| 2exo |
CRYSTAL STRUCTURE OF THE CATALYTIC DOMAIN OF THE BETA-1,4-GLYCANASE CEX FROM CELLULOMONAS FIMI |
19.6 |
59.9 |
X-RAY DIFFRACTION |
GOOD
|
| 2exr |
X-Ray Structure of Cytokinin Oxidase/Dehydrogenase (CKX) From Arabidopsis Thaliana AT5G21482 |
23.5 |
75.8 |
X-RAY DIFFRACTION |
REASONABLE
|
| 2exs |
TRAP3 (engineered TRAP) |
18.1 |
62.9 |
X-RAY DIFFRACTION |
REASONABLE
|
| 2ext |
TRAP4 (engineered TRAP) |
18.1 |
65.8 |
X-RAY DIFFRACTION |
GOOD
|
| 2exu |
Crystal Structure of Saccharomyces cerevisiae transcription elongation factors Spt4-Spt5NGN domain |
21.7 |
71.0 |
X-RAY DIFFRACTION |
GOOD
|
| 2exv |
Crystal structure of the F7A mutant of the cytochrome c551 from Pseudomonas aeruginosa |
18.2 |
61.9 |
X-RAY DIFFRACTION |
GOOD
|
| 2exw |
Crystal structure of a EcClC-Fab complex in the absence of bound ions |
43.2 |
135.9 |
X-RAY DIFFRACTION |
GOOD
|
| 2exx |
Crystal structure of HSCARG from Homo sapiens in complex with NADP |
26.6 |
92.8 |
X-RAY DIFFRACTION |
GOOD
|
| 2exy |
Crystal structure of the E148Q Mutant of EcClC, Fab complexed in absence of bound ions |
43.1 |
135.7 |
X-RAY DIFFRACTION |
GOOD
|
| 2exz |
Crystal structure of Staphylococcal nuclease mutant T22C |
15.4 |
52.4 |
X-RAY DIFFRACTION |
GOOD
|
| 2ey1 |
Crystal structure of Staphylococcal nuclease mutant T22V |
15.6 |
51.5 |
X-RAY DIFFRACTION |
GOOD
|
| 2ey2 |
Crystal structure of Staphylococcal nuclease mutant T41C |
15.4 |
51.9 |
X-RAY DIFFRACTION |
GOOD
|
| 2ey4 |
Crystal Structure of a Cbf5-Nop10-Gar1 Complex |
41.4 |
136.6 |
X-RAY DIFFRACTION |
GOOD
|
| 2ey5 |
Crystal structure of Staphylococcal nuclease mutant T41S |
15.4 |
52.1 |
X-RAY DIFFRACTION |
GOOD
|
| 2ey6 |
Crystal structure of Staphylococcal nuclease mutant T41V |
15.4 |
55.5 |
X-RAY DIFFRACTION |
GOOD
|
| 2eya |
DMSO refined solution structure of crambin in acetone/water |
9.5 |
34.1 |
SOLUTION NMR |
GOOD
|
| 2eyb |
Water refined solution structure of crambin in ACETONE/WATER |
9.3 |
23.9 |
SOLUTION NMR |
REASONABLE
|
| 2eyc |
DMSO refined solution structure of crambin in dpc micelles |
9.3 |
33.4 |
SOLUTION NMR |
GOOD
|
| 2eyd |
Water refined solution structure of crambin in dpc micelles |
9.2 |
35.3 |
SOLUTION NMR |
GOOD
|
| 2eyf |
Crystal structure of Staphylococcal nuclease mutant T44V |
15.4 |
50.4 |
X-RAY DIFFRACTION |
GOOD
|
| 2eyh |
Crystal structure of Staphylococcal nuclease mutant T62S |
15.4 |
51.7 |
X-RAY DIFFRACTION |
GOOD
|
| 2eyi |
Crystal structure of the actin-binding domain of human alpha-actinin 1 at 1.7 Angstrom resolution |
19.8 |
66.5 |
X-RAY DIFFRACTION |
REASONABLE
|
| 2eyj |
Crystal structure of Staphylococcal nuclease mutant T62V |
15.5 |
52.6 |
X-RAY DIFFRACTION |
GOOD
|
| 2eyl |
Crystal structure of Staphylococcal nuclease mutant T82S |
15.5 |
56.0 |
X-RAY DIFFRACTION |
GOOD
|
| 2eym |
Crystal structure of Staphylococcal nuclease mutant T120C |
15.6 |
50.1 |
X-RAY DIFFRACTION |
GOOD
|
| 2eyn |
Crystal structure of the actin-binding domain of human alpha-actinin 1 at 1.8 Angstrom resolution |
19.2 |
63.7 |
X-RAY DIFFRACTION |
GOOD
|
| 2eyo |
Crystal structure of Staphylococcal nuclease mutant T120S |
15.4 |
51.7 |
X-RAY DIFFRACTION |
GOOD
|
| 2eyp |
