| 1tg0 |
0.97-A structure of the SH3 domain of bbc1 |
12.7 |
40.0 |
X-RAY DIFFRACTION |
GOOD
|
| 1tg1 |
;Crystal Structure of the complex formed between russells viper phospholipase A2 and a designed peptide inhibitor PHQ-Leu-Val-Arg-Tyr at 1.2A resolution
; |
15.3 |
52.0 |
X-RAY DIFFRACTION |
GOOD
|
| 1tg2 |
Crystal structure of phenylalanine hydroxylase A313T mutant with 7,8-dihydrobiopterin bound |
19.8 |
59.0 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1tg3 |
Effect of Shuttle Location and pH Environment on H+ Transfer in Human Carbonic Anhydrase II |
18.7 |
58.9 |
X-RAY DIFFRACTION |
GOOD
|
| 1tg4 |
;Design of specific inhibitors of groupII phospholipase A2(PLA2): Crystal structure of the complex formed between russells viper PLA2 and designed peptide Phe-Leu-Ala-Tyr-Lys at 1.7A resolution
; |
15.4 |
53.6 |
X-RAY DIFFRACTION |
GOOD
|
| 1tg5 |
Crystal structures of plant 4-hydroxyphenylpyruvate dioxygenases complexed with DAS645 |
21.6 |
71.8 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1tg6 |
Crystallography and mutagenesis point to an essential role for the N-terminus of human mitochondrial ClpP |
36.8 |
106.7 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1tg7 |
Native structure of beta-galactosidase from Penicillium sp. |
31.0 |
107.6 |
X-RAY DIFFRACTION |
GOOD
|
| 1tg8 |
The structure of Dengue virus E glycoprotein |
33.8 |
128.4 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1tg9 |
Effect of Shuttle Location and pH Environment on H+ Transfer in Human Carbonic Anhydrase II |
18.8 |
59.1 |
X-RAY DIFFRACTION |
GOOD
|
| 1tgb |
;CRYSTAL STRUCTURE OF BOVINE TRYPSINOGEN AT 1.8 ANGSTROMS RESOLUTION. II. CRYSTALLOGRAPHIC REFINEMENT, REFINED CRYSTAL STRUCTURE AND COMPARISON WITH BOVINE TRYPSIN
; |
17.2 |
53.4 |
X-RAY DIFFRACTION |
GOOD
|
| 1tgc |
ON THE DISORDERED ACTIVATION DOMAIN IN TRYPSINOGEN. CHEMICAL LABELLING AND LOW-TEMPERATURE CRYSTALLOGRAPHY |
17.2 |
53.3 |
X-RAY DIFFRACTION |
GOOD
|
| 1tge |
The structure of immature Dengue virus at 12.5 angstrom |
56.7 |
180.3 |
ELECTRON MICROSCOPY |
GOOD
|
| 1tgg |
RH3 DESIGNED RIGHT-HANDED COILED COIL TRIMER |
17.0 |
58.1 |
X-RAY DIFFRACTION |
GOOD
|
| 1tgh |
TATA BINDING PROTEIN (TBP)/DNA COMPLEX |
19.2 |
64.7 |
X-RAY DIFFRACTION |
GOOD
|
| 1tgj |
HUMAN TRANSFORMING GROWTH FACTOR-BETA 3, CRYSTALLIZED FROM DIOXANE |
18.3 |
67.2 |
X-RAY DIFFRACTION |
GOOD
|
| 1tgk |
HUMAN TRANSFORMING GROWTH FACTOR BETA 3, CRYSTALLIZED FROM PEG 4000 |
18.1 |
72.1 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1tgl |
A SERINE PROTEASE TRIAD FORMS THE CATALYTIC CENTRE OF A TRIACYLGLYCEROL LIPASE |
17.6 |
50.3 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1tgm |
Crystal structure of a complex formed between group II phospholipase A2 and aspirin at 1.86 A resolution |
15.3 |
54.0 |
X-RAY DIFFRACTION |
GOOD
|
| 1tgn |
STRUCTURE OF BOVINE TRYPSINOGEN AT 1.9 ANGSTROMS RESOLUTION |
17.3 |
52.3 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1tgo |
THERMOSTABLE B TYPE DNA POLYMERASE FROM THERMOCOCCUS GORGONARIUS |
31.3 |
97.1 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1tgr |
Crystal Structure of mini-IGF-1(2) |
15.7 |
52.3 |
X-RAY DIFFRACTION |
GOOD
|
| 1tgs |
;THREE-DIMENSIONAL STRUCTURE OF THE COMPLEX BETWEEN PANCREATIC SECRETORY INHIBITOR (KAZAL TYPE) AND TRYPSINOGEN AT 1.8 ANGSTROMS RESOLUTION. STRUCTURE SOLUTION, CRYSTALLOGRAPHIC REFINEMENT AND PRELIMINARY STRUCTURAL INTERPRETATION
; |
18.9 |
61.2 |
X-RAY DIFFRACTION |
GOOD
|
| 1tgt |
ON THE DISORDERED ACTIVATION DOMAIN IN TRYPSINOGEN. CHEMICAL LABELLING AND LOW-TEMPERATURE CRYSTALLOGRAPHY |
17.3 |
55.2 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1tgu |
The crystal structure of bovine liver catalase without NADPH |
36.3 |
