| 1g4y |
1.60 A CRYSTAL STRUCTURE OF THE GATING DOMAIN FROM SMALL CONDUCTANCE POTASSIUM CHANNEL COMPLEXED WITH CALCIUM-CALMODULIN |
25.4 |
83.4 |
X-RAY DIFFRACTION |
GOOD
|
| 1g50 |
CRYSTAL STRUCTURE OF A WILD TYPE HER ALPHA LBD AT 2.9 ANGSTROM RESOLUTION |
34.3 |
111.5 |
X-RAY DIFFRACTION |
GOOD
|
| 1g51 |
ASPARTYL TRNA SYNTHETASE FROM THERMUS THERMOPHILUS AT 2.4 A RESOLUTION |
34.9 |
125.8 |
X-RAY DIFFRACTION |
GOOD
|
| 1g52 |
CARBONIC ANHYDRASE II COMPLEXED WITH 4-(AMINOSULFONYL)-N-[(2,3-DIFLUOROPHENYL)METHYL]-BENZAMIDE |
18.6 |
64.5 |
X-RAY DIFFRACTION |
GOOD
|
| 1g53 |
CARBONIC ANHYDRASE II COMPLEXED WITH 4-(AMINOSULFONYL)-N-[(2,6-DIFLUOROPHENYL)METHYL]-BENZAMIDE |
18.6 |
58.7 |
X-RAY DIFFRACTION |
GOOD
|
| 1g54 |
CARBONIC ANHYDRASE II COMPLEXED WITH 4-(AMINOSULFONYL)-N-[(2,3,4,5,6-PENTAFLUOROPHENYL)METHYL]-BENZAMIDE |
18.6 |
58.6 |
X-RAY DIFFRACTION |
GOOD
|
| 1g55 |
Structure of human DNMT2, an enigmatic DNA methyltransferase homologue |
22.4 |
78.0 |
X-RAY DIFFRACTION |
GOOD
|
| 1g57 |
CRYSTAL STRUCTURE OF 3,4-DIHYDROXY-2-BUTANONE 4-PHOSPHATE SYNTHASE |
22.4 |
85.2 |
X-RAY DIFFRACTION |
GOOD
|
| 1g58 |
CRYSTAL STRUCTURE OF 3,4-DIHYDROXY-2-BUTANONE 4-PHOSPHATE SYNTHASE GOLD DERIVATIVE |
22.0 |
74.0 |
X-RAY DIFFRACTION |
GOOD
|
| 1g59 |
GLUTAMYL-TRNA SYNTHETASE COMPLEXED WITH TRNA(GLU). |
52.2 |
149.5 |
X-RAY DIFFRACTION |
GOOD
|
| 1g5a |
AMYLOSUCRASE FROM NEISSERIA POLYSACCHAREA |
26.2 |
86.6 |
X-RAY DIFFRACTION |
GOOD
|
| 1g5b |
BACTERIOPHAGE LAMBDA SER/THR PROTEIN PHOSPHATASE |
32.8 |
105.8 |
X-RAY DIFFRACTION |
GOOD
|
| 1g5c |
;CRYSTAL STRUCTURE OF THE 'CAB' TYPE BETA CLASS CARBONIC ANHYDRASE FROM METHANOBACTERIUM THERMOAUTOTROPHICUM
; |
39.0 |
132.3 |
X-RAY DIFFRACTION |
GOOD
|
| 1g5d |
NMR STRUCTURE OF AN OLIGONUCLEOTIDE CONTAINING AN ABASIC SITE: ALPHA ANOMER |
13.8 |
44.4 |
SOLUTION NMR |
GOOD
|
| 1g5e |
NMR STRUCTURE OF AN OLIGONUCLEOTIDE CONTAINING AN ABASIC SITE: BETA ANOMER |
13.8 |
42.3 |
SOLUTION NMR |
GOOD
|
| 1g5f |
STRUCTURE OF LINB COMPLEXED WITH 1,2-DICHLOROETHANE |
18.8 |
59.8 |
X-RAY DIFFRACTION |
GOOD
|
| 1g5g |
FRAGMENT OF FUSION PROTEIN FROM NEWCASTLE DISEASE VIRUS |
48.7 |
170.6 |
X-RAY DIFFRACTION |
GOOD
|
| 1g5h |
CRYSTAL STRUCTURE OF THE ACCESSORY SUBUNIT OF MURINE MITOCHONDRIAL POLYMERASE GAMMA |
39.3 |
139.8 |
X-RAY DIFFRACTION |
GOOD
|
| 1g5i |
CRYSTAL STRUCTURE OF THE ACCESSORY SUBUNIT OF MURINE MITOCHONDRIAL POLYMERASE GAMMA |
39.2 |
140.1 |
X-RAY DIFFRACTION |
GOOD
|
| 1g5j |
COMPLEX OF BCL-XL WITH PEPTIDE FROM BAD |
18.2 |
55.5 |
SOLUTION NMR |
GOOD
|
| 1g5k |
;NMR Structrure of d(CCAAAGXACTGGG), X is a 3'-phosphoglycolate, 5'-phosphate gapped lesion, 10 structures
; |
13.9 |
46.5 |
SOLUTION NMR |
GOOD
|
| 1g5l |
CO(III)-BLEOMYCIN-OOH BOUND TO AN OLIGONUCLEOTIDE CONTAINING A PHOSPHOGLYCOLATE LESION |
— |
— |
SOLUTION NMR |
—
|
| 1g5m |
HUMAN BCL-2, ISOFORM 1 |
17.8 |
55.7 |
SOLUTION NMR |
GOOD
|
| 1g5n |
ANNEXIN V COMPLEX WITH HEPARIN OLIGOSACCHARIDES |
23.4 |
78.2 |
X-RAY DIFFRACTION |
GOOD
|
| 1g5p |
NITROGENASE IRON PROTEIN FROM AZOTOBACTER VINELANDII |
25.0 |
76.3 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1g5q |
