| 2ay2 |
AROMATIC AMINO ACID AMINOTRANSFERASE WITH CYCLOHEXANE PROPIONIC ACID |
28.9 |
99.6 |
X-RAY DIFFRACTION |
GOOD
|
| 2ay3 |
AROMATIC AMINO ACID AMINOTRANSFERASE WITH 3-(3,4-DIMETHOXYPHENYL)PROPIONIC ACID |
28.9 |
99.0 |
X-RAY DIFFRACTION |
GOOD
|
| 2ay4 |
AROMATIC AMINO ACID AMINOTRANSFERASE WITH 3-(P-TOLYL)PROPIONIC ACID |
28.9 |
99.1 |
X-RAY DIFFRACTION |
GOOD
|
| 2ay5 |
AROMATIC AMINO ACID AMINOTRANSFERASE WITH 3-INDOLEPROPIONIC ACID |
28.9 |
99.8 |
X-RAY DIFFRACTION |
GOOD
|
| 2ay6 |
AROMATIC AMINO ACID AMINOTRANSFERASE WITH 3-INDOLEBUTYRIC ACID |
28.9 |
99.2 |
X-RAY DIFFRACTION |
GOOD
|
| 2ay7 |
AROMATIC AMINO ACID AMINOTRANSFERASE WITH 4-PHENYLBUTYRIC ACID |
28.9 |
99.1 |
X-RAY DIFFRACTION |
GOOD
|
| 2ay8 |
AROMATIC AMINO ACID AMINOTRANSFERASE WITH 4-(2-THIENYL)BUTYRIC ACID |
28.9 |
101.8 |
X-RAY DIFFRACTION |
GOOD
|
| 2ay9 |
AROMATIC AMINO ACID AMINOTRANSFERASE WITH 5-PHENYLVALERIC ACID |
28.8 |
99.3 |
X-RAY DIFFRACTION |
GOOD
|
| 2aya |
Solution Structure of the C-Terminal 14 kDa Domain of the tau subunit from Escherichia coli DNA Polymerase III |
17.5 |
65.1 |
SOLUTION NMR |
REASONABLE
|
| 2ayb |
Crystal structure of HPV6a E2 DNA Binding Domain bound to a 16 base pair DNA target |
19.7 |
62.5 |
X-RAY DIFFRACTION |
GOOD
|
| 2ayd |
Crystal Structure of the C-terminal WRKY domainof AtWRKY1, an SA-induced and partially NPR1-dependent transcription factor |
13.9 |
47.7 |
X-RAY DIFFRACTION |
GOOD
|
| 2aye |
Crystal structure of the unliganded E2 DNA Binding Domain from HPV6a |
31.9 |
104.6 |
X-RAY DIFFRACTION |
GOOD
|
| 2ayg |
Crystal structure of HPV6a E2 DNA binding domain bound to an 18 base pair DNA target |
20.2 |
65.2 |
X-RAY DIFFRACTION |
GOOD
|
| 2ayh |
;CRYSTAL AND MOLECULAR STRUCTURE AT 1.6 ANGSTROMS RESOLUTION OF THE HYBRID BACILLUS ENDO-1,3-1,4-BETA-D-GLUCAN 4-GLUCANOHYDROLASE H(A16-M)
; |
17.4 |
54.5 |
X-RAY DIFFRACTION |
GOOD
|
| 2ayi |
Wild-type AmpT from Thermus thermophilus |
53.2 |
147.7 |
X-RAY DIFFRACTION |
GOOD
|
| 2ayj |
Solution structure of 50S ribosomal protein L40e from Sulfolobus solfataricus |
13.8 |
36.9 |
SOLUTION NMR |
REASONABLE
|
| 2ayk |
INHIBITOR-FREE CATALYTIC FRAGMENT OF HUMAN FIBROBLAST COLLAGENASE, NMR, MINIMIZED AVERAGE STRUCTURE |
16.7 |
52.1 |
SOLUTION NMR |
GOOD
|
| 2ayl |
;2.0 Angstrom Crystal Structure of Manganese Protoporphyrin IX-reconstituted Ovine Prostaglandin H2 Synthase-1 Complexed With Flurbiprofen
; |
32.6 |
102.7 |
X-RAY DIFFRACTION |
GOOD
|
| 2aym |
Solution Structure of Drosophila melanogaster SNF RBD2 |
12.0 |
36.0 |
SOLUTION NMR |
GOOD
|
| 2ayn |
Structure of USP14, a proteasome-associated deubiquitinating enzyme |
37.5 |
129.2 |
X-RAY DIFFRACTION |
GOOD
|
| 2ayo |
Structure of USP14 bound to ubquitin aldehyde |
23.4 |
76.4 |
X-RAY DIFFRACTION |
GOOD
|
| 2ayp |
Crystal Structure of CHK1 with an Indol Inhibitor |
20.5 |
65.6 |
X-RAY DIFFRACTION |
GOOD
|
| 2ayq |
3-ISOPROPYLMALATE DEHYDROGENASE FROM THE MODERATE FACULTATIVE THERMOPHILE, BACILLUS COAGULANS |
28.6 |
90.1 |
X-RAY DIFFRACTION |
GOOD
|
| 2ayr |
A SERM Designed for the Treatment of Uterine Leiomyoma with Unique Tissue Specificity for Uterus and Ovaries in Rats |
20.0 |
62.4 |
X-RAY DIFFRACTION |
GOOD
|
| 2ays |
;A conserved non-metallic binding site in the C-terminal lobe of lactoferrin: Structure of the complex of C-terminal lobe of bovine lactoferrin with N-acetyl galactosamine at 1.86 A resolution
; |
20.7 |
69.4 |
X-RAY DIFFRACTION |
GOOD
|
| 2ayt |
The crystal structure of a protein disulfide oxidoreductase from aquifex aeolicus |
27.1 |
89.2 |
X-RAY DIFFRACTION |
GOOD
|
| 2ayu |
