| 1as7 |
STRUCTURE OF ALCALIGENES FAECALIS NITRITE REDUCTASE AT CRYO TEMPERATURE |
28.6 |
84.4 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1as8 |
STRUCTURE OF NITRITE BOUND TO REDUCED ALCALIGENES FAECALIS NITRITE REDUCTASE AT CRYO TEMPERATURE |
28.6 |
81.4 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1asa |
THE STRUCTURAL BASIS FOR THE REDUCED ACTIVITY OF THE Y226F(Y225F) ACTIVE SITE MUTANT OF E. COLI ASPARTATE AMINOTRANSFERASE |
22.5 |
67.5 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1asb |
THE STRUCTURAL BASIS FOR THE REDUCED ACTIVITY OF THE D223A(D222A) ACTIVE SITE MUTANT OF E. COLI ASPARTATE AMINOTRANSFERASE |
22.8 |
69.7 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1asc |
THE STRUCTURAL BASIS FOR THE REDUCED ACTIVITY OF THE D223A(D222A) ACTIVE SITE MUTANT OF E. COLI ASPARTATE AMINOTRANSFERASE |
22.5 |
68.1 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1asd |
THE STRUCTURE OF WILD TYPE E. COLI ASPARTATE AMINOTRANSFERASE RECONSTITUTED WITH N-MEPLP |
22.7 |
69.7 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1ase |
THE STRUCTURE OF WILD TYPE E. COLI ASPARTATE AMINOTRANSFERASE RECONSTITUTED WITH PLP-N-OXIDE |
22.4 |
68.1 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1asf |
THE STRUCTURAL BASIS FOR THE REDUCED ACTIVITY OF THE Y226F(Y225F) ACTIVE SITE MUTANT OF E. COLI ASPARTATE AMINOTRANSFERASE |
22.7 |
69.4 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1asg |
THE STRUCTURAL BASIS FOR THE REDUCED ACTIVITY OF THE Y226F(Y225F) ACTIVE SITE MUTANT OF E. COLI ASPARTATE AMINOTRANSFERASE |
22.6 |
68.4 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1ash |
THE STRUCTURE OF ASCARIS HEMOGLOBIN DOMAIN I AT 2.2 ANGSTROMS RESOLUTION: MOLECULAR FEATURES OF OXYGEN AVIDITY |
16.5 |
51.9 |
X-RAY DIFFRACTION |
GOOD
|
| 1asj |
P1/MAHONEY POLIOVIRUS, AT CRYOGENIC TEMPERATURE |
29.9 |
95.7 |
X-RAY DIFFRACTION |
GOOD
|
| 1ask |
NUCLEAR TRANSPORT FACTOR 2 (NTF2) H66A MUTANT |
19.1 |
61.2 |
X-RAY DIFFRACTION |
GOOD
|
| 1asl |
;CRYSTAL STRUCTURES OF ESCHERICHIA COLI ASPARTATE AMINOTRANSFERASE IN TWO CONFORMATIONS: COMPARISON OF AN UNLIGANDED OPEN AND TWO LIGANDED CLOSED FORMS
; |
28.4 |
96.1 |
X-RAY DIFFRACTION |
GOOD
|
| 1asm |
;CRYSTAL STRUCTURES OF ESCHERICHIA COLI ASPARTATE AMINOTRANSFERASE IN TWO CONFORMATIONS: COMPARISON OF AN UNLIGANDED OPEN AND TWO LIGANDED CLOSED FORMS
; |
28.4 |
96.3 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1asn |
;CRYSTAL STRUCTURES OF ESCHERICHIA COLI ASPARTATE AMINOTRANSFERASE IN TWO CONFORMATIONS: COMPARISON OF AN UNLIGANDED OPEN AND TWO LIGANDED CLOSED FORMS
; |
28.8 |
95.6 |
X-RAY DIFFRACTION |
GOOD
|
| 1aso |
;X-RAY STRUCTURES AND MECHANISTIC IMPLICATIONS OF THREE FUNCTIONAL DERIVATIVES OF ASCORBATE OXIDASE FROM ZUCCHINI: REDUCED-, PEROXIDE-, AND AZIDE-FORMS
