| 1xyc |
;X-RAY CRYSTALLOGRAPHIC STRUCTURES OF D-XYLOSE ISOMERASE-SUBSTRATE COMPLEXES POSITION THE SUBSTRATE AND PROVIDE EVIDENCE FOR METAL MOVEMENT DURING CATALYSIS
; |
31.1 |
99.0 |
X-RAY DIFFRACTION |
GOOD
|
| 1xyd |
NMR Solution Structure of Rat Zinc-Calcium-S100B, 20 Structures |
16.8 |
53.0 |
SOLUTION NMR |
GOOD
|
| 1xye |
T-to-THigh Transitions in Human Hemoglobin: alpha Y42A deoxy low salt |
24.9 |
71.0 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1xyf |
ENDO-1,4-BETA-XYLANASE FROM STREPTOMYCES OLIVACEOVIRIDIS |
32.0 |
98.2 |
X-RAY DIFFRACTION |
GOOD
|
| 1xyg |
X-RAY STRUCTURE OF GENE PRODUCT FROM ARABIDOPSIS THALIANA AT2G19940 |
32.8 |
96.0 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1xyh |
Crystal Structure of Recombinant Human Cyclophilin J |
15.9 |
58.4 |
X-RAY DIFFRACTION |
GOOD
|
| 1xyi |
Hyperthermophile chromosomal protein Sac7d double mutant Val26Ala/Met29Ala in complex with DNA GCGATCGC |
14.6 |
47.0 |
X-RAY DIFFRACTION |
GOOD
|
| 1xyj |
NMR Structure of the cat prion protein |
15.4 |
52.1 |
SOLUTION NMR |
GOOD
|
| 1xyk |
NMR Structure of the canine prion protein |
15.2 |
52.4 |
SOLUTION NMR |
GOOD
|
| 1xyl |
;THE ROLE OF THE DIVALENT METAL ION IN SUGAR BINDING, RING OPENING, AND ISOMERIZATION BY D-XYLOSE ISOMERASE: REPLACEMENT OF A CATALYTIC METAL BY AN AMINO-ACID
; |
31.3 |
97.7 |
X-RAY DIFFRACTION |
GOOD
|
| 1xym |
;THE ROLE OF THE DIVALENT METAL ION IN SUGAR BINDING, RING OPENING, AND ISOMERIZATION BY D-XYLOSE ISOMERASE: REPLACEMENT OF A CATALYTIC METAL BY AN AMINO-ACID
; |
31.3 |
97.0 |
X-RAY DIFFRACTION |
GOOD
|
| 1xyn |
STRUCTURAL COMPARISON OF TWO MAJOR ENDO-1,4-BETA-XYLANASES FROM TRICHODREMA REESEI |
16.2 |
48.1 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1xyo |
STRUCTURAL COMPARISON OF TWO MAJOR ENDO-1,4-BETA-XYLANASES FROM TRICHODREMA REESEI |
25.9 |
81.6 |
X-RAY DIFFRACTION |
GOOD
|
| 1xyp |
STRUCTURAL COMPARISON OF TWO MAJOR ENDO-1,4-BETA-XYLANASES FROM TRICHODREMA REESEI |
25.9 |
82.5 |
X-RAY DIFFRACTION |
GOOD
|
| 1xyq |
NMR structure of the pig prion protein |
15.5 |
54.0 |
SOLUTION NMR |
GOOD
|
| 1xyr |
Poliovirus 135S cell entry intermediate |
29.3 |
92.3 |
ELECTRON MICROSCOPY |
GOOD
|
| 1xys |
CATALYTIC CORE OF XYLANASE A E246C MUTANT |
26.4 |
79.3 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1xyu |
Solution structure of the sheep prion protein with polymorphism H168 |
15.4 |
54.6 |
SOLUTION NMR |
GOOD
|
| 1xyv |
Low Temperature (100K) Crystal Structure Of Flavodoxin Mutant S64C, monomer, semiquinone state |
15.4 |
49.8 |
X-RAY DIFFRACTION |
GOOD
|
| 1xyw |
elk prion protein |
15.5 |
55.0 |
SOLUTION NMR |
GOOD
|
| 1xyx |
mouse prion protein fragment 121-231 |
15.8 |
55.4 |
SOLUTION NMR |
REASONABLE
|
| 1xyy |
Low Temperature (100K) Crystal Structure Of Flavodoxin Mutant S64C, homodimer, oxidised state |
15.6 |
49.0 |
X-RAY DIFFRACTION |
GOOD
|
| 1xyz |
A COMMON PROTEIN FOLD AND SIMILAR ACTIVE SITE IN TWO DISTINCT FAMILIES OF BETA-GLYCANASES |
28.3 |
90.0 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1xz0 |
Crystal structure of CD1a in complex with a synthetic mycobactin lipopeptide |
36.3 |
130.9 |
X-RAY DIFFRACTION |
GOOD
|
| 1xz1 |
Complex of halothane with apoferritin |
19.1 |
74.8 |
X-RAY DIFFRACTION |
GOOD
|
| 1xz2 |
wild-type hemoglobin deoxy no-salt |
