| 1bgx |
TAQ POLYMERASE IN COMPLEX WITH TP7, AN INHIBITORY FAB |
36.4 |
118.3 |
X-RAY DIFFRACTION |
GOOD
|
| 1bgy |
CYTOCHROME BC1 COMPLEX FROM BOVINE |
54.7 |
172.3 |
X-RAY DIFFRACTION |
GOOD
|
| 1bgz |
S8 RRNA BINDING SITE FROM E. COLI, NMR, 6 STRUCTURES |
12.9 |
46.1 |
SOLUTION NMR |
REASONABLE
|
| 1bh0 |
STRUCTURE OF A GLUCAGON ANALOG |
14.5 |
54.6 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1bh1 |
STRUCTURAL STUDIES OF D-PRO MELITTIN, NMR, 20 STRUCTURES |
10.7 |
37.2 |
SOLUTION NMR |
REASONABLE
|
| 1bh2 |
A326S MUTANT OF AN INHIBITORY ALPHA SUBUNIT |
21.4 |
71.5 |
X-RAY DIFFRACTION |
GOOD
|
| 1bh3 |
E1M, A116K MUTANT OF RH. BLASTICA PORIN |
20.7 |
68.3 |
X-RAY DIFFRACTION |
GOOD
|
| 1bh4 |
CIRCULIN A FROM CHASSALIA PARVIFLORA, NMR, 12 STRUCTURES |
7.7 |
30.9 |
SOLUTION NMR |
GOOD
|
| 1bh5 |
HUMAN GLYOXALASE I Q33E, E172Q DOUBLE MUTANT |
31.4 |
117.1 |
X-RAY DIFFRACTION |
GOOD
|
| 1bh6 |
SUBTILISIN DY IN COMPLEX WITH THE SYNTHETIC INHIBITOR N-BENZYLOXYCARBONYL-ALA-PRO-PHE-CHLOROMETHYL KETONE |
17.8 |
55.6 |
X-RAY DIFFRACTION |
GOOD
|
| 1bh7 |
A LOW ENERGY STRUCTURE FOR THE FINAL CYTOPLASMIC LOOP OF BAND 3, NMR, MINIMIZED AVERAGE STRUCTURE |
12.9 |
41.2 |
SOLUTION NMR |
EXCELLENT
|
| 1bh8 |
HTAFII18/HTAFII28 HETERODIMER CRYSTAL STRUCTURE |
16.7 |
55.3 |
X-RAY DIFFRACTION |
GOOD
|
| 1bh9 |
HTAFII18/HTAFII28 HETERODIMER CRYSTAL STRUCTURE WITH BOUND PCMBS |
16.8 |
53.4 |
X-RAY DIFFRACTION |
GOOD
|
| 1bha |
;THREE-DIMENSIONAL STRUCTURE OF (1-71) BACTERIOOPSIN SOLUBILIZED IN METHANOL-CHLOROFORM AND SDS MICELLES DETERMINED BY 15N-1H HETERONUCLEAR NMR SPECTROSCOPY
; |
14.2 |
51.8 |
SOLUTION NMR |
REASONABLE
|
| 1bhb |
;Three-dimensional structure of (1-71) bacterioopsin solubilized in methanol-chloroform and SDS micelles determined by 15N-1H heteronuclear NMR spectroscopy
; |
14.9 |
60.7 |
SOLUTION NMR |
REASONABLE
|
| 1bhc |
BOVINE PANCREATIC TRYPSIN INHIBITOR CRYSTALLIZED FROM THIOCYANATE |
23.7 |
83.9 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1bhd |
SECOND CALPONIN HOMOLOGY DOMAIN FROM UTROPHIN |
29.7 |
89.8 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1bhe |
POLYGALACTURONASE FROM ERWINIA CAROTOVORA SSP. CAROTOVORA |
21.6 |
70.1 |
X-RAY DIFFRACTION |
GOOD
|
| 1bhf |
P56LCK SH2 DOMAIN INHIBITOR COMPLEX |
14.8 |
50.2 |
X-RAY DIFFRACTION |
GOOD
|
| 1bhg |
HUMAN BETA-GLUCURONIDASE AT 2.6 A RESOLUTION |
40.7 |
135.2 |
X-RAY DIFFRACTION |
GOOD
|
| 1bhh |
FREE P56LCK SH2 DOMAIN |
21.2 |
77.2 |
X-RAY DIFFRACTION |
GOOD
|
| 1bhi |
STRUCTURE OF TRANSACTIVATION DOMAIN OF CRE-BP1/ATF-2, NMR, 20 STRUCTURES |
10.9 |
48.2 |
SOLUTION NMR |
REASONABLE
|
| 1bhj |
CRYSTAL STRUCTURE OF APO-GLYCINE N-METHYLTRANSFERASE (GNMT) |
27.6 |
89.7 |
X-RAY DIFFRACTION |
GOOD
|
| 1bhl |
CACODYLATED CATALYTIC DOMAIN OF HIV-1 INTEGRASE |
16.3 |
53.8 |
X-RAY DIFFRACTION |
GOOD
|
| 1bhm |
RESTRICTION ENDONUCLEASE BAMHI COMPLEX WITH DNA |
22.9 |
74.6 |
X-RAY DIFFRACTION |
GOOD
|
| 1bhn |
NUCLEOSIDE DIPHOSPHATE KINASE ISOFORM A FROM BOVINE RETINA |
28.6 |
88.5 |
X-RAY DIFFRACTION |
GOOD
|
| 1bho |
MAC-1 I DOMAIN MAGNESIUM COMPLEX |
25.8 |
78.1 |
