ? . 15 LEU B CD2 2350 ATOM 1400 N N . SER B 2350 16 . -9.331 16.391 41.209 1.00 17.94 ? ? ? ? ? . 16 SER B N 2350 ATOM 1401 C CA . SER B 2350 16 . -10.680 16.929 41.064 1.00 18.12 ? ? ? ? ? . 16 SER B CA 2350 ATOM 1402 C C . SER B 2350 16 . -10.613 18.305 40.430 1.00 16.87 ? ? ? ? ? . 16 SER B C 2350 ATOM 1403 O O . SER B 2350 16 . -9.533 18.879 40.272 1.00 17.19 ? ? ? ? ? . 16 SER B O 2350 ATOM 1404 C CB . SER B 2350 16 . -11.370 17.023 42.422 1.00 19.13 ? ? ? ? ? . 16 SER B CB 2350 ATOM 1405 O OG . SER B 2350 16 . -10.823 18.059 43.187 1.00 22.41 ? ? ? ? ? . 16 SER B OG 2350 ATOM 1406 N N . LYS B 2350 17 . -11.782 18.828 40.086 1.00 15.53 ? ? ? ? ? . 17 LYS B N 2350 ATOM 1407 C CA . LYS B 2350 17 . -11.903 20.175 39.539 1.00 16.49 ? ? ? ? ? . 17 LYS B CA 2350 ATOM 1408 C C . LYS B 2350 17 . -11.794 21.268 40.598 1.00 15.39 ? ? ? ? ? . 17 LYS B C 2350 ATOM 1409 O O . LYS B 2350 17 . -11.669 22.438 40.252 1.00 13.92 ? ? ? ? ? . 17 LYS B O 2350 ATOM 1410 C CB . LYS B 2350 17 . -13.215 20.305 38.757 1.00 18.01 ? ? ? ? ? . 17 LYS B CB 2350 ATOM 1411 C CG . LYS B 2350 17 . -13.335 19.299 37.622 1.00 19.88 ? ? ? ? ? . 17 LYS B CG 2350 ATOM 1412 C CD . LYS B 2350 17 . -12.060 19.234 36.794 1.00 21.42 ? ? ? ? ? . 17 LYS B CD 2350 ATOM 1413 C CE . LYS B 2350 17 . -12.221 18.350 35.596 1.00 22.48 ? ? ? ? ? . 17 LYS B CE 2350 ATOM 1414 N NZ . LYS B 2350 17 . -11.123 18.520 34.616 1.00 19.77 ? ? ? ? ? 1+ 17 LYS B NZ 2350 ATOM 1415 N N . SER B 2350 18 . -11.851 20.881 41.874 1.00 15.35 ? ? ? ? ? . 18 SER B N 2350 ATOM 1416 C CA . SER B 2350 18 . -11.747 21.801 43.005 1.00 16.54 ? ? ? ? ? . 18 SER B CA 2350 ATOM 1417 C C . SER B 2350 18 . -10.391 21.703 43.686 1.00 17.70 ? ? ? ? ? . 18 SER B C 2350 ATOM 1418 O O . SER B 2350 18 . -10.142 22.414 44.649 1.00 19.21 ? ? ? ? ? . 18 SER B O 2350 ATOM 1419 C CB . SER B 2350 18 . -12.863 21.496 44.015 1.00 17.01 ? ? ? ? ? . 18 SER B CB 2350 ATOM 1420 O OG . SER B 2350 18 . -12.878 20.104 44.333 1.00 19.03 ? ? ? ? ? . 18 SER B OG 2350 ATOM 1421 N N . GLY B 2350 19 . -9.511 20.850 43.167 1.00 20.26 ? ? ? ? ? . 19 GLY B N 2350 ATOM 1422 C CA . GLY B 2350 19 . -8.183 20.625 43.734 1.00 23.91 ? ? ? ? ? . 19 GLY B CA 2350 ATOM 1423 C C . GLY B 2350 19 . -7.970 19.137 43.899 1.00 29.48 ? ? ? ? ? . 19 GLY B C 2350 ATOM 1424 O O . GLY B 2350 19 . -7.881 18.400 42.908 1.00 35.30 ? ? ? ? ? . 19 GLY B O 2350 ATOM 1425 N N . GLU B 2350 20 . -7.904 18.693 45.150 1.00 33.35 ? ? ? ? ? . 20 GLU B N 2350 ATOM 1426 C CA . GLU B 2350 20 . -7.828 17.270 45.476 1.00 34.73 ? ? ? ? ? . 20 GLU B CA 2350 ATOM 1427 C C . GLU B 2350 20 . -9.006 16.904 46.383 1.00 32.98 ? ? ? ? ? . 20 GLU B C 2350 ATOM 1428 O O . GLU B 2350 20 . -9.526 17.757 47.117 1.00 31.53 ? ? ? ? ? . 20 GLU B O 2350 ATOM 1429 C CB . GLU B 2350 20 . -6.491 16.945 46.160 1.00 42.13 ? ? ? ? ? . 20 GLU B CB 2350 ATOM 1430 C CG . GLU B 2350 20 . -5.367 16.492 45.220 1.00 47.38 ? ? ? ? ? . 20 GLU B CG 2350 ATOM 1431 C CD . GLU B 2350 20 . -4.580 17.617 44.549 1.00 54.02 ? ? ? ? ? . 20 GLU B CD 2350 ATOM 1432 O OE1 . GLU B 2350 20 . -4.618 18.780 45.019 1.00 57.55 ? ? ? ? ? . 20 GLU B OE1 2350 ATOM 1433 O OE2 . GLU B 2350 20 . -3.893 17.325 43.539 1.00 54.84 ? ? ? ? ? 1- 20 GLU B OE2 2350 ATOM 1434 N N . VAL B 2350 21 . -9.449 15.651 46.305 1.00 27.54 ? ? ? ? ? . 21 VAL B N 2350 ATOM 1435 C CA . VAL B 2350 21 . -10.457 15.135 47.231 1.00 23.77 ? ? ? ? ? . 21 VAL B CA 2350 ATOM 1436 C C . VAL B 2350 21 . -9.976 13.792 47.753 1.00 21.10 ? ? ? ? ? . 21 VAL B C 2350 ATOM 1437 O O . VAL B 2350 21 . -9.420 12.984 47.009 1.00 22.82 ? ? ? ? ? . 21 VAL B O 2350 ATOM 1438 C CB . VAL B 2350 21 . -11.882 15.041 46.615 1.00 25.46 ? ? ? ? ? . 21 VAL B CB 2350 ATOM 1439 C CG1 . VAL B 2350 21 . -12.259 16.337 45.908 1.00 26.17 ? ? ? ? ? . 21 VAL B CG1 2350 ATOM 1440 C CG2 . VAL B 2350 21 . -12.032 13.874 45.654 1.00 27.50 ? ? ? ? ? . 21 VAL B CG2 2350 ATOM 1441 N N . SER B 2350 22 . -10.156 13.584 49.049 1.00 19.01 ? ? ? ? ? . 22 SER B N 2350 ATOM 1442 C CA . SER B 2350 22 . -9.832 12.319 49.690 1.00 17.12 ? ? ? ? ? . 22 SER B CA 2350 ATOM 1443 C C . SER B 2350 22 . -10.837 11.257 49.280 1.00 16.89 ? ? ? ? ? . 22 SER B C 2350 ATOM 1444 O O . SER B 2350 22 . -11.969 11.559 48.900 1.00 16.17 ? ? ? ? ? . 22 SER B O 2350 ATOM 1445 C CB . SER B 2350 22 . -9.882 12.477 51.201 1.00 17.47 ? ? ? ? ? . 22 SER B CB 2350 ATOM 1446 O OG . SER B 2350 22 . -11.186 12.875 51.610 1.00 18.10 ? ? ? ? ? . 22 SER B OG 2350 ATOM 1447 N N . LEU B 2350 23 . -10.439 10.000 49.383 1.00 16.00 ? ? ? ? ? . 23 LEU B N 2350 ATOM 1448 C CA . LEU B 2350 23 . -11.392 8.910 49.209 1.00 16.76 ? ? ? ? ? . 23 LEU B CA 2350 ATOM 1449 C C . LEU B 2350 23 . -12.551 9.038 50.208 1.00 14.79 ? ? ? ? ? . 23 LEU B C 2350 ATOM 1450 O O . LEU B 2350 23 . -13.717 8.880 49.845 1.00 15.73 ? ? ? ? ? . 23 LEU B O 2350 ATOM 1451 C CB . LEU B 2350 23 . -10.689 7.563 49.369 1.00 17.74 ? ? ? ? ? . 23 LEU B CB 2350 ATOM 1452 C CG . LEU B 2350 23 . -9.584 7.244 48.339 1.00 17.52 ? ? ? ? ? . 23 LEU B CG 2350 ATOM 1453 C CD1 . LEU B 2350 23 . -9.084 5.812 48.539 1.00 18.55 ? ? ? ? ? . 23 LEU B CD1 2350 ATOM 1454 C CD2 . LEU B 2350 23 . -10.077 7.420 46.929 1.00 19.15 ? ? ? ? ? . 23 LEU B CD2 2350 ATOM 1455 N N . GLY B 2350 24 . -12.223 9.375 51.449 1.00 14.46 ? ? ? ? ? . 24 GLY B N 2350 ATOM 1456 C CA . GLY B 2350 24 . -13.214 9.637 52.492 1.00 14.61 ? ? ? ? ? . 24 GLY B CA 2350 ATOM 1457 C C . GLY B 2350 24 . -14.315 10.639 52.178 1.00 14.98 ? ? ? ? ? . 24 GLY B C 2350 ATOM 1458 O O . GLY B 2350 24 . -15.447 10.508 52.685 1.00 13.90 ? ? ? ? ? . 24 GLY B O 2350 ATOM 1459 N N A SER B 2350 25 . -14.002 11.639 51.359 0.33 14.74 ? ? ? ? ? . 25 SER B N 2350 ATOM 1460 N N B SER B 2350 25 . -13.985 11.632 51.354 0.67 14.83 ? ? ? ? ? . 25 SER B N 2350 ATOM 1461 C CA A SER B 2350 25 . -14.990 12.634 50.953 0.33 15.11 ? ? ? ? ? . 25 SER B CA 2350 ATOM 1462 C CA B SER B 2350 25 . -14.956 12.633 50.907 0.67 15.70 ? ? ? ? ? . 25 SER B CA 2350 ATOM 1463 C C A SER B 2350 25 . -16.139 12.061 50.107 0.33 14.62 ? ? ? ? ? . 25 SER B C 2350 ATOM 1464 C C B SER B 2350 25 . -16.142 12.045 50.133 0.67 14.69 ? ? ? ? ? . 25 SER B C 2350 ATOM 1465 O O A SER B 2350 25 . -17.161 12.727 49.940 0.33 14.68 ? ? ? ? ? . 25 SER B O 2350 ATOM 1466 O O B SER B 2350 25 . -17.192 12.679 50.049 0.67 14.89 ? ? ? ? ? . 25 SER B O 2350 ATOM 1467 C CB A SER B 2350 25 . -14.312 13.771 50.192 0.33 15.75 ? ? ? ? ? . 25 SER B CB 2350 ATOM 1468 C CB B SER B 2350 25 . -14.277 13.710 50.050 0.67 17.08 ? ? ? ? ? . 25 SER B CB 2350 ATOM 1469 O OG A SER B 2350 25 . -13.934 13.355 48.898 0.33 15.76 ? ? ? ? ? . 25 SER B OG 2350 ATOM 1470 O OG B SER B 2350 25 . -13.378 14.486 50.832 0.67 17.83 ? ? ? ? ? . 25 SER B OG 2350 ATOM 1471 N N . LEU B 2350 26 . -15.971 10.843 49.583 1.00 14.64 ? ? ? ? ? . 26 LEU B N 2350 ATOM 1472 C CA . LEU B 2350 26 . -17.013 10.154 48.810 1.00 14.28 ? ? ? ? ? . 26 LEU B CA 2350 ATOM 1473 C C . LEU B 2350 26 . -17.907 9.246 49.653 1.00 13.59 ? ? ? ? ? . 26 LEU B C 2350 ATOM 1474 O O . LEU B 2350 26 . -18.662 8.454 49.099 1.00 13.08 ? ? ? ? ? . 26 LEU B O 2350 ATOM 1475 C CB . LEU B 2350 26 . -16.349 9.345 47.686 1.00 14.88 ? ? ? ? ? . 26 LEU B CB 2350 ATOM 1476 C CG . LEU B 2350 26 . -15.426 10.153 46.765 1.00 15.17 ? ? ? ? ? . 26 LEU B CG 2350 ATOM 1477 C CD1 . LEU B 2350 26 . -14.967 9.289 45.614 1.00 17.04 ? ? ? ? ? . 26 LEU B CD1 2350 ATOM 1478 C CD2 . LEU B 2350 26 . -16.139 11.406 46.266 1.00 16.62 ? ? ? ? ? . 26 LEU B CD2 2350 ATOM 1479 N N . VAL B 2350 27 . -17.834 9.368 50.978 1.00 14.28 ? ? ? ? ? . 27 VAL B N 2350 ATOM 1480 C CA . VAL B 2350 27 . -18.698 8.635 51.891 1.00 15.50 ? ? ? ? ? . 27 VAL B CA 2350 ATOM 1481 C C . VAL B 2350 27 . -20.162 8.724 51.441 1.00 15.84 ? ? ? ? ? . 27 VAL B C 2350 ATOM 1482 O O . VAL B 2350 27 . -20.649 9.800 51.054 1.00 14.49 ? ? ? ? ? . 27 VAL B O 2350 ATOM 1483 C CB . VAL B 2350 27 . -18.547 9.163 53.351 1.00 16.29 ? ? ? ? ? . 27 VAL B CB 2350 ATOM 1484 C CG1 . VAL B 2350 27 . -18.972 10.632 53.485 1.00 15.80 ? ? ? ? ? . 27 VAL B CG1 2350 ATOM 1485 C CG2 . VAL B 2350 27 . -19.296 8.283 54.345 1.00 16.28 ? ? ? ? ? . 27 VAL B CG2 2350 ATOM 1486 N N . GLY B 2350 28 . -20.824 7.572 51.443 1.00 15.56 ? ? ? ? ? . 28 GLY B N 2350 ATOM 1487 C CA . GLY B 2350 28 . -22.236 7.472 51.117 1.00 17.43 ? ? ? ? ? . 28 GLY B CA 2350 ATOM 1488 C C . GLY B 2350 28 . -22.560 7.471 49.633 1.00 17.56 ? ? ? ? ? . 28 GLY B C 2350 ATOM 1489 O O . GLY B 2350 28 . -23.721 7.312 49.289 1.00 16.53 ? ? ? ? ? . 28 GLY B O 2350 ATOM 1490 N N . LYS B 2350 29 . -21.558 7.614 48.749 1.00 18.00 ? ? ? ? ? . 29 LYS B N 2350 ATOM 1491 C CA A LYS B 2350 29 . -21.810 7.728 47.306 0.68 17.72 ? ? ? ? ? . 29 LYS B CA 2350 ATOM 1492 C CA B LYS B 2350 29 . -21.809 7.727 47.308 0.32 17.27 ? ? ? ? ? . 29 LYS B CA 2350 ATOM 1493 C C . LYS B 2350 29 . -21.633 6.400 46.590 1.00 17.35 ? ? ? ? ? . 29 LYS B C 2350 ATOM 1494 O O . LYS B 2350 29 . -21.001 5.464 47.114 1.00 16.43 ? ? ? ? ? . 29 LYS B O 2350 ATOM 1495 C CB A LYS B 2350 29 . -20.896 8.779 46.665 0.68 18.98 ? ? ? ? ? . 29 LYS B CB 2350 ATOM 1496 C CB B LYS B 2350 29 . -20.890 8.777 46.675 0.32 17.40 ? ? ? ? ? . 29 LYS B CB 2350 ATOM 1497 C CG A LYS B 2350 29 . -21.075 10.175 47.237 0.68 20.34 ? ? ? ? ? . 29 LYS B CG 2350 ATOM 1498 C CG B LYS B 2350 29 . -21.159 10.185 47.167 0.32 17.58 ? ? ? ? ? . 29 LYS B CG 2350 ATOM 1499 C CD A LYS B 2350 29 . -20.626 11.246 46.260 0.68 21.02 ? ? ? ? ? . 29 LYS B CD 2350 ATOM 1500 C CD B LYS B 2350 29 . -20.246 11.205 46.514 0.32 17.42 ? ? ? ? ? . 29 LYS B CD 2350 ATOM 1501 C CE A LYS B 2350 29 . -20.516 12.609 46.928 0.68 21.70 ? ? ? ? ? . 29 LYS B CE 2350 ATOM 1502 C CE B LYS B 2350 29 . -20.670 12.621 46.874 0.32 17.47 ? ? ? ? ? . 29 LYS B CE 2350 ATOM 1503 N NZ A LYS B 2350 29 . -21.730 13.052 47.665 0.68 19.96 ? ? ? ? ? 1+ 29 LYS B NZ 2350 ATOM 1504 N NZ B LYS B 2350 29 . -21.930 13.032 46.203 0.32 16.73 ? ? ? ? ? 1+ 29 LYS B NZ 2350 ATOM 1505 N N . THR B 2350 30 . -22.222 6.329 45.404 1.00 16.11 ? ? ? ? ? . 30 THR B N 2350 ATOM 1506 C CA . THR B 2350 30 . -21.922 5.287 44.433 1.00 16.62 ? ? ? ? ? . 30 THR B CA 2350 ATOM 1507 C C . THR B 2350 30 . -20.765 5.868 43.640 1.00 16.77 ? ? ? ? ? . 30 THR B C 2350 ATOM 1508 O O . THR B 2350 30 . -20.761 7.061 43.352 1.00 15.79 ? ? ? ? ? . 30 THR B O 2350 ATOM 1509 C CB . THR B 2350 30 . -23.134 4.990 43.527 1.00 16.40 ? ? ? ? ? . 30 THR B CB 2350 ATOM 1510 C CG2 . THR B 2350 30 . -22.788 3.993 42.435 1.00 17.05 ? ? ? ? ? . 30 THR B CG2 2350 ATOM 1511 O OG1 . THR B 2350 30 . -24.174 4.432 44.329 1.00 16.31 ? ? ? ? ? . 30 THR B OG1 2350 ATOM 1512 N N . VAL B 2350 31 . -19.755 5.048 43.335 1.00 16.50 ? ? ? ? ? . 31 VAL B N 2350 ATOM 1513 C CA . VAL B 2350 31 . -18.612 5.519 42.588 1.00 16.20 ? ? ? ? ? . 31 VAL B CA 2350 ATOM 1514 C C . VAL B 2350 31 . -18.434 4.641 41.355 1.00 16.54 ? ? ? ? ? . 31 VAL B C 2350 ATOM 1515 O O . VAL B 2350 31 . -18.420 3.411 41.466 1.00 17.66 ? ? ? ? ? . 31 VAL B O 2350 ATOM 1516 C CB . VAL B 2350 31 . -17.335 5.511 43.452 1.00 17.15 ? ? ? ? ? . 31 VAL B CB 2350 ATOM 1517 C CG1 . VAL B 2350 31 . -16.106 5.860 42.622 1.00 18.31 ? ? ? ? ? . 31 VAL B CG1 2350 ATOM 1518 C CG2 . VAL B 2350 31 . -17.513 6.471 44.623 1.00 18.02 ? ? ? ? ? . 31 VAL B CG2 2350 ATOM 1519 N N . PHE B 2350 32 . -18.278 5.289 40.205 1.00 15.33 ? ? ? ? ? . 32 PHE B N 2350 ATOM 1520 C CA . PHE B 2350 32 . -17.954 4.605 38.959 1.00 15.97 ? ? ? ? ? . 32 PHE B CA 2350 ATOM 1521 C C . PHE B 2350 32 . -16.463 4.743 38.690 1.00 17.33 ? ? ? ? ? . 32 PHE B C 2350 ATOM 1522 O O . PHE B 2350 32 . -15.955 5.860 38.580 1.00 17.87 ? ? ? ? ? . 32 PHE B O 2350 ATOM 1523 C CB . PHE B 2350 32 . -18.704 5.203 37.795 1.00 15.59 ? ? ? ? ? . 32 PHE B CB 2350 ATOM 1524 C CG . PHE B 2350 32 . -20.174 4.974 37.825 1.00 16.67 ? ? ? ? ? . 32 PHE B CG 2350 ATOM 1525 C CD1 . PHE B 2350 32 . -20.695 3.707 37.597 1.00 16.26 ? ? ? ? ? . 32 PHE B CD1 2350 ATOM 1526 C CD2 . PHE B 2350 32 . -21.052 6.023 38.060 1.00 18.11 ? ? ? ? ? . 32 PHE B CD2 2350 ATOM 1527 C CE1 . PHE B 2350 32 . -22.049 3.483 37.605 1.00 16.54 ? ? ? ? ? . 32 PHE B CE1 2350 ATOM 1528 C CE2 . PHE B 2350 32 . -22.423 5.801 38.050 1.00 19.09 ? ? ? ? ? . 32 PHE B CE2 2350 ATOM 1529 C CZ . PHE B 2350 32 . -22.914 4.524 37.828 1.00 17.79 ? ? ? ? ? . 32 PHE B CZ 2350 ATOM 1530 N N . LEU B 2350 33 . -15.776 3.614 38.563 1.00 18.19 ? ? ? ? ? . 33 LEU B N 2350 ATOM 1531 C CA . LEU B 2350 33 . -14.390 3.613 38.108 1.00 16.59 ? ? ? ? ? . 33 LEU B CA 2350 ATOM 1532 C C . LEU B 2350 33 . -14.442 3.462 36.600 1.00 16.50 ? ? ? ? ? . 33 LEU B C 2350 ATOM 1533 O O . LEU B 2350 33 . -14.938 2.453 36.105 1.00 15.95 ? ? ? ? ? . 33 LEU B O 2350 ATOM 1534 C CB . LEU B 2350 33 . -13.592 2.478 38.746 1.00 17.76 ? ? ? ? ? . 33 LEU B CB 2350 ATOM 1535 C CG . LEU B 2350 33 . -13.565 2.381 40.272 1.00 17.52 ? ? ? ? ? . 33 LEU B CG 2350 ATOM 1536 C CD1 . LEU B 2350 33 . -12.655 1.235 40.659 1.00 20.03 ? ? ? ? ? . 33 LEU B CD1 2350 ATOM 1537 C CD2 . LEU B 2350 33 . -13.101 3.681 40.919 1.00 18.78 ? ? ? ? ? . 33 LEU B CD2 2350 ATOM 1538 N N . TYR B 2350 34 . -13.955 4.487 35.892 1.00 15.29 ? ? ? ? ? . 34 TYR B N 2350 ATOM 1539 C CA . TYR B 2350 34 . -14.051 4.587 34.456 1.00 15.84 ? ? ? ? ? . 34 TYR B CA 2350 ATOM 1540 C C . TYR B 2350 34 . -12.697 4.264 33.844 1.00 16.40 ? ? ? ? ? . 34 TYR B C 2350 ATOM 1541 O O . TYR B 2350 34 . -11.798 5.117 33.844 1.00 16.02 ? ? ? ? ? . 34 TYR B O 2350 ATOM 1542 C CB . TYR B 2350 34 . -14.539 5.978 34.030 1.00 16.34 ? ? ? ? ? . 34 TYR B CB 2350 ATOM 1543 C CG . TYR B 2350 34 . -14.638 6.174 32.511 1.00 16.48 ? ? ? ? ? . 34 TYR B CG 2350 ATOM 1544 C CD1 . TYR B 2350 34 . -14.960 5.108 31.653 1.00 16.84 ? ? ? ? ? . 34 TYR B CD1 2350 ATOM 1545 C CD2 . TYR B 2350 34 . -14.424 7.419 31.932 1.00 17.38 ? ? ? ? ? . 34 TYR B CD2 2350 ATOM 1546 C CE1 . TYR B 2350 34 . -15.060 5.286 30.293 1.00 17.26 ? ? ? ? ? . 34 TYR B CE1 2350 ATOM 1547 C CE2 . TYR B 2350 34 . -14.528 7.603 30.558 1.00 17.55 ? ? ? ? ? . 34 TYR B CE2 2350 ATOM 1548 C CZ . TYR B 2350 34 . -14.850 6.534 29.747 1.00 17.57 ? ? ? ? ? . 34 TYR B CZ 2350 ATOM 1549 O OH . TYR B 2350 34 . -14.931 6.690 28.388 1.00 18.64 ? ? ? ? ? . 34 TYR B OH 2350 ATOM 1550 N N . PHE B 2350 35 . -12.559 3.025 33.358 1.00 16.94 ? ? ? ? ? . 35 PHE B N 2350 ATOM 1551 C CA . PHE B 2350 35 . -11.319 2.588 32.702 1.00 16.15 ? ? ? ? ? . 35 PHE B CA 2350 ATOM 1552 C C . PHE B 2350 35 . -11.357 3.088 31.269 1.00 15.95 ? ? ? ? ? . 35 PHE B C 2350 ATOM 1553 O O . PHE B 2350 35 . -12.252 2.733 30.502 1.00 15.83 ? ? ? ? ? . 35 PHE B O 2350 ATOM 1554 C CB . PHE B 2350 35 . -11.131 1.073 32.787 1.00 16.88 ? ? ? ? ? . 35 PHE B CB 2350 ATOM 1555 C CG . PHE B 2350 35 . -10.865 0.569 34.181 1.00 17.15 ? ? ? ? ? . 35 PHE B CG 2350 ATOM 1556 C CD1 . PHE B 2350 35 . -11.887 0.445 35.101 1.00 17.70 ? ? ? ? ? . 35 PHE B CD1 2350 ATOM 1557 C CD2 . PHE B 2350 35 . -9.573 0.220 34.578 1.00 18.87 ? ? ? ? ? . 35 PHE B CD2 2350 ATOM 1558 C CE1 . PHE B 2350 35 . -11.643 -0.049 36.378 1.00 18.55 ? ? ? ? ? . 35 PHE B CE1 2350 ATOM 1559 C CE2 . PHE B 2350 35 . -9.317 -0.256 35.858 1.00 18.03 ? ? ? ? ? . 35 PHE B CE2 2350 ATOM 1560 C CZ . PHE B 2350 35 . -10.352 -0.385 36.761 1.00 20.83 ? ? ? ? ? . 35 PHE B CZ 2350 ATOM 1561 N N . SER B 2350 36 . -10.401 3.940 30.922 1.00 16.18 ? ? ? ? ? . 36 SER B N 2350 ATOM 1562 C CA . SER B 2350 36 . -10.418 4.655 29.654 1.00 16.32 ? ? ? ? ? . 36 SER B CA 2350 ATOM 1563 C C . SER B 2350 36 . -8.995 5.030 29.241 1.00 14.78 ? ? ? ? ? . 36 SER B C 2350 ATOM 1564 O O . SER B 2350 36 . -8.040 4.734 29.954 1.00 14.88 ? ? ? ? ? . 36 SER B O 2350 ATOM 1565 C CB . SER B 2350 36 . -11.285 5.920 29.788 1.00 17.87 ? ? ? ? ? . 36 SER B CB 2350 ATOM 1566 O OG . SER B 2350 36 . -11.535 6.503 28.519 1.00 18.57 ? ? ? ? ? . 36 SER B OG 2350 ATOM 1567 N N . ALA B 2350 37 . -8.857 5.660 28.080 1.00 15.35 ? ? ? ? ? . 37 ALA B N 2350 ATOM 1568 C CA . ALA B 2350 37 . -7.567 6.159 27.613 1.00 15.61 ? ? ? ? ? . 37 ALA B CA 2350 ATOM 1569 C C . ALA B 2350 37 . -7.805 7.204 26.551 1.00 16.69 ? ? ? ? ? . 37 ALA B C 2350 ATOM 1570 O O . ALA B 2350 37 . -8.754 7.075 25.778 1.00 16.13 ? ? ? ? ? . 37 ALA B O 2350 ATOM 1571 C CB . ALA B 2350 37 . -6.728 5.014 27.031 1.00 15.54 ? ? ? ? ? . 37 ALA B CB 2350 ATOM 1572 N N . SER B 2350 38 . -6.913 8.197 26.489 1.00 15.71 ? ? ? ? ? . 38 SER B N 2350 ATOM 1573 C CA . SER B 2350 38 . -7.072 9.335 25.581 1.00 17.09 ? ? ? ? ? . 38 SER B CA 2350 ATOM 1574 C C . SER B 2350 38 . -7.153 8.953 24.102 1.00 19.07 ? ? ? ? ? . 38 SER B C 2350 ATOM 1575 O O . SER B 2350 38 . -7.854 9.606 23.326 1.00 20.98 ? ? ? ? ? . 38 SER B O 2350 ATOM 1576 C CB . SER B 2350 38 . -5.941 10.335 25.773 1.00 15.69 ? ? ? ? ? . 38 SER B CB 2350 ATOM 1577 O OG . SER B 2350 38 . -4.701 9.809 25.396 1.00 15.44 ? ? ? ? ? . 38 SER B OG 2350 ATOM 1578 N N . TRP B 2350 39 . -6.463 7.874 23.742 1.00 17.71 ? ? ? ? ? . 39 TRP B N 2350 ATOM 1579 C CA . TRP B 2350 39 . -6.253 7.475 22.352 1.00 17.15 ? ? ? ? ? . 39 TRP B CA 2350 ATOM 1580 C C . TRP B 2350 39 . -7.121 6.299 21.897 1.00 17.30 ? ? ? ? ? . 39 TRP B C 2350 ATOM 1581 O O . TRP B 2350 39 . -7.026 5.902 20.745 1.00 15.89 ? ? ? ? ? . 39 TRP B O 2350 ATOM 1582 C CB . TRP B 2350 39 . -4.757 7.203 22.076 1.00 17.52 ? ? ? ? ? . 39 TRP B CB 2350 ATOM 1583 C CG . TRP B 2350 39 . -4.007 6.714 23.240 1.00 17.35 ? ? ? ? ? . 39 TRP B CG 2350 ATOM 1584 C CD1 . TRP B 2350 39 . -3.045 7.391 23.940 1.00 17.10 ? ? ? ? ? . 39 TRP B CD1 2350 ATOM 1585 C CD2 . TRP B 2350 39 . -4.166 5.451 23.891 1.00 16.65 ? ? ? ? ? . 39 TRP B CD2 2350 ATOM 1586 C CE2 . TRP B 2350 39 . -3.278 5.437 24.986 1.00 16.51 ? ? ? ? ? . 39 TRP B CE2 2350 ATOM 1587 C CE3 . TRP B 2350 39 . -4.985 4.334 23.666 1.00 17.15 ? ? ? ? ? . 39 TRP B CE3 2350 ATOM 1588 N NE1 . TRP B 2350 39 . -2.611 6.633 24.990 1.00 18.33 ? ? ? ? ? . 39 TRP B NE1 2350 ATOM 1589 C CZ2 . TRP B 2350 39 . -3.158 4.343 25.842 1.00 16.73 ? ? ? ? ? . 39 TRP B CZ2 2350 ATOM 1590 C CZ3 . TRP B 2350 39 . -4.871 3.244 24.540 1.00 17.40 ? ? ? ? ? . 39 TRP B CZ3 2350 ATOM 1591 C CH2 . TRP B 2350 39 . -3.974 3.272 25.619 1.00 17.72 ? ? ? ? ? . 39 TRP B CH2 2350 ATOM 1592 N N A CYS B 2350 40 . -7.942 5.730 22.791 0.50 17.64 ? ? ? ? ? . 40 CYS B N 2350 ATOM 1593 N N B CYS B 2350 40 . -7.980 5.787 22.782 0.50 17.88 ? ? ? ? ? . 40 CYS B N 2350 ATOM 1594 C CA A CYS B 2350 40 . -8.768 4.570 22.439 0.50 16.86 ? ? ? ? ? . 40 CYS B CA 2350 ATOM 1595 C CA B CYS B 2350 40 . -8.812 4.625 22.494 0.50 17.28 ? ? ? ? ? . 40 CYS B CA 2350 ATOM 1596 C C A CYS B 2350 40 . -10.035 5.057 21.740 0.50 16.54 ? ? ? ? ? . 40 CYS B C 2350 ATOM 1597 C C B CYS B 2350 40 . -10.071 5.074 21.747 0.50 16.75 ? ? ? ? ? . 40 CYS B C 2350 ATOM 1598 O O A CYS B 2350 40 . -10.790 5.824 22.317 0.50 16.77 ? ? ? ? ? . 40 CYS B O 2350 ATOM 1599 O O B CYS B 2350 40 . -10.858 5.829 22.299 0.50 16.99 ? ? ? ? ? . 40 CYS B O 2350 ATOM 1600 C CB A CYS B 2350 40 . -9.121 3.740 23.677 0.50 17.14 ? ? ? ? ? . 40 CYS B CB 2350 ATOM 1601 C CB B CYS B 2350 40 . -9.167 3.943 23.820 0.50 18.03 ? ? ? ? ? . 40 CYS B CB 2350 ATOM 1602 S SG A CYS B 2350 40 . -10.007 2.211 23.268 0.50 17.57 ? ? ? ? ? . 40 CYS B SG 2350 ATOM 1603 S SG B CYS B 2350 40 . -10.605 2.859 23.744 0.50 19.19 ? ? ? ? ? . 40 CYS B SG 2350 ATOM 1604 N N . PRO B 2350 41 . -10.253 4.654 20.475 1.00 16.94 ? ? ? ? ? . 41 PRO B N 2350 ATOM 1605 C CA . PRO B 2350 41 . -11.436 5.180 19.741 1.00 18.45 ? ? ? ? ? . 41 PRO B CA 2350 ATOM 1606 C C . PRO B 2350 41 . -12.810 4.984 20.378 1.00 17.82 ? ? ? ? ? . 41 PRO B C 2350 ATOM 1607 O O . PRO B 2350 41 . -13.539 5.965 20.492 1.00 16.82 ? ? ? ? ? . 41 PRO B O 2350 ATOM 1608 C CB . PRO B 2350 41 . -11.343 4.521 18.355 1.00 16.98 ? ? ? ? ? . 41 PRO B CB 2350 ATOM 1609 C CG . PRO B 2350 41 . -9.900 4.161 18.206 1.00 16.89 ? ? ? ? ? . 41 PRO B CG 2350 ATOM 1610 C CD . PRO B 2350 41 . -9.375 3.873 19.578 1.00 17.21 ? ? ? ? ? . 41 PRO B CD 2350 ATOM 1611 N N . PRO B 2350 42 . -13.155 3.755 20.820 1.00 18.29 ? ? ? ? ? . 42 PRO B N 2350 ATOM 1612 C CA . PRO B 2350 42 . -14.458 3.621 21.485 1.00 18.49 ? ? ? ? ? . 42 PRO B CA 2350 ATOM 1613 C C . PRO B 2350 42 . -14.634 4.453 22.767 1.00 18.34 ? ? ? ? ? . 42 PRO B C 2350 ATOM 1614 O O . PRO B 2350 42 . -15.752 4.859 23.076 1.00 17.26 ? ? ? ? ? . 42 PRO B O 2350 ATOM 1615 C CB . PRO B 2350 42 . -14.575 2.107 21.771 1.00 18.19 ? ? ? ? ? . 42 PRO B CB 2350 ATOM 1616 C CG . PRO B 2350 42 . -13.212 1.574 21.649 1.00 19.06 ? ? ? ? ? . 42 PRO B CG 2350 ATOM 1617 C CD . PRO B 2350 42 . -12.479 2.450 20.676 1.00 18.40 ? ? ? ? ? . 42 PRO B CD 2350 ATOM 1618 N N . CYS B 2350 43 . -13.552 4.727 23.492 1.00 17.22 ? ? ? ? ? . 43 CYS B N 2350 ATOM 1619 C CA . CYS B 2350 43 . -13.627 5.660 24.616 1.00 18.95 ? ? ? ? ? . 43 CYS B CA 2350 ATOM 1620 C C . CYS B 2350 43 . -14.010 7.054 24.154 1.00 18.30 ? ? ? ? ? . 43 CYS B C 2350 ATOM 1621 O O . CYS B 2350 43 . -14.776 7.731 24.840 1.00 17.47 ? ? ? ? ? . 43 CYS B O 2350 ATOM 1622 C CB . CYS B 2350 43 . -12.315 5.731 25.400 1.00 17.93 ? ? ? ? ? . 43 CYS B CB 2350 ATOM 1623 S SG . CYS B 2350 43 . -11.945 4.205 26.268 1.00 18.83 ? ? ? ? ? . 43 CYS B SG 2350 ATOM 1624 N N . ARG B 2350 44 . -13.488 7.475 22.999 1.00 18.41 ? ? ? ? ? . 44 ARG B N 2350 ATOM 1625 C CA . ARG B 2350 44 . -13.821 8.784 22.446 1.00 20.27 ? ? ? ? ? . 44 ARG B CA 2350 ATOM 1626 C C . ARG B 2350 44 . -15.314 8.919 22.195 1.00 18.08 ? ? ? ? ? . 44 ARG B C 2350 ATOM 1627 O O . ARG B 2350 44 . -15.884 9.989 22.410 1.00 17.78 ? ? ? ? ? . 44 ARG B O 2350 ATOM 1628 C CB . ARG B 2350 44 . -13.015 9.091 21.174 1.00 24.38 ? ? ? ? ? . 44 ARG B CB 2350 ATOM 1629 C CG . ARG B 2350 44 . -11.547 9.283 21.467 1.00 31.65 ? ? ? ? ? . 44 ARG B CG 2350 ATOM 1630 C CD . ARG B 2350 44 . -10.774 9.731 20.250 1.00 40.06 ? ? ? ? ? . 44 ARG B CD 2350 ATOM 1631 N NE . ARG B 2350 44 . -9.418 10.139 20.614 1.00 46.56 ? ? ? ? ? . 44 ARG B NE 2350 ATOM 1632 C CZ . ARG B 2350 44 . -8.478 10.527 19.754 1.00 50.40 ? ? ? ? ? . 44 ARG B CZ 2350 ATOM 1633 N NH1 . ARG B 2350 44 . -8.722 10.569 18.443 1.00 54.07 ? ? ? ? ? 1+ 44 ARG B NH1 2350 ATOM 1634 N NH2 . ARG B 2350 44 . -7.276 10.876 20.209 1.00 53.44 ? ? ? ? ? . 44 ARG B NH2 2350 ATOM 1635 N N . GLY B 2350 45 . -15.947 7.823 21.783 1.00 17.67 ? ? ? ? ? . 45 GLY B N 2350 ATOM 1636 C CA . GLY B 2350 45 . -17.390 7.801 21.531 1.00 17.84 ? ? ? ? ? . 45 GLY B CA 2350 ATOM 1637 C C . GLY B 2350 45 . -18.247 7.720 22.782 1.00 17.44 ? ? ? ? ? . 45 GLY B C 2350 ATOM 1638 O O . GLY B 2350 45 . -19.403 8.161 22.779 1.00 19.73 ? ? ? ? ? . 45 GLY B O 2350 ATOM 1639 N N . PHE B 2350 46 . -17.694 7.155 23.848 1.00 16.57 ? ? ? ? ? . 46 PHE B N 2350 ATOM 1640 C CA . PHE B 2350 46 . -18.431 6.950 25.088 1.00 17.20 ? ? ? ? ? . 46 PHE B CA 2350 ATOM 1641 C C . PHE B 2350 46 . -18.295 8.104 26.090 1.00 16.63 ? ? ? ? ? . 46 PHE B C 2350 ATOM 1642 O O . PHE B 2350 46 . -19.269 8.470 26.755 1.00 18.09 ? ? ? ? ? . 46 PHE B O 2350 ATOM 1643 C CB . PHE B 2350 46 . -18.031 5.622 25.739 1.00 15.59 ? ? ? ? ? . 46 PHE B CB 2350 ATOM 1644 C CG . PHE B 2350 46 . -18.777 5.345 26.999 1.00 16.81 ? ? ? ? ? . 46 PHE B CG 2350 ATOM 1645 C CD1 . PHE B 2350 46 . -20.168 5.219 26.980 1.00 16.35 ? ? ? ? ? . 46 PHE B CD1 2350 ATOM 1646 C CD2 . PHE B 2350 46 . -18.108 5.247 28.225 1.00 16.40 ? ? ? ? ? . 46 PHE B CD2 2350 ATOM 1647 C CE1 . PHE B 2350 46 . -20.867 4.988 28.154 1.00 16.37 ? ? ? ? ? . 46 PHE B CE1 2350 ATOM 1648 C CE2 . PHE B 2350 46 . -18.811 5.004 29.398 1.00 16.33 ? ? ? ? ? . 46 PHE B CE2 2350 ATOM 1649 C CZ . PHE B 2350 46 . -20.198 4.887 29.358 1.00 15.99 ? ? ? ? ? . 46 PHE B CZ 2350 ATOM 1650 N N . THR B 2350 47 . -17.106 8.685 26.208 1.00 15.70 ? ? ? ? ? . 47 THR B N 2350 ATOM 1651 C CA . THR B 2350 47 . -16.868 9.714 27.226 1.00 16.94 ? ? ? ? ? . 47 THR B CA 2350 ATOM 1652 C C . THR B 2350 47 . -17.912 10.856 27.243 1.00 17.07 ? ? ? ? ? . 47 THR B C 2350 ATOM 1653 O O . THR B 2350 47 . -18.349 11.248 28.330 1.00 16.48 ? ? ? ? ? . 47 THR B O 2350 ATOM 1654 C CB . THR B 2350 47 . -15.430 10.247 27.148 1.00 19.26 ? ? ? ? ? . 47 THR B CB 2350 ATOM 1655 C CG2 . THR B 2350 47 . -15.210 11.385 28.149 1.00 19.34 ? ? ? ? ? . 47 THR B CG2 2350 ATOM 1656 O OG1 . THR B 2350 47 . -14.530 9.163 27.429 1.00 19.80 ? ? ? ? ? . 47 THR B OG1 2350 ATOM 1657 N N . PRO B 2350 48 . -18.331 11.370 26.060 1.00 16.50 ? ? ? ? ? . 48 PRO B N 2350 ATOM 1658 C CA . PRO B 2350 48 . -19.352 12.439 26.034 1.00 16.75 ? ? ? ? ? . 48 PRO B CA 2350 ATOM 1659 C C . PRO B 2350 48 . -20.719 11.979 26.525 1.00 16.05 ? ? ? ? ? . 48 PRO B C 2350 ATOM 1660 O O . PRO B 2350 48 . -21.466 12.765 27.119 1.00 15.03 ? ? ? ? ? . 48 PRO B O 2350 ATOM 1661 C CB . PRO B 2350 48 . -19.442 12.835 24.547 1.00 17.41 ? ? ? ? ? . 48 PRO B CB 2350 ATOM 1662 C CG . PRO B 2350 48 . -18.246 12.261 23.903 1.00 17.90 ? ? ? ? ? . 48 PRO B CG 2350 ATOM 1663 C CD . PRO B 2350 48 . -17.832 11.072 24.704 1.00 18.03 ? ? ? ? ? . 48 PRO B CD 2350 ATOM 1664 N N . VAL B 2350 49 . -21.026 10.710 26.278 1.00 17.45 ? ? ? ? ? . 49 VAL B N 2350 ATOM 1665 C CA . VAL B 2350 49 . -22.276 10.119 26.729 1.00 18.57 ? ? ? ? ? . 49 VAL B CA 2350 ATOM 1666 C C . VAL B 2350 49 . -22.243 10.048 28.251 1.00 18.24 ? ? ? ? ? . 49 VAL B C 2350 ATOM 1667 O O . VAL B 2350 49 . -23.231 10.387 28.905 1.00 17.34 ? ? ? ? ? . 49 VAL B O 2350 ATOM 1668 C CB . VAL B 2350 49 . -22.505 8.703 26.161 1.00 21.18 ? ? ? ? ? . 49 VAL B CB 2350 ATOM 1669 C CG1 . VAL B 2350 49 . -23.853 8.147 26.632 1.00 23.32 ? ? ? ? ? . 49 VAL B CG1 2350 ATOM 1670 C CG2 . VAL B 2350 49 . -22.452 8.736 24.642 1.00 22.14 ? ? ? ? ? . 49 VAL B CG2 2350 ATOM 1671 N N . LEU B 2350 50 . -21.105 9.619 28.801 1.00 16.45 ? ? ? ? ? . 50 LEU B N 2350 ATOM 1672 C CA . LEU B 2350 50 . -20.964 9.533 30.254 1.00 17.01 ? ? ? ? ? . 50 LEU B CA 2350 ATOM 1673 C C . LEU B 2350 50 . -20.941 10.909 30.894 1.00 16.78 ? ? ? ? ? . 50 LEU B C 2350 ATOM 1674 O O . LEU B 2350 50 . -21.522 11.097 31.961 1.00 16.95 ? ? ? ? ? . 50 LEU B O 2350 ATOM 1675 C CB . LEU B 2350 50 . -19.728 8.714 30.655 1.00 17.57 ? ? ? ? ? . 50 LEU B CB 2350 ATOM 1676 C CG . LEU B 2350 50 . -19.486 8.477 32.154 1.00 17.08 ? ? ? ? ? . 50 LEU B CG 2350 ATOM 1677 C CD1 . LEU B 2350 50 . -20.623 7.695 32.799 1.00 17.71 ? ? ? ? ? . 50 LEU B CD1 2350 ATOM 1678 C CD2 . LEU B 2350 50 . -18.162 7.773 32.395 1.00 18.09 ? ? ? ? ? . 50 LEU B CD2 2350 ATOM 1679 N N . ALA B 2350 51 . -20.295 11.876 30.246 1.00 16.81 ? ? ? ? ? . 51 ALA B N 2350 ATOM 1680 C CA . ALA B 2350 51 . -20.333 13.269 30.722 1.00 15.97 ? ? ? ? ? . 51 ALA B CA 2350 ATOM 1681 C C . ALA B 2350 51 . -21.736 13.853 30.774 1.00 15.65 ? ? ? ? ? . 51 ALA B C 2350 ATOM 1682 O O . ALA B 2350 51 . -22.077 14.546 31.726 1.00 16.02 ? ? ? ? ? . 51 ALA B O 2350 ATOM 1683 C CB . ALA B 2350 51 . -19.426 14.156 29.890 1.00 14.73 ? ? ? ? ? . 51 ALA B CB 2350 ATOM 1684 N N . GLU B 2350 52 . -22.551 13.592 29.758 1.00 15.19 ? ? ? ? ? . 52 GLU B N 2350 ATOM 1685 C CA . GLU B 2350 52 . -23.941 14.038 29.776 1.00 16.90 ? ? ? ? ? . 52 GLU B CA 2350 ATOM 1686 C C . GLU B 2350 52 . -24.716 13.377 30.923 1.00 16.11 ? ? ? ? ? . 52 GLU B C 2350 ATOM 1687 O O . GLU B 2350 52 . -25.475 14.047 31.617 1.00 15.24 ? ? ? ? ? . 52 GLU B O 2350 ATOM 1688 C CB . GLU B 2350 52 . -24.619 13.757 28.426 1.00 19.85 ? ? ? ? ? . 52 GLU B CB 2350 ATOM 1689 C CG . GLU B 2350 52 . -26.027 14.336 28.294 1.00 21.97 ? ? ? ? ? . 52 GLU B CG 2350 ATOM 1690 C CD . GLU B 2350 52 . -26.678 14.037 26.951 1.00 26.15 ? ? ? ? ? . 52 GLU B CD 2350 ATOM 1691 O OE1 . GLU B 2350 52 . -25.970 13.605 26.008 1.00 26.88 ? ? ? ? ? . 52 GLU B OE1 2350 ATOM 1692 O OE2 . GLU B 2350 52 . -27.911 14.232 26.850 1.00 26.62 ? ? ? ? ? 