| 1l22 |
CONTRIBUTIONS OF LEFT-HANDED HELICAL RESIDUES TO THE STRUCTURE AND STABILITY OF BACTERIOPHAGE T4 LYSOZYME |
17.4 |
57.6 |
X-RAY DIFFRACTION |
GOOD
|
| 1l23 |
ENHANCED PROTEIN THERMOSTABILITY FROM SITE-DIRECTED MUTATIONS THAT DECREASE THE ENTROPY OF UNFOLDING |
17.5 |
58.2 |
X-RAY DIFFRACTION |
GOOD
|
| 1l24 |
ENHANCED PROTEIN THERMOSTABILITY FROM SITE-DIRECTED MUTATIONS THAT DECREASE THE ENTROPY OF UNFOLDING |
17.5 |
58.7 |
X-RAY DIFFRACTION |
GOOD
|
| 1l25 |
REPLACEMENTS OF PRO86 IN PHAGE T4 LYSOZYME EXTEND AN ALPHA-HELIX BUT DO NOT ALTER PROTEIN STABILITY |
17.5 |
58.1 |
X-RAY DIFFRACTION |
GOOD
|
| 1l26 |
REPLACEMENTS OF PRO86 IN PHAGE T4 LYSOZYME EXTEND AN ALPHA-HELIX BUT DO NOT ALTER PROTEIN STABILITY |
17.6 |
58.0 |
X-RAY DIFFRACTION |
GOOD
|
| 1l27 |
REPLACEMENTS OF PRO86 IN PHAGE T4 LYSOZYME EXTEND AN ALPHA-HELIX BUT DO NOT ALTER PROTEIN STABILITY |
17.6 |
58.2 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1l28 |
REPLACEMENTS OF PRO86 IN PHAGE T4 LYSOZYME EXTEND AN ALPHA-HELIX BUT DO NOT ALTER PROTEIN STABILITY |
17.5 |
58.7 |
X-RAY DIFFRACTION |
GOOD
|
| 1l29 |
REPLACEMENTS OF PRO86 IN PHAGE T4 LYSOZYME EXTEND AN ALPHA-HELIX BUT DO NOT ALTER PROTEIN STABILITY |
17.5 |
60.7 |
X-RAY DIFFRACTION |
GOOD
|
| 1l2a |
;The Crystal Structure and Catalytic Mechanism of Cellobiohydrolase CelS, the Major Enzymatic Component of the Clostridium thermocellum cellulosome
; |
49.5 |
157.5 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1l2b |
MutM (Fpg) DNA End-Product Structure |
21.3 |
67.1 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1l2c |
MutM (Fpg)-DNA Estranged Thymine Mismatch Recognition Complex |
21.1 |
67.1 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1l2d |
MutM (Fpg)-DNA Estranged Guanine Mismatch Recognition Complex |
21.1 |
66.4 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1l2e |
Human Kallikrein 6 (hK6) Active Form with benzamidine inhibitor |
17.5 |
54.6 |
X-RAY DIFFRACTION |
GOOD
|
| 1l2f |
Crystal structure of NusA from Thermotoga maritima: a structure-based role of the N-terminal domain |
34.3 |
120.9 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1l2g |
Structure of a C-terminally truncated form of glycoprotein D from HSV-1 |
57.7 |
164.4 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1l2h |
Crystal structure of Interleukin 1-beta F42W/W120F mutant |
16.1 |
51.4 |
X-RAY DIFFRACTION |
GOOD
|
| 1l2i |
;Human Estrogen Receptor alpha Ligand-binding Domain in Complex with (R,R)-5,11-cis-diethyl-5,6,11,12-tetrahydrochrysene-2,8-diol and a Glucocorticoid Receptor Interacting Protein 1 NR box II Peptide
; |
23.6 |
82.5 |
X-RAY DIFFRACTION |
GOOD
|
| 1l2j |
Human Estrogen Receptor beta Ligand-binding Domain in Complex with (R,R)-5,11-cis-diethyl-5,6,11,12-tetrahydrochrysene-2,8-diol |
30.5 |
100.8 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1l2k |
Neutron Structure Determination of Sperm Whale Met-Myoglobin at 1.5A Resolution. |
16.9 |
52.0 |
NEUTRON DIFFRACTION |
EXCELLENT
|
| 1l2l |
Crystal structure of ADP-dependent glucokinase from a Pyrococcus Horikoshii |
23.8 |
76.9 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1l2m |
;Minimized Average Structure of the N-terminal, DNA-binding domain of the replication initiation protein from a geminivirus (Tomato yellow leaf curl virus-Sardinia)
; |
16.1 |
57.3 |
SOLUTION NMR |
GOOD
|
| 1l2n |
Smt3 Solution Structure |
19.4 |
71.8 |
SOLUTION NMR |
REASONABLE
|
| 1l2o |
SCALLOP MYOSIN S1-ADP-p-PDM IN THE ACTIN-DETACHED CONFORMATION |
47.3 |
164.6 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1l2p |
ATP Synthase b Subunit Dimerization Domain |
25.4 |
100.4 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1l2q |
Crystal Structure of the Methanosarcina barkeri Monomethylamine Methyltransferase (MtmB) |
