| 1gur |
GURMARIN, A SWEET TASTE-SUPPRESSING POLYPEPTIDE, NMR, 10 STRUCTURES |
52.7 |
139.6 |
SOLUTION NMR |
REASONABLE
|
| 1gus |
MopII from Clostridium pasteurianum (apo1) |
20.4 |
61.4 |
X-RAY DIFFRACTION |
GOOD
|
| 1gut |
MopII from Clostridium pasteurianum (apo2) |
20.6 |
62.3 |
X-RAY DIFFRACTION |
GOOD
|
| 1guu |
CRYSTAL STRUCTURE OF C-MYB R1 |
11.9 |
37.5 |
X-RAY DIFFRACTION |
GOOD
|
| 1guv |
Structure of human chitotriosidase |
21.1 |
70.9 |
X-RAY DIFFRACTION |
GOOD
|
| 1guw |
;STRUCTURE OF THE CHROMODOMAIN FROM MOUSE HP1beta IN COMPLEX WITH THE LYSINE 9-METHYL HISTONE H3 N-TERMINAL PEPTIDE, NMR, 25 STRUCTURES
; |
16.0 |
42.4 |
SOLUTION NMR |
REASONABLE
|
| 1gux |
RB POCKET BOUND TO E7 LXCXE MOTIF |
23.9 |
76.2 |
X-RAY DIFFRACTION |
GOOD
|
| 1guy |
Structural Basis for Thermophilic Protein Stability: Structures of Thermophilic and Mesophilic Malate Dehydrogenases |
27.5 |
85.4 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1guz |
Structural Basis for Thermophilic Protein Stability: Structures of Thermophilic and Mesophilic Malate Dehydrogenases |
31.1 |
93.0 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1gv0 |
Structural Basis for Thermophilic Protein Stability: Structures of Thermophilic and Mesophilic Malate Dehydrogenases |
26.1 |
86.8 |
X-RAY DIFFRACTION |
GOOD
|
| 1gv1 |
Structural Basis for Thermophilic Protein Stability: Structures of Thermophilic and Mesophilic Malate Dehydrogenases |
31.7 |
94.4 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1gv2 |
CRYSTAL STRUCTURE OF C-MYB R2R3 |
16.1 |
52.2 |
X-RAY DIFFRACTION |
GOOD
|
| 1gv3 |
The 2.0 Angstrom resolution structure of the catalytic portion of a cyanobacterial membrane-bound manganese superoxide dismutase |
23.7 |
74.1 |
X-RAY DIFFRACTION |
GOOD
|
| 1gv4 |
Murine apoptosis-inducing factor (AIF) |
34.0 |
108.0 |
X-RAY DIFFRACTION |
GOOD
|
| 1gv5 |
CRYSTAL STRUCTURE OF C-MYB R2 |
11.6 |
40.4 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1gv6 |
Solution structure of alfa-L-LNA:DNA duplex |
12.0 |
34.7 |
SOLUTION NMR |
GOOD
|
| 1gv7 |
ARH-I, an angiogenin/RNase A chimera |
15.4 |
50.0 |
X-RAY DIFFRACTION |
GOOD
|
| 1gv8 |
18 kDa fragment of N-II domain of duck ovotransferrin |
16.0 |
57.6 |
X-RAY DIFFRACTION |
GOOD
|
| 1gv9 |
p58/ERGIC-53 |
17.6 |
54.5 |
X-RAY DIFFRACTION |
GOOD
|
| 1gvc |
18kDa N-II domain fragment of duck ovotransferrin + NTA |
15.9 |
57.4 |
X-RAY DIFFRACTION |
GOOD
|
| 1gvd |
CRYSTAL STRUCTURE OF C-MYB R2 V103L MUTANT |
12.0 |
39.2 |
X-RAY DIFFRACTION |
GOOD
|
| 1gve |
Aflatoxin aldehyde reductase (AKR7A1) from Rat Liver |
28.1 |
89.3 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1gvf |
Structure of tagatose-1,6-bisphosphate aldolase |
26.3 |
92.5 |
X-RAY DIFFRACTION |
GOOD
|
| 1gvg |
Crystal Structure of Clavaminate Synthase with Nitric Oxide |
19.9 |
64.7 |
X-RAY DIFFRACTION |
GOOD
|
| 1gvh |
The X-ray structure of ferric Escherichia coli flavohemoglobin reveals an unespected geometry of the distal heme pocket |
23.4 |
75.9 |
X-RAY DIFFRACTION |
GOOD
|
| 1gvi |
Thermus maltogenic amylase in complex with beta-CD |
33.5 |
106.5 |
X-RAY DIFFRACTION |
