9NY5

LmuABC_apo

Summary for 9NY5

• Entry DOI: 10.2210/pdb9ny5/pdb
• EMDB information: 49922
• Descriptor: LmuC, ABC-three component systems C-terminal domain-containing protein, DUF3732 domain-containing protein (3 entities in total)
• Functional Keywords: lmuabc_apo, dna binding protein
• Biological source: Vibrio cholerae; More
• Total number of polymer chains: 4
• Total formula weight: 214347.57

Authors

Chakravarti, A.,Zhang, Z. (deposition date: 2025-03-26, release date: 2025-12-17)

Primary citation

Haudiquet, M.,Chakravarti, A.,Zhang, Z.,Ramirez, J.L.,Herrero Del Valle, A.,Olinares, P.D.B.,Lavenir, R.,Ahmed, M.A.,de la Cruz, M.J.,Chait, B.T.,Sternberg, S.H.,Bernheim, A.,Patel, D.J.
Structural basis for Lamassu-based antiviral immunity and its evolution from DNA repair machinery.
Proc.Natl.Acad.Sci.USA, 122:e2519643122-e2519643122, 2025

PubMed Abstract: Bacterial immune systems exhibit remarkable diversity and modularity, as a consequence of the continuous selective pressures imposed by phage predation. Despite recent mechanistic advances, the evolutionary origins of many antiphage immune systems remain elusive, especially for those that encode homologs of the structural maintenance of chromosomes (SMC) superfamily, which are essential for chromosome maintenance and DNA repair across domains of life. Here, we elucidate the structural basis and evolutionary emergence of Lamassu, a bacterial immune system family featuring diverse effectors but a core conserved SMC-like sensor. Using cryo-EM, we determined structures of the Lamassu complex in both apo- and dsDNA-bound states, revealing unexpected stoichiometry and topological architectures. We further demonstrate how Lamassu specifically senses dsDNA ends in vitro and phage replication origins in vivo, thereby triggering the formation of LmuA tetramers that activate its Cap4 nuclease domain. Our findings reveal that Lamassu evolved via exaptation of the bacterial Rad50-Mre11 DNA repair system to form a compact, modular sensor for viral replication, exemplifying how cellular machinery can be co-opted for novel immune functions.

PubMed: 41252147
DOI: 10.1073/pnas.2519643122

Experimental method

ELECTRON MICROSCOPY (3.21 Å)