| 1l83 |
A CAVITY-CONTAINING MUTANT OF T4 LYSOZYME IS STABILIZED BY BURIED BENZENE |
17.4 |
58.5 |
X-RAY DIFFRACTION |
GOOD
|
| 1l84 |
A CAVITY-CONTAINING MUTANT OF T4 LYSOZYME IS STABILIZED BY BURIED BENZENE |
17.4 |
61.9 |
X-RAY DIFFRACTION |
GOOD
|
| 1l85 |
;SIMILAR HYDROPHOBIC REPLACEMENTS OF LEU 99 AND PHE 153 WITHIN THE CORE OF T4 LYSOZYME HAVE DIFFERENT STRUCTURAL AND THERMODYNAMIC CONSEQUENCES
; |
17.4 |
59.5 |
X-RAY DIFFRACTION |
GOOD
|
| 1l86 |
;SIMILAR HYDROPHOBIC REPLACEMENTS OF LEU 99 AND PHE 153 WITHIN THE CORE OF T4 LYSOZYME HAVE DIFFERENT STRUCTURAL AND THERMODYNAMIC CONSEQUENCES
; |
17.4 |
58.4 |
X-RAY DIFFRACTION |
GOOD
|
| 1l87 |
;SIMILAR HYDROPHOBIC REPLACEMENTS OF LEU 99 AND PHE 153 WITHIN THE CORE OF T4 LYSOZYME HAVE DIFFERENT STRUCTURAL AND THERMODYNAMIC CONSEQUENCES
; |
17.4 |
58.5 |
X-RAY DIFFRACTION |
GOOD
|
| 1l88 |
;SIMILAR HYDROPHOBIC REPLACEMENTS OF LEU 99 AND PHE 153 WITHIN THE CORE OF T4 LYSOZYME HAVE DIFFERENT STRUCTURAL AND THERMODYNAMIC CONSEQUENCES
; |
17.4 |
69.1 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1l89 |
;SIMILAR HYDROPHOBIC REPLACEMENTS OF LEU 99 AND PHE 153 WITHIN THE CORE OF T4 LYSOZYME HAVE DIFFERENT STRUCTURAL AND THERMODYNAMIC CONSEQUENCES
; |
17.4 |
60.1 |
X-RAY DIFFRACTION |
GOOD
|
| 1l8a |
E. COLI PYRUVATE DEHYDROGENASE |
34.1 |
105.9 |
X-RAY DIFFRACTION |
GOOD
|
| 1l8b |
;Cocrystal Structure of the Messenger RNA 5' Cap-binding Protein (eIF4E) bound to 7-methylGpppG
; |
23.9 |
76.9 |
X-RAY DIFFRACTION |
GOOD
|
| 1l8c |
STRUCTURAL BASIS FOR HIF-1ALPHA/CBP RECOGNITION IN THE CELLULAR HYPOXIC RESPONSE |
15.4 |
50.8 |
SOLUTION NMR |
REASONABLE
|
| 1l8d |
Rad50 coiled-coil Zn hook |
29.9 |
116.0 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1l8f |
Structure of 20K-endoglucanase from Melanocarpus albomyces at 1.8 A |
16.6 |
48.3 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1l8g |
;Crystal structure of PTP1B complexed with 7-(1,1-Dioxo-1H-benzo[d]isothiazol-3-yloxymethyl)-2-(oxalyl-amino)-4,7-dihydro-5H-thieno[2,3-c]pyran-3-carboxylic acid
; |
20.0 |
66.1 |
X-RAY DIFFRACTION |
GOOD
|
| 1l8h |
DNA PROTECTION AND BINDING BY E. COLI DPS PROTEIN |
36.4 |
100.2 |
X-RAY DIFFRACTION |
GOOD
|
| 1l8i |
Dna Protection and Binding by E. Coli DPS Protein |
36.6 |
100.6 |
X-RAY DIFFRACTION |
GOOD
|
| 1l8j |
Crystal Structure of the Endothelial Protein C Receptor and Bound Phospholipid Molecule |
17.9 |
57.0 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1l8k |
T Cell Protein-Tyrosine Phosphatase Structure |
19.9 |
65.2 |
X-RAY DIFFRACTION |
GOOD
|
| 1l8l |
Molecular basis for the local confomational rearrangement of human phosphoserine phosphatase |
