| 1aqp |
RIBONUCLEASE A COPPER COMPLEX |
15.2 |
50.1 |
X-RAY DIFFRACTION |
GOOD
|
| 1aqq |
AG-SUBSTITUTED METALLOTHIONEIN FROM SACCHAROMYCES CEREVISIAE, NMR, 10 STRUCTURES |
7.9 |
30.3 |
SOLUTION NMR |
GOOD
|
| 1aqr |
CU-METALLOTHIONEIN FROM SACCHAROMYCES CEREVISIAE, NMR, MINIMIZED AVERAGE STRUCTURE |
9.8 |
34.8 |
SOLUTION NMR |
REASONABLE
|
| 1aqs |
CU-METALLOTHIONEIN FROM SACCHAROMYCES CEREVISIAE, NMR, 10 STRUCTURES |
8.6 |
36.0 |
SOLUTION NMR |
REASONABLE
|
| 1aqt |
EPSILON SUBUNIT OF F1F0-ATP SYNTHASE FROM ESCHERICHIA COLI |
17.3 |
60.9 |
X-RAY DIFFRACTION |
GOOD
|
| 1aqu |
ESTROGEN SULFOTRANSFERASE WITH BOUND INACTIVE COFACTOR PAP AND 17-BETA ESTRADIOL |
28.6 |
91.3 |
X-RAY DIFFRACTION |
GOOD
|
| 1aqv |
GLUTATHIONE S-TRANSFERASE IN COMPLEX WITH P-BROMOBENZYLGLUTATHIONE |
22.0 |
64.4 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1aqw |
GLUTATHIONE S-TRANSFERASE IN COMPLEX WITH GLUTATHIONE |
35.5 |
117.3 |
X-RAY DIFFRACTION |
GOOD
|
| 1aqx |
GLUTATHIONE S-TRANSFERASE IN COMPLEX WITH MEISENHEIMER COMPLEX |
35.3 |
116.1 |
X-RAY DIFFRACTION |
GOOD
|
| 1aqy |
ESTROGEN SULFOTRANSFERASE WITH PAP |
28.8 |
90.7 |
X-RAY DIFFRACTION |
GOOD
|
| 1aqz |
CRYSTAL STRUCTURE OF A HIGHLY SPECIFIC ASPERGILLUS RIBOTOXIN, RESTRICTOCIN |
23.5 |
83.5 |
X-RAY DIFFRACTION |
GOOD
|
| 1ar0 |
NUCLEAR TRANSPORT FACTOR 2 (NTF2) E42K MUTANT |
19.1 |
60.4 |
X-RAY DIFFRACTION |
GOOD
|
| 1ar1 |
;Structure at 2.7 Angstrom Resolution of the Paracoccus Denitrificans two-subunit Cytochrome C Oxidase Complexed with an Antibody Fv Fragment
; |
33.9 |
115.0 |
X-RAY DIFFRACTION |
GOOD
|
| 1ar2 |
DISULFIDE-FREE IMMUNOGLOBULIN FRAGMENT |
14.4 |
50.2 |
X-RAY DIFFRACTION |
GOOD
|
| 1ar4 |
X-RAY STRUCTURE ANALYSIS OF THE CAMBIALISTIC SUPEROXIDE DISMUTASE FROM PROPIONIBACTERIUM SHERMANII ACTIVE WITH FE OR MN |
23.8 |
78.5 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1ar5 |
X-RAY STRUCTURE OF THE CAMBIALISTIC SUPEROXIDE DISMUTASE FROM PROPIONIBACTERIUM SHERMANII ACTIVE WITH FE OR MN |
23.8 |
78.0 |
X-RAY DIFFRACTION |
GOOD
|
| 1ar6 |
P1/MAHONEY POLIOVIRUS, DOUBLE MUTANT V1160I +P1095S |
29.9 |
95.7 |
X-RAY DIFFRACTION |
GOOD
|
| 1ar7 |
P1/MAHONEY POLIOVIRUS, DOUBLE MUTANT P1095S + H2142Y |
29.9 |
95.7 |
X-RAY DIFFRACTION |
GOOD
|
| 1ar8 |
P1/MAHONEY POLIOVIRUS, MUTANT P1095S |
30.1 |
95.7 |
