[English] 日本語
Yorodumi- PDB-1qyx: Crystal structure of human estrogenic 17beta-hydroxysteroid dehyd... -
+Open data
-Basic information
Entry | Database: PDB / ID: 1qyx | ||||||
---|---|---|---|---|---|---|---|
Title | Crystal structure of human estrogenic 17beta-hydroxysteroid dehydrogenase complex with androstenedione and NADP | ||||||
Components | Estradiol 17 beta-dehydrogenase 1 | ||||||
Keywords | OXIDOREDUCTASE / 17bHSD1 / androstenedione / C19-steroid / NADP binding | ||||||
Function / homology | Function and homology information 17-beta-hydroxysteroid dehydrogenase (NADP+) activity / 3(or 17)beta-hydroxysteroid dehydrogenase / estradiol binding / estrogen biosynthetic process / testosterone dehydrogenase [NAD(P)+] activity / cellular response to metal ion / Estrogen biosynthesis / : / testosterone biosynthetic process / testosterone dehydrogenase (NAD+) activity ...17-beta-hydroxysteroid dehydrogenase (NADP+) activity / 3(or 17)beta-hydroxysteroid dehydrogenase / estradiol binding / estrogen biosynthetic process / testosterone dehydrogenase [NAD(P)+] activity / cellular response to metal ion / Estrogen biosynthesis / : / testosterone biosynthetic process / testosterone dehydrogenase (NAD+) activity / testosterone 17-beta-dehydrogenase (NADP+) activity / 17beta-estradiol 17-dehydrogenase / estradiol 17-beta-dehydrogenase [NAD(P)+] activity / steroid biosynthetic process / estrogen metabolic process / NADP+ binding / lysosome organization / The canonical retinoid cycle in rods (twilight vision) / small molecule binding / catalytic activity / adipose tissue development / skeletal muscle tissue development / steroid binding / bone development / NADP binding / gene expression / protein homodimerization activity / cytosol / cytoplasm Similarity search - Function | ||||||
Biological species | Homo sapiens (human) | ||||||
Method | X-RAY DIFFRACTION / SYNCHROTRON / FOURIER SYNTHESIS / Resolution: 1.89 Å | ||||||
Authors | Shi, R. / Lin, S.X. | ||||||
Citation | Journal: J.Biol.Chem. / Year: 2004 Title: Cofactor hydrogen bonding onto the protein main chain is conserved in the short chain dehydrogenase/reductase family and contributes to nicotinamide orientation. Authors: Shi, R. / Lin, S.X. | ||||||
History |
| ||||||
Remark 600 | HETEROGEN Several atoms belonging to Nicotinamide part of HETNAM 'NAP' could not be modeled and are ...HETEROGEN Several atoms belonging to Nicotinamide part of HETNAM 'NAP' could not be modeled and are missing from the coordinates |
-Structure visualization
Structure viewer | Molecule: MolmilJmol/JSmol |
---|
-Downloads & links
-Download
PDBx/mmCIF format | 1qyx.cif.gz | 72.7 KB | Display | PDBx/mmCIF format |
---|---|---|---|---|
PDB format | pdb1qyx.ent.gz | 51.6 KB | Display | PDB format |
PDBx/mmJSON format | 1qyx.json.gz | Tree view | PDBx/mmJSON format | |
Others | Other downloads |
-Validation report
Summary document | 1qyx_validation.pdf.gz | 513.7 KB | Display | wwPDB validaton report |
---|---|---|---|---|
Full document | 1qyx_full_validation.pdf.gz | 520.3 KB | Display | |
Data in XML | 1qyx_validation.xml.gz | 8.4 KB | Display | |
Data in CIF | 1qyx_validation.cif.gz | 12.5 KB | Display | |
Arichive directory | https://data.pdbj.org/pub/pdb/validation_reports/qy/1qyx ftp://data.pdbj.org/pub/pdb/validation_reports/qy/1qyx | HTTPS FTP |
-Related structure data
Related structure data | 1qyvC 1qywC 1jtvS S: Starting model for refinement C: citing same article (ref.) |
---|---|
Similar structure data |
-Links
-Assembly
Deposited unit |
| ||||||||
---|---|---|---|---|---|---|---|---|---|
1 |
| ||||||||
Unit cell |
| ||||||||
Details | The second part of the biological assembly (homodimer) is generated by the two fold axis: -X, Y, -Z. |
-Components
#1: Protein | Mass: 34887.828 Da / Num. of mol.: 1 / Source method: isolated from a natural source / Source: (natural) Homo sapiens (human) / Tissue: placenta References: UniProt: P14061, 17beta-estradiol 17-dehydrogenase |
---|---|
#2: Chemical | ChemComp-ASD / |
#3: Chemical | ChemComp-NAP / |
#4: Chemical | ChemComp-GOL / |
#5: Water | ChemComp-HOH / |
-Experimental details
-Experiment
Experiment | Method: X-RAY DIFFRACTION / Number of used crystals: 1 |
---|
-Sample preparation
Crystal | Density Matthews: 2.32 Å3/Da / Density % sol: 46.97 % |
---|---|
Crystal grow | Temperature: 300 K / Method: vapor diffusion, hanging drop / pH: 7.5 Details: PEG 4000, magnisum chloride, beta-octylglucoside, HEPES, glycerol, soaking with testosterone and NADP, pH 7.5, VAPOR DIFFUSION, HANGING DROP, temperature 300K |
-Data collection
Diffraction | Mean temperature: 100 K |
---|---|
Diffraction source | Source: SYNCHROTRON / Site: NSLS / Beamline: X8C / Wavelength: 0.9795 Å |
Detector | Type: ADSC QUANTUM 4 / Detector: CCD / Date: Oct 10, 2000 / Details: mirrors |
Radiation | Protocol: SINGLE WAVELENGTH / Monochromatic (M) / Laue (L): M / Scattering type: x-ray |
Radiation wavelength | Wavelength: 0.9795 Å / Relative weight: 1 |
Reflection | Resolution: 1.89→30 Å / Num. all: 65964 / Num. obs: 24387 / % possible obs: 95.4 % / Observed criterion σ(I): 2 / Redundancy: 2.7 % / Biso Wilson estimate: 21.4 Å2 / Rmerge(I) obs: 0.046 |
Reflection shell | Resolution: 1.89→1.96 Å / Redundancy: 2.58 % / Rmerge(I) obs: 0.289 / Mean I/σ(I) obs: 2 / Num. unique all: 2478 / % possible all: 93.6 |
-Processing
Software |
| ||||||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Refinement | Method to determine structure: FOURIER SYNTHESIS Starting model: PDB entry 1JTV Resolution: 1.89→10 Å / Isotropic thermal model: isotropic / Cross valid method: THROUGHOUT / σ(F): 0 / σ(I): 1 / Stereochemistry target values: Engh & Huber
| ||||||||||||||||
Displacement parameters | Biso mean: 37.7 Å2 | ||||||||||||||||
Refinement step | Cycle: LAST / Resolution: 1.89→10 Å
| ||||||||||||||||
Refine LS restraints |
| ||||||||||||||||
LS refinement shell | Resolution: 1.89→1.97 Å
|