+Open data
-Basic information
Entry | Database: PDB / ID: 1b01 | ||||||
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Title | TRANSCRIPTIONAL REPRESSOR COPG/DNA COMPLEX | ||||||
Components |
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Keywords | GENE REGULATION/DNA / TRANSCRIPTIONAL REPRESSOR / DNA-BINDING PROTEIN / PLASMID / PROTEIN-DNA COMPLEX / GENE REGULATION-DNA complex | ||||||
Function / homology | Function and homology information plasmid maintenance / protein-DNA complex / sequence-specific DNA binding / regulation of DNA-templated transcription Similarity search - Function | ||||||
Biological species | Streptococcus agalactiae (bacteria) | ||||||
Method | X-RAY DIFFRACTION / SYNCHROTRON / MIRAS / Resolution: 2.56 Å | ||||||
Authors | Gomis-Rueth, F.X. / Sola, M. / Acebo, P. / Parraga, A. / Guasch, A. / Eritja, R. / Gonzalez, A. / Espinosa, M. / del Solar, G. / Coll, M. | ||||||
Citation | Journal: EMBO J. / Year: 1998 Title: The structure of plasmid-encoded transcriptional repressor CopG unliganded and bound to its operator. Authors: Gomis-Ruth, F.X. / Sola, M. / Acebo, P. / Parraga, A. / Guasch, A. / Eritja, R. / Gonzalez, A. / Espinosa, M. / del Solar, G. / Coll, M. #1: Journal: FEBS Lett. / Year: 1998 Title: Overexpression, Purification, Crystallization and Preliminary X-Ray Diffraction Analysis of the Pmv158-Encoded Plasmid Transcriptional Repressor Protein Copg Authors: Gomis-Rueth, F.X. / Sola, M. / Perez-Luque, R. / Acebo, P. / Alda, M.T. / Gonzalez, A. / Espinosa, M. / del Solar, G. / Coll, M. | ||||||
History |
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-Structure visualization
Structure viewer | Molecule: MolmilJmol/JSmol |
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-Downloads & links
-Download
PDBx/mmCIF format | 1b01.cif.gz | 49.2 KB | Display | PDBx/mmCIF format |
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PDB format | pdb1b01.ent.gz | 34.4 KB | Display | PDB format |
PDBx/mmJSON format | 1b01.json.gz | Tree view | PDBx/mmJSON format | |
Others | Other downloads |
-Validation report
Arichive directory | https://data.pdbj.org/pub/pdb/validation_reports/b0/1b01 ftp://data.pdbj.org/pub/pdb/validation_reports/b0/1b01 | HTTPS FTP |
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-Related structure data
-Links
-Assembly
Deposited unit |
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1 |
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Unit cell |
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Noncrystallographic symmetry (NCS) | NCS oper: (Code: given Matrix: (-0.36851, -0.861028, -0.350473), Vector: |
-Components
#1: DNA chain | Mass: 5749.738 Da / Num. of mol.: 1 / Source method: obtained synthetically | ||
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#2: DNA chain | Mass: 5900.820 Da / Num. of mol.: 1 / Source method: obtained synthetically | ||
#3: Protein/peptide | Mass: 5124.092 Da / Num. of mol.: 2 / Fragment: DNA-BINDING PROTEIN Source method: isolated from a genetically manipulated source Source: (gene. exp.) Streptococcus agalactiae (bacteria) / Strain: PLS1 / Cellular location: PLASMID PMV158 / Plasmid: PMV158 / Production host: Escherichia coli (E. coli) / References: UniProt: P13920 #4: Water | ChemComp-HOH / | |
-Experimental details
-Experiment
Experiment | Method: X-RAY DIFFRACTION / Number of used crystals: 3 |
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-Sample preparation
Crystal | Density Matthews: 2.23 Å3/Da / Density % sol: 45 % | ||||||||||||||||||||
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Crystal grow | Method: vapor diffusion, hanging drop / pH: 6.7 / Details: MPD, HEPES, pH 6.70, VAPOR DIFFUSION, HANGING DROP | ||||||||||||||||||||
Components of the solutions |
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Crystal | *PLUS | ||||||||||||||||||||
Crystal grow | *PLUS PH range low: 7.5 / PH range high: 6.7 | ||||||||||||||||||||
Components of the solutions | *PLUS
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-Data collection
Diffraction | Mean temperature: 100 K |
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Diffraction source | Source: SYNCHROTRON / Site: EMBL/DESY, HAMBURG / Beamline: X31 / Wavelength: 1.5418 |
Detector | Type: MARRESEARCH / Detector: IMAGE PLATE |
Radiation | Monochromator: GRAPHITE / Protocol: SINGLE WAVELENGTH / Monochromatic (M) / Laue (L): M / Scattering type: x-ray |
Radiation wavelength | Wavelength: 1.5418 Å / Relative weight: 1 |
Reflection | Resolution: 1.6→19.61 Å / Num. obs: 91693 / % possible obs: 98.1 % / Redundancy: 5 % / Rmerge(I) obs: 0.08 / Net I/σ(I): 10.3 |
Reflection shell | Resolution: 1.6→1.69 Å / Rmerge(I) obs: 0.126 / Mean I/σ(I) obs: 3 / % possible all: 96.4 |
Reflection | *PLUS Highest resolution: 2.56 Å / Lowest resolution: 19.86 Å / Num. obs: 6252 / % possible obs: 96.3 % / Redundancy: 5.9 % / Num. measured all: 78954 / Rmerge(I) obs: 0.062 |
Reflection shell | *PLUS Highest resolution: 2.56 Å / Lowest resolution: 2.7 Å / % possible obs: 86.8 % / Rmerge(I) obs: 0.455 / Mean I/σ(I) obs: 1.7 |
-Processing
Software |
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Refinement | Method to determine structure: MIRAS / Resolution: 2.56→20 Å / Cross valid method: THROUGHOUT / σ(F): 2 Details: THE COMPLEX SET UP FOR CRYSTALLIZATION WAS MADE UP BY A COPG DIMER-OF-DIMERS AND A 19-BP DSDNA. AS THE DNA MOIETY IS PRESENT IN DUAL OCCUPANCY, A CRYSTALLOGRAPHIC DYAD IS CREATED. ...Details: THE COMPLEX SET UP FOR CRYSTALLIZATION WAS MADE UP BY A COPG DIMER-OF-DIMERS AND A 19-BP DSDNA. AS THE DNA MOIETY IS PRESENT IN DUAL OCCUPANCY, A CRYSTALLOGRAPHIC DYAD IS CREATED. ACCORDINGLY, THE CRYSTALLOGRAPHIC ASYMMETRIC UNIT COMPRISES HALF A PROTEIN/DNA COMPLEX, THAT IS, A COPG DIMER AND HALF DSDNA. THE DNA PART HAS BEEN MODELLED WITH THE TWO OBSERVED ORIENTATIONS, EACH WITH OCCUPANCY 0.5. IN THIS MODEL, DNA CHAIN E PAIRS CHAIN F AND CHAIN G DOES SO WITH CHAIN H.
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Refinement step | Cycle: LAST / Resolution: 2.56→20 Å
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Refine LS restraints |
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