1- 52 GLU B OE2 2350 ATOM 1693 N N . PHE B 2350 53 . -24.530 12.071 31.114 1.00 15.37 ? ? ? ? ? . 53 PHE B N 2350 ATOM 1694 C CA . PHE B 2350 53 . -25.170 11.341 32.218 1.00 15.90 ? ? ? ? ? . 53 PHE B CA 2350 ATOM 1695 C C . PHE B 2350 53 . -24.736 11.927 33.577 1.00 15.68 ? ? ? ? ? . 53 PHE B C 2350 ATOM 1696 O O . PHE B 2350 53 . -25.548 12.161 34.459 1.00 14.25 ? ? ? ? ? . 53 PHE B O 2350 ATOM 1697 C CB . PHE B 2350 53 . -24.829 9.842 32.131 1.00 18.04 ? ? ? ? ? . 53 PHE B CB 2350 ATOM 1698 C CG . PHE B 2350 53 . -25.649 8.979 33.042 1.00 17.72 ? ? ? ? ? . 53 PHE B CG 2350 ATOM 1699 C CD1 . PHE B 2350 53 . -26.890 8.471 32.625 1.00 19.59 ? ? ? ? ? . 53 PHE B CD1 2350 ATOM 1700 C CD2 . PHE B 2350 53 . -25.192 8.667 34.325 1.00 18.36 ? ? ? ? ? . 53 PHE B CD2 2350 ATOM 1701 C CE1 . PHE B 2350 53 . -27.646 7.665 33.479 1.00 20.58 ? ? ? ? ? . 53 PHE B CE1 2350 ATOM 1702 C CE2 . PHE B 2350 53 . -25.952 7.882 35.182 1.00 18.63 ? ? ? ? ? . 53 PHE B CE2 2350 ATOM 1703 C CZ . PHE B 2350 53 . -27.186 7.397 34.765 1.00 19.12 ? ? ? ? ? . 53 PHE B CZ 2350 ATOM 1704 N N . TYR B 2350 54 . -23.443 12.174 33.711 1.00 16.22 ? ? ? ? ? . 54 TYR B N 2350 ATOM 1705 C CA . TYR B 2350 54 . -22.864 12.791 34.900 1.00 16.80 ? ? ? ? ? . 54 TYR B CA 2350 ATOM 1706 C C . TYR B 2350 54 . -23.456 14.164 35.194 1.00 17.12 ? ? ? ? ? . 54 TYR B C 2350 ATOM 1707 O O . TYR B 2350 54 . -23.868 14.429 36.330 1.00 14.13 ? ? ? ? ? . 54 TYR B O 2350 ATOM 1708 C CB . TYR B 2350 54 . -21.349 12.901 34.733 1.00 17.77 ? ? ? ? ? . 54 TYR B CB 2350 ATOM 1709 C CG . TYR B 2350 54 . -20.606 13.433 35.935 1.00 17.67 ? ? ? ? ? . 54 TYR B CG 2350 ATOM 1710 C CD1 . TYR B 2350 54 . -20.241 12.595 36.984 1.00 19.54 ? ? ? ? ? . 54 TYR B CD1 2350 ATOM 1711 C CD2 . TYR B 2350 54 . -20.236 14.774 36.011 1.00 17.99 ? ? ? ? ? . 54 TYR B CD2 2350 ATOM 1712 C CE1 . TYR B 2350 54 . -19.553 13.086 38.099 1.00 18.82 ? ? ? ? ? . 54 TYR B CE1 2350 ATOM 1713 C CE2 . TYR B 2350 54 . -19.542 15.265 37.108 1.00 18.99 ? ? ? ? ? . 54 TYR B CE2 2350 ATOM 1714 C CZ . TYR B 2350 54 . -19.210 14.418 38.151 1.00 18.31 ? ? ? ? ? . 54 TYR B CZ 2350 ATOM 1715 O OH . TYR B 2350 54 . -18.510 14.930 39.221 1.00 18.74 ? ? ? ? ? . 54 TYR B OH 2350 ATOM 1716 N N . GLU B 2350 55 . -23.489 15.046 34.191 1.00 17.50 ? ? ? ? ? . 55 GLU B N 2350 ATOM 1717 C CA . GLU B 2350 55 . -24.071 16.376 34.399 1.00 19.67 ? ? ? ? ? . 55 GLU B CA 2350 ATOM 1718 C C . GLU B 2350 55 . -25.528 16.272 34.838 1.00 17.98 ? ? ? ? ? . 55 GLU B C 2350 ATOM 1719 O O . GLU B 2350 55 . -25.945 16.968 35.744 1.00 16.25 ? ? ? ? ? . 55 GLU B O 2350 ATOM 1720 C CB . GLU B 2350 55 . -23.941 17.257 33.149 1.00 24.87 ? ? ? ? ? . 55 GLU B CB 2350 ATOM 1721 C CG . GLU B 2350 55 . -22.527 17.753 32.894 1.00 31.42 ? ? ? ? ? . 55 GLU B CG 2350 ATOM 1722 C CD . GLU B 2350 55 . -22.014 18.658 34.006 1.00 38.94 ? ? ? ? ? . 55 GLU B CD 2350 ATOM 1723 O OE1 . GLU B 2350 55 . -22.737 19.618 34.387 1.00 43.93 ? ? ? ? ? . 55 GLU B OE1 2350 ATOM 1724 O OE2 . GLU B 2350 55 . -20.895 18.399 34.497 1.00 41.82 ? ? ? ? ? 1- 55 GLU B OE2 2350 ATOM 1725 N N . LYS B 2350 56 . -26.280 15.360 34.222 1.00 18.56 ? ? ? ? ? . 56 LYS B N 2350 ATOM 1726 C CA . LYS B 2350 56 . -27.717 15.217 34.507 1.00 18.98 ? ? ? ? ? . 56 LYS B CA 2350 ATOM 1727 C C . LYS B 2350 56 . -28.025 14.710 35.903 1.00 17.58 ? ? ? ? ? . 56 LYS B C 2350 ATOM 1728 O O . LYS B 2350 56 . -28.974 15.184 36.534 1.00 16.83 ? ? ? ? ? . 56 LYS B O 2350 ATOM 1729 C CB . LYS B 2350 56 . -28.402 14.254 33.521 1.00 23.33 ? ? ? ? ? . 56 LYS B CB 2350 ATOM 1730 C CG . LYS B 2350 56 . -29.299 14.920 32.482 1.00 28.96 ? ? ? ? ? . 56 LYS B CG 2350 ATOM 1731 C CD . LYS B 2350 56 . -30.217 13.890 31.823 1.00 29.28 ? ? ? ? ? . 56 LYS B CD 2350 ATOM 1732 C CE . LYS B 2350 56 . -31.047 14.501 30.712 1.00 29.01 ? ? ? ? ? . 56 LYS B CE 2350 ATOM 1733 N NZ . LYS B 2350 56 . -31.705 13.489 29.836 1.00 28.78 ? ? ? ? ? 1+ 56 LYS B NZ 2350 ATOM 1734 N N . HIS B 2350 57 . -27.267 13.711 36.347 1.00 15.89 ? ? ? ? ? . 57 HIS B N 2350 ATOM 1735 C CA . HIS B 2350 57 . -27.678 12.856 37.452 1.00 17.69 ? ? ? ? ? . 57 HIS B CA 2350 ATOM 1736 C C . HIS B 2350 57 . -26.739 12.753 38.653 1.00 17.22 ? ? ? ? ? . 57 HIS B C 2350 ATOM 1737 O O . HIS B 2350 57 . -27.149 12.180 39.658 1.00 18.59 ? ? ? ? ? . 57 HIS B O 2350 ATOM 1738 C CB . HIS B 2350 57 . -27.888 11.412 36.953 1.00 17.02 ? ? ? ? ? . 57 HIS B CB 2350 ATOM 1739 C CG . HIS B 2350 57 . -28.825 11.286 35.801 1.00 17.81 ? ? ? ? ? . 57 HIS B CG 2350 ATOM 1740 C CD2 . HIS B 2350 57 . -28.639 10.754 34.565 1.00 18.89 ? ? ? ? ? . 57 HIS B CD2 2350 ATOM 1741 N ND1 . HIS B 2350 57 . -30.140 11.681 35.855 1.00 17.57 ? ? ? ? ? . 57 HIS B ND1 2350 ATOM 1742 C CE1 . HIS B 2350 57 . -30.718 11.440 34.689 1.00 17.83 ? ? ? ? ? . 57 HIS B CE1 2350 ATOM 1743 N NE2 . HIS B 2350 57 . -29.833 10.862 33.894 1.00 17.22 ? ? ? ? ? . 57 HIS B NE2 2350 ATOM 1744 N N . HIS B 2350 58 . -25.498 13.238 38.573 1.00 15.59 ? ? ? ? ? . 58 HIS B N 2350 ATOM 1745 C CA . HIS B 2350 58 . -24.536 12.887 39.623 1.00 16.06 ? ? ? ? ? . 58 HIS B CA 2350 ATOM 1746 C C . HIS B 2350 58 . -24.926 13.425 41.003 1.00 14.76 ? ? ? ? ? . 58 HIS B C 2350 ATOM 1747 O O . HIS B 2350 58 . -24.618 12.803 41.994 1.00 16.12 ? ? ? ? ? . 58 HIS B O 2350 ATOM 1748 C CB . HIS B 2350 58 . -23.088 13.220 39.230 1.00 16.88 ? ? ? ? ? . 58 HIS B CB 2350 ATOM 1749 C CG . HIS B 2350 58 . -22.647 14.619 39.541 1.00 17.89 ? ? ? ? ? . 58 HIS B CG 2350 ATOM 1750 C CD2 . HIS B 2350 58 . -21.806 15.090 40.492 1.00 19.39 ? ? ? ? ? . 58 HIS B CD2 2350 ATOM 1751 N ND1 . HIS B 2350 58 . -23.009 15.708 38.780 1.00 18.72 ? ? ? ? ? . 58 HIS B ND1 2350 ATOM 1752 C CE1 . HIS B 2350 58 . -22.454 16.798 39.280 1.00 19.42 ? ? ? ? ? . 58 HIS B CE1 2350 ATOM 1753 N NE2 . HIS B 2350 58 . -21.713 16.449 40.316 1.00 20.87 ? ? ? ? ? . 58 HIS B NE2 2350 ATOM 1754 N N . VAL B 2350 59 . -25.648 14.545 41.065 1.00 16.39 ? ? ? ? ? . 59 VAL B N 2350 ATOM 1755 C CA . VAL B 2350 59 . -26.130 15.053 42.350 1.00 16.87 ? ? ? ? ? . 59 VAL B CA 2350 ATOM 1756 C C . VAL B 2350 59 . -27.353 14.277 42.829 1.00 17.10 ? ? ? ? ? . 59 VAL B C 2350 ATOM 1757 O O . VAL B 2350 59 . -27.352 13.747 43.950 1.00 16.17 ? ? ? ? ? . 59 VAL B O 2350 ATOM 1758 C CB . VAL B 2350 59 . -26.425 16.570 42.292 1.00 18.85 ? ? ? ? ? . 59 VAL B CB 2350 ATOM 1759 C CG1 . VAL B 2350 59 . -27.056 17.055 43.595 1.00 19.93 ? ? ? ? ? . 59 VAL B CG1 2350 ATOM 1760 C CG2 . VAL B 2350 59 . -25.131 17.324 42.014 1.00 19.28 ? ? ? ? ? . 59 VAL B CG2 2350 ATOM 1761 N N . ALA B 2350 60 . -28.393 14.211 41.992 1.00 16.61 ? ? ? ? ? . 60 ALA B N 2350 ATOM 1762 C CA . ALA B 2350 60 . -29.643 13.560 42.375 1.00 16.62 ? ? ? ? ? . 60 ALA B CA 2350 ATOM 1763 C C . ALA B 2350 60 . -29.499 12.083 42.675 1.00 16.56 ? ? ? ? ? . 60 ALA B C 2350 ATOM 1764 O O . ALA B 2350 60 . -30.263 11.552 43.487 1.00 16.27 ? ? ? ? ? . 60 ALA B O 2350 ATOM 1765 C CB . ALA B 2350 60 . -30.707 13.767 41.307 1.00 18.55 ? ? ? ? ? . 60 ALA B CB 2350 ATOM 1766 N N . LYS B 2350 61 . -28.543 11.427 42.013 1.00 15.97 ? ? ? ? ? . 61 LYS B N 2350 ATOM 1767 C CA . LYS B 2350 61 . -28.281 10.007 42.207 1.00 16.67 ? ? ? ? ? . 61 LYS B CA 2350 ATOM 1768 C C . LYS B 2350 61 . -26.993 9.747 42.998 1.00 16.95 ? ? ? ? ? . 61 LYS B C 2350 ATOM 1769 O O . LYS B 2350 61 . -26.540 8.604 43.087 1.00 17.30 ? ? ? ? ? . 61 LYS B O 2350 ATOM 1770 C CB . LYS B 2350 61 . -28.262 9.295 40.847 1.00 17.50 ? ? ? ? ? . 61 LYS B CB 2350 ATOM 1771 C CG . LYS B 2350 61 . -29.620 9.367 40.155 1.00 17.98 ? ? ? ? ? . 61 LYS B CG 2350 ATOM 1772 C CD . LYS B 2350 61 . -29.665 8.512 38.910 1.00 18.06 ? ? ? ? ? . 61 LYS B CD 2350 ATOM 1773 C CE . LYS B 2350 61 . -30.940 8.764 38.114 1.00 18.72 ? ? ? ? ? . 61 LYS B CE 2350 ATOM 1774 N NZ . LYS B 2350 61 . -32.150 8.403 38.884 1.00 18.99 ? ? ? ? ? 1+ 61 LYS B NZ 2350 ATOM 1775 N N . ASN B 2350 62 . -26.411 10.816 43.549 1.00 16.07 ? ? ? ? ? . 62 ASN B N 2350 ATOM 1776 C CA . ASN B 2350 62 . -25.332 10.747 44.530 1.00 15.99 ? ? ? ? ? . 62 ASN B CA 2350 ATOM 1777 C C . ASN B 2350 62 . -24.176 9.821 44.109 1.00 15.20 ? ? ? ? ? . 62 ASN B C 2350 ATOM 1778 O O . ASN B 2350 62 . -23.870 8.839 44.786 1.00 14.78 ? ? ? ? ? . 62 ASN B O 2350 ATOM 1779 C CB . ASN B 2350 62 . -25.899 10.343 45.905 1.00 18.04 ? ? ? ? ? . 62 ASN B CB 2350 ATOM 1780 C CG . ASN B 2350 62 . -24.956 10.670 47.054 1.00 17.36 ? ? ? ? ? . 62 ASN B CG 2350 ATOM 1781 N ND2 . ASN B 2350 62 . -24.904 9.799 48.057 1.00 16.56 ? ? ? ? ? . 62 ASN B ND2 2350 ATOM 1782 O OD1 . ASN B 2350 62 . -24.296 11.703 47.042 1.00 21.05 ? ? ? ? ? . 62 ASN B OD1 2350 ATOM 1783 N N . PHE B 2350 63 . -23.568 10.132 42.966 1.00 14.72 ? ? ? ? ? . 63 PHE B N 2350 ATOM 1784 C CA . PHE B 2350 63 . -22.431 9.358 42.491 1.00 15.39 ? ? ? ? ? . 63 PHE B CA 2350 ATOM 1785 C C . PHE B 2350 63 . -21.308 10.231 42.009 1.00 15.90 ? ? ? ? ? . 63 PHE B C 2350 ATOM 1786 O O . PHE B 2350 63 . -21.496 11.409 41.735 1.00 16.12 ? ? ? ? ? . 63 PHE B O 2350 ATOM 1787 C CB . PHE B 2350 63 . -22.814 8.338 41.395 1.00 16.32 ? ? ? ? ? . 63 PHE B CB 2350 ATOM 1788 C CG . PHE B 2350 63 . -23.291 8.943 40.089 1.00 17.02 ? ? ? ? ? . 63 PHE B CG 2350 ATOM 1789 C CD1 . PHE B 2350 63 . -22.385 9.329 39.099 1.00 18.25 ? ? ? ? ? . 63 PHE B CD1 2350 ATOM 1790 C CD2 . PHE B 2350 63 . -24.659 9.059 39.814 1.00 17.83 ? ? ? ? ? . 63 PHE B CD2 2350 ATOM 1791 C CE1 . PHE B 2350 63 . -22.829 9.859 37.889 1.00 18.50 ? ? ? ? ? . 63 PHE B CE1 2350 ATOM 1792 C CE2 . PHE B 2350 63 . -25.104 9.590 38.605 1.00 17.77 ? ? ? ? ? . 63 PHE B CE2 2350 ATOM 1793 C CZ . PHE B 2350 63 . -24.191 9.996 37.644 1.00 18.65 ? ? ? ? ? . 63 PHE B CZ 2350 ATOM 1794 N N . GLU B 2350 64 . -20.136 9.618 41.915 1.00 16.66 ? ? ? ? ? . 64 GLU B N 2350 ATOM 1795 C CA . GLU B 2350 64 . -18.989 10.231 41.263 1.00 17.84 ? ? ? ? ? . 64 GLU B CA 2350 ATOM 1796 C C . GLU B 2350 64 . -18.421 9.274 40.226 1.00 17.11 ? ? ? ? ? . 64 GLU B C 2350 ATOM 1797 O O . GLU B 2350 64 . -18.650 8.068 40.282 1.00 18.90 ? ? ? ? ? . 64 GLU B O 2350 ATOM 1798 C CB . GLU B 2350 64 . -17.894 10.592 42.270 1.00 19.70 ? ? ? ? ? . 64 GLU B CB 2350 ATOM 1799 C CG . GLU B 2350 64 . -18.038 11.949 42.930 1.00 22.91 ? ? ? ? ? . 64 GLU B CG 2350 ATOM 1800 C CD . GLU B 2350 64 . -17.795 13.134 42.007 1.00 23.63 ? ? ? ? ? . 64 GLU B CD 2350 ATOM 1801 O OE1 . GLU B 2350 64 . -17.573 12.954 40.778 1.00 20.92 ? ? ? ? ? . 64 GLU B OE1 2350 ATOM 1802 O OE2 . GLU B 2350 64 . -17.832 14.269 42.539 1.00 26.83 ? ? ? ? ? 1- 64 GLU B OE2 2350 ATOM 1803 N N . VAL B 2350 65 . -17.685 9.852 39.284 1.00 16.75 ? ? ? ? ? . 65 VAL B N 2350 ATOM 1804 C CA . VAL B 2350 65 . -16.929 9.114 38.290 1.00 16.81 ? ? ? ? ? . 65 VAL B CA 2350 ATOM 1805 C C . VAL B 2350 65 . -15.455 9.398 38.559 1.00 16.59 ? ? ? ? ? . 65 VAL B C 2350 ATOM 1806 O O . VAL B 2350 65 . -15.063 10.553 38.710 1.00 17.30 ? ? ? ? ? . 65 VAL B O 2350 ATOM 1807 C CB . VAL B 2350 65 . -17.326 9.539 36.864 1.00 18.23 ? ? ? ? ? . 65 VAL B CB 2350 ATOM 1808 C CG1 . VAL B 2350 65 . -16.423 8.884 35.833 1.00 18.75 ? ? ? ? ? . 65 VAL B CG1 2350 ATOM 1809 C CG2 . VAL B 2350 65 . -18.799 9.198 36.599 1.00 18.08 ? ? ? ? ? . 65 VAL B CG2 2350 ATOM 1810 N N . VAL B 2350 66 . -14.658 8.334 38.648 1.00 16.92 ? ? ? ? ? . 66 VAL B N 2350 ATOM 1811 C CA . VAL B 2350 66 . -13.201 8.450 38.793 1.00 16.10 ? ? ? ? ? . 66 VAL B CA 2350 ATOM 1812 C C . VAL B 2350 66 . -12.561 7.811 37.574 1.00 16.81 ? ? ? ? ? . 66 VAL B C 2350 ATOM 1813 O O . VAL B 2350 66 . -12.656 6.601 37.384 1.00 14.43 ? ? ? ? ? . 66 VAL B O 2350 ATOM 1814 C CB . VAL B 2350 66 . -12.690 7.736 40.048 1.00 15.87 ? ? ? ? ? . 66 VAL B CB 2350 ATOM 1815 C CG1 . VAL B 2350 66 . -11.174 7.884 40.168 1.00 16.03 ? ? ? ? ? . 66 VAL B CG1 2350 ATOM 1816 C CG2 . VAL B 2350 66 . -13.411 8.247 41.289 1.00 17.08 ? ? ? ? ? . 66 VAL B CG2 2350 ATOM 1817 N N . LEU B 2350 67 . -11.904 8.632 36.753 1.00 16.88 ? ? ? ? ? . 67 LEU B N 2350 ATOM 1818 C CA . LEU B 2350 67 . -11.100 8.120 35.642 1.00 16.83 ? ? ? ? ? . 67 LEU B CA 2350 ATOM 1819 C C . LEU B 2350 67 . -9.926 7.249 36.120 1.00 15.67 ? ? ? ? ? . 67 LEU B C 2350 ATOM 1820 O O . LEU B 2350 67 . -9.163 7.640 36.994 1.00 15.86 ? ? ? ? ? . 67 LEU B O 2350 ATOM 1821 C CB . LEU B 2350 67 . -10.535 9.290 34.811 1.00 16.36 ? ? ? ? ? . 67 LEU B CB 2350 ATOM 1822 C CG . LEU B 2350 67 . -9.493 8.998 33.735 1.00 16.45 ? ? ? ? ? . 67 LEU B CG 2350 ATOM 1823 C CD1 . LEU B 2350 67 . -10.126 8.191 32.623 1.00 16.86 ? ? ? ? ? . 67 LEU B CD1 2350 ATOM 1824 C CD2 . LEU B 2350 67 . -8.919 10.311 33.205 1.00 16.53 ? ? ? ? ? . 67 LEU B CD2 2350 ATOM 1825 N N A ILE B 2350 68 . -9.823 6.056 35.548 0.67 17.20 ? ? ? ? ? . 68 ILE B N 2350 ATOM 1826 N N B ILE B 2350 68 . -9.793 6.074 35.515 0.33 16.39 ? ? ? ? ? . 68 ILE B N 2350 ATOM 1827 C CA A ILE B 2350 68 . -8.662 5.189 35.698 0.67 16.28 ? ? ? ? ? . 68 ILE B CA 2350 ATOM 1828 C CA B ILE B 2350 68 . -8.637 5.209 35.708 0.33 15.93 ? ? ? ? ? . 68 ILE B CA 2350 ATOM 1829 C C A ILE B 2350 68 . -8.110 5.096 34.288 0.67 16.36 ? ? ? ? ? . 68 ILE B C 2350 ATOM 1830 C C B ILE B 2350 68 . -8.022 5.007 34.337 0.33 16.33 ? ? ? ? ? . 68 ILE B C 2350 ATOM 1831 O O A ILE B 2350 68 . -8.657 4.376 33.452 0.67 13.87 ? ? ? ? ? . 68 ILE B O 2350 ATOM 1832 O O B ILE B 2350 68 . -8.400 4.098 33.598 0.33 15.33 ? ? ? ? ? . 68 ILE B O 2350 ATOM 1833 C CB A ILE B 2350 68 . -9.034 3.787 36.222 0.67 16.98 ? ? ? ? ? . 68 ILE B CB 2350 ATOM 1834 C CB B ILE B 2350 68 . -9.031 3.868 36.330 0.33 15.94 ? ? ? ? ? . 68 ILE B CB 2350 ATOM 1835 C CG1 A ILE B 2350 68 . -9.950 3.865 37.462 0.67 17.02 ? ? ? ? ? . 68 ILE B CG1 2350 ATOM 1836 C CG2 A ILE B 2350 68 . -7.776 2.987 36.527 0.67 18.01 ? ? ? ? ? . 68 ILE B CG2 2350 ATOM 1837 C CG1 B ILE B 2350 68 . -9.732 4.115 37.670 0.33 15.51 ? ? ? ? ? . 68 ILE B CG1 2350 ATOM 1838 C CG2 B ILE B 2350 68 . -7.803 2.996 36.521 0.33 16.40 ? ? ? ? ? . 68 ILE B CG2 2350 ATOM 1839 C CD1 A ILE B 2350 68 . -9.327 4.506 38.681 0.67 17.83 ? ? ? ? ? . 68 ILE B CD1 2350 ATOM 1840 C CD1 B ILE B 2350 68 . -9.736 2.920 38.593 0.33 15.36 ? ? ? ? ? . 68 ILE B CD1 2350 ATOM 1841 N N . SER B 2350 69 . -7.064 5.870 34.018 1.00 16.47 ? ? ? ? ? . 69 SER B N 2350 ATOM 1842 C CA . SER B 2350 69 . -6.527 5.995 32.667 1.00 16.62 ? ? ? ? ? . 69 SER B CA 2350 ATOM 1843 C C . SER B 2350 69 . -5.413 5.016 32.337 1.00 16.16 ? ? ? ? ? . 69 SER B C 2350 ATOM 1844 O O . SER B 2350 69 . -4.464 4.866 33.110 1.00 16.34 ? ? ? ? ? . 69 SER B O 2350 ATOM 1845 C CB . SER B 2350 69 . -5.983 7.406 32.474 1.00 18.73 ? ? ? ? ? . 69 SER B CB 2350 ATOM 1846 O OG . SER B 2350 69 . -5.408 7.522 31.182 1.00 19.30 ? ? ? ? ? . 69 SER B OG 2350 ATOM 1847 N N . TRP B 2350 70 . -5.493 4.412 31.150 1.00 16.99 ? ? ? ? ? . 70 TRP B N 2350 ATOM 1848 C CA . TRP B 2350 70 . -4.410 3.551 30.621 1.00 17.24 ? ? ? ? ? . 70 TRP B CA 2350 ATOM 1849 C C . TRP B 2350 70 . -3.265 4.371 29.990 1.00 16.18 ? ? ? ? ? . 70 TRP B C 2350 ATOM 1850 O O . TRP B 2350 70 . -2.248 3.798 29.603 1.00 14.77 ? ? ? ? ? . 70 TRP B O 2350 ATOM 1851 C CB . TRP B 2350 70 . -4.944 2.531 29.584 1.00 18.94 ? ? ? ? ? . 70 TRP B CB 2350 ATOM 1852 C CG . TRP B 2350 70 . -4.583 1.101 29.898 1.00 20.10 ? ? ? ? ? . 70 TRP B CG 2350 ATOM 1853 C CD1 . TRP B 2350 70 . -3.473 0.425 29.498 1.00 22.08 ? ? ? ? ? . 70 TRP B CD1 2350 ATOM 1854 C CD2 . TRP B 2350 70 . -5.346 0.183 30.687 1.00 21.73 ? ? ? ? ? . 70 TRP B CD2 2350 ATOM 1855 C CE2 . TRP B 2350 70 . -4.629 -1.029 30.731 1.00 23.54 ? ? ? ? ? . 70 TRP B CE2 2350 ATOM 1856 C CE3 . TRP B 2350 70 . -6.561 0.272 31.369 1.00 22.88 ? ? ? ? ? . 70 TRP B CE3 2350 ATOM 1857 N NE1 . TRP B 2350 70 . -3.492 -0.856 29.994 1.00 23.05 ? ? ? ? ? . 70 TRP B NE1 2350 ATOM 1858 C CZ2 . TRP B 2350 70 . -5.096 -2.154 31.412 1.00 24.12 ? ? ? ? ? . 70 TRP B CZ2 2350 ATOM 1859 C CZ3 . TRP B 2350 70 . -7.028 -0.849 32.056 1.00 25.08 ? ? ? ? ? . 70 TRP B CZ3 2350 ATOM 1860 C CH2 . TRP B 2350 70 . -6.287 -2.046 32.077 1.00 24.62 ? ? ? ? ? . 70 TRP B CH2 2350 ATOM 1861 N N . ASP B 2350 71 . -3.418 5.697 29.885 1.00 16.38 ? ? ? ? ? . 71 ASP B N 2350 ATOM 1862 C CA . ASP B 2350 71 . -2.354 6.535 29.343 1.00 15.76 ? ? ? ? ? . 71 ASP B CA 2350 ATOM 1863 C C . ASP B 2350 71 . -1.033 6.307 30.099 1.00 14.95 ? ? ? ? ? . 71 ASP B C 2350 ATOM 1864 O O . ASP B 2350 71 . -1.014 6.240 31.328 1.00 15.32 ? ? ? ? ? . 71 ASP B O 2350 ATOM 1865 C CB . ASP B 2350 71 . -2.711 8.034 29.397 1.00 16.06 ? ? ? ? ? . 71 ASP B CB 2350 ATOM 1866 C CG . ASP B 2350 71 . -3.700 8.447 28.335 1.00 17.20 ? ? ? ? ? . 71 ASP B CG 2350 ATOM 1867 O OD1 . ASP B 2350 71 . -4.912 8.326 28.574 1.00 21.58 ? ? ? ? ? . 71 ASP B OD1 2350 ATOM 1868 O OD2 . ASP B 2350 71 . -3.291 8.929 27.260 1.00 17.68 ? ? ? ? ? 1- 71 ASP B OD2 2350 ATOM 1869 N N A GLU B 2350 72 . 0.053 6.175 29.353 0.51 14.50 ? ? ? ? ? . 72 GLU B N 2350 ATOM 1870 N N B GLU B 2350 72 . 0.048 6.158 29.342 0.49 14.34 ? ? ? ? ? . 72 GLU B N 2350 ATOM 1871 C CA A GLU B 2350 72 . 1.384 6.076 29.938 0.51 15.09 ? ? ? ? ? . 72 GLU B CA 2350 ATOM 1872 C CA B GLU B 2350 72 . 1.392 6.048 29.893 0.49 14.83 ? ? ? ? ? . 72 GLU B CA 2350 ATOM 1873 C C A GLU B 2350 72 . 2.188 7.360 29.820 0.51 14.34 ? ? ? ? ? . 72 GLU B C 2350 ATOM 1874 C C B GLU B 2350 72 . 2.186 7.348 29.808 0.49 14.17 ? ? ? ? ? . 72 GLU B C 2350 ATOM 1875 O O A GLU B 2350 72 . 3.306 7.430 30.334 0.51 13.00 ? ? ? ? ? . 72 GLU B O 2350 ATOM 1876 O O B GLU B 2350 72 . 3.298 7.415 30.335 0.49 12.82 ? ? ? ? ? . 72 GLU B O 2350 ATOM 1877 C CB A GLU B 2350 72 . 2.134 4.920 29.293 0.51 16.83 ? ? ? ? ? . 72 GLU B CB 2350 ATOM 1878 C CB B GLU B 2350 72 . 2.140 4.927 29.174 0.49 16.27 ? ? ? ? ? . 72 GLU B CB 2350 ATOM 1879 C CG A GLU B 2350 72 . 1.517 3.586 29.664 0.51 17.87 ? ? ? ? ? . 72 GLU B CG 2350 ATOM 1880 C CG B GLU B 2350 72 . 1.469 3.580 29.387 0.49 17.30 ? ? ? ? ? . 72 GLU B CG 2350 ATOM 1881 C CD A GLU B 2350 72 . 2.172 2.446 28.936 0.51 19.88 ? ? ? ? ? . 72 GLU B CD 2350 ATOM 1882 C CD B GLU B 2350 72 . 2.111 2.458 28.599 0.49 18.87 ? ? ? ? ? . 72 GLU B CD 2350 ATOM 1883 O OE1 A GLU B 2350 72 . 1.971 2.368 27.706 0.51 20.25 ? ? ? ? ? . 72 GLU B OE1 2350 ATOM 1884 O OE2 A GLU B 2350 72 . 2.872 1.640 29.592 0.51 21.48 ? ? ? ? ? 1- 72 GLU B OE2 2350 ATOM 1885 O OE1 B GLU B 2350 72 . 3.225 2.644 28.064 0.49 19.35 ? ? ? ? ? . 72 GLU B OE1 2350 ATOM 1886 O OE2 B GLU B 2350 72 . 1.490 1.377 28.529 0.49 19.70 ? ? ? ? ? 1- 72 GLU B OE2 2350 ATOM 1887 N N . ASN B 2350 73 . 1.620 8.362 29.146 1.00 14.22 ? ? ? ? ? . 73 ASN B N 2350 ATOM 1888 C CA . ASN B 2350 73 . 2.251 9.653 28.963 1.00 14.56 ? ? ? ? ? . 73 ASN B CA 2350 ATOM 1889 C C . ASN B 2350 73 . 1.516 10.611 29.883 1.00 15.20 ? ? ? ? ? . 73 ASN B C 2350 ATOM 1890 O O . ASN B 2350 73 . 0.299 10.782 29.768 1.00 15.15 ? ? ? ? ? . 73 ASN B O 2350 ATOM 1891 C CB . ASN B 2350 73 . 2.150 10.099 27.501 1.00 14.97 ? ? ? ? ? . 73 ASN B CB 2350 ATOM 1892 C CG . ASN B 2350 73 . 2.796 11.461 27.255 1.00 15.06 ? ? ? ? ? . 73 ASN B CG 2350 ATOM 1893 N ND2 . ASN B 2350 73 . 3.898 11.497 26.492 1.00 15.07 ? ? ? ? ? . 73 ASN B ND2 2350 ATOM 1894 O OD1 . ASN B 2350 73 . 2.309 12.465 27.753 1.00 14.79 ? ? ? ? ? . 73 ASN B OD1 2350 ATOM 1895 N N . GLU B 2350 74 . 2.250 11.208 30.814 1.00 15.32 ? ? ? ? ? . 74 GLU B N 2350 ATOM 1896 C CA . GLU B 2350 74 . 1.641 12.062 31.821 1.00 16.81 ? ? ? ? ? . 74 GLU B CA 2350 ATOM 1897 C C . GLU B 2350 74 . 0.997 13.322 31.235 1.00 15.94 ? ? ? ? ? . 74 GLU B C 2350 ATOM 1898 O O . GLU B 2350 74 . -0.087 13.721 31.687 1.00 16.38 ? ? ? ? ? . 74 GLU B O 2350 ATOM 1899 C CB . GLU B 2350 74 . 2.655 12.452 32.883 1.00 18.51 ? ? ? ? ? . 74 GLU B CB 2350 ATOM 1900 C CG . GLU B 2350 74 . 2.018 13.159 34.065 1.00 19.35 ? ? ? ? ? . 74 GLU B CG 2350 ATOM 1901 C CD . GLU B 2350 74 . 2.949 13.330 35.236 1.00 22.88 ? ? ? ? ? . 74 GLU B CD 2350 ATOM 1902 O OE1 . GLU B 2350 74 . 4.143 12.951 35.150 1.00 24.64 ? ? ? ? ? . 74 GLU B OE1 2350 ATOM 1903 O OE2 . GLU B 2350 74 . 2.481 13.867 36.255 1.00 25.05 ? ? ? ? ? 1- 74 GLU B OE2 2350 ATOM 1904 N N A SER B 2350 75 . 1.651 13.941 30.251 0.50 15.90 ? ? ? ? ? . 75 SER B N 2350 ATOM 1905 N N B SER B 2350 75 . 1.656 13.941 30.256 0.50 15.68 ? ? ? ? ? . 75 SER B N 2350 ATOM 1906 C CA A SER B 2350 75 . 1.104 15.148 29.605 0.50 15.77 ? ? ? ? ? . 75 SER B CA 2350 ATOM 1907 C CA B SER B 2350 75 . 1.115 15.142 29.594 0.50 15.45 ? ? ? ? ? . 75 SER B CA 2350 ATOM 1908 C C A SER B 2350 75 . -0.230 14.839 28.908 0.50 14.77 ? ? ? ? ? . 75 SER B C 2350 ATOM 1909 C C B SER B 2350 75 . -0.228 14.835 28.914 0.50 14.59 ? ? ? ? ? . 75 SER B C 2350 ATOM 1910 O O A SER B 2350 75 . -1.188 15.609 29.019 0.50 13.57 ? ? ? ? ? . 75 SER B O 2350 ATOM 1911 O O B SER B 2350 75 . -1.187 15.601 29.041 0.50 13.40 ? ? ? ? ? . 75 SER B O 2350 ATOM 1912 C CB A SER B 2350 75 . 2.122 15.753 28.623 0.50 16.44 ? ? ? ? ? . 75 SER B CB 2350 ATOM 1913 C CB B SER B 2350 75 . 2.128 15.696 28.582 0.50 15.81 ? ? ? ? ? . 75 SER B CB 2350 ATOM 1914 O OG A SER B 2350 75 . 2.210 15.005 27.421 0.50 16.71 ? ? ? ? ? . 75 SER B OG 2350 ATOM 1915 O OG B SER B 2350 75 . 1.655 16.888 27.982 0.50 15.64 ? ? ? ? ? . 75 SER B OG 2350 ATOM 1916 N N . ASP B 2350 76 . -0.291 13.701 28.218 1.00 14.38 ? ? ? ? ? . 76 ASP B N 2350 ATOM 1917 C CA . ASP B 2350 76 . -1.538 13.224 27.581 1.00 14.89 ? ? ? ? ? . 76 ASP B CA 2350 ATOM 1918 C C . ASP B 2350 76 . -2.647 12.977 28.614 1.00 15.39 ? ? ? ? ? . 76 ASP B C 2350 ATOM 1919 O O . ASP B 2350 76 . -3.806 13.366 28.415 1.00 14.77 ? ? ? ? ? . 76 ASP B O 2350 ATOM 1920 C CB . ASP B 2350 76 . -1.311 11.899 26.823 1.00 16.41 ? ? ? ? ? . 76 ASP B CB 2350 ATOM 1921 C CG . ASP B 2350 76 . -0.498 12.050 25.540 1.00 17.78 ? ? ? ? ? . 76 ASP B CG 2350 ATOM 1922 O OD1 . ASP B 2350 76 . -0.205 13.182 25.087 1.00 18.98 ? ? ? ? ? . 76 ASP B OD1 2350 ATOM 1923 O OD2 . ASP B 2350 76 . -0.156 10.993 24.968 1.00 18.58 ? ? ? ? ? 1- 76 ASP B OD2 2350 ATOM 1924 N N . PHE B 2350 77 . -2.289 12.316 29.706 1.00 14.34 ? ? ? ? ? . 77 PHE B N 2350 ATOM 1925 C CA . PHE B 2350 77 . -3.213 12.106 30.819 1.00 15.15 ? ? ? ? ? . 77 PHE B CA 2350 ATOM 1926 C C . PHE B 2350 77 . -3.856 13.408 31.312 1.00 15.18 ? ? ? ? ? . 77 PHE B C 2350 ATOM 1927 O O . PHE B 2350 77 . -5.078 13.505 31.385 1.00 14.13 ? ? ? ? ? . 77 PHE B O 2350 ATOM 1928 C CB . PHE B 2350 77 . -2.497 11.412 31.980 1.00 15.59 ? ? ? ? ? . 77 PHE B CB 2350 ATOM 1929 C CG . PHE B 2350 77 . -3.292 11.375 33.246 1.00 15.99 ? ? ? ? ? . 77 PHE B CG 2350 ATOM 1930 C CD1 . PHE B 2350 77 . -4.276 10.423 33.429 1.00 18.33 ? ? ? ? ? . 77 PHE B CD1 2350 ATOM 1931 C CD2 . PHE B 2350 77 . -3.055 12.289 34.261 1.00 16.11 ? ? ? ? ? . 77 PHE B CD2 2350 ATOM 1932 C CE1 . PHE B 2350 77 . -5.023 10.386 34.604 1.00 18.64 ? ? ? ? ? . 77 PHE B CE1 2350 ATOM 1933 C CE2 . PHE B 2350 77 . -3.798 12.256 35.433 1.00 17.39 ? ? ? ? ? . 77 PHE B CE2 2350 ATOM 1934 C CZ . PHE B 2350 77 . -4.772 11.305 35.607 1.00 16.62 ? ? ? ? ? . 77 PHE B CZ 2350 ATOM 1935 N N . HIS B 2350 78 . -3.030 14.390 31.644 1.00 15.40 ? ? ? ? ? . 78 HIS B N 2350 ATOM 1936 C CA . HIS B 2350 78 . -3.555 15.661 32.155 1.00 17.09 ? ? ? ? ? . 78 HIS B CA 2350 ATOM 1937 C C . HIS B 2350 78 . -4.412 16.407 31.136 1.00 17.40 ? ? ? ? ? . 78 HIS B C 2350 ATOM 1938 O O . HIS B 2350 78 . -5.402 17.034 31.503 1.00 17.56 ? ? ? ? ? . 78 HIS B O 2350 ATOM 1939 C CB . HIS B 2350 78 . -2.430 16.539 32.692 1.00 17.58 ? ? ? ? ? . 78 HIS B CB 2350 ATOM 1940 C CG . HIS B 2350 78 . -1.902 16.063 34.007 1.00 20.23 ? ? ? ? ? . 78 HIS B CG 2350 ATOM 1941 C CD2 . HIS B 2350 78 . -2.519 15.881 35.199 1.00 22.72 ? ? ? ? ? . 78 HIS B CD2 2350 ATOM 1942 N ND1 . HIS B 2350 78 . -0.596 15.675 34.190 1.00 22.98 ? ? ? ? ? . 78 HIS B ND1 2350 ATOM 1943 C CE1 . HIS B 2350 78 . -0.427 15.287 35.441 1.00 22.39 ? ? ? ? ? . 78 HIS B CE1 2350 ATOM 1944 N NE2 . HIS B 2350 78 . -1.577 15.400 36.074 1.00 22.36 ? ? ? ? ? . 78 HIS B NE2 2350 ATOM 1945 N N . ASP B 2350 79 . -4.044 16.334 29.863 1.00 17.23 ? ? ? ? ? . 79 ASP B N 2350 ATOM 1946 C CA . ASP B 2350 79 . -4.809 17.007 28.812 1.00 18.76 ? ? ? ? ? . 79 ASP B CA 2350 ATOM 1947 C C . ASP B 2350 79 . -6.208 16.401 28.687 1.00 16.45 ? ? ? ? ? . 79 ASP B C 2350 ATOM 1948 O O . ASP B 2350 79 . -7.200 17.117 28.642 1.00 15.60 ? ? ? ? ? . 79 ASP B O 2350 ATOM 1949 C CB . ASP B 2350 79 . -4.066 16.918 27.481 1.00 20.61 ? ? ? ? ? . 79 ASP B CB 2350 ATOM 1950 C CG . ASP B 2350 79 . -4.800 17.602 26.350 1.00 24.25 ? ? ? ? ? . 79 ASP B CG 2350 ATOM 1951 O OD1 . ASP B 2350 79 . -4.755 18.849 26.268 1.00 26.86 ? ? ? ? ? . 79 ASP B OD1 2350 ATOM 1952 O OD2 . ASP B 2350 79 . -5.416 16.883 25.534 1.00 27.35 ? ? ? ? ? 1- 79 ASP B OD2 2350 ATOM 1953 N N A TYR B 2350 80 . -6.218 15.075 28.656 0.75 17.30 ? ? ? ? ? . 80 TYR B N 2350 ATOM 1954 N N B TYR B 2350 80 . -6.333 15.079 28.645 0.25 15.42 ? ? ? ? ? . 80 TYR B N 2350 ATOM 1955 C CA A TYR B 2350 80 . -7.403 14.258 28.526 0.75 17.12 ? ? ? ? ? . 80 TYR B CA 2350 ATOM 1956 C CA B TYR B 2350 80 . -7.669 14.505 28.437 0.25 14.69 ? ? ? ? ? . 80 TYR B CA 2350 ATOM 1957 C C A TYR B 2350 80 . -8.387 14.510 29.684 0.75 17.25 ? ? ? ? ? . 80 TYR B C 2350 ATOM 1958 C C B TYR B 2350 80 . -8.505 14.348 29.715 0.25 15.60 ? ? ? ? ? . 80 TYR B C 2350 ATOM 1959 O O A TYR B 2350 80 . -9.548 14.887 29.472 0.75 17.68 ? ? ? ? ? . 80 TYR B O 2350 ATOM 1960 O O B TYR B 2350 80 . -9.730 14.238 29.614 0.25 15.85 ? ? ? ? ? . 80 TYR B O 2350 ATOM 1961 C CB A TYR B 2350 80 . -6.947 12.779 28.473 0.75 19.75 ? ? ? ? ? . 80 TYR B CB 2350 ATOM 1962 C CB B TYR B 2350 80 . -7.620 13.232 27.594 0.25 13.59 ? ? ? ? ? . 80 TYR B CB 2350 ATOM 1963 C CG A TYR B 2350 80 . -8.040 11.764 28.299 0.75 19.82 ? ? ? ? ? . 80 TYR B CG 2350 ATOM 1964 C CG B TYR B 2350 80 . -7.652 11.923 28.323 0.25 12.64 ? ? ? ? ? . 80 TYR B CG 2350 ATOM 1965 C CD1 A TYR B 2350 80 . -9.071 11.977 27.394 0.75 22.62 ? ? ? ? ? . 80 TYR B CD1 2350 ATOM 1966 C CD2 A TYR B 2350 80 . -8.031 10.564 29.011 0.75 20.66 ? ? ? ? ? . 80 TYR B CD2 2350 ATOM 1967 C CD1 B TYR B 2350 80 . -6.607 11.540 29.141 0.25 12.20 ? ? ? ? ? . 80 TYR B CD1 2350 ATOM 1968 C CD2 B TYR B 2350 80 . -8.709 11.040 28.144 0.25 12.38 ? ? ? ? ? . 80 TYR B CD2 2350 ATOM 1969 C CE1 A TYR B 2350 80 . -10.072 11.043 27.217 0.75 21.39 ? ? ? ? ? . 80 TYR B CE1 2350 ATOM 1970 C CE2 A TYR B 2350 80 . -9.026 9.619 28.828 0.75 19.95 ? ? ? ? ? . 80 TYR B CE2 2350 ATOM 1971 C CE1 B TYR B 2350 80 . -6.623 10.325 29.788 0.25 12.04 ? ? ? ? ? . 80 TYR B CE1 2350 ATOM 1972 C CE2 B TYR B 2350 80 . -8.730 9.820 28.776 0.25 12.02 ? ? ? ? ? . 80 TYR B CE2 2350 ATOM 1973 C CZ A TYR B 2350 80 . -10.042 9.862 27.921 0.75 20.46 ? ? ? ? ? . 80 TYR B CZ 2350 ATOM 1974 C CZ B TYR B 2350 80 . -7.686 9.470 29.596 0.25 11.93 ? ? ? ? ? . 80 TYR B CZ 2350 ATOM 1975 O OH A TYR B 2350 80 . -11.080 8.979 27.733 0.75 19.80 ? ? ? ? ? . 80 TYR B OH 2350 ATOM 1976 O OH B TYR B 2350 80 . -7.698 8.260 30.223 0.25 11.61 ? ? ? ? ? . 80 TYR B OH 2350 ATOM 1977 N N . TYR B 2350 81 . -7.879 14.343 30.898 1.00 16.13 ? ? ? ? ? . 81 TYR B N 2350 ATOM 1978 C CA . TYR B 2350 81 . -8.640 14.508 32.140 1.00 16.72 ? ? ? ? ? . 81 TYR B CA 2350 ATOM 1979 C C . TYR B 2350 81 . -9.094 15.980 32.334 1.00 17.50 ? ? ? ? ? . 81 TYR B C 2350 ATOM 1980 O O . TYR B 2350 81 . -10.201 16.233 32.822 1.00 16.04 ? ? ? ? ? . 81 TYR B O 2350 ATOM 1981 C CB . TYR B 2350 81 . -7.863 13.991 33.382 1.00 17.47 ? ? ? ? ? . 81 TYR B CB 2350 ATOM 1982 C CG . TYR B 2350 81 . -8.551 14.403 34.640 1.00 17.17 ? ? ? ? ? . 81 TYR B CG 2350 ATOM 1983 C CD1 . TYR B 2350 81 . -9.853 13.975 34.896 1.00 17.53 ? ? ? ? ? . 81 TYR B CD1 2350 ATOM 1984 C CD2 . TYR B 2350 81 . -7.970 15.303 35.523 1.00 17.37 ? ? ? ? ? . 