| 1js8 |
Structure of a Functional Unit from Octopus Hemocyanin |
29.7 |
99.6 |
X-RAY DIFFRACTION |
GOOD
|
| 1js9 |
Brome Mosaic Virus |
31.1 |
124.7 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1jsa |
MYRISTOYLATED RECOVERIN WITH TWO CALCIUMS BOUND, NMR, 24 STRUCTURES |
18.3 |
68.2 |
SOLUTION NMR |
REASONABLE
|
| 1jsc |
Crystal Structure of the Catalytic Subunit of Yeast Acetohydroxyacid Synthase: A target for Herbicidal Inhibitors |
31.9 |
110.8 |
X-RAY DIFFRACTION |
GOOD
|
| 1jsd |
CRYSTAL STRUCTURE OF SWINE H9 HAEMAGGLUTININ |
36.5 |
131.5 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1jse |
FULL-MATRIX LEAST-SQUARES REFINEMENT OF TURKEY LYSOZYME |
15.2 |
50.4 |
X-RAY DIFFRACTION |
GOOD
|
| 1jsf |
FULL-MATRIX LEAST-SQUARES REFINEMENT OF HUMAN LYSOZYME |
15.7 |
51.0 |
X-RAY DIFFRACTION |
GOOD
|
| 1jsg |
CRYSTAL STRUCTURE OF P14TCL1, AN ONCOGENE PRODUCT INVOLVED IN T-CELL PROLYMPHOCYTIC LEUKEMIA, REVEALS A NOVEL B-BARREL TOPOLOGY |
15.4 |
52.9 |
X-RAY DIFFRACTION |
GOOD
|
| 1jsh |
CRYSTAL STRUCTURE OF H9 HAEMAGGLUTININ COMPLEXED WITH LSTA RECEPTOR ANALOG |
36.5 |
135.0 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1jsi |
CRYSTAL STRUCTURE OF H9 HAEMAGGLUTININ BOUND TO LSTC RECEPTOR ANALOG |
36.7 |
124.1 |
X-RAY DIFFRACTION |
SUSPICIOUS
|
| 1jsl |
Crystal structure of Erwinia chrysanthemi L-asparaginase complexed with 6-HYDROXY-D-NORLEUCINE |
30.1 |
88.8 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1jsm |
STRUCTURE OF H5 AVIAN HAEMAGGLUTININ |
36.4 |
134.5 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1jsn |
STRUCTURE OF AVIAN H5 HAEMAGGLUTININ COMPLEXED WITH LSTA RECEPTRO ANALOG |
36.5 |
133.0 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1jso |
STRUCTURE OF AVIAN H5 HAEMAGGLUTININ BOUND TO LSTC RECEPTOR ANALOG |
36.4 |
134.6 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1jsp |
NMR Structure of CBP Bromodomain in complex with p53 peptide |
17.9 |
47.9 |
SOLUTION NMR |
REASONABLE
|
| 1jsr |
CRYSTAL STRUCTURE OF ERWINIA CHRYSANTHEMI L-ASPARAGINASE COMPLEXED WITH 6-HYDROXY-L-NORLEUCINE |
30.1 |
89.7 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1jss |
Crystal structure of the Mus musculus cholesterol-regulated START protein 4 (StarD4). |
27.2 |
87.3 |
X-RAY DIFFRACTION |
GOOD
|
| 1jst |
PHOSPHORYLATED CYCLIN-DEPENDENT KINASE-2 BOUND TO CYCLIN A |
34.6 |
113.2 |
X-RAY DIFFRACTION |
GOOD
|
| 1jsu |
P27(KIP1)/CYCLIN A/CDK2 COMPLEX |
27.1 |
81.5 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1jsv |
The structure of cyclin-dependent kinase 2 (CDK2) in complex with 4-[(6-amino-4-pyrimidinyl)amino]benzenesulfonamide |
20.6 |
67.6 |
X-RAY DIFFRACTION |
GOOD
|
| 1jsw |
NATIVE L-ASPARTATE AMMONIA LYASE |
36.1 |
114.8 |
X-RAY DIFFRACTION |
GOOD
|
| 1jsx |
Crystal Structure of the Escherichia coli Glucose-Inhibited Division Protein B (GidB) |
17.8 |
57.7 |
X-RAY DIFFRACTION |
GOOD
|
| 1jsy |
Crystal structure of bovine arrestin-2 |
25.9 |
94.2 |
X-RAY DIFFRACTION |
GOOD
|
| 1jsz |
Crystal Structure Analysis of N7,9-dimethylguanine-VP39 complex |
20.2 |
61.3 |
X-RAY DIFFRACTION |
GOOD
|
| 1jt0 |
Crystal structure of a cooperative QacR-DNA complex |
36.2 |
122.9 |
X-RAY DIFFRACTION |
GOOD
|
| 1jt2 |
STRUCTURAL BASIS FOR THE SUBSTRATE SPECIFICITY OF THE FERUL DOMAIN OF THE CELLULOSOMAL XYLANASE Z FROM C. THERMOCELLUM |
18.4 |
58.3 |
X-RAY DIFFRACTION |
GOOD
|
| 1jt3 |
Human Acidic Fibroblast Growth Factor. 141 Amino Acid Form with Amino Histidine Tag AND LEU 73 REPLACED BY VAL (L73V) |
21.4 |
74.6 |
X-RAY DIFFRACTION |
GOOD
