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Yorodumi- PDB-3j1v: A refined model of the prototypical Salmonella typhimurium T3SS b... -
+Open data
-Basic information
Entry | Database: PDB / ID: 3j1v | ||||||
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Title | A refined model of the prototypical Salmonella typhimurium T3SS basal body reveals the molecular basis for its assembly | ||||||
Components | Protein InvG | ||||||
Keywords | CELL INVASION / T3SS / Secretin | ||||||
Function / homology | Function and homology information type III protein secretion system complex / type II protein secretion system complex / protein secretion by the type III secretion system / protein secretion / cell outer membrane / identical protein binding Similarity search - Function | ||||||
Biological species | Salmonella enterica subsp. enterica serovar Typhimurium (bacteria) | ||||||
Method | ELECTRON MICROSCOPY / single particle reconstruction / cryo EM / Resolution: 11.7 Å | ||||||
Authors | Sgourakis, N.G. / Bergeron, J.R.C. / Strynadka, N.J.C. / Baker, D. | ||||||
Citation | Journal: Science / Year: 2011 Title: Three-dimensional model of Salmonella's needle complex at subnanometer resolution. Authors: Oliver Schraidt / Thomas C Marlovits / Abstract: Type III secretion systems (T3SSs) are essential virulence factors used by many Gram-negative bacteria to inject proteins that make eukaryotic host cells accessible to invasion. The T3SS core ...Type III secretion systems (T3SSs) are essential virulence factors used by many Gram-negative bacteria to inject proteins that make eukaryotic host cells accessible to invasion. The T3SS core structure, the needle complex (NC), is a ~3.5 megadalton-sized, oligomeric, membrane-embedded complex. Analyzing cryo-electron microscopy images of top views of NCs or NC substructures from Salmonella typhimurium revealed a 24-fold symmetry for the inner rings and a 15-fold symmetry for the outer rings, giving an overall C3 symmetry. Local refinement and averaging showed the organization of the central core and allowed us to reconstruct a subnanometer composite structure of the NC, which together with confident docking of atomic structures reveal insights into its overall organization and structural requirements during assembly. | ||||||
History |
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Remark 0 | THIS ENTRY 3J1V CONTAINS A STRUCTURAL MODEL FIT TO AN ELECTRON MICROSCOPY MAP (EMD-1875) DETERMINED ...THIS ENTRY 3J1V CONTAINS A STRUCTURAL MODEL FIT TO AN ELECTRON MICROSCOPY MAP (EMD-1875) DETERMINED ORIGINALLY BY AUTHORS: O.SCHRAIDT, T.C.MARLOVITS |
-Structure visualization
Movie |
Movie viewer |
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Structure viewer | Molecule: MolmilJmol/JSmol |
-Downloads & links
-Download
PDBx/mmCIF format | 3j1v.cif.gz | 350 KB | Display | PDBx/mmCIF format |
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PDB format | pdb3j1v.ent.gz | 283 KB | Display | PDB format |
PDBx/mmJSON format | 3j1v.json.gz | Tree view | PDBx/mmJSON format | |
Others | Other downloads |
-Validation report
Summary document | 3j1v_validation.pdf.gz | 754.1 KB | Display | wwPDB validaton report |
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Full document | 3j1v_full_validation.pdf.gz | 753.7 KB | Display | |
Data in XML | 3j1v_validation.xml.gz | 39.6 KB | Display | |
Data in CIF | 3j1v_validation.cif.gz | 67.8 KB | Display | |
Arichive directory | https://data.pdbj.org/pub/pdb/validation_reports/j1/3j1v ftp://data.pdbj.org/pub/pdb/validation_reports/j1/3j1v | HTTPS FTP |
-Related structure data
Related structure data | 1875M 3j1wC 3j1xC 4g08C 4g1iC 4g2sC M: map data used to model this data C: citing same article (ref.) |
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Similar structure data |
-Links
-Assembly
Deposited unit |
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1 |
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-Components
#1: Protein | Mass: 17694.172 Da / Num. of mol.: 15 / Fragment: UNP residues 22-178 Source method: isolated from a genetically manipulated source Source: (gene. exp.) Salmonella enterica subsp. enterica serovar Typhimurium (bacteria) Gene: invG, STM2898 / Production host: Escherichia coli (E. coli) / References: UniProt: P35672 |
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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 |
-Sample preparation
Component |
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Buffer solution | pH: 7.5 / Details: 10mM Tris-HCl (pH 7.5) 0.5mM NaCl 0.1% LDAO | ||||||||||||
Specimen | Embedding applied: NO / Shadowing applied: NO / Staining applied: NO / Vitrification applied: YES | ||||||||||||
Vitrification | Cryogen name: ETHANE |
-Electron microscopy imaging
Experimental equipment | Model: Tecnai Polara / Image courtesy: FEI Company |
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Microscopy | Model: FEI POLARA 300 |
Electron gun | Electron source: FIELD EMISSION GUN / Accelerating voltage: 300 kV / Illumination mode: FLOOD BEAM |
Electron lens | Mode: BRIGHT FIELD / Nominal magnification: 93000 X |
Image recording | Film or detector model: GENERIC CCD |
Radiation | Protocol: SINGLE WAVELENGTH / Monochromatic (M) / Laue (L): M / Scattering type: x-ray |
Radiation wavelength | Relative weight: 1 |
-Processing
EM software |
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Symmetry | Point symmetry: C15 (15 fold cyclic) | ||||||||||||
3D reconstruction | Resolution: 11.7 Å / Resolution method: FSC 0.5 CUT-OFF / Num. of particles: 37171 / Symmetry type: POINT | ||||||||||||
Atomic model building | Space: REAL | ||||||||||||
Refinement step | Cycle: LAST
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