24.9 |
70.8 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1xz3 |
Complex of apoferritin with isoflurane |
19.1 |
69.3 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1xz4 |
;Intersubunit Interactions Associated with Tyr42alpha Stabilize the Quaternary-T Tetramer but are not Major Quaternary Constraints in Deoxyhemoglobin: alphaY42A deoxyhemoglobin no-salt
; |
24.9 |
70.5 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1xz5 |
T-to-THigh Quaternary Transitions in Human Hemoglobin: alphaL91A deoxy low-salt |
24.8 |
70.0 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1xz6 |
Mutant ABO(H) blood group glycosyltransferase A |
19.7 |
68.0 |
X-RAY DIFFRACTION |
GOOD
|
| 1xz7 |
T-to-THigh Quaternary Transitions in Human Hemoglobin: alphaR92A deoxy low-salt |
24.9 |
70.2 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1xz8 |
Pyrr, The Regulator Of The Pyrimidine Biosynthetic Operon In Bacillus caldolyticus, Nucleotide-bound form |
22.1 |
67.8 |
X-RAY DIFFRACTION |
GOOD
|
| 1xz9 |
Structure of AF-6 PDZ domain |
13.5 |
47.7 |
SOLUTION NMR |
GOOD
|
| 1xza |
FUSARIUM SOLANI CUTINASE MUTANT WITH SER 129 REPLACED BY CYS |
16.6 |
52.9 |
X-RAY DIFFRACTION |
GOOD
|
| 1xzb |
FUSARIUM SOLANI CUTINASE MUTANT WITH SER 129 REPLACED BY CYS COMPLEX WITH MERCURY ACETATE |
16.3 |
53.5 |
X-RAY DIFFRACTION |
GOOD
|
| 1xzc |
FUSARIUM SOLANI CUTINASE MUTANT WITH SER 129 REPLACED BY CYS COMPLEX WITH PARA-SULFUROUSPHENYL MERCURY |
16.5 |
52.4 |
X-RAY DIFFRACTION |
GOOD
|
| 1xzd |
FUSARIUM SOLANI CUTINASE MUTANT WITH SER 213 REPLACED BY CYS |
16.4 |
52.4 |
X-RAY DIFFRACTION |
GOOD
|
| 1xze |
FUSARIUM SOLANI CUTINASE MUTANT WITH SER 92 REPLACED BY CYS |
16.5 |
53.3 |
X-RAY DIFFRACTION |
GOOD
|
| 1xzf |
FUSARIUM SOLANI CUTINASE MUTANT WITH THR 144 REPLACED BY CYS |
16.5 |
53.8 |
X-RAY DIFFRACTION |
GOOD
|
| 1xzg |
FUSARIUM SOLANI CUTINASE MUTANT WITH THR 45 REPLACED BY ALA |
16.5 |
52.9 |
X-RAY DIFFRACTION |
GOOD
|
| 1xzh |
FUSARIUM SOLANI CUTINASE MUTANT WITH THR 80 REPLACED BY PRO |
16.5 |
52.0 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1xzi |
FUSARIUM SOLANI CUTINASE MUTANT WITH THR 119 REPLACED BY HIS |
16.5 |
52.4 |
X-RAY DIFFRACTION |
GOOD
|
| 1xzj |
FUSARIUM SOLANI CUTINASE MUTANT WITH THR 38 REPLACED BY PHE |
16.6 |
52.6 |
X-RAY DIFFRACTION |
GOOD
|
| 1xzk |
FUSARIUM SOLANI CUTINASE COMPLEX WITH DI(ISOPROPYL)PHOSPHATE |
26.2 |
85.9 |
X-RAY DIFFRACTION |
GOOD
|
| 1xzl |
FUSARIUM SOLANI CUTINASE COMPLEX WITH N-HEXYLPHOSPHONATE ETHYL ESTER |
16.5 |
52.8 |
X-RAY DIFFRACTION |
GOOD
|
| 1xzm |
FUSARIUM SOLANI CUTINASE COMPLEX WITH N-UNDECYL O-METHYL CHLORO PHOSPHONATE ESTER |
16.5 |
52.4 |
X-RAY DIFFRACTION |
GOOD
|
| 1xzn |
PYRR, THE REGULATOR OF THE PYRIMIDINE BIOSYNTHETIC OPERON IN BACILLUS CALDOLYTICUS, sulfate-bound form |
22.1 |
67.7 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1xzo |
Identification of a disulfide switch in BsSco, a member of the Sco family of cytochrome c oxidase assembly proteins |
23.7 |
74.6 |
X-RAY DIFFRACTION |
GOOD
|
| 1xzp |
Structure of the GTP-binding protein TrmE from Thermotoga maritima |
29.7 |
94.4 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1xzq |
Structure of the GTP-binding protein TrmE from Thermotoga maritima complexed with 5-formyl-THF |
29.4 |
92.6 |
X-RAY DIFFRACTION |
EXCELLENT
|