; |
34.9 |
118.7 |
X-RAY DIFFRACTION |
GOOD
|
| 1asp |
;X-RAY STRUCTURES AND MECHANISTIC IMPLICATIONS OF THREE FUNCTIONAL DERIVATIVES OF ASCORBATE OXIDASE FROM ZUCCHINI: REDUCED-, PEROXIDE-, AND AZIDE-FORMS
; |
34.9 |
121.7 |
X-RAY DIFFRACTION |
GOOD
|
| 1asq |
;X-RAY STRUCTURES AND MECHANISTIC IMPLICATIONS OF THREE FUNCTIONAL DERIVATIVES OF ASCORBATE OXIDASE FROM ZUCCHINI: REDUCED-, PEROXIDE-, AND AZIDE-FORMS
; |
34.9 |
127.9 |
X-RAY DIFFRACTION |
GOOD
|
| 1ass |
APICAL DOMAIN OF THE CHAPERONIN FROM THERMOPLASMA ACIDOPHILUM |
18.4 |
68.2 |
X-RAY DIFFRACTION |
GOOD
|
| 1ast |
STRUCTURE OF ASTACIN AND IMPLICATIONS FOR ACTIVATION OF ASTACINS AND ZINC-LIGATION OF COLLAGENASES |
17.5 |
55.7 |
X-RAY DIFFRACTION |
GOOD
|
| 1asu |
AVIAN SARCOMA VIRUS INTEGRASE CATALYTIC CORE DOMAIN CRYSTALLIZED FROM 2% PEG 400, 2M AMMONIUM SULFATE, HEPES PH 7.5 |
18.0 |
62.1 |
X-RAY DIFFRACTION |
GOOD
|
| 1asv |
Avian sarcoma virus integrase catalytic core domain |
16.4 |
53.8 |
X-RAY DIFFRACTION |
GOOD
|
| 1asw |
;AVIAN SARCOMA VIRUS INTEGRASE CATALYTIC CORE DOMAIN CRYSTALLIZED FROM 20% PEG 4000, 10% ISOPROPANOL, HEPES PH 7.5 USING SELENOMETHIONINE SUBSTITUTED PROTEIN; DATA COLLECTED AT-165 DEGREES C
; |
16.9 |
56.7 |
X-RAY DIFFRACTION |
GOOD
|
| 1asx |
APICAL DOMAIN OF THE CHAPERONIN FROM THERMOPLASMA ACIDOPHILUM |
17.7 |
48.6 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1asy |
CLASS II AMINOACYL TRANSFER RNA SYNTHETASES: CRYSTAL STRUCTURE OF YEAST ASPARTYL-TRNA SYNTHETASE COMPLEXED WITH TRNA ASP |
38.6 |
124.4 |
X-RAY DIFFRACTION |
GOOD
|
| 1asz |
THE ACTIVE SITE OF YEAST ASPARTYL-TRNA SYNTHETASE: STRUCTURAL AND FUNCTIONAL ASPECTS OF THE AMINOACYLATION REACTION |
38.5 |
129.2 |
X-RAY DIFFRACTION |
GOOD
|
| 1at0 |
17-kDA fragment of hedgehog C-terminal autoprocessing domain |
15.6 |
49.2 |
X-RAY DIFFRACTION |
GOOD
|
| 1at1 |
;CRYSTAL STRUCTURES OF PHOSPHONOACETAMIDE LIGATED T AND PHOSPHONOACETAMIDE AND MALONATE LIGATED R STATES OF ASPARTATE CARBAMOYLTRANSFERASE AT 2.8-ANGSTROMS RESOLUTION AND NEUTRAL P*H
; |
38.5 |
117.4 |
X-RAY DIFFRACTION |
GOOD
|
| 1at3 |
HERPES SIMPLEX VIRUS TYPE II PROTEASE |
25.5 |
83.5 |
X-RAY DIFFRACTION |
GOOD
|
| 1at4 |
INTRAMOLECULAR DNA TRIPLEX CONTAINING A NON-NUCLEOTIDE LINKER (GAGAGA-X-TCTCCT-X-CTCTCT), NMR, 7 STRUCTURES |
9.6 |
29.2 |
SOLUTION NMR |
GOOD
|
| 1at5 |
HEN EGG WHITE LYSOZYME WITH A SUCCINIMIDE RESIDUE |
15.2 |
51.8 |
X-RAY DIFFRACTION |
GOOD
|
| 1at6 |
HEN EGG WHITE LYSOZYME WITH A ISOASPARTATE RESIDUE |
15.2 |
51.3 |
X-RAY DIFFRACTION |
GOOD
|
| 1at9 |
STRUCTURE OF BACTERIORHODOPSIN AT 3.0 ANGSTROM DETERMINED BY ELECTRON CRYSTALLOGRAPHY |
19.5 |
65.7 |
ELECTRON CRYSTALLOGRAPHY |
