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8Q3Z

Crystal structure of cA4-bound Can2 from Thermoanaerobacter brockii

Summary for 8Q3Z
Entry DOI10.2210/pdb8q3z/pdb
Related PRD IDPRD_002431
DescriptorDUF1887 family protein, Cyclic tetraadenosine monophosphate (cA4), MANGANESE (II) ION (3 entities in total)
Functional Keywordscan2, cyclic oligoadenylates, ca4, carf, crispr ancillary nuclease, dna binding protein
Biological sourceThermoanaerobacter brockii subsp. finnii Ako-1
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Total number of polymer chains3
Total formula weight104182.69
Authors
Jungfer, K.,Sigg, A.,Jinek, M. (deposition date: 2023-08-04, release date: 2023-11-22, Last modification date: 2024-01-24)
Primary citationJungfer, K.,Sigg, A.,Jinek, M.
Substrate selectivity and catalytic activation of the type III CRISPR ancillary nuclease Can2.
Nucleic Acids Res., 52:462-473, 2024
Cited by
PubMed 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 molecular interactions underpinning its sequence preference for CA dinucleotides. Furthermore, we identify a molecular interaction relay linking the cA4 binding site and the nuclease catalytic site to enable divalent metal cation coordination and catalytic activation. These findings provide key insights into the molecular mechanisms of Can2 nucleases in type III CRISPR-Cas immunity and may guide their technological development for nucleic acid detection applications.
PubMed: 38033326
DOI: 10.1093/nar/gkad1102
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (3.15 Å)
Structure validation

238582

数据于2025-07-09公开中

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