+Open data
-Basic information
Entry | Database: EMDB / ID: EMD-5720 | |||||||||
---|---|---|---|---|---|---|---|---|---|---|
Title | Structure of the Yersinia enterocolitica secretin YscC | |||||||||
Map data | Reconstruction of YscC secretin | |||||||||
Sample |
| |||||||||
Keywords | type III secretion system / Yersinia enterocolitica / Gram-negative bacteria / YscC / secretin / cryo-electron microscopy / outer membrane | |||||||||
Function / homology | Function and homology information type III protein secretion system complex / protein secretion by the type III secretion system / cell outer membrane / identical protein binding Similarity search - Function | |||||||||
Biological species | Yersinia enterocolitica (bacteria) | |||||||||
Method | single particle reconstruction / cryo EM / Resolution: 15.0 Å | |||||||||
Authors | Kowal J / Chami M / Ringler P / Muller AS / Kudryashev M / Castano-Diez D / Amstutz M / Cornelis GR / Stahlberg H / Engel A | |||||||||
Citation | Journal: Structure / Year: 2013 Title: Structure of the dodecameric Yersinia enterocolitica secretin YscC and its trypsin-resistant core. Authors: Julia Kowal / Mohamed Chami / Philippe Ringler / Shirley A Müller / Mikhail Kudryashev / Daniel Castaño-Díez / Marlise Amstutz / Guy R Cornelis / Henning Stahlberg / Andreas Engel / Abstract: The type III secretion system machinery, also known as the injectisome, delivers bacterial effector proteins into eukaryotic cells during infection. The outer membrane YscC secretin is a major part ...The type III secretion system machinery, also known as the injectisome, delivers bacterial effector proteins into eukaryotic cells during infection. The outer membrane YscC secretin is a major part of Yersinia enterocolitica's injectisome and is among the first components to assemble, solely assisted by its pilotin, YscW. We have determined the three-dimensional structures of the native complex and its protease-resistant core to 12 Å resolution by cryo-electron microscopy (cryo-EM) and show that YscC forms a dodecameric complex. Cryo-EM of YscC reconstituted into proteoliposomes defines the secretin's membrane-spanning region. Native YscC consists of an outer membrane ring connected via a thin cylindrical wall to a conical, periplasmic region that exposes N-terminal petals connected by flexible linkers. These petals harbor the binding site of YscD, a component of the inner membrane ring. A change in their orientation adapts the length of the YscC secretin and facilitates its interaction with YscD. | |||||||||
History |
|
-Structure visualization
Movie |
Movie viewer |
---|---|
Structure viewer | EM map: SurfViewMolmilJmol/JSmol |
Supplemental images |
-Downloads & links
-EMDB archive
Map data | emd_5720.map.gz | 7.9 MB | EMDB map data format | |
---|---|---|---|---|
Header (meta data) | emd-5720-v30.xml emd-5720.xml | 11.1 KB 11.1 KB | Display Display | EMDB header |
Images | emd_5720.png | 59.4 KB | ||
Archive directory | http://ftp.pdbj.org/pub/emdb/structures/EMD-5720 ftp://ftp.pdbj.org/pub/emdb/structures/EMD-5720 | HTTPS FTP |
-Validation report
Summary document | emd_5720_validation.pdf.gz | 78.2 KB | Display | EMDB validaton report |
---|---|---|---|---|
Full document | emd_5720_full_validation.pdf.gz | 77.3 KB | Display | |
Data in XML | emd_5720_validation.xml.gz | 494 B | Display | |
Arichive directory | https://ftp.pdbj.org/pub/emdb/validation_reports/EMD-5720 ftp://ftp.pdbj.org/pub/emdb/validation_reports/EMD-5720 | HTTPS FTP |
-Related structure data
-Links
EMDB pages | EMDB (EBI/PDBe) / EMDataResource |
---|---|
Related items in Molecule of the Month |
-Map
File | Download / File: emd_5720.map.gz / Format: CCP4 / Size: 12.1 MB / Type: IMAGE STORED AS FLOATING POINT NUMBER (4 BYTES) | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Annotation | Reconstruction of YscC secretin | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Projections & slices | Image control
Images are generated by Spider. | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Voxel size | X=Y=Z: 1.95 Å | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Density |
| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Symmetry | Space group: 1 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Details | EMDB XML:
CCP4 map header:
|
-Supplemental data
-Sample components
-Entire : YscC secretin from Yersinia enterocolitica
Entire | Name: YscC secretin from Yersinia enterocolitica |
---|---|
Components |
|
-Supramolecule #1000: YscC secretin from Yersinia enterocolitica
Supramolecule | Name: YscC secretin from Yersinia enterocolitica / type: sample / ID: 1000 / Details: Sample contained detergent DDM / Oligomeric state: 12 / Number unique components: 1 |
---|---|
Molecular weight | Experimental: 900 KDa / Theoretical: 768 KDa / Method: Gel filtration, Superose 6 30/100 GL column |
-Macromolecule #1: YscC secretin
Macromolecule | Name: YscC secretin / type: protein_or_peptide / ID: 1 / Oligomeric state: Dodecamer / Recombinant expression: Yes |
---|---|
Source (natural) | Organism: Yersinia enterocolitica (bacteria) / Strain: W22703 / synonym: Yersinia / Location in cell: outer membrane |
Molecular weight | Theoretical: 768 KDa |
Recombinant expression | Organism: Yersinia enterocolitica (bacteria) / Recombinant strain: W22703 / Recombinant plasmid: pMA6, pRS6 |
Sequence | UniProtKB: Type 3 secretion system secretin |
-Experimental details
-Structure determination
Method | cryo EM |
---|---|
Processing | single particle reconstruction |
Aggregation state | particle |
-Sample preparation
Concentration | 0.2 mg/mL |
---|---|
Buffer | pH: 7.8 Details: 10 mM Tris-HCl, 100 mM NaCl, 0.1 mM EDTA, 0.04% DDM |
Grid | Details: 200 mesh Cu grid, covered with a very thin additional continuous carbon film, glow-discharged |
Vitrification | Cryogen name: ETHANE / Chamber humidity: 95 % / Instrument: FEI VITROBOT MARK IV / Method: Plunging immediately after blotting. |
-Electron microscopy
Microscope | FEI/PHILIPS CM200FEG |
---|---|
Date | Oct 1, 2010 |
Image recording | Category: FILM / Film or detector model: KODAK SO-163 FILM / Digitization - Scanner: PRIMESCAN / Digitization - Sampling interval: 5 µm / Number real images: 100 / Average electron dose: 20 e/Å2 |
Electron beam | Acceleration voltage: 200 kV / Electron source: FIELD EMISSION GUN |
Electron optics | Illumination mode: FLOOD BEAM / Imaging mode: BRIGHT FIELD / Cs: 2 mm / Nominal defocus max: 3.5 µm / Nominal defocus min: 1.0 µm / Nominal magnification: 50000 |
Sample stage | Specimen holder model: GATAN LIQUID NITROGEN |
-Image processing
Details | Particles were selected using Boxer/EMAN1.9. Image processing was done using EMAN2. |
---|---|
CTF correction | Details: each particle |
Final reconstruction | Algorithm: OTHER / Resolution.type: BY AUTHOR / Resolution: 15.0 Å / Resolution method: FSC 0.5 CUT-OFF / Software - Name: EMAN2 Details: Mask parameters were optimized to minimize the influence of a flexible N-terminal domain that impaired projection alignment. Number images used: 35000 |
Final two d classification | Number classes: 240 |