29.1 |
100.9 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1l8n |
;The 1.5A crystal structure of alpha-D-glucuronidase from Bacillus stearothermophilus T-1, complexed with 4-O-methyl-glucuronic acid and xylotriose
; |
27.0 |
89.8 |
X-RAY DIFFRACTION |
GOOD
|
| 1l8o |
Molecular basis for the local conformational rearrangement of human phosphoserine phosphatase |
29.1 |
102.7 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1l8p |
Mg-phosphonoacetohydroxamate complex of S39A yeast enolase 1 |
44.8 |
146.5 |
X-RAY DIFFRACTION |
GOOD
|
| 1l8q |
CRYSTAL STRUCTURE OF DNA REPLICATION INITIATION FACTOR |
25.7 |
78.9 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1l8r |
Structure of the Retinal Determination Protein Dachshund Reveals a DNA-Binding Motif |
20.0 |
65.1 |
X-RAY DIFFRACTION |
GOOD
|
| 1l8s |
CARBOXYLIC ESTER HYDROLASE COMPLEX (DIMERIC PLA2 + LPC-ether + ACETATE + PHOSPHATE IONS) |
19.3 |
59.3 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1l8t |
;Crystal Structure Of 3',5"-Aminoglycoside Phosphotransferase Type IIIa ADP Kanamycin A Complex
; |
19.5 |
62.1 |
X-RAY DIFFRACTION |
GOOD
|
| 1l8v |
Crystal Structure of a Mutant (C109G,G212C) P4-P6 Domain of the Group I Intron from Tetrahymena Thermophilia |
33.9 |
119.3 |
X-RAY DIFFRACTION |
GOOD
|
| 1l8w |
Crystal Structure of Lyme Disease Variable Surface Antigen VlsE of Borrelia burgdorferi |
37.6 |
151.8 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1l8x |
Crystal Structure of Ferrochelatase from the Yeast, Saccharomyces cerevisiae, with Cobalt(II) as the Substrate Ion |
27.8 |
87.5 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1l8y |
Solution structure of HMG box 5 in human upstream binding factor |
17.0 |
66.0 |
SOLUTION NMR |
REASONABLE
|
| 1l8z |
Solution structure of HMG box 5 in human upstream binding factor |
17.0 |
61.1 |
SOLUTION NMR |
GOOD
|
| 1l90 |
;SIMILAR HYDROPHOBIC REPLACEMENTS OF LEU 99 AND PHE 153 WITHIN THE CORE OF T4 LYSOZYME HAVE DIFFERENT STRUCTURAL AND THERMODYNAMIC CONSEQUENCES
; |
17.5 |
58.6 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1l91 |
;SIMILAR HYDROPHOBIC REPLACEMENTS OF LEU 99 AND PHE 153 WITHIN THE CORE OF T4 LYSOZYME HAVE DIFFERENT STRUCTURAL AND THERMODYNAMIC CONSEQUENCES
; |
17.5 |
60.4 |
X-RAY DIFFRACTION |
GOOD
|
| 1l92 |
;SIMILAR HYDROPHOBIC REPLACEMENTS OF LEU 99 AND PHE 153 WITHIN THE CORE OF T4 LYSOZYME HAVE DIFFERENT STRUCTURAL AND THERMODYNAMIC CONSEQUENCES
; |
17.5 |
58.6 |
X-RAY DIFFRACTION |
GOOD
|
| 1l93 |
;SIMILAR HYDROPHOBIC REPLACEMENTS OF LEU 99 AND PHE 153 WITHIN THE CORE OF T4 LYSOZYME HAVE DIFFERENT STRUCTURAL AND THERMODYNAMIC CONSEQUENCES
