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Open data
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Basic information
| Entry | Database: PDB / ID: 7mud | |||||||||||||||
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| Title | Legionella pneumophila Dot/Icm T4SS OMC | |||||||||||||||
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Keywords | TRANSLOCASE / Dot/Icm / Secretion / T4SS | |||||||||||||||
| Function / homology | Function and homology information | |||||||||||||||
| Biological species | ![]() | |||||||||||||||
| Method | ELECTRON MICROSCOPY / single particle reconstruction / cryo EM / Resolution: 2.8 Å | |||||||||||||||
Authors | Sheedlo, M.J. / Durie, C.L. / Swanson, M. / Lacy, D.B. / Ohi, M.D. | |||||||||||||||
| Funding support | United States, 4items
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Citation | Journal: Elife / Year: 2021Title: Cryo-EM reveals new species-specific proteins and symmetry elements in the Dot/Icm T4SS. Authors: Michael J Sheedlo / Clarissa L Durie / Jeong Min Chung / Louise Chang / Jacquelyn Roberts / Michele Swanson / Dana Borden Lacy / Melanie D Ohi / ![]() Abstract: is an opportunistic pathogen that causes the potentially fatal pneumonia known as Legionnaires' disease. The pathology associated with infection depends on bacterial delivery of effector proteins ... is an opportunistic pathogen that causes the potentially fatal pneumonia known as Legionnaires' disease. The pathology associated with infection depends on bacterial delivery of effector proteins into the host via the membrane spanning Dot/Icm type IV secretion system (T4SS). We have determined sub-3.0 Å resolution maps of the Dot/Icm T4SS core complex by single particle cryo-EM. The high-resolution structural analysis has allowed us to identify proteins encoded outside the Dot/Icm genetic locus that contribute to the core T4SS structure. We can also now define two distinct areas of symmetry mismatch, one that connects the C18 periplasmic ring (PR) and the C13 outer membrane cap (OMC) and one that connects the C13 OMC with a 16-fold symmetric dome. Unexpectedly, the connection between the PR and OMC is DotH, with five copies sandwiched between the OMC and PR to accommodate the symmetry mismatch. Finally, we observe multiple conformations in the reconstructions that indicate flexibility within the structure. | |||||||||||||||
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Structure visualization
| Movie |
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| Structure viewer | Molecule: Molmil Jmol/JSmol |
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Downloads & links
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Download
| PDBx/mmCIF format | 7mud.cif.gz | 3 MB | Display | PDBx/mmCIF format |
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| PDB format | pdb7mud.ent.gz | Display | PDB format | |
| PDBx/mmJSON format | 7mud.json.gz | Tree view | PDBx/mmJSON format | |
| Others | Other downloads |
-Validation report
| Summary document | 7mud_validation.pdf.gz | 1.1 MB | Display | wwPDB validaton report |
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| Full document | 7mud_full_validation.pdf.gz | 1.1 MB | Display | |
| Data in XML | 7mud_validation.xml.gz | 356.5 KB | Display | |
| Data in CIF | 7mud_validation.cif.gz | 582.7 KB | Display | |
| Arichive directory | https://data.pdbj.org/pub/pdb/validation_reports/mu/7mud ftp://data.pdbj.org/pub/pdb/validation_reports/mu/7mud | HTTPS FTP |
-Related structure data
| Related structure data | ![]() 24005MC ![]() 7mucC ![]() 7mueC ![]() 7muqC ![]() 7musC ![]() 7muvC ![]() 7muwC ![]() 7muyC M: map data used to model this data C: citing same article ( |
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| Similar structure data |
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Links
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Assembly
| Deposited unit | ![]()
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| 1 |
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Components
-Protein , 8 types, 117 molecules ACBCCCDCECFCGCHCICJCKCLCMCADAdBDBdCDCdDDDdEDEdFDFdGDGdHDHdID...
| #1: Protein | Mass: 34162.441 Da / Num. of mol.: 13 / Source method: isolated from a natural source / Source: (natural) ![]() #2: Protein | Mass: 17860.678 Da / Num. of mol.: 26 / Source method: isolated from a natural source / Source: (natural) ![]() #3: Protein | Mass: 38958.926 Da / Num. of mol.: 13 / Source method: isolated from a natural source / Source: (natural) ![]() #4: Protein | Mass: 21096.492 Da / Num. of mol.: 13 / Source method: isolated from a natural source / Source: (natural) ![]() #5: Protein | Mass: 27582.047 Da / Num. of mol.: 13 / Source method: isolated from a natural source / Source: (natural) ![]() #6: Protein | Mass: 36095.367 Da / Num. of mol.: 13 / Source method: isolated from a natural source / Source: (natural) ![]() #7: Protein | Mass: 13598.854 Da / Num. of mol.: 13 / Source method: isolated from a natural source / Source: (natural) ![]() #9: Protein | Mass: 29729.969 Da / Num. of mol.: 13 / Source method: isolated from a natural source / Source: (natural) ![]() |
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-Protein/peptide , 1 types, 13 molecules AUBUCUDUEUFUGUHUIUJUKULUMU
| #8: Protein/peptide | Mass: 783.958 Da / Num. of mol.: 13 / Source method: isolated from a natural source / Source: (natural) ![]() |
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-Details
| Has protein modification | Y |
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| Sequence details | The protein fragment sequence could not be directly identified as the sample was purified from a ...The protein fragment sequence could not be directly identified as the sample was purified from a native source. |
-Experimental details
-Experiment
| Experiment | Method: ELECTRON MICROSCOPY |
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| EM experiment | Aggregation state: PARTICLE / 3D reconstruction method: single particle reconstruction |
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Sample preparation
| Component | Name: Legionella pneumophila Dot/Icm T4SS OMC / Type: COMPLEX / Entity ID: all / Source: NATURAL |
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| Molecular weight | Experimental value: NO |
| Source (natural) | Organism: ![]() |
| Buffer solution | pH: 8 |
| Specimen | Embedding applied: NO / Shadowing applied: NO / Staining applied: NO / Vitrification applied: YES |
| Vitrification | Cryogen name: ETHANE |
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Electron microscopy imaging
| Experimental equipment | ![]() Model: Titan Krios / Image courtesy: FEI Company |
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| Microscopy | Model: FEI TITAN KRIOS |
| Electron gun | Electron source: FIELD EMISSION GUN / Accelerating voltage: 300 kV / Illumination mode: FLOOD BEAM |
| Electron lens | Mode: BRIGHT FIELD |
| Image recording | Electron dose: 50 e/Å2 / Film or detector model: GATAN K3 (6k x 4k) |
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Processing
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| CTF correction | Type: PHASE FLIPPING AND AMPLITUDE CORRECTION | ||||||||||||||||||||||||
| 3D reconstruction | Resolution: 2.8 Å / Resolution method: FSC 0.143 CUT-OFF / Num. of particles: 84886 / Symmetry type: POINT | ||||||||||||||||||||||||
| Atomic model building | Protocol: AB INITIO MODEL | ||||||||||||||||||||||||
| Refinement | Cross valid method: NONE Stereochemistry target values: GeoStd + Monomer Library + CDL v1.2 | ||||||||||||||||||||||||
| Displacement parameters | Biso mean: 55.33 Å2 | ||||||||||||||||||||||||
| Refine LS restraints |
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