| 1ea1 |
Cytochrome P450 14 alpha-sterol demethylase (CYP51) from Mycobacterium tuberculosis in complex with fluconazole |
1 |
1 |
X-RAY DIFFRACTION |
| 1ea2 |
Pseudoreversion of the Catalytic Activity of Y14F by the Additional Tyrosine-to-Phenylalanine Substitution(s) in the Hydrogen Bond Network of Delta-5-3-Ketosteroid Isomerase from Pheudomonas putida Biotype B |
1 |
1 |
X-RAY DIFFRACTION |
| 1ea3 |
Influenza virus M1 protein |
2 |
2 |
X-RAY DIFFRACTION |
| 1ea4 |
TRANSCRIPTIONAL REPRESSOR COPG/22bp dsDNA COMPLEX |
4 |
4 |
X-RAY DIFFRACTION |
| 1ea5 |
NATIVE ACETYLCHOLINESTERASE (E.C. 3.1.1.7) FROM TORPEDO CALIFORNICA at 1.8A resolution |
1 |
1 |
X-RAY DIFFRACTION |
| 1ea6 |
N-terminal 40kDa fragment of NhPMS2 complexed with ADP |
2 |
2 |
X-RAY DIFFRACTION |
| 1ea7 |
Sphericase |
1 |
1 |
X-RAY DIFFRACTION |
| 1ea8 |
Apolipoprotein E3 22kD fragment LYS146GLU mutant |
1 |
1 |
X-RAY DIFFRACTION |
| 1ea9 |
Cyclomaltodextrinase |
2 |
2 |
X-RAY DIFFRACTION |
| 1eaa |
ATOMIC STRUCTURE OF THE CUBIC CORE OF THE PYRUVATE DEHYDROGENASE MULTIENZYME COMPLEX |
1 |
1 |
X-RAY DIFFRACTION |
| 1eab |
ATOMIC STRUCTURE OF THE CUBIC CORE OF THE PYRUVATE DEHYDROGENASE MULTIENZYME COMPLEX |
1 |
1 |
X-RAY DIFFRACTION |
| 1eac |
ATOMIC STRUCTURE OF THE CUBIC CORE OF THE PYRUVATE DEHYDROGENASE MULTIENZYME COMPLEX |
1 |
1 |
X-RAY DIFFRACTION |
| 1ead |
ATOMIC STRUCTURE OF THE CUBIC CORE OF THE PYRUVATE DEHYDROGENASE MULTIENZYME COMPLEX |
1 |
1 |
X-RAY DIFFRACTION |
| 1eae |
ATOMIC STRUCTURE OF THE CUBIC CORE OF THE PYRUVATE DEHYDROGENASE MULTIENZYME COMPLEX |
1 |
1 |
X-RAY DIFFRACTION |
| 1eaf |
ATOMIC STRUCTURE OF THE CUBIC CORE OF THE PYRUVATE DEHYDROGENASE MULTIENZYME COMPLEX |
1 |
1 |
X-RAY DIFFRACTION |
| 1eag |
Secreted aspartic proteinase (SAP2) from Candida albicans complexed with A70450 |
1 |
1 |
X-RAY DIFFRACTION |
| 1eah |
PV2L COMPLEXED WITH ANTIVIRAL AGENT SCH48973 |
1 |
6 |
X-RAY DIFFRACTION |
| 1eai |
COMPLEX OF ASCARIS CHYMOTRPSIN/ELASTASE INHIBITOR WITH PORCINE ELASTASE |
3 |
3 |
X-RAY DIFFRACTION |
| 1eaj |
DIMERIC STRUCTURE OF THE COXSACKIE VIRUS AND ADENOVIRUS RECEPTOR D1 DOMAIN AT 1.35 ANGSTROM RESOLUTION |
1 |
1 |
X-RAY DIFFRACTION |
| 1eak |
Catalytic domain of proMMP-2 E404Q mutant |
2 |
2 |
X-RAY DIFFRACTION |
| 1eal |
NMR STUDY OF ILEAL LIPID BINDING PROTEIN |
5 |
5 |
SOLUTION NMR |
| 1eam |
VACCINIA METHYLTRANSFERASE VP39 MUTANT (EC: 2.7.7.19) |
1 |
1 |
X-RAY DIFFRACTION |
| 1ean |
THE RUNX1 Runt domain at 1.70A resolution: A structural switch and specifically bound chloride ions modulate DNA binding |
1 |
1 |
X-RAY DIFFRACTION |
| 1eao |
THE RUNX1 Runt domain at 1.4A resolution: a structural switch and specifically bound chloride ions modulate DNA binding |
2 |
2 |
X-RAY DIFFRACTION |
| 1eap |
CRYSTAL STRUCTURE OF A CATALYTIC ANTIBODY WITH A SERINE PROTEASE ACTIVE SITE |
1 |
1 |
X-RAY DIFFRACTION |
| 1eaq |
The RUNX1 Runt domain at 1.25A resolution: A structural switch and specifically bound chloride ions modulate DNA binding |
2 |
2 |
X-RAY DIFFRACTION |
| 1ear |