; |
17.5 |
58.8 |
X-RAY DIFFRACTION |
GOOD
|
| 1l94 |
;SIMILAR HYDROPHOBIC REPLACEMENTS OF LEU 99 AND PHE 153 WITHIN THE CORE OF T4 LYSOZYME HAVE DIFFERENT STRUCTURAL AND THERMODYNAMIC CONSEQUENCES
; |
17.5 |
58.6 |
X-RAY DIFFRACTION |
GOOD
|
| 1l95 |
;SIMILAR HYDROPHOBIC REPLACEMENTS OF LEU 99 AND PHE 153 WITHIN THE CORE OF T4 LYSOZYME HAVE DIFFERENT STRUCTURAL AND THERMODYNAMIC CONSEQUENCES
; |
17.4 |
58.2 |
X-RAY DIFFRACTION |
GOOD
|
| 1l96 |
STRUCTURE OF A HINGE-BENDING BACTERIOPHAGE T4 LYSOZYME MUTANT, ILE3-> PRO |
17.5 |
60.9 |
X-RAY DIFFRACTION |
GOOD
|
| 1l97 |
STRUCTURE OF A HINGE-BENDING BACTERIOPHAGE T4 LYSOZYME MUTANT, ILE3-> PRO |
23.3 |
76.4 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1l98 |
;PERTURBATION OF TRP 138 IN T4 LYSOZYME BY MUTATIONS AT GLN 105 USED TO CORRELATE CHANGES IN STRUCTURE, STABILITY, SOLVATION, AND SPECTROSCOPIC PROPERTIES
; |
17.5 |
59.5 |
X-RAY DIFFRACTION |
GOOD
|
| 1l99 |
;PERTURBATION OF TRP 138 IN T4 LYSOZYME BY MUTATIONS AT GLN 105 USED TO CORRELATE CHANGES IN STRUCTURE, STABILITY, SOLVATION, AND SPECTROSCOPIC PROPERTIES
; |
17.5 |
59.8 |
X-RAY DIFFRACTION |
GOOD
|
| 1l9a |
CRYSTAL STRUCTURE OF SRP19 IN COMPLEX WITH THE S DOMAIN OF SIGNAL RECOGNITION PARTICLE RNA |
32.8 |
121.1 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1l9b |
;X-Ray Structure of the Cytochrome-c(2)-Photosynthetic Reaction Center Electron Transfer Complex from Rhodobacter sphaeroides in Type II Co-Crystals
; |
32.7 |
104.0 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1l9c |
Role of Histidine 269 in Catalysis by Monomeric Sarcosine Oxidase |
30.6 |
106.1 |
X-RAY DIFFRACTION |
GOOD
|
| 1l9d |
Role of Histidine 269 in Catalysis by Monomeric Sarcosine Oxidase |
33.0 |
108.9 |
X-RAY DIFFRACTION |
GOOD
|
| 1l9e |
Role of Histidine 269 in Catalysis by Monomeric Sarcosine Oxidase |
30.6 |
104.0 |
X-RAY DIFFRACTION |
GOOD
|
| 1l9g |
CRYSTAL STRUCTURE OF URACIL-DNA GLYCOSYLASE FROM T. MARITIMA |
17.3 |
55.9 |
X-RAY DIFFRACTION |
GOOD
|
| 1l9h |
Crystal structure of bovine rhodopsin at 2.6 angstroms RESOLUTION |
28.8 |
88.0 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1l9j |
;X-Ray Structure of the Cytochrome-c(2)-Photosynthetic Reaction Center Electron Transfer Complex from Rhodobacter sphaeroides in Type I Co-Crystals
; |
71.0 |
240.4 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1l9k |
dengue methyltransferase |
19.2 |
71.8 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1l9l |
GRANULYSIN FROM HUMAN CYTOLYTIC T LYMPHOCYTES |
13.9 |
43.9 |
X-RAY DIFFRACTION |
GOOD
|