| 13zq |
PanDDA analysis group deposition -- Crystal Structure of Enterovirus D68 3Dpol in complex with Z509756472 |
24.2 |
71.0 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 13zr |
PanDDA analysis group deposition -- Crystal Structure of Enterovirus D68 3Dpol in complex with Z53860899 |
24.2 |
70.2 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 13zs |
PanDDA analysis group deposition -- Crystal Structure of Enterovirus D68 3Dpol in complex with Z54226006 |
24.3 |
73.4 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 13zt |
PanDDA analysis group deposition -- Crystal Structure of Enterovirus D68 3Dpol in complex with Z55222357 |
24.2 |
71.2 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 13zu |
PanDDA analysis group deposition -- Crystal Structure of Enterovirus D68 3Dpol in complex with Z55993012 |
24.2 |
70.7 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 13zv |
PanDDA analysis group deposition -- Crystal Structure of Enterovirus D68 3Dpol in complex with Z56040660 |
24.0 |
71.2 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 13zw |
PanDDA analysis group deposition -- Crystal Structure of Enterovirus D68 3Dpol in complex with Z56755030 |
24.0 |
70.8 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 13zx |
PanDDA analysis group deposition -- Crystal Structure of Enterovirus D68 3Dpol in complex with Z56953052 |
24.3 |
71.5 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 13zy |
PanDDA analysis group deposition -- Crystal Structure of Enterovirus D68 3Dpol in complex with Z57260516 |
24.2 |
70.1 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 13zz |
PanDDA analysis group deposition -- Crystal Structure of Enterovirus D68 3Dpol in complex with Z57328552 |
24.2 |
70.2 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 140d |
;SOLUTION STRUCTURE OF A CONSERVED DNA SEQUENCE FROM THE HIV-1 GENOME: RESTRAINED MOLECULAR DYNAMICS SIMULATION WITH DISTANCE AND TORSION ANGLE RESTRAINTS DERIVED FROM TWO-DIMENSIONAL NMR SPECTRA
; |
13.9 |
44.1 |
SOLUTION NMR |
REASONABLE
|
| 140l |
ROLE OF BACKBONE FLEXIBILITY IN THE ACCOMMODATION OF VARIANTS THAT REPACK THE CORE OF T4 LYSOZYME |
17.5 |
58.7 |
X-RAY DIFFRACTION |
GOOD
|
| 141d |
;SOLUTION STRUCTURE OF A CONSERVED DNA SEQUENCE FROM THE HIV-1 GENOME: RESTRAINED MOLECULAR DYNAMICS SIMULATION WITH DISTANCE AND TORSION ANGLE RESTRAINTS DERIVED FROM TWO-DIMENSIONAL NMR SPECTRA
; |
13.9 |
44.8 |
SOLUTION NMR |
EXCELLENT
|
| 141l |
ROLE OF BACKBONE FLEXIBILITY IN THE ACCOMMODATION OF VARIANTS THAT REPACK THE CORE OF T4 LYSOZYME |
17.5 |
45.5 |
X-RAY DIFFRACTION |
REASONABLE
|
| 142d |