The structure of nucleosome assembly protein suggests a mechanism for histone binding and shuttling |
25.2 |
88.2 |
X-RAY DIFFRACTION |
GOOD
|
| 2ayv |
Crystal structure of a putative ubiquitin-conjugating enzyme E2 from Toxoplasma gondii |
— |
— |
X-RAY DIFFRACTION |
—
|
| 2ayw |
;Crystal Structure of the complex formed between trypsin and a designed synthetic highly potent inhibitor in the presence of benzamidine at 0.97 A resolution
; |
17.3 |
59.4 |
X-RAY DIFFRACTION |
GOOD
|
| 2ayx |
Solution structure of the E.coli RcsC C-terminus (residues 700-949) containing linker region and phosphoreceiver domain |
49.7 |
187.1 |
SOLUTION NMR |
REASONABLE
|
| 2ayy |
Solution structure of the E.coli RcsC C-terminus (residues 700-816) containing linker region |
17.4 |
49.0 |
SOLUTION NMR |
REASONABLE
|
| 2ayz |
Solution structure of the E.coli RcsC C-terminus (residues 817-949) containing phosphoreceiver domain |
15.1 |
62.4 |
SOLUTION NMR |
REASONABLE
|
| 2az0 |
Flock House virus B2-dsRNA Complex (P212121) |
19.8 |
62.5 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 2az1 |
Structure of a halophilic nucleoside diphosphate kinase from Halobacterium salinarum |
28.3 |
87.6 |
X-RAY DIFFRACTION |
GOOD
|
| 2az2 |
Flock House virus B2-dsRNA Complex (P4122) |
19.7 |
62.0 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 2az3 |
Structure of a halophilic nucleoside diphosphate kinase from Halobacterium salinarum in complex with CDP |
37.9 |
125.5 |
X-RAY DIFFRACTION |
GOOD
|
| 2az4 |
Crystal Structure of a Protein of Unknown Function from Enterococcus faecalis V583 |
32.7 |
103.9 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 2az5 |
Crystal Structure of TNF-alpha with a small molecule inhibitor |
26.5 |
82.9 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 2az8 |
HIV-1 Protease NL4-3 in complex with inhibitor, TL-3 |
14.8 |
53.8 |
X-RAY DIFFRACTION |
REASONABLE
|
| 2az9 |
HIV-1 Protease NL4-3 1X mutant |
14.8 |
52.8 |
X-RAY DIFFRACTION |
GOOD
|
| 2aza |
;STRUCTURE OF AZURIN FROM ALCALIGENES DENITRIFICANS. REFINEMENT AT 1.8 ANGSTROMS RESOLUTION AND COMPARISON OF THE TWO CRYSTALLOGRAPHICALLY INDEPENDENT MOLECULES
; |
21.1 |
76.9 |
X-RAY DIFFRACTION |
GOOD
|
| 2azb |
HIV-1 Protease NL4-3 3X mutant in complex with inhibitor, TL-3 |
14.6 |
52.3 |
X-RAY DIFFRACTION |
GOOD
|
| 2azc |
HIV-1 Protease NL4-3 6X mutant |
18.2 |
61.8 |
X-RAY DIFFRACTION |
GOOD
|
| 2azd |
;X-Ray studies on Maltodextrin Phosphorylase (MalP) Complexes: recognition of substrates and CATALYTIC mechanism of phosphorylase family
; |
39.1 |
130.9 |
X-RAY DIFFRACTION |
GOOD
|
| 2aze |
Structure of the Rb C-terminal domain bound to an E2F1-DP1 heterodimer |
23.9 |
84.0 |
X-RAY DIFFRACTION |
REASONABLE
|
| 2azh |
;Solution structure of iron-sulfur cluster assembly protein SUFU from Bacillus subtilis, with zinc bound at the active site. Northeast Structural Genomics Consortium target SR17
; |
15.2 |
55.1 |
SOLUTION NMR |
REASONABLE
|
| 2azj |
Crystal structure for the mutant D81C of Sulfolobus solfataricus hexaprenyl pyrophosphate synthase |
26.4 |
85.7 |
X-RAY DIFFRACTION |
GOOD
|
| 2azk |
Crystal structure for the mutant W136E of Sulfolobus solfataricus hexaprenyl pyrophosphate synthase |
26.4 |
81.8 |
X-RAY DIFFRACTION |
GOOD
|
| 2azl |
Crystal structure for the mutant F117E of Thermotoga maritima octaprenyl pyrophosphate synthase |
21.1 |
64.8 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 2azm |
Crystal structure of the MDC1 brct repeat in complex with the histone tail of gamma-H2AX |
29.6 |
96.9 |
X-RAY DIFFRACTION |
REASONABLE
|