| 1o02 |
Human mitochondrial aldehyde dehydrogenase complexed with NADH in the presence of Mg2+ |
61.9 |
179.3 |
X-RAY DIFFRACTION |
GOOD
|
| 1o03 |
;Structure of Pentavalent Phosphorous Intermediate of an Enzyme Catalyzed Phosphoryl transfer Reaction observed on cocrystallization with Glucose 6-phosphate
; |
18.3 |
62.8 |
X-RAY DIFFRACTION |
GOOD
|
| 1o04 |
Cys302Ser mutant of human mitochondrial aldehyde dehydrogenase complexed with NAD+ and Mg2+ |
62.0 |
178.9 |
X-RAY DIFFRACTION |
GOOD
|
| 1o05 |
Apo form of human mitochondrial aldehyde dehydrogenase |
61.9 |
180.7 |
X-RAY DIFFRACTION |
GOOD
|
| 1o06 |
Crystal structure of the Vps27p Ubiquitin Interacting Motif (UIM) |
11.3 |
41.7 |
X-RAY DIFFRACTION |
GOOD
|
| 1o07 |
Crystal Structure of the complex between Q120L/Y150E mutant of AmpC and a beta-lactam inhibitor (MXG) |
29.1 |
100.3 |
X-RAY DIFFRACTION |
GOOD
|
| 1o08 |
;Structure of Pentavalent Phosphorous Intermediate of an Enzyme Catalyzed Phosphoryl transfer Reaction observed on cocrystallization with Glucose 1-phosphate
; |
18.2 |
66.7 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1o0a |
BACTERIORHODOPSIN L INTERMEDIATE AT 1.62 A RESOLUTION |
18.5 |
64.4 |
X-RAY DIFFRACTION |
GOOD
|
| 1o0b |
CRYSTAL STRUCTURE OF L-GLUTAMINE AND AMPCPP BOUND TO GLUTAMINE AMINOACYL TRNA SYNTHETASE |
30.6 |
101.8 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1o0c |
CRYSTAL STRUCTURE OF L-GLUTAMATE AND AMPCPP BOUND TO GLUTAMINE AMINOACYL TRNA SYNTHETASE |
30.9 |
102.8 |
X-RAY DIFFRACTION |
GOOD
|
| 1o0d |
Human Thrombin complexed with a d-Phe-Pro-Arg-type Inhibitor and a C-terminal Hirudin derived exo-site inhibitor |
19.3 |
59.8 |
X-RAY DIFFRACTION |
GOOD
|
| 1o0e |
1.9 Angstrom Crystal Structure of a plant cysteine protease Ervatamin C |
22.7 |
72.6 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1o0f |
;RNASE A in complex with 3',5'-ADP
; |
21.3 |
77.0 |
X-RAY DIFFRACTION |
GOOD
|
| 1o0h |
;Ribonuclease A in complex with 5'-ADP
; |
21.2 |
74.5 |
X-RAY DIFFRACTION |
GOOD
|
| 1o0k |
Structure of the First Parallel DNA Quadruplex-drug Complex |
11.8 |
40.1 |
X-RAY DIFFRACTION |
GOOD
|
| 1o0l |
THE STRUCTURE OF BCL-W REVEALS A ROLE FOR THE C-TERMINAL RESIDUES IN MODULATING BIOLOGICAL ACTIVITY |
17.1 |
69.4 |
SOLUTION NMR |
REASONABLE
|
| 1o0m |
;Ribonuclease A in complex with uridine-2'-phosphate
; |
21.2 |
73.9 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1o0n |
;Ribonuclease A in complex with uridine-3'-phosphate
; |
21.3 |
76.6 |
X-RAY DIFFRACTION |
GOOD
|
| 1o0o |
;Ribonuclease A in complex with adenosine-2',5'-diphosphate
; |
21.4 |
75.1 |
X-RAY DIFFRACTION |
GOOD
|
| 1o0p |
Solution Structure of the third RNA Recognition Motif (RRM) of U2AF65 in complex with an N-terminal SF1 peptide |
14.5 |
46.9 |
SOLUTION NMR |
GOOD
|
| 1o0q |
Crystal structure of a cold adapted alkaline protease from Pseudomonas TAC II 18, co-crystallized with 1 mM EDTA |
25.4 |
90.7 |
X-RAY DIFFRACTION |
GOOD
|
| 1o0r |
Crystal structure of the catalytic domain of bovine beta1,4-galactosyltransferase complex with UDP-galactose |
36.4 |
115.6 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1o0s |
Crystal Structure of Ascaris suum Malic Enzyme Complexed with NADH |
37.9 |
126.0 |
X-RAY DIFFRACTION |
GOOD
|
| 1o0t |
CRYSTAL STRUCTURE OF A COLD ADAPTED ALKALINE PROTEASE FROM PSEUDOMONAS TAC II 18, CO-CRYSTALLIZED WITH 5 mM EDTA (5 DAYS) |
25.8 |
92.2 |
X-RAY DIFFRACTION |
GOOD
|
| 1o0v |
The crystal structure of IgE Fc reveals an asymmetrically bent conformation |
28.6 |