GOOD
|
| 1gvj |
ETS-1 DNA BINDING AND AUTOINHIBITORY DOMAINS |
22.4 |
74.5 |
X-RAY DIFFRACTION |
GOOD
|
| 1gvk |
Porcine pancreatic elastase acyl enzyme at 0.95 A resolution |
17.7 |
54.3 |
X-RAY DIFFRACTION |
GOOD
|
| 1gvl |
Human prokallikrein 6 (hK6)/ prozyme/ proprotease M/ proneurosin |
17.9 |
60.5 |
X-RAY DIFFRACTION |
GOOD
|
| 1gvm |
CHOLINE BINDING DOMAIN OF THE MAJOR AUTOLYSIN (C-LYTA) FROM STREPTOCOCCUS PNEUMONIAE |
41.7 |
153.2 |
X-RAY DIFFRACTION |
GOOD
|
| 1gvn |
Crystal Structure of the Plasmid Maintenance System epsilon/zeta: Meachnism of toxin inactivation and toxin function |
31.2 |
103.0 |
X-RAY DIFFRACTION |
GOOD
|
| 1gvo |
STRUCTURE OF PENTAERYTHRITOL TETRANITRATE REDUCTASE AND COMPLEXED WITH 2,4 DINITROPHENOL |
20.2 |
61.8 |
X-RAY DIFFRACTION |
GOOD
|
| 1gvp |
GENE V PROTEIN (SINGLE-STRANDED DNA BINDING PROTEIN) |
15.6 |
53.8 |
X-RAY DIFFRACTION |
GOOD
|
| 1gvq |
STRUCTURE OF PENTAERYTHRITOL TETRANITRATE REDUCTASE AND COMPLEXED WITH 2-CYCLOHEXENONE |
20.2 |
62.0 |
X-RAY DIFFRACTION |
GOOD
|
| 1gvr |
STRUCTURE OF PENTAERYTHRITOL TETRANITRATE REDUCTASE AND COMPLEXED WITH 2,4,6 TRINITROTOLUENE |
20.2 |
62.0 |
X-RAY DIFFRACTION |
GOOD
|
| 1gvs |
Structure of pentaerythritol tetranitrate reductase and complexed with picric acid |
20.2 |
62.0 |
X-RAY DIFFRACTION |
GOOD
|
| 1gvt |
Endothiapepsin complex with CP-80,794 |
20.6 |
65.3 |
X-RAY DIFFRACTION |
GOOD
|
| 1gvu |
Endothiapepsin complex with H189 |
20.8 |
66.5 |
X-RAY DIFFRACTION |
GOOD
|
| 1gvv |
Five Atomic Resolution Structures of Endothiapepsin Inhibitor Complexes; implications for the Aspartic Proteinase Mechanism |
20.3 |
77.6 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1gvw |
Endothiapepsin complex with PD-130,328 |
20.7 |
67.3 |
X-RAY DIFFRACTION |
GOOD
|
| 1gvx |
Endothiapepsin complexed with H256 |
21.0 |
66.1 |
X-RAY DIFFRACTION |
GOOD
|
| 1gvy |
Substrate distorsion by beta-mannanase from Pseudomonas cellulosa |
20.6 |
60.8 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1gvz |
Prostate Specific Antigen (PSA) from stallion seminal plasma |
17.7 |
53.0 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1gw0 |
Crystal Structure of Laccase from Melanocarpus albomyces in Four Copper Form |
33.8 |
104.8 |
X-RAY DIFFRACTION |
GOOD
|
| 1gw1 |
Substrate distortion by beta-mannanase from Pseudomonas cellulosa |
20.7 |
61.1 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1gw2 |
RECOMBINANT HORSERADISH PEROXIDASE C1A THR171SER IN COMPLEX WITH FERULIC ACID |
20.0 |
64.0 |
X-RAY DIFFRACTION |
GOOD
|
| 1gw3 |
THE HELIX-HINGE-HELIX STRUCTURAL MOTIF IN HUMAN APOLIPOPROTEIN A-I DETERMINED BY NMR SPECTROSCOPY, 1 STRUCTURE |
19.0 |
60.8 |
SOLUTION NMR |
GOOD
|
| 1gw4 |
THE HELIX-HINGE-HELIX STRUCTURAL MOTIF IN HUMAN APOLIPOPROTEIN A-I DETERMINED BY NMR SPECTROSCOPY, 1 STRUCTURE |
18.4 |
58.5 |
SOLUTION NMR |
REASONABLE
|
| 1gw6 |
STRUCTURE OF LEUKOTRIENE A4 HYDROLASE D375N MUTANT |
25.9 |
90.1 |
X-RAY DIFFRACTION |
GOOD
|
| 1gw7 |
QUASI-ATOMIC RESOLUTION MODEL OF BACTERIOPHAGE PRD1 CAPSID, OBTAINED BY COMBINED CRYO-EM AND X-RAY CRYSTALLOGRAPHY. |
58.4 |
188.3 |
ELECTRON MICROSCOPY |
GOOD
|