81 TYR B CD2 2350 ATOM 1985 C CE1 . TYR B 2350 81 . -10.531 14.408 36.021 1.00 17.74 ? ? ? ? ? . 81 TYR B CE1 2350 ATOM 1986 C CE2 . TYR B 2350 81 . -8.644 15.731 36.654 1.00 18.24 ? ? ? ? ? . 81 TYR B CE2 2350 ATOM 1987 C CZ . TYR B 2350 81 . -9.926 15.287 36.893 1.00 18.24 ? ? ? ? ? . 81 TYR B CZ 2350 ATOM 1988 O OH . TYR B 2350 81 . -10.599 15.711 38.016 1.00 18.62 ? ? ? ? ? . 81 TYR B OH 2350 ATOM 1989 N N . GLY B 2350 82 . -8.252 16.930 31.935 1.00 16.13 ? ? ? ? ? . 82 GLY B N 2350 ATOM 1990 C CA . GLY B 2350 82 . -8.599 18.338 31.970 1.00 16.93 ? ? ? ? ? . 82 GLY B CA 2350 ATOM 1991 C C . GLY B 2350 82 . -9.946 18.666 31.345 1.00 17.49 ? ? ? ? ? . 82 GLY B C 2350 ATOM 1992 O O . GLY B 2350 82 . -10.647 19.548 31.829 1.00 16.88 ? ? ? ? ? . 82 GLY B O 2350 ATOM 1993 N N . LYS B 2350 83 . -10.310 17.941 30.288 1.00 18.69 ? ? ? ? ? . 83 LYS B N 2350 ATOM 1994 C CA . LYS B 2350 83 . -11.560 18.194 29.551 1.00 20.72 ? ? ? ? ? . 83 LYS B CA 2350 ATOM 1995 C C . LYS B 2350 83 . -12.777 17.454 30.090 1.00 21.80 ? ? ? ? ? . 83 LYS B C 2350 ATOM 1996 O O . LYS B 2350 83 . -13.892 17.664 29.595 1.00 21.26 ? ? ? ? ? . 83 LYS B O 2350 ATOM 1997 C CB . LYS B 2350 83 . -11.357 17.854 28.073 1.00 21.83 ? ? ? ? ? . 83 LYS B CB 2350 ATOM 1998 C CG . LYS B 2350 83 . -10.329 18.748 27.429 1.00 22.78 ? ? ? ? ? . 83 LYS B CG 2350 ATOM 1999 C CD . LYS B 2350 83 . -10.121 18.447 25.961 1.00 24.60 ? ? ? ? ? . 83 LYS B CD 2350 ATOM 2000 C CE . LYS B 2350 83 . -8.850 19.122 25.477 1.00 28.02 ? ? ? ? ? . 83 LYS B CE 2350 ATOM 2001 N NZ . LYS B 2350 83 . -8.602 18.925 24.023 1.00 30.17 ? ? ? ? ? 1+ 83 LYS B NZ 2350 ATOM 2002 N N . MET B 2350 84 . -12.563 16.577 31.073 1.00 20.82 ? ? ? ? ? . 84 MET B N 2350 ATOM 2003 C CA . MET B 2350 84 . -13.635 15.814 31.708 1.00 21.27 ? ? ? ? ? . 84 MET B CA 2350 ATOM 2004 C C . MET B 2350 84 . -14.193 16.598 32.884 1.00 22.00 ? ? ? ? ? . 84 MET B C 2350 ATOM 2005 O O . MET B 2350 84 . -13.534 17.523 33.357 1.00 23.51 ? ? ? ? ? . 84 MET B O 2350 ATOM 2006 C CB . MET B 2350 84 . -13.118 14.469 32.193 1.00 19.77 ? ? ? ? ? . 84 MET B CB 2350 ATOM 2007 C CG . MET B 2350 84 . -12.706 13.549 31.072 1.00 19.50 ? ? ? ? ? . 84 MET B CG 2350 ATOM 2008 S SD . MET B 2350 84 . -11.882 12.101 31.749 1.00 19.88 ? ? ? ? ? . 84 MET B SD 2350 ATOM 2009 C CE . MET B 2350 84 . -11.718 11.109 30.270 1.00 20.94 ? ? ? ? ? . 84 MET B CE 2350 ATOM 2010 N N . PRO B 2350 85 . -15.411 16.248 33.352 1.00 20.76 ? ? ? ? ? . 85 PRO B N 2350 ATOM 2011 C CA . PRO B 2350 85 . -16.043 17.010 34.433 1.00 19.33 ? ? ? ? ? . 85 PRO B CA 2350 ATOM 2012 C C . PRO B 2350 85 . -15.858 16.459 35.847 1.00 18.20 ? ? ? ? ? . 85 PRO B C 2350 ATOM 2013 O O . PRO B 2350 85 . -16.214 17.136 36.814 1.00 18.87 ? ? ? ? ? . 85 PRO B O 2350 ATOM 2014 C CB . PRO B 2350 85 . -17.523 16.975 34.043 1.00 20.30 ? ? ? ? ? . 85 PRO B CB 2350 ATOM 2015 C CG . PRO B 2350 85 . -17.690 15.664 33.349 1.00 20.64 ? ? ? ? ? . 85 PRO B CG 2350 ATOM 2016 C CD . PRO B 2350 85 . -16.360 15.315 32.717 1.00 19.64 ? ? ? ? ? . 85 PRO B CD 2350 ATOM 2017 N N . TRP B 2350 86 . -15.245 15.279 35.975 1.00 16.54 ? ? ? ? ? . 86 TRP B N 2350 ATOM 2018 C CA . TRP B 2350 86 . -15.322 14.466 37.192 1.00 16.95 ? ? ? ? ? . 86 TRP B CA 2350 ATOM 2019 C C . TRP B 2350 86 . -13.931 14.316 37.872 1.00 16.70 ? ? ? ? ? . 86 TRP B C 2350 ATOM 2020 O O . TRP B 2350 86 . -13.138 15.253 37.827 1.00 18.08 ? ? ? ? ? . 86 TRP B O 2350 ATOM 2021 C CB . TRP B 2350 86 . -15.991 13.136 36.856 1.00 17.51 ? ? ? ? ? . 86 TRP B CB 2350 ATOM 2022 C CG . TRP B 2350 86 . -15.446 12.465 35.622 1.00 17.81 ? ? ? ? ? . 86 TRP B CG 2350 ATOM 2023 C CD1 . TRP B 2350 86 . -14.152 12.120 35.374 1.00 17.90 ? ? ? ? ? . 86 TRP B CD1 2350 ATOM 2024 C CD2 . TRP B 2350 86 . -16.185 12.099 34.457 1.00 17.07 ? ? ? ? ? . 86 TRP B CD2 2350 ATOM 2025 C CE2 . TRP B 2350 86 . -15.268 11.526 33.545 1.00 17.35 ? ? ? ? ? . 86 TRP B CE2 2350 ATOM 2026 C CE3 . TRP B 2350 86 . -17.535 12.187 34.096 1.00 17.36 ? ? ? ? ? . 86 TRP B CE3 2350 ATOM 2027 N NE1 . TRP B 2350 86 . -14.037 11.558 34.135 1.00 17.06 ? ? ? ? ? . 86 TRP B NE1 2350 ATOM 2028 C CZ2 . TRP B 2350 86 . -15.654 11.038 32.287 1.00 16.49 ? ? ? ? ? . 86 TRP B CZ2 2350 ATOM 2029 C CZ3 . TRP B 2350 86 . -17.925 11.708 32.854 1.00 17.25 ? ? ? ? ? . 86 TRP B CZ3 2350 ATOM 2030 C CH2 . TRP B 2350 86 . -16.984 11.145 31.953 1.00 17.92 ? ? ? ? ? . 86 TRP B CH2 2350 ATOM 2031 N N . LEU B 2350 87 . -13.625 13.161 38.465 1.00 16.41 ? ? ? ? ? . 87 LEU B N 2350 ATOM 2032 C CA . LEU B 2350 87 . -12.401 12.963 39.230 1.00 14.55 ? ? ? ? ? . 87 LEU B CA 2350 ATOM 2033 C C . LEU B 2350 87 . -11.466 12.019 38.498 1.00 16.57 ? ? ? ? ? . 87 LEU B C 2350 ATOM 2034 O O . LEU B 2350 87 . -11.854 11.400 37.515 1.00 17.83 ? ? ? ? ? . 87 LEU B O 2350 ATOM 2035 C CB . LEU B 2350 87 . -12.740 12.359 40.588 1.00 15.07 ? ? ? ? ? . 87 LEU B CB 2350 ATOM 2036 C CG . LEU B 2350 87 . -13.758 13.084 41.461 1.00 15.98 ? ? ? ? ? . 87 LEU B CG 2350 ATOM 2037 C CD1 . LEU B 2350 87 . -13.923 12.349 42.771 1.00 17.46 ? ? ? ? ? . 87 LEU B CD1 2350 ATOM 2038 C CD2 . LEU B 2350 87 . -13.319 14.486 41.736 1.00 17.54 ? ? ? ? ? . 87 LEU B CD2 2350 ATOM 2039 N N . ALA B 2350 88 . -10.230 11.911 38.973 1.00 16.57 ? ? ? ? ? . 88 ALA B N 2350 ATOM 2040 C CA . ALA B 2350 88 . -9.283 10.961 38.396 1.00 16.36 ? ? ? ? ? . 88 ALA B CA 2350 ATOM 2041 C C . ALA B 2350 88 . -8.323 10.412 39.434 1.00 15.96 ? ? ? ? ? . 88 ALA B C 2350 ATOM 2042 O O . ALA B 2350 88 . -7.891 11.115 40.346 1.00 15.90 ? ? ? ? ? . 88 ALA B O 2350 ATOM 2043 C CB . ALA B 2350 88 . -8.501 11.609 37.260 1.00 17.50 ? ? ? ? ? . 88 ALA B CB 2350 ATOM 2044 N N . LEU B 2350 89 . -7.990 9.136 39.275 1.00 17.02 ? ? ? ? ? . 89 LEU B N 2350 ATOM 2045 C CA . LEU B 2350 89 . -6.879 8.537 40.014 1.00 16.46 ? ? ? ? ? . 89 LEU B CA 2350 ATOM 2046 C C . LEU B 2350 89 . -5.615 9.205 39.475 1.00 16.33 ? ? ? ? ? . 89 LEU B C 2350 ATOM 2047 O O . LEU B 2350 89 . -5.440 9.269 38.238 1.00 16.60 ? ? ? ? ? . 89 LEU B O 2350 ATOM 2048 C CB . LEU B 2350 89 . -6.824 7.035 39.770 1.00 17.31 ? ? ? ? ? . 89 LEU B CB 2350 ATOM 2049 C CG . LEU B 2350 89 . -5.809 6.233 40.587 1.00 18.05 ? ? ? ? ? . 89 LEU B CG 2350 ATOM 2050 C CD1 . LEU B 2350 89 . -6.200 6.221 42.055 1.00 20.17 ? ? ? ? ? . 89 LEU B CD1 2350 ATOM 2051 C CD2 . LEU B 2350 89 . -5.715 4.824 40.026 1.00 18.99 ? ? ? ? ? . 89 LEU B CD2 2350 ATOM 2052 N N . PRO B 2350 90 . -4.742 9.705 40.367 1.00 16.37 ? ? ? ? ? . 90 PRO B N 2350 ATOM 2053 C CA . PRO B 2350 90 . -3.571 10.431 39.892 1.00 16.40 ? ? ? ? ? . 90 PRO B CA 2350 ATOM 2054 C C . PRO B 2350 90 . -2.658 9.608 38.990 1.00 16.81 ? ? ? ? ? . 90 PRO B C 2350 ATOM 2055 O O . PRO B 2350 90 . -2.636 8.362 39.054 1.00 15.83 ? ? ? ? ? . 90 PRO B O 2350 ATOM 2056 C CB . PRO B 2350 90 . -2.851 10.810 41.181 1.00 17.22 ? ? ? ? ? . 90 PRO B CB 2350 ATOM 2057 C CG . PRO B 2350 90 . -3.955 10.949 42.178 1.00 18.64 ? ? ? ? ? . 90 PRO B CG 2350 ATOM 2058 C CD . PRO B 2350 90 . -4.875 9.819 41.833 1.00 17.87 ? ? ? ? ? . 90 PRO B CD 2350 ATOM 2059 N N . PHE B 2350 91 . -1.912 10.306 38.150 1.00 16.95 ? ? ? ? ? . 91 PHE B N 2350 ATOM 2060 C CA . PHE B 2350 91 . -0.984 9.620 37.268 1.00 16.32 ? ? ? ? ? . 91 PHE B CA 2350 ATOM 2061 C C . PHE B 2350 91 . 0.043 8.771 38.029 1.00 16.14 ? ? ? ? ? . 91 PHE B C 2350 ATOM 2062 O O . PHE B 2350 91 . 0.493 7.737 37.501 1.00 15.16 ? ? ? ? ? . 91 PHE B O 2350 ATOM 2063 C CB . PHE B 2350 91 . -0.273 10.597 36.345 1.00 15.66 ? ? ? ? ? . 91 PHE B CB 2350 ATOM 2064 C CG . PHE B 2350 91 . 0.595 9.920 35.332 1.00 15.90 ? ? ? ? ? . 91 PHE B CG 2350 ATOM 2065 C CD1 . PHE B 2350 91 . 0.040 9.360 34.195 1.00 16.28 ? ? ? ? ? . 91 PHE B CD1 2350 ATOM 2066 C CD2 . PHE B 2350 91 . 1.970 9.805 35.545 1.00 14.93 ? ? ? ? ? . 91 PHE B CD2 2350 ATOM 2067 C CE1 . PHE B 2350 91 . 0.850 8.722 33.258 1.00 16.87 ? ? ? ? ? . 91 PHE B CE1 2350 ATOM 2068 C CE2 . PHE B 2350 91 . 2.779 9.154 34.629 1.00 15.84 ? ? ? ? ? . 91 PHE B CE2 2350 ATOM 2069 C CZ . PHE B 2350 91 . 2.225 8.610 33.484 1.00 15.95 ? ? ? ? ? . 91 PHE B CZ 2350 ATOM 2070 N N . ASP B 2350 92 . 0.414 9.169 39.251 1.00 17.39 ? ? ? ? ? . 92 ASP B N 2350 ATOM 2071 C CA . ASP B 2350 92 . 1.409 8.390 40.023 1.00 19.84 ? ? ? ? ? . 92 ASP B CA 2350 ATOM 2072 C C . ASP B 2350 92 . 0.920 7.009 40.500 1.00 18.70 ? ? ? ? ? . 92 ASP B C 2350 ATOM 2073 O O . ASP B 2350 92 . 1.689 6.251 41.095 1.00 17.34 ? ? ? ? ? . 92 ASP B O 2350 ATOM 2074 C CB . ASP B 2350 92 . 2.017 9.195 41.182 1.00 23.77 ? ? ? ? ? . 92 ASP B CB 2350 ATOM 2075 C CG . ASP B 2350 92 . 1.025 9.518 42.290 1.00 27.83 ? ? ? ? ? . 92 ASP B CG 2350 ATOM 2076 O OD1 . ASP B 2350 92 . -0.133 9.067 42.259 1.00 32.30 ? ? ? ? ? . 92 ASP B OD1 2350 ATOM 2077 O OD2 . ASP B 2350 92 . 1.423 10.254 43.209 1.00 34.80 ? ? ? ? ? 1- 92 ASP B OD2 2350 ATOM 2078 N N . GLN B 2350 93 . -0.349 6.696 40.239 1.00 16.99 ? ? ? ? ? . 93 GLN B N 2350 ATOM 2079 C CA . GLN B 2350 93 . -0.886 5.361 40.461 1.00 17.43 ? ? ? ? ? . 93 GLN B CA 2350 ATOM 2080 C C . GLN B 2350 93 . -0.942 4.506 39.196 1.00 16.35 ? ? ? ? ? . 93 GLN B C 2350 ATOM 2081 O O . GLN B 2350 93 . -1.478 3.408 39.235 1.00 16.83 ? ? ? ? ? . 93 GLN B O 2350 ATOM 2082 C CB . GLN B 2350 93 . -2.288 5.477 41.064 1.00 18.99 ? ? ? ? ? . 93 GLN B CB 2350 ATOM 2083 C CG . GLN B 2350 93 . -2.320 6.261 42.358 1.00 20.51 ? ? ? ? ? . 93 GLN B CG 2350 ATOM 2084 C CD . GLN B 2350 93 . -1.539 5.571 43.445 1.00 22.84 ? ? ? ? ? . 93 GLN B CD 2350 ATOM 2085 N NE2 . GLN B 2350 93 . -0.516 6.241 43.965 1.00 22.79 ? ? ? ? ? . 93 GLN B NE2 2350 ATOM 2086 O OE1 . GLN B 2350 93 . -1.836 4.424 43.797 1.00 23.59 ? ? ? ? ? . 93 GLN B OE1 2350 ATOM 2087 N N . ARG B 2350 94 . -0.395 4.997 38.082 1.00 17.24 ? ? ? ? ? . 94 ARG B N 2350 ATOM 2088 C CA . ARG B 2350 94 . -0.444 4.275 36.806 1.00 16.88 ? ? ? ? ? . 94 ARG B CA 2350 ATOM 2089 C C . ARG B 2350 94 . 0.105 2.829 36.885 1.00 16.61 ? ? ? ? ? . 94 ARG B C 2350 ATOM 2090 O O . ARG B 2350 94 . -0.405 1.942 36.208 1.00 17.97 ? ? ? ? ? . 94 ARG B O 2350 ATOM 2091 C CB . ARG B 2350 94 . 0.281 5.072 35.707 1.00 17.63 ? ? ? ? ? . 94 ARG B CB 2350 ATOM 2092 C CG . ARG B 2350 94 . 0.329 4.393 34.334 1.00 19.00 ? ? ? ? ? . 94 ARG B CG 2350 ATOM 2093 C CD . ARG B 2350 94 . -1.058 4.079 33.804 1.00 17.72 ? ? ? ? ? . 94 ARG B CD 2350 ATOM 2094 N NE . ARG B 2350 94 . -1.060 3.417 32.503 1.00 17.08 ? ? ? ? ? . 94 ARG B NE 2350 ATOM 2095 C CZ . ARG B 2350 94 . -0.901 2.110 32.284 1.00 17.71 ? ? ? ? ? . 94 ARG B CZ 2350 ATOM 2096 N NH1 . ARG B 2350 94 . -0.665 1.259 33.283 1.00 19.74 ? ? ? ? ? 1+ 94 ARG B NH1 2350 ATOM 2097 N NH2 . ARG B 2350 94 . -0.952 1.649 31.033 1.00 16.77 ? ? ? ? ? . 94 ARG B NH2 2350 ATOM 2098 N N . SER B 2350 95 . 1.110 2.589 37.724 1.00 16.31 ? ? ? ? ? . 95 SER B N 2350 ATOM 2099 C CA . SER B 2350 95 . 1.672 1.234 37.903 1.00 16.21 ? ? ? ? ? . 95 SER B CA 2350 ATOM 2100 C C . SER B 2350 95 . 0.683 0.205 38.487 1.00 17.13 ? ? ? ? ? . 95 SER B C 2350 ATOM 2101 O O . SER B 2350 95 . 0.927 -0.996 38.403 1.00 19.32 ? ? ? ? ? . 95 SER B O 2350 ATOM 2102 C CB . SER B 2350 95 . 2.920 1.280 38.787 1.00 15.66 ? ? ? ? ? . 95 SER B CB 2350 ATOM 2103 O OG . SER B 2350 95 . 2.575 1.563 40.126 1.00 14.53 ? ? ? ? ? . 95 SER B OG 2350 ATOM 2104 N N . THR B 2350 96 . -0.421 0.682 39.062 1.00 16.77 ? ? ? ? ? . 96 THR B N 2350 ATOM 2105 C CA . THR B 2350 96 . -1.479 -0.163 39.608 1.00 16.98 ? ? ? ? ? . 96 THR B CA 2350 ATOM 2106 C C . THR B 2350 96 . -2.621 -0.451 38.641 1.00 16.70 ? ? ? ? ? . 96 THR B C 2350 ATOM 2107 O O . THR B 2350 96 . -3.480 -1.274 38.956 1.00 16.12 ? ? ? ? ? . 96 THR B O 2350 ATOM 2108 C CB . THR B 2350 96 . -2.103 0.475 40.877 1.00 16.65 ? ? ? ? ? . 96 THR B CB 2350 ATOM 2109 C CG2 . THR B 2350 96 . -1.027 0.868 41.859 1.00 16.78 ? ? ? ? ? . 96 THR B CG2 2350 ATOM 2110 O OG1 . THR B 2350 96 . -2.918 1.611 40.536 1.00 17.39 ? ? ? ? ? . 96 THR B OG1 2350 ATOM 2111 N N . VAL B 2350 97 . -2.645 0.212 37.484 1.00 15.95 ? ? ? ? ? . 97 VAL B N 2350 ATOM 2112 C CA . VAL B 2350 97 . -3.832 0.207 36.622 1.00 15.76 ? ? ? ? ? . 97 VAL B CA 2350 ATOM 2113 C C . VAL B 2350 97 . -4.077 -1.175 36.010 1.00 15.32 ? ? ? ? ? . 97 VAL B C 2350 ATOM 2114 O O . VAL B 2350 97 . -5.210 -1.640 36.009 1.00 15.15 ? ? ? ? ? . 97 VAL B O 2350 ATOM 2115 C CB . VAL B 2350 97 . -3.749 1.265 35.510 1.00 15.29 ? ? ? ? ? . 97 VAL B CB 2350 ATOM 2116 C CG1 . VAL B 2350 97 . -4.886 1.099 34.503 1.00 16.21 ? ? ? ? ? . 97 VAL B CG1 2350 ATOM 2117 C CG2 . VAL B 2350 97 . -3.809 2.652 36.114 1.00 16.16 ? ? ? ? ? . 97 VAL B CG2 2350 ATOM 2118 N N . SER B 2350 98 . -3.022 -1.815 35.518 1.00 16.70 ? ? ? ? ? . 98 SER B N 2350 ATOM 2119 C CA . SER B 2350 98 . -3.121 -3.162 34.944 1.00 17.78 ? ? ? ? ? . 98 SER B CA 2350 ATOM 2120 C C . SER B 2350 98 . -3.711 -4.159 35.943 1.00 17.26 ? ? ? ? ? . 98 SER B C 2350 ATOM 2121 O O . SER B 2350 98 . -4.674 -4.865 35.619 1.00 17.51 ? ? ? ? ? . 98 SER B O 2350 ATOM 2122 C CB . SER B 2350 98 . -1.752 -3.661 34.430 1.00 18.21 ? ? ? ? ? . 98 SER B CB 2350 ATOM 2123 O OG . SER B 2350 98 . -1.807 -5.045 34.069 1.00 20.56 ? ? ? ? ? . 98 SER B OG 2350 ATOM 2124 N N . GLU B 2350 99 . -3.143 -4.226 37.148 1.00 17.06 ? ? ? ? ? . 99 GLU B N 2350 ATOM 2125 C CA . GLU B 2350 99 . -3.667 -5.155 38.154 1.00 17.20 ? ? ? ? ? . 99 GLU B CA 2350 ATOM 2126 C C . GLU B 2350 99 . -5.072 -4.783 38.623 1.00 17.25 ? ? ? ? ? . 99 GLU B C 2350 ATOM 2127 O O . GLU B 2350 99 . -5.868 -5.674 38.935 1.00 15.69 ? ? ? ? ? . 99 GLU B O 2350 ATOM 2128 C CB . GLU B 2350 99 . -2.720 -5.319 39.348 1.00 18.28 ? ? ? ? ? . 99 GLU B CB 2350 ATOM 2129 C CG . GLU B 2350 99 . -1.454 -6.112 39.035 1.00 19.77 ? ? ? ? ? . 99 GLU B CG 2350 ATOM 2130 C CD . GLU B 2350 99 . -1.704 -7.546 38.571 1.00 22.07 ? ? ? ? ? . 99 GLU B CD 2350 ATOM 2131 O OE1 . GLU B 2350 99 . -2.608 -8.234 39.099 1.00 21.98 ? ? ? ? ? . 99 GLU B OE1 2350 ATOM 2132 O OE2 . GLU B 2350 99 . -0.970 -7.999 37.671 1.00 22.99 ? ? ? ? ? 1- 99 GLU B OE2 2350 ATOM 2133 N N A LEU B 2350 100 . -5.370 -3.482 38.680 0.49 17.03 ? ? ? ? ? . 100 LEU B N 2350 ATOM 2134 N N B LEU B 2350 100 . -5.386 -3.488 38.661 0.51 16.95 ? ? ? ? ? . 100 LEU B N 2350 ATOM 2135 C CA A LEU B 2350 100 . -6.731 -3.011 38.953 0.49 18.24 ? ? ? ? ? . 100 LEU B CA 2350 ATOM 2136 C CA B LEU B 2350 100 . -6.748 -3.063 38.997 0.51 18.11 ? ? ? ? ? . 100 LEU B CA 2350 ATOM 2137 C C A LEU B 2350 100 . -7.730 -3.589 37.945 0.49 18.23 ? ? ? ? ? . 100 LEU B C 2350 ATOM 2138 C C B LEU B 2350 100 . -7.752 -3.577 37.944 0.51 18.21 ? ? ? ? ? . 100 LEU B C 2350 ATOM 2139 O O A LEU B 2350 100 . -8.764 -4.145 38.323 0.49 18.26 ? ? ? ? ? . 100 LEU B O 2350 ATOM 2140 O O B LEU B 2350 100 . -8.818 -4.088 38.298 0.51 18.44 ? ? ? ? ? . 100 LEU B O 2350 ATOM 2141 C CB A LEU B 2350 100 . -6.786 -1.489 38.904 0.49 18.06 ? ? ? ? ? . 100 LEU B CB 2350 ATOM 2142 C CB B LEU B 2350 100 . -6.832 -1.543 39.150 0.51 17.78 ? ? ? ? ? . 100 LEU B CB 2350 ATOM 2143 C CG A LEU B 2350 100 . -6.484 -0.751 40.200 0.49 18.12 ? ? ? ? ? . 100 LEU B CG 2350 ATOM 2144 C CG B LEU B 2350 100 . -8.092 -1.031 39.858 0.51 17.55 ? ? ? ? ? . 100 LEU B CG 2350 ATOM 2145 C CD1 A LEU B 2350 100 . -6.557 0.747 39.948 0.49 17.99 ? ? ? ? ? . 100 LEU B CD1 2350 ATOM 2146 C CD2 A LEU B 2350 100 . -7.443 -1.195 41.299 0.49 19.03 ? ? ? ? ? . 100 LEU B CD2 2350 ATOM 2147 C CD1 B LEU B 2350 100 . -8.094 -1.376 41.349 0.51 17.86 ? ? ? ? ? . 100 LEU B CD1 2350 ATOM 2148 C CD2 B LEU B 2350 100 . -8.232 0.466 39.661 0.51 18.12 ? ? ? ? ? . 100 LEU B CD2 2350 ATOM 2149 N N . GLY B 2350 101 . -7.400 -3.464 36.664 1.00 18.06 ? ? ? ? ? . 101 GLY B N 2350 ATOM 2150 C CA . GLY B 2350 101 . -8.206 -4.062 35.585 1.00 19.07 ? ? ? ? ? . 101 GLY B CA 2350 ATOM 2151 C C . GLY B 2350 101 . -8.386 -5.570 35.750 1.00 17.32 ? ? ? ? ? . 101 GLY B C 2350 ATOM 2152 O O . GLY B 2350 101 . -9.493 -6.087 35.597 1.00 18.58 ? ? ? ? ? . 101 GLY B O 2350 ATOM 2153 N N . LYS B 2350 102 . -7.307 -6.267 36.093 1.00 16.19 ? ? ? ? ? . 102 LYS B N 2350 ATOM 2154 C CA . LYS B 2350 102 . -7.359 -7.714 36.299 1.00 17.21 ? ? ? ? ? . 102 LYS B CA 2350 ATOM 2155 C C . LYS B 2350 102 . -8.251 -8.074 37.468 1.00 16.89 ? ? ? ? ? . 102 LYS B C 2350 ATOM 2156 O O . LYS B 2350 102 . -8.994 -9.048 37.402 1.00 15.61 ? ? ? ? ? . 102 LYS B O 2350 ATOM 2157 C CB . LYS B 2350 102 . -5.988 -8.296 36.592 1.00 19.27 ? ? ? ? ? . 102 LYS B CB 2350 ATOM 2158 C CG . LYS B 2350 102 . -5.054 -8.400 35.410 1.00 22.58 ? ? ? ? ? . 102 LYS B CG 2350 ATOM 2159 C CD . LYS B 2350 102 . -3.933 -9.364 35.782 1.00 25.96 ? ? ? ? ? . 102 LYS B CD 2350 ATOM 2160 C CE . LYS B 2350 102 . -2.604 -8.938 35.215 1.00 29.86 ? ? ? ? ? . 102 LYS B CE 2350 ATOM 2161 N NZ . LYS B 2350 102 . -1.511 -9.795 35.762 1.00 31.62 ? ? ? ? ? 1+ 102 LYS B NZ 2350 ATOM 2162 N N . THR B 2350 103 . -8.164 -7.288 38.538 1.00 16.61 ? ? ? ? ? . 103 THR B N 2350 ATOM 2163 C CA . THR B 2350 103 . -8.990 -7.508 39.735 1.00 17.16 ? ? ? ? ? . 103 THR B CA 2350 ATOM 2164 C C . THR B 2350 103 . -10.494 -7.450 39.412 1.00 16.65 ? ? ? ? ? . 103 THR B C 2350 ATOM 2165 O O . THR B 2350 103 . -11.278 -8.237 39.953 1.00 18.21 ? ? ? ? ? . 103 THR B O 2350 ATOM 2166 C CB . THR B 2350 103 . -8.658 -6.470 40.842 1.00 17.12 ? ? ? ? ? . 103 THR B CB 2350 ATOM 2167 C CG2 . THR B 2350 103 . -9.615 -6.587 42.020 1.00 17.45 ? ? ? ? ? . 103 THR B CG2 2350 ATOM 2168 O OG1 . THR B 2350 103 . -7.320 -6.677 41.310 1.00 16.38 ? ? ? ? ? . 103 THR B OG1 2350 ATOM 2169 N N . PHE B 2350 104 . -10.879 -6.530 38.536 1.00 15.70 ? ? ? ? ? . 104 PHE B N 2350 ATOM 2170 C CA . PHE B 2350 104 . -12.294 -6.337 38.179 1.00 17.76 ? ? ? ? ? . 104 PHE B CA 2350 ATOM 2171 C C . PHE B 2350 104 . -12.747 -7.074 36.907 1.00 18.79 ? ? ? ? ? . 104 PHE B C 2350 ATOM 2172 O O . PHE B 2350 104 . -13.915 -6.939 36.501 1.00 20.78 ? ? ? ? ? . 104 PHE B O 2350 ATOM 2173 C CB . PHE B 2350 104 . -12.604 -4.847 38.050 1.00 17.44 ? ? ? ? ? . 104 PHE B CB 2350 ATOM 2174 C CG . PHE B 2350 104 . -12.388 -4.055 39.319 1.00 19.30 ? ? ? ? ? . 104 PHE B CG 2350 ATOM 2175 C CD1 . PHE B 2350 104 . -12.955 -4.455 40.525 1.00 20.46 ? ? ? ? ? . 104 PHE B CD1 2350 ATOM 2176 C CD2 . PHE B 2350 104 . -11.632 -2.877 39.301 1.00 19.35 ? ? ? ? ? . 104 PHE B CD2 2350 ATOM 2177 C CE1 . PHE B 2350 104 . -12.761 -3.707 41.684 1.00 20.50 ? ? ? ? ? . 104 PHE B CE1 2350 ATOM 2178 C CE2 . PHE B 2350 104 . -11.446 -2.126 40.453 1.00 20.68 ? ? ? ? ? . 104 PHE B CE2 2350 ATOM 2179 C CZ . PHE B 2350 104 . -12.012 -2.547 41.646 1.00 20.25 ? ? ? ? ? . 104 PHE B CZ 2350 ATOM 2180 N N . GLY B 2350 105 . -11.847 -7.847 36.306 1.00 16.85 ? ? ? ? ? . 105 GLY B N 2350 ATOM 2181 C CA . GLY B 2350 105 . -12.113 -8.598 35.074 1.00 18.18 ? ? ? ? ? . 105 GLY B CA 2350 ATOM 2182 C C . GLY B 2350 105 . -12.337 -7.691 33.882 1.00 18.23 ? ? ? ? ? . 105 GLY B C 2350 ATOM 2183 O O . GLY B 2350 105 . -13.190 -7.968 33.053 1.00 19.24 ? ? ? ? ? . 105 GLY B O 2350 ATOM 2184 N N . VAL B 2350 106 . -11.565 -6.611 33.802 1.00 17.92 ? ? ? ? ? . 106 VAL B N 2350 ATOM 2185 C CA . VAL B 2350 106 . -11.660 -5.655 32.700 1.00 18.96 ? ? ? ? ? . 106 VAL B CA 2350 ATOM 2186 C C . VAL B 2350 106 . -10.959 -6.293 31.498 1.00 19.83 ? ? ? ? ? . 106 VAL B C 2350 ATOM 2187 O O . VAL B 2350 106 . -9.751 -6.549 31.544 1.00 21.37 ? ? ? ? ? . 106 VAL B O 2350 ATOM 2188 C CB . VAL B 2350 106 . -11.004 -4.288 33.060 1.00 17.64 ? ? ? ? ? . 106 VAL B CB 2350 ATOM 2189 C CG1 . VAL B 2350 106 . -10.986 -3.352 31.858 1.00 18.20 ? ? ? ? ? . 106 VAL B CG1 2350 ATOM 2190 C CG2 . VAL B 2350 106 . -11.722 -3.622 34.235 1.00 17.98 ? ? ? ? ? . 106 VAL B CG2 2350 ATOM 2191 N N . GLU B 2350 107 . -11.727 -6.593 30.452 1.00 18.84 ? ? ? ? ? . 107 GLU B N 2350 ATOM 2192 C CA . GLU B 2350 107 . -11.218 -7.272 29.245 1.00 21.13 ? ? ? ? ? . 107 GLU B CA 2350 ATOM 2193 C C . GLU B 2350 107 . -11.037 -6.331 28.051 1.00 18.68 ? ? ? ? ? . 107 GLU B C 2350 ATOM 2194 O O . GLU B 2350 107 . -10.450 -6.722 27.037 1.00 18.15 ? ? ? ? ? . 107 GLU B O 2350 ATOM 2195 C CB . GLU B 2350 107 . -12.152 -8.423 28.848 1.00 24.82 ? ? ? ? ? . 107 GLU B CB 2350 ATOM 2196 C CG . GLU B 2350 107 . -12.270 -9.529 29.884 1.00 28.31 ? ? ? ? ? . 107 GLU B CG 2350 ATOM 2197 C CD . GLU B 2350 107 . -10.950 -10.220 30.205 1.00 34.01 ? ? ? ? ? . 107 GLU B CD 2350 ATOM 2198 O OE1 . GLU B 2350 107 . -10.734 -10.534 31.395 1.00 44.29 ? ? ? ? ? . 107 GLU B OE1 2350 ATOM 2199 O OE2 . GLU B 2350 107 . -10.126 -10.442 29.289 1.00 32.07 ? ? ? ? ? 1- 107 GLU B OE2 2350 ATOM 2200 N N . SER B 2350 108 . -11.561 -5.118 28.175 1.00 17.73 ? ? ? ? ? . 108 SER B N 2350 ATOM 2201 C CA . SER B 2350 108 . -11.397 -4.071 27.175 1.00 17.33 ? ? ? ? ? . 108 SER B CA 2350 ATOM 2202 C C . SER B 2350 108 . -11.818 -2.738 27.778 1.00 15.74 ? ? ? ? ? . 108 SER B C 2350 ATOM 2203 O O . SER B 2350 108 . -12.361 -2.699 28.876 1.00 15.99 ? ? ? ? ? . 108 SER B O 2350 ATOM 2204 C CB . SER B 2350 108 . -12.256 -4.347 25.952 1.00 19.74 ? ? ? ? ? . 108 SER B CB 2350 ATOM 2205 O OG . SER B 2350 108 . -13.625 -4.264 26.285 1.00 22.41 ? ? ? ? ? . 108 SER B OG 2350 ATOM 2206 N N . ILE B 2350 109 . -11.559 -1.649 27.067 1.00 14.80 ? ? ? ? ? . 109 ILE B N 2350 ATOM 2207 C CA . ILE B 2350 109 . -12.072 -0.339 27.467 1.00 15.47 ? ? ? ? ? . 109 ILE B CA 2350 ATOM 2208 C C . ILE B 2350 109 . -12.845 0.251 26.296 1.00 16.17 ? ? ? ? ? . 109 ILE B C 2350 ATOM 2209 O O . ILE B 2350 109 . -12.602 -0.128 25.144 1.00 16.27 ? ? ? ? ? . 109 ILE B O 2350 ATOM 2210 C CB . ILE B 2350 109 . -10.972 0.632 27.987 1.00 16.02 ? ? ? ? ? . 109 ILE B CB 2350 ATOM 2211 C CG1 . ILE B 2350 109 . -9.961 0.967 26.903 1.00 15.75 ? ? ? ? ? . 109 ILE B CG1 2350 ATOM 2212 C CG2 . ILE B 2350 109 . -10.282 0.054 29.216 1.00 15.93 ? ? ? ? ? . 109 ILE B CG2 2350 ATOM 2213 C CD1 . ILE B 2350 109 . -8.993 2.067 27.266 1.00 16.37 ? ? ? ? ? . 109 ILE B CD1 2350 ATOM 2214 N N . PRO B 2350 110 . -13.792 1.170 26.568 1.00 16.95 ? ? ? ? ? . 110 PRO B N 2350 ATOM 2215 C CA . PRO B 2350 110 . -14.237 1.696 27.863 1.00 16.22 ? ? ? ? ? . 110 PRO B CA 2350 ATOM 2216 C C . PRO B 2350 110 . -14.920 0.644 28.734 1.00 17.60 ? ? ? ? ? . 110 PRO B C 2350 ATOM 2217 O O . PRO B 2350 110 . -15.617 -0.236 28.202 1.00 16.52 ? ? ? ? ? . 110 PRO B O 2350 ATOM 2218 C CB . PRO B 2350 110 . -15.259 2.765 27.461 1.00 18.10 ? ? ? ? ? . 110 PRO B CB 2350 ATOM 2219 C CG . PRO B 2350 110 . -15.822 2.275 26.186 1.00 18.28 ? ? ? ? ? . 110 PRO B CG 2350 ATOM 2220 C CD . PRO B 2350 110 . -14.652 1.644 25.470 1.00 17.16 ? ? ? ? ? . 110 PRO B CD 2350 ATOM 2221 N N . THR B 2350 111 . -14.694 0.716 30.045 1.00 16.11 ? ? ? ? ? . 111 THR B N 2350 ATOM 2222 C CA . THR B 2350 111 . -15.409 -0.126 31.022 1.00 17.84 ? ? ? ? ? . 111 THR B CA 2350 ATOM 2223 C C . THR B 2350 111 . -15.693 0.701 32.267 1.00 15.92 ? ? ? ? ? . 111 THR B C 2350 ATOM 2224 O O . THR B 2350 111 . -14.854 1.488 32.684 1.00 16.14 ? ? ? ? ? . 111 THR B O 2350 ATOM 2225 C CB . THR B 2350 111 . -14.610 -1.402 31.404 1.00 19.98 ? ? ? ? ? . 111 THR B CB 2350 ATOM 2226 C CG2 . THR B 2350 111 . -15.277 -2.166 32.547 1.00 23.70 ? ? ? ? ? . 111 THR B CG2 2350 ATOM 2227 O OG1 . THR B 2350 111 . -14.558 -2.285 30.281 1.00 20.70 ? ? ? ? ? . 111 THR B OG1 2350 ATOM 2228 N N . LEU B 2350 112 . -16.896 0.545 32.814 1.00 16.09 ? ? ? ? ? . 112 LEU B N 2350 ATOM 2229 C CA . LEU B 2350 112 . -17.268 1.097 34.111 1.00 16.65 ? ? ? ? ? . 112 LEU B CA 2350 ATOM 2230 C C . LEU B 2350 112 . -17.415 -0.020 35.152 1.00 16.97 ? ? ? ? ? . 112 LEU B C 2350 ATOM 2231 O O . LEU B 2350 112 . -18.046 -1.039 34.895 1.00 15.77 ? ? ? ? ? . 112 LEU B O 2350 ATOM 2232 C CB . LEU B 2350 112 . -18.584 1.885 34.009 1.00 17.47 ? ? ? ? ? . 112 LEU B CB 2350 ATOM 2233 C CG . LEU B 2350 112 . -18.569 3.198 33.214 1.00 18.01 ? ? ? ? ? . 112 LEU B CG 2350 ATOM 2234 C CD1 . LEU B 2350 112 . -19.969 3.779 33.085 1.00 18.77 ? ? ? ? ? . 112 LEU B CD1 2350 ATOM 2235 C CD2 . LEU B 2350 112 . -17.646 4.216 33.837 1.00 17.16 ? ? ? ? ? . 112 LEU B CD2 2350 ATOM 2236 N N . ILE B 2350 113 . -16.826 0.192 36.329 1.00 17.00 ? ? ? ? ? . 113 ILE B N 2350 ATOM 2237 C CA . ILE B 2350 113 . -17.007 -0.670 37.479 1.00 16.38 ? ? ? ? ? . 113 ILE B CA 2350 ATOM 2238 C C . ILE B 2350 113 . -17.716 0.177 38.540 1.00 16.37 ? ? ? ? ? . 113 ILE B C 2350 ATOM 2239 O O . ILE B 2350 113 . -17.248 1.255 38.896 1.00 16.22 ? ? ? ? ? . 113 ILE B O 2350 ATOM 2240 C CB . ILE B 2350 113 . -15.657 -1.185 38.022 1.00 17.79 ? ? ? ? ? . 113 ILE B CB 2350 ATOM 2241 C CG1 . ILE B 2350 113 . -14.838 -1.867 36.895 1.00 17.85 ? ? ? ? ? . 113 ILE B CG1 2350 ATOM 2242 C CG2 . ILE B 2350 113 . -15.877 -2.141 39.192 1.00 18.54 ? ? ? ? ? . 113 ILE B CG2 2350 ATOM 2243 C CD1 . ILE B 2350 113 . -15.488 -3.095 36.280 1.00 18.47 ? ? ? ? ? . 113 ILE B CD1 2350 ATOM 2244 N N . THR B 2350 114 . -18.842 -0.325 39.028 1.00 15.43 ? ? ? ? ? . 114 THR B N 2350 ATOM 2245 C CA . THR B 2350 114 . -19.682 0.402 39.975 1.00 16.48 ? ? ? ? ? . 114 THR B CA 2350 ATOM 2246 C C . THR B 2350 114 . -19.412 -0.113 41.381 1.00 16.42 ? ? ? ? ? . 114 THR B C 2350 ATOM 2247 O O . THR B 2350 114 . -19.584 -1.308 41.647 1.00 16.58 ? ? ? ? ? . 114 THR B O 2350 ATOM 2248 C CB . THR B 2350 114 . -21.168 0.225 39.621 1.00 15.92 ? ? ? ? ? . 114 THR B CB 2350 ATOM 2249 C CG2 . THR B 2350 114 . -22.027 1.243 40.350 1.00 16.26 ? ? ? ? ? . 114 THR B CG2 2350 ATOM 2250 O OG1 . THR B 2350 114 . -21.344 0.401 38.213 1.00 15.73 ? ? ? ? ? . 114 THR B OG1 2350 ATOM 2251 N N . ILE B 2350 115 . -18.990 0.787 42.273 1.00 16.90 ? ? ? ? ? . 115 ILE B N 2350 ATOM 2252 C CA . ILE B 2350 115 . -18.544 0.407 43.625 1.00 17.54 ? ? ? ? ? . 115 ILE B CA 2350 ATOM 2253 C C . ILE B 2350 115 . -19.263 1.239 44.688 1.00 16.17 ? ? ? ? ? . 115 ILE B C 2350 ATOM 2254 O O . ILE B 2350 115 . -19.466 2.428 44.522 1.00 15.85 ? ? ? ? ? . 115 ILE B O 2350 ATOM 2255 C CB . ILE B 2350 115 . -17.015 0.585 43.794 1.00 20.42 ? ? ? ? ? . 115 ILE B CB 2350 ATOM 2256 C CG1 . ILE B 2350 115 . -16.282 -0.201 42.713 1.00 23.68 ? ? ? ? ? . 115 ILE B CG1 2350 ATOM 2257 C CG2 . ILE B 2350 115 . -16.553 0.099 45.166 1.00 21.05 ? ? ? ? ? . 115 ILE B CG2 2350 ATOM 2258 C CD1 . ILE B 2350 115 . -14.778 -0.142 42.803 1.00 25.90 ? ? ? ? ? . 115 ILE B CD1 2350 ATOM 2259 N N . ASN B 2350 116 . -19.662 0.582 45.767 1.00 16.90 ? ? ? ? ? . 116 ASN B N 2350 ATOM 2260 C CA . ASN B 2350 116 . -20.147 1.263 46.971 1.00 16.70 ? ? ? ? ? . 116 ASN B CA 2350 ATOM 2261 C C . ASN B 2350 116 . -18.931 1.852 47.702 1.00 16.05 ? ? ? ? ? . 116 ASN B C 2350 ATOM 2262 O O . ASN B 2350 116 . -18.058 1.101 48.162 1.00 15.37 ? ? ? ? ? . 116 ASN B O 2350 ATOM 2263 C CB . ASN B 2350 116 . -20.874 0.266 47.859 1.00 17.51 ? ? ? ? ? . 116 ASN B CB 2350 ATOM 2264 C CG . ASN B 2350 116 . -21.445 0.897 49.111 1.00 20.14 ? ? ? ? ? . 116 ASN B CG 2350 ATOM 2265 N ND2 . ASN B 2350 116 . -22.754 0.873 49.224 1.00 25.82 ? ? ? ? ? . 116 ASN B ND2 2350 ATOM 2266 O OD1 . ASN B 2350 116 . -20.714 1.380 49.974 1.00 18.71 ? ? ? ? ? . 116 ASN B OD1 2350 ATOM 2267 N N . ALA B 2350 117 . -18.896 3.176 47.829 1.00 16.79 ? ? ? ? ? . 117 ALA B N 2350 ATOM 2268 C CA . ALA B 2350 117 . -17.761 3.890 48.455 1.00 17.20 ? ? ? ? ? . 117 ALA B CA 2350 ATOM 2269 C C . ALA B 2350 117 . -17.479 3.493 49.908 1.00 17.04 ? ? ? ? ? . 117 ALA B C 2350 ATOM 2270 O O . ALA B 2350 117 . -16.322 3.460 50.323 1.00 16.84 ? ? ? ? ? . 117 ALA B O 2350 ATOM 2271 C CB . ALA B 2350 117 . -17.982 5.391 48.369 1.00 17.96 ? ? ? ? ? . 117 ALA B CB 2350 ATOM 2272 N N . ASP B 2350 118 . -18.530 3.193 50.676 1.00 16.23 ? ? ? ? ? . 118 ASP B N 2350 ATOM 2273 C CA . ASP B 2350 118 . -18.388 2.829 52.092 1.00 16.61 ? ? ? ? ? . 118 ASP B CA 2350 ATOM 2274 C C . ASP B 2350 118 . -17.863 1.421 52.371 1.00 16.96 ? ? ? ? ? . 