|
| 1jt4 |
Human Acidic Fibroblast Growth Factor. 141 Amino Acid Form with Amino Terminal His Tag AND VAL 109 REPLACED BY LEU (V109L) |
21.3 |
71.2 |
X-RAY DIFFRACTION |
GOOD
|
| 1jt5 |
;Human Acidic Fibroblast Growth Factor. 141 Amino Acid Form with Amino Terminal His Tag AND LEU 73 REPLACED BY VAL AND VAL 109 REPLACED BY LEU (L73V/V109L)
; |
21.5 |
69.5 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1jt6 |
Crystal structure of the multidrug binding protein QacR bound to dequalinium |
35.3 |
117.4 |
X-RAY DIFFRACTION |
GOOD
|
| 1jt7 |
;Human Acidic Fibroblast Growth Factor. 141 Amino Acid Form with Amino Terminal His Tag AND LEU 44 REPLACED BY PHE AND LEU 73 REPLACED BY VAL AND VAL 109 REPLACED BY LEU (L44F/L73V/V109L)
; |
39.9 |
136.8 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1jt8 |
ARCHAEAL INITIATION FACTOR-1A, AIF-1A |
16.1 |
60.2 |
SOLUTION NMR |
REASONABLE
|
| 1jt9 |
Structure of the mutant F174A T form of the Glucosamine-6-Phosphate deaminase from E.coli |
18.7 |
59.6 |
X-RAY DIFFRACTION |
GOOD
|
| 1jta |
Crystal Structure of Pectate Lyase A (C2 form) |
20.5 |
64.6 |
X-RAY DIFFRACTION |
GOOD
|
| 1jtb |
LIPID TRANSFER PROTEIN COMPLEXED WITH PALMITOYL COENZYME A, NMR, 16 STRUCTURES |
12.5 |
37.7 |
SOLUTION NMR |
GOOD
|
| 1jtc |
Human Acidic Fibroblast Growth Factor. 141 Amino Acid Form with Amino Terminal His Tag AND LEU 44 REPLACED BY PHE (L44F) |
39.8 |
130.2 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1jtd |
Crystal structure of beta-lactamase inhibitor protein-II in complex with TEM-1 beta-lactamase |
24.4 |
78.1 |
X-RAY DIFFRACTION |
GOOD
|
| 1jte |
Crystal Structure Analysis of VP39 F180W mutant |
20.2 |
61.8 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1jtf |
Crystal Structure Analysis of VP39-F180W mutant and m7GpppG complex |
20.1 |
61.7 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1jtg |
CRYSTAL STRUCTURE OF TEM-1 BETA-LACTAMASE / BETA-LACTAMASE INHIBITOR PROTEIN COMPLEX |
33.0 |
110.5 |
X-RAY DIFFRACTION |
GOOD
|
| 1jth |
;Crystal structure and biophysical properties of a complex between the N-terminal region of SNAP25 and the SNARE region of syntaxin 1a
; |
27.1 |
104.1 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1jti |
;Loop-inserted Structure of P1-P1' Cleaved Ovalbumin Mutant R339T
; |
29.8 |
92.4 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1jtj |
Solution structure of HIV-1Lai mutated SL1 hairpin |
12.6 |
42.2 |
SOLUTION NMR |
GOOD
|
| 1jtk |
Crystal structure of cytidine deaminase from Bacillus subtilis in complex with the inhibitor tetrahydrodeoxyuridine |
19.9 |
62.6 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1jtl |
The crystal structure of d(GGCCAATTGG) Complexed with Distamycin |
13.1 |
46.1 |
X-RAY DIFFRACTION |
GOOD
|
| 1jtm |
;Alternative Structures of a Sequence Extended T4 Lysozyme Show that the Highly Conserved Beta-Sheet has Weak Intrinsic Folding Propensity
; |
17.2 |
58.0 |
X-RAY DIFFRACTION |
GOOD
|
| 1jtn |
;Alternative Structures of a Sequence Extended T4 Lysozyme Show that the Highly Conserved Beta-Sheet Region has weak intrinsic Folding Propensity
; |
24.8 |
75.7 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1jto |
Degenerate interfaces in antigen-antibody complexes |
29.5 |
92.9 |
X-RAY DIFFRACTION |
GOOD
|
| 1jtp |
Degenerate interfaces in antigen-antibody complexes |
29.5 |
95.0 |
X-RAY DIFFRACTION |
GOOD
|
| 1jtq |
E. coli TS Complex with dUMP and the Pyrrolo(2,3-d)pyrimidine-based Antifolate LY341770 |
24.4 |
73.6 |
X-RAY DIFFRACTION |
EXCELLENT
|