| 2gcb |
G51S/S52T double mutant of L. casei FPGS |
22.9 |
71.4 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 2gcc |
SOLUTION STRUCTURE OF THE GCC-BOX BINDING DOMAIN, NMR, MINIMIZED MEAN STRUCTURE |
13.7 |
48.1 |
SOLUTION NMR |
GOOD
|
| 2gcd |
TAO2 kinase domain-staurosporine structure |
28.6 |
97.6 |
X-RAY DIFFRACTION |
GOOD
|
| 2gce |
;The 1,1-proton transfer reaction mechanism by alpha-methylacyl-CoA racemase is catalyzed by an aspartate/histidine pair and involves a smooth, methionine-rich surface for binding the fatty acyl moiety
; |
48.5 |
164.1 |
X-RAY DIFFRACTION |
REASONABLE
|
| 2gcf |
Solution structure of the N-terminal domain of the coppper(I) ATPase PacS in its apo form |
12.3 |
42.4 |
SOLUTION NMR |
REASONABLE
|
| 2gcg |
Ternary Crystal Structure of Human Glyoxylate Reductase/Hydroxypyruvate Reductase |
41.5 |
126.7 |
X-RAY DIFFRACTION |
GOOD
|
| 2gch |
REFINED CRYSTAL STRUCTURE OF GAMMA-CHYMOTRYPSIN AT 1.9 ANGSTROMS RESOLUTION |
17.4 |
54.7 |
X-RAY DIFFRACTION |
GOOD
|
| 2gci |
;The 1,1-proton transfer reaction mechanism by alpha-methylacyl-CoA racemase is catalyzed by an asparte/histidine pair and involves a smooth, methionine-rich surface for binding the fatty acyl moiety
; |
38.8 |
131.5 |
X-RAY DIFFRACTION |
GOOD
|
| 2gcj |
Crystal Structure of the Pob3 middle domain |
35.1 |
116.0 |
X-RAY DIFFRACTION |
GOOD
|
| 2gcl |
Structure of the Pob3 Middle domain |
26.6 |
83.1 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 2gcn |
Crystal structure of the human RhoC-GDP complex |
17.1 |
57.2 |
X-RAY DIFFRACTION |
REASONABLE
|
| 2gco |
Crystal structure of the human RhoC-GppNHp complex |
25.0 |
83.9 |
X-RAY DIFFRACTION |
GOOD
|
| 2gcp |
Crystal structure of the human RhoC-GSP complex |
16.9 |
56.0 |
X-RAY DIFFRACTION |
GOOD
|
| 2gcq |
;Fully ligated E.Coli Adenylosuccinate Synthetase with GTP, 2'-deoxy-IMP and Hadacidin
; |
22.5 |
74.5 |
X-RAY DIFFRACTION |
GOOD
|
| 2gcs |
Pre-cleavage state of the Thermoanaerobacter tengcongensis glmS ribozyme |
28.4 |
107.0 |
X-RAY DIFFRACTION |
GOOD
|
| 2gct |
;STRUCTURE OF GAMMA-CHYMOTRYPSIN IN THE RANGE PH 2.0 TO PH 10.5 SUGGESTS THAT GAMMA-CHYMOTRYPSIN IS A COVALENT ACYL-ENZYME ADDUCT AT LOW PH
; |
17.5 |
54.4 |
X-RAY DIFFRACTION |
GOOD
|
| 2gcu |
X-Ray Structure of Gene Product from Arabidopsis Thaliana At1g53580 |
32.0 |
102.1 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 2gcv |
Post-cleavage state of the Thermoanaerobacter tengcongensis glmS ribozyme |
28.3 |
106.7 |
X-RAY DIFFRACTION |
GOOD
|
| 2gcx |
Solution Structure of Ferrous Iron Transport Protein A (FeoA) of Klebsiella pneumoniae |
12.4 |
38.2 |
SOLUTION NMR |
GOOD
|
| 2gcy |
humanized antibody C25 Fab fragment |
25.1 |
79.8 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 2gcz |
Solution Structure of alpha-Conotoxin OmIA |
5.6 |
20.2 |
SOLUTION NMR |
GOOD
|
| 2gd0 |
;The 1,1-proton transfer reaction mechanism by alpha-methylacyl-CoA racemase is catalyzed by an aspartate/histidine pair and involves a smooth, methionine-rich surface for binding the fatty acyl moiety
; |
38.6 |
124.4 |
X-RAY DIFFRACTION |
GOOD
|
| 2gd1 |
COENZYME-INDUCED CONFORMATIONAL CHANGES IN GLYCERALDEHYDE-3-PHOSPHATE DEHYDROGENASE FROM BACILLUS STEAROTHERMOPHILLUS |
32.9 |
97.9 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 2gd2 |
;The 1,1-proton transfer reaction mechanism by alpha-methylacyl-CoA racemase is catalyzed by an aspartate/histidine pair and involves a smooth, methionine-rich surface for binding the fatty acyl moiety
; |
38.9 |
131.9 |
X-RAY DIFFRACTION |
