+Open data
-Basic information
Entry | Database: EMDB / ID: EMD-7612 | |||||||||
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Title | Cytoplasmic ATPase in a Type IV Secretion Machine | |||||||||
Map data | Cytoplasmic ATPase complex | |||||||||
Sample |
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Biological species | Legionella pneumophila (bacteria) | |||||||||
Method | subtomogram averaging / cryo EM / Resolution: 33.0 Å | |||||||||
Authors | Liu J / Hu B | |||||||||
Citation | Journal: Nat Microbiol / Year: 2018 Title: A unique cytoplasmic ATPase complex defines the Legionella pneumophila type IV secretion channel. Authors: David Chetrit / Bo Hu / Peter J Christie / Craig R Roy / Jun Liu / Abstract: Type IV secretion systems (T4SSs) are complex machines used by bacteria to deliver protein and DNA complexes into target host cells. Conserved ATPases are essential for T4SS function, but how they ...Type IV secretion systems (T4SSs) are complex machines used by bacteria to deliver protein and DNA complexes into target host cells. Conserved ATPases are essential for T4SS function, but how they coordinate their activities to promote substrate transfer remains poorly understood. Here, we show that the DotB ATPase associates with the Dot-Icm T4SS at the Legionella cell pole through interactions with the DotO ATPase. The structure of the Dot-Icm apparatus was solved in situ by cryo-electron tomography at 3.5 nm resolution and the cytoplasmic complex was solved at 3.0 nm resolution. These structures revealed a cell envelope-spanning channel that connects to the cytoplasmic complex. Further analysis revealed a hexameric assembly of DotO dimers associated with the inner membrane complex, and a DotB hexamer associated with the base of this cytoplasmic complex. The assembly of a DotB-DotO energy complex creates a cytoplasmic channel that directs the translocation of substrates through the T4SS. These data define distinct stages in Dot-Icm machine biogenesis, advance our understanding of channel activation, and identify an envelope-spanning T4SS channel. | |||||||||
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_7612.map.gz | 1.3 MB | EMDB map data format | |
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Header (meta data) | emd-7612-v30.xml emd-7612.xml | 8 KB 8 KB | Display Display | EMDB header |
Images | emd_7612.png | 94.8 KB | ||
Archive directory | http://ftp.pdbj.org/pub/emdb/structures/EMD-7612 ftp://ftp.pdbj.org/pub/emdb/structures/EMD-7612 | HTTPS FTP |
-Validation report
Summary document | emd_7612_validation.pdf.gz | 78.1 KB | Display | EMDB validaton report |
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Full document | emd_7612_full_validation.pdf.gz | 77.2 KB | Display | |
Data in XML | emd_7612_validation.xml.gz | 494 B | Display | |
Arichive directory | https://ftp.pdbj.org/pub/emdb/validation_reports/EMD-7612 ftp://ftp.pdbj.org/pub/emdb/validation_reports/EMD-7612 | HTTPS FTP |
-Related structure data
-Links
EMDB pages | EMDB (EBI/PDBe) / EMDataResource |
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-Map
File | Download / File: emd_7612.map.gz / Format: CCP4 / Size: 1.5 MB / Type: IMAGE STORED AS FLOATING POINT NUMBER (4 BYTES) | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Annotation | Cytoplasmic ATPase complex | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Projections & slices | Image control
Images are generated by Spider. generated in cubic-lattice coordinate | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Voxel size | X=Y=Z: 5 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 : Type IV secretion machine
Entire | Name: Type IV secretion machine |
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Components |
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-Supramolecule #1: Type IV secretion machine
Supramolecule | Name: Type IV secretion machine / type: complex / ID: 1 / Parent: 0 |
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Source (natural) | Organism: Legionella pneumophila (bacteria) |
-Experimental details
-Structure determination
Method | cryo EM |
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Processing | subtomogram averaging |
Aggregation state | cell |
-Sample preparation
Buffer | pH: 7 |
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Grid | Model: Quantifoil R2/2 / Material: COPPER / Mesh: 200 / Support film - Material: CARBON / Pretreatment - Type: GLOW DISCHARGE / Pretreatment - Atmosphere: AIR |
Vitrification | Cryogen name: ETHANE |
-Electron microscopy
Microscope | FEI POLARA 300 |
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Image recording | Film or detector model: GATAN K2 SUMMIT (4k x 4k) / Detector mode: COUNTING / Average exposure time: 1.0 sec. / Average electron dose: 1.5 e/Å2 |
Electron beam | Acceleration voltage: 300 kV / Electron source: FIELD EMISSION GUN |
Electron optics | Illumination mode: FLOOD BEAM / Imaging mode: BRIGHT FIELD |
Experimental equipment | Model: Tecnai Polara / Image courtesy: FEI Company |
-Image processing
Final reconstruction | Resolution.type: BY AUTHOR / Resolution: 33.0 Å / Resolution method: FSC 0.5 CUT-OFF / Number subtomograms used: 5000 |
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Extraction | Number tomograms: 1000 / Number images used: 5000 / Method: manually |
CTF correction | Software - Name: IMOD (ver. 4.9.6) |
Final angle assignment | Type: OTHER |