118 ASP B C 2350 ATOM 2275 O O . ASP B 2350 118 . -17.174 1.215 53.368 1.00 16.07 ? ? ? ? ? . 118 ASP B O 2350 ATOM 2276 C CB . ASP B 2350 118 . -19.737 2.982 52.822 1.00 18.01 ? ? ? ? ? . 118 ASP B CB 2350 ATOM 2277 C CG . ASP B 2350 118 . -20.237 4.389 52.815 1.00 19.29 ? ? ? ? ? . 118 ASP B CG 2350 ATOM 2278 O OD1 . ASP B 2350 118 . -19.439 5.311 52.540 1.00 17.79 ? ? ? ? ? . 118 ASP B OD1 2350 ATOM 2279 O OD2 . ASP B 2350 118 . -21.440 4.585 53.062 1.00 19.94 ? ? ? ? ? 1- 118 ASP B OD2 2350 ATOM 2280 N N . THR B 2350 119 . -18.225 0.452 51.526 1.00 16.79 ? ? ? ? ? . 119 THR B N 2350 ATOM 2281 C CA . THR B 2350 119 . -17.870 -0.963 51.759 1.00 16.25 ? ? ? ? ? . 119 THR B CA 2350 ATOM 2282 C C . THR B 2350 119 . -16.845 -1.529 50.766 1.00 15.04 ? ? ? ? ? . 119 THR B C 2350 ATOM 2283 O O . THR B 2350 119 . -16.168 -2.523 51.061 1.00 15.85 ? ? ? ? ? . 119 THR B O 2350 ATOM 2284 C CB . THR B 2350 119 . -19.130 -1.849 51.728 1.00 15.66 ? ? ? ? ? . 119 THR B CB 2350 ATOM 2285 C CG2 . THR B 2350 119 . -20.150 -1.347 52.749 1.00 16.06 ? ? ? ? ? . 119 THR B CG2 2350 ATOM 2286 O OG1 . THR B 2350 119 . -19.708 -1.815 50.418 1.00 16.00 ? ? ? ? ? . 119 THR B OG1 2350 ATOM 2287 N N . GLY B 2350 120 . -16.742 -0.913 49.600 1.00 14.05 ? ? ? ? ? . 120 GLY B N 2350 ATOM 2288 C CA . GLY B 2350 120 . -15.979 -1.465 48.502 1.00 15.89 ? ? ? ? ? . 120 GLY B CA 2350 ATOM 2289 C C . GLY B 2350 120 . -16.681 -2.581 47.748 1.00 16.20 ? ? ? ? ? . 120 GLY B C 2350 ATOM 2290 O O . GLY B 2350 120 . -16.062 -3.214 46.898 1.00 18.41 ? ? ? ? ? . 120 GLY B O 2350 ATOM 2291 N N . ALA B 2350 121 . -17.958 -2.821 48.022 1.00 17.23 ? ? ? ? ? . 121 ALA B N 2350 ATOM 2292 C CA . ALA B 2350 121 . -18.705 -3.859 47.317 1.00 17.65 ? ? ? ? ? . 121 ALA B CA 2350 ATOM 2293 C C . ALA B 2350 121 . -18.873 -3.430 45.858 1.00 18.18 ? ? ? ? ? . 121 ALA B C 2350 ATOM 2294 O O . ALA B 2350 121 . -19.147 -2.257 45.572 1.00 16.95 ? ? ? ? ? . 121 ALA B O 2350 ATOM 2295 C CB . ALA B 2350 121 . -20.064 -4.092 47.957 1.00 19.25 ? ? ? ? ? . 121 ALA B CB 2350 ATOM 2296 N N . ILE B 2350 122 . -18.699 -4.386 44.947 1.00 18.05 ? ? ? ? ? . 122 ILE B N 2350 ATOM 2297 C CA . ILE B 2350 122 . -18.941 -4.164 43.525 1.00 18.12 ? ? ? ? ? . 122 ILE B CA 2350 ATOM 2298 C C . ILE B 2350 122 . -20.440 -4.340 43.276 1.00 20.59 ? ? ? ? ? . 122 ILE B C 2350 ATOM 2299 O O . ILE B 2350 122 . -20.977 -5.455 43.410 1.00 19.10 ? ? ? ? ? . 122 ILE B O 2350 ATOM 2300 C CB . ILE B 2350 122 . -18.156 -5.143 42.628 1.00 20.60 ? ? ? ? ? . 122 ILE B CB 2350 ATOM 2301 C CG1 . ILE B 2350 122 . -16.683 -5.237 43.056 1.00 21.44 ? ? ? ? ? . 122 ILE B CG1 2350 ATOM 2302 C CG2 . ILE B 2350 122 . -18.285 -4.741 41.163 1.00 20.26 ? ? ? ? ? . 122 ILE B CG2 2350 ATOM 2303 C CD1 . ILE B 2350 122 . -15.966 -3.917 43.167 1.00 22.79 ? ? ? ? ? . 122 ILE B CD1 2350 ATOM 2304 N N . ILE B 2350 123 . -21.091 -3.220 42.955 1.00 19.17 ? ? ? ? ? . 123 ILE B N 2350 ATOM 2305 C CA . ILE B 2350 123 . -22.524 -3.148 42.665 1.00 19.40 ? ? ? ? ? . 123 ILE B CA 2350 ATOM 2306 C C . ILE B 2350 123 . -22.828 -3.699 41.282 1.00 20.40 ? ? ? ? ? . 123 ILE B C 2350 ATOM 2307 O O . ILE B 2350 123 . -23.866 -4.326 41.074 1.00 21.80 ? ? ? ? ? . 123 ILE B O 2350 ATOM 2308 C CB . ILE B 2350 123 . -23.019 -1.673 42.737 1.00 19.90 ? ? ? ? ? . 123 ILE B CB 2350 ATOM 2309 C CG1 . ILE B 2350 123 . -23.002 -1.193 44.187 1.00 20.39 ? ? ? ? ? . 123 ILE B CG1 2350 ATOM 2310 C CG2 . ILE B 2350 123 . -24.415 -1.498 42.128 1.00 20.67 ? ? ? ? ? . 123 ILE B CG2 2350 ATOM 2311 C CD1 . ILE B 2350 123 . -23.096 0.301 44.351 1.00 19.36 ? ? ? ? ? . 123 ILE B CD1 2350 ATOM 2312 N N . GLY B 2350 124 . -21.937 -3.423 40.337 1.00 18.81 ? ? ? ? ? . 124 GLY B N 2350 ATOM 2313 C CA . GLY B 2350 124 . -22.146 -3.798 38.949 1.00 18.93 ? ? ? ? ? . 124 GLY B CA 2350 ATOM 2314 C C . GLY B 2350 124 . -20.917 -3.561 38.098 1.00 18.59 ? ? ? ? ? . 124 GLY B C 2350 ATOM 2315 O O . GLY B 2350 124 . -19.977 -2.870 38.514 1.00 17.42 ? ? ? ? ? . 124 GLY B O 2350 ATOM 2316 N N . THR B 2350 125 . -20.915 -4.183 36.918 1.00 16.72 ? ? ? ? ? . 125 THR B N 2350 ATOM 2317 C CA . THR B 2350 125 . -19.809 -4.078 35.974 1.00 18.21 ? ? ? ? ? . 125 THR B CA 2350 ATOM 2318 C C . THR B 2350 125 . -20.260 -3.682 34.544 1.00 18.06 ? ? ? ? ? . 125 THR B C 2350 ATOM 2319 O O . THR B 2350 125 . -19.433 -3.643 33.641 1.00 17.16 ? ? ? ? ? . 125 THR B O 2350 ATOM 2320 C CB . THR B 2350 125 . -19.051 -5.431 35.924 1.00 17.85 ? ? ? ? ? . 125 THR B CB 2350 ATOM 2321 C CG2 . THR B 2350 125 . -18.663 -5.884 37.328 1.00 19.30 ? ? ? ? ? . 125 THR B CG2 2350 ATOM 2322 O OG1 . THR B 2350 125 . -19.902 -6.432 35.363 1.00 17.40 ? ? ? ? ? . 125 THR B OG1 2350 ATOM 2323 N N . GLN B 2350 126 . -21.554 -3.380 34.350 1.00 17.06 ? ? ? ? ? . 126 GLN B N 2350 ATOM 2324 C CA . GLN B 2350 126 . -22.139 -3.200 33.006 1.00 18.96 ? ? ? ? ? . 126 GLN B CA 2350 ATOM 2325 C C . GLN B 2350 126 . -22.612 -1.762 32.731 1.00 16.18 ? ? ? ? ? . 126 GLN B C 2350 ATOM 2326 O O . GLN B 2350 126 . -23.266 -1.519 31.717 1.00 16.00 ? ? ? ? ? . 126 GLN B O 2350 ATOM 2327 C CB . GLN B 2350 126 . -23.318 -4.179 32.800 1.00 21.53 ? ? ? ? ? . 126 GLN B CB 2350 ATOM 2328 C CG . GLN B 2350 126 . -22.997 -5.639 33.127 1.00 26.65 ? ? ? ? ? . 126 GLN B CG 2350 ATOM 2329 C CD . GLN B 2350 126 . -21.992 -6.255 32.163 1.00 33.54 ? ? ? ? ? . 126 GLN B CD 2350 ATOM 2330 N NE2 . GLN B 2350 126 . -20.900 -6.819 32.704 1.00 32.18 ? ? ? ? ? . 126 GLN B NE2 2350 ATOM 2331 O OE1 . GLN B 2350 126 . -22.197 -6.230 30.944 1.00 36.43 ? ? ? ? ? . 126 GLN B OE1 2350 ATOM 2332 N N . ALA B 2350 127 . -22.264 -0.808 33.593 1.00 16.05 ? ? ? ? ? . 127 ALA B N 2350 ATOM 2333 C CA . ALA B 2350 127 . -22.760 0.564 33.436 1.00 15.75 ? ? ? ? ? . 127 ALA B CA 2350 ATOM 2334 C C . ALA B 2350 127 . -22.341 1.243 32.141 1.00 15.23 ? ? ? ? ? . 127 ALA B C 2350 ATOM 2335 O O . ALA B 2350 127 . -23.034 2.142 31.687 1.00 15.93 ? ? ? ? ? . 127 ALA B O 2350 ATOM 2336 C CB . ALA B 2350 127 . -22.400 1.425 34.627 1.00 15.67 ? ? ? ? ? . 127 ALA B CB 2350 ATOM 2337 N N . ARG B 2350 128 . -21.240 0.798 31.530 1.00 14.93 ? ? ? ? ? . 128 ARG B N 2350 ATOM 2338 C CA . ARG B 2350 128 . -20.830 1.298 30.206 1.00 15.96 ? ? ? ? ? . 128 ARG B CA 2350 ATOM 2339 C C . ARG B 2350 128 . -21.925 1.121 29.144 1.00 15.06 ? ? ? ? ? . 128 ARG B C 2350 ATOM 2340 O O . ARG B 2350 128 . -22.027 1.926 28.218 1.00 15.65 ? ? ? ? ? . 128 ARG B O 2350 ATOM 2341 C CB . ARG B 2350 128 . -19.519 0.644 29.737 1.00 17.36 ? ? ? ? ? . 128 ARG B CB 2350 ATOM 2342 C CG . ARG B 2350 128 . -19.030 1.060 28.355 1.00 18.28 ? ? ? ? ? . 128 ARG B CG 2350 ATOM 2343 C CD . ARG B 2350 128 . -19.475 0.089 27.261 1.00 18.70 ? ? ? ? ? . 128 ARG B CD 2350 ATOM 2344 N NE . ARG B 2350 128 . -18.961 0.461 25.948 1.00 20.10 ? ? ? ? ? . 128 ARG B NE 2350 ATOM 2345 C CZ . ARG B 2350 128 . -19.426 1.445 25.180 1.00 19.13 ? ? ? ? ? . 128 ARG B CZ 2350 ATOM 2346 N NH1 . ARG B 2350 128 . -20.456 2.197 25.558 1.00 19.69 ? ? ? ? ? 1+ 128 ARG B NH1 2350 ATOM 2347 N NH2 . ARG B 2350 128 . -18.859 1.668 24.002 1.00 18.47 ? ? ? ? ? . 128 ARG B NH2 2350 ATOM 2348 N N . THR B 2350 129 . -22.702 0.051 29.241 1.00 15.09 ? ? ? ? ? . 129 THR B N 2350 ATOM 2349 C CA . THR B 2350 129 . -23.852 -0.119 28.355 1.00 14.80 ? ? ? ? ? . 129 THR B CA 2350 ATOM 2350 C C . THR B 2350 129 . -25.135 0.426 28.952 1.00 15.27 ? ? ? ? ? . 129 THR B C 2350 ATOM 2351 O O . THR B 2350 129 . -25.954 0.976 28.224 1.00 15.86 ? ? ? ? ? . 129 THR B O 2350 ATOM 2352 C CB . THR B 2350 129 . -24.066 -1.592 27.963 1.00 15.34 ? ? ? ? ? . 129 THR B CB 2350 ATOM 2353 C CG2 . THR B 2350 129 . -22.915 -2.076 27.139 1.00 15.87 ? ? ? ? ? . 129 THR B CG2 2350 ATOM 2354 O OG1 . THR B 2350 129 . -24.144 -2.393 29.141 1.00 16.33 ? ? ? ? ? . 129 THR B OG1 2350 ATOM 2355 N N . ARG B 2350 130 . -25.323 0.275 30.262 1.00 15.00 ? ? ? ? ? . 130 ARG B N 2350 ATOM 2356 C CA . ARG B 2350 130 . -26.568 0.715 30.893 1.00 17.13 ? ? ? ? ? . 130 ARG B CA 2350 ATOM 2357 C C . ARG B 2350 130 . -26.825 2.216 30.730 1.00 15.71 ? ? ? ? ? . 130 ARG B C 2350 ATOM 2358 O O . ARG B 2350 130 . -27.975 2.620 30.566 1.00 15.21 ? ? ? ? ? . 130 ARG B O 2350 ATOM 2359 C CB . ARG B 2350 130 . -26.612 0.354 32.379 1.00 17.49 ? ? ? ? ? . 130 ARG B CB 2350 ATOM 2360 C CG . ARG B 2350 130 . -26.602 -1.128 32.693 1.00 19.40 ? ? ? ? ? . 130 ARG B CG 2350 ATOM 2361 C CD . ARG B 2350 130 . -27.939 -1.798 32.398 1.00 23.34 ? ? ? ? ? . 130 ARG B CD 2350 ATOM 2362 N NE . ARG B 2350 130 . -27.856 -3.263 32.477 1.00 25.67 ? ? ? ? ? . 130 ARG B NE 2350 ATOM 2363 C CZ . ARG B 2350 130 . -27.249 -4.044 31.578 1.00 29.30 ? ? ? ? ? . 130 ARG B CZ 2350 ATOM 2364 N NH1 . ARG B 2350 130 . -26.635 -3.522 30.505 1.00 32.20 ? ? ? ? ? 1+ 130 ARG B NH1 2350 ATOM 2365 N NH2 . ARG B 2350 130 . -27.232 -5.363 31.757 1.00 30.69 ? ? ? ? ? . 130 ARG B NH2 2350 ATOM 2366 N N . VAL B 2350 131 . -25.762 3.019 30.763 1.00 17.22 ? ? ? ? ? . 131 VAL B N 2350 ATOM 2367 C CA . VAL B 2350 131 . -25.866 4.465 30.546 1.00 18.71 ? ? ? ? ? . 131 VAL B CA 2350 ATOM 2368 C C . VAL B 2350 131 . -26.491 4.773 29.164 1.00 18.50 ? ? ? ? ? . 131 VAL B C 2350 ATOM 2369 O O . VAL B 2350 131 . -27.324 5.668 29.033 1.00 18.95 ? ? ? ? ? . 131 VAL B O 2350 ATOM 2370 C CB . VAL B 2350 131 . -24.483 5.156 30.689 1.00 19.83 ? ? ? ? ? . 131 VAL B CB 2350 ATOM 2371 C CG1 . VAL B 2350 131 . -24.538 6.599 30.221 1.00 22.90 ? ? ? ? ? . 131 VAL B CG1 2350 ATOM 2372 C CG2 . VAL B 2350 131 . -23.979 5.076 32.124 1.00 19.15 ? ? ? ? ? . 131 VAL B CG2 2350 ATOM 2373 N N . ILE B 2350 132 . -26.120 3.994 28.158 1.00 16.67 ? ? ? ? ? . 132 ILE B N 2350 ATOM 2374 C CA . ILE B 2350 132 . -26.661 4.145 26.812 1.00 16.90 ? ? ? ? ? . 132 ILE B CA 2350 ATOM 2375 C C . ILE B 2350 132 . -28.113 3.643 26.739 1.00 16.29 ? ? ? ? ? . 132 ILE B C 2350 ATOM 2376 O O . ILE B 2350 132 . -28.967 4.263 26.096 1.00 16.44 ? ? ? ? ? . 132 ILE B O 2350 ATOM 2377 C CB . ILE B 2350 132 . -25.800 3.359 25.799 1.00 17.24 ? ? ? ? ? . 132 ILE B CB 2350 ATOM 2378 C CG1 . ILE B 2350 132 . -24.362 3.915 25.762 1.00 20.53 ? ? ? ? ? . 132 ILE B CG1 2350 ATOM 2379 C CG2 . ILE B 2350 132 . -26.477 3.315 24.433 1.00 17.11 ? ? ? ? ? . 132 ILE B CG2 2350 ATOM 2380 C CD1 . ILE B 2350 132 . -24.119 5.034 24.790 1.00 24.40 ? ? ? ? ? . 132 ILE B CD1 2350 ATOM 2381 N N A GLU B 2350 133 . -28.423 2.510 27.395 0.00 20.00 ? ? ? ? ? . 133 GLU B N 2350 ATOM 2382 N N B GLU B 2350 133 . -28.382 2.515 27.392 1.00 16.20 ? ? ? ? ? . 133 GLU B N 2350 ATOM 2383 C CA A GLU B 2350 133 . -29.761 1.917 27.397 0.00 20.00 ? ? ? ? ? . 133 GLU B CA 2350 ATOM 2384 C CA B GLU B 2350 133 . -29.721 1.911 27.407 1.00 16.09 ? ? ? ? ? . 133 GLU B CA 2350 ATOM 2385 C C A GLU B 2350 133 . -30.756 2.689 28.261 0.00 20.00 ? ? ? ? ? . 133 GLU B C 2350 ATOM 2386 C C B GLU B 2350 133 . -30.751 2.681 28.240 1.00 15.31 ? ? ? ? ? . 133 GLU B C 2350 ATOM 2387 O O A GLU B 2350 133 . -31.968 2.622 28.042 0.00 20.00 ? ? ? ? ? . 133 GLU B O 2350 ATOM 2388 O O B GLU B 2350 133 . -31.953 2.593 27.972 1.00 13.81 ? ? ? ? ? . 133 GLU B O 2350 ATOM 2389 C CB A GLU B 2350 133 . -29.692 0.475 27.901 0.00 20.00 ? ? ? ? ? . 133 GLU B CB 2350 ATOM 2390 C CB B GLU B 2350 133 . -29.641 0.482 27.956 1.00 17.60 ? ? ? ? ? . 133 GLU B CB 2350 ATOM 2391 C CG A GLU B 2350 133 . -28.792 -0.432 27.085 0.00 20.00 ? ? ? ? ? . 133 GLU B CG 2350 ATOM 2392 C CG B GLU B 2350 133 . -28.771 -0.446 27.118 1.00 18.12 ? ? ? ? ? . 133 GLU B CG 2350 ATOM 2393 C CD A GLU B 2350 133 . -28.619 -1.805 27.715 0.00 20.00 ? ? ? ? ? . 133 GLU B CD 2350 ATOM 2394 C CD B GLU B 2350 133 . -28.629 -1.834 27.719 1.00 23.40 ? ? ? ? ? . 133 GLU B CD 2350 ATOM 2395 O OE1 A GLU B 2350 133 . -29.026 -1.980 28.883 0.00 20.00 ? ? ? ? ? . 133 GLU B OE1 2350 ATOM 2396 O OE2 A GLU B 2350 133 . -28.080 -2.710 27.040 0.00 20.00 ? ? ? ? ? 1- 133 GLU B OE2 2350 ATOM 2397 O OE1 B GLU B 2350 133 . -29.036 -2.035 28.889 1.00 26.51 ? ? ? ? ? . 133 GLU B OE1 2350 ATOM 2398 O OE2 B GLU B 2350 133 . -28.127 -2.736 27.000 1.00 24.92 ? ? ? ? ? 1- 133 GLU B OE2 2350 ATOM 2399 N N . ASP B 2350 134 . -30.272 3.427 29.234 1.00 14.63 ? ? ? ? ? . 134 ASP B N 2350 ATOM 2400 C CA . ASP B 2350 134 . -31.098 4.039 30.257 1.00 14.66 ? ? ? ? ? . 134 ASP B CA 2350 ATOM 2401 C C . ASP B 2350 134 . -30.534 5.443 30.535 1.00 14.28 ? ? ? ? ? . 134 ASP B C 2350 ATOM 2402 O O . ASP B 2350 134 . -29.995 5.697 31.610 1.00 14.15 ? ? ? ? ? . 134 ASP B O 2350 ATOM 2403 C CB . ASP B 2350 134 . -31.029 3.145 31.494 1.00 14.80 ? ? ? ? ? . 134 ASP B CB 2350 ATOM 2404 C CG . ASP B 2350 134 . -31.928 3.600 32.640 1.00 15.67 ? ? ? ? ? . 134 ASP B CG 2350 ATOM 2405 O OD1 . ASP B 2350 134 . -32.885 4.373 32.428 1.00 15.40 ? ? ? ? ? . 134 ASP B OD1 2350 ATOM 2406 O OD2 . ASP B 2350 134 . -31.670 3.133 33.784 1.00 16.14 ? ? ? ? ? 1- 134 ASP B OD2 2350 ATOM 2407 N N . PRO B 2350 135 . -30.624 6.355 29.549 1.00 14.67 ? ? ? ? ? . 135 PRO B N 2350 ATOM 2408 C CA . PRO B 2350 135 . -29.977 7.677 29.718 1.00 14.78 ? ? ? ? ? . 135 PRO B CA 2350 ATOM 2409 C C . PRO B 2350 135 . -30.502 8.548 30.877 1.00 14.89 ? ? ? ? ? . 135 PRO B C 2350 ATOM 2410 O O . PRO B 2350 135 . -29.768 9.410 31.374 1.00 15.32 ? ? ? ? ? . 135 PRO B O 2350 ATOM 2411 C CB . PRO B 2350 135 . -30.218 8.381 28.373 1.00 15.25 ? ? ? ? ? . 135 PRO B CB 2350 ATOM 2412 C CG . PRO B 2350 135 . -30.790 7.356 27.446 1.00 16.44 ? ? ? ? ? . 135 PRO B CG 2350 ATOM 2413 C CD . PRO B 2350 135 . -31.390 6.272 28.292 1.00 15.89 ? ? ? ? ? . 135 PRO B CD 2350 ATOM 2414 N N . ASP B 2350 136 . -31.757 8.355 31.277 1.00 15.18 ? ? ? ? ? . 136 ASP B N 2350 ATOM 2415 C CA . ASP B 2350 136 . -32.283 9.049 32.464 1.00 15.63 ? ? ? ? ? . 136 ASP B CA 2350 ATOM 2416 C C . ASP B 2350 136 . -32.159 8.264 33.780 1.00 16.54 ? ? ? ? ? . 136 ASP B C 2350 ATOM 2417 O O . ASP B 2350 136 . -32.680 8.702 34.820 1.00 16.53 ? ? ? ? ? . 136 ASP B O 2350 ATOM 2418 C CB . ASP B 2350 136 . -33.708 9.558 32.208 1.00 16.92 ? ? ? ? ? . 136 ASP B CB 2350 ATOM 2419 C CG . ASP B 2350 136 . -33.724 10.785 31.317 1.00 17.19 ? ? ? ? ? . 136 ASP B CG 2350 ATOM 2420 O OD1 . ASP B 2350 136 . -32.848 11.663 31.491 1.00 19.61 ? ? ? ? ? . 136 ASP B OD1 2350 ATOM 2421 O OD2 . ASP B 2350 136 . -34.608 10.885 30.447 1.00 16.73 ? ? ? ? ? 1- 136 ASP B OD2 2350 ATOM 2422 N N . GLY B 2350 137 . -31.429 7.139 33.740 1.00 15.48 ? ? ? ? ? . 137 GLY B N 2350 ATOM 2423 C CA . GLY B 2350 137 . -31.066 6.372 34.932 1.00 15.18 ? ? ? ? ? . 137 GLY B CA 2350 ATOM 2424 C C . GLY B 2350 137 . -32.218 5.870 35.764 1.00 15.76 ? ? ? ? ? . 137 GLY B C 2350 ATOM 2425 O O . GLY B 2350 137 . -32.130 5.846 37.003 1.00 14.72 ? ? ? ? ? . 137 GLY B O 2350 ATOM 2426 N N . ALA B 2350 138 . -33.317 5.498 35.102 1.00 16.78 ? ? ? ? ? . 138 ALA B N 2350 ATOM 2427 C CA . ALA B 2350 138 . -34.455 4.902 35.790 1.00 16.69 ? ? ? ? ? . 138 ALA B CA 2350 ATOM 2428 C C . ALA B 2350 138 . -34.043 3.709 36.648 1.00 16.56 ? ? ? ? ? . 138 ALA B C 2350 ATOM 2429 O O . ALA B 2350 138 . -34.481 3.599 37.787 1.00 16.42 ? ? ? ? ? . 138 ALA B O 2350 ATOM 2430 C CB . ALA B 2350 138 . -35.529 4.493 34.796 1.00 17.21 ? ? ? ? ? . 138 ALA B CB 2350 ATOM 2431 N N . ASN B 2350 139 . -33.158 2.866 36.111 1.00 15.91 ? ? ? ? ? . 139 ASN B N 2350 ATOM 2432 C CA . ASN B 2350 139 . -32.708 1.642 36.777 1.00 16.24 ? ? ? ? ? . 139 ASN B CA 2350 ATOM 2433 C C . ASN B 2350 139 . -31.351 1.739 37.470 1.00 16.81 ? ? ? ? ? . 139 ASN B C 2350 ATOM 2434 O O . ASN B 2350 139 . -30.799 0.732 37.912 1.00 17.05 ? ? ? ? ? . 139 ASN B O 2350 ATOM 2435 C CB . ASN B 2350 139 . -32.759 0.500 35.767 1.00 18.11 ? ? ? ? ? . 139 ASN B CB 2350 ATOM 2436 C CG . ASN B 2350 139 . -34.194 0.133 35.404 1.00 19.83 ? ? ? ? ? . 139 ASN B CG 2350 ATOM 2437 N ND2 . ASN B 2350 139 . -34.481 0.024 34.124 1.00 20.88 ? ? ? ? ? . 139 ASN B ND2 2350 ATOM 2438 O OD1 . ASN B 2350 139 . -35.032 -0.029 36.280 1.00 23.51 ? ? ? ? ? . 139 ASN B OD1 2350 ATOM 2439 N N . PHE B 2350 140 . -30.828 2.958 37.598 1.00 16.22 ? ? ? ? ? . 140 PHE B N 2350 ATOM 2440 C CA . PHE B 2350 140 . -29.580 3.208 38.327 1.00 17.64 ? ? ? ? ? . 140 PHE B CA 2350 ATOM 2441 C C . PHE B 2350 140 . -29.668 2.659 39.767 1.00 18.96 ? ? ? ? ? . 140 PHE B C 2350 ATOM 2442 O O . PHE B 2350 140 . -30.713 2.807 40.414 1.00 15.66 ? ? ? ? ? . 140 PHE B O 2350 ATOM 2443 C CB . PHE B 2350 140 . -29.310 4.724 38.347 1.00 18.45 ? ? ? ? ? . 140 PHE B CB 2350 ATOM 2444 C CG . PHE B 2350 140 . -28.154 5.125 39.214 1.00 17.77 ? ? ? ? ? . 140 PHE B CG 2350 ATOM 2445 C CD1 . PHE B 2350 140 . -28.314 5.281 40.581 1.00 18.71 ? ? ? ? ? . 140 PHE B CD1 2350 ATOM 2446 C CD2 . PHE B 2350 140 . -26.902 5.336 38.662 1.00 19.83 ? ? ? ? ? . 140 PHE B CD2 2350 ATOM 2447 C CE1 . PHE B 2350 140 . -27.247 5.635 41.388 1.00 19.21 ? ? ? ? ? . 140 PHE B CE1 2350 ATOM 2448 C CE2 . PHE B 2350 140 . -25.839 5.721 39.469 1.00 18.92 ? ? ? ? ? . 140 PHE B CE2 2350 ATOM 2449 C CZ . PHE B 2350 140 . -26.017 5.858 40.828 1.00 18.52 ? ? ? ? ? . 140 PHE B CZ 2350 ATOM 2450 N N . PRO B 2350 141 . -28.576 2.041 40.288 1.00 20.41 ? ? ? ? ? . 141 PRO B N 2350 ATOM 2451 C CA . PRO B 2350 141 . -27.244 1.803 39.717 1.00 20.11 ? ? ? ? ? . 141 PRO B CA 2350 ATOM 2452 C C . PRO B 2350 141 . -27.077 0.490 38.928 1.00 21.32 ? ? ? ? ? . 141 PRO B C 2350 ATOM 2453 O O . PRO B 2350 141 . -25.948 0.030 38.762 1.00 24.20 ? ? ? ? ? . 141 PRO B O 2350 ATOM 2454 C CB . PRO B 2350 141 . -26.362 1.785 40.961 1.00 20.66 ? ? ? ? ? . 141 PRO B CB 2350 ATOM 2455 C CG . PRO B 2350 141 . -27.208 1.126 41.985 1.00 20.62 ? ? ? ? ? . 141 PRO B CG 2350 ATOM 2456 C CD . PRO B 2350 141 . -28.635 1.561 41.690 1.00 22.19 ? ? ? ? ? . 141 PRO B CD 2350 ATOM 2457 N N . TRP B 2350 142 . -28.183 -0.093 38.455 1.00 22.13 ? ? ? ? ? . 142 TRP B N 2350 ATOM 2458 C CA . TRP B 2350 142 . -28.196 -1.272 37.585 1.00 22.88 ? ? ? ? ? . 142 TRP B CA 2350 ATOM 2459 C C . TRP B 2350 142 . -27.597 -2.535 38.225 1.00 27.43 ? ? ? ? ? . 142 TRP B C 2350 ATOM 2460 O O . TRP B 2350 142 . -26.693 -3.159 37.664 1.00 28.69 ? ? ? ? ? . 142 TRP B O 2350 ATOM 2461 C CB . TRP B 2350 142 . -27.548 -0.969 36.234 1.00 20.48 ? ? ? ? ? . 142 TRP B CB 2350 ATOM 2462 C CG . TRP B 2350 142 . -28.048 0.278 35.596 1.00 19.57 ? ? ? ? ? . 142 TRP B CG 2350 ATOM 2463 C CD1 . TRP B 2350 142 . -29.266 0.468 35.016 1.00 19.51 ? ? ? ? ? . 142 TRP B CD1 2350 ATOM 2464 C CD2 . TRP B 2350 142 . -27.335 1.514 35.462 1.00 19.44 ? ? ? ? ? . 142 TRP B CD2 2350 ATOM 2465 C CE2 . TRP B 2350 142 . -28.188 2.417 34.783 1.00 18.08 ? ? ? ? ? . 142 TRP B CE2 2350 ATOM 2466 C CE3 . TRP B 2350 142 . -26.049 1.947 35.837 1.00 19.06 ? ? ? ? ? . 142 TRP B CE3 2350 ATOM 2467 N NE1 . TRP B 2350 142 . -29.356 1.750 34.516 1.00 19.65 ? ? ? ? ? . 142 TRP B NE1 2350 ATOM 2468 C CZ2 . TRP B 2350 142 . -27.801 3.720 34.473 1.00 17.32 ? ? ? ? ? . 142 TRP B CZ2 2350 ATOM 2469 C CZ3 . TRP B 2350 142 . -25.667 3.235 35.533 1.00 19.30 ? ? ? ? ? . 142 TRP B CZ3 2350 ATOM 2470 C CH2 . TRP B 2350 142 . -26.541 4.114 34.851 1.00 19.76 ? ? ? ? ? . 142 TRP B CH2 2350 ATOM 2471 N N . PRO B 2350 143 . -28.131 -2.929 39.393 1.00 31.65 ? ? ? ? ? . 143 PRO B N 2350 ATOM 2472 C CA . PRO B 2350 143 . -27.712 -4.186 40.002 1.00 36.16 ? ? ? ? ? . 143 PRO B CA 2350 ATOM 2473 C C . PRO B 2350 143 . -28.212 -5.407 39.215 1.00 39.42 ? ? ? ? ? . 143 PRO B C 2350 ATOM 2474 O O . PRO B 2350 143 . -29.291 -5.370 38.615 1.00 36.58 ? ? ? ? ? . 143 PRO B O 2350 ATOM 2475 C CB . PRO B 2350 143 . -28.372 -4.127 41.381 1.00 35.00 ? ? ? ? ? . 143 PRO B CB 2350 ATOM 2476 C CG . PRO B 2350 143 . -29.627 -3.370 41.132 1.00 33.72 ? ? ? ? ? . 143 PRO B CG 2350 ATOM 2477 C CD . PRO B 2350 143 . -29.212 -2.291 40.169 1.00 31.42 ? ? ? ? ? . 143 PRO B CD 2350 ATOM 2478 N N . ASN B 2350 144 . -27.436 -6.486 39.261 1.00 48.21 ? ? ? ? ? . 144 ASN B N 2350 ATOM 2479 C CA . ASN B 2350 144 . -27.747 -7.734 38.535 1.00 49.64 ? ? ? ? ? . 144 ASN B CA 2350 ATOM 2480 C C . ASN B 2350 144 . -29.042 -8.395 39.025 1.00 46.88 ? ? ? ? ? . 144 ASN B C 2350 ATOM 2481 O O . ASN B 2350 144 . -29.532 -8.104 40.119 1.00 43.00 ? ? ? ? ? . 144 ASN B O 2350 ATOM 2482 C CB . ASN B 2350 144 . -26.590 -8.735 38.669 1.00 49.51 ? ? ? ? ? . 144 ASN B CB 2350 ATOM 2483 C CG . ASN B 2350 144 . -25.262 -8.155 38.222 1.00 53.00 ? ? ? ? ? . 144 ASN B CG 2350 ATOM 2484 N ND2 . ASN B 2350 144 . -25.061 -8.087 36.913 1.00 55.30 ? ? ? ? ? . 144 ASN B ND2 2350 ATOM 2485 O OD1 . ASN B 2350 144 . -24.441 -7.737 39.047 1.00 49.90 ? ? ? ? ? . 144 ASN B OD1 2350 ATOM 2486 O OXT . ASN B 2350 144 . -29.634 -9.235 38.341 1.00 41.41 ? ? ? ? ? 1- 144 ASN B OXT 2350 # data_SASDEB4_MODEL_2351 # _sas_model.id 2351 _sas_model.type_of_model atomic _sas_model.version . _sas_model.symmetry . _sas_model.comment . _sas_model.fitting_id 1706 _sas_model.radius . # loop_ _atom_site.group_PDB _atom_site.id _atom_site.type_symbol _atom_site.label_atom_id _atom_site.label_alt_id _atom_site.label_comp_id _atom_site.label_asym_id _atom_site.label_entity_id _atom_site.label_seq_id _atom_site.pdbx_PDB_ins_code _atom_site.Cartn_x _atom_site.Cartn_y _atom_site.Cartn_z _atom_site.occupancy _atom_site.B_iso_or_equiv _atom_site.Cartn_x_esd _atom_site.Cartn_y_esd _atom_site.Cartn_z_esd _atom_site.occupancy_esd _atom_site.B_iso_or_equiv_esd _atom_site.pdbx_formal_charge _atom_site.auth_seq_id _atom_site.auth_comp_id _atom_site.auth_asym_id _atom_site.auth_atom_id _atom_site.pdbx_PDB_model_num ATOM 1 N N . MET A 2351 1 . 1.498 -29.784 9.466 1.00 42.34 ? ? ? ? ? . 1 MET A N 2351 ATOM 2 C CA . MET A 2351 1 . 1.362 -28.330 9.713 1.00 38.79 ? ? ? ? ? . 1 MET A CA 2351 ATOM 3 C C . MET A 2351 1 . 2.451 -27.795 10.648 1.00 34.46 ? ? ? ? ? . 1 MET A C 2351 ATOM 4 O O . MET A 2351 1 . 3.019 -28.519 11.476 1.00 28.07 ? ? ? ? ? . 1 MET A O 2351 ATOM 5 C CB . MET A 2351 1 . -0.032 -28.003 10.280 1.00 43.44 ? ? ? ? ? . 1 MET A CB 2351 ATOM 6 C CG . MET A 2351 1 . -1.163 -28.074 9.261 1.00 48.34 ? ? ? ? ? . 1 MET A CG 2351 ATOM 7 S SD . MET A 2351 1 . -1.096 -26.763 8.019 1.00 56.59 ? ? ? ? ? . 1 MET A SD 2351 ATOM 8 C CE . MET A 2351 1 . -1.944 -27.553 6.650 1.00 53.77 ? ? ? ? ? . 1 MET A CE 2351 ATOM 9 N N . SER A 2351 2 . 2.702 -26.498 10.518 1.00 31.58 ? ? ? ? ? . 2 SER A N 2351 ATOM 10 C CA . SER A 2351 2 . 3.686 -25.813 11.340 1.00 29.58 ? ? ? ? ? . 2 SER A CA 2351 ATOM 11 C C . SER A 2351 2 . 3.179 -25.647 12.742 1.00 28.87 ? ? ? ? ? . 2 SER A C 2351 ATOM 12 O O . SER A 2351 2 . 1.976 -25.688 12.985 1.00 24.92 ? ? ? ? ? . 2 SER A O 2351 ATOM 13 C CB . SER A 2351 2 . 3.985 -24.427 10.800 1.00 31.81 ? ? ? ? ? . 2 SER A CB 2351 ATOM 14 O OG . SER A 2351 2 . 2.955 -23.494 11.097 1.00 29.45 ? ? ? ? ? . 2 SER A OG 2351 ATOM 15 N N . GLY A 2351 3 . 4.105 -25.396 13.653 1.00 26.92 ? ? ? ? ? . 3 GLY A N 2351 ATOM 16 C CA . GLY A 2351 3 . 3.752 -25.062 15.022 1.00 27.19 ? ? ? ? ? . 3 GLY A CA 2351 ATOM 17 C C . GLY A 2351 3 . 3.057 -23.717 15.142 1.00 26.26 ? ? ? ? ? . 3 GLY A C 2351 ATOM 18 O O . GLY A 2351 3 . 2.392 -23.466 16.134 1.00 31.06 ? ? ? ? ? . 3 GLY A O 2351 ATOM 19 N N . LEU A 2351 4 . 3.204 -22.842 14.148 1.00 27.31 ? ? ? ? ? . 4 LEU A N 2351 ATOM 20 C CA . LEU A 2351 4 . 2.393 -21.618 14.096 1.00 28.14 ? ? ? ? ? . 4 LEU A CA 2351 ATOM 21 C C . LEU A 2351 4 . 0.907 -21.935 13.926 1.00 26.94 ? ? ? ? ? . 4 LEU A C 2351 ATOM 22 O O . LEU A 2351 4 . 0.070 -21.235 14.495 1.00 25.83 ? ? ? ? ? . 4 LEU A O 2351 ATOM 23 C CB . LEU A 2351 4 . 2.859 -20.661 12.988 1.00 31.30 ? ? ? ? ? . 4 LEU A CB 2351 ATOM 24 C CG . LEU A 2351 4 . 4.018 -19.719 13.288 1.00 32.68 ? ? ? ? ? . 4 LEU A CG 2351 ATOM 25 C CD1 . LEU A 2351 4 . 4.270 -18.858 12.063 1.00 34.49 ? ? ? ? ? . 4 LEU A CD1 2351 ATOM 26 C CD2 . LEU A 2351 4 . 3.718 -18.844 14.497 1.00 34.30 ? ? ? ? ? . 4 LEU A CD2 2351 ATOM 27 N N . ALA A 2351 5 . 0.579 -22.994 13.176 1.00 26.99 ? ? ? ? ? . 5 ALA A N 2351 ATOM 28 C CA . ALA A 2351 5 . -0.817 -23.451 13.048 1.00 29.14 ? ? ? ? ? . 5 ALA A CA 2351 ATOM 29 C C . ALA A 2351 5 . -1.502 -23.807 14.377 1.00 31.57 ? ? ? ? ? . 5 ALA A C 2351 ATOM 30 O O . ALA A 2351 5 . -2.722 -23.642 14.499 1.00 38.23 ? ? ? ? ? . 5 ALA A O 2351 ATOM 31 C CB . ALA A 2351 5 . -0.923 -24.626 12.077 1.00 32.07 ? ? ? ? ? . 5 ALA A CB 2351 ATOM 32 N N . LYS A 2351 6 . -0.746 -24.274 15.372 1.00 28.88 ? ? ? ? ? . 6 LYS A N 2351 ATOM 33 C CA . LYS A 2351 6 . -1.337 -24.554 16.690 1.00 28.76 ? ? ? ? ? . 6 LYS A CA 2351 ATOM 34 C C . LYS A 2351 6 . -1.895 -23.293 17.343 1.00 24.63 ? ? ? ? ? . 6 LYS A C 2351 ATOM 35 O O . LYS A 2351 6 . -2.853 -23.372 18.095 1.00 25.15 ? ? ? ? ? . 6 LYS A O 2351 ATOM 36 C CB . LYS A 2351 6 . -0.356 -25.256 17.646 1.00 32.13 ? ? ? ? ? . 6 LYS A CB 2351 ATOM 37 C CG . LYS A 2351 6 . 0.511 -24.341 18.526 1.00 31.95 ? ? ? ? ? . 6 LYS A CG 2351 ATOM 38 C CD . LYS A 2351 6 . 1.607 -25.092 19.277 1.00 33.12 ? ? ? ? ? . 6 LYS A CD 2351 ATOM 39 C CE . LYS A 2351 6 . 2.655 -25.712 18.350 1.00 32.32 ? ? ? ? ? . 6 LYS A CE 2351 ATOM 40 N NZ . LYS A 2351 6 . 3.554 -26.649 19.060 1.00 28.93 ? ? ? ? ? 1+ 6 LYS A NZ 2351 ATOM 41 N N . TYR A 2351 7 . -1.273 -22.149 17.060 1.00 23.51 ? ? ? ? ? . 7 TYR A N 2351 ATOM 42 C CA . TYR A 2351 7 . -1.713 -20.858 17.597 1.00 24.18 ? ? ? ? ? . 7 TYR A CA 2351 ATOM 43 C C . TYR A 2351 7 . -2.735 -20.147 16.721 1.00 25.86 ? ? ? ? ? . 7 TYR A C 2351 ATOM 44 O O . TYR A 2351 7 . -3.549 -19.381 17.235 1.00 25.45 ? ? ? ? ? . 7 TYR A O 2351 ATOM 45 C CB . TYR A 2351 7 . -0.526 -19.931 17.799 1.00 22.86 ? ? ? ? ? . 7 TYR A CB 2351 ATOM 46 C CG . TYR A 2351 7 . 0.519 -20.473 18.741 1.00 20.79 ? ? ? ? ? . 7 TYR A CG 2351 ATOM 47 C CD1 . TYR A 2351 7 . 0.199 -20.788 20.060 1.00 19.65 ? ? ? ? ? . 7 TYR A CD1 2351 ATOM 48 C CD2 . TYR A 2351 7 . 1.841 -20.635 18.325 1.00 19.30 ? ? ? ? ? . 7 TYR A CD2 2351 ATOM 49 C CE1 . TYR A 2351 7 . 1.162 -21.270 20.934 1.00 19.28 ? ? ? ? ? . 7 TYR A CE1 2351 ATOM 50 C CE2 . TYR A 2351 7 . 2.805 -21.114 19.186 1.00 19.91 ? ? ? ? ? . 7 TYR A CE2 2351 ATOM 51 C CZ . TYR A 2351 7 . 2.462 -21.430 20.493 1.00 19.68 ? ? ? ? ? . 7 TYR A CZ 2351 ATOM 52 O OH . TYR A 2351 7 . 3.427 -21.901 21.354 1.00 19.23 ? ? ? ? ? . 7 TYR A OH 2351 ATOM 53 N N . LEU A 2351 8 . -2.711 -20.410 15.413 1.00 25.61 ? ? ? ? ? . 8 LEU A N 2351 ATOM 54 C CA . LEU A 2351 8 . -3.604 -19.742 14.468 1.00 27.57 ? ? ? ? ? . 8 LEU A CA 2351 ATOM 55 C C . LEU A 2351 8 . -4.522 -20.703 13.671 1.00 30.41 ? ? ? ? ? . 8 LEU A C 2351 ATOM 56 O O . LEU A 2351 8 . -4.503 -20.676 12.444 1.00 31.20 ? ? ? ? ? . 8 LEU A O 2351 ATOM 57 C CB . LEU A 2351 8 . -2.750 -18.882 13.517 1.00 26.23 ? ? ? ? ? . 8 LEU A CB 2351 ATOM 58 C CG . LEU A 2351 8 . -1.810 -17.852 14.164 1.00 24.95 ? ? ? ? ? . 8 LEU A CG 2351 ATOM 59 C CD1 . LEU A 2351 8 . -0.828 -17.290 13.142 1.00 26.14 ? ? ? ? ? . 8 LEU A CD1 2351 ATOM 60 C CD2 . LEU A 2351 8 . -2.602 -16.730 14.822 1.00 25.27 ? ? ? ? ? . 8 LEU A CD2 2351 ATOM 61 N N A PRO A 2351 9 . -5.300 -21.558 14.376 0.49 34.84 ? ? ? ? ? . 9 PRO A N 2351 ATOM 62 N N B PRO A 2351 9 . -5.359 -21.503 14.365 0.51 33.67 ? ? ? ? ? . 9 PRO A N 2351 ATOM 63 C CA A PRO A 2351 9 . -6.293 -22.381 13.700 0.49 37.05 ? ? ? ? ? . 9 PRO A CA 2351 ATOM 64 C CA B PRO A 2351 9 . -6.175 -22.534 13.697 0.51 35.34 ? ? ? ? ? . 9 PRO A CA 2351 ATOM 65 C C A PRO A 2351 9 . -7.506 -21.519 13.432 0.49 38.35 ? ? ? ? ? . 9 PRO A C 2351 ATOM 66 C C B PRO A 2351 9 . -7.186 -22.013 12.660 0.51 36.39 ? ? ? ? ? . 9 PRO A C 2351 ATOM 67 O O A PRO A 2351 9 . -8.118 -21.001 14.366 0.49 39.55 ? ? ? ? ? . 9 PRO A O 2351 ATOM 68 O O B PRO A 2351 9 . -7.420 -22.691 11.657 0.51 37.00 ? ? ? ? ? . 9 PRO A O 2351 ATOM 69 C CB A PRO A 2351 9 . -6.624 -23.442 14.742 0.49 36.54 ? ? ? ? ? . 9 PRO A CB 2351 ATOM 70 C CB B PRO A 2351 9 . -6.909 -23.210 14.865 0.51 34.76 ? ? ? ? ? . 