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8RK6

Baseplate core of bacteriophage JBD30 computed in C3 symmetry

This is a non-PDB format compatible entry.
Summary for 8RK6
Entry DOI10.2210/pdb8rk6/pdb
EMDB information19262
DescriptorDUF2163 domain-containing protein, Virion structural protein, Tip attachment protein J domain-containing protein, ... (4 entities in total)
Functional Keywordsbacteriophage jbd30, virion, baseplate core, baseplate upper protein, distal tail protein, baseplate hub protein, virus
Biological sourcePseudomonas phage JBD30
More
Total number of polymer chains3
Total formula weight172096.83
Authors
Valentova, L.,Fuzik, T.,Plevka, P. (deposition date: 2023-12-23, release date: 2024-08-14, Last modification date: 2024-10-16)
Primary citationValentova, L.,Fuzik, T.,Novacek, J.,Hlavenkova, Z.,Pospisil, J.,Plevka, P.
Structure and replication of Pseudomonas aeruginosa phage JBD30.
Embo J., 43:4384-4405, 2024
Cited by
PubMed Abstract: Bacteriophages are the most abundant biological entities on Earth, but our understanding of many aspects of their lifecycles is still incomplete. Here, we have structurally analysed the infection cycle of the siphophage Casadabanvirus JBD30. Using its baseplate, JBD30 attaches to Pseudomonas aeruginosa via the bacterial type IV pilus, whose subsequent retraction brings the phage to the bacterial cell surface. Cryo-electron microscopy structures of the baseplate-pilus complex show that the tripod of baseplate receptor-binding proteins attaches to the outer bacterial membrane. The tripod and baseplate then open to release three copies of the tape-measure protein, an event that is followed by DNA ejection. JBD30 major capsid proteins assemble into procapsids, which expand by 7% in diameter upon filling with phage dsDNA. The DNA-filled heads are finally joined with 180-nm-long tails, which bend easily because flexible loops mediate contacts between the successive discs of major tail proteins. It is likely that the structural features and replication mechanisms described here are conserved among siphophages that utilize the type IV pili for initial cell attachment.
PubMed: 39143239
DOI: 10.1038/s44318-024-00195-1
PDB entries with the same primary citation
Experimental method
ELECTRON MICROSCOPY (3.6 Å)
Structure validation

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