X-RAY DIFFRACTION |
GOOD
|
| 1bhp |
STRUCTURE OF BETA-PUROTHIONIN AT ROOM TEMPERATURE AND 1.7 ANGSTROMS RESOLUTION |
10.9 |
39.2 |
X-RAY DIFFRACTION |
GOOD
|
| 1bhq |
MAC-1 I DOMAIN CADMIUM COMPLEX |
25.7 |
78.6 |
X-RAY DIFFRACTION |
GOOD
|
| 1bhr |
;2'-DEOXY-ISOGUANOSINE BASE PAIRED TO THYMIDINE, NMR, MINIMIZED AVERAGE STRUCTURE
; |
13.7 |
47.2 |
SOLUTION NMR |
GOOD
|
| 1bhs |
HUMAN ESTROGENIC 17BETA-HYDROXYSTEROID DEHYDROGENASE |
20.9 |
65.0 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1bht |
NK1 FRAGMENT OF HUMAN HEPATOCYTE GROWTH FACTOR |
21.8 |
68.6 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1bhu |
;THE 3D STRUCTURE OF THE STREPTOMYCES METALLOPROTEINASE INHIBITOR, SMPI, ISOLATED FROM STREPTOMYCES NIGRESCENS TK-23, NMR, MINIMIZED AVERAGE STRUCTURE
; |
13.7 |
44.4 |
SOLUTION NMR |
GOOD
|
| 1bhw |
LOW TEMPERATURE MIDDLE RESOLUTION STRUCTURE OF XYLOSE ISOMERASE FROM MASC DATA |
32.9 |
100.9 |
X-RAY DIFFRACTION |
GOOD
|
| 1bhx |
X-RAY STRUCTURE OF THE COMPLEX OF HUMAN ALPHA THROMBIN WITH THE INHIBITOR SDZ 229-357 |
19.0 |
57.8 |
X-RAY DIFFRACTION |
GOOD
|
| 1bhy |
LOW TEMPERATURE MIDDLE RESOLUTION STRUCTURE OF P64K FROM MASC DATA |
25.0 |
84.7 |
X-RAY DIFFRACTION |
GOOD
|
| 1bhz |
LOW TEMPERATURE MIDDLE RESOLUTION STRUCTURE OF HEN EGG WHITE LYSOZYME FROM MASC DATA |
15.2 |
56.9 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1bi0 |
STRUCTURE OF APO-AND HOLO-DIPHTHERIA TOXIN REPRESSOR |
22.0 |
70.2 |
X-RAY DIFFRACTION |
GOOD
|
| 1bi1 |
STRUCTURE OF APO-AND HOLO-DIPHTHERIA TOXIN REPRESSOR |
21.9 |
70.1 |
X-RAY DIFFRACTION |
GOOD
|
| 1bi2 |
STRUCTURE OF APO-AND HOLO-DIPHTHERIA TOXIN REPRESSOR |
24.2 |
73.5 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1bi3 |
STRUCTURE OF APO-AND HOLO-DIPHTHERIA TOXIN REPRESSOR |
24.1 |
73.5 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1bi4 |
CATALYTIC DOMAIN OF HIV-1 INTEGRASE |
26.7 |
82.9 |
X-RAY DIFFRACTION |
GOOD
|
| 1bi5 |
CHALCONE SYNTHASE FROM ALFALFA |
22.2 |
81.1 |
X-RAY DIFFRACTION |
GOOD
|
| 1bi6 |
NMR STRUCTURE OF BROMELAIN INHIBITOR VI FROM PINEAPPLE STEM |
11.9 |
43.5 |
SOLUTION NMR |
GOOD
|
| 1bi7 |
MECHANISM OF G1 CYCLIN DEPENDENT KINASE INHIBITION FROM THE STRUCTURE OF THE CDK6-P16INK4A TUMOR SUPPRESSOR COMPLEX |
22.9 |
74.9 |
X-RAY DIFFRACTION |
GOOD
|
| 1bi8 |
MECHANISM OF G1 CYCLIN DEPENDENT KINASE INHIBITION FROM THE STRUCTURES CDK6-P19INK4D INHIBITOR COMPLEX |
35.8 |
110.0 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1bi9 |
RETINAL DEHYDROGENASE TYPE TWO WITH NAD BOUND |
37.8 |
114.3 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1bia |
THE E. COLI BIOTIN HOLOENZYME SYNTHETASE(SLASH)BIO REPRESSOR CRYSTAL STRUCTURE DELINEATES THE BIOTIN AND DNA-BINDING DOMAINS |
22.3 |
86.4 |
X-RAY DIFFRACTION |
GOOD
|
| 1bib |
THE E. COLI BIOTIN HOLOENZYME SYNTHETASE(SLASH)BIO REPRESSOR CRYSTAL STRUCTURE DELINEATES THE BIOTIN AND DNA-BINDING DOMAINS |
21.9 |
75.8 |
X-RAY DIFFRACTION |
GOOD
|
| 1bic |
CRYSTALLOGRAPHIC ANALYSIS OF THR-200-> HIS HUMAN CARBONIC ANHYDRASE II AND ITS COMPLEX WITH THE SUBSTRATE, HCO3- |
18.7 |
59.5 |
X-RAY DIFFRACTION |
GOOD
|