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Yorodumi- PDB-4x67: Crystal structure of elongating yeast RNA polymerase II stalled a... -
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Open data
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Basic information
| Entry | Database: PDB / ID: 4x67 | ||||||||||||
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| Title | Crystal structure of elongating yeast RNA polymerase II stalled at oxidative Cyclopurine DNA lesions. | ||||||||||||
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Keywords | TRANSCRIPTION/DNA / pol II elongation complex oxidative Cyclopurine DNA lesions / TRANSCRIPTION-DNA complex | ||||||||||||
| Function / homology | Function and homology informationRNA Polymerase I Transcription Initiation / Processing of Capped Intron-Containing Pre-mRNA / RNA Polymerase III Transcription Initiation From Type 2 Promoter / RNA Pol II CTD phosphorylation and interaction with CE / Formation of the Early Elongation Complex / mRNA Capping / RNA polymerase II transcribes snRNA genes / termination of RNA polymerase II transcription / TP53 Regulates Transcription of DNA Repair Genes / RNA Polymerase II Promoter Escape ...RNA Polymerase I Transcription Initiation / Processing of Capped Intron-Containing Pre-mRNA / RNA Polymerase III Transcription Initiation From Type 2 Promoter / RNA Pol II CTD phosphorylation and interaction with CE / Formation of the Early Elongation Complex / mRNA Capping / RNA polymerase II transcribes snRNA genes / termination of RNA polymerase II transcription / TP53 Regulates Transcription of DNA Repair Genes / RNA Polymerase II Promoter Escape / RNA Polymerase II Transcription Pre-Initiation And Promoter Opening / RNA Polymerase II Transcription Initiation / RNA Polymerase II Transcription Initiation And Promoter Clearance / termination of RNA polymerase III transcription / RNA Polymerase II Pre-transcription Events / RNA-templated transcription / Formation of TC-NER Pre-Incision Complex / transcription initiation at RNA polymerase III promoter / RNA Polymerase I Promoter Escape / termination of RNA polymerase I transcription / nucleolar large rRNA transcription by RNA polymerase I / Gap-filling DNA repair synthesis and ligation in TC-NER / transcription initiation at RNA polymerase I promoter / Estrogen-dependent gene expression / maintenance of transcriptional fidelity during transcription elongation by RNA polymerase II / transcription by RNA polymerase III / Dual incision in TC-NER / translesion synthesis / RNA polymerase I complex / transcription elongation by RNA polymerase I / RNA polymerase III complex / RNA polymerase II, core complex / tRNA transcription by RNA polymerase III / transcription by RNA polymerase I / transcription-coupled nucleotide-excision repair / transcription initiation at RNA polymerase II promoter / transcription elongation by RNA polymerase II / ribonucleoside binding / DNA-directed RNA polymerase / cytoplasmic stress granule / DNA-directed RNA polymerase activity / peroxisome / ribosome biogenesis / nucleic acid binding / transcription by RNA polymerase II / protein dimerization activity / mRNA binding / nucleolus / mitochondrion / DNA binding / zinc ion binding / nucleoplasm / metal ion binding / nucleus / cytoplasm Similarity search - Function | ||||||||||||
| Biological species | ![]() synthetic construct (others) | ||||||||||||
| Method | X-RAY DIFFRACTION / SYNCHROTRON / MOLECULAR REPLACEMENT / molecular replacement / Resolution: 4.1 Å | ||||||||||||
Authors | Wang, L. / Chong, J. / Wang, D. | ||||||||||||
| Funding support | United States, 3items
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Citation | Journal: Proc.Natl.Acad.Sci.USA / Year: 2015Title: Mechanism of RNA polymerase II bypass of oxidative cyclopurine DNA lesions. Authors: Walmacq, C. / Wang, L. / Chong, J. / Scibelli, K. / Lubkowska, L. / Gnatt, A. / Brooks, P.J. / Wang, D. / Kashlev, M. | ||||||||||||
| History |
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Structure visualization
| Structure viewer | Molecule: Molmil Jmol/JSmol |
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Downloads & links
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Download
| PDBx/mmCIF format | 4x67.cif.gz | 750.1 KB | Display | PDBx/mmCIF format |
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| PDB format | pdb4x67.ent.gz | 584.4 KB | Display | PDB format |
| PDBx/mmJSON format | 4x67.json.gz | Tree view | PDBx/mmJSON format | |
| Others | Other downloads |
-Validation report
| Summary document | 4x67_validation.pdf.gz | 568.2 KB | Display | wwPDB validaton report |
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| Full document | 4x67_full_validation.pdf.gz | 706.8 KB | Display | |
| Data in XML | 4x67_validation.xml.gz | 141.4 KB | Display | |
| Data in CIF | 4x67_validation.cif.gz | 187.5 KB | Display | |
| Arichive directory | https://data.pdbj.org/pub/pdb/validation_reports/x6/4x67 ftp://data.pdbj.org/pub/pdb/validation_reports/x6/4x67 | HTTPS FTP |
-Related structure data
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Links
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Assembly
| Deposited unit | ![]()
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| Unit cell |
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Components
-DNA-directed RNA polymerase II subunit ... , 5 types, 5 molecules ABCIK
| #1: Protein | Mass: 191821.578 Da / Num. of mol.: 1 / Source method: isolated from a natural source Source: (natural) ![]() Strain: ATCC 204508 / S288c / References: UniProt: P04050 |
