| 1bn6 |
HALOALKANE DEHALOGENASE FROM A RHODOCOCCUS SPECIES |
19.1 |
58.3 |
X-RAY DIFFRACTION |
GOOD
|
| 1bn7 |
HALOALKANE DEHALOGENASE FROM A RHODOCOCCUS SPECIES |
19.1 |
59.6 |
X-RAY DIFFRACTION |
GOOD
|
| 1bn8 |
BACILLUS SUBTILIS PECTATE LYASE |
21.7 |
66.2 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1bn9 |
RESPONSE ELEMENT OF THE ORPHAN NUCLEAR RECEPTOR REV-ERB BETA |
15.9 |
53.6 |
SOLUTION NMR |
GOOD
|
| 1bna |
STRUCTURE OF A B-DNA DODECAMER. CONFORMATION AND DYNAMICS |
13.7 |
46.5 |
X-RAY DIFFRACTION |
GOOD
|
| 1bnb |
;SOLUTION STRUCTURE OF BOVINE NEUTROPHIL BETA-DEFENSIN 12: THE PEPTIDE FOLD OF THE BETA-DEFENSINS IS IDENTICAL TO THAT OF THE CLASSICAL DEFENSINS
; |
8.3 |
28.5 |
SOLUTION NMR |
GOOD
|
| 1bnc |
THREE-DIMENSIONAL STRUCTURE OF THE BIOTIN CARBOXYLASE SUBUNIT OF ACETYL-COA CARBOXYLASE |
31.5 |
121.2 |
X-RAY DIFFRACTION |
GOOD
|
| 1bnd |
STRUCTURE OF THE BRAIN-DERIVED NEUROTROPHIC FACTOR(SLASH)NEUROTROPHIN 3 HETERODIMER |
20.4 |
68.5 |
X-RAY DIFFRACTION |
GOOD
|
| 1bne |
BARNASE A43C/S80C DISULFIDE MUTANT |
26.2 |
80.4 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1bnf |
BARNASE T70C/S92C DISULFIDE MUTANT |
25.9 |
80.2 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1bng |
BARNASE S85C/H102C DISULFIDE MUTANT |
26.1 |
79.9 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1bni |
BARNASE WILDTYPE STRUCTURE AT PH 6.0 |
26.3 |
82.4 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1bnj |
BARNASE WILDTYPE STRUCTURE AT PH 9.0 |
26.2 |
82.5 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1bnk |
HUMAN 3-METHYLADENINE DNA GLYCOSYLASE COMPLEXED TO DNA |
19.5 |
61.7 |
X-RAY DIFFRACTION |
GOOD
|
| 1bnl |
ZINC DEPENDENT DIMERS OBSERVED IN CRYSTALS OF HUMAN ENDOSTATIN |
36.3 |
109.8 |
X-RAY DIFFRACTION |
GOOD
|
| 1bnm |
CARBONIC ANHYDRASE II INHIBITOR |
18.5 |
58.1 |
X-RAY DIFFRACTION |
GOOD
|
| 1bnn |
CARBONIC ANHYDRASE II INHIBITOR |
18.5 |
59.0 |
X-RAY DIFFRACTION |
GOOD
|
| 1bno |
NMR SOLUTION STRUCTURE OF THE N-TERMINAL DOMAIN OF DNA POLYMERASE BETA, MINIMIZED AVERAGE STRUCTURE |
16.1 |
63.0 |
SOLUTION NMR |
GOOD
|
| 1bnp |
NMR SOLUTION STRUCTURE OF THE N-TERMINAL DOMAIN OF DNA POLYMERASE BETA, 55 STRUCTURES |
15.4 |
41.4 |
SOLUTION NMR |
REASONABLE
|
| 1bnq |
CARBONIC ANHYDRASE II INHIBITOR |
18.5 |
58.0 |
X-RAY DIFFRACTION |
GOOD
|
| 1bnr |
BARNASE |
13.7 |
44.7 |
SOLUTION NMR |
GOOD
|
| 1bns |
STRUCTURAL STUDIES OF BARNASE MUTANTS |
26.1 |
80.8 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1bnt |
CARBONIC ANHYDRASE II INHIBITOR |
18.4 |
57.1 |
X-RAY DIFFRACTION |
GOOD
|
| 1bnu |
CARBONIC ANHYDRASE II INHIBITOR |
18.5 |
57.7 |
X-RAY DIFFRACTION |
GOOD
|
| 1bnv |
CARBONIC ANHYDRASE II INHIBITOR |
18.5 |
59.0 |
X-RAY DIFFRACTION |
GOOD
|
| 1bnw |
CARBONIC ANHYDRASE II INHIBITOR |
18.5 |
59.2 |
X-RAY DIFFRACTION |
GOOD
|
| 1bnx |
;STRUCTURAL STUDIES ON THE EFFECTS OF THE DELETION IN THE RED CELL ANION EXCHANGER (BAND3, AE1) ASSOCIATED WITH SOUTH EAST ASIAN OVALOCYTOSIS.