108.8 |
X-RAY DIFFRACTION |
GOOD
|
| 1tgv |
Structure of E. coli Uridine Phosphorylase complexed with 5-Fluorouridine and sulfate |
22.4 |
68.4 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1tgx |
;X-RAY STRUCTURE AT 1.55 A OF TOXIN GAMMA, A CARDIOTOXIN FROM NAJA NIGRICOLLIS VENOM. CRYSTAL PACKING REVEALS A MODEL FOR INSERTION INTO MEMBRANES
; |
16.8 |
55.1 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1tgy |
Structure of E. coli Uridine Phosphorylase complexed with uracil and ribose 1-phosphate |
22.6 |
71.0 |
X-RAY DIFFRACTION |
GOOD
|
| 1tgz |
Structure of human Senp2 in complex with SUMO-1 |
21.0 |
68.4 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1th0 |
Structure of human Senp2 |
29.8 |
95.3 |
X-RAY DIFFRACTION |
GOOD
|
| 1th1 |
Beta-catenin in complex with a phosphorylated APC 20aa repeat fragment |
42.6 |
159.9 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1th2 |
crystal structure of NADPH depleted bovine liver catalase complexed with azide |
36.4 |
110.0 |
X-RAY DIFFRACTION |
GOOD
|
| 1th3 |
Crystal structure of NADPH depleted bovine live catalase complexed with cyanide |
36.4 |
111.1 |
X-RAY DIFFRACTION |
GOOD
|
| 1th4 |
crystal structure of NADPH depleted bovine liver catalase complexed with 3-amino-1,2,4-triazole |
36.4 |
110.1 |
X-RAY DIFFRACTION |
GOOD
|
| 1th5 |
Solution structure of C-terminal domain of NifU-like protein from Oryza sativa |
12.0 |
41.0 |
SOLUTION NMR |
REASONABLE
|
| 1th6 |
Crystal structure of phospholipase A2 in complex with atropine at 1.23A resolution |
15.3 |
52.5 |
X-RAY DIFFRACTION |
GOOD
|
| 1th7 |
Crystal Structure of an Archaeal Sm Protein from Sulfolobus solfataricus |
30.8 |
89.4 |
X-RAY DIFFRACTION |
GOOD
|
| 1th8 |
;Crystal Structures of the ADP and ATP bound forms of the Bacillus Anti-sigma factor SpoIIAB in complex with the Anti-anti-sigma SpoIIAA: inhibitory complex with ADP, crystal form II
; |
19.9 |
64.5 |
X-RAY DIFFRACTION |
GOOD
|
| 1th9 |
Effect of Shuttle Location and pH Environment on H+ Transfer in Human Carbonic Anhydrase II |
18.7 |
58.0 |
X-RAY DIFFRACTION |
GOOD
|
| 1tha |
;MECHANISM OF MOLECULAR RECOGNITION. STRUCTURAL ASPECTS OF 3,3'-DIIODO-L-THYRONINE BINDING TO HUMAN SERUM TRANSTHYRETIN
; |
19.1 |
64.2 |
X-RAY DIFFRACTION |
GOOD
|
| 1thb |
REFINEMENT OF A PARTIALLY OXYGENATED T STATE HAEMOGLOBIN AT 1.5 ANGSTROMS RESOLUTION |
24.4 |
72.7 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1thc |
;CRYSTAL STRUCTURE DETERMINATION AT 2.3A OF HUMAN TRANSTHYRETIN-3',5'-DIBROMO-2',4,4',6-TETRA-HYDROXYAURONE COMPLEX
; |
18.9 |
62.4 |
X-RAY DIFFRACTION |
GOOD
|
| 1thd |
COMPLEX ORGANIZATION OF DENGUE VIRUS E PROTEIN AS REVEALED BY 9.5 ANGSTROM CRYO-EM RECONSTRUCTION |
51.3 |
180.7 |
ELECTRON MICROSCOPY |
GOOD
|
| 1the |
;CRYSTAL STRUCTURES OF RECOMBINANT RAT CATHEPSIN B AND A CATHEPSIN B-INHIBITOR COMPLEX: IMPLICATIONS FOR STRUCTURE-BASED INHIBITOR DESIGN
; |
23.9 |
82.0 |
X-RAY DIFFRACTION |
GOOD
|
| 1thf |
CYCLASE SUBUNIT OF IMIDAZOLEGLYCEROLPHOSPHATE SYNTHASE FROM THERMOTOGA MARITIMA |
18.7 |
57.9 |
X-RAY DIFFRACTION |
GOOD
|
| 1thg |
1.8 ANGSTROMS REFINED STRUCTURE OF THE LIPASE FROM GEOTRICHUM CANDIDUM |
23.6 |
71.3 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1thi |
CRYSTAL STRUCTURES OF TWO INTENSELY SWEET PROTEINS |
16.7 |
55.9 |
X-RAY DIFFRACTION |
GOOD
|
| 1thj |
CARBONIC ANHYDRASE FROM METHANOSARCINA |
24.4 |
75.1 |
X-RAY DIFFRACTION |
GOOD
|
| 1thk |
Effect of Shuttle Location and pH Environment on H+ Transfer in Human Carbonic Anhydrase II |
18.8 |
58.7 |
X-RAY DIFFRACTION |
GOOD
|
| 1thl |
Thermolysin complexed with a novel glutaramide derivative, n-(1-(2(r,s)-carboxy-4-phenylbutyl) cyclopentylcarbonyl)-(s)-tryptophan |
20.3 |
67.6 |
X-RAY DIFFRACTION |
GOOD
|