| 1yuf |
TYPE ALPHA TRANSFORMING GROWTH FACTOR, NMR, 16 MODELS WITHOUT ENERGY MINIMIZATION |
11.8 |
51.5 |
SOLUTION NMR |
REASONABLE
|
| 1yug |
TYPE ALPHA TRANSFORMING GROWTH FACTOR, NMR, 15 MODELS AFTER ECEPP/3 ENERGY MINIMIZATION |
11.8 |
51.4 |
SOLUTION NMR |
REASONABLE
|
| 1yuh |
FAB FRAGMENT |
36.9 |
117.3 |
X-RAY DIFFRACTION |
GOOD
|
| 1yui |
SOLUTION NMR STRUCTURE OF THE GAGA FACTOR/DNA COMPLEX, REGULARIZED MEAN STRUCTURE |
15.3 |
53.9 |
SOLUTION NMR |
REASONABLE
|
| 1yuj |
SOLUTION NMR STRUCTURE OF THE GAGA FACTOR/DNA COMPLEX, 50 STRUCTURES |
14.4 |
47.5 |
SOLUTION NMR |
GOOD
|
| 1yuk |
The crystal structure of the PSI/Hybrid domain/ I-EGF1 segment from the human integrin beta2 at 1.8 resolution |
23.4 |
87.7 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1yul |
Crystal Structure of Nicotinic Acid Mononucleotide Adenylyltransferase from Pseudomonas aeruginosa |
18.4 |
66.8 |
X-RAY DIFFRACTION |
GOOD
|
| 1yum |
Crystal Structure of Nicotinic Acid Mononucleotide Adenylyltransferase from Pseudomonas aeruginosa |
30.7 |
86.7 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1yun |
Crystal Structure of Nicotinic Acid Mononucleotide Adenylyltransferase from Pseudomonas aeruginosa |
29.1 |
104.1 |
X-RAY DIFFRACTION |
GOOD
|
| 1yuo |
;Optimisation of the surface electrostatics as a strategy for cold adaptation of uracil-DNA N-glycosylase (UNG)from atlantic cod (Gadus morhua)
; |
18.2 |
58.8 |
X-RAY DIFFRACTION |
GOOD
|
| 1yup |
Reindeer beta-lactoglobulin |
43.9 |
161.3 |
X-RAY DIFFRACTION |
GOOD
|
| 1yur |
Solution structure of apo-S100A13 (minimized mean structure) |
18.2 |
55.5 |
SOLUTION NMR |
GOOD
|
| 1yus |
Solution structure of apo-S100A13 |
17.2 |
53.4 |
SOLUTION NMR |
GOOD
|
| 1yut |
Solution structure of Calcium-S100A13 (minimized mean structure) |
18.5 |
58.4 |
SOLUTION NMR |
GOOD
|
| 1yuu |
Solution structure of Calcium-S100A13 |
17.7 |
56.4 |
SOLUTION NMR |
GOOD
|
| 1yuw |
crystal structure of bovine hsc70(aa1-554)E213A/D214A mutant |
28.8 |
97.9 |
X-RAY DIFFRACTION |
GOOD
|
| 1yux |
Mixed valant state of nigerythrin |
21.8 |
74.0 |
X-RAY DIFFRACTION |
GOOD
|
| 1yuy |
HEPATITIS C VIRUS NS5B RNA-DEPENDENT RNA POLYMERASE GENOTYPE 2a |
25.0 |
74.9 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1yuz |
Partially Reduced State of Nigerythrin |
21.9 |
76.1 |
X-RAY DIFFRACTION |
GOOD
|
| 1yv0 |
Crystal structure of skeletal muscle troponin in the Ca2+-free state |
29.1 |
96.3 |
X-RAY DIFFRACTION |
GOOD
|
| 1yv1 |
Fully reduced state of nigerythrin (all ferrous) |
21.9 |
72.5 |
X-RAY DIFFRACTION |
GOOD
|
| 1yv2 |
Hepatitis C virus NS5B RNA-dependent RNA Polymerase genotype 2a |
25.6 |
76.3 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1yv3 |
The structural basis of blebbistatin inhibition and specificity for myosin II |
28.6 |
92.2 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1yv4 |
X-ray structure of M23L onconase at 100K |
14.7 |
50.8 |
X-RAY DIFFRACTION |
GOOD
|
| 1yv5 |
Human farnesyl diphosphate synthase complexed with Mg and risedronate |
21.4 |
69.9 |
X-RAY DIFFRACTION |
GOOD
|
| 1yv6 |
X-ray structure of M23L onconase at 298K |
14.8 |
51.2 |
X-RAY DIFFRACTION |
GOOD
|
| 1yv7 |
X-ray structure of (C87S,des103-104) onconase |
14.7 |
51.2 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1yv8 |
Solution structure of crambin in acetone/water mixed solvent |
9.2 |
32.1 |
SOLUTION NMR |
REASONABLE
|
| 1yv9 |
Crystal structure of a HAD-like phosphatase from Enterococcus faecalis V583 |
24.7 |
87.3 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1yva |
NMR solution structure of crambin in DPC micelles |
9.0 |
29.9 |
SOLUTION NMR |
GOOD
|
| 1yvb |
the Plasmodium falciparum Cysteine Protease Falcipain-2 |
24.7 |
88.2 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1yvc |
;Solution structure of the conserved protein from the gene locus MMP0076 of Methanococcus maripaludis. Northeast Structural Genomics target MrR5.