9 PRO A CB 2351 ATOM 71 C CG A PRO A 2351 9 . -6.535 -22.693 16.022 0.49 36.43 ? ? ? ? ? . 9 PRO A CG 2351 ATOM 72 C CG B PRO A 2351 9 . -6.953 -22.172 15.932 0.51 34.10 ? ? ? ? ? . 9 PRO A CG 2351 ATOM 73 C CD A PRO A 2351 9 . -5.375 -21.751 15.840 0.49 36.25 ? ? ? ? ? . 9 PRO A CD 2351 ATOM 74 C CD B PRO A 2351 9 . -5.641 -21.459 15.815 0.51 34.53 ? ? ? ? ? . 9 PRO A CD 2351 ATOM 75 N N A GLY A 2351 10 . -7.850 -21.363 12.165 0.49 38.66 ? ? ? ? ? . 10 GLY A N 2351 ATOM 76 N N B GLY A 2351 10 . -7.776 -20.841 12.911 0.51 35.97 ? ? ? ? ? . 10 GLY A N 2351 ATOM 77 C CA A GLY A 2351 10 . -8.786 -20.329 11.768 0.49 37.94 ? ? ? ? ? . 10 GLY A CA 2351 ATOM 78 C CA B GLY A 2351 10 . -8.733 -20.217 11.981 0.51 36.27 ? ? ? ? ? . 10 GLY A CA 2351 ATOM 79 C C A GLY A 2351 10 . -8.121 -19.416 10.757 0.49 37.83 ? ? ? ? ? . 10 GLY A C 2351 ATOM 80 C C B GLY A 2351 10 . -8.107 -19.480 10.800 0.51 37.15 ? ? ? ? ? . 10 GLY A C 2351 ATOM 81 O O A GLY A 2351 10 . -8.796 -18.870 9.876 0.49 37.03 ? ? ? ? ? . 10 GLY A O 2351 ATOM 82 O O B GLY A 2351 10 . -8.798 -19.134 9.836 0.51 37.06 ? ? ? ? ? . 10 GLY A O 2351 ATOM 83 N N . ALA A 2351 11 . -6.803 -19.231 10.888 1.00 36.15 ? ? ? ? ? . 11 ALA A N 2351 ATOM 84 C CA . ALA A 2351 11 . -6.026 -18.586 9.835 1.00 35.46 ? ? ? ? ? . 11 ALA A CA 2351 ATOM 85 C C . ALA A 2351 11 . -5.687 -19.603 8.758 1.00 36.66 ? ? ? ? ? . 11 ALA A C 2351 ATOM 86 O O . ALA A 2351 11 . -5.713 -20.816 8.988 1.00 35.61 ? ? ? ? ? . 11 ALA A O 2351 ATOM 87 C CB . ALA A 2351 11 . -4.743 -17.992 10.401 1.00 34.28 ? ? ? ? ? . 11 ALA A CB 2351 ATOM 88 N N . THR A 2351 12 . -5.403 -19.089 7.571 1.00 35.16 ? ? ? ? ? . 12 THR A N 2351 ATOM 89 C CA . THR A 2351 12 . -4.620 -19.821 6.582 1.00 34.41 ? ? ? ? ? . 12 THR A CA 2351 ATOM 90 C C . THR A 2351 12 . -3.465 -18.927 6.157 1.00 30.55 ? ? ? ? ? . 12 THR A C 2351 ATOM 91 O O . THR A 2351 12 . -2.309 -19.284 6.369 1.00 33.15 ? ? ? ? ? . 12 THR A O 2351 ATOM 92 C CB . THR A 2351 12 . -5.447 -20.322 5.371 1.00 37.60 ? ? ? ? ? . 12 THR A CB 2351 ATOM 93 C CG2 . THR A 2351 12 . -5.624 -21.844 5.441 1.00 41.25 ? ? ? ? ? . 12 THR A CG2 2351 ATOM 94 O OG1 . THR A 2351 12 . -6.745 -19.707 5.356 1.00 40.05 ? ? ? ? ? . 12 THR A OG1 2351 ATOM 95 N N . ASN A 2351 13 . -3.761 -17.760 5.589 1.00 24.01 ? ? ? ? ? . 13 ASN A N 2351 ATOM 96 C CA . ASN A 2351 13 . -2.702 -16.909 5.058 1.00 21.19 ? ? ? ? ? . 13 ASN A CA 2351 ATOM 97 C C . ASN A 2351 13 . -2.485 -15.671 5.897 1.00 19.45 ? ? ? ? ? . 13 ASN A C 2351 ATOM 98 O O . ASN A 2351 13 . -3.378 -15.222 6.620 1.00 21.50 ? ? ? ? ? . 13 ASN A O 2351 ATOM 99 C CB . ASN A 2351 13 . -2.997 -16.518 3.609 1.00 23.60 ? ? ? ? ? . 13 ASN A CB 2351 ATOM 100 C CG . ASN A 2351 13 . -3.062 -17.718 2.683 1.00 25.11 ? ? ? ? ? . 13 ASN A CG 2351 ATOM 101 N ND2 . ASN A 2351 13 . -4.029 -17.717 1.771 1.00 24.16 ? ? ? ? ? . 13 ASN A ND2 2351 ATOM 102 O OD1 . ASN A 2351 13 . -2.256 -18.644 2.795 1.00 28.41 ? ? ? ? ? . 13 ASN A OD1 2351 ATOM 103 N N . LEU A 2351 14 . -1.277 -15.134 5.781 1.00 16.54 ? ? ? ? ? . 14 LEU A N 2351 ATOM 104 C CA . LEU A 2351 14 . -0.881 -13.881 6.390 1.00 15.38 ? ? ? ? ? . 14 LEU A CA 2351 ATOM 105 C C . LEU A 2351 14 . -0.723 -12.879 5.271 1.00 15.70 ? ? ? ? ? . 14 LEU A C 2351 ATOM 106 O O . LEU A 2351 14 . -0.384 -13.251 4.152 1.00 16.70 ? ? ? ? ? . 14 LEU A O 2351 ATOM 107 C CB . LEU A 2351 14 . 0.455 -14.057 7.118 1.00 15.56 ? ? ? ? ? . 14 LEU A CB 2351 ATOM 108 C CG . LEU A 2351 14 . 0.466 -15.081 8.254 1.00 15.33 ? ? ? ? ? . 14 LEU A CG 2351 ATOM 109 C CD1 . LEU A 2351 14 . 1.865 -15.199 8.824 1.00 16.03 ? ? ? ? ? . 14 LEU A CD1 2351 ATOM 110 C CD2 . LEU A 2351 14 . -0.512 -14.706 9.360 1.00 14.84 ? ? ? ? ? . 14 LEU A CD2 2351 ATOM 111 N N . LEU A 2351 15 . -0.963 -11.610 5.571 1.00 15.63 ? ? ? ? ? . 15 LEU A N 2351 ATOM 112 C CA . LEU A 2351 15 . -0.692 -10.536 4.620 1.00 16.16 ? ? ? ? ? . 15 LEU A CA 2351 ATOM 113 C C . LEU A 2351 15 . 0.817 -10.328 4.485 1.00 16.48 ? ? ? ? ? . 15 LEU A C 2351 ATOM 114 O O . LEU A 2351 15 . 1.537 -10.488 5.458 1.00 15.72 ? ? ? ? ? . 15 LEU A O 2351 ATOM 115 C CB . LEU A 2351 15 . -1.302 -9.224 5.088 1.00 15.78 ? ? ? ? ? . 15 LEU A CB 2351 ATOM 116 C CG . LEU A 2351 15 . -2.774 -9.203 5.473 1.00 16.53 ? ? ? ? ? . 15 LEU A CG 2351 ATOM 117 C CD1 . LEU A 2351 15 . -3.169 -7.778 5.854 1.00 17.40 ? ? ? ? ? . 15 LEU A CD1 2351 ATOM 118 C CD2 . LEU A 2351 15 . -3.657 -9.742 4.356 1.00 15.86 ? ? ? ? ? . 15 LEU A CD2 2351 ATOM 119 N N . SER A 2351 16 . 1.274 -9.967 3.289 1.00 16.81 ? ? ? ? ? . 16 SER A N 2351 ATOM 120 C CA . SER A 2351 16 . 2.659 -9.490 3.089 1.00 18.19 ? ? ? ? ? . 16 SER A CA 2351 ATOM 121 C C . SER A 2351 16 . 2.617 -8.199 2.266 1.00 19.91 ? ? ? ? ? . 16 SER A C 2351 ATOM 122 O O . SER A 2351 16 . 1.553 -7.749 1.839 1.00 18.64 ? ? ? ? ? . 16 SER A O 2351 ATOM 123 C CB . SER A 2351 16 . 3.525 -10.544 2.378 1.00 19.00 ? ? ? ? ? . 16 SER A CB 2351 ATOM 124 O OG . SER A 2351 16 . 3.353 -10.503 0.969 1.00 19.59 ? ? ? ? ? . 16 SER A OG 2351 ATOM 125 N N . LYS A 2351 17 . 3.780 -7.614 2.027 1.00 21.51 ? ? ? ? ? . 17 LYS A N 2351 ATOM 126 C CA . LYS A 2351 17 . 3.855 -6.435 1.165 1.00 24.73 ? ? ? ? ? . 17 LYS A CA 2351 ATOM 127 C C . LYS A 2351 17 . 3.444 -6.732 -0.283 1.00 25.66 ? ? ? ? ? . 17 LYS A C 2351 ATOM 128 O O . LYS A 2351 17 . 3.019 -5.819 -0.983 1.00 27.03 ? ? ? ? ? . 17 LYS A O 2351 ATOM 129 C CB . LYS A 2351 17 . 5.262 -5.832 1.197 1.00 25.50 ? ? ? ? ? . 17 LYS A CB 2351 ATOM 130 C CG . LYS A 2351 17 . 5.682 -5.273 2.551 1.00 25.81 ? ? ? ? ? . 17 LYS A CG 2351 ATOM 131 C CD . LYS A 2351 17 . 4.736 -4.187 3.056 1.00 28.95 ? ? ? ? ? . 17 LYS A CD 2351 ATOM 132 C CE . LYS A 2351 17 . 3.753 -4.693 4.113 1.00 28.57 ? ? ? ? ? . 17 LYS A CE 2351 ATOM 133 N NZ . LYS A 2351 17 . 2.971 -3.562 4.702 1.00 25.15 ? ? ? ? ? 1+ 17 LYS A NZ 2351 ATOM 134 N N . SER A 2351 18 . 3.555 -7.992 -0.712 1.00 25.74 ? ? ? ? ? . 18 SER A N 2351 ATOM 135 C CA . SER A 2351 18 . 3.177 -8.416 -2.070 1.00 30.18 ? ? ? ? ? . 18 SER A CA 2351 ATOM 136 C C . SER A 2351 18 . 2.143 -9.546 -2.074 1.00 32.37 ? ? ? ? ? . 18 SER A C 2351 ATOM 137 O O . SER A 2351 18 . 2.384 -10.619 -2.635 1.00 35.88 ? ? ? ? ? . 18 SER A O 2351 ATOM 138 C CB . SER A 2351 18 . 4.431 -8.893 -2.797 1.00 31.94 ? ? ? ? ? . 18 SER A CB 2351 ATOM 139 O OG . SER A 2351 18 . 4.959 -10.040 -2.149 1.00 33.68 ? ? ? ? ? . 18 SER A OG 2351 ATOM 140 N N . GLY A 2351 19 . 0.995 -9.323 -1.452 1.00 31.20 ? ? ? ? ? . 19 GLY A N 2351 ATOM 141 C CA . GLY A 2351 19 . -0.034 -10.370 -1.395 1.00 32.15 ? ? ? ? ? . 19 GLY A CA 2351 ATOM 142 C C . GLY A 2351 19 . 0.276 -11.471 -0.382 1.00 31.51 ? ? ? ? ? . 19 GLY A C 2351 ATOM 143 O O . GLY A 2351 19 . 1.310 -11.458 0.288 1.00 33.38 ? ? ? ? ? . 19 GLY A O 2351 ATOM 144 N N . GLU A 2351 20 . -0.629 -12.434 -0.282 1.00 26.41 ? ? ? ? ? . 20 GLU A N 2351 ATOM 145 C CA . GLU A 2351 20 . -0.691 -13.290 0.884 1.00 24.83 ? ? ? ? ? . 20 GLU A CA 2351 ATOM 146 C C . GLU A 2351 20 . 0.330 -14.411 0.824 1.00 21.95 ? ? ? ? ? . 20 GLU A C 2351 ATOM 147 O O . GLU A 2351 20 . 0.679 -14.879 -0.254 1.00 20.93 ? ? ? ? ? . 20 GLU A O 2351 ATOM 148 C CB . GLU A 2351 20 . -2.102 -13.854 1.040 1.00 28.97 ? ? ? ? ? . 20 GLU A CB 2351 ATOM 149 C CG . GLU A 2351 20 . -3.156 -12.772 1.249 1.00 29.83 ? ? ? ? ? . 20 GLU A CG 2351 ATOM 150 C CD . GLU A 2351 20 . -4.539 -13.321 1.561 1.00 31.70 ? ? ? ? ? . 20 GLU A CD 2351 ATOM 151 O OE1 . GLU A 2351 20 . -4.814 -14.491 1.202 1.00 33.49 ? ? ? ? ? . 20 GLU A OE1 2351 ATOM 152 O OE2 . GLU A 2351 20 . -5.349 -12.565 2.154 1.00 34.19 ? ? ? ? ? 1- 20 GLU A OE2 2351 ATOM 153 N N . VAL A 2351 21 . 0.799 -14.822 1.996 1.00 18.14 ? ? ? ? ? . 21 VAL A N 2351 ATOM 154 C CA . VAL A 2351 21 . 1.739 -15.940 2.130 1.00 18.05 ? ? ? ? ? . 21 VAL A CA 2351 ATOM 155 C C . VAL A 2351 21 . 1.210 -16.964 3.137 1.00 16.57 ? ? ? ? ? . 21 VAL A C 2351 ATOM 156 O O . VAL A 2351 21 . 0.519 -16.610 4.089 1.00 15.65 ? ? ? ? ? . 21 VAL A O 2351 ATOM 157 C CB . VAL A 2351 21 . 3.150 -15.466 2.542 1.00 18.57 ? ? ? ? ? . 21 VAL A CB 2351 ATOM 158 C CG1 . VAL A 2351 21 . 3.672 -14.437 1.540 1.00 19.84 ? ? ? ? ? . 21 VAL A CG1 2351 ATOM 159 C CG2 . VAL A 2351 21 . 3.176 -14.922 3.970 1.00 17.16 ? ? ? ? ? . 21 VAL A CG2 2351 ATOM 160 N N . SER A 2351 22 . 1.533 -18.230 2.906 1.00 15.34 ? ? ? ? ? . 22 SER A N 2351 ATOM 161 C CA . SER A 2351 22 . 1.073 -19.315 3.767 1.00 16.37 ? ? ? ? ? . 22 SER A CA 2351 ATOM 162 C C . SER A 2351 22 . 1.872 -19.345 5.061 1.00 16.62 ? ? ? ? ? . 22 SER A C 2351 ATOM 163 O O . SER A 2351 22 . 3.000 -18.826 5.142 1.00 15.98 ? ? ? ? ? . 22 SER A O 2351 ATOM 164 C CB . SER A 2351 22 . 1.237 -20.655 3.056 1.00 17.61 ? ? ? ? ? . 22 SER A CB 2351 ATOM 165 O OG . SER A 2351 22 . 2.618 -20.887 2.815 1.00 17.06 ? ? ? ? ? . 22 SER A OG 2351 ATOM 166 N N . LEU A 2351 23 . 1.305 -19.988 6.072 1.00 17.27 ? ? ? ? ? . 23 LEU A N 2351 ATOM 167 C CA . LEU A 2351 23 . 2.058 -20.286 7.290 1.00 17.54 ? ? ? ? ? . 23 LEU A CA 2351 ATOM 168 C C . LEU A 2351 23 . 3.271 -21.187 6.998 1.00 15.71 ? ? ? ? ? . 23 LEU A C 2351 ATOM 169 O O . LEU A 2351 23 . 4.357 -20.961 7.555 1.00 15.68 ? ? ? ? ? . 23 LEU A O 2351 ATOM 170 C CB . LEU A 2351 23 . 1.158 -20.925 8.354 1.00 19.09 ? ? ? ? ? . 23 LEU A CB 2351 ATOM 171 C CG . LEU A 2351 23 . 0.047 -20.044 8.926 1.00 19.85 ? ? ? ? ? . 23 LEU A CG 2351 ATOM 172 C CD1 . LEU A 2351 23 . -0.781 -20.855 9.912 1.00 20.80 ? ? ? ? ? . 23 LEU A CD1 2351 ATOM 173 C CD2 . LEU A 2351 23 . 0.588 -18.800 9.598 1.00 20.11 ? ? ? ? ? . 23 LEU A CD2 2351 ATOM 174 N N . GLY A 2351 24 . 3.092 -22.170 6.110 1.00 14.87 ? ? ? ? ? . 24 GLY A N 2351 ATOM 175 C CA . GLY A 2351 24 . 4.183 -23.039 5.652 1.00 14.51 ? ? ? ? ? . 24 GLY A CA 2351 ATOM 176 C C . GLY A 2351 24 . 5.381 -22.325 5.024 1.00 14.47 ? ? ? ? ? . 24 GLY A C 2351 ATOM 177 O O . GLY A 2351 24 . 6.505 -22.845 5.067 1.00 12.91 ? ? ? ? ? . 24 GLY A O 2351 ATOM 178 N N . SER A 2351 25 . 5.160 -21.133 4.454 1.00 14.24 ? ? ? ? ? . 25 SER A N 2351 ATOM 179 C CA . SER A 2351 25 . 6.248 -20.339 3.852 1.00 14.58 ? ? ? ? ? . 25 SER A CA 2351 ATOM 180 C C . SER A 2351 25 . 7.295 -19.881 4.877 1.00 15.23 ? ? ? ? ? . 25 SER A C 2351 ATOM 181 O O . SER A 2351 25 . 8.425 -19.538 4.510 1.00 15.85 ? ? ? ? ? . 25 SER A O 2351 ATOM 182 C CB . SER A 2351 25 . 5.691 -19.131 3.076 1.00 14.16 ? ? ? ? ? . 25 SER A CB 2351 ATOM 183 O OG . SER A 2351 25 . 5.236 -18.112 3.943 1.00 13.91 ? ? ? ? ? . 25 SER A OG 2351 ATOM 184 N N . LEU A 2351 26 . 6.900 -19.862 6.153 1.00 15.28 ? ? ? ? ? . 26 LEU A N 2351 ATOM 185 C CA . LEU A 2351 26 . 7.770 -19.517 7.262 1.00 15.71 ? ? ? ? ? . 26 LEU A CA 2351 ATOM 186 C C . LEU A 2351 26 . 8.551 -20.698 7.831 1.00 13.64 ? ? ? ? ? . 26 LEU A C 2351 ATOM 187 O O . LEU A 2351 26 . 9.162 -20.554 8.882 1.00 12.80 ? ? ? ? ? . 26 LEU A O 2351 ATOM 188 C CB . LEU A 2351 26 . 6.938 -18.882 8.384 1.00 17.44 ? ? ? ? ? . 26 LEU A CB 2351 ATOM 189 C CG . LEU A 2351 26 . 6.047 -17.702 7.946 1.00 20.26 ? ? ? ? ? . 26 LEU A CG 2351 ATOM 190 C CD1 . LEU A 2351 26 . 5.260 -17.143 9.118 1.00 22.13 ? ? ? ? ? . 26 LEU A CD1 2351 ATOM 191 C CD2 . LEU A 2351 26 . 6.881 -16.637 7.276 1.00 23.52 ? ? ? ? ? . 26 LEU A CD2 2351 ATOM 192 N N . VAL A 2351 27 . 8.555 -21.833 7.132 1.00 13.12 ? ? ? ? ? . 27 VAL A N 2351 ATOM 193 C CA . VAL A 2351 27 . 9.321 -23.014 7.537 1.00 13.59 ? ? ? ? ? . 27 VAL A CA 2351 ATOM 194 C C . VAL A 2351 27 . 10.754 -22.634 7.923 1.00 13.89 ? ? ? ? ? . 27 VAL A C 2351 ATOM 195 O O . VAL A 2351 27 . 11.416 -21.850 7.236 1.00 13.58 ? ? ? ? ? . 27 VAL A O 2351 ATOM 196 C CB . VAL A 2351 27 . 9.281 -24.133 6.469 1.00 12.77 ? ? ? ? ? . 27 VAL A CB 2351 ATOM 197 C CG1 . VAL A 2351 27 . 9.896 -23.694 5.145 1.00 12.72 ? ? ? ? ? . 27 VAL A CG1 2351 ATOM 198 C CG2 . VAL A 2351 27 . 9.933 -25.428 6.964 1.00 13.09 ? ? ? ? ? . 27 VAL A CG2 2351 ATOM 199 N N . GLY A 2351 28 . 11.165 -23.100 9.095 1.00 14.31 ? ? ? ? ? . 28 GLY A N 2351 ATOM 200 C CA . GLY A 2351 28 . 12.540 -22.930 9.573 1.00 14.56 ? ? ? ? ? . 28 GLY A CA 2351 ATOM 201 C C . GLY A 2351 28 . 12.871 -21.574 10.159 1.00 13.61 ? ? ? ? ? . 28 GLY A C 2351 ATOM 202 O O . GLY A 2351 28 . 14.008 -21.365 10.620 1.00 13.45 ? ? ? ? ? . 28 GLY A O 2351 ATOM 203 N N . LYS A 2351 29 . 11.900 -20.657 10.167 1.00 14.17 ? ? ? ? ? . 29 LYS A N 2351 ATOM 204 C CA . LYS A 2351 29 . 12.110 -19.302 10.657 1.00 14.57 ? ? ? ? ? . 29 LYS A CA 2351 ATOM 205 C C . LYS A 2351 29 . 11.932 -19.163 12.159 1.00 14.89 ? ? ? ? ? . 29 LYS A C 2351 ATOM 206 O O . LYS A 2351 29 . 11.235 -19.949 12.797 1.00 14.69 ? ? ? ? ? . 29 LYS A O 2351 ATOM 207 C CB . LYS A 2351 29 . 11.153 -18.306 9.975 1.00 15.81 ? ? ? ? ? . 29 LYS A CB 2351 ATOM 208 C CG . LYS A 2351 29 . 11.404 -18.134 8.484 1.00 16.45 ? ? ? ? ? . 29 LYS A CG 2351 ATOM 209 C CD . LYS A 2351 29 . 12.316 -16.947 8.202 1.00 17.42 ? ? ? ? ? . 29 LYS A CD 2351 ATOM 210 C CE . LYS A 2351 29 . 12.498 -16.708 6.715 1.00 17.30 ? ? ? ? ? . 29 LYS A CE 2351 ATOM 211 N NZ . LYS A 2351 29 . 13.044 -17.885 5.999 1.00 19.11 ? ? ? ? ? 1+ 29 LYS A NZ 2351 ATOM 212 N N . THR A 2351 30 . 12.603 -18.156 12.701 1.00 14.18 ? ? ? ? ? . 30 THR A N 2351 ATOM 213 C CA . THR A 2351 30 . 12.220 -17.550 13.977 1.00 14.27 ? ? ? ? ? . 30 THR A CA 2351 ATOM 214 C C . THR A 2351 30 . 11.144 -16.525 13.641 1.00 15.54 ? ? ? ? ? . 30 THR A C 2351 ATOM 215 O O . THR A 2351 30 . 11.293 -15.738 12.701 1.00 15.21 ? ? ? ? ? . 30 THR A O 2351 ATOM 216 C CB . THR A 2351 30 . 13.423 -16.869 14.660 1.00 15.36 ? ? ? ? ? . 30 THR A CB 2351 ATOM 217 C CG2 . THR A 2351 30 . 12.991 -16.093 15.905 1.00 17.24 ? ? ? ? ? . 30 THR A CG2 2351 ATOM 218 O OG1 . THR A 2351 30 . 14.393 -17.861 15.017 1.00 15.76 ? ? ? ? ? . 30 THR A OG1 2351 ATOM 219 N N . VAL A 2351 31 . 10.046 -16.537 14.380 1.00 14.34 ? ? ? ? ? . 31 VAL A N 2351 ATOM 220 C CA . VAL A 2351 31 . 8.934 -15.639 14.093 1.00 15.79 ? ? ? ? ? . 31 VAL A CA 2351 ATOM 221 C C . VAL A 2351 31 . 8.663 -14.816 15.342 1.00 16.49 ? ? ? ? ? . 31 VAL A C 2351 ATOM 222 O O . VAL A 2351 31 . 8.590 -15.357 16.455 1.00 15.72 ? ? ? ? ? . 31 VAL A O 2351 ATOM 223 C CB . VAL A 2351 31 . 7.675 -16.424 13.645 1.00 17.31 ? ? ? ? ? . 31 VAL A CB 2351 ATOM 224 C CG1 . VAL A 2351 31 . 6.467 -15.506 13.473 1.00 19.83 ? ? ? ? ? . 31 VAL A CG1 2351 ATOM 225 C CG2 . VAL A 2351 31 . 7.959 -17.190 12.356 1.00 16.54 ? ? ? ? ? . 31 VAL A CG2 2351 ATOM 226 N N . PHE A 2351 32 . 8.564 -13.502 15.158 1.00 16.30 ? ? ? ? ? . 32 PHE A N 2351 ATOM 227 C CA . PHE A 2351 32 . 8.143 -12.616 16.214 1.00 16.84 ? ? ? ? ? . 32 PHE A CA 2351 ATOM 228 C C . PHE A 2351 32 . 6.687 -12.259 15.980 1.00 16.42 ? ? ? ? ? . 32 PHE A C 2351 ATOM 229 O O . PHE A 2351 32 . 6.341 -11.721 14.924 1.00 18.32 ? ? ? ? ? . 32 PHE A O 2351 ATOM 230 C CB . PHE A 2351 32 . 8.955 -11.336 16.217 1.00 19.26 ? ? ? ? ? . 32 PHE A CB 2351 ATOM 231 C CG . PHE A 2351 32 . 10.415 -11.530 16.494 1.00 19.00 ? ? ? ? ? . 32 PHE A CG 2351 ATOM 232 C CD1 . PHE A 2351 32 . 10.870 -11.695 17.797 1.00 19.12 ? ? ? ? ? . 32 PHE A CD1 2351 ATOM 233 C CD2 . PHE A 2351 32 . 11.344 -11.506 15.462 1.00 20.74 ? ? ? ? ? . 32 PHE A CD2 2351 ATOM 234 C CE1 . PHE A 2351 32 . 12.222 -11.839 18.070 1.00 19.85 ? ? ? ? ? . 32 PHE A CE1 2351 ATOM 235 C CE2 . PHE A 2351 32 . 12.707 -11.659 15.734 1.00 21.50 ? ? ? ? ? . 32 PHE A CE2 2351 ATOM 236 C CZ . PHE A 2351 32 . 13.134 -11.818 17.049 1.00 20.68 ? ? ? ? ? . 32 PHE A CZ 2351 ATOM 237 N N . LEU A 2351 33 . 5.849 -12.554 16.959 1.00 14.24 ? ? ? ? ? . 33 LEU A N 2351 ATOM 238 C CA . LEU A 2351 33 . 4.475 -12.091 16.982 1.00 14.81 ? ? ? ? ? . 33 LEU A CA 2351 ATOM 239 C C . LEU A 2351 33 . 4.477 -10.717 17.622 1.00 15.85 ? ? ? ? ? . 33 LEU A C 2351 ATOM 240 O O . LEU A 2351 33 . 4.880 -10.578 18.777 1.00 15.41 ? ? ? ? ? . 33 LEU A O 2351 ATOM 241 C CB . LEU A 2351 33 . 3.592 -13.056 17.779 1.00 15.00 ? ? ? ? ? . 33 LEU A CB 2351 ATOM 242 C CG . LEU A 2351 33 . 3.603 -14.485 17.239 1.00 16.27 ? ? ? ? ? . 33 LEU A CG 2351 ATOM 243 C CD1 . LEU A 2351 33 . 2.632 -15.324 18.051 1.00 17.02 ? ? ? ? ? . 33 LEU A CD1 2351 ATOM 244 C CD2 . LEU A 2351 33 . 3.259 -14.541 15.757 1.00 17.70 ? ? ? ? ? . 33 LEU A CD2 2351 ATOM 245 N N . TYR A 2351 34 . 4.035 -9.718 16.859 1.00 16.06 ? ? ? ? ? . 34 TYR A N 2351 ATOM 246 C CA . TYR A 2351 34 . 4.112 -8.329 17.268 1.00 15.69 ? ? ? ? ? . 34 TYR A CA 2351 ATOM 247 C C . TYR A 2351 34 . 2.721 -7.828 17.608 1.00 15.39 ? ? ? ? ? . 34 TYR A C 2351 ATOM 248 O O . TYR A 2351 34 . 1.965 -7.440 16.735 1.00 14.35 ? ? ? ? ? . 34 TYR A O 2351 ATOM 249 C CB . TYR A 2351 34 . 4.773 -7.466 16.198 1.00 16.16 ? ? ? ? ? . 34 TYR A CB 2351 ATOM 250 C CG . TYR A 2351 34 . 4.825 -5.977 16.516 1.00 16.03 ? ? ? ? ? . 34 TYR A CG 2351 ATOM 251 C CD1 . TYR A 2351 34 . 4.977 -5.516 17.821 1.00 16.83 ? ? ? ? ? . 34 TYR A CD1 2351 ATOM 252 C CD2 . TYR A 2351 34 . 4.769 -5.031 15.488 1.00 17.63 ? ? ? ? ? . 34 TYR A CD2 2351 ATOM 253 C CE1 . TYR A 2351 34 . 5.030 -4.159 18.098 1.00 17.21 ? ? ? ? ? . 34 TYR A CE1 2351 ATOM 254 C CE2 . TYR A 2351 34 . 4.829 -3.670 15.759 1.00 17.31 ? ? ? ? ? . 34 TYR A CE2 2351 ATOM 255 C CZ . TYR A 2351 34 . 4.965 -3.243 17.069 1.00 16.44 ? ? ? ? ? . 34 TYR A CZ 2351 ATOM 256 O OH . TYR A 2351 34 . 5.016 -1.898 17.366 1.00 17.87 ? ? ? ? ? . 34 TYR A OH 2351 ATOM 257 N N . PHE A 2351 35 . 2.438 -7.854 18.898 1.00 15.23 ? ? ? ? ? . 35 PHE A N 2351 ATOM 258 C CA . PHE A 2351 35 . 1.192 -7.354 19.477 1.00 16.74 ? ? ? ? ? . 35 PHE A CA 2351 ATOM 259 C C . PHE A 2351 35 . 1.248 -5.831 19.553 1.00 16.39 ? ? ? ? ? . 35 PHE A C 2351 ATOM 260 O O . PHE A 2351 35 . 2.115 -5.268 20.223 1.00 17.11 ? ? ? ? ? . 35 PHE A O 2351 ATOM 261 C CB . PHE A 2351 35 . 0.966 -7.980 20.843 1.00 17.16 ? ? ? ? ? . 35 PHE A CB 2351 ATOM 262 C CG . PHE A 2351 35 . 0.735 -9.454 20.782 1.00 18.26 ? ? ? ? ? . 35 PHE A CG 2351 ATOM 263 C CD1 . PHE A 2351 35 . 1.802 -10.330 20.795 1.00 18.94 ? ? ? ? ? . 35 PHE A CD1 2351 ATOM 264 C CD2 . PHE A 2351 35 . -0.552 -9.974 20.684 1.00 19.43 ? ? ? ? ? . 35 PHE A CD2 2351 ATOM 265 C CE1 . PHE A 2351 35 . 1.605 -11.695 20.708 1.00 19.02 ? ? ? ? ? . 35 PHE A CE1 2351 ATOM 266 C CE2 . PHE A 2351 35 . -0.759 -11.344 20.614 1.00 19.14 ? ? ? ? ? . 35 PHE A CE2 2351 ATOM 267 C CZ . PHE A 2351 35 . 0.321 -12.205 20.626 1.00 19.19 ? ? ? ? ? . 35 PHE A CZ 2351 ATOM 268 N N . SER A 2351 36 . 0.344 -5.181 18.822 1.00 17.49 ? ? ? ? ? . 36 SER A N 2351 ATOM 269 C CA . SER A 2351 36 . 0.415 -3.732 18.583 1.00 18.12 ? ? ? ? ? . 36 SER A CA 2351 ATOM 270 C C . SER A 2351 36 . -0.954 -3.153 18.254 1.00 17.25 ? ? ? ? ? . 36 SER A C 2351 ATOM 271 O O . SER A 2351 36 . -1.942 -3.878 18.155 1.00 16.75 ? ? ? ? ? . 36 SER A O 2351 ATOM 272 C CB . SER A 2351 36 . 1.391 -3.425 17.436 1.00 19.11 ? ? ? ? ? . 36 SER A CB 2351 ATOM 273 O OG . SER A 2351 36 . 1.744 -2.041 17.380 1.00 20.12 ? ? ? ? ? . 36 SER A OG 2351 ATOM 274 N N . ALA A 2351 37 . -0.999 -1.835 18.129 1.00 16.02 ? ? ? ? ? . 37 ALA A N 2351 ATOM 275 C CA . ALA A 2351 37 . -2.210 -1.132 17.705 1.00 17.21 ? ? ? ? ? . 37 ALA A CA 2351 ATOM 276 C C . ALA A 2351 37 . -1.822 0.227 17.163 1.00 16.58 ? ? ? ? ? . 37 ALA A C 2351 ATOM 277 O O . ALA A 2351 37 . -0.894 0.865 17.681 1.00 16.07 ? ? ? ? ? . 37 ALA A O 2351 ATOM 278 C CB . ALA A 2351 37 . -3.176 -0.987 18.865 1.00 16.09 ? ? ? ? ? . 37 ALA A CB 2351 ATOM 279 N N . SER A 2351 38 . -2.538 0.673 16.134 1.00 16.09 ? ? ? ? ? . 38 SER A N 2351 ATOM 280 C CA . SER A 2351 38 . -2.180 1.894 15.393 1.00 15.94 ? ? ? ? ? . 38 SER A CA 2351 ATOM 281 C C . SER A 2351 38 . -2.215 3.154 16.234 1.00 16.06 ? ? ? ? ? . 38 SER A C 2351 ATOM 282 O O . SER A 2351 38 . -1.492 4.108 15.933 1.00 15.57 ? ? ? ? ? . 38 SER A O 2351 ATOM 283 C CB . SER A 2351 38 . -3.111 2.110 14.198 1.00 15.53 ? ? ? ? ? . 38 SER A CB 2351 ATOM 284 O OG . SER A 2351 38 . -4.417 2.483 14.611 1.00 13.61 ? ? ? ? ? . 38 SER A OG 2351 ATOM 285 N N . TRP A 2351 39 . -3.083 3.153 17.250 1.00 14.29 ? ? ? ? ? . 39 TRP A N 2351 ATOM 286 C CA . TRP A 2351 39 . -3.327 4.323 18.102 1.00 15.81 ? ? ? ? ? . 39 TRP A CA 2351 ATOM 287 C C . TRP A 2351 39 . -2.576 4.292 19.439 1.00 15.54 ? ? ? ? ? . 39 TRP A C 2351 ATOM 288 O O . TRP A 2351 39 . -2.677 5.230 20.197 1.00 14.28 ? ? ? ? ? . 39 TRP A O 2351 ATOM 289 C CB . TRP A 2351 39 . -4.835 4.560 18.336 1.00 16.03 ? ? ? ? ? . 39 TRP A CB 2351 ATOM 290 C CG . TRP A 2351 39 . -5.696 3.342 18.284 1.00 17.02 ? ? ? ? ? . 39 TRP A CG 2351 ATOM 291 C CD1 . TRP A 2351 39 . -6.597 3.017 17.301 1.00 16.62 ? ? ? ? ? . 39 TRP A CD1 2351 ATOM 292 C CD2 . TRP A 2351 39 . -5.734 2.265 19.233 1.00 17.48 ? ? ? ? ? . 39 TRP A CD2 2351 ATOM 293 C CE2 . TRP A 2351 39 . -6.689 1.329 18.758 1.00 16.65 ? ? ? ? ? . 39 TRP A CE2 2351 ATOM 294 C CE3 . TRP A 2351 39 . -5.061 2.002 20.438 1.00 17.08 ? ? ? ? ? . 39 TRP A CE3 2351 ATOM 295 N NE1 . TRP A 2351 39 . -7.186 1.815 17.579 1.00 16.89 ? ? ? ? ? . 39 TRP A NE1 2351 ATOM 296 C CZ2 . TRP A 2351 39 . -6.978 0.143 19.435 1.00 17.13 ? ? ? ? ? . 39 TRP A CZ2 2351 ATOM 297 C CZ3 . TRP A 2351 39 . -5.351 0.824 21.116 1.00 17.20 ? ? ? ? ? . 39 TRP A CZ3 2351 ATOM 298 C CH2 . TRP A 2351 39 . -6.305 -0.098 20.607 1.00 17.58 ? ? ? ? ? . 39 TRP A CH2 2351 ATOM 299 N N A CYS A 2351 40 . -1.820 3.233 19.710 0.50 15.53 ? ? ? ? ? . 40 CYS A N 2351 ATOM 300 N N B CYS A 2351 40 . -1.828 3.220 19.708 0.50 15.76 ? ? ? ? ? . 40 CYS A N 2351 ATOM 301 C CA A CYS A 2351 40 . -1.099 3.113 20.973 0.50 15.94 ? ? ? ? ? . 40 CYS A CA 2351 ATOM 302 C CA B CYS A 2351 40 . -1.048 3.086 20.945 0.50 16.31 ? ? ? ? ? . 40 CYS A CA 2351 ATOM 303 C C A CYS A 2351 40 . 0.252 3.841 20.875 0.50 15.63 ? ? ? ? ? . 40 CYS A C 2351 ATOM 304 C C B CYS A 2351 40 . 0.259 3.881 20.821 0.50 15.84 ? ? ? ? ? . 40 CYS A C 2351 ATOM 305 O O A CYS A 2351 40 . 1.104 3.413 20.104 0.50 15.01 ? ? ? ? ? . 40 CYS A O 2351 ATOM 306 O O B CYS A 2351 40 . 1.084 3.541 19.979 0.50 15.24 ? ? ? ? ? . 40 CYS A O 2351 ATOM 307 C CB A CYS A 2351 40 . -0.881 1.639 21.293 0.50 17.19 ? ? ? ? ? . 40 CYS A CB 2351 ATOM 308 C CB B CYS A 2351 40 . -0.732 1.603 21.194 0.50 17.85 ? ? ? ? ? . 40 CYS A CB 2351 ATOM 309 S SG A CYS A 2351 40 . -0.070 1.366 22.877 0.50 18.83 ? ? ? ? ? . 40 CYS A SG 2351 ATOM 310 S SG B CYS A 2351 40 . 0.692 1.280 22.270 0.50 20.15 ? ? ? ? ? . 40 CYS A SG 2351 ATOM 311 N N . PRO A 2351 41 . 0.452 4.940 21.641 1.00 15.67 ? ? ? ? ? . 41 PRO A N 2351 ATOM 312 C CA . PRO A 2351 41 . 1.703 5.735 21.475 1.00 16.29 ? ? ? ? ? . 41 PRO A CA 2351 ATOM 313 C C . PRO A 2351 41 . 3.027 4.964 21.556 1.00 17.16 ? ? ? ? ? . 41 PRO A C 2351 ATOM 314 O O . PRO A 2351 41 . 3.835 5.088 20.625 1.00 16.58 ? ? ? ? ? . 41 PRO A O 2351 ATOM 315 C CB . PRO A 2351 41 . 1.589 6.838 22.534 1.00 16.29 ? ? ? ? ? . 41 PRO A CB 2351 ATOM 316 C CG . PRO A 2351 41 . 0.113 6.972 22.756 1.00 17.02 ? ? ? ? ? . 41 PRO A CG 2351 ATOM 317 C CD . PRO A 2351 41 . -0.466 5.598 22.594 1.00 16.25 ? ? ? ? ? . 41 PRO A CD 2351 ATOM 318 N N . PRO A 2351 42 . 3.238 4.137 22.603 1.00 16.73 ? ? ? ? ? . 42 PRO A N 2351 ATOM 319 C CA . PRO A 2351 42 . 4.509 3.413 22.587 1.00 16.97 ? ? ? ? ? . 42 PRO A CA 2351 ATOM 320 C C . PRO A 2351 42 . 4.682 2.470 21.399 1.00 17.31 ? ? ? ? ? . 42 PRO A C 2351 ATOM 321 O O . PRO A 2351 42 . 5.815 2.236 21.007 1.00 18.01 ? ? ? ? ? . 42 PRO A O 2351 ATOM 322 C CB . PRO A 2351 42 . 4.524 2.635 23.913 1.00 18.24 ? ? ? ? ? . 42 PRO A CB 2351 ATOM 323 C CG . PRO A 2351 42 . 3.144 2.716 24.442 1.00 20.34 ? ? ? ? ? . 42 PRO A CG 2351 ATOM 324 C CD . PRO A 2351 42 . 2.500 3.930 23.859 1.00 17.99 ? ? ? ? ? . 42 PRO A CD 2351 ATOM 325 N N . CYS A 2351 43 . 3.583 1.953 20.830 1.00 17.08 ? ? ? ? ? . 43 CYS A N 2351 ATOM 326 C CA . CYS A 2351 43 . 3.654 1.131 19.615 1.00 17.71 ? ? ? ? ? . 43 CYS A CA 2351 ATOM 327 C C . CYS A 2351 43 . 4.071 1.965 18.412 1.00 18.28 ? ? ? ? ? . 43 CYS A C 2351 ATOM 328 O O . CYS A 2351 43 . 4.896 1.539 17.592 1.00 17.92 ? ? ? ? ? . 43 CYS A O 2351 ATOM 329 C CB . CYS A 2351 43 . 2.302 0.486 19.283 1.00 16.62 ? ? ? ? ? . 43 CYS A CB 2351 ATOM 330 S SG . CYS A 2351 43 . 1.804 -0.806 20.436 1.00 17.97 ? ? ? ? ? . 43 CYS A SG 2351 ATOM 331 N N . ARG A 2351 44 . 3.472 3.148 18.300 1.00 18.14 ? ? ? ? ? . 44 ARG A N 2351 ATOM 332 C CA . ARG A 2351 44 . 3.794 4.048 17.197 1.00 19.48 ? ? ? ? ? . 44 ARG A CA 2351 ATOM 333 C C . ARG A 2351 44 . 5.273 4.436 17.232 1.00 18.72 ? ? ? ? ? . 44 ARG A C 2351 ATOM 334 O O . ARG A 2351 44 . 5.871 4.609 16.184 1.00 18.31 ? ? ? ? ? . 44 ARG A O 2351 ATOM 335 C CB . ARG A 2351 44 . 2.889 5.272 17.211 1.00 19.31 ? ? ? ? ? . 44 ARG A CB 2351 ATOM 336 C CG . ARG A 2351 44 . 1.429 4.933 16.938 1.00 20.47 ? ? ? ? ? . 44 ARG A CG 2351 ATOM 337 C CD . ARG A 2351 44 . 0.501 5.909 17.620 1.00 25.71 ? ? ? ? ? . 44 ARG A CD 2351 ATOM 338 N NE . ARG A 2351 44 . 0.489 7.222 16.986 1.00 27.26 ? ? ? ? ? . 44 ARG A NE 2351 ATOM 339 C CZ . ARG A 2351 44 . -0.417 7.656 16.109 1.00 32.49 ? ? ? ? ? . 44 ARG A CZ 2351 ATOM 340 N NH1 . ARG A 2351 44 . -1.424 6.879 15.692 1.00 36.29 ? ? ? ? ? 1+ 44 ARG A NH1 2351 ATOM 341 N NH2 . ARG A 2351 44 . -0.309 8.895 15.634 1.00 31.30 ? ? ? ? ? . 44 ARG A NH2 2351 ATOM 342 N N . GLY A 2351 45 . 5.852 4.549 18.432 1.00 16.87 ? ? ? ? ? . 45 GLY A N 2351 ATOM 343 C CA . GLY A 2351 45 . 7.291 4.825 18.587 1.00 16.30 ? ? ? ? ? . 45 GLY A CA 2351 ATOM 344 C C . GLY A 2351 45 . 8.197 3.625 18.399 1.00 17.31 ? ? ? ? ? . 45 GLY A C 2351 ATOM 345 O O . GLY A 2351 45 . 9.343 3.761 17.968 1.00 16.80 ? ? ? ? ? . 45 GLY A O 2351 ATOM 346 N N . PHE A 2351 46 . 7.690 2.440 18.711 1.00 17.16 ? ? ? ? ? . 46 PHE A N 2351 ATOM 347 C CA . PHE A 2351 46 . 8.479 1.220 18.586 1.00 16.13 ? ? ? ? ? . 46 PHE A CA 2351 ATOM 348 C C . PHE A 2351 46 . 8.512 0.651 17.162 1.00 16.60 ? ? ? ? ? . 46 PHE A C 2351 ATOM 349 O O . PHE A 2351 46 . 9.535 0.198 16.710 1.00 16.70 ? ? ? ? ? . 46 PHE A O 2351 ATOM 350 C CB . PHE A 2351 46 . 7.967 0.150 19.541 1.00 15.86 ? ? ? ? ? . 46 PHE A CB 2351 ATOM 351 C CG . PHE A 2351 46 . 8.771 -1.108 19.489 1.00 16.05 ? ? ? ? ? . 46 PHE A CG 2351 ATOM 352 C CD1 . PHE A 2351 46 . 10.130 -1.082 19.799 1.00 17.33 ? ? ? ? ? . 46 PHE A CD1 2351 ATOM 353 C CD2 . PHE A 2351 46 . 8.199 -2.300 19.084 1.00 17.49 ? ? ? ? ? . 46 PHE A CD2 2351 ATOM 354 C CE1 . PHE A 2351 46 . 10.889 -2.235 19.714 1.00 18.28 ? ? ? ? ? . 46 PHE A CE1 2351 ATOM 355 C CE2 . PHE A 2351 46 . 8.954 -3.462 19.011 1.00 17.09 ? ? ? ? ? . 46 PHE A CE2 2351 ATOM 356 C CZ . PHE A 2351 46 . 10.300 -3.424 19.324 1.00 17.72 ? ? ? ? ? . 46 PHE A CZ 2351 ATOM 357 N N . THR A 2351 47 . 7.376 0.671 16.476 1.00 16.70 ? ? ? ? ? . 47 THR A N 2351 ATOM 358 C CA . THR A 2351 47 . 7.269 0.187 15.102 1.00 15.83 ? ? ? ? ? . 47 THR A CA 2351 ATOM 359 C C . THR A 2351 47 . 8.421 0.636 14.151 1.00 16.94 ? ? ? ? ? . 47 THR A C 2351 ATOM 360 O O . THR A 2351 47 . 9.011 -0.218 13.479 1.00 16.96 ? ? ? ? ? . 47 THR A O 2351 ATOM 361 C CB . THR A 2351 47 . 5.867 0.510 14.547 1.00 16.66 ? ? ? ? ? . 47 THR A CB 2351 ATOM 362 C CG2 . THR A 2351 47 . 5.752 0.297 13.034 1.00 16.80 ? ? ? ? ? . 47 THR A CG2 2351 ATOM 363 O OG1 . THR A 2351 47 . 4.915 -0.318 15.229 1.00 18.14 ? ? ? ? ? . 47 THR A OG1 2351 ATOM 364 N N . PRO A 2351 48 . 8.758 1.947 14.112 1.00 16.14 ? ? ? ? ? . 48 PRO A N 2351 ATOM 365 C CA . PRO A 2351 48 . 9.871 2.352 13.228 1.00 15.16 ? ? ? ? ? . 48 PRO A CA 2351 ATOM 366 C C . PRO A 2351 48 . 11.242 1.798 13.654 1.00 15.43 ? ? ? ? ? . 48 PRO A C 2351 ATOM 367 O O . PRO A 2351 48 . 12.110 1.557 12.800 1.00 15.62 ? ? ? ? ? . 48 PRO A O 2351 ATOM 368 C CB . PRO A 2351 48 . 9.825 3.888 13.265 1.00 15.95 ? ? ? ? ? . 48 PRO A CB 2351 ATOM 369 C CG . PRO A 2351 48 . 9.028 4.237 14.475 1.00 16.18 ? ? ? ? ? . 