;SOLUTION STRUCTURE OF A CONSERVED DNA SEQUENCE FROM THE HIV-1 GENOME: RESTRAINED MOLECULAR DYNAMICS SIMULATION WITH DISTANCE AND TORSION ANGLE RESTRAINTS DERIVED FROM TWO-DIMENSIONAL NMR SPECTRA
; |
13.7 |
44.3 |
SOLUTION NMR |
EXCELLENT
|
| 142l |
ROLE OF BACKBONE FLEXIBILITY IN THE ACCOMMODATION OF VARIANTS THAT REPACK THE CORE OF T4 LYSOZYME |
17.4 |
59.0 |
X-RAY DIFFRACTION |
GOOD
|
| 143d |
SOLUTION STRUCTURE OF THE HUMAN TELOMERIC REPEAT D(AG3[T2AG3]3) OF THE G-QUADRUPLEX |
10.5 |
37.0 |
SOLUTION NMR |
GOOD
|
| 143l |
ROLE OF BACKBONE FLEXIBILITY IN THE ACCOMMODATION OF VARIANTS THAT REPACK THE CORE OF T4 LYSOZYME |
17.4 |
58.0 |
X-RAY DIFFRACTION |
GOOD
|
| 144d |
MINOR GROOVE BINDING OF SN6999 TO AN ALKYLATED DNA: MOLECULAR STRUCTURE OF D(CGC[E6G]AATTCGCG)-SN6999 COMPLEX |
13.8 |
48.1 |
X-RAY DIFFRACTION |
GOOD
|
| 144l |
ROLE OF BACKBONE FLEXIBILITY IN THE ACCOMMODATION OF VARIANTS THAT REPACK THE CORE OF T4 LYSOZYME |
17.5 |
60.1 |
X-RAY DIFFRACTION |
REASONABLE
|
| 145d |
;Structure and thermodynamics of nonalternating C/G base pairs in Z-DNA: the 1.3 angstroms crystal structure of the asymmetric hexanucleotide D(M(5)CGGGM(5) CG)/D(M(5)CGCCM(5)CG)
; |
9.4 |
30.8 |
X-RAY DIFFRACTION |
GOOD
|
| 145l |
ROLE OF BACKBONE FLEXIBILITY IN THE ACCOMMODATION OF VARIANTS THAT REPACK THE CORE OF T4 LYSOZYME |
17.4 |
58.4 |
X-RAY DIFFRACTION |
GOOD
|
| 146d |
SOLUTION STRUCTURE OF THE MITHRAMYCIN DIMER-DNA COMPLEX |
9.9 |
33.0 |
SOLUTION NMR |
GOOD
|
| 146l |
ROLE OF BACKBONE FLEXIBILITY IN THE ACCOMMODATION OF VARIANTS THAT REPACK THE CORE OF T4 LYSOZYME |
17.4 |
58.8 |
X-RAY DIFFRACTION |
GOOD
|
| 147l |
ROLE OF BACKBONE FLEXIBILITY IN THE ACCOMMODATION OF VARIANTS THAT REPACK THE CORE OF T4 LYSOZYME |
17.4 |
61.1 |
X-RAY DIFFRACTION |
GOOD
|
| 148d |
THREE-DIMENSIONAL SOLUTION STRUCTURE OF THE THROMBIN BINDING DNA APTAMER D(GGTTGGTGTGGTTGG) |
9.2 |
27.7 |
SOLUTION NMR |
REASONABLE
|
| 148l |
A COVALENT ENZYME-SUBSTRATE INTERMEDIATE WITH SACCHARIDE DISTORTION IN A MUTANT T4 LYSOZYME |
17.2 |
57.9 |
X-RAY DIFFRACTION |
GOOD
|
| 149d |
SOLUTION STRUCTURE OF A PYRIMIDINE(DOT)PURINE(DOT) PYRIMIDINE DNA TRIPLEX CONTAINING T(DOT)AT, C+(DOT)GC AND G(DOT)TA TRIPLES |
10.5 |
31.3 |
SOLUTION NMR |
EXCELLENT
|
| 149l |
CONSERVATION OF SOLVENT-BINDING SITES IN 10 CRYSTAL FORMS OF T4 LYSOZYME |
17.7 |
59.7 |
X-RAY DIFFRACTION |
GOOD
|
| 14aa |
PanDDA analysis group deposition of ground-state model of Enterovirus D68 3Dpol |
24.2 |
70.8 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 14gs |
GLUTATHIONE S-TRANSFERASE P1-1 APO FORM 1 |
21.9 |
64.5 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 150d |
