| 1qn0 |
SOLUTION STRUCTURE OF DESULFOVIBRIO GIGAS FERROCYTOCHROME C3, NMR, 20 STRUCTURES |
14.2 |
47.4 |
SOLUTION NMR |
GOOD
|
| 1qn1 |
SOLUTION STRUCTURE OF DESULFOVIBRIO GIGAS FERRICYTOCHROME C3, NMR, 15 STRUCTURES |
14.2 |
48.4 |
SOLUTION NMR |
GOOD
|
| 1qn2 |
cytochrome cH from Methylobacterium extorquens |
23.2 |
71.3 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1qn3 |
;Crystal structure of the C(-25) Adenovirus major late promoter TATA box variant bound to wild-type TBP (Arabidopsis thaliana TBP isoform 2). TATA element recognition by the TATA box-binding protein has been conserved throughout evolution.
; |
34.4 |
116.4 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1qn4 |
;Crystal structure of the T(-24) Adenovirus major late promoter TATA box variant bound to wild-type TBP (Arabidopsis thaliana TBP isoform 2). TATA element recognition by the TATA box-binding protein has been conserved throughout evolution.
; |
34.4 |
114.1 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1qn5 |
;Crystal structure of the G(-26) Adenovirus major late promoter TATA box variant bound to wild-type TBP (Arabidopsis thaliana TBP isoform 2). TATA element recognition by the TATA box-binding protein has been conserved throughout evolution.
; |
34.5 |
124.1 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1qn6 |
;Crystal structure of the T(-26) Adenovirus major late promoter TATA box variant bound to wild-type TBP (Arabidopsis thaliana TBP isoform 2). TATA element recognition by the TATA box-binding protein has been conserved throughout evolution.
; |
34.4 |
116.7 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1qn7 |
;Crystal structure of the T(-27) Adenovirus major late promoter TATA box variant bound to wild-type TBP (Arabidopsis thaliana TBP isoform 2). TATA element recognition by the TATA box-binding protein has been conserved throughout evolution.
; |
34.3 |
117.6 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1qn8 |
;Crystal structure of the T(-28) Adenovirus major late promoter TATA box variant bound to wild-type TBP (Arabidopsis thaliana TBP isoform 2). TATA element recognition by the TATA box-binding protein has been conserved throughout evolution.
; |
34.4 |
116.2 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1qn9 |
;Crystal structure of the C(-29) Adenovirus major late promoter TATA box variant bound to wild-type TBP (Arabidopsis thaliana TBP isoform 2). TATA element recognition by the TATA box-binding protein has been conserved throughout evolution.
; |
34.5 |
117.5 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1qna |
;Crystal structure of the T(-30) Adenovirus major late promoter TATA box variant bound to wild-type TBP (Arabidopsis thaliana TBP isoform 2). TATA element recognition by the TATA box-binding protein has been conserved throughout evolution.
; |
34.5 |
116.2 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1qnb |
;Crystal structure of the T(-25) Adenovirus major late promoter TATA box variant bound to wild-type TBP (Arabidopsis thaliana TBP isoform 2). TATA element recognition by the TATA box-binding protein has been conserved throughout evolution.
; |
34.5 |
118.2 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1qnc |
;Crystal structure of the A(-31) Adenovirus major late promoter TATA box variant bound to wild-type TBP (Arabidopsis thaliana TBP isoform 2). TATA element recognition by the TATA box-binding protein has been conserved throughout evolution.
; |
34.4 |
117.2 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1qnd |
STEROL CARRIER PROTEIN-2, NMR, 20 STRUCTURES |
14.2 |
47.2 |
SOLUTION NMR |
REASONABLE
|
| 1qne |
Crystal structure of the Adenovirus major late promoter TATA box bound to wild-type TBP (Arabidopsis thaliana TBP isoform 2). |
34.4 |
117.1 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1qnf |
STRUCTURE OF PHOTOLYASE |
24.4 |
80.5 |
X-RAY DIFFRACTION |
GOOD
|
| 1qng |
Plasmodium falciparum Cyclophilin complexed with Cyclosporin A |
15.8 |
48.3 |
X-RAY DIFFRACTION |
GOOD
|
| 1qnh |
Plasmodium falciparum Cyclophilin (double mutant) complexed with Cyclosporin A |
