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Yorodumi- PDB-8x6g: Cryo-EM structure of Staphylococcus aureus sigB-dependent RNAP-pr... -
+Open data
-Basic information
Entry | Database: PDB / ID: 8x6g | ||||||
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Title | Cryo-EM structure of Staphylococcus aureus sigB-dependent RNAP-promoter open complex | ||||||
Components |
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Keywords | TRANSCRIPTION / RNA polymerase / Staphylococcus aureus / sigB | ||||||
Function / homology | Function and homology information sigma factor activity / DNA-directed RNA polymerase complex / DNA-templated transcription initiation / ribonucleoside binding / DNA-directed 5'-3' RNA polymerase activity / DNA-directed RNA polymerase / protein dimerization activity / DNA-templated transcription / regulation of DNA-templated transcription / magnesium ion binding ...sigma factor activity / DNA-directed RNA polymerase complex / DNA-templated transcription initiation / ribonucleoside binding / DNA-directed 5'-3' RNA polymerase activity / DNA-directed RNA polymerase / protein dimerization activity / DNA-templated transcription / regulation of DNA-templated transcription / magnesium ion binding / DNA binding / zinc ion binding / cytoplasm Similarity search - Function | ||||||
Biological species | Staphylococcus aureus (bacteria) | ||||||
Method | ELECTRON MICROSCOPY / single particle reconstruction / cryo EM / Resolution: 3.3 Å | ||||||
Authors | Yuan, L. / Xu, L. / Liu, Q. / Feng, Y. | ||||||
Funding support | China, 1items
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Citation | Journal: Nat Commun / Year: 2024 Title: Structural basis of promoter recognition by Staphylococcus aureus RNA polymerase. Authors: Linggang Yuan / Qingyang Liu / Liqiao Xu / Bing Wu / Yu Feng / Abstract: Bacterial RNAP needs to form holoenzyme with σ factors to initiate transcription. While Staphylococcus aureus σ controls housekeeping functions, S. aureus σ regulates virulence, biofilm formation, ...Bacterial RNAP needs to form holoenzyme with σ factors to initiate transcription. While Staphylococcus aureus σ controls housekeeping functions, S. aureus σ regulates virulence, biofilm formation, persistence, cell internalization, membrane transport, and antimicrobial resistance. Besides the sequence difference, the spacers between the -35 element and -10 element of σ regulated promoters are shorter than those of σ regulated promoters. Therefore, how σ recognizes and initiates transcription from target promoters can not be inferred from that of the well studied σ. Here, we report the cryo-EM structures of S. aureus RNAP-promoter open complexes comprising σ and σ, respectively. Structural analyses, in combination with biochemical experiments, reveal the structural basis for the promoter specificity of S. aureus transcription. Although the -10 element of σ regulated promoters is recognized by domain σ as single-stranded DNA, the -10 element of σ regulated promoters is co-recognized by domains σ and σ as double-stranded DNA, accounting for the short spacers of σ regulated promoters. S. aureus RNAP is a validated target of antibiotics, and our structures pave the way for rational drug design targeting S. aureus RNAP. | ||||||
History |
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-Structure visualization
Structure viewer | Molecule: MolmilJmol/JSmol |
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-Downloads & links
-Download
PDBx/mmCIF format | 8x6g.cif.gz | 691.7 KB | Display | PDBx/mmCIF format |
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PDB format | pdb8x6g.ent.gz | 549.1 KB | Display | PDB format |
PDBx/mmJSON format | 8x6g.json.gz | Tree view | PDBx/mmJSON format | |
Others | Other downloads |
-Validation report
Summary document | 8x6g_validation.pdf.gz | 1.5 MB | Display | wwPDB validaton report |
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Full document | 8x6g_full_validation.pdf.gz | 1.5 MB | Display | |
Data in XML | 8x6g_validation.xml.gz | 88.7 KB | Display | |
