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Yorodumi- PDB-8f1i: SigN RNA polymerase early-melted intermediate bound to mismatch f... -
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Open data
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Basic information
| Entry | Database: PDB / ID: 8f1i | ||||||
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| Title | SigN RNA polymerase early-melted intermediate bound to mismatch fragment dhsU36mm1 (-12T) | ||||||
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Keywords | TRANSCRIPTION/DNA / promoter-bound / initiation / DNA melting / transcription bubble nucleation / TRANSCRIPTION / TRANSCRIPTION-DNA complex | ||||||
| Function / homology | Function and homology informationarginine metabolic process / DNA-binding transcription activator activity / RNA polymerase complex / submerged biofilm formation / cellular response to cell envelope stress / regulation of DNA-templated transcription initiation / sigma factor activity / bacterial-type flagellum assembly / bacterial-type RNA polymerase core enzyme binding / cytosolic DNA-directed RNA polymerase complex ...arginine metabolic process / DNA-binding transcription activator activity / RNA polymerase complex / submerged biofilm formation / cellular response to cell envelope stress / regulation of DNA-templated transcription initiation / sigma factor activity / bacterial-type flagellum assembly / bacterial-type RNA polymerase core enzyme binding / cytosolic DNA-directed RNA polymerase complex / bacterial-type flagellum-dependent cell motility / nitrate assimilation / nucleotidyltransferase activity / regulation of DNA-templated transcription elongation / transcription elongation factor complex / transcription antitermination / cell motility / DNA-templated transcription initiation / protein-DNA complex / ribonucleoside binding / DNA-directed RNA polymerase / DNA-directed RNA polymerase activity / response to heat / protein-containing complex assembly / intracellular iron ion homeostasis / transcription cis-regulatory region binding / protein dimerization activity / response to antibiotic / regulation of DNA-templated transcription / positive regulation of DNA-templated transcription / magnesium ion binding / DNA binding / zinc ion binding / membrane / cytoplasm / cytosol Similarity search - Function | ||||||
| Biological species | ![]() ![]() Aquifex aeolicus (bacteria) | ||||||
| Method | ELECTRON MICROSCOPY / single particle reconstruction / cryo EM / Resolution: 3 Å | ||||||
Authors | Mueller, A.U. / Chen, J. / Darst, S.A. | ||||||
| Funding support | United States, 1items
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Citation | Journal: Proc Natl Acad Sci U S A / Year: 2023Title: A general mechanism for transcription bubble nucleation in bacteria. Authors: Andreas U Mueller / James Chen / Mengyu Wu / Courtney Chiu / B Tracy Nixon / Elizabeth A Campbell / Seth A Darst / ![]() Abstract: Bacterial transcription initiation requires σ factors for nucleation of the transcription bubble. The canonical housekeeping σ factor, σ, nucleates DNA melting via recognition of conserved bases ...Bacterial transcription initiation requires σ factors for nucleation of the transcription bubble. The canonical housekeeping σ factor, σ, nucleates DNA melting via recognition of conserved bases of the promoter -10 motif, which are unstacked and captured in pockets of σ. By contrast, the mechanism of transcription bubble nucleation and formation during the unrelated σ-mediated transcription initiation is poorly understood. Herein, we combine structural and biochemical approaches to establish that σ, like σ, captures a flipped, unstacked base in a pocket formed between its N-terminal region I (RI) and extra-long helix features. Strikingly, RI inserts into the nascent bubble to stabilize the nucleated bubble prior to engagement of the obligate ATPase activator. Our data suggest a general paradigm of transcription initiation that requires σ factors to nucleate an early melted intermediate prior to productive RNA synthesis. | ||||||
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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 | 8f1i.cif.gz | 780.1 KB | Display | PDBx/mmCIF format |
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| PDB format | pdb8f1i.ent.gz | 616.6 KB | Display | PDB format |
| PDBx/mmJSON format | 8f1i.json.gz | Tree view | PDBx/mmJSON format | |
| Others | Other downloads |
-Validation report
| Summary document | 8f1i_validation.pdf.gz | 919 KB | Display | wwPDB validaton report |
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| Full document | 8f1i_full_validation.pdf.gz | 947.6 KB | Display | |
| Data in XML | 8f1i_validation.xml.gz | 92.3 KB | Display | |
| Data in CIF | 8f1i_validation.cif.gz | 142.7 KB | Display | |
| Arichive directory | https://data.pdbj.org/pub/pdb/validation_reports/f1/8f1i ftp://data.pdbj.org/pub/pdb/validation_reports/f1/8f1i | HTTPS FTP |
-Related structure data
| Related structure data | ![]() 28797MC ![]() 8f1jC ![]() 8f1kC C: citing same article ( M: map data used to model this data |
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| Similar structure data | Similarity search - Function & homology F&H Search |
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Links
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Assembly
| Deposited unit | ![]()
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Components
-DNA chain , 2 types, 4 molecules ACBD
| #1: DNA chain | Mass: 11071.182 Da / Num. of mol.: 2 / Source method: obtained synthetically / Source: (synth.) ![]() Aquifex aeolicus (bacteria) / References: GenBank: AE000657.1#7: DNA chain | Mass: 11045.092 Da / Num. of mol.: 2 / Source method: obtained synthetically / Source: (synth.) ![]() Aquifex aeolicus (bacteria) / References: GenBank: AE000657.1 |
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-DNA-directed RNA polymerase subunit ... , 4 types, 5 molecules GHIJK
| #2: Protein | Mass: 36558.680 Da / Num. of mol.: 2 Source method: isolated from a genetically manipulated source Source: (gene. exp.) ![]() ![]() #3: Protein | | Mass: 150820.875 Da / Num. of mol.: 1 Source method: isolated from a genetically manipulated source Source: (gene. exp.) ![]() Gene: rpoB, groN, nitB, rif, ron, stl, stv, tabD, b3987, JW3950 Production host: ![]() #4: Protein | | Mass: 158105.672 Da / Num. of mol.: 1 Source method: isolated from a genetically manipulated source Source: (gene. exp.) ![]() ![]() #5: Protein | | Mass: 10249.547 Da / Num. of mol.: 1 Source method: isolated from a genetically manipulated source Source: (gene. exp.) ![]() ![]() |
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-Protein , 1 types, 1 molecules M
| #6: Protein | Mass: 54406.906 Da / Num. of mol.: 1 Source method: isolated from a genetically manipulated source Source: (gene. exp.) ![]() ![]() |
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-Non-polymers , 3 types, 11 molecules 




