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7AE0

Cryo-EM structure of an extracellular contractile injection system in marine bacterium Algoriphagus machipongonensis, the sheath-tube module in extended state.

This is a non-PDB format compatible entry.
Summary for 7AE0
Entry DOI10.2210/pdb7ae0/pdb
EMDB information11734 11735
DescriptorPutative phage tail sheath protein FI, Phage tail protein (2 entities in total)
Functional Keywordsextracellular contractile injection system, structural protein
Biological sourceAlgoriphagus machipongonensis
More
Total number of polymer chains36
Total formula weight1668500.95
Authors
Xu, J.,Ericson, C.,Feldmueller, M.,Lien, Y.W.,Pilhofer, M. (deposition date: 2020-09-17, release date: 2022-02-16, Last modification date: 2024-07-10)
Primary citationXu, J.,Ericson, C.F.,Lien, Y.W.,Rutaganira, F.U.N.,Eisenstein, F.,Feldmuller, M.,King, N.,Pilhofer, M.
Identification and structure of an extracellular contractile injection system from the marine bacterium Algoriphagus machipongonensis.
Nat Microbiol, 7:397-410, 2022
Cited by
PubMed Abstract: Contractile injection systems (CISs) are phage tail-like nanomachines, mediating bacterial cell-cell interactions as either type VI secretion systems (T6SSs) or extracellular CISs (eCISs). Bioinformatic studies uncovered a phylogenetic group of hundreds of putative CIS gene clusters that are highly diverse and widespread; however, only four systems have been characterized. Here we studied a putative CIS gene cluster in the marine bacterium Algoriphagus machipongonensis. Using an integrative approach, we show that the system is compatible with an eCIS mode of action. Our cryo-electron microscopy structure revealed several features that differ from those seen in other CISs: a 'cap adaptor' located at the distal end, a 'plug' exposed to the tube lumen, and a 'cage' formed by massive extensions of the baseplate. These elements are conserved in other CISs, and our genetic tools identified that they are required for assembly, cargo loading and function. Furthermore, our atomic model highlights specific evolutionary hotspots and will serve as a framework for understanding and re-engineering CISs.
PubMed: 35165385
DOI: 10.1038/s41564-022-01059-2
PDB entries with the same primary citation
Experimental method
ELECTRON MICROSCOPY (2.4 Å)
Structure validation

240971

数据于2025-08-27公开中

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