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- PDB-5bke: Crystal structure of AAD-2 in complex with Mn(II) and N-oxalylglycine -
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Open data
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Basic information
Entry | Database: PDB / ID: 5bke | ||||||
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Title | Crystal structure of AAD-2 in complex with Mn(II) and N-oxalylglycine | ||||||
![]() | Alpha-ketoglutarate-dependent 2,4-dichlorophenoxyacetate dioxygenase | ||||||
![]() | OXIDOREDUCTASE / dioxygenase / herbicide degradation | ||||||
Function / homology | ![]() Oxidoreductases; Acting on paired donors, with incorporation or reduction of molecular oxygen; With 2-oxoglutarate as one donor, and incorporation of one atom of oxygen into each donor / dioxygenase activity Similarity search - Function | ||||||
Biological species | ![]() | ||||||
Method | ![]() ![]() ![]() | ||||||
![]() | Chekan, J.R. / Nair, S.K. | ||||||
![]() | ![]() Title: Molecular basis for enantioselective herbicide degradation imparted by aryloxyalkanoate dioxygenases in transgenic plants. Authors: Chekan, J.R. / Ongpipattanakul, C. / Wright, T.R. / Zhang, B. / Bollinger Jr., J.M. / Rajakovich, L.J. / Krebs, C. / Cicchillo, R.M. / Nair, S.K. | ||||||
History |
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Structure visualization
Structure viewer | Molecule: ![]() ![]() |
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Downloads & links
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Download
PDBx/mmCIF format | ![]() | 423.9 KB | Display | ![]() |
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PDB format | ![]() | 342.8 KB | Display | ![]() |
PDBx/mmJSON format | ![]() | Tree view | ![]() | |
Others | ![]() |
-Validation report
Summary document | ![]() | 5.1 MB | Display | ![]() |
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Full document | ![]() | 5.1 MB | Display | |
Data in XML | ![]() | 83.5 KB | Display | |
Data in CIF | ![]() | 122.1 KB | Display | |
Arichive directory | ![]() ![]() | HTTPS FTP |
-Related structure data
Related structure data | ![]() 5bk9C ![]() 5bkbC ![]() 5bkcC ![]() 5bkdC ![]() 1gqwS C: citing same article ( S: Starting model for refinement |
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Similar structure data |
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Links
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Assembly
Deposited unit | ![]()
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Unit cell |
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Components
#1: Protein | Mass: 33693.996 Da / Num. of mol.: 7 Source method: isolated from a genetically manipulated source Source: (gene. exp.) ![]() Strain: JCM 10833 / IAM 13628 / NBRC 14792 / USDA 110 / Gene: tfdA / Production host: ![]() ![]() References: UniProt: Q89UC4, Oxidoreductases; Acting on paired donors, with incorporation or reduction of molecular oxygen; With 2-oxoglutarate as one donor, and incorporation of one atom of oxygen into each donor #2: Chemical | ChemComp-MN / #3: Chemical | ChemComp-OGA / #4: Chemical | ChemComp-K / #5: Water | ChemComp-HOH / | |
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-Experimental details
-Experiment
Experiment | Method: ![]() |
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Sample preparation
Crystal | Density Matthews: 2.52 Å3/Da / Density % sol: 51.16 % |
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Crystal grow | Temperature: 289 K / Method: vapor diffusion, hanging drop / pH: 6 Details: 22% PEG 4000 40 mM LiSO4 0.1 M MES pH 6.0 10 mg/mL AAD-2 Cryo: 15% ethylene glycol |
-Data collection
Diffraction | Mean temperature: 100 K / Serial crystal experiment: N |
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Diffraction source | Source: ![]() ![]() ![]() |
Detector | Type: MARMOSAIC 300 mm CCD / Detector: CCD / Date: Apr 25, 2015 |
Radiation | Protocol: SINGLE WAVELENGTH / Monochromatic (M) / Laue (L): M / Scattering type: x-ray |
Radiation wavelength | Wavelength: 0.9787 Å / Relative weight: 1 |
Reflection | Resolution: 2.15→50 Å / Num. obs: 127502 / % possible obs: 99 % / Redundancy: 4.6 % / Rsym value: 0.088 / Net I/σ(I): 16.1 |
Reflection shell | Resolution: 2.15→2.19 Å / Num. unique obs: 5910 / CC1/2: 0.742 / Rsym value: 0.72 / % possible all: 92.6 |
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Processing
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Refinement | Method to determine structure: ![]() Starting model: 1GQW Resolution: 2.15→25 Å / Cor.coef. Fo:Fc: 0.948 / Cor.coef. Fo:Fc free: 0.92 / SU B: 5.69 / SU ML: 0.145 / Cross valid method: THROUGHOUT / ESU R: 0.278 / ESU R Free: 0.211 / Details: HYDROGENS HAVE BEEN USED IF PRESENT IN THE INPUT
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Solvent computation | Ion probe radii: 0.8 Å / Shrinkage radii: 0.8 Å / VDW probe radii: 1.2 Å | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Displacement parameters | Biso mean: 35.038 Å2
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Refinement step | Cycle: 1 / Resolution: 2.15→25 Å
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Refine LS restraints |
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