48 PRO A CG 2351 ATOM 370 C CD . PRO A 2351 48 . 8.057 3.109 14.670 1.00 16.84 ? ? ? ? ? . 48 PRO A CD 2351 ATOM 371 N N . VAL A 2351 49 . 11.421 1.568 14.952 1.00 15.24 ? ? ? ? ? . 49 VAL A N 2351 ATOM 372 C CA . VAL A 2351 49 . 12.653 0.979 15.497 1.00 15.00 ? ? ? ? ? . 49 VAL A CA 2351 ATOM 373 C C . VAL A 2351 49 . 12.738 -0.490 15.080 1.00 16.44 ? ? ? ? ? . 49 VAL A C 2351 ATOM 374 O O . VAL A 2351 49 . 13.785 -0.970 14.589 1.00 17.54 ? ? ? ? ? . 49 VAL A O 2351 ATOM 375 C CB . VAL A 2351 49 . 12.683 1.119 17.046 1.00 14.01 ? ? ? ? ? . 49 VAL A CB 2351 ATOM 376 C CG1 . VAL A 2351 49 . 13.850 0.377 17.659 1.00 13.62 ? ? ? ? ? . 49 VAL A CG1 2351 ATOM 377 C CG2 . VAL A 2351 49 . 12.703 2.591 17.436 1.00 13.12 ? ? ? ? ? . 49 VAL A CG2 2351 ATOM 378 N N . LEU A 2351 50 . 11.629 -1.205 15.264 1.00 16.04 ? ? ? ? ? . 50 LEU A N 2351 ATOM 379 C CA . LEU A 2351 50 . 11.549 -2.607 14.859 1.00 16.65 ? ? ? ? ? . 50 LEU A CA 2351 ATOM 380 C C . LEU A 2351 50 . 11.728 -2.754 13.346 1.00 16.14 ? ? ? ? ? . 50 LEU A C 2351 ATOM 381 O O . LEU A 2351 50 . 12.392 -3.689 12.896 1.00 17.52 ? ? ? ? ? . 50 LEU A O 2351 ATOM 382 C CB . LEU A 2351 50 . 10.228 -3.235 15.291 1.00 17.24 ? ? ? ? ? . 50 LEU A CB 2351 ATOM 383 C CG . LEU A 2351 50 . 10.134 -4.760 15.088 1.00 18.60 ? ? ? ? ? . 50 LEU A CG 2351 ATOM 384 C CD1 . LEU A 2351 50 . 11.292 -5.525 15.736 1.00 18.52 ? ? ? ? ? . 50 LEU A CD1 2351 ATOM 385 C CD2 . LEU A 2351 50 . 8.808 -5.265 15.625 1.00 20.67 ? ? ? ? ? . 50 LEU A CD2 2351 ATOM 386 N N . ALA A 2351 51 . 11.158 -1.827 12.578 1.00 15.16 ? ? ? ? ? . 51 ALA A N 2351 ATOM 387 C CA . ALA A 2351 51 . 11.350 -1.791 11.114 1.00 16.39 ? ? ? ? ? . 51 ALA A CA 2351 ATOM 388 C C . ALA A 2351 51 . 12.807 -1.689 10.702 1.00 16.39 ? ? ? ? ? . 51 ALA A C 2351 ATOM 389 O O . ALA A 2351 51 . 13.234 -2.388 9.789 1.00 16.12 ? ? ? ? ? . 51 ALA A O 2351 ATOM 390 C CB . ALA A 2351 51 . 10.558 -0.659 10.489 1.00 16.94 ? ? ? ? ? . 51 ALA A CB 2351 ATOM 391 N N . GLU A 2351 52 . 13.571 -0.833 11.380 1.00 15.83 ? ? ? ? ? . 52 GLU A N 2351 ATOM 392 C CA . GLU A 2351 52 . 15.018 -0.741 11.136 1.00 17.29 ? ? ? ? ? . 52 GLU A CA 2351 ATOM 393 C C . GLU A 2351 52 . 15.738 -2.056 11.452 1.00 16.77 ? ? ? ? ? . 52 GLU A C 2351 ATOM 394 O O . GLU A 2351 52 . 16.547 -2.538 10.644 1.00 17.83 ? ? ? ? ? . 52 GLU A O 2351 ATOM 395 C CB . GLU A 2351 52 . 15.655 0.398 11.929 1.00 19.04 ? ? ? ? ? . 52 GLU A CB 2351 ATOM 396 C CG . GLU A 2351 52 . 15.197 1.779 11.502 1.00 23.10 ? ? ? ? ? . 52 GLU A CG 2351 ATOM 397 C CD . GLU A 2351 52 . 15.652 2.158 10.111 1.00 27.07 ? ? ? ? ? . 52 GLU A CD 2351 ATOM 398 O OE1 . GLU A 2351 52 . 16.805 1.871 9.753 1.00 26.53 ? ? ? ? ? . 52 GLU A OE1 2351 ATOM 399 O OE2 . GLU A 2351 52 . 14.838 2.741 9.372 1.00 35.08 ? ? ? ? ? 1- 52 GLU A OE2 2351 ATOM 400 N N . PHE A 2351 53 . 15.440 -2.626 12.617 1.00 17.09 ? ? ? ? ? . 53 PHE A N 2351 ATOM 401 C CA . PHE A 2351 53 . 15.961 -3.927 13.008 1.00 17.72 ? ? ? ? ? . 53 PHE A CA 2351 ATOM 402 C C . PHE A 2351 53 . 15.659 -5.004 11.960 1.00 18.04 ? ? ? ? ? . 53 PHE A C 2351 ATOM 403 O O . PHE A 2351 53 . 16.544 -5.765 11.559 1.00 17.15 ? ? ? ? ? . 53 PHE A O 2351 ATOM 404 C CB . PHE A 2351 53 . 15.394 -4.344 14.367 1.00 17.66 ? ? ? ? ? . 53 PHE A CB 2351 ATOM 405 C CG . PHE A 2351 53 . 16.073 -5.523 14.955 1.00 17.72 ? ? ? ? ? . 53 PHE A CG 2351 ATOM 406 C CD1 . PHE A 2351 53 . 17.204 -5.365 15.759 1.00 19.84 ? ? ? ? ? . 53 PHE A CD1 2351 ATOM 407 C CD2 . PHE A 2351 53 . 15.613 -6.800 14.692 1.00 18.67 ? ? ? ? ? . 53 PHE A CD2 2351 ATOM 408 C CE1 . PHE A 2351 53 . 17.855 -6.470 16.294 1.00 18.69 ? ? ? ? ? . 53 PHE A CE1 2351 ATOM 409 C CE2 . PHE A 2351 53 . 16.250 -7.909 15.237 1.00 19.49 ? ? ? ? ? . 53 PHE A CE2 2351 ATOM 410 C CZ . PHE A 2351 53 . 17.381 -7.740 16.022 1.00 19.50 ? ? ? ? ? . 53 PHE A CZ 2351 ATOM 411 N N . TYR A 2351 54 . 14.402 -5.066 11.538 1.00 18.62 ? ? ? ? ? . 54 TYR A N 2351 ATOM 412 C CA . TYR A 2351 54 . 13.957 -5.985 10.484 1.00 16.78 ? ? ? ? ? . 54 TYR A CA 2351 ATOM 413 C C . TYR A 2351 54 . 14.740 -5.808 9.197 1.00 17.12 ? ? ? ? ? . 54 TYR A C 2351 ATOM 414 O O . TYR A 2351 54 . 15.274 -6.777 8.637 1.00 16.38 ? ? ? ? ? . 54 TYR A O 2351 ATOM 415 C CB . TYR A 2351 54 . 12.465 -5.744 10.204 1.00 17.54 ? ? ? ? ? . 54 TYR A CB 2351 ATOM 416 C CG . TYR A 2351 54 . 11.834 -6.704 9.220 1.00 17.88 ? ? ? ? ? . 54 TYR A CG 2351 ATOM 417 C CD1 . TYR A 2351 54 . 11.284 -7.902 9.655 1.00 17.99 ? ? ? ? ? . 54 TYR A CD1 2351 ATOM 418 C CD2 . TYR A 2351 54 . 11.783 -6.414 7.859 1.00 18.12 ? ? ? ? ? . 54 TYR A CD2 2351 ATOM 419 C CE1 . TYR A 2351 54 . 10.703 -8.787 8.776 1.00 17.40 ? ? ? ? ? . 54 TYR A CE1 2351 ATOM 420 C CE2 . TYR A 2351 54 . 11.201 -7.294 6.965 1.00 18.18 ? ? ? ? ? . 54 TYR A CE2 2351 ATOM 421 C CZ . TYR A 2351 54 . 10.656 -8.477 7.430 1.00 18.40 ? ? ? ? ? . 54 TYR A CZ 2351 ATOM 422 O OH . TYR A 2351 54 . 10.066 -9.352 6.548 1.00 18.64 ? ? ? ? ? . 54 TYR A OH 2351 ATOM 423 N N . GLU A 2351 55 . 14.825 -4.567 8.729 1.00 18.35 ? ? ? ? ? . 55 GLU A N 2351 ATOM 424 C CA . GLU A 2351 55 . 15.479 -4.298 7.450 1.00 19.54 ? ? ? ? ? . 55 GLU A CA 2351 ATOM 425 C C . GLU A 2351 55 . 16.941 -4.728 7.457 1.00 17.47 ? ? ? ? ? . 55 GLU A C 2351 ATOM 426 O O . GLU A 2351 55 . 17.426 -5.225 6.444 1.00 16.00 ? ? ? ? ? . 55 GLU A O 2351 ATOM 427 C CB . GLU A 2351 55 . 15.344 -2.832 7.037 1.00 23.35 ? ? ? ? ? . 55 GLU A CB 2351 ATOM 428 C CG . GLU A 2351 55 . 13.904 -2.394 6.757 1.00 27.78 ? ? ? ? ? . 55 GLU A CG 2351 ATOM 429 C CD . GLU A 2351 55 . 13.379 -2.755 5.374 1.00 33.34 ? ? ? ? ? . 55 GLU A CD 2351 ATOM 430 O OE1 . GLU A 2351 55 . 13.957 -3.640 4.695 1.00 38.81 ? ? ? ? ? . 55 GLU A OE1 2351 ATOM 431 O OE2 . GLU A 2351 55 . 12.365 -2.144 4.970 1.00 33.79 ? ? ? ? ? 1- 55 GLU A OE2 2351 ATOM 432 N N . LYS A 2351 56 . 17.630 -4.527 8.582 1.00 17.29 ? ? ? ? ? . 56 LYS A N 2351 ATOM 433 C CA . LYS A 2351 56 . 19.040 -4.884 8.705 1.00 17.51 ? ? ? ? ? . 56 LYS A CA 2351 ATOM 434 C C . LYS A 2351 56 . 19.255 -6.396 8.816 1.00 15.74 ? ? ? ? ? . 56 LYS A C 2351 ATOM 435 O O . LYS A 2351 56 . 20.181 -6.935 8.183 1.00 16.74 ? ? ? ? ? . 56 LYS A O 2351 ATOM 436 C CB . LYS A 2351 56 . 19.699 -4.158 9.902 1.00 20.10 ? ? ? ? ? . 56 LYS A CB 2351 ATOM 437 C CG . LYS A 2351 56 . 21.202 -4.417 10.024 1.00 22.06 ? ? ? ? ? . 56 LYS A CG 2351 ATOM 438 C CD . LYS A 2351 56 . 21.921 -3.570 11.086 1.00 24.35 ? ? ? ? ? . 56 LYS A CD 2351 ATOM 439 C CE . LYS A 2351 56 . 23.451 -3.707 10.942 1.00 26.58 ? ? ? ? ? . 56 LYS A CE 2351 ATOM 440 N NZ . LYS A 2351 56 . 24.320 -2.988 11.937 1.00 24.67 ? ? ? ? ? 1+ 56 LYS A NZ 2351 ATOM 441 N N . HIS A 2351 57 . 18.415 -7.076 9.599 1.00 14.57 ? ? ? ? ? . 57 HIS A N 2351 ATOM 442 C CA . HIS A 2351 57 . 18.718 -8.424 10.085 1.00 15.29 ? ? ? ? ? . 57 HIS A CA 2351 ATOM 443 C C . HIS A 2351 57 . 17.814 -9.569 9.624 1.00 15.31 ? ? ? ? ? . 57 HIS A C 2351 ATOM 444 O O . HIS A 2351 57 . 18.170 -10.726 9.880 1.00 16.33 ? ? ? ? ? . 57 HIS A O 2351 ATOM 445 C CB . HIS A 2351 57 . 18.690 -8.468 11.612 1.00 15.83 ? ? ? ? ? . 57 HIS A CB 2351 ATOM 446 C CG . HIS A 2351 57 . 19.586 -7.481 12.281 1.00 16.66 ? ? ? ? ? . 57 HIS A CG 2351 ATOM 447 C CD2 . HIS A 2351 57 . 19.312 -6.513 13.190 1.00 18.19 ? ? ? ? ? . 57 HIS A CD2 2351 ATOM 448 N ND1 . HIS A 2351 57 . 20.944 -7.457 12.094 1.00 16.54 ? ? ? ? ? . 57 HIS A ND1 2351 ATOM 449 C CE1 . HIS A 2351 57 . 21.471 -6.502 12.836 1.00 18.76 ? ? ? ? ? . 57 HIS A CE1 2351 ATOM 450 N NE2 . HIS A 2351 57 . 20.502 -5.918 13.519 1.00 17.63 ? ? ? ? ? . 57 HIS A NE2 2351 ATOM 451 N N . HIS A 2351 58 . 16.668 -9.294 8.996 1.00 15.07 ? ? ? ? ? . 58 HIS A N 2351 ATOM 452 C CA . HIS A 2351 58 . 15.663 -10.363 8.809 1.00 15.32 ? ? ? ? ? . 58 HIS A CA 2351 ATOM 453 C C . HIS A 2351 58 . 16.142 -11.508 7.916 1.00 15.60 ? ? ? ? ? . 58 HIS A C 2351 ATOM 454 O O . HIS A 2351 58 . 15.814 -12.666 8.172 1.00 16.71 ? ? ? ? ? . 58 HIS A O 2351 ATOM 455 C CB . HIS A 2351 58 . 14.270 -9.838 8.384 1.00 16.50 ? ? ? ? ? . 58 HIS A CB 2351 ATOM 456 C CG . HIS A 2351 58 . 14.110 -9.576 6.917 1.00 16.28 ? ? ? ? ? . 58 HIS A CG 2351 ATOM 457 C CD2 . HIS A 2351 58 . 13.530 -10.314 5.939 1.00 17.28 ? ? ? ? ? . 58 HIS A CD2 2351 ATOM 458 N ND1 . HIS A 2351 58 . 14.514 -8.401 6.318 1.00 18.08 ? ? ? ? ? . 58 HIS A ND1 2351 ATOM 459 C CE1 . HIS A 2351 58 . 14.236 -8.449 5.025 1.00 19.03 ? ? ? ? ? . 58 HIS A CE1 2351 ATOM 460 N NE2 . HIS A 2351 58 . 13.622 -9.592 4.773 1.00 19.90 ? ? ? ? ? . 58 HIS A NE2 2351 ATOM 461 N N . VAL A 2351 59 . 16.953 -11.183 6.909 1.00 14.27 ? ? ? ? ? . 59 VAL A N 2351 ATOM 462 C CA . VAL A 2351 59 . 17.521 -12.205 6.060 1.00 14.71 ? ? ? ? ? . 59 VAL A CA 2351 ATOM 463 C C . VAL A 2351 59 . 18.661 -12.908 6.783 1.00 14.94 ? ? ? ? ? . 59 VAL A C 2351 ATOM 464 O O . VAL A 2351 59 . 18.645 -14.134 6.937 1.00 14.29 ? ? ? ? ? . 59 VAL A O 2351 ATOM 465 C CB . VAL A 2351 59 . 17.994 -11.612 4.722 1.00 14.66 ? ? ? ? ? . 59 VAL A CB 2351 ATOM 466 C CG1 . VAL A 2351 59 . 18.666 -12.682 3.873 1.00 14.25 ? ? ? ? ? . 59 VAL A CG1 2351 ATOM 467 C CG2 . VAL A 2351 59 . 16.805 -10.993 3.980 1.00 14.94 ? ? ? ? ? . 59 VAL A CG2 2351 ATOM 468 N N . ALA A 2351 60 . 19.645 -12.144 7.246 1.00 15.73 ? ? ? ? ? . 60 ALA A N 2351 ATOM 469 C CA . ALA A 2351 60 . 20.864 -12.747 7.823 1.00 17.51 ? ? ? ? ? . 60 ALA A CA 2351 ATOM 470 C C . ALA A 2351 60 . 20.557 -13.591 9.054 1.00 16.03 ? ? ? ? ? . 60 ALA A C 2351 ATOM 471 O O . ALA A 2351 60 . 21.143 -14.653 9.242 1.00 15.29 ? ? ? ? ? . 60 ALA A O 2351 ATOM 472 C CB . ALA A 2351 60 . 21.898 -11.674 8.149 1.00 18.78 ? ? ? ? ? . 60 ALA A CB 2351 ATOM 473 N N . LYS A 2351 61 . 19.598 -13.149 9.864 1.00 14.83 ? ? ? ? ? . 61 LYS A N 2351 ATOM 474 C CA . LYS A 2351 61 . 19.226 -13.871 11.088 1.00 15.73 ? ? ? ? ? . 61 LYS A CA 2351 ATOM 475 C C . LYS A 2351 61 . 17.927 -14.693 10.936 1.00 17.18 ? ? ? ? ? . 61 LYS A C 2351 ATOM 476 O O . LYS A 2351 61 . 17.409 -15.236 11.923 1.00 18.10 ? ? ? ? ? . 61 LYS A O 2351 ATOM 477 C CB . LYS A 2351 61 . 19.132 -12.891 12.265 1.00 15.99 ? ? ? ? ? . 61 LYS A CB 2351 ATOM 478 C CG . LYS A 2351 61 . 20.452 -12.166 12.504 1.00 18.28 ? ? ? ? ? . 61 LYS A CG 2351 ATOM 479 C CD . LYS A 2351 61 . 20.439 -11.283 13.741 1.00 20.10 ? ? ? ? ? . 61 LYS A CD 2351 ATOM 480 C CE . LYS A 2351 61 . 21.754 -10.505 13.895 1.00 20.17 ? ? ? ? ? . 61 LYS A CE 2351 ATOM 481 N NZ . LYS A 2351 61 . 22.893 -11.355 14.328 1.00 19.55 ? ? ? ? ? 1+ 61 LYS A NZ 2351 ATOM 482 N N . ASN A 2351 62 . 17.428 -14.784 9.701 1.00 16.86 ? ? ? ? ? . 62 ASN A N 2351 ATOM 483 C CA . ASN A 2351 62 . 16.360 -15.705 9.305 1.00 16.87 ? ? ? ? ? . 62 ASN A CA 2351 ATOM 484 C C . ASN A 2351 62 . 15.135 -15.622 10.221 1.00 16.20 ? ? ? ? ? . 62 ASN A C 2351 ATOM 485 O O . ASN A 2351 62 . 14.743 -16.606 10.871 1.00 15.82 ? ? ? ? ? . 62 ASN A O 2351 ATOM 486 C CB . ASN A 2351 62 . 16.895 -17.137 9.242 1.00 17.98 ? ? ? ? ? . 62 ASN A CB 2351 ATOM 487 C CG . ASN A 2351 62 . 15.989 -18.059 8.453 1.00 17.03 ? ? ? ? ? . 62 ASN A CG 2351 ATOM 488 N ND2 . ASN A 2351 62 . 15.720 -19.247 8.994 1.00 15.43 ? ? ? ? ? . 62 ASN A ND2 2351 ATOM 489 O OD1 . ASN A 2351 62 . 15.544 -17.708 7.365 1.00 16.98 ? ? ? ? ? . 62 ASN A OD1 2351 ATOM 490 N N . PHE A 2351 63 . 14.555 -14.436 10.284 1.00 15.83 ? ? ? ? ? . 63 PHE A N 2351 ATOM 491 C CA . PHE A 2351 63 . 13.315 -14.245 11.005 1.00 15.98 ? ? ? ? ? . 63 PHE A CA 2351 ATOM 492 C C . PHE A 2351 63 . 12.272 -13.479 10.209 1.00 16.65 ? ? ? ? ? . 63 PHE A C 2351 ATOM 493 O O . PHE A 2351 63 . 12.540 -12.876 9.147 1.00 14.62 ? ? ? ? ? . 63 PHE A O 2351 ATOM 494 C CB . PHE A 2351 63 . 13.555 -13.608 12.392 1.00 15.93 ? ? ? ? ? . 63 PHE A CB 2351 ATOM 495 C CG . PHE A 2351 63 . 14.065 -12.191 12.351 1.00 16.47 ? ? ? ? ? . 63 PHE A CG 2351 ATOM 496 C CD1 . PHE A 2351 63 . 13.192 -11.131 12.154 1.00 17.02 ? ? ? ? ? . 63 PHE A CD1 2351 ATOM 497 C CD2 . PHE A 2351 63 . 15.419 -11.914 12.539 1.00 17.98 ? ? ? ? ? . 63 PHE A CD2 2351 ATOM 498 C CE1 . PHE A 2351 63 . 13.646 -9.823 12.123 1.00 16.99 ? ? ? ? ? . 63 PHE A CE1 2351 ATOM 499 C CE2 . PHE A 2351 63 . 15.874 -10.605 12.516 1.00 17.17 ? ? ? ? ? . 63 PHE A CE2 2351 ATOM 500 C CZ . PHE A 2351 63 . 14.992 -9.562 12.310 1.00 17.23 ? ? ? ? ? . 63 PHE A CZ 2351 ATOM 501 N N . GLU A 2351 64 . 11.065 -13.521 10.753 1.00 16.63 ? ? ? ? ? . 64 GLU A N 2351 ATOM 502 C CA . GLU A 2351 64 . 9.931 -12.790 10.211 1.00 16.06 ? ? ? ? ? . 64 GLU A CA 2351 ATOM 503 C C . GLU A 2351 64 . 9.161 -12.165 11.375 1.00 16.89 ? ? ? ? ? . 64 GLU A C 2351 ATOM 504 O O . GLU A 2351 64 . 9.251 -12.634 12.498 1.00 16.07 ? ? ? ? ? . 64 GLU A O 2351 ATOM 505 C CB . GLU A 2351 64 . 9.043 -13.756 9.433 1.00 17.67 ? ? ? ? ? . 64 GLU A CB 2351 ATOM 506 C CG . GLU A 2351 64 . 7.934 -13.109 8.651 1.00 20.12 ? ? ? ? ? . 64 GLU A CG 2351 ATOM 507 C CD . GLU A 2351 64 . 8.458 -12.085 7.676 1.00 20.42 ? ? ? ? ? . 64 GLU A CD 2351 ATOM 508 O OE1 . GLU A 2351 64 . 8.489 -10.901 8.045 1.00 19.99 ? ? ? ? ? . 64 GLU A OE1 2351 ATOM 509 O OE2 . GLU A 2351 64 . 8.839 -12.477 6.559 1.00 20.73 ? ? ? ? ? 1- 64 GLU A OE2 2351 ATOM 510 N N . VAL A 2351 65 . 8.413 -11.107 11.097 1.00 16.69 ? ? ? ? ? . 65 VAL A N 2351 ATOM 511 C CA . VAL A 2351 65 . 7.578 -10.458 12.100 1.00 15.86 ? ? ? ? ? . 65 VAL A CA 2351 ATOM 512 C C . VAL A 2351 65 . 6.140 -10.529 11.600 1.00 14.98 ? ? ? ? ? . 65 VAL A C 2351 ATOM 513 O O . VAL A 2351 65 . 5.879 -10.397 10.391 1.00 14.44 ? ? ? ? ? . 65 VAL A O 2351 ATOM 514 C CB . VAL A 2351 65 . 8.066 -9.013 12.345 1.00 17.34 ? ? ? ? ? . 65 VAL A CB 2351 ATOM 515 C CG1 . VAL A 2351 65 . 7.112 -8.225 13.239 1.00 18.32 ? ? ? ? ? . 65 VAL A CG1 2351 ATOM 516 C CG2 . VAL A 2351 65 . 9.464 -9.038 12.945 1.00 18.63 ? ? ? ? ? . 65 VAL A CG2 2351 ATOM 517 N N . VAL A 2351 66 . 5.212 -10.798 12.517 1.00 14.94 ? ? ? ? ? . 66 VAL A N 2351 ATOM 518 C CA . VAL A 2351 66 . 3.791 -10.901 12.186 1.00 15.77 ? ? ? ? ? . 66 VAL A CA 2351 ATOM 519 C C . VAL A 2351 66 . 3.013 -9.926 13.068 1.00 16.12 ? ? ? ? ? . 66 VAL A C 2351 ATOM 520 O O . VAL A 2351 66 . 2.954 -10.091 14.287 1.00 18.95 ? ? ? ? ? . 66 VAL A O 2351 ATOM 521 C CB . VAL A 2351 66 . 3.248 -12.327 12.365 1.00 15.17 ? ? ? ? ? . 66 VAL A CB 2351 ATOM 522 C CG1 . VAL A 2351 66 . 1.807 -12.407 11.883 1.00 14.64 ? ? ? ? ? . 66 VAL A CG1 2351 ATOM 523 C CG2 . VAL A 2351 66 . 4.127 -13.332 11.615 1.00 15.43 ? ? ? ? ? . 66 VAL A CG2 2351 ATOM 524 N N . LEU A 2351 67 . 2.413 -8.925 12.441 1.00 14.97 ? ? ? ? ? . 67 LEU A N 2351 ATOM 525 C CA . LEU A 2351 67 . 1.558 -7.976 13.155 1.00 15.42 ? ? ? ? ? . 67 LEU A CA 2351 ATOM 526 C C . LEU A 2351 67 . 0.311 -8.673 13.669 1.00 14.43 ? ? ? ? ? . 67 LEU A C 2351 ATOM 527 O O . LEU A 2351 67 . -0.406 -9.315 12.914 1.00 15.61 ? ? ? ? ? . 67 LEU A O 2351 ATOM 528 C CB . LEU A 2351 67 . 1.134 -6.830 12.239 1.00 16.16 ? ? ? ? ? . 67 LEU A CB 2351 ATOM 529 C CG . LEU A 2351 67 . 0.138 -5.813 12.822 1.00 16.89 ? ? ? ? ? . 67 LEU A CG 2351 ATOM 530 C CD1 . LEU A 2351 67 . 0.748 -5.117 14.038 1.00 18.06 ? ? ? ? ? . 67 LEU A CD1 2351 ATOM 531 C CD2 . LEU A 2351 67 . -0.302 -4.804 11.764 1.00 16.86 ? ? ? ? ? . 67 LEU A CD2 2351 ATOM 532 N N . ILE A 2351 68 . 0.069 -8.515 14.959 1.00 16.21 ? ? ? ? ? . 68 ILE A N 2351 ATOM 533 C CA . ILE A 2351 68 . -1.140 -8.969 15.618 1.00 16.24 ? ? ? ? ? . 68 ILE A CA 2351 ATOM 534 C C . ILE A 2351 68 . -1.759 -7.692 16.195 1.00 16.84 ? ? ? ? ? . 68 ILE A C 2351 ATOM 535 O O . ILE A 2351 68 . -1.309 -7.202 17.220 1.00 16.78 ? ? ? ? ? . 68 ILE A O 2351 ATOM 536 C CB . ILE A 2351 68 . -0.842 -9.969 16.752 1.00 15.81 ? ? ? ? ? . 68 ILE A CB 2351 ATOM 537 C CG1 . ILE A 2351 68 . 0.100 -11.106 16.287 1.00 15.85 ? ? ? ? ? . 68 ILE A CG1 2351 ATOM 538 C CG2 . ILE A 2351 68 . -2.143 -10.534 17.291 1.00 16.11 ? ? ? ? ? . 68 ILE A CG2 2351 ATOM 539 C CD1 . ILE A 2351 68 . -0.444 -11.963 15.172 1.00 15.85 ? ? ? ? ? . 68 ILE A CD1 2351 ATOM 540 N N . SER A 2351 69 . -2.769 -7.158 15.519 1.00 18.12 ? ? ? ? ? . 69 SER A N 2351 ATOM 541 C CA . SER A 2351 69 . -3.262 -5.825 15.839 1.00 18.34 ? ? ? ? ? . 69 SER A CA 2351 ATOM 542 C C . SER A 2351 69 . -4.568 -5.818 16.640 1.00 17.36 ? ? ? ? ? . 69 SER A C 2351 ATOM 543 O O . SER A 2351 69 . -5.517 -6.553 16.339 1.00 15.89 ? ? ? ? ? . 69 SER A O 2351 ATOM 544 C CB . SER A 2351 69 . -3.454 -5.013 14.563 1.00 20.93 ? ? ? ? ? . 69 SER A CB 2351 ATOM 545 O OG . SER A 2351 69 . -3.970 -3.726 14.871 1.00 22.79 ? ? ? ? ? . 69 SER A OG 2351 ATOM 546 N N . TRP A 2351 70 . -4.612 -4.932 17.630 1.00 17.71 ? ? ? ? ? . 70 TRP A N 2351 ATOM 547 C CA . TRP A 2351 70 . -5.849 -4.612 18.370 1.00 17.54 ? ? ? ? ? . 70 TRP A CA 2351 ATOM 548 C C . TRP A 2351 70 . -6.788 -3.654 17.619 1.00 16.23 ? ? ? ? ? . 70 TRP A C 2351 ATOM 549 O O . TRP A 2351 70 . -7.870 -3.325 18.129 1.00 15.84 ? ? ? ? ? . 70 TRP A O 2351 ATOM 550 C CB . TRP A 2351 70 . -5.522 -4.043 19.773 1.00 18.64 ? ? ? ? ? . 70 TRP A CB 2351 ATOM 551 C CG . TRP A 2351 70 . -5.764 -5.026 20.876 1.00 18.49 ? ? ? ? ? . 70 TRP A CG 2351 ATOM 552 C CD1 . TRP A 2351 70 . -6.897 -5.175 21.635 1.00 20.30 ? ? ? ? ? . 70 TRP A CD1 2351 ATOM 553 C CD2 . TRP A 2351 70 . -4.846 -6.010 21.326 1.00 19.25 ? ? ? ? ? . 70 TRP A CD2 2351 ATOM 554 C CE2 . TRP A 2351 70 . -5.481 -6.736 22.357 1.00 20.72 ? ? ? ? ? . 70 TRP A CE2 2351 ATOM 555 C CE3 . TRP A 2351 70 . -3.546 -6.347 20.958 1.00 20.16 ? ? ? ? ? . 70 TRP A CE3 2351 ATOM 556 N NE1 . TRP A 2351 70 . -6.733 -6.207 22.522 1.00 19.85 ? ? ? ? ? . 70 TRP A NE1 2351 ATOM 557 C CZ2 . TRP A 2351 70 . -4.852 -7.783 23.021 1.00 20.72 ? ? ? ? ? . 70 TRP A CZ2 2351 ATOM 558 C CZ3 . TRP A 2351 70 . -2.918 -7.378 21.619 1.00 21.27 ? ? ? ? ? . 70 TRP A CZ3 2351 ATOM 559 C CH2 . TRP A 2351 70 . -3.570 -8.090 22.638 1.00 22.10 ? ? ? ? ? . 70 TRP A CH2 2351 ATOM 560 N N . ASP A 2351 71 . -6.400 -3.183 16.430 1.00 14.95 ? ? ? ? ? . 71 ASP A N 2351 ATOM 561 C CA . ASP A 2351 71 . -7.261 -2.280 15.672 1.00 15.71 ? ? ? ? ? . 71 ASP A CA 2351 ATOM 562 C C . ASP A 2351 71 . -8.605 -2.930 15.328 1.00 14.08 ? ? ? ? ? . 71 ASP A C 2351 ATOM 563 O O . ASP A 2351 71 . -8.633 -4.074 14.887 1.00 13.83 ? ? ? ? ? . 71 ASP A O 2351 ATOM 564 C CB . ASP A 2351 71 . -6.575 -1.838 14.377 1.00 16.40 ? ? ? ? ? . 71 ASP A CB 2351 ATOM 565 C CG . ASP A 2351 71 . -5.488 -0.813 14.617 1.00 16.78 ? ? ? ? ? . 71 ASP A CG 2351 ATOM 566 O OD1 . ASP A 2351 71 . -5.861 0.357 14.863 1.00 16.06 ? ? ? ? ? . 71 ASP A OD1 2351 ATOM 567 O OD2 . ASP A 2351 71 . -4.277 -1.173 14.553 1.00 18.80 ? ? ? ? ? 1- 71 ASP A OD2 2351 ATOM 568 N N . GLU A 2351 72 . -9.689 -2.197 15.550 1.00 13.55 ? ? ? ? ? . 72 GLU A N 2351 ATOM 569 C CA A GLU A 2351 72 . -11.051 -2.601 15.169 0.66 14.70 ? ? ? ? ? . 72 GLU A CA 2351 ATOM 570 C CA B GLU A 2351 72 . -11.003 -2.662 15.116 0.34 14.17 ? ? ? ? ? . 72 GLU A CA 2351 ATOM 571 C C . GLU A 2351 72 . -11.544 -1.845 13.940 1.00 14.43 ? ? ? ? ? . 72 GLU A C 2351 ATOM 572 O O . GLU A 2351 72 . -12.612 -2.162 13.403 1.00 15.02 ? ? ? ? ? . 72 GLU A O 2351 ATOM 573 C CB A GLU A 2351 72 . -12.032 -2.365 16.325 0.66 15.58 ? ? ? ? ? . 72 GLU A CB 2351 ATOM 574 C CB B GLU A 2351 72 . -11.951 -2.732 16.315 0.34 14.14 ? ? ? ? ? . 72 GLU A CB 2351 ATOM 575 C CG A GLU A 2351 72 . -11.825 -3.284 17.523 0.66 17.74 ? ? ? ? ? . 72 GLU A CG 2351 ATOM 576 C CG B GLU A 2351 72 . -11.456 -3.763 17.335 0.34 14.63 ? ? ? ? ? . 72 GLU A CG 2351 ATOM 577 C CD A GLU A 2351 72 . -12.840 -3.071 18.643 0.66 18.62 ? ? ? ? ? . 72 GLU A CD 2351 ATOM 578 C CD B GLU A 2351 72 . -12.487 -4.156 18.381 0.34 15.00 ? ? ? ? ? . 72 GLU A CD 2351 ATOM 579 O OE1 A GLU A 2351 72 . -13.397 -1.946 18.785 0.66 20.42 ? ? ? ? ? . 72 GLU A OE1 2351 ATOM 580 O OE2 A GLU A 2351 72 . -13.078 -4.039 19.399 0.66 18.80 ? ? ? ? ? 1- 72 GLU A OE2 2351 ATOM 581 O OE1 B GLU A 2351 72 . -13.558 -3.519 18.446 0.34 15.59 ? ? ? ? ? . 72 GLU A OE1 2351 ATOM 582 O OE2 B GLU A 2351 72 . -12.220 -5.118 19.141 0.34 14.77 ? ? ? ? ? 1- 72 GLU A OE2 2351 ATOM 583 N N . ASN A 2351 73 . -10.789 -0.830 13.505 1.00 14.08 ? ? ? ? ? . 73 ASN A N 2351 ATOM 584 C CA . ASN A 2351 73 . -11.154 -0.041 12.336 1.00 14.22 ? ? ? ? ? . 73 ASN A CA 2351 ATOM 585 C C . ASN A 2351 73 . -10.271 -0.425 11.153 1.00 13.82 ? ? ? ? ? . 73 ASN A C 2351 ATOM 586 O O . ASN A 2351 73 . -9.048 -0.290 11.203 1.00 13.41 ? ? ? ? ? . 73 ASN A O 2351 ATOM 587 C CB . ASN A 2351 73 . -11.065 1.455 12.613 1.00 15.75 ? ? ? ? ? . 73 ASN A CB 2351 ATOM 588 C CG . ASN A 2351 73 . -11.382 2.282 11.378 1.00 16.44 ? ? ? ? ? . 73 ASN A CG 2351 ATOM 589 N ND2 . ASN A 2351 73 . -12.576 2.835 11.326 1.00 16.80 ? ? ? ? ? . 73 ASN A ND2 2351 ATOM 590 O OD1 . ASN A 2351 73 . -10.571 2.366 10.456 1.00 17.63 ? ? ? ? ? . 73 ASN A OD1 2351 ATOM 591 N N . GLU A 2351 74 . -10.908 -0.880 10.082 1.00 12.83 ? ? ? ? ? . 74 GLU A N 2351 ATOM 592 C CA . GLU A 2351 74 . -10.164 -1.428 8.942 1.00 13.34 ? ? ? ? ? . 74 GLU A CA 2351 ATOM 593 C C . GLU A 2351 74 . -9.264 -0.399 8.251 1.00 12.42 ? ? ? ? ? . 74 GLU A C 2351 ATOM 594 O O . GLU A 2351 74 . -8.163 -0.752 7.810 1.00 12.27 ? ? ? ? ? . 74 GLU A O 2351 ATOM 595 C CB . GLU A 2351 74 . -11.098 -2.104 7.937 1.00 13.28 ? ? ? ? ? . 74 GLU A CB 2351 ATOM 596 C CG . GLU A 2351 74 . -10.322 -2.877 6.864 1.00 14.42 ? ? ? ? ? . 74 GLU A CG 2351 ATOM 597 C CD . GLU A 2351 74 . -11.098 -3.992 6.185 1.00 15.31 ? ? ? ? ? . 74 GLU A CD 2351 ATOM 598 O OE1 . GLU A 2351 74 . -12.342 -4.043 6.291 1.00 16.61 ? ? ? ? ? . 74 GLU A OE1 2351 ATOM 599 O OE2 . GLU A 2351 74 . -10.428 -4.814 5.521 1.00 16.63 ? ? ? ? ? 1- 74 GLU A OE2 2351 ATOM 600 N N A SER A 2351 75 . -9.716 0.852 8.158 0.50 12.08 ? ? ? ? ? . 75 SER A N 2351 ATOM 601 N N B SER A 2351 75 . -9.720 0.852 8.162 0.50 12.17 ? ? ? ? ? . 75 SER A N 2351 ATOM 602 C CA A SER A 2351 75 . -8.889 1.908 7.555 0.50 12.63 ? ? ? ? ? . 75 SER A CA 2351 ATOM 603 C CA B SER A 2351 75 . -8.902 1.929 7.582 0.50 12.79 ? ? ? ? ? . 75 SER A CA 2351 ATOM 604 C C A SER A 2351 75 . -7.615 2.172 8.375 0.50 12.99 ? ? ? ? ? . 75 SER A C 2351 ATOM 605 C C B SER A 2351 75 . -7.614 2.148 8.378 0.50 13.06 ? ? ? ? ? . 75 SER A C 2351 ATOM 606 O O A SER A 2351 75 . -6.534 2.346 7.802 0.50 12.87 ? ? ? ? ? . 75 SER A O 2351 ATOM 607 O O B SER A 2351 75 . -6.530 2.275 7.797 0.50 12.91 ? ? ? ? ? . 75 SER A O 2351 ATOM 608 C CB A SER A 2351 75 . -9.691 3.193 7.344 0.50 12.19 ? ? ? ? ? . 75 SER A CB 2351 ATOM 609 C CB B SER A 2351 75 . -9.687 3.235 7.505 0.50 12.53 ? ? ? ? ? . 75 SER A CB 2351 ATOM 610 O OG A SER A 2351 75 . -9.929 3.865 8.562 0.50 12.51 ? ? ? ? ? . 75 SER A OG 2351 ATOM 611 O OG B SER A 2351 75 . -11.042 2.992 7.190 0.50 12.90 ? ? ? ? ? . 75 SER A OG 2351 ATOM 612 N N . ASP A 2351 76 . -7.737 2.174 9.705 1.00 13.63 ? ? ? ? ? . 76 ASP A N 2351 ATOM 613 C CA . ASP A 2351 76 . -6.574 2.273 10.604 1.00 14.12 ? ? ? ? ? . 76 ASP A CA 2351 ATOM 614 C C . ASP A 2351 76 . -5.635 1.088 10.406 1.00 14.27 ? ? ? ? ? . 76 ASP A C 2351 ATOM 615 O O . ASP A 2351 76 . -4.413 1.264 10.305 1.00 15.60 ? ? ? ? ? . 76 ASP A O 2351 ATOM 616 C CB . ASP A 2351 76 . -6.999 2.328 12.092 1.00 15.22 ? ? ? ? ? . 76 ASP A CB 2351 ATOM 617 C CG . ASP A 2351 76 . -7.739 3.609 12.471 1.00 17.74 ? ? ? ? ? . 76 ASP A CG 2351 ATOM 618 O OD1 . ASP A 2351 76 . -7.583 4.650 11.792 1.00 18.03 ? ? ? ? ? . 76 ASP A OD1 2351 ATOM 619 O OD2 . ASP A 2351 76 . -8.511 3.555 13.461 1.00 18.66 ? ? ? ? ? 1- 76 ASP A OD2 2351 ATOM 620 N N . PHE A 2351 77 . -6.198 -0.116 10.328 1.00 13.52 ? ? ? ? ? . 77 PHE A N 2351 ATOM 621 C CA . PHE A 2351 77 . -5.377 -1.318 10.207 1.00 14.12 ? ? ? ? ? . 77 PHE A CA 2351 ATOM 622 C C . PHE A 2351 77 . -4.500 -1.258 8.952 1.00 13.79 ? ? ? ? ? . 77 PHE A C 2351 ATOM 623 O O . PHE A 2351 77 . -3.297 -1.442 9.049 1.00 14.65 ? ? ? ? ? . 77 PHE A O 2351 ATOM 624 C CB . PHE A 2351 77 . -6.250 -2.570 10.169 1.00 14.39 ? ? ? ? ? . 77 PHE A CB 2351 ATOM 625 C CG . PHE A 2351 77 . -5.489 -3.825 9.863 1.00 14.28 ? ? ? ? ? . 77 PHE A CG 2351 ATOM 626 C CD1 . PHE A 2351 77 . -4.882 -4.561 10.885 1.00 14.15 ? ? ? ? ? . 77 PHE A CD1 2351 ATOM 627 C CD2 . PHE A 2351 77 . -5.389 -4.282 8.545 1.00 13.66 ? ? ? ? ? . 77 PHE A CD2 2351 ATOM 628 C CE1 . PHE A 2351 77 . -4.198 -5.736 10.592 1.00 14.66 ? ? ? ? ? . 77 PHE A CE1 2351 ATOM 629 C CE2 . PHE A 2351 77 . -4.715 -5.450 8.263 1.00 14.31 ? ? ? ? ? . 77 PHE A CE2 2351 ATOM 630 C CZ . PHE A 2351 77 . -4.106 -6.167 9.277 1.00 13.75 ? ? ? ? ? . 77 PHE A CZ 2351 ATOM 631 N N . HIS A 2351 78 . -5.105 -0.968 7.800 1.00 13.17 ? ? ? ? ? . 78 HIS A N 2351 ATOM 632 C CA . HIS A 2351 78 . -4.363 -1.017 6.526 1.00 15.15 ? ? ? ? ? . 78 HIS A CA 2351 ATOM 633 C C . HIS A 2351 78 . -3.291 0.066 6.463 1.00 16.44 ? ? ? ? ? . 78 HIS A C 2351 ATOM 634 O O . HIS A 2351 78 . -2.177 -0.197 6.034 1.00 18.01 ? ? ? ? ? . 78 HIS A O 2351 ATOM 635 C CB . HIS A 2351 78 . -5.293 -0.947 5.327 1.00 15.24 ? ? ? ? ? . 78 HIS A CB 2351 ATOM 636 C CG . HIS A 2351 78 . -6.138 -2.171 5.161 1.00 16.20 ? ? ? ? ? . 78 HIS A CG 2351 ATOM 637 C CD2 . HIS A 2351 78 . -7.474 -2.321 5.042 1.00 16.05 ? ? ? ? ? . 78 HIS A CD2 2351 ATOM 638 N ND1 . HIS A 2351 78 . -5.603 -3.438 5.092 1.00 16.80 ? ? ? ? ? . 78 HIS A ND1 2351 ATOM 639 C CE1 . HIS A 2351 78 . -6.577 -4.317 4.956 1.00 16.55 ? ? ? ? ? . 78 HIS A CE1 2351 ATOM 640 N NE2 . HIS A 2351 78 . -7.722 -3.664 4.911 1.00 16.79 ? ? ? ? ? . 78 HIS A NE2 2351 ATOM 641 N N . ASP A 2351 79 . -3.634 1.265 6.931 1.00 16.68 ? ? ? ? ? . 79 ASP A N 2351 ATOM 642 C CA . ASP A 2351 79 . -2.676 2.375 7.024 1.00 16.83 ? ? ? ? ? . 79 ASP A CA 2351 ATOM 643 C C . ASP A 2351 79 . -1.470 2.068 7.917 1.00 15.94 ? ? ? ? ? . 79 ASP A C 2351 ATOM 644 O O . ASP A 2351 79 . -0.336 2.356 7.523 1.00 17.28 ? ? ? ? ? . 79 ASP A O 2351 ATOM 645 C CB . ASP A 2351 79 . -3.376 3.617 7.558 1.00 17.23 ? ? ? ? ? . 79 ASP A CB 2351 ATOM 646 C CG . ASP A 2351 79 . -2.424 4.781 7.759 1.00 20.48 ? ? ? ? ? . 79 ASP A CG 2351 ATOM 647 O OD1 . ASP A 2351 79 . -2.084 5.421 6.759 1.00 20.77 ? ? ? ? ? . 79 ASP A OD1 2351 ATOM 648 O OD2 . ASP A 2351 79 . -2.011 5.037 8.914 1.00 25.19 ? ? ? ? ? 1- 79 ASP A OD2 2351 ATOM 649 N N . TYR A 2351 80 . -1.730 1.494 9.099 1.00 14.61 ? ? ? ? ? . 80 TYR A N 2351 ATOM 650 C CA . TYR A 2351 80 . -0.697 1.179 10.096 1.00 17.20 ? ? ? ? ? . 80 TYR A CA 2351 ATOM 651 C C . TYR A 2351 80 . 0.221 0.072 9.590 1.00 17.19 ? ? ? ? ? . 80 TYR A C 2351 ATOM 652 O O . TYR A 2351 80 . 1.447 0.196 9.633 1.00 16.67 ? ? ? ? ? . 80 TYR A O 2351 ATOM 653 C CB . TYR A 2351 80 . -1.340 0.758 11.427 1.00 18.55 ? ? ? ? ? . 80 TYR A CB 2351 ATOM 654 C CG . TYR A 2351 80 . -0.396 0.484 12.583 1.00 18.63 ? ? ? ? ? . 80 TYR A CG 2351 ATOM 655 C CD1 . TYR A 2351 80 . 0.683 1.323 12.833 1.00 23.04 ? ? ? ? ? . 80 TYR A CD1 2351 ATOM 656 C CD2 . TYR A 2351 80 . -0.627 -0.565 13.480 1.00 20.76 ? ? ? ? ? . 80 TYR A CD2 2351 ATOM 657 C CE1 . TYR A 2351 80 . 1.538 1.105 13.894 1.00 22.93 ? ? ? ? ? . 80 TYR A CE1 2351 ATOM 658 C CE2 . TYR A 2351 80 . 0.226 -0.795 14.558 1.00 21.46 ? ? ? ? ? . 80 TYR A CE2 2351 ATOM 659 C CZ . TYR A 2351 80 . 1.316 0.057 14.752 1.00 22.68 ? ? ? ? ? . 80 TYR A CZ 2351 ATOM 660 O OH . TYR A 2351 80 . 2.212 -0.095 15.781 1.00 22.57 ? ? ? ? ? . 80 TYR A OH 2351 ATOM 661 N N . TYR A 2351 81 . -0.381 -1.002 9.092 1.00 17.50 ? ? ? ? ? . 81 TYR A N 2351 ATOM 662 C CA . TYR A 2351 81 . 0.379 -2.102 8.498 1.00 16.24 ? ? ? ? ? . 81 TYR A CA 2351 ATOM 663 C C . TYR A 2351 81 . 1.140 -1.652 7.227 1.00 18.13 ? ? ? ? ? . 81 TYR A C 2351 ATOM 664 O O . TYR A 2351 81 . 2.207 -2.185 6.913 1.00 15.85 ? ? ? ? ? . 81 TYR A O 2351 ATOM 665 C CB . TYR A 2351 81 . -0.539 -3.302 8.214 1.00 16.74 ? ? ? ? ? . 81 TYR A CB 2351 ATOM 666 C CG . TYR A 2351 81 . 