| 1cqd |
THE 2.1 ANGSTROM STRUCTURE OF A CYSTEINE PROTEASE WITH PROLINE SPECIFICITY FROM GINGER RHIZOME, ZINGIBER OFFICINALE |
32.4 |
108.5 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1cqe |
PROSTAGLANDIN H2 SYNTHASE-1 COMPLEX WITH FLURBIPROFEN |
32.4 |
100.5 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1cqf |
THE COMPLEX OF THE MUTATED SHIGA TOXIN B SUBUNIT AND GB3 TRISACCHARIDE |
22.2 |
67.2 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1cqg |
;HIGH RESOLUTION SOLUTION NMR STRUCTURE OF MIXED DISULFIDE INTERMEDIATE BETWEEN HUMAN THIOREDOXIN (C35A, C62A, C69A, C73A) MUTANT AND A 13 RESIDUE PEPTIDE COMPRISING ITS TARGET SITE IN HUMAN REF-1 (RESIDUES 59-71 OF THE P50 SUBUNIT OF NFKB), NMR, 31 STRUCTURES
; |
13.8 |
43.7 |
SOLUTION NMR |
GOOD
|
| 1cqh |
;HIGH RESOLUTION SOLUTION NMR STRUCTURE OF MIXED DISULFIDE INTERMEDIATE BETWEEN HUMAN THIOREDOXIN (C35A, C62A, C69A, C73A) MUTANT AND A 13 RESIDUE PEPTIDE COMPRISING ITS TARGET SITE IN HUMAN REF-1 (RESIDUES 59-71 OF THE P50 SUBUNIT OF NFKB), NMR, MINIMIZED AVERAGE STRUCTURE
; |
15.0 |
49.1 |
SOLUTION NMR |
GOOD
|
| 1cqi |
Crystal Structure of the Complex of ADP and MG2+ with Dephosphorylated E. Coli Succinyl-CoA Synthetase |
36.3 |
119.2 |
X-RAY DIFFRACTION |
GOOD
|
| 1cqj |
CRYSTAL STRUCTURE OF DEPHOSPHORYLATED E. COLI SUCCINYL-COA SYNTHETASE |
35.9 |
116.8 |
X-RAY DIFFRACTION |
GOOD
|
| 1cqk |
CRYSTAL STRUCTURE OF THE CH3 DOMAIN FROM THE MAK33 ANTIBODY |
18.2 |
57.8 |
X-RAY DIFFRACTION |
GOOD
|
| 1cql |
NMR STRUCTURE OF SRP RNA DOMAIN IV |
19.8 |
75.3 |
SOLUTION NMR |
REASONABLE
|
| 1cqm |
;PROTEIN AGGREGATION AND ALZHEIMER'S DISEASE: CRYSTALLOGRAPHIC ANALYSIS OF THE PHENOMENON. ENGINEERED VERSION OF THE RIBOSOMAL PROTEIN S6 USED AS A STABLE SCAFFOLD TO STUDY OLIGOMERIZATION.
; |
24.6 |
83.6 |
X-RAY DIFFRACTION |
GOOD
|
| 1cqn |
;PROTEIN AGGREGATION AND ALZHEIMER'S DISEASE: CRYSTALLOGRAPHIC ANALYSIS OF THE PHENOMENON. ENGINEERED VERSION OF THE RIBOSOMAL PROTEIN S6 USED AS A STABLE SCAFFOLD TO STUDY OLIGOMERIZATION.
