+Open data
-Basic information
Entry | Database: PDB / ID: 8ivh | ||||||
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Title | crystal structure of SulE mutant | ||||||
Components | Alpha/beta fold hydrolase | ||||||
Keywords | HYDROLASE / Complex / SulE / mutant | ||||||
Function / homology | Function and homology information Hydrolases; Acting on ester bonds; Carboxylic-ester hydrolases / hydrolase activity Similarity search - Function | ||||||
Biological species | Hansschlegelia zhihuaiae (bacteria) | ||||||
Method | X-RAY DIFFRACTION / SYNCHROTRON / MOLECULAR REPLACEMENT / Resolution: 1.45 Å | ||||||
Authors | Liu, B. / He, J. / Ran, T. / Wang, W. | ||||||
Funding support | China, 1items
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Citation | Journal: To Be Published Title: crystal structure of SulE mutant Authors: Liu, B. / He, J. / Ran, T. / Wang, W. | ||||||
History |
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-Structure visualization
Structure viewer | Molecule: MolmilJmol/JSmol |
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-Downloads & links
-Download
PDBx/mmCIF format | 8ivh.cif.gz | 171.1 KB | Display | PDBx/mmCIF format |
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PDB format | pdb8ivh.ent.gz | 131.1 KB | Display | PDB format |
PDBx/mmJSON format | 8ivh.json.gz | Tree view | PDBx/mmJSON format | |
Others | Other downloads |
-Validation report
Summary document | 8ivh_validation.pdf.gz | 2 MB | Display | wwPDB validaton report |
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Full document | 8ivh_full_validation.pdf.gz | 2 MB | Display | |
Data in XML | 8ivh_validation.xml.gz | 35.7 KB | Display | |
Data in CIF | 8ivh_validation.cif.gz | 54.9 KB | Display | |
Arichive directory | https://data.pdbj.org/pub/pdb/validation_reports/iv/8ivh ftp://data.pdbj.org/pub/pdb/validation_reports/iv/8ivh | HTTPS FTP |
-Related structure data
Related structure data | 8iw8C 8j7iC 8j7lC 8golS S: Starting model for refinement C: citing same article (ref.) |
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Similar structure data | Similarity search - Function & homologyF&H Search |
-Links
-Assembly
Deposited unit |
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1 |
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Unit cell |
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-Components
#1: Protein | Mass: 41092.234 Da / Num. of mol.: 2 / Mutation: S209A,H333A Source method: isolated from a genetically manipulated source Source: (gene. exp.) Hansschlegelia zhihuaiae (bacteria) / Gene: EK403_17710 / Production host: Escherichia coli (E. coli) / References: UniProt: G9I933 #2: Chemical | #3: Chemical | #4: Chemical | #5: Water | ChemComp-HOH / | Has ligand of interest | Y | |
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-Experimental details
-Experiment
Experiment | Method: X-RAY DIFFRACTION / Number of used crystals: 1 |
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-Sample preparation
Crystal | Density Matthews: 2.47 Å3/Da / Density % sol: 50.22 % |
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Crystal grow | Temperature: 277 K / Method: vapor diffusion, sitting drop / Details: PEG |
-Data collection
Diffraction | Mean temperature: 100 K / Serial crystal experiment: N |
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Diffraction source | Source: SYNCHROTRON / Site: SSRF / Beamline: BL18U1 / Wavelength: 0.9791 Å |
Detector | Type: DECTRIS PILATUS 6M / Detector: PIXEL / Date: Jan 1, 2023 |
Radiation | Protocol: SINGLE WAVELENGTH / Monochromatic (M) / Laue (L): M / Scattering type: x-ray |
Radiation wavelength | Wavelength: 0.9791 Å / Relative weight: 1 |
Reflection | Resolution: 1.45→24.43 Å / Num. obs: 132910 / % possible obs: 94.6 % / Redundancy: 4.5 % / CC1/2: 0.998 / Rpim(I) all: 0.034 / Net I/σ(I): 15 |
Reflection shell | Resolution: 1.45→1.49 Å / Num. unique obs: 6159 / CC1/2: 0.639 / Rpim(I) all: 0.439 |
-Processing
Software |
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Refinement | Method to determine structure: MOLECULAR REPLACEMENT Starting model: 8GOL Resolution: 1.45→24.35 Å / Cross valid method: FREE R-VALUE Stereochemistry target values: GeoStd + Monomer Library + CDL v1.2
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Displacement parameters | Biso mean: 17.52 Å2 | ||||||||||||||||||||||||
Refinement step | Cycle: LAST / Resolution: 1.45→24.35 Å
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Refine LS restraints |
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