[English] 日本語
![](img/lk-miru.gif)
- PDB-2bv0: Crystal Structure of Protocatechuate 3,4-Dioxygenase from Acineto... -
+
Open data
-
Basic information
Entry | Database: PDB / ID: 2bv0 | ||||||
---|---|---|---|---|---|---|---|
Title | Crystal Structure of Protocatechuate 3,4-Dioxygenase from Acinetobacter Sp. ADP1 Mutant R133H in Complex with Protocatechuate. | ||||||
![]() |
| ||||||
![]() | OXIDOREDUCTASE / DIOXYGENASE / AROMATIC DEGRADATION / NON-HEME IRON / BETA-SANDWICH / MIXED ALPHA/BETA STRUCTURE | ||||||
Function / homology | ![]() protocatechuate 3,4-dioxygenase / protocatechuate 3,4-dioxygenase activity / 3,4-dihydroxybenzoate catabolic process / beta-ketoadipate pathway / ferric iron binding Similarity search - Function | ||||||
Biological species | ![]() | ||||||
Method | ![]() ![]() | ||||||
![]() | Vetting, M.W. / Valley, M.P. / D'Argenio, D.A. / Ornston, L.N. / Lipscomb, J.D. / Ohlendorf, D.H. | ||||||
![]() | ![]() Title: Crystallographic Studies of Intradiol Dioxygenases. Authors: Vetting, M.W. | ||||||
History |
| ||||||
Remark 700 | SHEET THE SHEET STRUCTURE OF THIS MOLECULE IS BIFURCATED. IN ORDER TO REPRESENT THIS FEATURE IN ... SHEET THE SHEET STRUCTURE OF THIS MOLECULE IS BIFURCATED. IN ORDER TO REPRESENT THIS FEATURE IN THE SHEET RECORDS BELOW, TWO SHEETS ARE DEFINED. |
-
Structure visualization
Structure viewer | Molecule: ![]() ![]() |
---|
-
Downloads & links
-
Download
PDBx/mmCIF format | ![]() | 109.2 KB | Display | ![]() |
---|---|---|---|---|
PDB format | ![]() | 82.1 KB | Display | ![]() |
PDBx/mmJSON format | ![]() | Tree view | ![]() | |
Others | ![]() |
-Validation report
Summary document | ![]() | 450.3 KB | Display | ![]() |
---|---|---|---|---|
Full document | ![]() | 456.3 KB | Display | |
Data in XML | ![]() | 20.5 KB | Display | |
Data in CIF | ![]() | 29.9 KB | Display | |
Arichive directory | ![]() ![]() | HTTPS FTP |
-Related structure data
Related structure data | ![]() 2buuC ![]() 2buwC ![]() 2buxC ![]() 2buyC ![]() 1eo2S S: Starting model for refinement C: citing same article ( |
---|---|
Similar structure data |
-
Links
-
Assembly
Deposited unit | ![]()
| ||||||||
---|---|---|---|---|---|---|---|---|---|
1 | ![]()
| x 12||||||||
Unit cell |
| ||||||||
Components on special symmetry positions |
| ||||||||
Details | THE PHYSIOLOGICAL STATE OF THE MOLECULE IS A (AB)12DODECAMER. |
-
Components
#1: Protein | Mass: 23489.053 Da / Num. of mol.: 1 / Mutation: YES Source method: isolated from a genetically manipulated source Source: (gene. exp.) ![]() ![]() ![]() References: UniProt: P20371, protocatechuate 3,4-dioxygenase |
---|---|
#2: Protein | Mass: 27583.031 Da / Num. of mol.: 1 Source method: isolated from a genetically manipulated source Source: (gene. exp.) ![]() ![]() ![]() References: UniProt: P20372, protocatechuate 3,4-dioxygenase |
#3: Chemical | ChemComp-FE / |
#4: Chemical | ChemComp-DHB / |
#5: Water | ChemComp-HOH / |
Compound details | ENGINEERED |
-Experimental details
-Experiment
Experiment | Method: ![]() |
---|
-
Sample preparation
Crystal | Density Matthews: 2.61 Å3/Da / Density % sol: 52.8 % Description: CRYSTAL WAS SOAKED IN 2.0 M AMMONIUM SULFATE, 100 MM TRIS PH 8.5, 30 MM PROTOCATECHUATE WITHIN AN ANEROBIC ENVIRONMENT PRIOR TO DATA COLLECTION. |
---|---|
Crystal grow | pH: 8.5 Details: 1.8 M AMMONIUM SULFATE, 100 MM TRIS-MALEATE PH 7.5, 0.08% PEG4000 PROTEIN AT 20 MG/ML |
-Data collection
Diffraction | Mean temperature: 292 K |
---|---|
Diffraction source | Source: ![]() |
Detector | Type: RIGAKU RAXIS IV / Detector: IMAGE PLATE / Details: OSMIC CONFOCAL MAXFLUX OPTICS |
Radiation | Protocol: SINGLE WAVELENGTH / Monochromatic (M) / Laue (L): M / Scattering type: x-ray |
Radiation wavelength | Wavelength: 1.5418 Å / Relative weight: 1 |
Reflection | Resolution: 1.8→30 Å / Num. obs: 46726 / % possible obs: 99.5 % / Observed criterion σ(I): 0 / Redundancy: 3.4 % / Rmerge(I) obs: 0.04 / Net I/σ(I): 17.1 |
Reflection shell | Resolution: 1.8→1.85 Å / Redundancy: 3.4 % / Rmerge(I) obs: 0.26 / Mean I/σ(I) obs: 5.8 / % possible all: 99.5 |
-
Processing
Software |
| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Refinement | Method to determine structure: ![]() Starting model: PDB ENTRY 1EO2 Resolution: 1.8→30 Å / Cross valid method: THROUGHOUT / σ(F): 0
| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Displacement parameters | Biso mean: 26.8 Å2 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Refinement step | Cycle: LAST / Resolution: 1.8→30 Å
| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Refine LS restraints |
| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
LS refinement shell | Resolution: 1.8→1.86 Å /
|