; |
26.4 |
87.3 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1cqo |
NMR STRUCTURE OF THE PALINDROMIC DNA DECAMER D(GCGTTAACGC)2 |
12.2 |
38.9 |
SOLUTION NMR |
GOOD
|
| 1cqp |
CRYSTAL STRUCTURE ANALYSIS OF THE COMPLEX LFA-1 (CD11A) I-DOMAIN / LOVASTATIN AT 2.6 A RESOLUTION |
25.7 |
79.5 |
X-RAY DIFFRACTION |
GOOD
|
| 1cqq |
TYPE 2 RHINOVIRUS 3C PROTEASE WITH AG7088 INHIBITOR |
16.5 |
53.6 |
X-RAY DIFFRACTION |
GOOD
|
| 1cqr |
CRYSTAL STRUCTURE OF THE STROMELYSIN CATALYTIC DOMAIN AT 2.0 A RESOLUTION |
23.6 |
85.1 |
X-RAY DIFFRACTION |
GOOD
|
| 1cqs |
CRYSTAL STRUCTURE OF D103E MUTANT WITH EQUILENINEOF KSI IN PSEUDOMONAS PUTIDA |
19.4 |
62.6 |
X-RAY DIFFRACTION |
GOOD
|
| 1cqt |
CRYSTAL STRUCTURE OF A TERNARY COMPLEX CONTAINING AN OCA-B PEPTIDE, THE OCT-1 POU DOMAIN, AND AN OCTAMER ELEMENT |
31.0 |
109.2 |
X-RAY DIFFRACTION |
GOOD
|
| 1cqu |
SOLUTION STRUCTURE OF THE N-TERMINAL DOMAIN OF RIBOSOMAL PROTEIN L9 |
12.5 |
33.2 |
SOLUTION NMR |
REASONABLE
|
| 1cqv |
CRYSTAL STRUCTURE OF STAPHYLOCOCCAL ENTEROTOXIN C2 AT 100K CRYSTALLIZED AT PH 5.0 |
18.8 |
59.7 |
X-RAY DIFFRACTION |
GOOD
|
| 1cqw |
NAI COCRYSTALLISED WITH HALOALKANE DEHALOGENASE FROM A RHODOCOCCUS SPECIES |
18.9 |
63.5 |
X-RAY DIFFRACTION |
GOOD
|
| 1cqx |
Crystal structure of the flavohemoglobin from Alcaligenes eutrophus at 1.75 A resolution |
33.9 |
117.6 |
X-RAY DIFFRACTION |
GOOD
|
| 1cqy |
STARCH BINDING DOMAIN OF BACILLUS CEREUS BETA-AMYLASE |
14.5 |
49.3 |
X-RAY DIFFRACTION |
GOOD
|
| 1cqz |
CRYSTAL STRUCTURE OF MURINE SOLUBLE EPOXIDE HYDROLASE. |
32.5 |
100.7 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1cr0 |
CRYSTAL STRUCTURE OF THE HELICASE DOMAIN OF THE GENE4 PROTEIN OF BACTERIOPHAGE T7 |
19.8 |
74.2 |
X-RAY DIFFRACTION |
GOOD
|
| 1cr1 |
CRYSTAL STRUCTURE OF THE HELICASE DOMAIN OF THE GENE 4 PROTEIN OF BACTERIOPHAGE T7: COMPLEX WITH DTTP |
19.7 |
51.3 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1cr2 |
CRYSTAL STRUCTURE OF THE HELICASE DOMAIN OF THE GENE 4 PROTEIN OF BACTERIOPHAGE T7: COMPLEX WITH DATP |
19.9 |
77.7 |
X-RAY DIFFRACTION |
GOOD
|
| 1cr3 |
SOLUTION CONFORMATION OF THE (+)TRANS-ANTI-BENZO[G]CHRYSENE-DA ADDUCT OPPOSITE DT IN A DNA DUPLEX |
14.3 |
38.6 |
SOLUTION NMR |
REASONABLE
|
| 1cr4 |
CRYSTAL STRUCTURE OF THE HELICASE DOMAIN OF THE GENE 4 PROTEIN OF BACTERIOPHAGE T7: COMPLEX WITH DTDP |
19.8 |
74.1 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1cr5 |
N-TERMINAL DOMAIN OF SEC18P |
33.1 |
98.5 |
X-RAY DIFFRACTION |
GOOD
|
| 1cr6 |
CRYSTAL STRUCTURE OF MURINE SOLUBLE EPOXIDE HYDROLASE COMPLEXED WITH CPU INHIBITOR |
32.3 |
101.0 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1cr7 |
PEANUT LECTIN-LACTOSE COMPLEX MONOCLINIC FORM |
51.2 |
145.9 |
X-RAY DIFFRACTION |
GOOD
|
| 1cr8 |
LOW DENSITY LIPOPROTEIN RECEPTOR-RELATED PROTEIN COMPLEMENT REPEAT 8 |
21.1 |
68.2 |
SOLUTION NMR |
GOOD
|