GOOD
|
| 2gd3 |
NMR structure of S14G-humanin in 30% TFE solution |
13.2 |
47.9 |
SOLUTION NMR |
REASONABLE
|
| 2gd4 |
Crystal Structure of the Antithrombin-S195A Factor Xa-Pentasaccharide Complex |
54.7 |
202.1 |
X-RAY DIFFRACTION |
REASONABLE
|
| 2gd5 |
Structural basis for budding by the ESCRTIII factor CHMP3 |
33.3 |
107.8 |
X-RAY DIFFRACTION |
GOOD
|
| 2gd6 |
;The 1,1-proton transfer reaction mechanism by alpha-methylacyl-CoA racemase is catalyzed by an aspartate/histidine pair and involves a smooth, methionine-rich surface for binding the fatty acyl moiety
; |
38.9 |
132.5 |
X-RAY DIFFRACTION |
REASONABLE
|
| 2gd7 |
The Structure of the Cyclin T-binding domain of Hexim1 reveals the molecular basis for regulation of transcription elongation |
38.4 |
149.5 |
SOLUTION NMR |
SUSPICIOUS
|
| 2gd8 |
Crystal structure analysis of the human carbonic anhydrase II in complex with a 2-substituted estradiol bis-sulfamate |
18.6 |
57.9 |
X-RAY DIFFRACTION |
GOOD
|
| 2gd9 |
Crystal structure of a putative dihydrofolate reductase (bsu40760, yyap) from bacillus subtilis at 2.30 A resolution |
24.1 |
81.0 |
X-RAY DIFFRACTION |
GOOD
|
| 2gda |
REFINED SOLUTION STRUCTURE OF THE GLUCOCORTICOID RECEPTOR DNA-BINDING DOMAIN |
11.8 |
41.3 |
SOLUTION NMR |
REASONABLE
|
| 2gdc |
Structure of Vinculin VD1 / IpaA560-633 complex |
26.2 |
98.7 |
X-RAY DIFFRACTION |
REASONABLE
|
| 2gdd |
Human beta II tryptase with inhibitor CRA-27592 |
33.3 |
101.7 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 2gde |
Thrombin in complex with inhibitor |
19.1 |
57.1 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 2gdf |
Crystal structure of Dioclea violacea seed lectin |
29.7 |
87.1 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 2gdg |
Crystal structure of covalently modified macrophage inhibitory factor |
20.0 |
63.5 |
X-RAY DIFFRACTION |
GOOD
|
| 2gdi |
Crystal structure of thiamine pyrophosphate-specific riboswitch in complex with thiamine pyrophosphate |
38.8 |
130.4 |
X-RAY DIFFRACTION |
SUSPICIOUS
|
| 2gdj |
Delta-62 RADA recombinase in complex with AMP-PNP and magnesium |
18.3 |
59.0 |
X-RAY DIFFRACTION |
REASONABLE
|
| 2gdl |
Fowlicidin-2: NMR structure of antimicrobial peptide |
11.3 |
41.9 |
SOLUTION NMR |
GOOD
|
| 2gdm |
LEGHEMOGLOBIN (OXY) |
16.4 |
50.8 |
X-RAY DIFFRACTION |
GOOD
|
| 2gdn |
Crystal structure of the Mycobacterium tuberculosis beta-lactamase |
18.7 |
60.2 |
X-RAY DIFFRACTION |
REASONABLE
|
| 2gdo |
4-(Aminoalkylamino)-3-Benzimidazole-Quinolinones As Potent CHK1 Inhibitors |
20.7 |
72.6 |
X-RAY DIFFRACTION |
GOOD
|
| 2gdq |
Crystal structure of mandelate racemase/muconate lactonizing enzyme from Bacillus subtilis at 1.8 A resolution |
29.3 |
93.7 |
X-RAY DIFFRACTION |
GOOD
|
| 2gdr |
Crystal structure of a bacterial glutathione transferase |
38.6 |
111.7 |
X-RAY DIFFRACTION |
GOOD
|
| 2gds |
Interrupting the Hydrogen Bonding Network at the Active Site of Human Manganese Superoxide Dismutase |
28.5 |
83.9 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 2gdt |
NMR Structure of the nonstructural protein 1 (nsp1) from the SARS coronavirus |
14.3 |
45.4 |
SOLUTION NMR |
GOOD
|
| 2gdu |
E232Q mutant of sucrose phosphorylase from BIFIDOBACTERIUM ADOLESCENTIS in complex with sucrose |
33.1 |
112.4 |
X-RAY DIFFRACTION |
GOOD
|
| 2gdv |
Sucrose phosphorylase from BIFIDOBACTERIUM ADOLESCENTIS reacted with sucrose |
33.1 |
114.0 |
X-RAY DIFFRACTION |
REASONABLE
|
| 2gdw |
Solution structure of the B. brevis TycC3-PCP in A/H-state |
12.3 |
46.9 |
SOLUTION NMR |
GOOD
|