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Yorodumi- EMDB-14171: CryoEM structure of bacterial transcription intermediate complex ... -
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Open data
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Basic information
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| Title | CryoEM structure of bacterial transcription intermediate complex mediated by activator PspF | |||||||||
Map data | Local filtered map | |||||||||
Sample |
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Keywords | RNA polymerase / AAA protein / transcription regulation / cryoEM / TRANSCRIPTION | |||||||||
| Function / homology | Function and homology informationregulation of cellular response to stress / DNA-binding transcription activator activity / RNA polymerase complex / submerged biofilm formation / cellular response to cell envelope stress / phosphorelay signal transduction system / regulation of DNA-templated transcription initiation / sigma factor activity / bacterial-type flagellum assembly / bacterial-type RNA polymerase core enzyme binding ...regulation of cellular response to stress / DNA-binding transcription activator activity / RNA polymerase complex / submerged biofilm formation / cellular response to cell envelope stress / phosphorelay signal transduction system / 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 / cis-regulatory region sequence-specific DNA binding / nucleotidyltransferase activity / DNA-directed RNA polymerase complex / 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 / transcription regulator complex / sequence-specific DNA binding / intracellular iron ion homeostasis / protein dimerization activity / response to antibiotic / negative regulation of DNA-templated transcription / regulation of DNA-templated transcription / positive regulation of DNA-templated transcription / magnesium ion binding / ATP hydrolysis activity / DNA binding / zinc ion binding / ATP binding / identical protein binding / membrane / cytoplasm / cytosol Similarity search - Function | |||||||||
| Biological species | ![]() Klebsiella pneumoniae (bacteria) | |||||||||
| Method | single particle reconstruction / cryo EM / Resolution: 3.5 Å | |||||||||
Authors | Ye FZ / Zhang XD | |||||||||
| Funding support | United Kingdom, 1 items
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Citation | Journal: Sci Adv / Year: 2022Title: Mechanisms of DNA opening revealed in AAA+ transcription complex structures. Authors: Fuzhou Ye / Forson Gao / Xiaojiao Liu / Martin Buck / Xiaodong Zhang / ![]() Abstract: Gene transcription is carried out by RNA polymerase (RNAP) and requires the conversion of the initial closed promoter complex, where DNA is double stranded, to a transcription-competent open promoter ...Gene transcription is carried out by RNA polymerase (RNAP) and requires the conversion of the initial closed promoter complex, where DNA is double stranded, to a transcription-competent open promoter complex, where DNA is opened up. In bacteria, RNAP relies on σ factors for its promoter specificities. Using a special form of sigma factor (σ), which forms a stable closed complex and requires its activator that belongs to the AAA+ ATPases (ATPases associated with diverse cellular activities), we obtained cryo-electron microscopy structures of transcription initiation complexes that reveal a previously unidentified process of DNA melting opening. The σ amino terminus threads through the locally opened up DNA and then becomes enclosed by the AAA+ hexameric ring in the activator-bound intermediate complex. Our structures suggest how ATP hydrolysis by the AAA+ activator could remove the σ inhibition while helping to open up DNA, using σ amino-terminal peptide as a pry bar. | |||||||||
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Structure visualization
| Supplemental images |
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Downloads & links
-EMDB archive
| Map data | emd_14171.map.gz | 49.6 MB | EMDB map data format | |
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| Header (meta data) | emd-14171-v30.xml emd-14171.xml | 31 KB 31 KB | Display Display | EMDB header |
| Images | emd_14171.png | 168.6 KB | ||
| Filedesc metadata | emd-14171.cif.gz | 10 KB | ||
| Others | emd_14171_additional_1.map.gz emd_14171_additional_2.map.gz | 49.3 MB 45.9 MB | ||
| Archive directory | http://ftp.pdbj.org/pub/emdb/structures/EMD-14171 ftp://ftp.pdbj.org/pub/emdb/structures/EMD-14171 | HTTPS FTP |
-Validation report
| Summary document | emd_14171_validation.pdf.gz | 414.6 KB | Display | EMDB validaton report |
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| Full document | emd_14171_full_validation.pdf.gz | 414.2 KB | Display | |
| Data in XML | emd_14171_validation.xml.gz | 6.1 KB | Display | |
| Data in CIF | emd_14171_validation.cif.gz | 7 KB | Display | |
| Arichive directory | https://ftp.pdbj.org/pub/emdb/validation_reports/EMD-14171 ftp://ftp.pdbj.org/pub/emdb/validation_reports/EMD-14171 | HTTPS FTP |
