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Yorodumi- PDB-7aoz: Atomic structure of the poxvirus transcription initiation complex... -
+Open data
-Basic information
Entry | Database: PDB / ID: 7aoz | ||||||
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Title | Atomic structure of the poxvirus transcription initiation complex in conformation 1 | ||||||
Components |
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Keywords | TRANSCRIPTION / Vaccinia / Virus / RNA polymerase / DNA-dependent / pre-initiation complex / PIC / initially melted / poxvirus / poxviridae | ||||||
Function / homology | Function and homology information viral transcription / RNA polymerase I activity / DNA-directed RNA polymerase complex / nucleotidyltransferase activity / DNA-templated transcription termination / virion component / ribonucleoside binding / DNA-directed 5'-3' RNA polymerase activity / DNA-directed RNA polymerase / DNA-binding transcription factor activity ...viral transcription / RNA polymerase I activity / DNA-directed RNA polymerase complex / nucleotidyltransferase activity / DNA-templated transcription termination / virion component / ribonucleoside binding / DNA-directed 5'-3' RNA polymerase activity / DNA-directed RNA polymerase / DNA-binding transcription factor activity / DNA-templated transcription / DNA binding / zinc ion binding / metal ion binding Similarity search - Function | ||||||
Biological species | Vaccinia virus GLV-1h68 | ||||||
Method | ELECTRON MICROSCOPY / single particle reconstruction / cryo EM / Resolution: 2.85 Å | ||||||
Authors | Grimm, C. / Bartuli, J. / Fischer, U. | ||||||
Funding support | Germany, 1items
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Citation | Journal: Nat Struct Mol Biol / Year: 2021 Title: Structural basis of the complete poxvirus transcription initiation process. Authors: Clemens Grimm / Julia Bartuli / Bettina Boettcher / Aladar A Szalay / Utz Fischer / Abstract: Poxviruses express their genes in the cytoplasm of infected cells using a virus-encoded multi-subunit polymerase (vRNAP) and unique transcription factors. We present cryo-EM structures that uncover ...Poxviruses express their genes in the cytoplasm of infected cells using a virus-encoded multi-subunit polymerase (vRNAP) and unique transcription factors. We present cryo-EM structures that uncover the complete transcription initiation phase of the poxvirus vaccinia. In the pre-initiation complex, the heterodimeric early transcription factor VETFs/l adopts an arc-like shape spanning the polymerase cleft and anchoring upstream and downstream promoter elements. VETFI emerges as a TBP-like protein that inserts asymmetrically into the DNA major groove, triggers DNA melting, ensures promoter recognition and enforces transcription directionality. The helicase VETFs fosters promoter melting and the phospho-peptide domain (PPD) of vRNAP subunit Rpo30 enables transcription initiation. An unprecedented upstream promoter scrunching mechanism assisted by the helicase NPH-I probably fosters promoter escape and transition into elongation. Our structures shed light on unique mechanisms of poxviral gene expression and aid the understanding of thus far unexplained universal principles in transcription. | ||||||
History |
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-Structure visualization
Movie |
Movie viewer |
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Structure viewer | Molecule: MolmilJmol/JSmol |
-Downloads & links
-Download
PDBx/mmCIF format | 7aoz.cif.gz | 720.9 KB | Display | PDBx/mmCIF format |
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PDB format | pdb7aoz.ent.gz | 571.2 KB | Display | PDB format |
PDBx/mmJSON format | 7aoz.json.gz | Tree view | PDBx/mmJSON format | |
Others | Other downloads |
-Validation report
Summary document | 7aoz_validation.pdf.gz | 832.4 KB | Display | wwPDB validaton report |
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Full document | 7aoz_full_validation.pdf.gz | 854 KB | Display | |
Data in XML | 7aoz_validation.xml.gz | 88.1 KB | Display | |
Data in CIF | 7aoz_validation.cif.gz | 144.4 KB | Display | |
Arichive directory | https://data.pdbj.org/pub/pdb/validation_reports/ao/7aoz ftp://data.pdbj.org/pub/pdb/validation_reports/ao/7aoz | HTTPS FTP |
-Related structure data
Related structure data | 11848MC 7amvC 7aofC 7aohC 7ap8C 7ap9C M: map data used to model this data 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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-Components
-DNA-directed RNA polymerase ... , 7 types, 7 molecules ACEFGJS