GOOD
|
| 1ata |
;HIGH-RESOLUTION STRUCTURE OF ASCARIS TRYPSIN INHIBITOR IN SOLUTION: DIRECT EVIDENCE FOR A PH INDUCED CONFORMATIONAL TRANSITION IN THE REACTIVE SITE
; |
12.9 |
44.0 |
SOLUTION NMR |
GOOD
|
| 1atb |
;HIGH-RESOLUTION STRUCTURE OF ASCARIS TRYPSIN INHIBITOR IN SOLUTION: DIRECT EVIDENCE FOR A PH INDUCED CONFORMATIONAL TRANSITION IN THE REACTIVE SITE
; |
13.0 |
48.6 |
SOLUTION NMR |
GOOD
|
| 1atd |
;HIGH-RESOLUTION STRUCTURE OF ASCARIS TRYPSIN INHIBITOR IN SOLUTION: DIRECT EVIDENCE FOR A PH INDUCED CONFORMATIONAL TRANSITION IN THE REACTIVE SITE
; |
11.6 |
44.8 |
SOLUTION NMR |
GOOD
|
| 1ate |
;HIGH-RESOLUTION STRUCTURE OF ASCARIS TRYPSIN INHIBITOR IN SOLUTION: DIRECT EVIDENCE FOR A PH INDUCED CONFORMATIONAL TRANSITION IN THE REACTIVE SITE
; |
11.6 |
44.8 |
SOLUTION NMR |
GOOD
|
| 1atg |
AZOTOBACTER VINELANDII PERIPLASMIC MOLYBDATE-BINDING PROTEIN |
18.7 |
60.7 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1ath |
THE INTACT AND CLEAVED HUMAN ANTITHROMBIN III COMPLEX AS A MODEL FOR SERPIN-PROTEINASE INTERACTIONS |
36.7 |
122.9 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1ati |
CRYSTAL STRUCTURE OF GLYCYL-TRNA SYNTHETASE FROM THERMUS THERMOPHILUS |
30.4 |
95.7 |
X-RAY DIFFRACTION |
GOOD
|
| 1atj |
RECOMBINANT HORSERADISH PEROXIDASE C1A |
40.9 |
130.7 |
X-RAY DIFFRACTION |
GOOD
|
| 1atk |
CRYSTAL STRUCTURE OF THE CYSTEINE PROTEASE HUMAN CATHEPSIN K IN COMPLEX WITH THE COVALENT INHIBITOR E-64 |
17.5 |
56.8 |
X-RAY DIFFRACTION |
GOOD
|
| 1atl |
Structural interaction of natural and synthetic inhibitors with the VENOM METALLOPROTEINASE, ATROLYSIN C (FORM-D) |
25.2 |
82.5 |
X-RAY DIFFRACTION |
GOOD
|
| 1atn |
Atomic structure of the actin:DNASE I complex |
30.8 |
96.9 |
X-RAY DIFFRACTION |
GOOD
|
| 1ato |
THE STRUCTURE OF THE ISOLATED, CENTRAL HAIRPIN OF THE HDV ANTIGENOMIC RIBOZYME, NMR, 10 STRUCTURES |
12.2 |
42.0 |
SOLUTION NMR |
GOOD
|
| 1atp |
;2.2 angstrom refined crystal structure of the catalytic subunit of cAMP-dependent protein kinase complexed with MNATP and a peptide inhibitor
; |
21.1 |
66.8 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1atr |
THREONINE 204 OF THE CHAPERONE PROTEIN HSC70 INFLUENCES THE STRUCTURE OF THE ACTIVE SITE BUT IS NOT ESSENTIAL FOR ATP HYDROLYSIS |
22.3 |
71.9 |
X-RAY DIFFRACTION |
GOOD
|
| 1ats |
THREONINE 204 OF THE CHAPERONE PROTEIN HSC70 INFLUENCES THE STRUCTURE OF THE ACTIVE SITE BUT IS NOT ESSENTIAL FOR ATP HYDROLYSIS |
22.3 |
72.7 |
X-RAY DIFFRACTION |
GOOD
|
| 1att |
CRYSTAL STRUCTURE OF CLEAVED BOVINE ANTITHROMBIN III AT 3.2 ANGSTROMS RESOLUTION |
40.2 |
129.8 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1atu |
UNCLEAVED ALPHA-1-ANTITRYPSIN |
23.3 |
76.4 |
X-RAY DIFFRACTION |
GOOD
|