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- PDB-7dib: Crystal structure of D-threonine aldolase from Filomicrobium marinum -
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Open data
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Basic information
Entry | Database: PDB / ID: 7dib | ||||||
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Title | Crystal structure of D-threonine aldolase from Filomicrobium marinum | ||||||
![]() | D-threonine aldolase | ||||||
![]() | BIOSYNTHETIC PROTEIN / aldolase / PLP-dependent enzyme | ||||||
Function / homology | ![]() | ||||||
Biological species | ![]() | ||||||
Method | ![]() ![]() ![]() ![]() | ||||||
![]() | Seo, H. / Kim, K.-J. | ||||||
![]() | ![]() Title: Cbeta-Selective Aldol Addition of d-Threonine Aldolase by Spatial Constraint of Aldehyde Binding. Authors: Park, S.-H. / Seo, H. / Seok, J. / Kim, H. / Kwon, K.K. / Yeom, S.-J. / Lee, S.-G. / Kim, K.-J. | ||||||
History |
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Structure visualization
Structure viewer | Molecule: ![]() ![]() |
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Downloads & links
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Download
PDBx/mmCIF format | ![]() | 150.7 KB | Display | ![]() |
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PDB format | ![]() | 116.7 KB | Display | ![]() |
PDBx/mmJSON format | ![]() | Tree view | ![]() | |
Others | ![]() |
-Validation report
Summary document | ![]() | 453.6 KB | Display | ![]() |
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Full document | ![]() | 460.8 KB | Display | |
Data in XML | ![]() | 27.7 KB | Display | |
Data in CIF | ![]() | 37.9 KB | Display | |
Arichive directory | ![]() ![]() | HTTPS FTP |
-Related structure data
Related structure data | ![]() 4v15S 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: 42495.023 Da / Num. of mol.: 2 Source method: isolated from a genetically manipulated source Details: The sequence "MGSSHHHHHHSSGLVPRGSH" are derived from pET28a vector. Source: (gene. exp.) ![]() Gene: YBN1229_v1_3680 / Plasmid: pET28a / Production host: ![]() ![]() #2: Water | ChemComp-HOH / | Has ligand of interest | Y | |
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-Experimental details
-Experiment
Experiment | Method: ![]() |
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Sample preparation
Crystal | Density Matthews: 2.43 Å3/Da / Density % sol: 49.44 % |
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Crystal grow | Temperature: 298 K / Method: vapor diffusion, sitting drop / pH: 4.6 Details: PEG 400, Sodium acetate tribasic, Cadmium chloride hydrate |
-Data collection
Diffraction | Mean temperature: 100 K / Serial crystal experiment: N |
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Diffraction source | Source: ![]() ![]() |
Detector | Type: ADSC QUANTUM 270 / Detector: CCD / Date: Sep 17, 2018 |
Radiation | Monochromator: Double Crystal Monochromator / Protocol: SINGLE WAVELENGTH / Monochromatic (M) / Laue (L): M / Scattering type: x-ray |
Radiation wavelength | Wavelength: 0.97934 Å / Relative weight: 1 |
Reflection | Resolution: 2.2→50 Å / Num. obs: 41469 / % possible obs: 96.1 % / Redundancy: 4 % / CC1/2: 0.982 / Rmerge(I) obs: 0.082 / Net I/σ(I): 19.3 |
Reflection shell | Resolution: 2.2→2.24 Å / Rmerge(I) obs: 0.398 / Mean I/σ(I) obs: 3.3 / Num. unique obs: 1981 / CC1/2: 0.585 |
-Phasing
Phasing | Method: ![]() |
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Processing
Software |
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Refinement | Method to determine structure: ![]() Starting model: 4v15 Resolution: 2.2→31.3 Å / Cor.coef. Fo:Fc: 0.935 / Cor.coef. Fo:Fc free: 0.907 / SU B: 7.593 / SU ML: 0.183 / Cross valid method: THROUGHOUT / σ(F): 0 / ESU R: 0.276 / ESU R Free: 0.217 / Stereochemistry target values: MAXIMUM LIKELIHOOD Details: HYDROGENS HAVE BEEN ADDED IN THE RIDING POSITIONS U VALUES : REFINED INDIVIDUALLY
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Solvent computation | Ion probe radii: 0.8 Å / Shrinkage radii: 0.8 Å / VDW probe radii: 1.2 Å / Solvent model: MASK | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Displacement parameters | Biso max: 125.36 Å2 / Biso mean: 31.372 Å2 / Biso min: 12.8 Å2
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Refinement step | Cycle: final / Resolution: 2.2→31.3 Å
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Refine LS restraints |
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LS refinement shell | Resolution: 2.2→2.253 Å / Rfactor Rfree error: 0
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