Data in CIF | 8x6g_validation.cif.gz | 135.4 KB | Display | |
Arichive directory | https://data.pdbj.org/pub/pdb/validation_reports/x6/8x6g ftp://data.pdbj.org/pub/pdb/validation_reports/x6/8x6g | HTTPS FTP |
-Related structure data
Related structure data | 38088MC 8x6fC M: map data used to model this data C: citing same article (ref.) |
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Similar structure data | Similarity search - Function & homologyF&H Search |
-Links
-Assembly
Deposited unit |
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1 |
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-Components
-DNA-directed RNA polymerase subunit ... , 5 types, 6 molecules ABCDFG
#1: Protein | Mass: 35052.656 Da / Num. of mol.: 2 Source method: isolated from a genetically manipulated source Source: (gene. exp.) Staphylococcus aureus (bacteria) / Gene: rpoA / Production host: Escherichia coli (E. coli) / References: UniProt: A0A0D1GTM7 #2: Protein | | Mass: 133381.312 Da / Num. of mol.: 1 Source method: isolated from a genetically manipulated source Source: (gene. exp.) Staphylococcus aureus (bacteria) / Gene: rpoB / Production host: Escherichia coli (E. coli) / References: UniProt: W8UT31 #3: Protein | | Mass: 135594.266 Da / Num. of mol.: 1 Source method: isolated from a genetically manipulated source Source: (gene. exp.) Staphylococcus aureus (bacteria) / Gene: rpoC / Production host: Escherichia coli (E. coli) / References: UniProt: A0A2C6P019 #5: Protein | | Mass: 8161.236 Da / Num. of mol.: 1 Source method: isolated from a genetically manipulated source Source: (gene. exp.) Staphylococcus aureus (bacteria) / Gene: rpoZ / Production host: Escherichia coli (E. coli) / References: UniProt: W8UYF2 #6: Protein | | Mass: 8764.739 Da / Num. of mol.: 1 Source method: isolated from a genetically manipulated source Source: (gene. exp.) Staphylococcus aureus (bacteria) / Gene: rnpZA / Production host: Escherichia coli (E. coli) / References: UniProt: A0A7I0YN47 |
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-Protein , 2 types, 2 molecules EH
#4: Protein | Mass: 20893.010 Da / Num. of mol.: 1 Source method: isolated from a genetically manipulated source Source: (gene. exp.) Staphylococcus aureus (bacteria) / Gene: rpoE / Production host: Escherichia coli (E. coli) / References: UniProt: A0A7I0YLU8 |
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#7: Protein | Mass: 29474.559 Da / Num. of mol.: 1 Source method: isolated from a genetically manipulated source Source: (gene. exp.) Staphylococcus aureus (bacteria) / Gene: sigB / Production host: Escherichia coli (E. coli) / References: UniProt: A0A390QYZ6 |
-DNA chain , 2 types, 2 molecules TN
#8: DNA chain | Mass: 21360.715 Da / Num. of mol.: 1 / Source method: obtained synthetically / Source: (synth.) Staphylococcus aureus (bacteria) |
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#9: DNA chain | Mass: 21771.047 Da / Num. of mol.: 1 / Source method: obtained synthetically / Source: (synth.) Staphylococcus aureus (bacteria) |
-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: sigB-dependent RNAP-promoter open complex / Type: COMPLEX / Entity ID: all / Source: RECOMBINANT |
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Source (natural) | Organism: Staphylococcus aureus (bacteria) |
Source (recombinant) | Organism: Escherichia coli (E. coli) |
Buffer solution | pH: 7.5 |
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 / Nominal defocus max: 2000 nm / Nominal defocus min: 1000 nm |
Image recording | Electron dose: 51 e/Å2 / Film or detector model: FEI FALCON IV (4k x 4k) |
-Processing
EM software | Name: PHENIX / Version: 1.20.1_4487: / Category: model refinement | ||||||||||||||||||||||||
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CTF correction | Type: PHASE FLIPPING AND AMPLITUDE CORRECTION | ||||||||||||||||||||||||
3D reconstruction | Resolution: 3.3 Å / Resolution method: FSC 0.143 CUT-OFF / Num. of particles: 95089 / Symmetry type: POINT | ||||||||||||||||||||||||
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