0.157 -4.417 7.487 1.00 15.44 ? ? ? ? ? . 81 TYR A CG 2351 ATOM 667 C CD1 . TYR A 2351 81 . 1.326 -4.962 7.996 1.00 15.29 ? ? ? ? ? . 81 TYR A CD1 2351 ATOM 668 C CD2 . TYR A 2351 81 . -0.327 -4.903 6.270 1.00 16.27 ? ? ? ? ? . 81 TYR A CD2 2351 ATOM 669 C CE1 . TYR A 2351 81 . 1.991 -5.974 7.330 1.00 16.12 ? ? ? ? ? . 81 TYR A CE1 2351 ATOM 670 C CE2 . TYR A 2351 81 . 0.337 -5.915 5.598 1.00 16.03 ? ? ? ? ? . 81 TYR A CE2 2351 ATOM 671 C CZ . TYR A 2351 81 . 1.494 -6.446 6.138 1.00 15.55 ? ? ? ? ? . 81 TYR A CZ 2351 ATOM 672 O OH . TYR A 2351 81 . 2.175 -7.436 5.481 1.00 15.91 ? ? ? ? ? . 81 TYR A OH 2351 ATOM 673 N N . GLY A 2351 82 . 0.590 -0.673 6.520 1.00 17.41 ? ? ? ? ? . 82 GLY A N 2351 ATOM 674 C CA . GLY A 2351 82 . 1.289 0.024 5.435 1.00 18.28 ? ? ? ? ? . 82 GLY A CA 2351 ATOM 675 C C . GLY A 2351 82 . 2.637 0.633 5.811 1.00 20.09 ? ? ? ? ? . 82 GLY A C 2351 ATOM 676 O O . GLY A 2351 82 . 3.493 0.785 4.952 1.00 24.29 ? ? ? ? ? . 82 GLY A O 2351 ATOM 677 N N . LYS A 2351 83 . 2.831 0.980 7.081 1.00 22.68 ? ? ? ? ? . 83 LYS A N 2351 ATOM 678 C CA . LYS A 2351 83 . 4.127 1.471 7.568 1.00 25.21 ? ? ? ? ? . 83 LYS A CA 2351 ATOM 679 C C . LYS A 2351 83 . 5.180 0.368 7.755 1.00 24.73 ? ? ? ? ? . 83 LYS A C 2351 ATOM 680 O O . LYS A 2351 83 . 6.347 0.694 7.939 1.00 27.09 ? ? ? ? ? . 83 LYS A O 2351 ATOM 681 C CB . LYS A 2351 83 . 3.966 2.226 8.900 1.00 27.32 ? ? ? ? ? . 83 LYS A CB 2351 ATOM 682 C CG . LYS A 2351 83 . 3.068 3.460 8.822 1.00 28.44 ? ? ? ? ? . 83 LYS A CG 2351 ATOM 683 C CD . LYS A 2351 83 . 2.696 3.960 10.213 1.00 29.59 ? ? ? ? ? . 83 LYS A CD 2351 ATOM 684 C CE . LYS A 2351 83 . 1.544 4.950 10.191 1.00 32.72 ? ? ? ? ? . 83 LYS A CE 2351 ATOM 685 N NZ . LYS A 2351 83 . 2.009 6.314 9.830 1.00 33.48 ? ? ? ? ? 1+ 83 LYS A NZ 2351 ATOM 686 N N . MET A 2351 84 . 4.781 -0.911 7.691 1.00 19.28 ? ? ? ? ? . 84 MET A N 2351 ATOM 687 C CA . MET A 2351 84 . 5.594 -2.020 8.159 1.00 17.95 ? ? ? ? ? . 84 MET A CA 2351 ATOM 688 C C . MET A 2351 84 . 6.094 -2.867 6.992 1.00 17.98 ? ? ? ? ? . 84 MET A C 2351 ATOM 689 O O . MET A 2351 84 . 5.361 -3.039 6.022 1.00 18.70 ? ? ? ? ? . 84 MET A O 2351 ATOM 690 C CB . MET A 2351 84 . 4.741 -2.887 9.073 1.00 18.33 ? ? ? ? ? . 84 MET A CB 2351 ATOM 691 C CG . MET A 2351 84 . 4.178 -2.120 10.259 1.00 17.16 ? ? ? ? ? . 84 MET A CG 2351 ATOM 692 S SD . MET A 2351 84 . 3.073 -3.159 11.216 1.00 18.23 ? ? ? ? ? . 84 MET A SD 2351 ATOM 693 C CE . MET A 2351 84 . 2.572 -2.030 12.508 1.00 19.33 ? ? ? ? ? . 84 MET A CE 2351 ATOM 694 N N . PRO A 2351 85 . 7.327 -3.413 7.084 1.00 15.09 ? ? ? ? ? . 85 PRO A N 2351 ATOM 695 C CA . PRO A 2351 85 . 7.898 -4.245 6.004 1.00 14.89 ? ? ? ? ? . 85 PRO A CA 2351 ATOM 696 C C . PRO A 2351 85 . 7.578 -5.746 6.060 1.00 14.31 ? ? ? ? ? . 85 PRO A C 2351 ATOM 697 O O . PRO A 2351 85 . 7.878 -6.490 5.111 1.00 16.07 ? ? ? ? ? . 85 PRO A O 2351 ATOM 698 C CB . PRO A 2351 85 . 9.418 -4.058 6.204 1.00 13.50 ? ? ? ? ? . 85 PRO A CB 2351 ATOM 699 C CG . PRO A 2351 85 . 9.557 -3.858 7.671 1.00 14.27 ? ? ? ? ? . 85 PRO A CG 2351 ATOM 700 C CD . PRO A 2351 85 . 8.354 -3.051 8.079 1.00 14.84 ? ? ? ? ? . 85 PRO A CD 2351 ATOM 701 N N . TRP A 2351 86 . 7.021 -6.177 7.179 1.00 14.39 ? ? ? ? ? . 86 TRP A N 2351 ATOM 702 C CA . TRP A 2351 86 . 6.848 -7.584 7.527 1.00 15.05 ? ? ? ? ? . 86 TRP A CA 2351 ATOM 703 C C . TRP A 2351 86 . 5.414 -8.087 7.212 1.00 14.93 ? ? ? ? ? . 86 TRP A C 2351 ATOM 704 O O . TRP A 2351 86 . 4.763 -7.552 6.308 1.00 15.89 ? ? ? ? ? . 86 TRP A O 2351 ATOM 705 C CB . TRP A 2351 86 . 7.249 -7.774 8.986 1.00 16.09 ? ? ? ? ? . 86 TRP A CB 2351 ATOM 706 C CG . TRP A 2351 86 . 6.594 -6.805 9.948 1.00 16.38 ? ? ? ? ? . 86 TRP A CG 2351 ATOM 707 C CD1 . TRP A 2351 86 . 5.277 -6.720 10.275 1.00 16.39 ? ? ? ? ? . 86 TRP A CD1 2351 ATOM 708 C CD2 . TRP A 2351 86 . 7.254 -5.759 10.661 1.00 16.60 ? ? ? ? ? . 86 TRP A CD2 2351 ATOM 709 C CE2 . TRP A 2351 86 . 6.275 -5.092 11.428 1.00 16.59 ? ? ? ? ? . 86 TRP A CE2 2351 ATOM 710 C CE3 . TRP A 2351 86 . 8.580 -5.340 10.752 1.00 17.11 ? ? ? ? ? . 86 TRP A CE3 2351 ATOM 711 N NE1 . TRP A 2351 86 . 5.074 -5.703 11.176 1.00 17.10 ? ? ? ? ? . 86 TRP A NE1 2351 ATOM 712 C CZ2 . TRP A 2351 86 . 6.576 -4.003 12.239 1.00 16.34 ? ? ? ? ? . 86 TRP A CZ2 2351 ATOM 713 C CZ3 . TRP A 2351 86 . 8.880 -4.259 11.571 1.00 16.26 ? ? ? ? ? . 86 TRP A CZ3 2351 ATOM 714 C CH2 . TRP A 2351 86 . 7.883 -3.601 12.300 1.00 16.70 ? ? ? ? ? . 86 TRP A CH2 2351 ATOM 715 N N . LEU A 2351 87 . 4.947 -9.122 7.918 1.00 14.24 ? ? ? ? ? . 87 LEU A N 2351 ATOM 716 C CA . LEU A 2351 87 . 3.666 -9.781 7.638 1.00 14.03 ? ? ? ? ? . 87 LEU A CA 2351 ATOM 717 C C . LEU A 2351 87 . 2.585 -9.335 8.606 1.00 13.87 ? ? ? ? ? . 87 LEU A C 2351 ATOM 718 O O . LEU A 2351 87 . 2.870 -8.625 9.570 1.00 15.16 ? ? ? ? ? . 87 LEU A O 2351 ATOM 719 C CB . LEU A 2351 87 . 3.834 -11.298 7.738 1.00 14.67 ? ? ? ? ? . 87 LEU A CB 2351 ATOM 720 C CG . LEU A 2351 87 . 4.941 -11.933 6.902 1.00 15.26 ? ? ? ? ? . 87 LEU A CG 2351 ATOM 721 C CD1 . LEU A 2351 87 . 4.898 -13.451 7.044 1.00 17.71 ? ? ? ? ? . 87 LEU A CD1 2351 ATOM 722 C CD2 . LEU A 2351 87 . 4.848 -11.552 5.423 1.00 15.24 ? ? ? ? ? . 87 LEU A CD2 2351 ATOM 723 N N . ALA A 2351 88 . 1.338 -9.735 8.355 1.00 14.07 ? ? ? ? ? . 88 ALA A N 2351 ATOM 724 C CA . ALA A 2351 88 . 0.243 -9.403 9.270 1.00 13.95 ? ? ? ? ? . 88 ALA A CA 2351 ATOM 725 C C . ALA A 2351 88 . -0.837 -10.476 9.311 1.00 14.05 ? ? ? ? ? . 88 ALA A C 2351 ATOM 726 O O . ALA A 2351 88 . -1.203 -11.084 8.292 1.00 13.51 ? ? ? ? ? . 88 ALA A O 2351 ATOM 727 C CB . ALA A 2351 88 . -0.376 -8.068 8.919 1.00 14.60 ? ? ? ? ? . 88 ALA A CB 2351 ATOM 728 N N . LEU A 2351 89 . -1.325 -10.720 10.521 1.00 14.21 ? ? ? ? ? . 89 LEU A N 2351 ATOM 729 C CA . LEU A 2351 89 . -2.521 -11.514 10.693 1.00 14.62 ? ? ? ? ? . 89 LEU A CA 2351 ATOM 730 C C . LEU A 2351 89 . -3.619 -10.667 10.045 1.00 15.33 ? ? ? ? ? . 89 LEU A C 2351 ATOM 731 O O . LEU A 2351 89 . -3.754 -9.482 10.397 1.00 16.78 ? ? ? ? ? . 89 LEU A O 2351 ATOM 732 C CB . LEU A 2351 89 . -2.799 -11.754 12.179 1.00 15.84 ? ? ? ? ? . 89 LEU A CB 2351 ATOM 733 C CG . LEU A 2351 89 . -4.017 -12.623 12.472 1.00 17.67 ? ? ? ? ? . 89 LEU A CG 2351 ATOM 734 C CD1 . LEU A 2351 89 . -3.789 -14.077 12.038 1.00 17.19 ? ? ? ? ? . 89 LEU A CD1 2351 ATOM 735 C CD2 . LEU A 2351 89 . -4.381 -12.542 13.948 1.00 18.01 ? ? ? ? ? . 89 LEU A CD2 2351 ATOM 736 N N . PRO A 2351 90 . -4.369 -11.236 9.079 1.00 15.61 ? ? ? ? ? . 90 PRO A N 2351 ATOM 737 C CA . PRO A 2351 90 . -5.337 -10.408 8.338 1.00 15.39 ? ? ? ? ? . 90 PRO A CA 2351 ATOM 738 C C . PRO A 2351 90 . -6.419 -9.804 9.235 1.00 16.09 ? ? ? ? ? . 90 PRO A C 2351 ATOM 739 O O . PRO A 2351 90 . -6.743 -10.365 10.289 1.00 17.53 ? ? ? ? ? . 90 PRO A O 2351 ATOM 740 C CB . PRO A 2351 90 . -5.942 -11.382 7.316 1.00 15.62 ? ? ? ? ? . 90 PRO A CB 2351 ATOM 741 C CG . PRO A 2351 90 . -5.047 -12.581 7.294 1.00 15.55 ? ? ? ? ? . 90 PRO A CG 2351 ATOM 742 C CD . PRO A 2351 90 . -4.440 -12.653 8.660 1.00 15.71 ? ? ? ? ? . 90 PRO A CD 2351 ATOM 743 N N . PHE A 2351 91 . -6.969 -8.674 8.808 1.00 15.01 ? ? ? ? ? . 91 PHE A N 2351 ATOM 744 C CA . PHE A 2351 91 . -8.012 -7.972 9.554 1.00 15.12 ? ? ? ? ? . 91 PHE A CA 2351 ATOM 745 C C . PHE A 2351 91 . -9.234 -8.855 9.838 1.00 14.96 ? ? ? ? ? . 91 PHE A C 2351 ATOM 746 O O . PHE A 2351 91 . -9.821 -8.765 10.919 1.00 14.30 ? ? ? ? ? . 91 PHE A O 2351 ATOM 747 C CB . PHE A 2351 91 . -8.419 -6.696 8.808 1.00 14.17 ? ? ? ? ? . 91 PHE A CB 2351 ATOM 748 C CG . PHE A 2351 91 . -9.368 -5.827 9.575 1.00 14.33 ? ? ? ? ? . 91 PHE A CG 2351 ATOM 749 C CD1 . PHE A 2351 91 . -8.907 -5.015 10.596 1.00 14.03 ? ? ? ? ? . 91 PHE A CD1 2351 ATOM 750 C CD2 . PHE A 2351 91 . -10.718 -5.837 9.293 1.00 14.08 ? ? ? ? ? . 91 PHE A CD2 2351 ATOM 751 C CE1 . PHE A 2351 91 . -9.778 -4.214 11.312 1.00 14.13 ? ? ? ? ? . 91 PHE A CE1 2351 ATOM 752 C CE2 . PHE A 2351 91 . -11.593 -5.031 10.000 1.00 14.14 ? ? ? ? ? . 91 PHE A CE2 2351 ATOM 753 C CZ . PHE A 2351 91 . -11.125 -4.227 11.017 1.00 13.32 ? ? ? ? ? . 91 PHE A CZ 2351 ATOM 754 N N . ASP A 2351 92 . -9.589 -9.745 8.906 1.00 15.56 ? ? ? ? ? . 92 ASP A N 2351 ATOM 755 C CA . ASP A 2351 92 . -10.703 -10.677 9.134 1.00 17.16 ? ? ? ? ? . 92 ASP A CA 2351 ATOM 756 C C . ASP A 2351 92 . -10.492 -11.723 10.253 1.00 16.55 ? ? ? ? ? . 92 ASP A C 2351 ATOM 757 O O . ASP A 2351 92 . -11.442 -12.405 10.630 1.00 15.77 ? ? ? ? ? . 92 ASP A O 2351 ATOM 758 C CB . ASP A 2351 92 . -11.183 -11.323 7.817 1.00 19.89 ? ? ? ? ? . 92 ASP A CB 2351 ATOM 759 C CG . ASP A 2351 92 . -10.238 -12.389 7.264 1.00 22.49 ? ? ? ? ? . 92 ASP A CG 2351 ATOM 760 O OD1 . ASP A 2351 92 . -9.083 -12.505 7.702 1.00 25.02 ? ? ? ? ? . 92 ASP A OD1 2351 ATOM 761 O OD2 . ASP A 2351 92 . -10.682 -13.123 6.358 1.00 28.11 ? ? ? ? ? 1- 92 ASP A OD2 2351 ATOM 762 N N . GLN A 2351 93 . -9.265 -11.838 10.772 1.00 18.68 ? ? ? ? ? . 93 GLN A N 2351 ATOM 763 C CA . GLN A 2351 93 . -8.950 -12.682 11.938 1.00 19.24 ? ? ? ? ? . 93 GLN A CA 2351 ATOM 764 C C . GLN A 2351 93 . -8.865 -11.918 13.267 1.00 19.92 ? ? ? ? ? . 93 GLN A C 2351 ATOM 765 O O . GLN A 2351 93 . -8.488 -12.498 14.294 1.00 19.87 ? ? ? ? ? . 93 GLN A O 2351 ATOM 766 C CB . GLN A 2351 93 . -7.613 -13.387 11.705 1.00 21.09 ? ? ? ? ? . 93 GLN A CB 2351 ATOM 767 C CG . GLN A 2351 93 . -7.585 -14.287 10.491 1.00 22.02 ? ? ? ? ? . 93 GLN A CG 2351 ATOM 768 C CD . GLN A 2351 93 . -8.625 -15.367 10.592 1.00 22.70 ? ? ? ? ? . 93 GLN A CD 2351 ATOM 769 N NE2 . GLN A 2351 93 . -9.587 -15.348 9.687 1.00 24.75 ? ? ? ? ? . 93 GLN A NE2 2351 ATOM 770 O OE1 . GLN A 2351 93 . -8.582 -16.194 11.502 1.00 26.33 ? ? ? ? ? . 93 GLN A OE1 2351 ATOM 771 N N . ARG A 2351 94 . -9.195 -10.629 13.268 1.00 18.83 ? ? ? ? ? . 94 ARG A N 2351 ATOM 772 C CA . ARG A 2351 94 . -9.008 -9.798 14.473 1.00 18.44 ? ? ? ? ? . 94 ARG A CA 2351 ATOM 773 C C . ARG A 2351 94 . -9.787 -10.249 15.731 1.00 20.01 ? ? ? ? ? . 94 ARG A C 2351 ATOM 774 O O . ARG A 2351 94 . -9.382 -9.946 16.856 1.00 21.06 ? ? ? ? ? . 94 ARG A O 2351 ATOM 775 C CB . ARG A 2351 94 . -9.362 -8.352 14.163 1.00 18.84 ? ? ? ? ? . 94 ARG A CB 2351 ATOM 776 C CG . ARG A 2351 94 . -10.833 -8.137 13.869 1.00 17.70 ? ? ? ? ? . 94 ARG A CG 2351 ATOM 777 C CD . ARG A 2351 94 . -11.074 -6.817 13.167 1.00 17.62 ? ? ? ? ? . 94 ARG A CD 2351 ATOM 778 N NE . ARG A 2351 94 . -12.479 -6.584 12.868 1.00 16.14 ? ? ? ? ? . 94 ARG A NE 2351 ATOM 779 C CZ . ARG A 2351 94 . -13.172 -7.168 11.890 1.00 15.93 ? ? ? ? ? . 94 ARG A CZ 2351 ATOM 780 N NH1 . ARG A 2351 94 . -12.618 -8.075 11.077 1.00 15.88 ? ? ? ? ? 1+ 94 ARG A NH1 2351 ATOM 781 N NH2 . ARG A 2351 94 . -14.447 -6.844 11.720 1.00 15.41 ? ? ? ? ? . 94 ARG A NH2 2351 ATOM 782 N N . SER A 2351 95 . -10.894 -10.966 15.554 1.00 18.52 ? ? ? ? ? . 95 SER A N 2351 ATOM 783 C CA . SER A 2351 95 . -11.631 -11.517 16.704 1.00 19.63 ? ? ? ? ? . 95 SER A CA 2351 ATOM 784 C C . SER A 2351 95 . -10.806 -12.529 17.529 1.00 20.04 ? ? ? ? ? . 95 SER A C 2351 ATOM 785 O O . SER A 2351 95 . -11.153 -12.802 18.675 1.00 23.68 ? ? ? ? ? . 95 SER A O 2351 ATOM 786 C CB . SER A 2351 95 . -12.957 -12.140 16.257 1.00 19.52 ? ? ? ? ? . 95 SER A CB 2351 ATOM 787 O OG . SER A 2351 95 . -12.750 -13.290 15.451 1.00 19.99 ? ? ? ? ? . 95 SER A OG 2351 ATOM 788 N N . THR A 2351 96 . -9.726 -13.065 16.955 1.00 18.79 ? ? ? ? ? . 96 THR A N 2351 ATOM 789 C CA . THR A 2351 96 . -8.848 -14.022 17.638 1.00 19.20 ? ? ? ? ? . 96 THR A CA 2351 ATOM 790 C C . THR A 2351 96 . -7.699 -13.365 18.408 1.00 18.18 ? ? ? ? ? . 96 THR A C 2351 ATOM 791 O O . THR A 2351 96 . -7.004 -14.049 19.141 1.00 18.92 ? ? ? ? ? . 96 THR A O 2351 ATOM 792 C CB . THR A 2351 96 . -8.234 -15.045 16.647 1.00 18.50 ? ? ? ? ? . 96 THR A CB 2351 ATOM 793 C CG2 . THR A 2351 96 . -9.306 -15.722 15.827 1.00 19.51 ? ? ? ? ? . 96 THR A CG2 2351 ATOM 794 O OG1 . THR A 2351 96 . -7.308 -14.396 15.773 1.00 17.89 ? ? ? ? ? . 96 THR A OG1 2351 ATOM 795 N N . VAL A 2351 97 . -7.509 -12.050 18.253 1.00 17.87 ? ? ? ? ? . 97 VAL A N 2351 ATOM 796 C CA . VAL A 2351 97 . -6.369 -11.333 18.837 1.00 17.37 ? ? ? ? ? . 97 VAL A CA 2351 ATOM 797 C C . VAL A 2351 97 . -6.320 -11.387 20.366 1.00 17.80 ? ? ? ? ? . 97 VAL A C 2351 ATOM 798 O O . VAL A 2351 97 . -5.255 -11.611 20.940 1.00 20.08 ? ? ? ? ? . 97 VAL A O 2351 ATOM 799 C CB . VAL A 2351 97 . -6.303 -9.861 18.321 1.00 17.84 ? ? ? ? ? . 97 VAL A CB 2351 ATOM 800 C CG1 . VAL A 2351 97 . -5.371 -8.987 19.152 1.00 19.58 ? ? ? ? ? . 97 VAL A CG1 2351 ATOM 801 C CG2 . VAL A 2351 97 . -5.879 -9.848 16.855 1.00 18.67 ? ? ? ? ? . 97 VAL A CG2 2351 ATOM 802 N N . SER A 2351 98 . -7.446 -11.187 21.024 1.00 18.78 ? ? ? ? ? . 98 SER A N 2351 ATOM 803 C CA . SER A 2351 98 . -7.464 -11.238 22.490 1.00 21.28 ? ? ? ? ? . 98 SER A CA 2351 ATOM 804 C C . SER A 2351 98 . -7.035 -12.609 23.030 1.00 18.77 ? ? ? ? ? . 98 SER A C 2351 ATOM 805 O O . SER A 2351 98 . -6.158 -12.685 23.897 1.00 18.08 ? ? ? ? ? . 98 SER A O 2351 ATOM 806 C CB . SER A 2351 98 . -8.832 -10.833 23.032 1.00 25.06 ? ? ? ? ? . 98 SER A CB 2351 ATOM 807 O OG . SER A 2351 98 . -9.007 -9.449 22.802 1.00 31.85 ? ? ? ? ? . 98 SER A OG 2351 ATOM 808 N N . GLU A 2351 99 . -7.616 -13.681 22.496 1.00 19.69 ? ? ? ? ? . 99 GLU A N 2351 ATOM 809 C CA . GLU A 2351 99 . -7.262 -15.038 22.954 1.00 21.24 ? ? ? ? ? . 99 GLU A CA 2351 ATOM 810 C C . GLU A 2351 99 . -5.793 -15.374 22.682 1.00 17.41 ? ? ? ? ? . 99 GLU A C 2351 ATOM 811 O O . GLU A 2351 99 . -5.151 -16.025 23.503 1.00 15.18 ? ? ? ? ? . 99 GLU A O 2351 ATOM 812 C CB . GLU A 2351 99 . -8.204 -16.125 22.399 1.00 26.09 ? ? ? ? ? . 99 GLU A CB 2351 ATOM 813 C CG . GLU A 2351 99 . -9.552 -16.237 23.134 1.00 32.76 ? ? ? ? ? . 99 GLU A CG 2351 ATOM 814 C CD . GLU A 2351 99 . -9.435 -16.520 24.639 1.00 38.23 ? ? ? ? ? . 99 GLU A CD 2351 ATOM 815 O OE1 . GLU A 2351 99 . -10.112 -15.830 25.435 1.00 38.21 ? ? ? ? ? . 99 GLU A OE1 2351 ATOM 816 O OE2 . GLU A 2351 99 . -8.659 -17.420 25.035 1.00 43.04 ? ? ? ? ? 1- 99 GLU A OE2 2351 ATOM 817 N N A LEU A 2351 100 . -5.267 -14.922 21.547 0.62 17.52 ? ? ? ? ? . 100 LEU A N 2351 ATOM 818 N N B LEU A 2351 100 . -5.274 -14.931 21.535 0.38 17.54 ? ? ? ? ? . 100 LEU A N 2351 ATOM 819 C CA A LEU A 2351 100 . -3.843 -15.073 21.262 0.62 17.97 ? ? ? ? ? . 100 LEU A CA 2351 ATOM 820 C CA B LEU A 2351 100 . -3.842 -15.024 21.233 0.38 17.83 ? ? ? ? ? . 100 LEU A CA 2351 ATOM 821 C C A LEU A 2351 100 . -2.991 -14.334 22.306 0.62 17.34 ? ? ? ? ? . 100 LEU A C 2351 ATOM 822 C C B LEU A 2351 100 . -2.996 -14.330 22.297 0.38 17.23 ? ? ? ? ? . 100 LEU A C 2351 ATOM 823 O O A LEU A 2351 100 . -2.009 -14.887 22.811 0.62 17.52 ? ? ? ? ? . 100 LEU A O 2351 ATOM 824 O O B LEU A 2351 100 . -2.015 -14.895 22.788 0.38 17.39 ? ? ? ? ? . 100 LEU A O 2351 ATOM 825 C CB A LEU A 2351 100 . -3.512 -14.591 19.845 0.62 17.99 ? ? ? ? ? . 100 LEU A CB 2351 ATOM 826 C CB B LEU A 2351 100 . -3.539 -14.408 19.866 0.38 17.92 ? ? ? ? ? . 100 LEU A CB 2351 ATOM 827 C CG A LEU A 2351 100 . -2.154 -15.017 19.286 0.62 18.53 ? ? ? ? ? . 100 LEU A CG 2351 ATOM 828 C CG B LEU A 2351 100 . -3.832 -15.294 18.660 0.38 18.30 ? ? ? ? ? . 100 LEU A CG 2351 ATOM 829 C CD1 A LEU A 2351 100 . -2.036 -16.528 19.154 0.62 18.85 ? ? ? ? ? . 100 LEU A CD1 2351 ATOM 830 C CD2 A LEU A 2351 100 . -1.922 -14.346 17.940 0.62 18.72 ? ? ? ? ? . 100 LEU A CD2 2351 ATOM 831 C CD1 B LEU A 2351 100 . -3.529 -14.555 17.366 0.38 18.21 ? ? ? ? ? . 100 LEU A CD1 2351 ATOM 832 C CD2 B LEU A 2351 100 . -3.032 -16.584 18.760 0.38 18.99 ? ? ? ? ? . 100 LEU A CD2 2351 ATOM 833 N N . GLY A 2351 101 . -3.394 -13.112 22.652 1.00 16.30 ? ? ? ? ? . 101 GLY A N 2351 ATOM 834 C CA . GLY A 2351 101 . -2.751 -12.353 23.730 1.00 17.07 ? ? ? ? ? . 101 GLY A CA 2351 ATOM 835 C C . GLY A 2351 101 . -2.761 -13.100 25.058 1.00 16.31 ? ? ? ? ? . 101 GLY A C 2351 ATOM 836 O O . GLY A 2351 101 . -1.743 -13.175 25.749 1.00 16.49 ? ? ? ? ? . 101 GLY A O 2351 ATOM 837 N N . LYS A 2351 102 . -3.894 -13.712 25.373 1.00 16.43 ? ? ? ? ? . 102 LYS A N 2351 ATOM 838 C CA . LYS A 2351 102 . -4.015 -14.519 26.581 1.00 18.92 ? ? ? ? ? . 102 LYS A CA 2351 ATOM 839 C C . LYS A 2351 102 . -3.185 -15.794 26.544 1.00 17.88 ? ? ? ? ? . 102 LYS A C 2351 ATOM 840 O O . LYS A 2351 102 . -2.693 -16.236 27.592 1.00 17.27 ? ? ? ? ? . 102 LYS A O 2351 ATOM 841 C CB . LYS A 2351 102 . -5.471 -14.864 26.852 1.00 20.65 ? ? ? ? ? . 102 LYS A CB 2351 ATOM 842 C CG . LYS A 2351 102 . -6.288 -13.651 27.240 1.00 23.12 ? ? ? ? ? . 102 LYS A CG 2351 ATOM 843 C CD . LYS A 2351 102 . -7.765 -13.982 27.284 1.00 26.40 ? ? ? ? ? . 102 LYS A CD 2351 ATOM 844 C CE . LYS A 2351 102 . -8.599 -12.716 27.350 1.00 30.33 ? ? ? ? ? . 102 LYS A CE 2351 ATOM 845 N NZ . LYS A 2351 102 . -10.031 -13.013 27.641 1.00 32.61 ? ? ? ? ? 1+ 102 LYS A NZ 2351 ATOM 846 N N . THR A 2351 103 . -3.048 -16.401 25.367 1.00 16.42 ? ? ? ? ? . 103 THR A N 2351 ATOM 847 C CA . THR A 2351 103 . -2.195 -17.586 25.218 1.00 17.78 ? ? ? ? ? . 103 THR A CA 2351 ATOM 848 C C . THR A 2351 103 . -0.744 -17.326 25.664 1.00 17.24 ? ? ? ? ? . 103 THR A C 2351 ATOM 849 O O . THR A 2351 103 . -0.141 -18.175 26.318 1.00 18.04 ? ? ? ? ? . 103 THR A O 2351 ATOM 850 C CB . THR A 2351 103 . -2.246 -18.126 23.775 1.00 18.81 ? ? ? ? ? . 103 THR A CB 2351 ATOM 851 C CG2 . THR A 2351 103 . -1.316 -19.326 23.587 1.00 20.17 ? ? ? ? ? . 103 THR A CG2 2351 ATOM 852 O OG1 . THR A 2351 103 . -3.593 -18.515 23.477 1.00 20.80 ? ? ? ? ? . 103 THR A OG1 2351 ATOM 853 N N . PHE A 2351 104 . -0.216 -16.152 25.328 1.00 19.05 ? ? ? ? ? . 104 PHE A N 2351 ATOM 854 C CA . PHE A 2351 104 . 1.181 -15.790 25.614 1.00 19.38 ? ? ? ? ? . 104 PHE A CA 2351 ATOM 855 C C . PHE A 2351 104 . 1.370 -14.884 26.835 1.00 20.42 ? ? ? ? ? . 104 PHE A C 2351 ATOM 856 O O . PHE A 2351 104 . 2.509 -14.490 27.138 1.00 21.98 ? ? ? ? ? . 104 PHE A O 2351 ATOM 857 C CB . PHE A 2351 104 . 1.800 -15.141 24.379 1.00 19.21 ? ? ? ? ? . 104 PHE A CB 2351 ATOM 858 C CG . PHE A 2351 104 . 1.787 -16.032 23.169 1.00 18.31 ? ? ? ? ? . 104 PHE A CG 2351 ATOM 859 C CD1 . PHE A 2351 104 . 2.515 -17.212 23.163 1.00 18.08 ? ? ? ? ? . 104 PHE A CD1 2351 ATOM 860 C CD2 . PHE A 2351 104 . 1.042 -15.701 22.042 1.00 18.77 ? ? ? ? ? . 104 PHE A CD2 2351 ATOM 861 C CE1 . PHE A 2351 104 . 2.515 -18.044 22.052 1.00 19.62 ? ? ? ? ? . 104 PHE A CE1 2351 ATOM 862 C CE2 . PHE A 2351 104 . 1.023 -16.536 20.933 1.00 19.73 ? ? ? ? ? . 104 PHE A CE2 2351 ATOM 863 C CZ . PHE A 2351 104 . 1.766 -17.706 20.933 1.00 19.63 ? ? ? ? ? . 104 PHE A CZ 2351 ATOM 864 N N . GLY A 2351 105 . 0.278 -14.584 27.535 1.00 17.32 ? ? ? ? ? . 105 GLY A N 2351 ATOM 865 C CA . GLY A 2351 105 . 0.314 -13.721 28.702 1.00 17.53 ? ? ? ? ? . 105 GLY A CA 2351 ATOM 866 C C . GLY A 2351 105 . 0.695 -12.289 28.385 1.00 18.09 ? ? ? ? ? . 105 GLY A C 2351 ATOM 867 O O . GLY A 2351 105 . 1.374 -11.625 29.192 1.00 18.88 ? ? ? ? ? . 105 GLY A O 2351 ATOM 868 N N . VAL A 2351 106 . 0.237 -11.800 27.229 1.00 16.90 ? ? ? ? ? . 106 VAL A N 2351 ATOM 869 C CA . VAL A 2351 106 . 0.450 -10.401 26.824 1.00 17.15 ? ? ? ? ? . 106 VAL A CA 2351 ATOM 870 C C . VAL A 2351 106 . -0.420 -9.510 27.720 1.00 17.09 ? ? ? ? ? . 106 VAL A C 2351 ATOM 871 O O . VAL A 2351 106 . -1.656 -9.601 27.679 1.00 17.42 ? ? ? ? ? . 106 VAL A O 2351 ATOM 872 C CB . VAL A 2351 106 . 0.113 -10.177 25.338 1.00 16.91 ? ? ? ? ? . 106 VAL A CB 2351 ATOM 873 C CG1 . VAL A 2351 106 . 0.239 -8.706 24.946 1.00 17.76 ? ? ? ? ? . 106 VAL A CG1 2351 ATOM 874 C CG2 . VAL A 2351 106 . 1.032 -11.025 24.467 1.00 16.80 ? ? ? ? ? . 106 VAL A CG2 2351 ATOM 875 N N A GLU A 2351 107 . 0.231 -8.684 28.544 0.48 16.42 ? ? ? ? ? . 107 GLU A N 2351 ATOM 876 N N B GLU A 2351 107 . 0.226 -8.667 28.525 0.52 16.18 ? ? ? ? ? . 107 GLU A N 2351 ATOM 877 C CA A GLU A 2351 107 . -0.457 -7.789 29.486 0.48 17.61 ? ? ? ? ? . 107 GLU A CA 2351 ATOM 878 C CA B GLU A 2351 107 . -0.482 -7.782 29.455 0.52 17.47 ? ? ? ? ? . 107 GLU A CA 2351 ATOM 879 C C A GLU A 2351 107 . -0.440 -6.314 29.071 0.48 16.30 ? ? ? ? ? . 107 GLU A C 2351 ATOM 880 C C B GLU A 2351 107 . -0.383 -6.294 29.118 0.52 16.22 ? ? ? ? ? . 107 GLU A C 2351 ATOM 881 O O A GLU A 2351 107 . -1.159 -5.512 29.658 0.48 15.00 ? ? ? ? ? . 107 GLU A O 2351 ATOM 882 O O B GLU A 2351 107 . -0.983 -5.467 29.799 0.52 14.91 ? ? ? ? ? . 107 GLU A O 2351 ATOM 883 C CB A GLU A 2351 107 . 0.136 -7.934 30.885 0.48 18.90 ? ? ? ? ? . 107 GLU A CB 2351 ATOM 884 C CB B GLU A 2351 107 . -0.026 -8.061 30.878 0.52 18.53 ? ? ? ? ? . 107 GLU A CB 2351 ATOM 885 C CG A GLU A 2351 107 . -0.152 -9.282 31.527 0.48 20.28 ? ? ? ? ? . 107 GLU A CG 2351 ATOM 886 C CG B GLU A 2351 107 . -0.457 -9.445 31.335 0.52 19.46 ? ? ? ? ? . 107 GLU A CG 2351 ATOM 887 C CD A GLU A 2351 107 . -1.634 -9.612 31.585 0.48 20.99 ? ? ? ? ? . 107 GLU A CD 2351 ATOM 888 C CD B GLU A 2351 107 . -0.230 -9.688 32.809 0.52 20.69 ? ? ? ? ? . 107 GLU A CD 2351 ATOM 889 O OE1 A GLU A 2351 107 . -1.964 -10.810 31.716 0.48 22.80 ? ? ? ? ? . 107 GLU A OE1 2351 ATOM 890 O OE2 A GLU A 2351 107 . -2.475 -8.685 31.501 0.48 20.81 ? ? ? ? ? 1- 107 GLU A OE2 2351 ATOM 891 O OE1 B GLU A 2351 107 . 0.552 -8.941 33.435 0.52 21.77 ? ? ? ? ? . 107 GLU A OE1 2351 ATOM 892 O OE2 B GLU A 2351 107 . -0.834 -10.641 33.338 0.52 20.72 ? ? ? ? ? 1- 107 GLU A OE2 2351 ATOM 893 N N . SER A 2351 108 . 0.380 -5.969 28.081 1.00 15.68 ? ? ? ? ? . 108 SER A N 2351 ATOM 894 C CA . SER A 2351 108 . 0.383 -4.638 27.500 1.00 17.08 ? ? ? ? ? . 108 SER A CA 2351 ATOM 895 C C . SER A 2351 108 . 0.985 -4.755 26.112 1.00 16.89 ? ? ? ? ? . 108 SER A C 2351 ATOM 896 O O . SER A 2351 108 . 1.450 -5.829 25.729 1.00 17.73 ? ? ? ? ? . 108 SER A O 2351 ATOM 897 C CB . SER A 2351 108 . 1.213 -3.668 28.353 1.00 18.24 ? ? ? ? ? . 108 SER A CB 2351 ATOM 898 O OG . SER A 2351 108 . 2.566 -4.088 28.395 1.00 19.50 ? ? ? ? ? . 108 SER A OG 2351 ATOM 899 N N . ILE A 2351 109 . 0.943 -3.654 25.361 1.00 16.59 ? ? ? ? ? . 109 ILE A N 2351 ATOM 900 C CA . ILE A 2351 109 . 1.631 -3.552 24.077 1.00 16.95 ? ? ? ? ? . 109 ILE A CA 2351 ATOM 901 C C . ILE A 2351 109 . 2.424 -2.244 24.042 1.00 17.07 ? ? ? ? ? . 109 ILE A C 2351 ATOM 902 O O . ILE A 2351 109 . 2.119 -1.314 24.806 1.00 15.40 ? ? ? ? ? . 109 ILE A O 2351 ATOM 903 C CB . ILE A 2351 109 . 0.661 -3.621 22.878 1.00 16.61 ? ? ? ? ? . 109 ILE A CB 2351 ATOM 904 C CG1 . ILE A 2351 109 . -0.342 -2.464 22.916 1.00 16.67 ? ? ? ? ? . 109 ILE A CG1 2351 ATOM 905 C CG2 . ILE A 2351 109 . -0.070 -4.947 22.864 1.00 17.96 ? ? ? ? ? . 109 ILE A CG2 2351 ATOM 906 C CD1 . ILE A 2351 109 . -1.334 -2.459 21.764 1.00 17.14 ? ? ? ? ? . 109 ILE A CD1 2351 ATOM 907 N N . PRO A 2351 110 . 3.455 -2.163 23.184 1.00 17.10 ? ? ? ? ? . 110 PRO A N 2351 ATOM 908 C CA . PRO A 2351 110 . 3.969 -3.163 22.255 1.00 16.27 ? ? ? ? ? . 110 PRO A CA 2351 ATOM 909 C C . PRO A 2351 110 . 4.615 -4.367 22.957 1.00 16.00 ? ? ? ? ? . 110 PRO A C 2351 ATOM 910 O O . PRO A 2351 110 . 5.305 -4.213 23.960 1.00 15.22 ? ? ? ? ? . 110 PRO A O 2351 ATOM 911 C CB . PRO A 2351 110 . 5.004 -2.363 21.462 1.00 16.63 ? ? ? ? ? . 110 PRO A CB 2351 ATOM 912 C CG . PRO A 2351 110 . 5.544 -1.416 22.461 1.00 14.86 ? ? ? ? ? . 110 PRO A CG 2351 ATOM 913 C CD . PRO A 2351 110 . 4.334 -0.974 23.215 1.00 16.56 ? ? ? ? ? . 110 PRO A CD 2351 ATOM 914 N N . THR A 2351 111 . 4.358 -5.563 22.450 1.00 16.65 ? ? ? ? ? . 111 THR A N 2351 ATOM 915 C CA . THR A 2351 111 . 5.020 -6.757 22.952 1.00 16.87 ? ? ? ? ? . 111 THR A CA 2351 ATOM 916 C C . THR A 2351 111 . 5.390 -7.633 21.753 1.00 16.48 ? ? ? ? ? . 111 THR A C 2351 ATOM 917 O O . THR A 2351 111 . 4.610 -7.759 20.799 1.00 16.90 ? ? ? ? ? . 111 THR A O 2351 ATOM 918 C CB . THR A 2351 111 . 4.107 -7.527 23.939 1.00 17.53 ? ? ? ? ? . 111 THR A CB 2351 ATOM 919 C CG2 . THR A 2351 111 . 4.684 -8.888 24.316 1.00 18.56 ? ? ? ? ? . 111 THR A CG2 2351 ATOM 920 O OG1 . THR A 2351 111 . 3.924 -6.761 25.132 1.00 18.31 ? ? ? ? ? . 111 THR A OG1 2351 ATOM 921 N N . LEU A 2351 112 . 6.592 -8.200 21.806 1.00 15.48 ? ? ? ? ? . 112 LEU A N 2351 ATOM 922 C CA . LEU A 2351 112 . 7.032 -9.243 20.872 1.00 16.77 ? ? ? ? ? . 112 LEU A CA 2351 ATOM 923 C C . LEU A 2351 112 . 7.096 -10.595 21.590 1.00 17.72 ? ? ? ? ? . 112 LEU A C 2351 ATOM 924 O O . LEU A 2351 112 . 7.684 -10.706 22.669 1.00 18.56 ? ? ? ? ? . 112 LEU A O 2351 ATOM 925 C CB . LEU A 2351 112 . 8.420 -8.917 20.311 1.00 16.88 ? ? ? ? ? . 112 LEU A CB 2351 ATOM 926 C CG . LEU A 2351 112 . 8.521 -7.687 19.408 1.00 17.77 ? ? ? ? ? . 112 LEU A CG 2351 ATOM 927 C CD1 . LEU A 2351 112 . 9.973 -7.390 19.033 1.00 16.92 ? ? ? ? ? . 112 LEU A CD1 2351 ATOM 928 C CD2 . LEU A 2351 112 . 7.689 -7.898 18.153 1.00 19.55 ? ? ? ? ? . 112 LEU A CD2 2351 ATOM 929 N N . ILE A 2351 113 . 6.496 -11.617 20.990 1.00 15.87 ? ? ? ? ? . 113 ILE A N 2351 ATOM 930 C CA . ILE A 2351 113 . 6.651 -12.997 21.460 1.00 15.67 ? ? ? ? ? . 113 ILE A CA 2351 ATOM 931 C C . ILE A 2351 113 . 7.452 -13.761 20.404 1.00 16.43 ? ? ? ? ? . 113 ILE A C 2351 ATOM 932 O O . ILE A 2351 113 . 7.100 -13.752 19.241 1.00 17.53 ? ? ? ? ? . 113 ILE A O 2351 ATOM 933 C CB . ILE A 2351 113 . 5.284 -13.665 21.671 1.00 16.79 ? ? ? ? ? . 113 ILE A CB 2351 ATOM 934 C CG1 . ILE A 2351 113 . 4.438 -12.866 22.669 1.00 16.77 ? ? ? ? ? . 113 ILE A CG1 2351 ATOM 935 C CG2 . ILE A 2351 113 . 5.450 -15.106 22.132 1.00 16.45 ? ? ? ? ? . 113 ILE A CG2 2351 ATOM 936 C CD1 . ILE A 2351 113 . 5.059 -12.691 24.033 1.00 17.44 ? ? ? ? ? . 113 ILE A CD1 2351 ATOM 937 N N . THR A 2351 114 . 8.548 -14.395 20.806 1.00 15.64 ? ? ? ? ? . 114 THR A N 2351 ATOM 938 C CA . THR A 2351 114 . 9.432 -15.065 19.851 1.00 15.54 ? ? ? ? ? . 114 THR A CA 2351 ATOM 939 C C . THR A 2351 114 . 9.105 -16.535 19.804 1.00 16.03 ? ? ? ? ? . 114 THR A C 2351 ATOM 940 O O . THR A 2351 114 . 9.069 -17.201 20.843 1.00 15.89 ? ? ? ? ? . 114 THR A O 2351 ATOM 941 C CB . THR A 2351 114 . 10.899 -14.877 20.248 1.00 16.17 ? ? ? ? ? . 114 THR A CB 2351 ATOM 942 C CG2 . THR A 2351 114 . 11.843 -15.242 19.082 1.00 17.31 ? ? ? ? ? . 114 THR A CG2 2351 ATOM 943 O OG1 . THR A 2351 114 . 11.091 -13.522 20.641 1.00 16.08 ? ? ? ? ? . 114 THR A OG1 2351 ATOM 944 N N A ILE A 2351 115 . 8.888 -17.070 18.605 0.55 16.54 ? ? ? ? ? . 115 ILE A N 2351 ATOM 945 N N B ILE A 2351 115 . 8.876 -17.020 18.585 0.45 15.81 ? ? ? ? ? . 115 ILE A N 2351 ATOM 946 C CA A ILE A 2351 115 . 8.499 -18.473 18.450 0.55 16.27 ? ? ? ? ? . 115 ILE A CA 2351 ATOM 947 C CA B ILE A 2351 115 . 8.382 -18.358 18.324 0.45 15.23 ? ? ? ? ? . 115 ILE A CA 2351 ATOM 948 C C A ILE A 2351 115 . 9.340 -19.134 17.352 0.55 15.48 ? ? ? ? ? . 115 ILE A C 2351 ATOM 949 C C B ILE A 2351 115 . 9.324 -19.049 17.348 0.45 14.86 ? ? ? ? ? . 115 ILE A C 2351 ATOM 950 O O A ILE A 2351 115 . 9.682 -18.500 16.351 0.55 15.76 ? ? ? ? ? . 115 ILE A O 2351 ATOM 951 O O B ILE A 2351 115 . 9.872 -18.421 16.445 0.45 14.85 ? ? ? ? ? . 115 ILE A O 2351 ATOM 952 C CB A ILE A 2351 115 . 6.978 -18.584 18.143 0.55 16.88 ? ? ? ? ? . 115 ILE A CB 2351 ATOM 953 C CB B ILE A 2351 115 . 6.970 -18.282 17.698 0.45 14.58 ? ? ? ? ? . 115 ILE A CB 2351 ATOM 954 C CG1 A ILE A 2351 115 . 6.158 -18.040 19.325 0.55 17.01 ? ? ? ? ? . 115 ILE A CG1 2351 ATOM 955 C CG2 A ILE A 2351 115 . 6.558 -20.022 17.847 0.55 17.77 ? ? ? ? ? . 115 ILE A CG2 2351 ATOM 956 C CG1 B ILE A 2351 115 . 6.030 -17.511 18.630 0.45 13.86 ? ? ? ? ? . 115 ILE A CG1 2351 ATOM 957 C CG2 B ILE A 2351 115 . 6.416 -19.669 17.440 0.45 15.79 ? ? ? ? ? . 115 ILE A CG2 2351 ATOM 958 C CD1 A ILE A 2351 115 . 4.718 -17.741 18.993 0.55 18.59 ? ? ? ? ? . 115 ILE A CD1 2351 ATOM 959 C CD1 B ILE A 2351 115 . 5.831 -18.198 19.961 0.45 13.69 ? ? ? ? ? . 