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Yorodumi- PDB-7d7c: CryoEM structure of gp55-dependent RNA polymerase-promoter open c... -
+Open data
-Basic information
Entry | Database: PDB / ID: 7d7c | ||||||
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Title | CryoEM structure of gp55-dependent RNA polymerase-promoter open complex | ||||||
Components |
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Keywords | TRANSCRIPTION / RNA polymerase | ||||||
Function / homology | Function and homology information DNA-directed RNA polymerase complex / ribonucleoside binding / DNA-directed 5'-3' RNA polymerase activity / DNA-directed RNA polymerase / protein dimerization activity / DNA-templated transcription / magnesium ion binding / DNA binding / zinc ion binding / cytoplasm Similarity search - Function | ||||||
Biological species | Escherichia coli (E. coli) Escherichia coli 1-392-07_S4_C3 (bacteria) | ||||||
Method | ELECTRON MICROSCOPY / single particle reconstruction / cryo EM / Resolution: 3.6 Å | ||||||
Authors | Shi, J. / Wen, A. / Jin, S. / Feng, Y. | ||||||
Funding support | China, 1items
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Citation | Journal: Nat Commun / Year: 2021 Title: Transcription activation by a sliding clamp. Authors: Jing Shi / Aijia Wen / Sha Jin / Bo Gao / Yang Huang / Yu Feng / Abstract: Transcription activation of bacteriophage T4 late genes is accomplished by a transcription activation complex containing RNA polymerase (RNAP), the promoter specificity factor gp55, the coactivator ...Transcription activation of bacteriophage T4 late genes is accomplished by a transcription activation complex containing RNA polymerase (RNAP), the promoter specificity factor gp55, the coactivator gp33, and a universal component of cellular DNA replication, the sliding clamp gp45. Although genetic and biochemical studies have elucidated many aspects of T4 late gene transcription, no precise structure of the transcription machinery in the process is available. Here, we report the cryo-EM structures of a gp55-dependent RNAP-promoter open complex and an intact gp45-dependent transcription activation complex. The structures reveal the interactions between gp55 and the promoter DNA that mediate the recognition of T4 late promoters. In addition to the σR2 homology domain, gp55 has a helix-loop-helix motif that chaperons the template-strand single-stranded DNA of the transcription bubble. Gp33 contacts both RNAP and the upstream double-stranded DNA. Gp45 encircles the DNA and tethers RNAP to it, supporting the idea that gp45 switches the promoter search from three-dimensional diffusion mode to one-dimensional scanning mode. | ||||||
History |
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-Structure visualization
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Movie viewer |
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Structure viewer | Molecule: MolmilJmol/JSmol |
-Downloads & links
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PDBx/mmCIF format | 7d7c.cif.gz | 594.4 KB | Display | PDBx/mmCIF format |
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PDB format | pdb7d7c.ent.gz | 474.6 KB | Display | PDB format |
PDBx/mmJSON format | 7d7c.json.gz | Tree view | PDBx/mmJSON format | |
Others | Other downloads |
-Validation report
Summary document | 7d7c_validation.pdf.gz | 948.6 KB | Display | wwPDB validaton report |
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Full document | 7d7c_full_validation.pdf.gz | 1019.8 KB | Display | |
Data in XML | 7d7c_validation.xml.gz | 89.5 KB | Display | |
Data in CIF | 7d7c_validation.cif.gz | 138.6 KB | Display | |
Arichive directory | https://data.pdbj.org/pub/pdb/validation_reports/d7/7d7c ftp://data.pdbj.org/pub/pdb/validation_reports/d7/7d7c | HTTPS FTP |
-Related structure data
Related structure data | 30604MC 7d7dC 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 subunit ... , 3 types, 4 molecules ABCD
#1: Protein | Mass: 36558.680 Da / Num. of mol.: 2 Source method: isolated from a genetically manipulated source Source: (gene. exp.) Escherichia coli (E. coli) / Production host: Escherichia coli (E. coli) / References: UniProt: U9ZUN7, DNA-directed RNA polymerase #2: Protein | | Mass: 150820.875 Da / Num. of mol.: 1 Source method: isolated from a genetically manipulated source Source: (gene. exp.) Escherichia coli 1-392-07_S4_C3 (bacteria) Gene: rpoB, AD40_4833 / Production host: Escherichia coli (E. coli) References: UniProt: A0A080FHH4, DNA-directed RNA polymerase #3: Protein | | Mass: 155366.781 Da / Num. of mol.: 1 Source method: isolated from a genetically manipulated source Source: (gene. exp.) Escherichia coli (E. coli) / Production host: Escherichia coli (E. coli) / References: UniProt: D7Y6A2, DNA-directed RNA polymerase |
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-DNA chain , 2 types, 2 molecules TN
#4: DNA chain | Mass: 18203.668 Da / Num. of mol.: 1 / Source method: obtained synthetically / Source: (synth.) Escherichia coli (E. coli) |
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#6: DNA chain | Mass: 18155.713 Da / Num. of mol.: 1 / Source method: obtained synthetically / Source: (synth.) Escherichia coli (E. coli) |
-Protein , 1 types, 1 molecules F
#5: Protein | Mass: 21565.160 Da / Num. of mol.: 1 Source method: isolated from a genetically manipulated source Source: (gene. exp.) Escherichia coli (E. coli) / Production host: Escherichia coli (E. coli) |
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-Non-polymers , 2 types, 3 molecules
#7: Chemical | ChemComp-MG / |
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#8: Chemical |
-Details
Has ligand of interest | N |
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-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 | Name: gp55-dependent RNA polymerase-promoter open complex / Type: COMPLEX / Entity ID: #1-#6 / Source: MULTIPLE SOURCES |
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Molecular weight | Experimental value: NO |
Source (natural) | Organism: Thermus thermophilus (bacteria) |
Buffer solution | pH: 7.9 |
Specimen | Embedding applied: NO / Shadowing applied: NO / Staining applied: NO / Vitrification applied: YES |
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 |
Image recording | Electron dose: 59 e/Å2 / Film or detector model: GATAN K2 SUMMIT (4k x 4k) |
-Processing
CTF correction | Type: PHASE FLIPPING AND AMPLITUDE CORRECTION |
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3D reconstruction | Resolution: 3.6 Å / Resolution method: FSC 0.143 CUT-OFF / Num. of particles: 57776 / Symmetry type: POINT |