Crystal structure of Bacillus pasteurii UreE at 1.7 A. Type II crystal form. |
1 |
1 |
X-RAY DIFFRACTION |
| 1eas |
NONPEPTIDIC INHIBITORS OF HUMAN LEUKOCYTE ELASTASE. 3. DESIGN, SYNTHESIS, X-RAY CRYSTALLOGRAPHIC ANALYSIS, AND STRUCTURE-ACTIVITY RELATIONSHIPS FOR A SERIES OF ORALLY ACTIVE 3-AMINO-6-PHENYLPYRIDIN-2-ONE TRIFLUOROMETHYL KETONES |
1 |
1 |
X-RAY DIFFRACTION |
| 1eat |
NONPEPTIDIC INHIBITORS OF HUMAN LEUKOCYTE ELASTASE. 5. DESIGN, SYNTHESIS, AND X-RAY CRYSTALLOGRAPHY OF A SERIES OF ORALLY ACTIVE 5-AMINO-PYRIMIDIN-6-ONE-CONTAINING TRIFLUOROMETHYLKETONES |
1 |
1 |
X-RAY DIFFRACTION |
| 1eau |
NONPEPTIDIC INHIBITORS OF HUMAN LEUKOCYTE ELASTASE. 6. DESIGN OF A POTENT, INTRATRACHEALLY ACTIVE, PYRIDONE-BASED TRIFLUOROMETHYL KETONE |
1 |
1 |
X-RAY DIFFRACTION |
| 1eav |
Crystal Structures of Human Gephyrin and Plant Cnx1 G domains - Comparative Analysis and Functional Implications |
4 |
4 |
X-RAY DIFFRACTION |
| 1eaw |
Crystal structure of the MTSP1 (matriptase)-BPTI (aprotinin) complex |
2 |
2 |
X-RAY DIFFRACTION |
| 1eax |
Crystal structure of MTSP1 (matriptase) |
1 |
1 |
X-RAY DIFFRACTION |
| 1eay |
CHEY-BINDING (P2) DOMAIN OF CHEA IN COMPLEX WITH CHEY FROM ESCHERICHIA COLI |
2 |
2 |
X-RAY DIFFRACTION |
| 1eaz |
Crystal structure of the phosphoinositol (3,4)-bisphosphate binding PH domain of TAPP1 from human. |
1 |
1 |
X-RAY DIFFRACTION |
| 1eb0 |
Crystal structure of Bacillus pasteurii UreE at 1.85 A, phased by SIRAS. Type I crystal form. |
1 |
1 |
X-RAY DIFFRACTION |
| 1eb1 |
Complex structure of human thrombin with N-methyl-arginine inhibitor |
1 |
1 |
X-RAY DIFFRACTION |
| 1eb2 |
Trypsin inhibitor complex (BPO) |
1 |
1 |
X-RAY DIFFRACTION |
| 1eb3 |
YEAST 5-AMINOLAEVULINIC ACID DEHYDRATASE 4,7-DIOXOSEBACIC ACID COMPLEX |
1 |
1 |
X-RAY DIFFRACTION |
| 1eb4 |
Histidine Ammonia-Lyase (HAL) Mutant F329A from Pseudomonas putida |
1 |
1 |
X-RAY DIFFRACTION |
| 1eb6 |
Deuterolysin from Aspergillus oryzae |
1 |
1 |
X-RAY DIFFRACTION |
| 1eb7 |
Crystal structure of the di-haem cytochrome c peroxidase from Pseudomonas aeruginosa |
1 |
1 |
X-RAY DIFFRACTION |
| 1eb8 |
Structure Determinants of Substrate Specificity of Hydroxynitrile Lyase from Manihot esculenta |
1 |
1 |
X-RAY DIFFRACTION |
| 1eb9 |
Structure Determinants of Substrate Specificity of Hydroxynitrile Lyase from Manihot esculenta |
1 |
1 |
X-RAY DIFFRACTION |
| 1eba |
COMPLEX BETWEEN THE EXTRACELLULAR DOMAIN OF ERYTHROPOIETIN (EPO) RECEPTOR [EBP] AND AN INACTIVE PEPTIDE [EMP33] CONTAINS 3,5-DIBROMOTYROSINE IN POSITION 4 (DENOTED DBY) |
3 |
3 |
X-RAY DIFFRACTION |
| 1ebb |
Bacillus stearothermophilus YhfR |
1 |
1 |
X-RAY DIFFRACTION |
| 1ebc |
SPERM WHALE MET-MYOGLOBIN:CYANIDE COMPLEX |
1 |
1 |
X-RAY DIFFRACTION |
| 1ebd |
DIHYDROLIPOAMIDE DEHYDROGENASE COMPLEXED WITH THE BINDING DOMAIN OF THE DIHYDROLIPOAMIDE ACETYLASE |
1 |
1 |
X-RAY DIFFRACTION |
| 1ebe |
Laue diffraction study on the structure of cytochrome c peroxidase compound I |
1 |
1 |
X-RAY DIFFRACTION |
| 1ebf |
HOMOSERINE DEHYDROGENASE FROM S. CEREVISIAE COMPLEX WITH NAD+ |
1 |
1 |
X-RAY DIFFRACTION |