| 1ggy |
HUMAN FACTOR XIII WITH YTTERBIUM BOUND IN THE ION SITE |
36.4 |
119.3 |
X-RAY DIFFRACTION |
GOOD
|
| 1ggz |
CRYSTAL STRUCTURE OF THE CALMODULIN-LIKE PROTEIN (HCLP) FROM HUMAN EPITHELIAL CELLS |
23.3 |
73.5 |
X-RAY DIFFRACTION |
GOOD
|
| 1gh0 |
CRYSTAL STRUCTURE OF C-PHYCOCYANIN FROM SPIRULINA PLATENSIS |
64.8 |
202.6 |
X-RAY DIFFRACTION |
GOOD
|
| 1gh1 |
NMR STRUCTURES OF WHEAT NONSPECIFIC LIPID TRANSFER PROTEIN |
12.6 |
40.4 |
SOLUTION NMR |
GOOD
|
| 1gh2 |
Crystal structure of the catalytic domain of a new human thioredoxin-like protein |
14.0 |
42.5 |
X-RAY DIFFRACTION |
GOOD
|
| 1gh4 |
Structure of the triple mutant (K56M, K120M, K121M) of phospholipase A2 |
15.8 |
40.6 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1gh5 |
ANTIFUNGAL PROTEIN FROM STREPTOMYCES TENDAE TU901, NMR AVERAGE STRUCTURE |
13.8 |
46.4 |
SOLUTION NMR |
GOOD
|
| 1gh6 |
RETINOBLASTOMA POCKET COMPLEXED WITH SV40 LARGE T ANTIGEN |
30.5 |
104.7 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1gh7 |
CRYSTAL STRUCTURE OF THE COMPLETE EXTRACELLULAR DOMAIN OF THE BETA-COMMON RECEPTOR OF IL-3, IL-5, AND GM-CSF |
45.7 |
151.1 |
X-RAY DIFFRACTION |
GOOD
|
| 1gh8 |
SOLUTION STRUCTURE OF THE ARCHAEAL TRANSLATION ELONGATION FACTOR 1BETA FROM METHANOBACTERIUM THERMOAUTOTROPHICUM |
13.2 |
44.6 |
SOLUTION NMR |
REASONABLE
|
| 1gh9 |
SOLUTION STRUCTURE OF A 8.3 KDA PROTEIN (GENE MTH1184) FROM METHANOBACTERIUM THERMOAUTOTROPHICUM |
15.6 |
61.1 |
SOLUTION NMR |
REASONABLE
|
| 1gha |
A SECOND ACTIVE SITE IN CHYMOTRYPSIN? THE X-RAY CRYSTAL STRUCTURE OF N-ACETYL-D-TRYPTOPHAN BOUND TO GAMMA-CHYMOTRYPSIN |
17.4 |
53.2 |
X-RAY DIFFRACTION |
GOOD
|
| 1ghb |
A SECOND ACTIVE SITE IN CHYMOTRYPSIN? THE X-RAY CRYSTAL STRUCTURE OF N-ACETYL-D-TRYPTOPHAN BOUND TO GAMMA-CHYMOTRYPSIN |
17.4 |
53.5 |
X-RAY DIFFRACTION |
GOOD
|
| 1ghc |
;HOMO-AND HETERONUCLEAR TWO-DIMENSIONAL NMR STUDIES OF THE GLOBULAR DOMAIN OF HISTONE H1: FULL ASSIGNMENT, TERTIARY STRUCTURE, AND COMPARISON WITH THE GLOBULAR DOMAIN OF HISTONE H5
; |
12.1 |
42.4 |
SOLUTION NMR |
GOOD
|
| 1ghd |
Crystal structure of the glutaryl-7-aminocephalosporanic acid acylase by mad phasing |
26.6 |
81.2 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1ghe |
CRYSTAL STRUCTURE OF TABTOXIN RESISTANCE PROTEIN COMPLEXED WITH AN ACYL COENZYME A |
23.5 |
79.9 |
X-RAY DIFFRACTION |
GOOD
|
| 1ghf |
ANTI-ANTI-IDIOTYPE GH1002 FAB FRAGMENT |
25.7 |
77.1 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1ghg |
CRYSTAL STRUCTURE OF VANCOMYCIN AGLYCON |