; |
13.0 |
36.6 |
SOLUTION NMR |
REASONABLE
|
| 1yvd |
GppNHp-Bound Rab22 GTPase |
16.4 |
51.2 |
X-RAY DIFFRACTION |
GOOD
|
| 1yve |
ACETOHYDROXY ACID ISOMEROREDUCTASE COMPLEXED WITH NADPH, MAGNESIUM AND INHIBITOR IPOHA (N-HYDROXY-N-ISOPROPYLOXAMATE) |
41.2 |
126.2 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1yvf |
Hepatitis C virus NS5B RNA-dependent RNA polymerase complex with inhibitor PHA-00729145 |
25.0 |
75.7 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1yvg |
Structural analysis of the catalytic domain of tetanus neurotoxin |
22.8 |
71.1 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1yvh |
Crystal Structure of the c-Cbl TKB Domain in Complex with the APS pTyr-618 Phosphopeptide |
21.3 |
68.8 |
X-RAY DIFFRACTION |
GOOD
|
| 1yvi |
X-RAY STRUCTURE OF PUTATIVE HISTIDINE-CONTAINING PHOSPHOTRANSFER PROTEIN FROM RICE, AK104879 |
20.9 |
74.8 |
X-RAY DIFFRACTION |
GOOD
|
| 1yvj |
Crystal structure of the Jak3 kinase domain in complex with a staurosporine analogue |
20.8 |
68.9 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1yvk |
Crystal Structure of the Bacillis subtilis Acetyltransferase in complex with CoA, Northeast Structural Genomics Target SR237. |
27.1 |
88.7 |
X-RAY DIFFRACTION |
GOOD
|
| 1yvl |
Structure of Unphosphorylated STAT1 |
46.0 |
160.4 |
X-RAY DIFFRACTION |
GOOD
|
| 1yvm |
E. coli Methionine Aminopeptidase in complex with thiabendazole |
18.3 |
57.8 |
X-RAY DIFFRACTION |
GOOD
|
| 1yvn |
THE YEAST ACTIN VAL 159 ASN MUTANT COMPLEX WITH HUMAN GELSOLIN SEGMENT 1. |
25.3 |
86.6 |
X-RAY DIFFRACTION |
GOOD
|
| 1yvo |
hypothetical acetyltransferase from P.aeruginosa PA01 |
21.9 |
79.5 |
X-RAY DIFFRACTION |
GOOD
|
| 1yvp |
Ro autoantigen complexed with RNAs |
38.6 |
136.1 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1yvq |
The low salt (PEG) crystal structure of CO Hemoglobin E (betaE26K) approaching physiological pH (pH 7.5) |
24.6 |
71.3 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1yvr |
Ro autoantigen |
26.8 |
87.9 |
X-RAY DIFFRACTION |
GOOD
|
| 1yvs |
Trimeric domain swapped barnase |
22.2 |
78.8 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1yvt |
The high salt (phosphate) crystal structure of CO Hemoglobin E (Glu26Lys) at physiological pH (pH 7.35) |
20.2 |
60.2 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1yvu |
Crystal structure of A. aeolicus Argonaute |
28.9 |
90.9 |
X-RAY DIFFRACTION |
GOOD
|