#1: Protein | Mass: 146995.703 Da / Num. of mol.: 1 / Source method: isolated from a natural source / Source: (natural) Vaccinia virus GLV-1h68 / References: UniProt: Q1PIV1, DNA-directed RNA polymerase |
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#3: Protein | Mass: 35430.676 Da / Num. of mol.: 1 / Source method: isolated from a natural source / Source: (natural) Vaccinia virus GLV-1h68 / References: UniProt: Q49PG1, DNA-directed RNA polymerase |
#4: Protein | Mass: 21365.740 Da / Num. of mol.: 1 / Source method: isolated from a natural source / Source: (natural) Vaccinia virus GLV-1h68 / References: UniProt: A4GDF1, DNA-directed RNA polymerase |
#5: Protein | Mass: 19020.088 Da / Num. of mol.: 1 / Source method: isolated from a natural source / Source: (natural) Vaccinia virus GLV-1h68 / References: UniProt: Q49QC8, DNA-directed RNA polymerase |
#6: Protein | Mass: 17917.195 Da / Num. of mol.: 1 / Source method: isolated from a natural source / Source: (natural) Vaccinia virus GLV-1h68 / References: UniProt: Q49PL6, DNA-directed RNA polymerase |
#8: Protein | Mass: 7299.715 Da / Num. of mol.: 1 / Source method: isolated from a natural source / Source: (natural) Vaccinia virus GLV-1h68 / References: UniProt: Q49QI2, DNA-directed RNA polymerase |
#11: Protein | Mass: 29834.359 Da / Num. of mol.: 1 / Source method: isolated from a natural source / Source: (natural) Vaccinia virus GLV-1h68 / References: UniProt: H2DZ00, DNA-directed RNA polymerase |
-Protein , 2 types, 2 molecules BI
#2: Protein | Mass: 133526.859 Da / Num. of mol.: 1 / Source method: isolated from a natural source / Source: (natural) Vaccinia virus GLV-1h68 / References: UniProt: Q49PH2, DNA-directed RNA polymerase |
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#7: Protein | Mass: 93667.633 Da / Num. of mol.: 1 / Source method: isolated from a natural source / Source: (natural) Vaccinia virus GLV-1h68 / References: UniProt: Q1PIU7 |
-Synthetic promoter DNA oligomer, ... , 2 types, 2 molecules NT
#9: DNA chain | Mass: 18417.867 Da / Num. of mol.: 1 / Source method: obtained synthetically / Source: (synth.) Vaccinia virus GLV-1h68 |
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#12: DNA chain | Mass: 18547.941 Da / Num. of mol.: 1 / Source method: obtained synthetically / Source: (synth.) Vaccinia virus GLV-1h68 |
-RNA chain , 1 types, 1 molecules P
#10: RNA chain | Mass: 1578.032 Da / Num. of mol.: 1 / Source method: isolated from a natural source / Source: (natural) Vaccinia virus GLV-1h68 |
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-Non-polymers , 2 types, 5 molecules
#13: Chemical | ChemComp-MG / |
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#14: Chemical | ChemComp-ZN / |
-Details
Has ligand of interest | N |
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Has protein modification | Y |
-Experimental details
-Experiment
Experiment | Method: ELECTRON MICROSCOPY |
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EM experiment | Aggregation state: PARTICLE / 3D reconstruction method: single particle reconstruction |
-Sample preparation
Component |
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Molecular weight | Value: 0.67 MDa / Experimental value: NO | ||||||||||||||||||||||||
Source (natural) |
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Source (recombinant) | Organism: synthetic construct (others) | ||||||||||||||||||||||||
Buffer solution | pH: 7.5 | ||||||||||||||||||||||||
Specimen | Conc.: 0.15 mg/ml / Embedding applied: NO / Shadowing applied: NO / Staining applied: NO / Vitrification applied: YES Details: monodisperse sample prepared by sucrose gradient centrifugation | ||||||||||||||||||||||||
Specimen support | Grid material: COPPER / Grid type: Quantifoil | ||||||||||||||||||||||||
Vitrification | Cryogen name: ETHANE |
-Electron microscopy imaging
Experimental equipment | Model: Titan Krios / Image courtesy: FEI Company |
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Microscopy | Model: FEI TITAN KRIOS |
Electron gun | Electron source: FIELD EMISSION GUN / Accelerating voltage: 300 kV / Illumination mode: FLOOD BEAM |
Electron lens | Mode: BRIGHT FIELD |
Specimen holder | Specimen holder model: FEI TITAN KRIOS AUTOGRID HOLDER |
Image recording | Average exposure time: 74.99 sec. / Electron dose: 78.9 e/Å2 / Detector mode: COUNTING / Film or detector model: FEI FALCON III (4k x 4k) / Num. of grids imaged: 3 |
-Processing
CTF correction | Type: PHASE FLIPPING AND AMPLITUDE CORRECTION |
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3D reconstruction | Resolution: 2.85 Å / Resolution method: FSC 0.143 CUT-OFF / Num. of particles: 133467 / Symmetry type: POINT |