X-RAY DIFFRACTION |
GOOD
|
| 1ar9 |
P1/MAHONEY POLIOVIRUS, SINGLE SITE MUTANT H2142Y |
29.9 |
96.6 |
X-RAY DIFFRACTION |
GOOD
|
| 1arb |
THE PRIMARY STRUCTURE AND STRUCTURAL CHARACTERISTICS OF ACHROMOBACTER LYTICUS PROTEASE I, A LYSINE-SPECIFIC SERINE PROTEASE |
17.7 |
54.3 |
X-RAY DIFFRACTION |
GOOD
|
| 1arc |
THE PRIMARY STRUCTURE AND STRUCTURAL CHARACTERISTICS OF ACHROMOBACTER LYTICUS PROTEASE I, A LYSINE-SPECIFIC SERINE PROTEASE |
17.6 |
54.2 |
X-RAY DIFFRACTION |
GOOD
|
| 1ard |
STRUCTURES OF DNA-BINDING MUTANT ZINC FINGER DOMAINS: IMPLICATIONS FOR DNA BINDING |
9.5 |
41.2 |
SOLUTION NMR |
REASONABLE
|
| 1are |
STRUCTURES OF DNA-BINDING MUTANT ZINC FINGER DOMAINS: IMPLICATIONS FOR DNA BINDING |
9.5 |
41.8 |
SOLUTION NMR |
REASONABLE
|
| 1arf |
STRUCTURES OF DNA-BINDING MUTANT ZINC FINGER DOMAINS: IMPLICATIONS FOR DNA BINDING |
9.7 |
26.2 |
SOLUTION NMR |
REASONABLE
|
| 1arg |
;Aspartate aminotransferase, phospho-5'-pyridoxyl aspartate complex
; |
28.4 |
95.2 |
X-RAY DIFFRACTION |
GOOD
|
| 1arh |
ASPARTATE AMINOTRANSFERASE, Y225R/R386A MUTANT |
28.6 |
96.8 |
X-RAY DIFFRACTION |
GOOD
|
| 1ari |
Aspartate aminotransferase, W140H mutant, maleate complex |
28.6 |
96.8 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1arj |
ARG-BOUND TAR RNA, NMR |
13.7 |
47.9 |
SOLUTION NMR |
GOOD
|
| 1ark |
SH3 DOMAIN FROM HUMAN NEBULIN, NMR, 15 STRUCTURES |
22.1 |
74.0 |
SOLUTION NMR |
GOOD
|
| 1arl |
CARBOXYPEPTIDASE A WITH ZN REMOVED |
19.5 |
60.3 |
X-RAY DIFFRACTION |
GOOD
|
| 1arm |
CARBOXYPEPTIDASE A WITH ZN REPLACED BY HG |
19.4 |
61.7 |
X-RAY DIFFRACTION |
GOOD
|
| 1aro |
T7 RNA POLYMERASE COMPLEXED WITH T7 LYSOZYME |
32.1 |
98.1 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1arp |
;Crystal structure of the fungal peroxidase from Arthromyces ramosus at 1.9 angstroms resolution: structural comparisons with the lignin and cytochrome C peroxidases
; |
20.5 |
65.2 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1arq |
RELAXATION MATRIX REFINEMENT OF THE SOLUTION STRUCTURE OF THE ARC REPRESSOR |
14.4 |
49.5 |
SOLUTION NMR |
GOOD
|
| 1arr |
RELAXATION MATRIX REFINEMENT OF THE SOLUTION STRUCTURE OF THE ARC REPRESSOR |
15.6 |
53.1 |
SOLUTION NMR |
GOOD
|
| 1ars |
;X-RAY CRYSTALLOGRAPHIC STUDY OF PYRIDOXAL 5'-PHOSPHATE-TYPE ASPARTATE AMINOTRANSFERASES FROM ESCHERICHIA COLI IN OPEN AND CLOSED FORM
