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7MUV

Reconstruction of the Legionella pneumophila Dot/Icm T4SS 3DVA Map 3

This is a non-PDB format compatible entry.
Summary for 7MUV
Entry DOI10.2210/pdb7muv/pdb
EMDB information24023
DescriptorIcmE protein, DotC, DUF2807 domain-containing protein, ... (11 entities in total)
Functional Keywordsdot/icm, secretion, t4ss, translocase
Biological sourceLegionella pneumophila
More
Total number of polymer chains205
Total formula weight7563275.58
Authors
Sheedlo, M.J.,Durie, C.L.,Swanson, M.,Lacy, D.B.,Ohi, M.D. (deposition date: 2021-05-14, release date: 2021-10-06, Last modification date: 2024-10-16)
Primary citationSheedlo, M.J.,Durie, C.L.,Chung, J.M.,Chang, L.,Roberts, J.,Swanson, M.,Lacy, D.B.,Ohi, M.D.
Cryo-EM reveals new species-specific proteins and symmetry elements in the Legionella pneumophila Dot/Icm T4SS.
Elife, 10:-, 2021
Cited by
PubMed 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 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.
PubMed: 34519271
DOI: 10.7554/eLife.70427
PDB entries with the same primary citation
Experimental method
ELECTRON MICROSCOPY (4.6 Å)
Structure validation

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