14.1 |
46.4 |
X-RAY DIFFRACTION |
GOOD
|
| 1ghh |
SOLUTION STRUCTURE OF DINI |
13.3 |
46.3 |
SOLUTION NMR |
GOOD
|
| 1ghi |
STRUCTURE OF BETA-LACTAMASE GLU166ASP:ASN170GLN MUTANT |
18.7 |
65.3 |
X-RAY DIFFRACTION |
GOOD
|
| 1ghj |
;SOLUTION STRUCTURE OF THE LIPOYL DOMAIN OF THE 2-OXOGLUTARATE DEHYDROGENASE COMPLEX FROM AZOTOBACTER VINELAND II, NMR, MINIMIZED AVERAGE STRUCTURE
; |
14.2 |
49.7 |
SOLUTION NMR |
GOOD
|
| 1ghk |
;SOLUTION STRUCTURE OF THE LIPOYL DOMAIN OF THE 2-OXOGLUTARATE DEHYDROGENASE COMPLEX FROM AZOTOBACTER VINELAND II, NMR, 25 STRUCTURES
; |
12.9 |
44.6 |
SOLUTION NMR |
GOOD
|
| 1ghl |
THE THREE-DIMENSIONAL STRUCTURE OF PHEASANT AND GUINEA-FOWL EGG LYSOZYMES |
27.1 |
84.8 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1ghm |
;Structures of the acyl-enzyme complex of the staphylococcus aureus beta-lactamase mutant GLU166ASP:ASN170GLN with degraded cephaloridine
; |
18.6 |
59.6 |
X-RAY DIFFRACTION |
GOOD
|
| 1ghp |
;STRUCTURES OF THE ACYL-ENZYME COMPLEX OF THE STAPHYLOCOCCUS AUREUS BETA-LACTAMASE MUTANT GLU166ASP:ASN170GLN WITH DEGRADED BENZYLPENICILLIN
; |
18.6 |
66.9 |
X-RAY DIFFRACTION |
GOOD
|
| 1ghq |
CR2-C3D COMPLEX STRUCTURE |
30.6 |
99.3 |
X-RAY DIFFRACTION |
GOOD
|
| 1ghr |
THE THREE-DIMENSIONAL STRUCTURES OF TWO PLANT BETA-GLUCAN ENDOHYDROLASES WITH DISTINCT SUBSTRATE SPECIFICITIES |
19.9 |
59.2 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1ghs |
THE THREE-DIMENSIONAL STRUCTURES OF TWO PLANT BETA-GLUCAN ENDOHYDROLASES WITH DISTINCT SUBSTRATE SPECIFICITIES |
28.6 |
87.4 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1ght |
SOLUTION STRUCTURE OF THE CATALYTIC DOMAIN OF GAMMA DELTA RESOLVASE |
15.0 |
48.7 |
SOLUTION NMR |
GOOD
|
| 1ghu |
NMR solution structure of growth factor receptor-bound protein 2 (GRB2) SH2 domain, 24 structures |
13.2 |
39.6 |
SOLUTION NMR |
GOOD
|
| 1ghv |
A NOVEL SERINE PROTEASE INHIBITION MOTIF INVOLVING A MULTI-CENTERED SHORT HYDROGEN BONDING NETWORK AT THE ACTIVE SITE |
19.4 |
59.1 |
X-RAY DIFFRACTION |
GOOD
|
| 1ghw |
A NOVEL SERINE PROTEASE INHIBITION MOTIF INVOLVING A MULTI-CENTERED SHORT HYDROGEN BONDING NETWORK AT THE ACTIVE SITE |
19.3 |
62.4 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1ghx |
A NOVEL SERINE PROTEASE INHIBITION MOTIF INVOLVING A MULTI-CENTERED SHORT HYDROGEN BONDING NETWORK AT THE ACTIVE SITE |
19.4 |
59.4 |
X-RAY DIFFRACTION |
GOOD
|
| 1ghy |
A NOVEL SERINE PROTEASE INHIBITION MOTIF INVOLVING A MULTI-CENTERED SHORT HYDROGEN BONDING NETWORK AT THE ACTIVE SITE |