EPID H67N COMPLEXED WITH SUBSTRATE PEPTIDE DSYTC |
37.0 |
98.0 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1g5r |
THE THREE-DIMENSIONAL STRUCTURE OF ATP:CORRINOID ADENOSYLTRANSFERASE FROM SALMONELLA TYPHIMURIUM. APO FORM |
16.4 |
52.9 |
X-RAY DIFFRACTION |
GOOD
|
| 1g5s |
CRYSTAL STRUCTURE OF HUMAN CYCLIN DEPENDENT KINASE 2 (CDK2) IN COMPLEX WITH THE INHIBITOR H717 |
20.8 |
67.2 |
X-RAY DIFFRACTION |
GOOD
|
| 1g5t |
THE THREE-DIMENSIONAL STRUCTURE OF ATP:CORRINOID ADENOSYLTRANSFERASE FROM SALMONELLA TYPHIMURIUM. APO-ATP FORM |
16.4 |
52.4 |
X-RAY DIFFRACTION |
GOOD
|
| 1g5u |
LATEX PROFILIN HEVB8 |
19.8 |
65.7 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1g5v |
SOLUTION STRUCTURE OF THE TUDOR DOMAIN OF THE HUMAN SMN PROTEIN |
11.0 |
35.9 |
SOLUTION NMR |
GOOD
|
| 1g5w |
SOLUTION STRUCTURE OF HUMAN HEART-TYPE FATTY ACID BINDING PROTEIN |
14.4 |
42.2 |
SOLUTION NMR |
GOOD
|
| 1g5x |
The Structure of Beta-Ketoacyl-[Acyl Carrier Protein] Synthase I |
40.4 |
132.2 |
X-RAY DIFFRACTION |
GOOD
|
| 1g5y |
;THE 2.0 ANGSTROM RESOLUTION CRYSTAL STRUCTURE OF THE RXRALPHA LIGAND BINDING DOMAIN TETRAMER IN THE PRESENCE OF A NON-ACTIVATING RETINOIC ACID ISOMER.
; |
30.5 |
92.3 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1g5z |
CRYSTAL STRUCTURE OF LYME DISEASE ANTIGEN OUTER SURFACE PROTEIN C (OSPC) FROM BORRELIA BURGDORFERI STRAIN N40 |
20.3 |
73.4 |
X-RAY DIFFRACTION |
GOOD
|
| 1g60 |
Crystal Structure of Methyltransferase MboIIa (Moraxella bovis) |
25.3 |
81.7 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1g61 |
CRYSTAL STRUCTURE OF M.JANNASCHII EIF6 |
24.1 |
76.9 |
X-RAY DIFFRACTION |
GOOD
|
| 1g62 |
CRYSTAL STRUCTURE OF S.CEREVISIAE EIF6 |
17.2 |
53.3 |
X-RAY DIFFRACTION |
GOOD
|
| 1g63 |
PEPTIDYL-CYSTEINE DECARBOXYLASE EPID |
39.5 |
111.6 |
X-RAY DIFFRACTION |
GOOD
|
| 1g64 |
THE THREE-DIMENSIONAL STRUCTURE OF ATP:CORRINOID ADENOSYLTRANSFERASE FROM SALMONELLA TYPHIMURIUM. COBALAMIN/ATP TERNARY COMPLEX |
21.5 |
75.6 |
X-RAY DIFFRACTION |
GOOD
|
| 1g65 |
;Crystal structure of epoxomicin:20s proteasome reveals a molecular basis for selectivity of alpha,beta-epoxyketone proteasome inhibitors
; |
60.3 |
189.0 |
X-RAY DIFFRACTION |
GOOD
|
| 1g66 |
ACETYLXYLAN ESTERASE AT 0.90 ANGSTROM RESOLUTION |
16.6 |
56.4 |
X-RAY DIFFRACTION |
GOOD
|
| 1g67 |
THIAMIN PHOSPHATE SYNTHASE |
26.1 |
80.9 |
X-RAY DIFFRACTION |
GOOD
|
| 1g68 |
PSE-4 CARBENICILLINASE, WILD TYPE |
18.9 |
61.4 |
X-RAY DIFFRACTION |
GOOD
|
| 1g69 |
THIAMIN PHOSPHATE SYNTHASE |
25.8 |
80.7 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1g6a |
PSE-4 CARBENICILLINASE, R234K MUTANT |
18.9 |
61.5 |
X-RAY DIFFRACTION |
GOOD
|
| 1g6b |
CRYSTAL STRUCTURE OF P47S MUTANT OF FERREDOXIN I |
13.5 |
42.5 |
X-RAY DIFFRACTION |
GOOD
|
| 1g6c |
THIAMIN PHOSPHATE SYNTHASE |
25.8 |
81.4 |
X-RAY DIFFRACTION |
GOOD
|
| 1g6d |
STRUCTURE OF PEPTIDYL-D(CGCAATTGCG) IN THE PRESENCE OF ZINC IONS |
12.9 |
42.0 |
X-RAY DIFFRACTION |
GOOD
|
| 1g6e |
ANTIFUNGAL PROTEIN FROM STREPTOMYCES TENDAE TU901, 30-CONFORMERS ENSEMBLE |
12.7 |
41.7 |
SOLUTION NMR |
GOOD
|