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Yorodumi- EMDB-2637: Negative stain electron microscopy of Bacillus subtilis RNA polym... -
+Open data
-Basic information
Entry | Database: EMDB / ID: EMD-2637 | |||||||||
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Title | Negative stain electron microscopy of Bacillus subtilis RNA polymerase with YkzG-GFP fusion | |||||||||
Map data | Reconstruction of B. subtilis RNAP with YkzG-GFP fusion | |||||||||
Sample |
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Keywords | RNA polymerase / small subunit / transcription / Bacillus subtilis | |||||||||
Biological species | Bacillus subtilis (bacteria) | |||||||||
Method | single particle reconstruction / negative staining / Resolution: 24.0 Å | |||||||||
Authors | Keller A / Yang X / Korelusova J / Delumeau O / Krasny L / Lewis PJ | |||||||||
Citation | Journal: J Bacteriol / Year: 2014 Title: ε, a new subunit of RNA polymerase found in gram-positive bacteria. Authors: Andrew N Keller / Xiao Yang / Jana Wiedermannová / Olivier Delumeau / Libor Krásný / Peter J Lewis / Abstract: RNA polymerase in bacteria is a multisubunit protein complex that is essential for gene expression. We have identified a new subunit of RNA polymerase present in the high-A+T Firmicutes phylum of ...RNA polymerase in bacteria is a multisubunit protein complex that is essential for gene expression. We have identified a new subunit of RNA polymerase present in the high-A+T Firmicutes phylum of Gram-positive bacteria and have named it ε. Previously ε had been identified as a small protein (ω1) that copurified with RNA polymerase. We have solved the structure of ε by X-ray crystallography and show that it is not an ω subunit. Rather, ε bears remarkable similarity to the Gp2 family of phage proteins involved in the inhibition of host cell transcription following infection. Deletion of ε shows no phenotype and has no effect on the transcriptional profile of the cell. Determination of the location of ε within the assembly of RNA polymerase core by single-particle analysis suggests that it binds toward the downstream side of the DNA binding cleft. Due to the structural similarity of ε with Gp2 and the fact they bind similar regions of RNA polymerase, we hypothesize that ε may serve a role in protection from phage infection. | |||||||||
History |
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-Structure visualization
Movie |
Movie viewer |
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Structure viewer | EM map: SurfViewMolmilJmol/JSmol |
Supplemental images |
-Downloads & links
-EMDB archive
Map data | emd_2637.map.gz | 1.3 MB | EMDB map data format | |
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Header (meta data) | emd-2637-v30.xml emd-2637.xml | 7.7 KB 7.7 KB | Display Display | EMDB header |
Images | EMD-2637.png emd-2637.png | 131 KB 131 KB | ||
Archive directory | http://ftp.pdbj.org/pub/emdb/structures/EMD-2637 ftp://ftp.pdbj.org/pub/emdb/structures/EMD-2637 | HTTPS FTP |
-Validation report
Summary document | emd_2637_validation.pdf.gz | 211.3 KB | Display | EMDB validaton report |
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Full document | emd_2637_full_validation.pdf.gz | 210.5 KB | Display | |
Data in XML | emd_2637_validation.xml.gz | 5.2 KB | Display | |
Arichive directory | https://ftp.pdbj.org/pub/emdb/validation_reports/EMD-2637 ftp://ftp.pdbj.org/pub/emdb/validation_reports/EMD-2637 | HTTPS FTP |
-Related structure data
-Links
EMDB pages | EMDB (EBI/PDBe) / EMDataResource |
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-Map
File | Download / File: emd_2637.map.gz / Format: CCP4 / Size: 1.4 MB / Type: IMAGE STORED AS FLOATING POINT NUMBER (4 BYTES) | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Annotation | Reconstruction of B. subtilis RNAP with YkzG-GFP fusion | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Projections & slices | Image control
Images are generated by Spider. | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Voxel size | X=Y=Z: 3.6 Å | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Density |
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Symmetry | Space group: 1 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Details | EMDB XML:
CCP4 map header:
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-Supplemental data
-Sample components
-Entire : RNA polymerase YkzG-GFP
Entire | Name: RNA polymerase YkzG-GFP |
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Components |
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-Supramolecule #1000: RNA polymerase YkzG-GFP
Supramolecule | Name: RNA polymerase YkzG-GFP / type: sample / ID: 1000 / Number unique components: 1 |
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Molecular weight | Experimental: 430 KDa / Theoretical: 430 KDa |
-Macromolecule #1: RNA polymerase
Macromolecule | Name: RNA polymerase / type: protein_or_peptide / ID: 1 / Name.synonym: RNAP / Details: RNAP with YkzG-GFP fusion / Number of copies: 1 / Recombinant expression: Yes |
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Source (natural) | Organism: Bacillus subtilis (bacteria) / Strain: BS509 |
Molecular weight | Experimental: 430 KDa / Theoretical: 430 KDa |
Recombinant expression | Organism: Bacillus subtilis (bacteria) |
-Experimental details
-Structure determination
Method | negative staining |
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Processing | single particle reconstruction |
Aggregation state | particle |
-Sample preparation
Concentration | 1 mg/mL |
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Buffer | pH: 7.8 Details: 20 mM Tris-HCl , 150 mM NaCl, 10 mM MgCl2, 5% (v/v) glycerol and 1 mM DTT |
Staining | Type: NEGATIVE Details: The specimens were then stained with a 1 % (w/v) uranyl formate aqueous solution. |
Vitrification | Cryogen name: NONE / Instrument: OTHER |
-Electron microscopy
Microscope | FEI TECNAI F30 |
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Date | Dec 1, 2009 |
Image recording | Category: CCD / Film or detector model: GATAN ULTRASCAN 4000 (4k x 4k) / Number real images: 260 |
Electron beam | Acceleration voltage: 300 kV / Electron source: FIELD EMISSION GUN |
Electron optics | Illumination mode: FLOOD BEAM / Imaging mode: BRIGHT FIELD |
Sample stage | Specimen holder model: JEOL |
Experimental equipment | Model: Tecnai F30 / Image courtesy: FEI Company |
-Image processing
Final reconstruction | Applied symmetry - Point group: C1 (asymmetric) / Resolution.type: BY AUTHOR / Resolution: 24.0 Å / Resolution method: OTHER / Software - Name: EMAN2.8 / Number images used: 10104 |
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