9G9E
CryoEM structure of Enterococcus italicus Csm-crRNA complex bound to AMPNPP
Summary for 9G9E
| Entry DOI | 10.2210/pdb9g9e/pdb |
| EMDB information | 51149 |
| Descriptor | CRISPR system single-strand-specific deoxyribonuclease Cas10/Csm1 (subtype III-A), CRISPR system Cms protein Csm2, CRISPR system Cms endoribonuclease Csm3, ... (8 entities in total) |
| Functional Keywords | type iii-a crispr-cas rna-guided nuclease endoribonuclease cyclic oligoadenylate synthetase hd nuclease, rna binding protein |
| Biological source | Enterococcus italicus DSM 15952 More |
| Total number of polymer chains | 9 |
| Total formula weight | 285236.00 |
| Authors | |
| Primary citation | Jungfer, K.,Moravcik, S.,Garcia-Doval, C.,Knorlein, A.,Hall, J.,Jinek, M. Mechanistic determinants and dynamics of cA6 synthesis in type III CRISPR-Cas effector complexes. Nucleic Acids Res., 53:-, 2025 Cited by PubMed Abstract: Type III clustered regularly interspaced short palindromic repeats (CRISPR) and CRISPR-associated (Cas) systems (type III CRISPR-Cas systems) use guide RNAs to recognize RNA transcripts of foreign genetic elements, which triggers the generation of cyclic oligoadenylate (cOA) second messengers by the Cas10 subunit of the type III effector complex. In turn, cOAs bind and activate ancillary effector proteins to reinforce the host immune response. Type III systems utilize distinct cOAs, including cyclic tri- (cA3), tetra- (cA4) and hexa-adenylates (cA6). However, the molecular mechanisms dictating cOA product identity are poorly understood. Here we used cryoelectron microscopy to visualize the mechanism of cA6 biosynthesis by the Csm effector complex from Enterococcus italicus (EiCsm). We show that EiCsm synthesizes oligoadenylate nucleotides in 3'-5' direction using a set of conserved binding sites in the Cas10 Palm domains to determine the size of the nascent oligoadenylate chain. Our data also reveal that conformational dynamics induced by target RNA binding results in allosteric activation of Cas10 to trigger oligoadenylate synthesis. Mutations of a key structural element in Cas10 perturb cOA synthesis to favor cA3 and cA4 formation. Together, these results provide comprehensive insights into the dynamics of cOA synthesis in type III CRISPR-Cas systems and reveal key determinants of second messenger product selectivity, thereby illuminating potential avenues for their engineering. PubMed: 39817514DOI: 10.1093/nar/gkae1277 PDB entries with the same primary citation |
| Experimental method | ELECTRON MICROSCOPY (2.87 Å) |
Structure validation
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