; |
16.1 |
60.4 |
SOLUTION NMR |
REASONABLE
|
| 1bnz |
SSO7D HYPERTHERMOPHILE PROTEIN/DNA COMPLEX |
14.3 |
46.1 |
X-RAY DIFFRACTION |
GOOD
|
| 1bo0 |
MONOCYTE CHEMOATTRACTANT PROTEIN-3, NMR, MINIMIZED AVERAGE STRUCTURE |
15.6 |
60.5 |
SOLUTION NMR |
GOOD
|
| 1bo1 |
PHOSPHATIDYLINOSITOL PHOSPHATE KINASE TYPE II BETA |
34.0 |
115.4 |
X-RAY DIFFRACTION |
GOOD
|
| 1bo4 |
CRYSTAL STRUCTURE OF A GCN5-RELATED N-ACETYLTRANSFERASE: SERRATIA MARESCENS AMINOGLYCOSIDE 3-N-ACETYLTRANSFERASE |
21.3 |
73.0 |
X-RAY DIFFRACTION |
GOOD
|
| 1bo5 |
CRYSTAL STRUCTURE OF THE COMPLEX BETWEEN ESCHERICHIA COLI GLYCEROL KINASE AND THE ALLOSTERIC REGULATOR FRUCTOSE 1,6-BISPHOSPHATE. |
39.6 |
114.2 |
X-RAY DIFFRACTION |
GOOD
|
| 1bo6 |
ESTROGEN SULFOTRANSFERASE WITH INACTIVE COFACTOR PAP AND VANADATE |
28.0 |
90.2 |
X-RAY DIFFRACTION |
GOOD
|
| 1bo7 |
THYMIDYLATE SYNTHASE R179T MUTANT |
21.5 |
66.0 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1bo8 |
THYMIDYLATE SYNTHASE R178T MUTANT |
21.4 |
65.9 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1bo9 |
NMR SOLUTION STRUCTURE OF DOMAIN 1 OF HUMAN ANNEXIN I |
11.4 |
36.8 |
SOLUTION NMR |
GOOD
|
| 1boa |
HUMAN METHIONINE AMINOPEPTIDASE 2 COMPLEXED WITH ANGIOGENESIS INHIBITOR FUMAGILLIN |
21.0 |
66.2 |
X-RAY DIFFRACTION |
GOOD
|
| 1bob |
HISTONE ACETYLTRANSFERASE HAT1 FROM SACCHAROMYCES CEREVISIAE IN COMPLEX WITH ACETYL COENZYME A |
23.0 |
79.0 |
X-RAY DIFFRACTION |
GOOD
|
| 1boc |
;THE SOLUTION STRUCTURES OF MUTANT CALBINDIN D9K'S, AS DETERMINED BY NMR, SHOW THAT THE CALCIUM BINDING SITE CAN ADOPT DIFFERENT FOLDS
; |
12.2 |
38.7 |
SOLUTION NMR |
GOOD
|
| 1bod |
;THE SOLUTION STRUCTURES OF MUTANT CALBINDIN D9K'S, AS DETERMINED BY NMR, SHOW THAT THE CALCIUM BINDING SITE CAN ADOPT DIFFERENT FOLDS
; |
12.1 |
41.4 |
SOLUTION NMR |
GOOD
|
| 1boe |
;STRUCTURE OF THE IGF BINDING DOMAIN OF THE INSULIN-LIKE GROWTH FACTOR-BINDING PROTEIN-5 (IGFBP-5): IMPLICATIONS FOR IGF AND IGF-I RECEPTOR INTERACTIONS
; |
10.0 |
36.2 |
SOLUTION NMR |
GOOD
|
| 1bof |
GI-ALPHA-1 BOUND TO GDP AND MAGNESIUM |
23.4 |
83.1 |
X-RAY DIFFRACTION |
GOOD
|
| 1bog |
ANTI-P24 (HIV-1) FAB FRAGMENT CB41 COMPLEXED WITH AN EPITOPE-HOMOLOGOUS PEPTIDE |
25.9 |
78.4 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1boh |
SULFUR-SUBSTITUTED RHODANESE (ORTHORHOMBIC FORM) |
19.7 |
64.0 |
X-RAY DIFFRACTION |
GOOD
|
| 1boi |
N-TERMINALLY TRUNCATED RHODANESE |
19.8 |
63.7 |
X-RAY DIFFRACTION |
GOOD
|
| 1bol |
THE CRYSTAL STRUCTURE OF RIBONUCLEASE RH FROM RHIZOPUS NIVEUS AT 2.0 A RESOLUTION |
18.6 |
64.2 |
X-RAY DIFFRACTION |
GOOD
|
| 1bom |
;THREE-DIMENSIONAL STRUCTURE OF BOMBYXIN-II, AN INSULIN-RELATED BRAIN-SECRETORY PEPTIDE OF THE SILKMOTH BOMBYX MORI: COMPARISON WITH INSULIN AND RELAXIN
; |
12.6 |
43.6 |
SOLUTION NMR |
GOOD
|
| 1bon |
;THREE-DIMENSIONAL STRUCTURE OF BOMBYXIN-II, AN INSULIN-RELATED BRAIN-SECRETORY PEPTIDE OF THE SILKMOTH BOMBYX MORI: COMPARISON WITH INSULIN AND RELAXIN
; |
11.6 |
45.8 |
SOLUTION NMR |
REASONABLE
|
| 1boo |
PVUII DNA METHYLTRANSFERASE (CYTOSINE-N4-SPECIFIC) |
20.1 |
62.2 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1boq |
PRO REGION C-TERMINUS: PROTEASE ACTIVE SITE INTERACTIONS ARE CRITICAL IN CATALYZING THE FOLDING OF ALPHA-LYTIC PROTEASE |
16.2 |
51.7 |
X-RAY DIFFRACTION |
REASONABLE
|