| 1gq4 |
STRUCTURAL DETERMINANTS OF THE NHERF INTERACTION WITH BETA2AR AND PDGFR |
13.8 |
42.7 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1gq5 |
Structural Determinants of the NHERF Interaction with beta2-AR and PDGFR |
13.9 |
45.3 |
X-RAY DIFFRACTION |
GOOD
|
| 1gq6 |
PROCLAVAMINATE AMIDINO HYDROLASE FROM STREPTOMYCES CLAVULIGERUS |
28.6 |
85.8 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1gq7 |
PROCLAVAMINATE AMIDINO HYDROLASE FROM STREPTOMYCES CLAVULIGERUS |
33.5 |
99.7 |
X-RAY DIFFRACTION |
GOOD
|
| 1gq8 |
Pectin methylesterase from Carrot |
20.5 |
66.8 |
X-RAY DIFFRACTION |
GOOD
|
| 1gq9 |
THE STRUCTURE OF CMP:2-KETO-3-DEOXY-MANNO-OCTONIC ACID SYNTHETASE COMPLEXED WITH CTP at 100K |
27.1 |
91.1 |
X-RAY DIFFRACTION |
GOOD
|
| 1gqa |
;Cytochrome c' from Rhodobacter Spheriodes
; |
19.9 |
61.8 |
X-RAY DIFFRACTION |
GOOD
|
| 1gqb |
HUMAN MIR-RECEPTOR, REPEAT 11 |
24.0 |
79.2 |
X-RAY DIFFRACTION |
GOOD
|
| 1gqc |
THE STRUCTURE OF CMP:2-KETO-3-DEOXY-MANNO-OCTONIC ACID SYNTHETASE COMPLEXED WITH CMP-Kdo at 100K |
26.9 |
89.3 |
X-RAY DIFFRACTION |
GOOD
|
| 1gqe |
Polypeptide Chain Release Factor 2 (RF2) from Escherichia coli |
24.5 |
81.0 |
X-RAY DIFFRACTION |
GOOD
|
| 1gqf |
Crystal structure of human procaspase-7 |
25.6 |
81.4 |
X-RAY DIFFRACTION |
GOOD
|
| 1gqg |
Quercetin 2,3-dioxygenase in complex with the inhibitor diethyldithiocarbamate |
40.2 |
136.6 |
X-RAY DIFFRACTION |
GOOD
|
| 1gqh |
Quercetin 2,3-dioxygenase in complex with the inhibitor kojic acid |
40.6 |
137.9 |
X-RAY DIFFRACTION |
GOOD
|
| 1gqi |
Structure of Pseudomonas cellulosa alpha-D-glucuronidase |
34.7 |
107.7 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1gqj |
Structure of Pseudomonas cellulosa alpha-D-glucuronidase complexed with xylobiose |
34.6 |
108.3 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1gqk |
Structure of Pseudomonas cellulosa alpha-D-glucuronidase complexed with glucuronic acid |
34.6 |
108.3 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1gql |
Structure of Pseudomonas cellulosa alpha-D-glucuronidase complexed with glucuronic acid and xylotriose |
34.7 |
107.6 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1gqm |
The structure of S100A12 in a hexameric form and its proposed role in receptor signalling |
38.0 |
125.7 |
X-RAY DIFFRACTION |
GOOD
|
| 1gqn |
Native 3-dehydroquinase from Salmonella typhi |
18.4 |
56.2 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1gqo |
Type II Dehydroquinase from Bacillus subtilis |
53.8 |
166.8 |
X-RAY DIFFRACTION |
GOOD
|
| 1gqp |
APC10/DOC1 SUBUNIT OF S. cerevisiae |
25.1 |
81.4 |
X-RAY DIFFRACTION |
GOOD
|
| 1gqq |
MURC - Crystal structure of the apo-enzyme from Haemophilus influenzae |
37.0 |
130.3 |
X-RAY DIFFRACTION |
GOOD
|
| 1gqr |
ACETYLCHOLINESTERASE (E.C. 3.1.1.7) COMPLEXED WITH RIVASTIGMINE |
23.8 |
77.2 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1gqs |
ACETYLCHOLINESTERASE (E.C. 3.1.1.7) COMPLEXED WITH NAP |
23.9 |
76.2 |
X-RAY DIFFRACTION |
GOOD
|
| 1gqt |
Activation of Ribokinase by Monovalent Cations |
49.2 |
165.7 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1gqu |
Crystal structure of an alternating A-T oligonucleotide fragment with Hoogsteen base pairing |
13.7 |
50.9 |
X-RAY DIFFRACTION |
GOOD
|
| 1gqv |
Atomic Resolution (0.98A) Structure of Eosinophil-Derived Neurotoxin |
16.4 |
52.0 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1gqw |
Taurine/alpha-ketoglutarate Dioxygenase from Escherichia coli |
29.2 |
94.4 |
X-RAY DIFFRACTION |
