+ Open data
Open data
- Basic information
Basic information
| Entry | Database: PDB / ID: 4fj5 | ||||||
|---|---|---|---|---|---|---|---|
| Title | RB69 DNA polymerase ternary complex with dATP/dT | ||||||
|  Components | 
 | ||||||
|  Keywords | Transferase/DNA / dATP/dT / RB69pol / RB69 / quadruple / Transferase-DNA complex | ||||||
| Function / homology |  Function and homology information bidirectional double-stranded viral DNA replication / Hydrolases; Acting on ester bonds; Exodeoxyribonucleases producing 5'-phosphomonoesters / 3'-5' exonuclease activity / DNA-templated DNA replication / DNA-directed DNA polymerase / DNA-directed DNA polymerase activity / nucleotide binding / DNA binding / metal ion binding Similarity search - Function | ||||||
| Biological species |  Enterobacteria phage RB69 (virus) | ||||||
| Method |  X-RAY DIFFRACTION /  SYNCHROTRON /  MOLECULAR REPLACEMENT / Resolution: 2.05 Å | ||||||
|  Authors | Xia, S. / Wang, J. / Konigsberg, W.H. | ||||||
|  Citation |  Journal: J.Am.Chem.Soc. / Year: 2013 Title: DNA mismatch synthesis complexes provide insights into base selectivity of a B family DNA polymerase. Authors: Xia, S. / Wang, J. / Konigsberg, W.H. | ||||||
| History | 
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- Structure visualization
Structure visualization
| Structure viewer | Molecule:  Molmil  Jmol/JSmol | 
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- Downloads & links
Downloads & links
- Download
Download
| PDBx/mmCIF format |  4fj5.cif.gz | 235.1 KB | Display |  PDBx/mmCIF format | 
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| PDB format |  pdb4fj5.ent.gz | 180.5 KB | Display |  PDB format | 
| PDBx/mmJSON format |  4fj5.json.gz | Tree view |  PDBx/mmJSON format | |
| Others |  Other downloads | 
-Validation report
| Summary document |  4fj5_validation.pdf.gz | 801 KB | Display |  wwPDB validaton report | 
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| Full document |  4fj5_full_validation.pdf.gz | 805.6 KB | Display | |
| Data in XML |  4fj5_validation.xml.gz | 40.2 KB | Display | |
| Data in CIF |  4fj5_validation.cif.gz | 61.6 KB | Display | |
| Arichive directory |  https://data.pdbj.org/pub/pdb/validation_reports/fj/4fj5  ftp://data.pdbj.org/pub/pdb/validation_reports/fj/4fj5 | HTTPS FTP | 
-Related structure data
| Related structure data |  4fj7C  4fj8C  4fj9C  4fjgC  4fjhC  4fjiC  4fjjC  4fjkC  4fjlC  4fjmC  4fjnC  4fjxC  4fk0C  4fk2C  4fk4C C: citing same article ( | 
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| Similar structure data | 
- Links
Links
- Assembly
Assembly
| Deposited unit |  
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| 1 | 
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| Unit cell | 
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- Components
Components
-Protein , 1 types, 1 molecules A
| #1: Protein | Mass: 104448.867 Da / Num. of mol.: 1 / Mutation: D222A, D327A, L415A, L561A, S565G, Y567A Source method: isolated from a genetically manipulated source Source: (gene. exp.)  Enterobacteria phage RB69 (virus) / Gene: 43 / Production host:   Escherichia coli (E. coli) / References: UniProt: Q38087, DNA-directed DNA polymerase | 
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-DNA chain , 2 types, 2 molecules TP 
| #2: DNA chain | Mass: 5516.579 Da / Num. of mol.: 1 / Source method: obtained synthetically | 
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| #3: DNA chain | Mass: 3982.596 Da / Num. of mol.: 1 / Source method: obtained synthetically | 
-Non-polymers , 3 types, 760 molecules 




| #4: Chemical | ChemComp-DTP / | ||
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| #5: Chemical | ChemComp-CA / #6: Water | ChemComp-HOH / |  | 
-Experimental details
-Experiment
| Experiment | Method:  X-RAY DIFFRACTION / Number of used crystals: 1 | 
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- Sample preparation
Sample preparation
| Crystal | Density Matthews: 2.59 Å3/Da / Density % sol: 52.52 % | 
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| Crystal grow | Temperature: 298 K / Method: vapor diffusion / pH: 6.5 Details: 150 mM CaCl2, 10% (w/v) PEG 350 monomethyl ether (MME), and 100 mM sodium cacodylate pH 6.5, VAPOR DIFFUSION, temperature 298K | 
-Data collection
| Diffraction | Mean temperature: 110 K | 
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| Diffraction source | Source:  SYNCHROTRON / Site:  APS  / Beamline: 24-ID-E / Wavelength: 0.97 Å | 
| Detector | Type: APEX II CCD / Detector: CCD / Date: Oct 15, 2011 | 
| Radiation | Monochromator: Graphite / Protocol: SINGLE WAVELENGTH / Monochromatic (M) / Laue (L): M / Scattering type: x-ray | 
| Radiation wavelength | Wavelength: 0.97 Å / Relative weight: 1 | 
| Reflection | Resolution: 2.05→50 Å / Num. all: 74061 / Num. obs: 70263 / % possible obs: 94.9 % / Observed criterion σ(F): 3.2 / Observed criterion σ(I): 1.6 | 
| Reflection shell | Resolution: 2.05→2.12 Å / % possible all: 99.5 | 
- Processing
Processing
| Software | 
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| Refinement | Method to determine structure:  MOLECULAR REPLACEMENT / Resolution: 2.05→34.57 Å / Cor.coef. Fo:Fc: 0.955  / Cor.coef. Fo:Fc free: 0.925  / SU B: 4.329  / SU ML: 0.117  / Cross valid method: THROUGHOUT / ESU R: 0.193  / ESU R Free: 0.176  / Stereochemistry target values: MAXIMUM LIKELIHOOD / 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 / Solvent model: MASK | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Displacement parameters | Biso  mean: 30.84 Å2 
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| Refinement step | Cycle: LAST / Resolution: 2.05→34.57 Å 
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| Refine LS restraints | 
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| LS refinement shell | Resolution: 2.05→2.1 Å / Total num. of bins used: 20 
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