Crystal structure of Staphylococcal nuclease mutant T120V |
15.5 |
52.2 |
X-RAY DIFFRACTION |
GOOD
|
| 2eyq |
Crystal structure of Escherichia coli transcription-repair coupling factor |
46.4 |
152.0 |
X-RAY DIFFRACTION |
GOOD
|
| 2eyr |
;A structural basis for selection and cross-species reactivity of the semi-invariant NKT cell receptor in CD1d/glycolipid recognition
; |
25.2 |
76.5 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 2eys |
;A structural basis for selection and cross-species reactivity of the semi-invariant NKT cell receptor in CD1d/glycolipid recognition
; |
25.2 |
75.7 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 2eyt |
;A structural basis for selection and cross-species reactivity of the semi-invariant NKT cell receptor in CD1d/glycolipid recognition
; |
40.3 |
138.2 |
X-RAY DIFFRACTION |
GOOD
|
| 2eyu |
The Crystal Structure of the C-terminal Domain of Aquifex aeolicus PilT |
26.9 |
82.5 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 2eyv |
SH2 domain of CT10-Regulated Kinase |
17.6 |
64.6 |
SOLUTION NMR |
REASONABLE
|
| 2eyw |
N-terminal SH3 domain of CT10-Regulated Kinase |
16.3 |
63.5 |
SOLUTION NMR |
GOOD
|
| 2eyx |
C-Terminal SH3 domain of CT10-Regulated Kinase |
13.2 |
50.8 |
SOLUTION NMR |
GOOD
|
| 2eyy |
CT10-Regulated Kinase isoform I |
28.8 |
89.3 |
SOLUTION NMR |
REASONABLE
|
| 2eyz |
CT10-Regulated Kinase isoform II |
21.7 |
66.3 |
SOLUTION NMR |
EXCELLENT
|
| 2ez0 |
Crystal structure of the S107A/E148Q/Y445A mutant of EcClC, in complex with a FaB fragment |
42.9 |
135.2 |
X-RAY DIFFRACTION |
GOOD
|
| 2ez1 |
Holo tyrosine phenol-lyase from Citrobacter freundii at pH 8.0 |
29.4 |
114.3 |
X-RAY DIFFRACTION |
REASONABLE
|
| 2ez2 |
Apo tyrosine phenol-lyase from Citrobacter freundii at pH 8.0 |
29.1 |
91.0 |
X-RAY DIFFRACTION |
REASONABLE
|
| 2ez4 |
Pyruvate oxidase variant F479W |
34.3 |
112.5 |
X-RAY DIFFRACTION |
GOOD
|
| 2ez5 |
Solution Structure of the dNedd4 WW3* Domain- Comm LPSY Peptide Complex |
11.9 |
47.8 |
SOLUTION NMR |
GOOD
|
| 2ez6 |
Crystal structure of Aquifex aeolicus RNase III (D44N) complexed with product of double-stranded RNA processing |
26.4 |
84.1 |
X-RAY DIFFRACTION |
GOOD
|
| 2ez7 |
;Carbonic anhydrase activators. Activation of isozymes I, II, IV, VA, VII and XIV with L- and D-histidine and crystallographic analysis of their adducts with isoform II: engineering proton transfer processes within the active site of an enzyme
; |
18.6 |
58.5 |
X-RAY DIFFRACTION |
GOOD
|
| 2ez8 |
Pyruvate oxidase variant F479W in complex with reaction intermediate 2-lactyl-thiamin diphosphate |
34.4 |
112.7 |
X-RAY DIFFRACTION |
GOOD
|
| 2ez9 |
Pyruvate oxidase variant F479W in complex with reaction intermediate analogue 2-phosphonolactyl-thiamin diphosphate |
34.4 |
112.8 |
X-RAY DIFFRACTION |
REASONABLE
|
| 2eza |
AMINO TERMINAL DOMAIN OF ENZYME I FROM ESCHERICHIA COLI, NMR, RESTRAINED REGULARIZED MEAN STRUCTURE |
23.5 |
85.9 |
SOLUTION NMR |
GOOD
|
| 2ezb |
AMINO TERMINAL DOMAIN OF ENZYME I FROM ESCHERICHIA COLI, NMR, 14 STRUCTURES |
21.9 |
76.8 |
SOLUTION NMR |
GOOD
|
| 2ezc |
AMINO TERMINAL DOMAIN OF ENZYME I FROM ESCHERICHIA COLI, NMR, 14 STRUCTURES |
21.9 |
77.9 |
SOLUTION NMR |
GOOD
|