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| #2: Protein | Mass: 138937.297 Da / Num. of mol.: 1 / Source method: isolated from a natural source Source: (natural) ![]() Strain: ATCC 204508 / S288c / References: UniProt: P08518, DNA-directed RNA polymerase |
| #3: Protein | Mass: 35330.457 Da / Num. of mol.: 1 / Source method: isolated from a natural source Source: (natural) ![]() Strain: ATCC 204508 / S288c / References: UniProt: P16370 |
| #7: Protein | Mass: 14308.161 Da / Num. of mol.: 1 / Source method: isolated from a natural source Source: (natural) ![]() Strain: ATCC 204508 / S288c / References: UniProt: P27999 |
| #9: Protein | Mass: 13633.493 Da / Num. of mol.: 1 / Source method: isolated from a natural source Source: (natural) ![]() Strain: ATCC 204508 / S288c / References: UniProt: P38902 |
-DNA-directed RNA polymerases I, II, and III subunit ... , 5 types, 5 molecules EFHJL
| #4: Protein | Mass: 25117.094 Da / Num. of mol.: 1 / Source method: isolated from a natural source Source: (natural) ![]() Strain: ATCC 204508 / S288c / References: UniProt: P20434 |
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| #5: Protein | Mass: 17931.834 Da / Num. of mol.: 1 / Source method: isolated from a natural source Source: (natural) ![]() Strain: ATCC 204508 / S288c / References: UniProt: P20435 |
| #6: Protein | Mass: 16525.363 Da / Num. of mol.: 1 / Source method: isolated from a natural source Source: (natural) ![]() Strain: ATCC 204508 / S288c / References: UniProt: P20436 |
| #8: Protein | Mass: 8290.732 Da / Num. of mol.: 1 / Source method: isolated from a natural source Source: (natural) ![]() Strain: ATCC 204508 / S288c / References: UniProt: P22139 |
| #10: Protein | Mass: 7729.969 Da / Num. of mol.: 1 / Source method: isolated from a natural source Source: (natural) ![]() Strain: ATCC 204508 / S288c / References: UniProt: P40422 |
-RNA chain / DNA chain / Non-polymers , 3 types, 10 molecules RT

| #11: RNA chain | Mass: 2879.791 Da / Num. of mol.: 1 / Source method: obtained synthetically / Source: (synth.) synthetic construct (others) |
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| #12: DNA chain | Mass: 8950.771 Da / Num. of mol.: 1 / Source method: obtained synthetically / Source: (synth.) synthetic construct (others) |
| #13: Chemical | ChemComp-ZN / |
-Details
| Compound details | A 14 nt Non-Template DNA (CTG CTT ATC GGT AG) was not built into the final model due to the weak density |
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| Has protein modification | Y |
-Experimental details
-Experiment
| Experiment | Method: X-RAY DIFFRACTION / Number of used crystals: 1 |
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Sample preparation
| Crystal | Density Matthews: 3.66 Å3/Da / Density % sol: 66.36 % |
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| Crystal grow | Temperature: 293.15 K / Method: vapor diffusion, hanging drop Details: 390 mM (NH4)2HPO4/NaH2PO4, PH 5.9-6.3, 50 mM dioxane, 10 mM DTT, and 10.7% - 11.6% PEG6000 PH range: 5.9-6.3 |
-Data collection
| Diffraction | Mean temperature: 100 K | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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| Diffraction source | Source: SYNCHROTRON / Site: ALS / Beamline: 5.0.3 / Wavelength: 0.976 Å | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Detector | Type: ADSC QUANTUM 315r / Detector: CCD / Date: Oct 26, 2013 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Radiation | Protocol: SINGLE WAVELENGTH / Monochromatic (M) / Laue (L): M / Scattering type: x-ray | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Radiation wavelength | Wavelength: 0.976 Å / Relative weight: 1 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Reflection | Resolution: 4.1→50 Å / Num. obs: 46515 / % possible obs: 86 % / Redundancy: 2.7 % / Rmerge(I) obs: 0.222 / Rpim(I) all: 0.152 / Rrim(I) all: 0.27 / Χ2: 0.938 / Net I/av σ(I): 4.375 / Net I/σ(I): 3.6 / Num. measured all: 127175 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Reflection shell | Diffraction-ID: 1 / Rejects: _
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-Phasing
| Phasing | Method: molecular replacement | |||||||||
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| Phasing MR | Model details: Phaser MODE: MR_AUTO
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Processing
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| Refinement | Method to determine structure: MOLECULAR REPLACEMENT / Resolution: 4.1→50 Å / Cor.coef. Fo:Fc: 0.861 / Cor.coef. Fo:Fc free: 0.794 / WRfactor Rfree: 0.2637 / WRfactor Rwork: 0.2165 / FOM work R set: 0.7322 / SU Rfree: 1.1286 / Cross valid method: THROUGHOUT / σ(F): 0 / ESU R Free: 1.129 / Stereochemistry target values: MAXIMUM LIKELIHOODDetails: HYDROGENS HAVE BEEN ADDED IN THE RIDING POSITIONS U VALUES : REFINED INDIVIDUALLY
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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 max: 258.36 Å2 / Biso mean: 86.315 Å2 / Biso min: 30.87 Å2
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| Refinement step | Cycle: final / Resolution: 4.1→50 Å
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| Refine LS restraints |
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| LS refinement shell | Resolution: 4.098→4.204 Å / Total num. of bins used: 20
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X-RAY DIFFRACTION
United States, 3items
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