Substrate selectivity and catalytic activation of the type III CRISPR ancillary nuclease Can2.
Ontology highlight
ABSTRACT: Type III CRISPR-Cas systems provide adaptive immunity against foreign mobile genetic elements through RNA-guided interference. Sequence-specific recognition of RNA targets by the type III effector complex triggers the generation of cyclic oligoadenylate (cOA) second messengers that activate ancillary effector proteins, thus reinforcing the host immune response. The ancillary nuclease Can2 is activated by cyclic tetra-AMP (cA4); however, the mechanisms underlying cA4-mediated activation and substrate selectivity remain elusive. Here we report crystal structures of Thermoanaerobacter brockii Can2 (TbrCan2) in substrate- and product-bound complexes. We show that TbrCan2 is a single strand-selective DNase and RNase that binds substrates via a conserved SxTTS active site motif, and reveal molec
SUBMITTER: Jungfer K
PROVIDER: S-EPMC10783487 | biostudies-literature | 2024 Jan
REPOSITORIES: biostudies-literature
ACCESS DATA