GOOD
|
| 1gqy |
MURC - CRYSTAL STRUCTURE OF THE ENZYME FROM HAEMOPHILUS INFLUENZAE COMPLEXED WITH AMPPCP |
34.4 |
119.3 |
X-RAY DIFFRACTION |
GOOD
|
| 1gqz |
Refinement of Haemophilus influenzae Diaminopimelate epimerase at 1.7A |
19.5 |
56.6 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1gr0 |
myo-inositol 1-phosphate synthase from Mycobacterium tuberculosis in complex with NAD and zinc. |
21.2 |
77.5 |
X-RAY DIFFRACTION |
GOOD
|
| 1gr1 |
Structure of Ferredoxin-NADP+ Reductase with Glu 139 replaced by Lys (E139K) |
20.5 |
62.6 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1gr2 |
STRUCTURE OF A GLUTAMATE RECEPTOR LIGAND BINDING CORE (GLUR2) COMPLEXED WITH KAINATE |
19.3 |
61.6 |
X-RAY DIFFRACTION |
GOOD
|
| 1gr3 |
Structure of the human collagen X NC1 trimer |
16.0 |
57.0 |
X-RAY DIFFRACTION |
GOOD
|
| 1gr5 |
Solution Structure of apo GroEL by Cryo-Electron microscopy |
64.4 |
170.3 |
ELECTRON MICROSCOPY |
GOOD
|
| 1gr7 |
Crystal structure of the double mutant Cys3Ser/Ser100Pro from Pseudomonas Aeruginosa at 1.8 A resolution |
23.2 |
76.5 |
X-RAY DIFFRACTION |
GOOD
|
| 1gra |
;SUBSTRATE BINDING AND CATALYSIS BY GLUTATHIONE REDUCTASE AS DERIVED FROM REFINED ENZYME: SUBSTRATE CRYSTAL STRUCTURES AT 2 ANGSTROMS RESOLUTION
; |
24.7 |
76.6 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1grb |
;SUBSTRATE BINDING AND CATALYSIS BY GLUTATHIONE REDUCTASE AS DERIVED FROM REFINED ENZYME: SUBSTRATE CRYSTAL STRUCTURES AT 2 ANGSTROMS RESOLUTION
; |
24.5 |
77.2 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1grc |
;CRYSTAL STRUCTURE OF GLYCINAMIDE RIBONUCLEOTIDE TRANSFORMYLASE FROM ESCHERICHIA COLI AT 3.0 ANGSTROMS RESOLUTION: A TARGET ENZYME FOR CHEMOTHERAPY
; |
25.4 |
84.1 |
X-RAY DIFFRACTION |
GOOD
|
| 1gre |
;SUBSTRATE BINDING AND CATALYSIS BY GLUTATHIONE REDUCTASE AS DERIVED FROM REFINED ENZYME: SUBSTRATE CRYSTAL STRUCTURES AT 2 ANGSTROMS RESOLUTION
; |
24.8 |
76.3 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1grf |
;SUBSTRATE BINDING AND CATALYSIS BY GLUTATHIONE REDUCTASE AS DERIVED FROM REFINED ENZYME: SUBSTRATE CRYSTAL STRUCTURES AT 2 ANGSTROMS RESOLUTION
; |
24.9 |
91.3 |
X-RAY DIFFRACTION |
GOOD
|
| 1grg |
;SUBSTRATE BINDING AND CATALYSIS BY GLUTATHIONE REDUCTASE AS DERIVED FROM REFINED ENZYME: SUBSTRATE CRYSTAL STRUCTURES AT 2 ANGSTROMS RESOLUTION
; |
24.7 |
76.9 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1grh |
;INHIBITION OF HUMAN GLUTATHIONE REDUCTASE BY THE NITROSOUREA DRUGS 1,3-BIS(2-CHLOROETHYL)-1-NITROSOUREA AND 1-(2-CHLOROETHYL)-3-(2-HYDROXYETHYL)-1-NITROSOUREA
; |
24.9 |
75.5 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1gri |
GRB2 |
24.2 |
78.6 |
X-RAY DIFFRACTION |
GOOD
|
| 1grj |
GREA TRANSCRIPT CLEAVAGE FACTOR FROM ESCHERICHIA COLI |
21.9 |
76.2 |
X-RAY DIFFRACTION |
GOOD
|
| 1grl |
THE CRYSTAL STRUCTURE OF THE BACTERIAL CHAPERONIN GROEL AT 2.8 ANGSTROMS |
54.9 |
162.7 |
X-RAY DIFFRACTION |
GOOD
|
| 1grm |
REFINEMENT OF THE SPATIAL STRUCTURE OF THE GRAMICIDIN A TRANSMEMBRANE ION-CHANNEL (RUSSIAN) |
8.8 |
32.4 |
SOLUTION NMR |
REASONABLE
|
| 1grn |
CRYSTAL STRUCTURE OF THE CDC42/CDC42GAP/ALF3 COMPLEX. |
22.9 |
75.6 |
X-RAY DIFFRACTION |
GOOD
|
| 1gro |
REGULATORY AND CATALYTIC MECHANISMS IN ESCHERICHIA COLI ISOCITRATE DEHYDROGENASE: MULTIPLE ROLES FOR N115 |
23.4 |
75.0 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1grp |
REGULATORY AND CATALYTIC MECHANISMS IN ESCHERICHIA COLI ISOCITRATE DEHYDROGENASE: MULTIPLE ROLES FOR N115 |
23.5 |
75.7 |
X-RAY DIFFRACTION |
GOOD
|