-Related structure data
| Related structure data | ![]() 7qv9MC ![]() 9q90M ![]() 7qwpC ![]() 7qxiC M: atomic model generated by this map C: citing same article ( |
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| Similar structure data | Similarity search - Function & homology F&H Search |
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Links
| EMDB pages | EMDB (EBI/PDBe) / EMDataResource |
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| Related items in Molecule of the Month |
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Map
| File | Download / File: emd_14171.map.gz / Format: CCP4 / Size: 83.7 MB / Type: IMAGE STORED AS FLOATING POINT NUMBER (4 BYTES) | ||||||||||||||||||||||||||||||||||||
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| Annotation | Local filtered map | ||||||||||||||||||||||||||||||||||||
| Projections & slices | Image control
Images are generated by Spider. | ||||||||||||||||||||||||||||||||||||
| Voxel size | X=Y=Z: 1.1 Å | ||||||||||||||||||||||||||||||||||||
| Density |
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| Symmetry | Space group: 1 | ||||||||||||||||||||||||||||||||||||
| Details | EMDB XML:
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-Supplemental data
-Additional map: Focus refinement map
| File | emd_14171_additional_1.map | ||||||||||||
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| Annotation | Focus refinement map | ||||||||||||
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| Density Histograms |
-Additional map: Focus refinement map
| File | emd_14171_additional_2.map | ||||||||||||
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| Annotation | Focus refinement map | ||||||||||||
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| Density Histograms |
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Sample components
+Entire : Bacterial transcription intermediate complex mediated by PspF act...
+Supramolecule #1: Bacterial transcription intermediate complex mediated by PspF act...
+Macromolecule #1: DNA-directed RNA polymerase subunit alpha
+Macromolecule #2: DNA-directed RNA polymerase subunit beta
+Macromolecule #3: DNA-directed RNA polymerase subunit beta'
+Macromolecule #4: DNA-directed RNA polymerase subunit omega
+Macromolecule #7: Transcription activator PspF
+Macromolecule #8: RNA polymerase sigma-54 factor
+Macromolecule #5: Non-template promoter DNA
+Macromolecule #6: Template promoter DNA
+Macromolecule #9: ADENOSINE-5'-DIPHOSPHATE
+Macromolecule #10: ALUMINUM FLUORIDE
-Experimental details
-Structure determination
| Method | cryo EM |
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Processing | single particle reconstruction |
| Aggregation state | particle |
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Sample preparation
| Concentration | 3.5 mg/mL | |||||||||||||||
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| Buffer | pH: 8 Component:
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| Grid | Model: Quantifoil R2/2 / Material: COPPER / Mesh: 200 / Support film - Material: CARBON / Support film - topology: HOLEY / Pretreatment - Type: PLASMA CLEANING / Pretreatment - Time: 30 sec. | |||||||||||||||
| Vitrification | Cryogen name: ETHANE / Chamber humidity: 95 % / Chamber temperature: 277 K / Instrument: FEI VITROBOT MARK IV |
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Electron microscopy
| Microscope | FEI TITAN KRIOS |
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| Specialist optics | Energy filter - Name: GIF Bioquantum / Energy filter - Slit width: 20 eV |
| Image recording | Film or detector model: GATAN K3 (6k x 4k) / Digitization - Dimensions - Width: 5760 pixel / Digitization - Dimensions - Height: 4092 pixel / Number grids imaged: 1 / Number real images: 14780 / Average exposure time: 4.1 sec. / Average electron dose: 50.0 e/Å2 |
| Electron beam | Acceleration voltage: 300 kV / Electron source: FIELD EMISSION GUN |
| Electron optics | C2 aperture diameter: 50.0 µm / Illumination mode: FLOOD BEAM / Imaging mode: BRIGHT FIELD / Cs: 2.7 mm / Nominal defocus max: 2.6 µm / Nominal defocus min: 1.4000000000000001 µm / Nominal magnification: 81000 |
| Sample stage | Specimen holder model: FEI TITAN KRIOS AUTOGRID HOLDER / Cooling holder cryogen: NITROGEN |
| Experimental equipment | ![]() Model: Titan Krios / Image courtesy: FEI Company |
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Image processing
-Atomic model buiding 1
| Initial model | PDB ID: Chain - Source name: PDB / Chain - Initial model type: experimental model |
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| Refinement | Space: REAL / Protocol: RIGID BODY FIT |
| Output model | ![]() PDB-7qv9: ![]() PDB-9q90: |
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About Yorodumi



Keywords
Authors
United Kingdom, 1 items
Citation











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FIELD EMISSION GUN