| #8: Chemical | ChemComp-MG / | ||
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| #9: Chemical | | #10: Water | ChemComp-HOH / | |
-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 |
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Sample preparation
| Component | Name: EsN-dhsU36mm1 / Type: COMPLEX / Entity ID: #1-#7 / Source: MULTIPLE SOURCES | |||||||||||||||||||||||||
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| Buffer solution | pH: 8 | |||||||||||||||||||||||||
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| Specimen | Embedding applied: NO / Shadowing applied: NO / Staining applied: NO / Vitrification applied: YES | |||||||||||||||||||||||||
| Specimen support | Details: Chamber of self-built glow discharge unit was evacuated using a vacuum pump prior to application of voltage (no pressure and/or voltage readings available) Grid material: GOLD / Grid mesh size: 400 divisions/in. / Grid type: C-flat-1.2/1.3 | |||||||||||||||||||||||||
| Vitrification | Instrument: FEI VITROBOT MARK IV / Cryogen name: ETHANE / Humidity: 100 % / Chamber temperature: 295 K |
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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: 2500 nm / Nominal defocus min: 1000 nm |
| Image recording | Average exposure time: 2 sec. / Electron dose: 51 e/Å2 / Film or detector model: GATAN K3 (6k x 4k) / Num. of real images: 12294 Details: dose-fractionation, 0.05 seconds/frame (=40 frames total) |
| EM imaging optics | Energyfilter name: GIF Bioquantum / Energyfilter slit width: 20 eV |
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Processing
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| CTF correction | Type: PHASE FLIPPING AND AMPLITUDE CORRECTION | ||||||||||||||||||||||||
| 3D reconstruction | Resolution: 3 Å / Resolution method: FSC 0.143 CUT-OFF / Num. of particles: 602287 Details: Particle number and FSC resolution estimate of the full map provided Symmetry type: POINT | ||||||||||||||||||||||||
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About Yorodumi




Aquifex aeolicus (bacteria)
United States, 1items
Citation










PDBj







































gel filtration