87.6 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1o0w |
Crystal structure of Ribonuclease III (TM1102) from Thermotoga maritima at 2.0 A resolution |
28.1 |
98.9 |
X-RAY DIFFRACTION |
GOOD
|
| 1o0x |
Crystal structure of Methionine aminopeptidase (TM1478) from Thermotoga maritima at 1.90 A resolution |
18.2 |
56.3 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1o12 |
Crystal structure of N-acetylglucosamine-6-phosphate deacetylase (TM0814) from Thermotoga maritima at 2.5 A resolution |
30.9 |
97.3 |
X-RAY DIFFRACTION |
GOOD
|
| 1o13 |
Crystal structure of a putative dinitrogenase iron-molybdenum cofactor (tm1816) from thermotoga maritima at 1.83 A resolution |
14.8 |
48.7 |
X-RAY DIFFRACTION |
GOOD
|
| 1o15 |
;THEOPHYLLINE-BINDING RNA IN COMPLEX WITH THEOPHYLLINE, NMR, REGULARIZED MEAN STRUCTURE, REFINEMENT WITH TORSION ANGLE AND BASE-BASE POSITIONAL DATABASE POTENTIALS AND DIPOLAR COUPLINGS
; |
15.3 |
54.7 |
SOLUTION NMR |
REASONABLE
|
| 1o16 |
RECOMBINANT SPERM WHALE MYOGLOBIN H64D/V68S/D122N MUTANT (MET) |
16.6 |
51.9 |
X-RAY DIFFRACTION |
GOOD
|
| 1o17 |
ANTHRANILATE PHOSPHORIBOSYL-TRANSFERASE (TRPD) |
48.9 |
147.8 |
X-RAY DIFFRACTION |
GOOD
|
| 1o18 |
MOLECULAR MODELS OF AVERAGED RIGOR CROSSBRIDGES FROM TOMOGRAMS OF INSECT FLIGHT MUSCLE |
— |
302.8 |
ELECTRON MICROSCOPY |
EXCELLENT
|
| 1o19 |
MOLECULAR MODELS OF AVERAGED RIGOR CROSSBRIDGES FROM TOMOGRAMS OF INSECT FLIGHT MUSCLE |
— |
308.2 |
ELECTRON MICROSCOPY |
EXCELLENT
|
| 1o1a |
MOLECULAR MODELS OF AVERAGED RIGOR CROSSBRIDGES FROM TOMOGRAMS OF INSECT FLIGHT MUSCLE |
— |
309.0 |
ELECTRON MICROSCOPY |
EXCELLENT
|
| 1o1b |
MOLECULAR MODELS OF AVERAGED RIGOR CROSSBRIDGES FROM TOMOGRAMS OF INSECT FLIGHT MUSCLE |
— |
306.6 |
ELECTRON MICROSCOPY |
EXCELLENT
|
| 1o1c |
MOLECULAR MODELS OF AVERAGED RIGOR CROSSBRIDGES FROM TOMOGRAMS OF INSECT FLIGHT MUSCLE |
— |
305.8 |
ELECTRON MICROSCOPY |
EXCELLENT
|
| 1o1d |
MOLECULAR MODELS OF AVERAGED RIGOR CROSSBRIDGES FROM TOMOGRAMS OF INSECT FLIGHT MUSCLE |
— |
308.7 |
ELECTRON MICROSCOPY |
EXCELLENT
|
| 1o1e |
MOLECULAR MODELS OF AVERAGED RIGOR CROSSBRIDGES FROM TOMOGRAMS OF INSECT FLIGHT MUSCLE |
— |
303.3 |
ELECTRON MICROSCOPY |
EXCELLENT
|
| 1o1f |
MOLECULAR MODELS OF AVERAGED RIGOR CROSSBRIDGES FROM TOMOGRAMS OF INSECT FLIGHT MUSCLE |
— |
289.6 |
ELECTRON MICROSCOPY |
EXCELLENT
|
| 1o1g |
MOLECULAR MODELS OF AVERAGED RIGOR CROSSBRIDGES FROM TOMOGRAMS OF INSECT FLIGHT MUSCLE |
— |
305.1 |
ELECTRON MICROSCOPY |
EXCELLENT
|
| 1o1h |
STRUCTURE OF GLUCOSE ISOMERASE DERIVATIZED WITH KR. |
28.8 |
89.8 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1o1i |
Cyanomet hemoglobin (A-GLY-C:V1M,L29F,H58Q; B,D:V1M,L106W) |
20.5 |
60.9 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1o1j |
Deoxy hemoglobin (A-GLY-C:V1M,L29F,H58Q; B,D:V1M,L106W) |
24.8 |
70.7 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1o1k |
Deoxy hemoglobin (A,C:V1M; B,D:V1M,V67W) |
24.9 |
70.9 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1o1l |
Deoxy hemoglobin (A-GLY-C:V1M,L29W,H58Q; B,D:V1M) |
24.8 |
70.1 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1o1m |
Deoxy hemoglobin (A-GLYGLYGLY-C:V1M,L29F,H58Q B,D:V1M,V67W) |
24.9 |
70.1 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1o1n |
Deoxy hemoglobin (A-GLYGLYGLY-C:V1M,L29W; B,D:V1M) |
24.9 |
70.1 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1o1o |
Deoxy hemoglobin (A,C:V1M,V62L; B,D:V1M,V67L) |
24.8 |
69.4 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1o1p |
Deoxy hemoglobin (A-GLY-C:V1M; B,D:V1M,C93A,N108K) |
24.8 |
70.1 |
X-RAY DIFFRACTION |
EXCELLENT
|