GUANINE.1,N6-ETHENOADENINE BASE-PAIRS IN THE CRYSTAL STRUCTURE OF D(CGCGAATT(EDA)GCG) |
13.6 |
46.3 |
X-RAY DIFFRACTION |
GOOD
|
| 150l |
CONSERVATION OF SOLVENT-BINDING SITES IN 10 CRYSTAL FORMS OF T4 LYSOZYME |
30.9 |
101.5 |
X-RAY DIFFRACTION |
GOOD
|
| 151d |
DIVERSITY OF WATER RING SIZE AT DNA INTERFACES: HYDRATION AND DYNAMICS OF DNA-ANTHRACYCLINE COMPLEXES |
9.7 |
33.2 |
X-RAY DIFFRACTION |
GOOD
|
| 151l |
CONSERVATION OF SOLVENT-BINDING SITES IN 10 CRYSTAL FORMS OF T4 LYSOZYME |
17.8 |
60.0 |
X-RAY DIFFRACTION |
GOOD
|
| 152d |
DIVERSITY OF WATER RING SIZE AT DNA INTERFACES: HYDRATION AND DYNAMICS OF DNA-ANTHRACYCLINE COMPLEXES |
9.6 |
33.2 |
X-RAY DIFFRACTION |
GOOD
|
| 152l |
CONSERVATION OF SOLVENT-BINDING SITES IN 10 CRYSTAL FORMS OF T4 LYSOZYME |
17.1 |
57.3 |
X-RAY DIFFRACTION |
REASONABLE
|
| 153d |
CRYSTAL STRUCTURE OF A MISPAIRED DODECAMER, D(CGAGAATTC(O6ME)GCG)2, CONTAINING A CARCINOGENIC O6-METHYLGUANINE |
13.5 |
46.2 |
X-RAY DIFFRACTION |
REASONABLE
|
| 153l |
;THE REFINED STRUCTURES OF GOOSE LYSOZYME AND ITS COMPLEX WITH A BOUND TRISACCHARIDE SHOW THAT THE "GOOSE-TYPE LYSOZYMES LACK A CATALYTIC ASPARTATE
; |
16.2 |
49.1 |
X-RAY DIFFRACTION |
GOOD
|
| 154d |
DNA DISTORTION IN BIS-INTERCALATED COMPLEXES |
9.3 |
29.0 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 154l |
;THE REFINED STRUCTURES OF GOOSE LYSOZYME AND ITS COMPLEX WITH A BOUND TRISACCHARIDE SHOW THAT THE "GOOSE-TYPE LYSOZYMES LACK A CATALYTIC ASPARTATE
; |
16.2 |
49.6 |
X-RAY DIFFRACTION |
GOOD
|
| 155c |
THE STRUCTURE OF PARACOCCUS DENITRIFICANS CYTOCHROME C550 |
15.3 |
47.4 |
X-RAY DIFFRACTION |
GOOD
|
| 155l |
CONTROL OF ENZYME ACTIVITY BY AN ENGINEERED DISULFIDE BOND |
17.4 |
60.4 |
X-RAY DIFFRACTION |
GOOD
|
| 156d |
REFINED SOLUTION STRUCTURE OF THE DIMERIC QUADRUPLEX FORMED FROM THE OXYTRICHA TELOMERIC OLIGONUCLEOTIDE D(GGGGTTTTGGGG) |
10.4 |
34.1 |
SOLUTION NMR |
GOOD
|
| 156l |
CONTROL OF ENZYME ACTIVITY BY AN ENGINEERED DISULFIDE BOND |
17.4 |
61.9 |
X-RAY DIFFRACTION |
GOOD
|
| 157d |
CRYSTAL AND MOLECULAR STRUCTURE OF R(CGCGAAUUAGCG): AN RNA DUPLEX CONTAINING TWO G(ANTI).A(ANTI) BASE-PAIRS |
12.8 |
44.2 |
X-RAY DIFFRACTION |
GOOD
|
| 157l |
CONTROL OF ENZYME ACTIVITY BY AN ENGINEERED DISULFIDE BOND |
17.3 |
58.5 |
X-RAY DIFFRACTION |
GOOD
|
| 158d |
CRYSTALLOGRAPHIC ANALYSIS OF C-C-A-A-G-C-T-T-G-G AND ITS IMPLICATIONS FOR BENDING IN B-DNA |
12.5 |
43.0 |
X-RAY DIFFRACTION |
GOOD
|
| 158l |
CONTROL OF ENZYME ACTIVITY BY AN ENGINEERED DISULFIDE BOND |
17.4 |
61.1 |
X-RAY DIFFRACTION |
GOOD
|
| 159d |
SIDE BY SIDE BINDING OF TWO DISTAMYCIN A DRUGS IN THE MINOR GROOVE OF AN ALTERNATING B-DNA DUPLEX |
10.6 |
35.8 |
X-RAY DIFFRACTION |
GOOD
|