115 ILE A CD1 2351 ATOM 960 N N A ASN A 2351 116 . 9.696 -20.393 17.578 0.55 14.26 ? ? ? ? ? . 116 ASN A N 2351 ATOM 961 N N B ASN A 2351 116 . 9.528 -20.339 17.550 0.45 14.15 ? ? ? ? ? . 116 ASN A N 2351 ATOM 962 C CA A ASN A 2351 116 . 10.195 -21.272 16.531 0.55 14.49 ? ? ? ? ? . 116 ASN A CA 2351 ATOM 963 C CA B ASN A 2351 116 . 10.161 -21.166 16.547 0.45 14.57 ? ? ? ? ? . 116 ASN A CA 2351 ATOM 964 C C A ASN A 2351 116 . 8.994 -21.667 15.677 0.55 14.67 ? ? ? ? ? . 116 ASN A C 2351 ATOM 965 C C B ASN A 2351 116 . 9.036 -21.700 15.669 0.45 14.67 ? ? ? ? ? . 116 ASN A C 2351 ATOM 966 O O A ASN A 2351 116 . 8.060 -22.285 16.182 0.55 14.82 ? ? ? ? ? . 116 ASN A O 2351 ATOM 967 O O B ASN A 2351 116 . 8.204 -22.467 16.147 0.45 14.81 ? ? ? ? ? . 116 ASN A O 2351 ATOM 968 C CB A ASN A 2351 116 . 10.852 -22.511 17.146 0.55 14.78 ? ? ? ? ? . 116 ASN A CB 2351 ATOM 969 C CB B ASN A 2351 116 . 10.920 -22.308 17.211 0.45 15.08 ? ? ? ? ? . 116 ASN A CB 2351 ATOM 970 C CG A ASN A 2351 116 . 11.479 -23.433 16.108 0.55 14.39 ? ? ? ? ? . 116 ASN A CG 2351 ATOM 971 C CG B ASN A 2351 116 . 11.701 -23.154 16.220 0.45 15.35 ? ? ? ? ? . 116 ASN A CG 2351 ATOM 972 N ND2 A ASN A 2351 116 . 12.807 -23.467 16.077 0.55 15.51 ? ? ? ? ? . 116 ASN A ND2 2351 ATOM 973 O OD1 A ASN A 2351 116 . 10.785 -24.115 15.358 0.55 13.66 ? ? ? ? ? . 116 ASN A OD1 2351 ATOM 974 N ND2 B ASN A 2351 116 . 11.743 -24.447 16.470 0.45 15.08 ? ? ? ? ? . 116 ASN A ND2 2351 ATOM 975 O OD1 B ASN A 2351 116 . 12.279 -22.646 15.258 0.45 15.65 ? ? ? ? ? . 116 ASN A OD1 2351 ATOM 976 N N . ALA A 2351 117 . 9.000 -21.278 14.401 1.00 14.43 ? ? ? ? ? . 117 ALA A N 2351 ATOM 977 C CA . ALA A 2351 117 . 7.853 -21.558 13.494 1.00 15.56 ? ? ? ? ? . 117 ALA A CA 2351 ATOM 978 C C . ALA A 2351 117 . 7.501 -23.034 13.368 1.00 16.26 ? ? ? ? ? . 117 ALA A C 2351 ATOM 979 O O . ALA A 2351 117 . 6.317 -23.404 13.362 1.00 19.27 ? ? ? ? ? . 117 ALA A O 2351 ATOM 980 C CB . ALA A 2351 117 . 8.106 -20.984 12.098 1.00 15.32 ? ? ? ? ? . 117 ALA A CB 2351 ATOM 981 N N . ASP A 2351 118 . 8.530 -23.869 13.280 1.00 13.71 ? ? ? ? ? . 118 ASP A N 2351 ATOM 982 C CA . ASP A 2351 118 . 8.340 -25.280 12.997 1.00 13.63 ? ? ? ? ? . 118 ASP A CA 2351 ATOM 983 C C . ASP A 2351 118 . 7.697 -26.025 14.164 1.00 13.30 ? ? ? ? ? . 118 ASP A C 2351 ATOM 984 O O . ASP A 2351 118 . 6.772 -26.787 13.955 1.00 12.97 ? ? ? ? ? . 118 ASP A O 2351 ATOM 985 C CB . ASP A 2351 118 . 9.665 -25.950 12.628 1.00 13.67 ? ? ? ? ? . 118 ASP A CB 2351 ATOM 986 C CG . ASP A 2351 118 . 10.195 -25.494 11.295 1.00 14.35 ? ? ? ? ? . 118 ASP A CG 2351 ATOM 987 O OD1 . ASP A 2351 118 . 9.479 -24.785 10.536 1.00 13.29 ? ? ? ? ? . 118 ASP A OD1 2351 ATOM 988 O OD2 . ASP A 2351 118 . 11.353 -25.828 11.017 1.00 16.07 ? ? ? ? ? 1- 118 ASP A OD2 2351 ATOM 989 N N . THR A 2351 119 . 8.191 -25.774 15.372 1.00 13.59 ? ? ? ? ? . 119 THR A N 2351 ATOM 990 C CA . THR A 2351 119 . 7.739 -26.479 16.573 1.00 13.80 ? ? ? ? ? . 119 THR A CA 2351 ATOM 991 C C . THR A 2351 119 . 6.693 -25.695 17.356 1.00 13.84 ? ? ? ? ? . 119 THR A C 2351 ATOM 992 O O . THR A 2351 119 . 6.050 -26.256 18.241 1.00 15.00 ? ? ? ? ? . 119 THR A O 2351 ATOM 993 C CB . THR A 2351 119 . 8.912 -26.737 17.531 1.00 14.43 ? ? ? ? ? . 119 THR A CB 2351 ATOM 994 C CG2 . THR A 2351 119 . 10.039 -27.489 16.838 1.00 16.16 ? ? ? ? ? . 119 THR A CG2 2351 ATOM 995 O OG1 . THR A 2351 119 . 9.392 -25.493 18.029 1.00 14.78 ? ? ? ? ? . 119 THR A OG1 2351 ATOM 996 N N . GLY A 2351 120 . 6.550 -24.410 17.051 1.00 13.31 ? ? ? ? ? . 120 GLY A N 2351 ATOM 997 C CA . GLY A 2351 120 . 5.745 -23.482 17.845 1.00 15.55 ? ? ? ? ? . 120 GLY A CA 2351 ATOM 998 C C . GLY A 2351 120 . 6.291 -23.172 19.227 1.00 15.73 ? ? ? ? ? . 120 GLY A C 2351 ATOM 999 O O . GLY A 2351 120 . 5.607 -22.535 20.029 1.00 18.55 ? ? ? ? ? . 120 GLY A O 2351 ATOM 1000 N N . ALA A 2351 121 . 7.522 -23.581 19.519 1.00 15.46 ? ? ? ? ? . 121 ALA A N 2351 ATOM 1001 C CA . ALA A 2351 121 . 8.064 -23.394 20.865 1.00 15.87 ? ? ? ? ? . 121 ALA A CA 2351 ATOM 1002 C C . ALA A 2351 121 . 8.213 -21.904 21.136 1.00 15.57 ? ? ? ? ? . 121 ALA A C 2351 ATOM 1003 O O . ALA A 2351 121 . 8.585 -21.138 20.241 1.00 13.38 ? ? ? ? ? . 121 ALA A O 2351 ATOM 1004 C CB . ALA A 2351 121 . 9.389 -24.104 21.016 1.00 16.46 ? ? ? ? ? . 121 ALA A CB 2351 ATOM 1005 N N . ILE A 2351 122 . 7.880 -21.483 22.353 1.00 15.28 ? ? ? ? ? . 122 ILE A N 2351 ATOM 1006 C CA . ILE A 2351 122 . 8.156 -20.104 22.776 1.00 14.91 ? ? ? ? ? . 122 ILE A CA 2351 ATOM 1007 C C . ILE A 2351 122 . 9.641 -20.062 23.119 1.00 15.51 ? ? ? ? ? . 122 ILE A C 2351 ATOM 1008 O O . ILE A 2351 122 . 10.119 -20.875 23.900 1.00 16.67 ? ? ? ? ? . 122 ILE A O 2351 ATOM 1009 C CB . ILE A 2351 122 . 7.290 -19.669 23.961 1.00 15.79 ? ? ? ? ? . 122 ILE A CB 2351 ATOM 1010 C CG1 . ILE A 2351 122 . 5.823 -19.696 23.552 1.00 17.18 ? ? ? ? ? . 122 ILE A CG1 2351 ATOM 1011 C CG2 . ILE A 2351 122 . 7.689 -18.266 24.434 1.00 17.48 ? ? ? ? ? . 122 ILE A CG2 2351 ATOM 1012 C CD1 . ILE A 2351 122 . 4.864 -19.526 24.708 1.00 17.88 ? ? ? ? ? . 122 ILE A CD1 2351 ATOM 1013 N N A ILE A 2351 123 . 10.392 -19.155 22.503 0.47 13.95 ? ? ? ? ? . 123 ILE A N 2351 ATOM 1014 N N B ILE A 2351 123 . 10.323 -19.113 22.485 0.53 15.23 ? ? ? ? ? . 123 ILE A N 2351 ATOM 1015 C CA A ILE A 2351 123 . 11.809 -18.977 22.850 0.47 14.95 ? ? ? ? ? . 123 ILE A CA 2351 ATOM 1016 C CA B ILE A 2351 123 . 11.762 -18.894 22.572 0.53 17.28 ? ? ? ? ? . 123 ILE A CA 2351 ATOM 1017 C C A ILE A 2351 123 . 12.170 -17.581 23.356 0.47 15.02 ? ? ? ? ? . 123 ILE A C 2351 ATOM 1018 C C B ILE A 2351 123 . 12.096 -17.681 23.473 0.53 16.15 ? ? ? ? ? . 123 ILE A C 2351 ATOM 1019 O O A ILE A 2351 123 . 13.349 -17.281 23.543 0.47 15.33 ? ? ? ? ? . 123 ILE A O 2351 ATOM 1020 O O B ILE A 2351 123 . 13.152 -17.646 24.107 0.53 15.98 ? ? ? ? ? . 123 ILE A O 2351 ATOM 1021 C CB A ILE A 2351 123 . 12.723 -19.369 21.683 0.47 14.78 ? ? ? ? ? . 123 ILE A CB 2351 ATOM 1022 C CB B ILE A 2351 123 . 12.330 -18.807 21.116 0.53 19.50 ? ? ? ? ? . 123 ILE A CB 2351 ATOM 1023 C CG1 A ILE A 2351 123 . 12.353 -18.591 20.417 0.47 14.37 ? ? ? ? ? . 123 ILE A CG1 2351 ATOM 1024 C CG2 A ILE A 2351 123 . 12.618 -20.868 21.444 0.47 15.29 ? ? ? ? ? . 123 ILE A CG2 2351 ATOM 1025 C CG1 B ILE A 2351 123 . 13.033 -20.116 20.737 0.53 21.28 ? ? ? ? ? . 123 ILE A CG1 2351 ATOM 1026 C CG2 B ILE A 2351 123 . 13.317 -17.675 20.906 0.53 20.71 ? ? ? ? ? . 123 ILE A CG2 2351 ATOM 1027 C CD1 A ILE A 2351 123 . 13.153 -19.012 19.200 0.47 14.19 ? ? ? ? ? . 123 ILE A CD1 2351 ATOM 1028 C CD1 B ILE A 2351 123 . 12.135 -21.339 20.747 0.53 22.34 ? ? ? ? ? . 123 ILE A CD1 2351 ATOM 1029 N N . GLY A 2351 124 . 11.173 -16.729 23.568 1.00 15.77 ? ? ? ? ? . 124 GLY A N 2351 ATOM 1030 C CA . GLY A 2351 124 . 11.373 -15.508 24.323 1.00 15.97 ? ? ? ? ? . 124 GLY A CA 2351 ATOM 1031 C C . GLY A 2351 124 . 10.096 -14.707 24.394 1.00 15.46 ? ? ? ? ? . 124 GLY A C 2351 ATOM 1032 O O . GLY A 2351 124 . 9.193 -14.882 23.581 1.00 15.31 ? ? ? ? ? . 124 GLY A O 2351 ATOM 1033 N N . THR A 2351 125 . 10.008 -13.856 25.405 1.00 14.42 ? ? ? ? ? . 125 THR A N 2351 ATOM 1034 C CA . THR A 2351 125 . 8.920 -12.890 25.529 1.00 14.27 ? ? ? ? ? . 125 THR A CA 2351 ATOM 1035 C C . THR A 2351 125 . 9.371 -11.431 25.677 1.00 14.34 ? ? ? ? ? . 125 THR A C 2351 ATOM 1036 O O . THR A 2351 125 . 8.520 -10.535 25.770 1.00 13.54 ? ? ? ? ? . 125 THR A O 2351 ATOM 1037 C CB . THR A 2351 125 . 8.063 -13.230 26.766 1.00 15.10 ? ? ? ? ? . 125 THR A CB 2351 ATOM 1038 C CG2 . THR A 2351 125 . 7.560 -14.673 26.687 1.00 15.56 ? ? ? ? ? . 125 THR A CG2 2351 ATOM 1039 O OG1 . THR A 2351 125 . 8.859 -13.073 27.951 1.00 15.70 ? ? ? ? ? . 125 THR A OG1 2351 ATOM 1040 N N A GLN A 2351 126 . 10.689 -11.200 25.676 0.65 15.74 ? ? ? ? ? . 126 GLN A N 2351 ATOM 1041 N N B GLN A 2351 126 . 10.683 -11.184 25.692 0.35 15.08 ? ? ? ? ? . 126 GLN A N 2351 ATOM 1042 C CA A GLN A 2351 126 . 11.267 -9.893 25.996 0.65 16.74 ? ? ? ? ? . 126 GLN A CA 2351 ATOM 1043 C CA B GLN A 2351 126 . 11.214 -9.851 25.975 0.35 15.65 ? ? ? ? ? . 126 GLN A CA 2351 ATOM 1044 C C A GLN A 2351 126 . 11.938 -9.209 24.799 0.65 16.96 ? ? ? ? ? . 126 GLN A C 2351 ATOM 1045 C C B GLN A 2351 126 . 11.948 -9.214 24.801 0.35 16.17 ? ? ? ? ? . 126 GLN A C 2351 ATOM 1046 O O A GLN A 2351 126 . 12.672 -8.231 24.982 0.65 18.20 ? ? ? ? ? . 126 GLN A O 2351 ATOM 1047 O O B GLN A 2351 126 . 12.738 -8.285 25.009 0.35 17.02 ? ? ? ? ? . 126 GLN A O 2351 ATOM 1048 C CB A GLN A 2351 126 . 12.281 -10.056 27.137 0.65 17.82 ? ? ? ? ? . 126 GLN A CB 2351 ATOM 1049 C CB B GLN A 2351 126 . 12.138 -9.924 27.186 0.35 15.92 ? ? ? ? ? . 126 GLN A CB 2351 ATOM 1050 C CG A GLN A 2351 126 . 11.700 -10.649 28.418 0.65 19.05 ? ? ? ? ? . 126 GLN A CG 2351 ATOM 1051 C CG B GLN A 2351 126 . 11.370 -10.101 28.485 0.35 16.11 ? ? ? ? ? . 126 GLN A CG 2351 ATOM 1052 C CD A GLN A 2351 126 . 10.613 -9.780 29.040 0.65 21.28 ? ? ? ? ? . 126 GLN A CD 2351 ATOM 1053 C CD B GLN A 2351 126 . 12.269 -10.217 29.694 0.35 16.65 ? ? ? ? ? . 126 GLN A CD 2351 ATOM 1054 N NE2 A GLN A 2351 126 . 9.365 -10.244 28.979 0.65 21.64 ? ? ? ? ? . 126 GLN A NE2 2351 ATOM 1055 O OE1 A GLN A 2351 126 . 10.896 -8.711 29.578 0.65 24.99 ? ? ? ? ? . 126 GLN A OE1 2351 ATOM 1056 N NE2 B GLN A 2351 126 . 12.111 -9.296 30.636 0.35 16.48 ? ? ? ? ? . 126 GLN A NE2 2351 ATOM 1057 O OE1 B GLN A 2351 126 . 13.085 -11.133 29.790 0.35 16.80 ? ? ? ? ? . 126 GLN A OE1 2351 ATOM 1058 N N . ALA A 2351 127 . 11.681 -9.681 23.580 1.00 16.07 ? ? ? ? ? . 127 ALA A N 2351 ATOM 1059 C CA . ALA A 2351 127 . 12.365 -9.138 22.395 1.00 15.77 ? ? ? ? ? . 127 ALA A CA 2351 ATOM 1060 C C . ALA A 2351 127 . 12.118 -7.629 22.136 1.00 16.92 ? ? ? ? ? . 127 ALA A C 2351 ATOM 1061 O O . ALA A 2351 127 . 12.988 -6.961 21.574 1.00 16.61 ? ? ? ? ? . 127 ALA A O 2351 ATOM 1062 C CB . ALA A 2351 127 . 12.088 -9.962 21.152 1.00 15.60 ? ? ? ? ? . 127 ALA A CB 2351 ATOM 1063 N N A ARG A 2351 128 . 10.956 -7.112 22.537 0.56 17.01 ? ? ? ? ? . 128 ARG A N 2351 ATOM 1064 N N B ARG A 2351 128 . 10.970 -7.103 22.563 0.44 16.65 ? ? ? ? ? . 128 ARG A N 2351 ATOM 1065 C CA A ARG A 2351 128 . 10.675 -5.662 22.452 0.56 17.35 ? ? ? ? ? . 128 ARG A CA 2351 ATOM 1066 C CA B ARG A 2351 128 . 10.711 -5.658 22.477 0.44 16.75 ? ? ? ? ? . 128 ARG A CA 2351 ATOM 1067 C C A ARG A 2351 128 . 11.742 -4.852 23.213 0.56 17.98 ? ? ? ? ? . 128 ARG A C 2351 ATOM 1068 C C B ARG A 2351 128 . 11.832 -4.909 23.210 0.44 17.06 ? ? ? ? ? . 128 ARG A C 2351 ATOM 1069 O O A ARG A 2351 128 . 12.117 -3.754 22.795 0.56 19.74 ? ? ? ? ? . 128 ARG A O 2351 ATOM 1070 O O B ARG A 2351 128 . 12.397 -3.949 22.691 0.44 18.15 ? ? ? ? ? . 128 ARG A O 2351 ATOM 1071 C CB A ARG A 2351 128 . 9.263 -5.347 22.979 0.56 17.73 ? ? ? ? ? . 128 ARG A CB 2351 ATOM 1072 C CB B ARG A 2351 128 . 9.339 -5.312 23.066 0.44 16.87 ? ? ? ? ? . 128 ARG A CB 2351 ATOM 1073 C CG A ARG A 2351 128 . 8.870 -3.865 23.016 0.56 18.71 ? ? ? ? ? . 128 ARG A CG 2351 ATOM 1074 C CG B ARG A 2351 128 . 8.901 -3.861 22.874 0.44 17.49 ? ? ? ? ? . 128 ARG A CG 2351 ATOM 1075 C CD A ARG A 2351 128 . 9.128 -3.215 24.373 0.56 20.16 ? ? ? ? ? . 128 ARG A CD 2351 ATOM 1076 C CD B ARG A 2351 128 . 9.642 -2.916 23.804 0.44 18.39 ? ? ? ? ? . 128 ARG A CD 2351 ATOM 1077 N NE A ARG A 2351 128 . 8.614 -1.848 24.461 0.56 21.19 ? ? ? ? ? . 128 ARG A NE 2351 ATOM 1078 N NE B ARG A 2351 128 . 9.174 -1.532 23.713 0.44 18.67 ? ? ? ? ? . 128 ARG A NE 2351 ATOM 1079 C CZ A ARG A 2351 128 . 9.152 -0.774 23.876 0.56 22.12 ? ? ? ? ? . 128 ARG A CZ 2351 ATOM 1080 C CZ B ARG A 2351 128 . 8.307 -0.973 24.557 0.44 18.88 ? ? ? ? ? . 128 ARG A CZ 2351 ATOM 1081 N NH1 A ARG A 2351 128 . 10.245 -0.862 23.118 0.56 21.19 ? ? ? ? ? 1+ 128 ARG A NH1 2351 ATOM 1082 N NH2 A ARG A 2351 128 . 8.582 0.419 24.051 0.56 22.67 ? ? ? ? ? . 128 ARG A NH2 2351 ATOM 1083 N NH1 B ARG A 2351 128 . 7.788 -1.677 25.551 0.44 18.59 ? ? ? ? ? 1+ 128 ARG A NH1 2351 ATOM 1084 N NH2 B ARG A 2351 128 . 7.951 0.296 24.402 0.44 19.51 ? ? ? ? ? . 128 ARG A NH2 2351 ATOM 1085 N N A THR A 2351 129 . 12.197 -5.402 24.338 0.56 16.60 ? ? ? ? ? . 129 THR A N 2351 ATOM 1086 N N B THR A 2351 129 . 12.172 -5.391 24.401 0.44 16.19 ? ? ? ? ? . 129 THR A N 2351 ATOM 1087 C CA A THR A 2351 129 . 13.260 -4.819 25.151 0.56 15.90 ? ? ? ? ? . 129 THR A CA 2351 ATOM 1088 C CA B THR A 2351 129 . 13.262 -4.829 25.190 0.44 15.82 ? ? ? ? ? . 129 THR A CA 2351 ATOM 1089 C C A THR A 2351 129 . 14.648 -5.072 24.556 0.56 15.75 ? ? ? ? ? . 129 THR A C 2351 ATOM 1090 C C B THR A 2351 129 . 14.652 -5.082 24.590 0.44 15.77 ? ? ? ? ? . 129 THR A C 2351 ATOM 1091 O O A THR A 2351 129 . 15.501 -4.173 24.523 0.56 14.19 ? ? ? ? ? . 129 THR A O 2351 ATOM 1092 O O B THR A 2351 129 . 15.508 -4.188 24.583 0.44 14.57 ? ? ? ? ? . 129 THR A O 2351 ATOM 1093 C CB A THR A 2351 129 . 13.199 -5.413 26.563 0.56 16.22 ? ? ? ? ? . 129 THR A CB 2351 ATOM 1094 C CB B THR A 2351 129 . 13.239 -5.411 26.607 0.44 16.28 ? ? ? ? ? . 129 THR A CB 2351 ATOM 1095 C CG2 A THR A 2351 129 . 14.194 -4.750 27.499 0.56 16.27 ? ? ? ? ? . 129 THR A CG2 2351 ATOM 1096 O OG1 A THR A 2351 129 . 11.866 -5.240 27.067 0.56 15.54 ? ? ? ? ? . 129 THR A OG1 2351 ATOM 1097 C CG2 B THR A 2351 129 . 14.425 -4.927 27.397 0.44 16.31 ? ? ? ? ? . 129 THR A CG2 2351 ATOM 1098 O OG1 B THR A 2351 129 . 12.025 -5.011 27.257 0.44 16.08 ? ? ? ? ? . 129 THR A OG1 2351 ATOM 1099 N N . ARG A 2351 130 . 14.877 -6.301 24.106 1.00 15.66 ? ? ? ? ? . 130 ARG A N 2351 ATOM 1100 C CA . ARG A 2351 130 . 16.188 -6.692 23.577 1.00 16.35 ? ? ? ? ? . 130 ARG A CA 2351 ATOM 1101 C C . ARG A 2351 130 . 16.559 -5.897 22.320 1.00 15.65 ? ? ? ? ? . 130 ARG A C 2351 ATOM 1102 O O . ARG A 2351 130 . 17.720 -5.558 22.136 1.00 15.70 ? ? ? ? ? . 130 ARG A O 2351 ATOM 1103 C CB . ARG A 2351 130 . 16.246 -8.188 23.306 1.00 18.25 ? ? ? ? ? . 130 ARG A CB 2351 ATOM 1104 C CG . ARG A 2351 130 . 16.058 -9.052 24.544 1.00 20.23 ? ? ? ? ? . 130 ARG A CG 2351 ATOM 1105 C CD . ARG A 2351 130 . 17.267 -9.045 25.461 1.00 24.15 ? ? ? ? ? . 130 ARG A CD 2351 ATOM 1106 N NE . ARG A 2351 130 . 16.962 -9.671 26.747 1.00 26.08 ? ? ? ? ? . 130 ARG A NE 2351 ATOM 1107 C CZ . ARG A 2351 130 . 16.384 -9.059 27.784 1.00 29.65 ? ? ? ? ? . 130 ARG A CZ 2351 ATOM 1108 N NH1 . ARG A 2351 130 . 15.999 -7.782 27.725 1.00 30.49 ? ? ? ? ? 1+ 130 ARG A NH1 2351 ATOM 1109 N NH2 . ARG A 2351 130 . 16.171 -9.748 28.906 1.00 33.51 ? ? ? ? ? . 130 ARG A NH2 2351 ATOM 1110 N N . VAL A 2351 131 . 15.561 -5.570 21.501 1.00 15.55 ? ? ? ? ? . 131 VAL A N 2351 ATOM 1111 C CA . VAL A 2351 131 . 15.755 -4.735 20.300 1.00 16.06 ? ? ? ? ? . 131 VAL A CA 2351 ATOM 1112 C C . VAL A 2351 131 . 16.319 -3.355 20.678 1.00 15.16 ? ? ? ? ? . 131 VAL A C 2351 ATOM 1113 O O . VAL A 2351 131 . 17.149 -2.806 19.958 1.00 14.17 ? ? ? ? ? . 131 VAL A O 2351 ATOM 1114 C CB . VAL A 2351 131 . 14.431 -4.608 19.503 1.00 18.89 ? ? ? ? ? . 131 VAL A CB 2351 ATOM 1115 C CG1 . VAL A 2351 131 . 14.491 -3.492 18.465 1.00 19.08 ? ? ? ? ? . 131 VAL A CG1 2351 ATOM 1116 C CG2 . VAL A 2351 131 . 14.079 -5.950 18.859 1.00 21.65 ? ? ? ? ? . 131 VAL A CG2 2351 ATOM 1117 N N A ILE A 2351 132 . 15.856 -2.817 21.806 0.19 15.13 ? ? ? ? ? . 132 ILE A N 2351 ATOM 1118 N N B ILE A 2351 132 . 15.884 -2.809 21.816 0.81 15.27 ? ? ? ? ? . 132 ILE A N 2351 ATOM 1119 C CA A ILE A 2351 132 . 16.341 -1.547 22.332 0.19 15.00 ? ? ? ? ? . 132 ILE A CA 2351 ATOM 1120 C CA B ILE A 2351 132 . 16.395 -1.520 22.293 0.81 14.70 ? ? ? ? ? . 132 ILE A CA 2351 ATOM 1121 C C A ILE A 2351 132 . 17.808 -1.612 22.736 0.19 14.96 ? ? ? ? ? . 132 ILE A C 2351 ATOM 1122 C C B ILE A 2351 132 . 17.849 -1.630 22.707 0.81 14.54 ? ? ? ? ? . 132 ILE A C 2351 ATOM 1123 O O A ILE A 2351 132 . 18.613 -0.783 22.313 0.19 14.79 ? ? ? ? ? . 132 ILE A O 2351 ATOM 1124 O O B ILE A 2351 132 . 18.686 -0.831 22.296 0.81 13.48 ? ? ? ? ? . 132 ILE A O 2351 ATOM 1125 C CB A ILE A 2351 132 . 15.520 -1.130 23.564 0.19 14.92 ? ? ? ? ? . 132 ILE A CB 2351 ATOM 1126 C CB B ILE A 2351 132 . 15.575 -0.974 23.489 0.81 14.72 ? ? ? ? ? . 132 ILE A CB 2351 ATOM 1127 C CG1 A ILE A 2351 132 . 14.034 -1.319 23.280 0.19 15.02 ? ? ? ? ? . 132 ILE A CG1 2351 ATOM 1128 C CG2 A ILE A 2351 132 . 15.824 0.307 23.942 0.19 14.66 ? ? ? ? ? . 132 ILE A CG2 2351 ATOM 1129 C CG1 B ILE A 2351 132 . 14.149 -0.656 23.059 0.81 15.47 ? ? ? ? ? . 132 ILE A CG1 2351 ATOM 1130 C CG2 B ILE A 2351 132 . 16.235 0.255 24.089 0.81 13.99 ? ? ? ? ? . 132 ILE A CG2 2351 ATOM 1131 C CD1 A ILE A 2351 132 . 13.567 -0.581 22.051 0.19 15.23 ? ? ? ? ? . 132 ILE A CD1 2351 ATOM 1132 C CD1 B ILE A 2351 132 . 13.182 -0.605 24.230 0.81 16.62 ? ? ? ? ? . 132 ILE A CD1 2351 ATOM 1133 N N . GLU A 2351 133 . 18.144 -2.599 23.559 1.00 14.85 ? ? ? ? ? . 133 GLU A N 2351 ATOM 1134 C CA . GLU A 2351 133 . 19.500 -2.725 24.095 1.00 15.86 ? ? ? ? ? . 133 GLU A CA 2351 ATOM 1135 C C . GLU A 2351 133 . 20.510 -3.300 23.114 1.00 15.18 ? ? ? ? ? . 133 GLU A C 2351 ATOM 1136 O O . GLU A 2351 133 . 21.694 -3.025 23.243 1.00 14.71 ? ? ? ? ? . 133 GLU A O 2351 ATOM 1137 C CB . GLU A 2351 133 . 19.516 -3.523 25.385 1.00 18.34 ? ? ? ? ? . 133 GLU A CB 2351 ATOM 1138 C CG . GLU A 2351 133 . 19.099 -4.959 25.269 1.00 21.00 ? ? ? ? ? . 133 GLU A CG 2351 ATOM 1139 C CD . GLU A 2351 133 . 19.009 -5.600 26.628 1.00 24.62 ? ? ? ? ? . 133 GLU A CD 2351 ATOM 1140 O OE1 . GLU A 2351 133 . 17.888 -5.653 27.182 1.00 24.54 ? ? ? ? ? . 133 GLU A OE1 2351 ATOM 1141 O OE2 . GLU A 2351 133 . 20.070 -6.015 27.133 1.00 24.87 ? ? ? ? ? 1- 133 GLU A OE2 2351 ATOM 1142 N N . ASP A 2351 134 . 20.031 -4.102 22.163 1.00 15.80 ? ? ? ? ? . 134 ASP A N 2351 ATOM 1143 C CA . ASP A 2351 134 . 20.885 -4.847 21.228 1.00 16.53 ? ? ? ? ? . 134 ASP A CA 2351 ATOM 1144 C C . ASP A 2351 134 . 20.373 -4.627 19.798 1.00 16.35 ? ? ? ? ? . 134 ASP A C 2351 ATOM 1145 O O . ASP A 2351 134 . 19.922 -5.562 19.131 1.00 16.33 ? ? ? ? ? . 134 ASP A O 2351 ATOM 1146 C CB . ASP A 2351 134 . 20.881 -6.341 21.606 1.00 16.03 ? ? ? ? ? . 134 ASP A CB 2351 ATOM 1147 C CG . ASP A 2351 134 . 21.859 -7.184 20.769 1.00 16.81 ? ? ? ? ? . 134 ASP A CG 2351 ATOM 1148 O OD1 . ASP A 2351 134 . 22.869 -6.642 20.264 1.00 16.39 ? ? ? ? ? . 134 ASP A OD1 2351 ATOM 1149 O OD2 . ASP A 2351 134 . 21.614 -8.404 20.635 1.00 16.25 ? ? ? ? ? 1- 134 ASP A OD2 2351 ATOM 1150 N N . PRO A 2351 135 . 20.451 -3.379 19.309 1.00 15.65 ? ? ? ? ? . 135 PRO A N 2351 ATOM 1151 C CA . PRO A 2351 135 . 19.917 -3.103 17.962 1.00 16.45 ? ? ? ? ? . 135 PRO A CA 2351 ATOM 1152 C C . PRO A 2351 135 . 20.699 -3.798 16.828 1.00 17.49 ? ? ? ? ? . 135 PRO A C 2351 ATOM 1153 O O . PRO A 2351 135 . 20.164 -3.961 15.727 1.00 19.27 ? ? ? ? ? . 135 PRO A O 2351 ATOM 1154 C CB . PRO A 2351 135 . 20.036 -1.580 17.849 1.00 16.15 ? ? ? ? ? . 135 PRO A CB 2351 ATOM 1155 C CG . PRO A 2351 135 . 21.147 -1.228 18.767 1.00 15.72 ? ? ? ? ? . 135 PRO A CG 2351 ATOM 1156 C CD . PRO A 2351 135 . 21.003 -2.165 19.931 1.00 16.34 ? ? ? ? ? . 135 PRO A CD 2351 ATOM 1157 N N . ASP A 2351 136 . 21.943 -4.192 17.089 1.00 18.50 ? ? ? ? ? . 136 ASP A N 2351 ATOM 1158 C CA . ASP A 2351 136 . 22.709 -4.962 16.102 1.00 18.72 ? ? ? ? ? . 136 ASP A CA 2351 ATOM 1159 C C . ASP A 2351 136 . 22.475 -6.472 16.207 1.00 19.15 ? ? ? ? ? . 136 ASP A C 2351 ATOM 1160 O O . ASP A 2351 136 . 23.067 -7.249 15.446 1.00 18.36 ? ? ? ? ? . 136 ASP A O 2351 ATOM 1161 C CB . ASP A 2351 136 . 24.208 -4.659 16.203 1.00 19.68 ? ? ? ? ? . 136 ASP A CB 2351 ATOM 1162 C CG . ASP A 2351 136 . 24.951 -5.002 14.926 1.00 20.65 ? ? ? ? ? . 136 ASP A CG 2351 ATOM 1163 O OD1 . ASP A 2351 136 . 24.302 -4.958 13.849 1.00 19.34 ? ? ? ? ? . 136 ASP A OD1 2351 ATOM 1164 O OD2 . ASP A 2351 136 . 26.167 -5.316 14.990 1.00 18.99 ? ? ? ? ? 1- 136 ASP A OD2 2351 ATOM 1165 N N . GLY A 2351 137 . 21.644 -6.897 17.152 1.00 19.37 ? ? ? ? ? . 137 GLY A N 2351 ATOM 1166 C CA . GLY A 2351 137 . 21.276 -8.295 17.269 1.00 18.65 ? ? ? ? ? . 137 GLY A CA 2351 ATOM 1167 C C . GLY A 2351 137 . 22.434 -9.246 17.520 1.00 18.62 ? ? ? ? ? . 137 GLY A C 2351 ATOM 1168 O O . GLY A 2351 137 . 22.362 -10.405 17.126 1.00 17.20 ? ? ? ? ? . 137 GLY A O 2351 ATOM 1169 N N . ALA A 2351 138 . 23.489 -8.772 18.186 1.00 18.23 ? ? ? ? ? . 138 ALA A N 2351 ATOM 1170 C CA . ALA A 2351 138 . 24.618 -9.638 18.572 1.00 18.91 ? ? ? ? ? . 138 ALA A CA 2351 ATOM 1171 C C . ALA A 2351 138 . 24.172 -10.873 19.359 1.00 18.87 ? ? ? ? ? . 138 ALA A C 2351 ATOM 1172 O O . ALA A 2351 138 . 24.763 -11.937 19.209 1.00 18.45 ? ? ? ? ? . 138 ALA A O 2351 ATOM 1173 C CB . ALA A 2351 138 . 25.646 -8.865 19.388 1.00 19.07 ? ? ? ? ? . 138 ALA A CB 2351 ATOM 1174 N N . ASN A 2351 139 . 23.150 -10.721 20.207 1.00 17.91 ? ? ? ? ? . 139 ASN A N 2351 ATOM 1175 C CA . ASN A 2351 139 . 22.657 -11.826 21.042 1.00 18.78 ? ? ? ? ? . 139 ASN A CA 2351 ATOM 1176 C C . ASN A 2351 139 . 21.320 -12.415 20.575 1.00 18.34 ? ? ? ? ? . 139 ASN A C 2351 ATOM 1177 O O . ASN A 2351 139 . 20.716 -13.222 21.284 1.00 16.63 ? ? ? ? ? . 139 ASN A O 2351 ATOM 1178 C CB . ASN A 2351 139 . 22.558 -11.357 22.493 1.00 20.43 ? ? ? ? ? . 139 ASN A CB 2351 ATOM 1179 C CG . ASN A 2351 139 . 23.907 -11.007 23.077 1.00 22.54 ? ? ? ? ? . 139 ASN A CG 2351 ATOM 1180 N ND2 . ASN A 2351 139 . 24.033 -9.800 23.604 1.00 24.70 ? ? ? ? ? . 139 ASN A ND2 2351 ATOM 1181 O OD1 . ASN A 2351 139 . 24.826 -11.813 23.049 1.00 25.00 ? ? ? ? ? . 139 ASN A OD1 2351 ATOM 1182 N N . PHE A 2351 140 . 20.862 -12.019 19.387 1.00 19.01 ? ? ? ? ? . 140 PHE A N 2351 ATOM 1183 C CA . PHE A 2351 140 . 19.669 -12.603 18.768 1.00 20.41 ? ? ? ? ? . 140 PHE A CA 2351 ATOM 1184 C C . PHE A 2351 140 . 19.812 -14.133 18.747 1.00 20.42 ? ? ? ? ? . 140 PHE A C 2351 ATOM 1185 O O . PHE A 2351 140 . 20.913 -14.633 18.513 1.00 17.90 ? ? ? ? ? . 140 PHE A O 2351 ATOM 1186 C CB . PHE A 2351 140 . 19.522 -12.084 17.327 1.00 21.52 ? ? ? ? ? . 140 PHE A CB 2351 ATOM 1187 C CG . PHE A 2351 140 . 18.452 -12.782 16.532 1.00 22.24 ? ? ? ? ? . 140 PHE A CG 2351 ATOM 1188 C CD1 . PHE A 2351 140 . 18.719 -13.998 15.901 1.00 21.67 ? ? ? ? ? . 140 PHE A CD1 2351 ATOM 1189 C CD2 . PHE A 2351 140 . 17.181 -12.252 16.440 1.00 21.18 ? ? ? ? ? . 140 PHE A CD2 2351 ATOM 1190 C CE1 . PHE A 2351 140 . 17.745 -14.662 15.185 1.00 20.84 ? ? ? ? ? . 140 PHE A CE1 2351 ATOM 1191 C CE2 . PHE A 2351 140 . 16.205 -12.923 15.721 1.00 21.80 ? ? ? ? ? . 140 PHE A CE2 2351 ATOM 1192 C CZ . PHE A 2351 140 . 16.490 -14.121 15.089 1.00 20.62 ? ? ? ? ? . 140 PHE A CZ 2351 ATOM 1193 N N . PRO A 2351 141 . 18.713 -14.878 18.978 1.00 19.68 ? ? ? ? ? . 141 PRO A N 2351 ATOM 1194 C CA . PRO A 2351 141 . 17.322 -14.496 19.270 1.00 20.19 ? ? ? ? ? . 141 PRO A CA 2351 ATOM 1195 C C . PRO A 2351 141 . 17.031 -14.317 20.773 1.00 20.52 ? ? ? ? ? . 141 PRO A C 2351 ATOM 1196 O O . PRO A 2351 141 . 15.896 -14.485 21.219 1.00 20.28 ? ? ? ? ? . 141 PRO A O 2351 ATOM 1197 C CB . PRO A 2351 141 . 16.531 -15.649 18.667 1.00 20.58 ? ? ? ? ? . 141 PRO A CB 2351 ATOM 1198 C CG . PRO A 2351 141 . 17.408 -16.822 18.883 1.00 22.19 ? ? ? ? ? . 141 PRO A CG 2351 ATOM 1199 C CD . PRO A 2351 141 . 18.835 -16.342 18.841 1.00 21.97 ? ? ? ? ? . 141 PRO A CD 2351 ATOM 1200 N N . TRP A 2351 142 . 18.070 -13.962 21.521 1.00 19.76 ? ? ? ? ? . 142 TRP A N 2351 ATOM 1201 C CA . TRP A 2351 142 . 17.983 -13.534 22.901 1.00 21.33 ? ? ? ? ? . 142 TRP A CA 2351 ATOM 1202 C C . TRP A 2351 142 . 17.420 -14.620 23.822 1.00 25.77 ? ? ? ? ? . 142 TRP A C 2351 ATOM 1203 O O . TRP A 2351 142 . 16.345 -14.426 24.421 1.00 25.77 ? ? ? ? ? . 142 TRP A O 2351 ATOM 1204 C CB . TRP A 2351 142 . 17.210 -12.224 23.014 1.00 19.99 ? ? ? ? ? . 142 TRP A CB 2351 ATOM 1205 C CG . TRP A 2351 142 . 17.778 -11.119 22.165 1.00 18.70 ? ? ? ? ? . 142 TRP A CG 2351 ATOM 1206 C CD1 . TRP A 2351 142 . 18.994 -10.522 22.306 1.00 18.19 ? ? ? ? ? . 142 TRP A CD1 2351 ATOM 1207 C CD2 . TRP A 2351 142 . 17.132 -10.461 21.076 1.00 17.96 ? ? ? ? ? . 142 TRP A CD2 2351 ATOM 1208 C CE2 . TRP A 2351 142 . 18.022 -9.480 20.595 1.00 18.04 ? ? ? ? ? . 142 TRP A CE2 2351 ATOM 1209 C CE3 . TRP A 2351 142 . 15.890 -10.610 20.454 1.00 18.59 ? ? ? ? ? . 142 TRP A CE3 2351 ATOM 1210 N NE1 . TRP A 2351 142 . 19.156 -9.555 21.357 1.00 17.87 ? ? ? ? ? . 142 TRP A NE1 2351 ATOM 1211 C CZ2 . TRP A 2351 142 . 17.711 -8.645 19.516 1.00 17.55 ? ? ? ? ? . 142 TRP A CZ2 2351 ATOM 1212 C CZ3 . TRP A 2351 142 . 15.574 -9.787 19.397 1.00 19.05 ? ? ? ? ? . 142 TRP A CZ3 2351 ATOM 1213 C CH2 . TRP A 2351 142 . 16.486 -8.803 18.938 1.00 18.51 ? ? ? ? ? . 142 TRP A CH2 2351 ATOM 1214 N N A PRO A 2351 143 . 18.105 -15.758 23.889 0.43 25.91 ? ? ? ? ? . 143 PRO A N 2351 ATOM 1215 N N B PRO A 2351 143 . 18.145 -15.709 23.950 0.57 28.56 ? ? ? ? ? . 143 PRO A N 2351 ATOM 1216 C CA A PRO A 2351 143 . 17.728 -16.750 24.895 0.43 26.55 ? ? ? ? ? . 143 PRO A CA 2351 ATOM 1217 C CA B PRO A 2351 143 . 17.683 -16.682 24.925 0.57 30.66 ? ? ? ? ? . 143 PRO A CA 2351 ATOM 1218 C C A PRO A 2351 143 . 18.114 -16.109 26.241 0.43 27.90 ? ? ? ? ? . 143 PRO A C 2351 ATOM 1219 C C B PRO A 2351 143 . 18.148 -16.217 26.307 0.57 33.98 ? ? ? ? ? . 143 PRO A C 2351 ATOM 1220 O O A PRO A 2351 143 . 19.033 -15.280 26.295 0.43 29.57 ? ? ? ? ? . 143 PRO A O 2351 ATOM 1221 O O B PRO A 2351 143 . 17.516 -16.577 27.281 0.57 40.90 ? ? ? ? ? . 143 PRO A O 2351 ATOM 1222 C CB A PRO A 2351 143 . 18.662 -17.907 24.589 0.43 26.47 ? ? ? ? ? . 143 PRO A CB 2351 ATOM 1223 C CB B PRO A 2351 143 . 18.464 -17.930 24.540 0.57 31.72 ? ? ? ? ? . 143 PRO A CB 2351 ATOM 1224 C CG A PRO A 2351 143 . 19.869 -17.262 24.025 0.43 27.23 ? ? ? ? ? . 143 PRO A CG 2351 ATOM 1225 C CG B PRO A 2351 143 . 19.714 -17.418 23.925 0.57 32.06 ? ? ? ? ? . 143 PRO A CG 2351 ATOM 1226 C CD A PRO A 2351 143 . 19.399 -16.061 23.265 0.43 26.55 ? ? ? ? ? . 143 PRO A CD 2351 ATOM 1227 C CD B PRO A 2351 143 . 19.334 -16.157 23.214 0.57 30.24 ? ? ? ? ? . 143 PRO A CD 2351 ATOM 1228 N N A ASN A 2351 144 . 17.447 -16.445 27.332 0.43 29.72 ? ? ? ? ? . 144 ASN A N 2351 ATOM 1229 N N B ASN A 2351 144 . 19.154 -15.333 26.349 0.57 43.48 ? ? ? ? ? . 144 ASN A N 2351 ATOM 1230 C CA A ASN A 2351 144 . 17.845 -15.794 28.584 0.43 31.67 ? ? ? ? ? . 144 ASN A CA 2351 ATOM 1231 C CA B ASN A 2351 144 . 19.879 -14.941 27.567 0.57 41.21 ? ? ? ? ? . 144 ASN A CA 2351 ATOM 1232 C C A ASN A 2351 144 . 19.155 -16.376 29.126 0.43 34.18 ? ? ? ? ? . 144 ASN A C 2351 ATOM 1233 C C B ASN A 2351 144 . 19.928 -16.021 28.652 0.57 46.68 ? ? ? ? ? . 144 ASN A C 2351 ATOM 1234 O O A ASN A 2351 144 . 19.292 -16.688 30.295 0.43 37.95 ? ? ? ? ? . 144 ASN A O 2351 ATOM 1235 O O B ASN A 2351 144 . 20.998 -16.385 29.101 0.57 44.85 ? ? ? ? ? . 144 ASN A O 2351 ATOM 1236 C CB A ASN A 2351 144 . 16.725 -15.785 29.643 0.43 31.33 ? ? ? ? ? . 144 ASN A CB 2351 ATOM 1237 C CB B ASN A 2351 144 . 19.766 -13.486 28.103 0.57 37.67 ? ? ? ? ? . 144 ASN A CB 2351 ATOM 1238 C CG A ASN A 2351 144 . 16.683 -14.482 30.437 0.43 30.34 ? ? ? ? ? . 144 ASN A CG 2351 ATOM 1239 C CG B ASN A 2351 144 . 18.456 -12.779 27.779 0.57 32.86 ? ? ? ? ? . 144 ASN A CG 2351 ATOM 1240 N ND2 A ASN A 2351 144 . 15.880 -14.449 31.481 0.43 29.27 ? ? ? ? ? . 144 ASN A ND2 2351 ATOM 1241 O OD1 A ASN A 2351 144 . 17.350 -13.516 30.096 0.43 30.43 ? ? ? ? ? . 144 ASN A OD1 2351 ATOM 1242 N ND2 B ASN A 2351 144 . 18.201 -12.534 26.509 0.57 28.80 ? ? ? ? ? . 144 ASN A ND2 2351 ATOM 1243 O OD1 B ASN A 2351 144 . 17.731 -12.384 28.685 0.57 29.27 ? ? ? ? ? . 144 ASN A OD1 2351 ATOM 1244 O OXT A ASN A 2351 144 . 20.133 -16.520 28.420 0.43 34.42 ? ? ? ? ? 1- 144 ASN A OXT 2351 ATOM 1245 O OXT B ASN A 2351 144 . 18.927 -16.583 29.037 0.57 53.68 ? ? ? ? ? 1- 144 ASN A OXT 2351 #