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7YNA

Cryo-EM structure of Cas7-11-crRNA bound to target RNA-1

Summary for 7YNA
Entry DOI10.2210/pdb7yna/pdb
EMDB information33956
DescriptorCRISPR-associated RAMP family protein, crRNA (38-MER), Target RNA-1 (25-MER) (3 entities in total)
Functional Keywordscas7-11, crrna, crispr-cas, csx29, rna binding protein
Biological sourceDesulfonema ishimotonii
More
Total number of polymer chains3
Total formula weight209208.04
Authors
Huo, Y.,Dong, Q.,Zhao, H.,Jiang, T. (deposition date: 2022-07-30, release date: 2023-02-01, Last modification date: 2024-07-03)
Primary citationHuo, Y.,Zhao, H.,Dong, Q.,Jiang, T.
Cryo-EM structure and protease activity of the type III-E CRISPR-Cas effector.
Nat Microbiol, 8:522-532, 2023
Cited by
PubMed Abstract: The recently discovered type III-E CRISPR-Cas effector Cas7-11 shows promise when used as an RNA manipulation tool, but its structure and the mechanisms underlying its function remain unclear. Here we present four cryo-EM structures of Desulfonema ishimotonii Cas7-11-crRNA complex in pre-target and target RNA-bound states, and the cryo-EM structure of DiCas7-11-crRNA bound to its accessory protein DiCsx29. These data reveal structural elements for pre-crRNA processing, target RNA cleavage and regulation. Moreover, a 3' seed region of crRNA is involved in regulating RNA cleavage activity of DiCas7-11-crRNA-Csx29. Our analysis also shows that both the minimal mismatch of 4 nt to the 5' handle of crRNA and the minimal matching of the first 12 nt of the spacer by the target RNA are essential for triggering the protease activity of DiCas7-11-crRNA-Csx29 towards DiCsx30. Taken together, we propose that target RNA recognition and cleavage regulate and fine-tune the protease activity of DiCas7-11-crRNA-Csx29, thus preventing auto-immune responses.
PubMed: 36702942
DOI: 10.1038/s41564-022-01316-4
PDB entries with the same primary citation
Experimental method
ELECTRON MICROSCOPY (3.64 Å)
Structure validation

226707

數據於2024-10-30公開中

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