+Open data
-Basic information
Entry | Database: PDB / ID: 6waf | ||||||
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Title | Crystal Structure of SmcR N55I from Vibrio vulnificus | ||||||
Components | LuxR family transcriptional regulator | ||||||
Keywords | TRANSCRIPTION / quorum-sensing / transcription factor / DNA-binding protein | ||||||
Function / homology | Function and homology information transcription cis-regulatory region binding / DNA-binding transcription factor activity Similarity search - Function | ||||||
Biological species | Vibrio vulnificus (bacteria) | ||||||
Method | X-RAY DIFFRACTION / SYNCHROTRON / MOLECULAR REPLACEMENT / Resolution: 3.381 Å | ||||||
Authors | Newman, J.D. / Russell, M.M. / Gonzalez-Gutierrez, G. / van Kessel, J.C. | ||||||
Funding support | United States, 1items
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Citation | Journal: Nucleic Acids Res. / Year: 2021 Title: The DNA binding domain of the Vibrio vulnificus SmcR transcription factor is flexible and binds diverse DNA sequences. Authors: Newman, J.D. / Russell, M.M. / Fan, L. / Wang, Y.X. / Gonzalez-Gutierrez, G. / van Kessel, J.C. | ||||||
History |
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-Structure visualization
Structure viewer | Molecule: MolmilJmol/JSmol |
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-Downloads & links
-Download
PDBx/mmCIF format | 6waf.cif.gz | 174.2 KB | Display | PDBx/mmCIF format |
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PDB format | pdb6waf.ent.gz | 140.9 KB | Display | PDB format |
PDBx/mmJSON format | 6waf.json.gz | Tree view | PDBx/mmJSON format | |
Others | Other downloads |
-Validation report
Summary document | 6waf_validation.pdf.gz | 454.2 KB | Display | wwPDB validaton report |
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Full document | 6waf_full_validation.pdf.gz | 462.8 KB | Display | |
Data in XML | 6waf_validation.xml.gz | 16.8 KB | Display | |
Data in CIF | 6waf_validation.cif.gz | 21.6 KB | Display | |
Arichive directory | https://data.pdbj.org/pub/pdb/validation_reports/wa/6waf ftp://data.pdbj.org/pub/pdb/validation_reports/wa/6waf | HTTPS FTP |
-Related structure data
Related structure data | 6waeC 6wagC 6wahC 6waiC 3kz9S S: Starting model for refinement C: citing same article (ref.) |
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Similar structure data |
-Links
-Assembly
Deposited unit |
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1 |
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Unit cell |
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Components on special symmetry positions |
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-Components
#1: Protein | Mass: 23745.047 Da / Num. of mol.: 2 / Mutation: N55I Source method: isolated from a genetically manipulated source Source: (gene. exp.) Vibrio vulnificus (bacteria) Gene: smcR, vvpR, CRN32_08135, CRN52_17705, D8T54_02235, D8T65_23975, JS86_16400 Production host: Escherichia coli (E. coli) / References: UniProt: Q9L8G8 #2: Chemical | Has ligand of interest | N | Has protein modification | 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: 3.75 Å3/Da / Density % sol: 67.24 % |
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Crystal grow | Temperature: 293 K / Method: vapor diffusion, hanging drop Details: 0.2 M of Lithium Sulfate, 0.1 M Imidazole buffer pH 7.6-8 and 6-10% PEG3350 PH range: 7.6 - 8.0 |
-Data collection
Diffraction | Mean temperature: 100 K / Serial crystal experiment: N |
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Diffraction source | Source: SYNCHROTRON / Site: ALS / Beamline: 4.2.2 / Wavelength: 1.00003 Å |
Detector | Type: RDI CMOS_8M / Detector: CMOS / Date: Dec 7, 2017 |
Radiation | Protocol: SINGLE WAVELENGTH / Monochromatic (M) / Laue (L): M / Scattering type: x-ray |
Radiation wavelength | Wavelength: 1.00003 Å / Relative weight: 1 |
Reflection | Resolution: 3.38→46.38 Å / Num. obs: 9974 / % possible obs: 98.9 % / Redundancy: 3.4 % / CC1/2: 0.996 / Rpim(I) all: 0.09 / Rrim(I) all: 0.168 / Rsym value: 0.141 / Net I/σ(I): 6.4 |
Reflection shell | Resolution: 3.38→3.5 Å / Redundancy: 3.3 % / Mean I/σ(I) obs: 1.1 / Num. unique obs: 2051 / CC1/2: 0.605 / Rpim(I) all: 0.815 / Rrim(I) all: 1.476 / Rsym value: 1.223 / % possible all: 99.4 |
-Processing
Software |
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Refinement | Method to determine structure: MOLECULAR REPLACEMENT Starting model: 3kz9 Resolution: 3.381→46.375 Å / SU ML: 0.75 / Cross valid method: FREE R-VALUE / σ(F): 1.34 / Phase error: 39.67
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Solvent computation | Shrinkage radii: 0.9 Å / VDW probe radii: 1.11 Å | ||||||||||||||||||||||||||||||||||||||||
Refinement step | Cycle: LAST / Resolution: 3.381→46.375 Å
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Refine LS restraints |
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LS refinement shell |
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Refinement TLS params. | Method: refined / Origin x: 9.4476 Å / Origin y: -13.5835 Å / Origin z: 25.9465 Å
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Refinement TLS group | Selection details: all |