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Yorodumi- PDB-1s0o: Snapshots of replication through an abasic lesion: structural bas... -
+Open data
-Basic information
Entry | Database: PDB / ID: 1s0o | ||||||
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Title | Snapshots of replication through an abasic lesion: structural basis for base substitution and frameshift | ||||||
Components |
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Keywords | TRANSFERASE/DNA / abaic lesion / LESION BYPASS / POLYMERASE / TRANSFERASE-DNA COMPLEX | ||||||
Function / homology | Function and homology information error-prone translesion synthesis / DNA-templated DNA replication / damaged DNA binding / DNA-directed DNA polymerase / DNA-directed DNA polymerase activity / magnesium ion binding / cytoplasm Similarity search - Function | ||||||
Biological species | Sulfolobus solfataricus (archaea) | ||||||
Method | X-RAY DIFFRACTION / MOLECULAR REPLACEMENT / Resolution: 2.1 Å | ||||||
Authors | Ling, H. / Boudsocq, F. / Woodgate, R. / Yang, W. | ||||||
Citation | Journal: Mol.Cell / Year: 2004 Title: Snapshots of Replication through an Abasic Lesion; Structural Basis for Base Substitutions and Frameshifts. Authors: Ling, H. / Boudsocq, F. / Woodgate, R. / Yang, W. | ||||||
History |
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-Structure visualization
Structure viewer | Molecule: MolmilJmol/JSmol |
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-Downloads & links
-Download
PDBx/mmCIF format | 1s0o.cif.gz | 192.9 KB | Display | PDBx/mmCIF format |
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PDB format | pdb1s0o.ent.gz | 148.2 KB | Display | PDB format |
PDBx/mmJSON format | 1s0o.json.gz | Tree view | PDBx/mmJSON format | |
Others | Other downloads |
-Validation report
Summary document | 1s0o_validation.pdf.gz | 1.2 MB | Display | wwPDB validaton report |
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Full document | 1s0o_full_validation.pdf.gz | 1.2 MB | Display | |
Data in XML | 1s0o_validation.xml.gz | 36 KB | Display | |
Data in CIF | 1s0o_validation.cif.gz | 50.5 KB | Display | |
Arichive directory | https://data.pdbj.org/pub/pdb/validation_reports/s0/1s0o ftp://data.pdbj.org/pub/pdb/validation_reports/s0/1s0o | HTTPS FTP |
-Related structure data
Related structure data | 1n56C 1s0nC 1s10C 1jx4S 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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2 |
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Unit cell |
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-Components
-DNA chain , 2 types, 4 molecules CEDF
#1: DNA chain | Mass: 4081.659 Da / Num. of mol.: 2 / Source method: obtained synthetically #2: DNA chain | Mass: 5074.285 Da / Num. of mol.: 2 / Source method: obtained synthetically |
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-Protein , 1 types, 2 molecules AB
#3: Protein | Mass: 40257.879 Da / Num. of mol.: 2 Source method: isolated from a genetically manipulated source Source: (gene. exp.) Sulfolobus solfataricus (archaea) / Strain: P2 / Gene: dpo4 / Plasmid: pET22b / Species (production host): Escherichia coli / Production host: Escherichia coli BL21 (bacteria) / Strain (production host): BL21 / References: UniProt: Q97W02, DNA-directed DNA polymerase |
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-Non-polymers , 4 types, 386 molecules
#4: Chemical | ChemComp-CA / #5: Chemical | #6: Chemical | #7: Water | ChemComp-HOH / | |
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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: 2.84 Å3/Da / Density % sol: 56.34 % | ||||||||||||||||||||||||||||||||||||
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Crystal grow | Temperature: 295 K / Method: vapor diffusion, hanging drop / pH: 7 Details: PEG3350, Ca(AC)2, Hepes, pH 7.0, VAPOR DIFFUSION, HANGING DROP, temperature 295K | ||||||||||||||||||||||||||||||||||||
Components of the solutions |
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-Data collection
Diffraction | Mean temperature: 100 K |
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Diffraction source | Source: ROTATING ANODE / Type: RIGAKU RU200 / Wavelength: 1.5418 |
Detector | Type: RIGAKU RAXIS IV / Detector: IMAGE PLATE / Date: Jun 28, 2003 / Details: MIRRORS |
Radiation | Monochromator: MIRRORS / Protocol: SINGLE WAVELENGTH / Monochromatic (M) / Laue (L): M / Scattering type: x-ray |
Radiation wavelength | Wavelength: 1.5418 Å / Relative weight: 1 |
Reflection | Resolution: 2→30 Å / Num. obs: 69987 |
-Processing
Software |
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Refinement | Method to determine structure: MOLECULAR REPLACEMENT Starting model: PDB entry 1JX4 Resolution: 2.1→30 Å / σ(F): 0 / Stereochemistry target values: ENGH & HUBER
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Displacement parameters |
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Refinement step | Cycle: LAST / Resolution: 2.1→30 Å
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Refine LS restraints |
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Xplor file |
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