22.8 |
78.1 |
X-RAY DIFFRACTION |
GOOD
|
| 1qni |
Crystal Structure of Nitrous Oxide Reductase from Pseudomonas nautica, at 2.4A Resolution |
52.6 |
165.5 |
X-RAY DIFFRACTION |
GOOD
|
| 1qnj |
THE STRUCTURE OF NATIVE PORCINE PANCREATIC ELASTASE AT ATOMIC RESOLUTION (1.1 A) |
17.8 |
55.1 |
X-RAY DIFFRACTION |
GOOD
|
| 1qnk |
TRUNCATED HUMAN GROB[5-73], NMR, 20 STRUCTURES |
15.4 |
57.4 |
SOLUTION NMR |
GOOD
|
| 1qnl |
AMIDE RECEPTOR/NEGATIVE REGULATOR OF THE AMIDASE OPERON OF PSEUDOMONAS AERUGINOSA (AMIC) COMPLEXED WITH BUTYRAMIDE |
21.3 |
69.7 |
X-RAY DIFFRACTION |
GOOD
|
| 1qnm |
HUMAN MANGANESE SUPEROXIDE DISMUTASE MUTANT Q143N |
23.9 |
80.8 |
X-RAY DIFFRACTION |
GOOD
|
| 1qnn |
Cambialistic superoxide dismutase from Porphyromonas gingivalis |
30.1 |
98.6 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1qno |
The 3-D structure of a Trichoderma reesei b-mannanase from glycoside hydrolase family 5 |
20.1 |
59.8 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1qnp |
The 3-D structure of a Trichoderma reesei b-mannanase from glycoside hydrolase family 5 |
20.2 |
62.0 |
X-RAY DIFFRACTION |
GOOD
|
| 1qnq |
The 3-D structure of a Trichoderma reesei b-mannanase from glycoside hydrolase family 5 |
20.4 |
60.1 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1qnr |
The 3-D structure of a Trichoderma reesei b-mannanase from glycoside hydrolase family 5 |
20.3 |
60.4 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1qns |
The 3-D structure of a Trichoderma reesei b-mannanase from glycoside hydrolase family 5 |
20.1 |
59.3 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1qnt |
X-ray structure of human O6alkylguanine-DNA alkyltransferase |
16.9 |
52.8 |
X-RAY DIFFRACTION |
GOOD
|
| 1qnu |
Shiga-Like Toxin I B Subunit Complexed with the Bridged-Starfish Inhibitor |
22.9 |
70.2 |
X-RAY DIFFRACTION |
GOOD
|
| 1qnv |
yeast 5-aminolaevulinic acid dehydratase Lead (Pb) complex |
23.1 |
89.8 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1qnw |
lectin II from Ulex europaeus |
31.0 |
99.0 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1qnx |
Ves v 5, an allergen from Vespula vulgaris venom |
17.9 |
57.8 |
X-RAY DIFFRACTION |
GOOD
|
| 1qny |
X-ray refinement of D2O soaked crystal of concanavalin A |
18.6 |
63.2 |
X-RAY DIFFRACTION |
GOOD
|
| 1qnz |
NMR structure of the 0.5b anti-HIV antibody complex with the gp120 V3 peptide |
19.0 |
62.2 |
SOLUTION NMR |
REASONABLE
|
| 1qo0 |
Amide receptor of the amidase operon of Pseudomonas aeruginosa (AmiC) complexed with the negative regulator AmiR. |
36.3 |
118.0 |
X-RAY DIFFRACTION |
GOOD
|
| 1qo1 |
Molecular Architecture of the Rotary Motor in ATP Synthase from Yeast Mitochondria |
59.2 |
192.2 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1qo2 |
;Crystal structure of N-((5'-phosphoribosyl)-formimino)-5-aminoimidazol-4-carboxamid ribonucleotid isomerase (EC 3.1.3.15, HisA)
; |
26.4 |
85.3 |
X-RAY DIFFRACTION |
GOOD
|
| 1qo3 |
Complex between NK cell receptor Ly49A and its MHC class I ligand H-2Dd |
32.0 |
100.8 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1qo4 |
ARABIDOPSIS THALIANA PEROXIDASE A2 AT ROOM TEMPERATURE |
20.0 |
64.8 |
X-RAY DIFFRACTION |
GOOD
|
| 1qo5 |
Fructose 1,6-bisphosphate Aldolase from Human Liver Tissue |
— |
305.1 |
X-RAY DIFFRACTION |
GOOD
|
| 1qo6 |
Solution structure of a pair of modules from the gelatin-binding domain of fibronectin |
15.3 |
51.7 |
SOLUTION NMR |
GOOD
|
| 1qo7 |
Structure of Aspergillus niger epoxide hydrolase |
29.8 |
100.0 |
X-RAY DIFFRACTION |
GOOD
|
| 1qo8 |
The structure of the open conformation of a flavocytochrome c3 fumarate reductase |
34.5 |
110.2 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1qoa |
FERREDOXIN MUTATION C49S |
21.8 |
72.2 |
X-RAY DIFFRACTION |
GOOD
|
| 1qob |
FERREDOXIN MUTATION D62K |
21.6 |
71.8 |
X-RAY DIFFRACTION |
GOOD
|
| 1qof |
FERREDOXIN MUTATION Q70K |
21.7 |
72.1 |
X-RAY DIFFRACTION |
GOOD
|
| 1qog |
FERREDOXIN MUTATION S47A |
21.8 |
72.2 |
X-RAY DIFFRACTION |
GOOD
|
| 1qoh |
A MUTANT SHIGA-LIKE TOXIN IIE |
38.9 |
129.1 |
X-RAY DIFFRACTION |
GOOD
|