6SCE

Structure of a Type III CRISPR defence DNA nuclease activated by cyclic oligoadenylate

Summary for 6SCE

• Entry DOI: 10.2210/pdb6sce/pdb
• Descriptor: Uncharacterized protein, cyclic oligoadenylate (3 entities in total)
• Functional Keywords: crispr carf dna nuclease cyclic oligoadenylate thermus thermophilus, dna
• Biological source: Thermus thermophilus HB8; More
• Total number of polymer chains: 2
• Total formula weight: 73526.62

Authors

McMahon, S.A.,Zhu, W.,Graham, S.,White, M.F.,Gloster, T.M. (deposition date: 2019-07-24, release date: 2020-02-19, Last modification date: 2024-10-16)

Primary citation

McMahon, S.A.,Zhu, W.,Graham, S.,Rambo, R.,White, M.F.,Gloster, T.M.
Structure and mechanism of a Type III CRISPR defence DNA nuclease activated by cyclic oligoadenylate.
Nat Commun, 11:500-500, 2020

PubMed Abstract: The CRISPR system provides adaptive immunity against mobile genetic elements in prokaryotes. On binding invading RNA species, Type III CRISPR systems generate cyclic oligoadenylate (cOA) signalling molecules, potentiating a powerful immune response by activating downstream effector proteins, leading to viral clearance, cell dormancy or death. Here we describe the structure and mechanism of a cOA-activated CRISPR defence DNA endonuclease, CRISPR ancillary nuclease 1 (Can1). Can1 has a unique monomeric structure with two CRISPR associated Rossman fold (CARF) domains and two DNA nuclease-like domains. The crystal structure of the enzyme has been captured in the activated state, with a cyclic tetra-adenylate (cA) molecule bound at the core of the protein. cA binding reorganises the structure to license a metal-dependent DNA nuclease activity specific for nicking of supercoiled DNA. DNA nicking by Can1 is predicted to slow down viral replication kinetics by leading to the collapse of DNA replication forks.

PubMed: 31980625
DOI: 10.1038/s41467-019-14222-x

Experimental method

X-RAY DIFFRACTION (1.83 Å)