| 1cr9 |
CRYSTAL STRUCTURE OF THE ANTI-PRION FAB 3F4 |
25.2 |
80.1 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1cra |
THE COMPLEX BETWEEN HUMAN CARBONIC ANHYDRASE II AND THE AROMATIC INHIBITOR 1,2,4-TRIAZOLE |
18.7 |
58.8 |
X-RAY DIFFRACTION |
GOOD
|
| 1crb |
;CRYSTALLOGRAPHIC STUDIES ON A FAMILY OF CELLULAR LIPOPHILIC TRANSPORT PROTEINS. REFINEMENT OF P2 MYELIN PROTEIN AND THE STRUCTURE DETERMINATION AND REFINEMENT OF CELLULAR RETINOL-BINDING PROTEIN IN COMPLEX WITH ALL-TRANS-RETINOL
; |
15.5 |
47.0 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1crc |
CYTOCHROME C AT LOW IONIC STRENGTH |
20.8 |
66.9 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1cre |
CARDIOTOXIN II FROM TAIWAN COBRA VENOM, NAJA NAJA ATRA: STRUCTURE IN SOLUTION AND COMPARISION AMONG HOMOLOGOUS CARDIOTOXINS |
12.4 |
42.2 |
SOLUTION NMR |
GOOD
|
| 1crf |
CARDIOTOXIN II FROM TAIWAN COBRA VENOM, NAJA NAJA ATRA: STRUCTURE IN SOLUTION AND COMPARISION AMONG HOMOLOGOUS CARDIOTOXINS |
10.9 |
36.2 |
SOLUTION NMR |
GOOD
|
| 1crg |
THE ROLE OF A CONSERVED INTERNAL WATER MOLECULE AND ITS ASSOCIATED HYDROGEN BOND NETWORK IN CYTOCHROME C |
14.2 |
47.2 |
X-RAY DIFFRACTION |
GOOD
|
| 1crh |
THE ROLE OF A CONSERVED INTERNAL WATER MOLECULE AND ITS ASSOCIATED HYDROGEN BOND NETWORK IN CYTOCHROME C |
14.2 |
46.5 |
X-RAY DIFFRACTION |
GOOD
|
| 1cri |
THE ROLE OF A CONSERVED INTERNAL WATER MOLECULE AND ITS ASSOCIATED HYDROGEN BOND NETWORK IN CYTOCHROME C |
14.3 |
48.3 |
X-RAY DIFFRACTION |
GOOD
|
| 1crj |
THE ROLE OF A CONSERVED INTERNAL WATER MOLECULE AND ITS ASSOCIATED HYDROGEN BOND NETWORK IN CYTOCHROME C |
14.2 |
47.3 |
X-RAY DIFFRACTION |
GOOD
|
| 1crk |
MITOCHONDRIAL CREATINE KINASE |
45.5 |
146.1 |
X-RAY DIFFRACTION |
GOOD
|
| 1crl |
;INSIGHTS INTO INTERFACIAL ACTIVATION FROM AN 'OPEN' STRUCTURE OF CANDIDA RUGOSA LIPASE
; |
23.3 |
71.2 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1crm |
STRUCTURE AND FUNCTION OF CARBONIC ANHYDRASES |
18.4 |
58.4 |
X-RAY DIFFRACTION |
GOOD
|
| 1crn |
WATER STRUCTURE OF A HYDROPHOBIC PROTEIN AT ATOMIC RESOLUTION. PENTAGON RINGS OF WATER MOLECULES IN CRYSTALS OF CRAMBIN |
10.5 |
35.6 |
X-RAY DIFFRACTION |
GOOD
|
| 1crp |
THE SOLUTION STRUCTURE AND DYNAMICS OF RAS P21. GDP DETERMINED BY HETERONUCLEAR THREE AND FOUR DIMENSIONAL NMR SPECTROSCOPY |
15.9 |
45.9 |
SOLUTION NMR |
GOOD
|
| 1crq |
THE SOLUTION STRUCTURE AND DYNAMICS OF RAS P21. GDP DETERMINED BY HETERONUCLEAR THREE AND FOUR DIMENSIONAL NMR SPECTROSCOPY |
16.9 |
49.9 |
SOLUTION NMR |
EXCELLENT
|
| 1crr |
THE SOLUTION STRUCTURE AND DYNAMICS OF RAS P21. GDP DETERMINED BY HETERONUCLEAR THREE AND FOUR DIMENSIONAL NMR SPECTROSCOPY |
15.9 |
47.4 |
SOLUTION NMR |
EXCELLENT
|
| 1cru |
SOLUBLE QUINOPROTEIN GLUCOSE DEHYDROGENASE FROM ACINETOBACTER CALCOACETICUS IN COMPLEX WITH PQQ AND METHYLHYDRAZINE |
30.0 |
95.6 |
X-RAY DIFFRACTION |
EXCELLENT
|