19.4 |
60.7 |
X-RAY DIFFRACTION |
GOOD
|
| 1ghz |
A NOVEL SERINE PROTEASE INHIBITION MOTIF INVOLVING A MULTI-CENTERED SHORT HYDROGEN BONDING NETWORK AT THE ACTIVE SITE |
17.4 |
54.0 |
X-RAY DIFFRACTION |
GOOD
|
| 1gi0 |
A NOVEL SERINE PROTEASE INHIBITION MOTIF INVOLVING A MULTI-CENTERED SHORT HYDROGEN BONDING NETWORK AT THE ACTIVE SITE |
17.3 |
58.0 |
X-RAY DIFFRACTION |
GOOD
|
| 1gi1 |
A NOVEL SERINE PROTEASE INHIBITION MOTIF INVOLVING A MULTI-CENTERED SHORT HYDROGEN BONDING NETWORK AT THE ACTIVE SITE |
17.2 |
61.6 |
X-RAY DIFFRACTION |
GOOD
|
| 1gi2 |
A NOVEL SERINE PROTEASE INHIBITION MOTIF INVOLVING A MULTI-CENTERED SHORT HYDROGEN BONDING NETWORK AT THE ACTIVE SITE |
17.1 |
52.6 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1gi3 |
A NOVEL SERINE PROTEASE INHIBITION MOTIF INVOLVING A MULTI-CENTERED SHORT HYDROGEN BONDING NETWORK AT THE ACTIVE SITE |
17.2 |
54.8 |
X-RAY DIFFRACTION |
GOOD
|
| 1gi4 |
A NOVEL SERINE PROTEASE INHIBITION MOTIF INVOLVING A MULTI-CENTERED SHORT HYDROGEN BONDING NETWORK AT THE ACTIVE SITE |
17.2 |
52.7 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1gi5 |
A NOVEL SERINE PROTEASE INHIBITION MOTIF INVOLVING A MULTI-CENTERED SHORT HYDROGEN BONDING NETWORK AT THE ACTIVE SITE |
17.1 |
57.5 |
X-RAY DIFFRACTION |
GOOD
|
| 1gi6 |
A NOVEL SERINE PROTEASE INHIBITION MOTIF INVOLVING A MULTI-CENTERED SHORT HYDROGEN BONDING NETWORK AT THE ACTIVE SITE |
17.2 |
52.6 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1gi7 |
A NOVEL SERINE PROTEASE INHIBITION MOTIF INVOLVING A MULTI-CENTERED SHORT HYDROGEN BONDING NETWORK AT THE ACTIVE SITE |
18.5 |
65.6 |
X-RAY DIFFRACTION |
GOOD
|
| 1gi8 |
A NOVEL SERINE PROTEASE INHIBITION MOTIF INVOLVING A MULTI-CENTERED SHORT HYDROGEN BONDING NETWORK AT THE ACTIVE SITE |
18.5 |
59.8 |
X-RAY DIFFRACTION |
GOOD
|
| 1gi9 |
A NOVEL SERINE PROTEASE INHIBITION MOTIF INVOLVING A MULTI-CENTERED SHORT HYDROGEN BONDING NETWORK AT THE ACTIVE SITE |
18.5 |
59.7 |
X-RAY DIFFRACTION |
GOOD
|
| 1gia |
STRUCTURE OF ACTIVE CONFORMATIONS OF GIA1 AND THE MECHANISM OF GTP HYDROLYSIS |
21.3 |
70.7 |
X-RAY DIFFRACTION |
GOOD
|
| 1gib |
MU-CONOTOXIN GIIIB, NMR |
7.5 |
27.7 |
SOLUTION NMR |
GOOD
|
| 1gic |
CONCANAVALIN A COMPLEXED WITH METHYL ALPHA-D-GLUCOPYRANOSIDE |
25.9 |
84.0 |
X-RAY DIFFRACTION |
GOOD
|
| 1gid |
CRYSTAL STRUCTURE OF A GROUP I RIBOZYME DOMAIN: PRINCIPLES OF RNA PACKING |
33.3 |
118.4 |
X-RAY DIFFRACTION |
GOOD
|
| 1gif |
HUMAN GLYCOSYLATION-INHIBITING FACTOR |
20.0 |
59.0 |
X-RAY DIFFRACTION |
GOOD
|