21.9 |
69.0 |
X-RAY DIFFRACTION |
GOOD
|
| 1l2s |
X-ray crystal structure of AmpC beta-lactamase from E. coli in complex with a DOCK-predicted non-covalent inhibitor |
29.0 |
99.0 |
X-RAY DIFFRACTION |
GOOD
|
| 1l2t |
Dimeric Structure of MJ0796, a Bacterial ABC Transporter Cassette |
24.1 |
72.9 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1l2u |
;Orotidine 5'-monophosphate decarboxylase from E. coli
; |
23.3 |
80.2 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1l2w |
Crystal Structure of the Yersinia Virulence Effector YopE Chaperone-binding Domain in Complex with its Secretion Chaperone, SycE |
38.0 |
120.8 |
X-RAY DIFFRACTION |
GOOD
|
| 1l2x |
Atomic Resolution Crystal Structure of a Viral RNA Pseudoknot |
13.4 |
46.7 |
X-RAY DIFFRACTION |
GOOD
|
| 1l2y |
NMR Structure of Trp-Cage Miniprotein Construct TC5b |
6.8 |
24.1 |
SOLUTION NMR |
GOOD
|
| 1l2z |
CD2BP2-GYF domain in complex with proline-rich CD2 tail segment peptide |
12.1 |
40.4 |
SOLUTION NMR |
GOOD
|
| 1l30 |
REPLACEMENTS OF PRO86 IN PHAGE T4 LYSOZYME EXTEND AN ALPHA-HELIX BUT DO NOT ALTER PROTEIN STABILITY |
17.5 |
58.2 |
X-RAY DIFFRACTION |
GOOD
|
| 1l31 |
REPLACEMENTS OF PRO86 IN PHAGE T4 LYSOZYME EXTEND AN ALPHA-HELIX BUT DO NOT ALTER PROTEIN STABILITY |
17.5 |
58.4 |
X-RAY DIFFRACTION |
GOOD
|
| 1l32 |
REPLACEMENTS OF PRO86 IN PHAGE T4 LYSOZYME EXTEND AN ALPHA-HELIX BUT DO NOT ALTER PROTEIN STABILITY |
17.5 |
57.9 |
X-RAY DIFFRACTION |
GOOD
|
| 1l33 |
CONTRIBUTIONS OF LEFT-HANDED HELICAL RESIDUES TO THE STRUCTURE AND STABILITY OF BACTERIOPHAGE T4 LYSOZYME |
17.5 |
57.9 |
X-RAY DIFFRACTION |
GOOD
|
| 1l34 |
HIGH-RESOLUTION STRUCTURE OF THE TEMPERATURE-SENSITIVE MUTANT OF PHAGE LYSOZYME, ARG 96 (RIGHT ARROW) HIS |
17.5 |
58.5 |
X-RAY DIFFRACTION |
GOOD
|
| 1l35 |
;STRUCTURE OF A THERMOSTABLE DISULFIDE-BRIDGE MUTANT OF PHAGE T4 LYSOZYME SHOWS THAT AN ENGINEERED CROSSLINK IN A FLEXIBLE REGION DOES NOT INCREASE THE RIGIDITY OF THE FOLDED PROTEIN
; |
17.5 |
57.9 |
X-RAY DIFFRACTION |
GOOD
|
| 1l36 |
TOWARD A SIMPLIFICATION OF THE PROTEIN FOLDING PROBLEM: A STABILIZING POLYALANINE ALPHA-HELIX ENGINEERED IN T4 LYSOZYME |
17.4 |
58.2 |
X-RAY DIFFRACTION |
GOOD
|
| 1l37 |
CONTRIBUTIONS OF ENGINEERED SURFACE SALT BRIDGES TO THE STABILITY OF T4 LYSOZYME DETERMINED BY DIRECTED MUTAGENESIS |
17.5 |
58.0 |
X-RAY DIFFRACTION |
GOOD
|
| 1l38 |
CONTRIBUTIONS OF ENGINEERED SURFACE SALT BRIDGES TO THE STABILITY OF T4 LYSOZYME DETERMINED BY DIRECTED MUTAGENESIS |
17.5 |
59.3 |
X-RAY DIFFRACTION |
GOOD
|
| 1l39 |
CONTRIBUTIONS OF ENGINEERED SURFACE SALT BRIDGES TO THE STABILITY OF T4 LYSOZYME DETERMINED BY DIRECTED MUTAGENESIS |
17.5 |
58.3 |
X-RAY DIFFRACTION |
GOOD
|
| 1l3a |
Structure of the plant transcriptional regulator PBF-2 |
29.2 |
95.3 |
X-RAY DIFFRACTION |
GOOD
|
| 1l3b |
MT0146, THE PRECORRIN-6Y METHYLTRANSFERASE (CBIT) HOMOLOG FROM M. THERMOAUTOTROPHICUM, C2 SPACEGROUP W/ LONG CELL |
43.8 |
152.9 |
X-RAY DIFFRACTION |
GOOD
|
| 1l3c |
MT0146, THE PRECORRIN-6Y METHYLTRANSFERASE (CBIT) HOMOLOG FROM M. THERMOAUTOTROPHICUM, C2 SPACEGROUP WITH SHORT CELL |
28.5 |
85.6 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1l3d |
Low Resolution Crystal Structure of a Viral RNA Pseudoknot |
13.2 |
47.2 |
X-RAY DIFFRACTION |
GOOD
|
| 1l3e |
NMR Structures of the HIF-1alpha CTAD/p300 CH1 Complex |
16.4 |
67.2 |
SOLUTION NMR |
GOOD
|
| 1l3f |
Thermolysin in the Absence of Substrate has an Open Conformation |
20.3 |
67.3 |
X-RAY DIFFRACTION |
GOOD
|
| 1l3g |
NMR Structure of the DNA-binding Domain of Cell Cycle Protein, Mbp1(2-124) from Saccharomyces cerevisiae |
15.1 |
40.3 |
SOLUTION NMR |
REASONABLE
|
| 1l3h |
NMR structure of P41icf, a potent inhibitor of human cathepsin L |
11.3 |
32.3 |
SOLUTION NMR |
GOOD
|