; |
22.6 |
69.5 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1art |
;X-RAY CRYSTALLOGRAPHIC STUDY OF PYRIDOXAL 5'-PHOSPHATE-TYPE ASPARTATE AMINOTRANSFERASES FROM ESCHERICHIA COLI IN OPEN AND CLOSED FORM
; |
22.3 |
67.7 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1aru |
;CRYSTAL STRUCTURES OF CYANIDE-AND TRIIODIDE-BOUND FORMS OF ARTHROMYCES RAMOSUS PEROXIDASE AT DIFFERENT PH VALUES. PERTURBATIONS OF ACTIVE SITE RESIDUES AND THEIR IMPLICATION IN ENZYME CATALYSIS
; |
20.5 |
65.3 |
X-RAY DIFFRACTION |
GOOD
|
| 1arv |
;CRYSTAL STRUCTURES OF CYANIDE-AND TRIIODIDE-BOUND FORMS OF ARTHROMYCES RAMOSUS PEROXIDASE AT DIFFERENT PH VALUES. PERTURBATIONS OF ACTIVE SITE RESIDUES AND THEIR IMPLICATION IN ENZYME CATALYSIS
; |
20.5 |
66.7 |
X-RAY DIFFRACTION |
GOOD
|
| 1arw |
;CRYSTAL STRUCTURES OF CYANIDE-AND TRIIODIDE-BOUND FORMS OF ARTHROMYCES RAMOSUS PEROXIDASE AT DIFFERENT PH VALUES. PERTURBATIONS OF ACTIVE SITE RESIDUES AND THEIR IMPLICATION IN ENZYME CATALYSIS
; |
20.5 |
66.2 |
X-RAY DIFFRACTION |
GOOD
|
| 1arx |
;CRYSTAL STRUCTURES OF CYANIDE-AND TRIIODIDE-BOUND FORMS OF ARTHROMYCES RAMOSUS PEROXIDASE AT DIFFERENT PH VALUES. PERTURBATIONS OF ACTIVE SITE RESIDUES AND THEIR IMPLICATION IN ENZYME CATALYSIS
; |
20.2 |
65.3 |
X-RAY DIFFRACTION |
GOOD
|
| 1ary |
;CRYSTAL STRUCTURES OF CYANIDE-AND TRIIODIDE-BOUND FORMS OF ARTHROMYCES RAMOSUS PEROXIDASE AT DIFFERENT PH VALUES. PERTURBATIONS OF ACTIVE SITE RESIDUES AND THEIR IMPLICATION IN ENZYME CATALYSIS
; |
20.2 |
63.7 |
X-RAY DIFFRACTION |
GOOD
|
| 1arz |
ESCHERICHIA COLI DIHYDRODIPICOLINATE REDUCTASE IN COMPLEX WITH NADH AND 2,6 PYRIDINE DICARBOXYLATE |
32.3 |
103.3 |
X-RAY DIFFRACTION |
GOOD
|
| 1as0 |
GTP-GAMMA-S BOUND G42V GIA1 |
21.2 |
71.1 |
X-RAY DIFFRACTION |
GOOD
|
| 1as2 |
GDP+PI BOUND G42V GIA1 |
21.6 |
70.8 |
X-RAY DIFFRACTION |
GOOD
|
| 1as3 |
GDP BOUND G42V GIA1 |
23.3 |
82.7 |
X-RAY DIFFRACTION |
GOOD
|
| 1as4 |
CLEAVED ANTICHYMOTRYPSIN A349R |
22.6 |
72.3 |
X-RAY DIFFRACTION |
GOOD
|
| 1as5 |
SOLUTION STRUCTURE OF CONOTOXIN Y-PIIIE FROM CONUS PURPURASCENS, NMR, 14 STRUCTURES |
8.4 |
32.3 |
SOLUTION NMR |
GOOD
|
| 1as6 |
STRUCTURE OF NITRITE BOUND TO OXIDIZED ALCALIGENES FAECALIS NITRITE REDUCTASE AT CRYO TEMPERATURE |
28.5 |
84.1 |
X-RAY DIFFRACTION |
EXCELLENT
|