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7XI1

AcrIF 24

Summary for 7XI1
Entry DOI10.2210/pdb7xi1/pdb
Descriptoranti-CRISPR protein AcrIF24 (2 entities in total)
Functional Keywordsanti-crispr, acr, inhibitor of type i-f cascade, immune system
Biological sourcePseudomonas aeruginosa
Total number of polymer chains1
Total formula weight26066.43
Authors
Kim, G.E.,Park, H.H. (deposition date: 2022-04-11, release date: 2023-03-22, Last modification date: 2023-11-29)
Primary citationKim, G.E.,Lee, S.Y.,Birkholz, N.,Kamata, K.,Jeong, J.H.,Kim, Y.G.,Fineran, P.C.,Park, H.H.
Molecular basis of dual anti-CRISPR and auto-regulatory functions of AcrIF24.
Nucleic Acids Res., 50:11344-11358, 2022
Cited by
PubMed Abstract: CRISPR-Cas systems are adaptive immune systems in bacteria and archaea that provide resistance against phages and other mobile genetic elements. To fight against CRISPR-Cas systems, phages and archaeal viruses encode anti-CRISPR (Acr) proteins that inhibit CRISPR-Cas systems. The expression of acr genes is controlled by anti-CRISPR-associated (Aca) proteins encoded within acr-aca operons. AcrIF24 is a recently identified Acr that inhibits the type I-F CRISPR-Cas system. Interestingly, AcrIF24 was predicted to be a dual-function Acr and Aca. Here, we elucidated the crystal structure of AcrIF24 from Pseudomonas aeruginosa and identified its operator sequence within the regulated acr-aca operon promoter. The structure of AcrIF24 has a novel domain composition, with wing, head and body domains. The body domain is responsible for recognition of promoter DNA for Aca regulatory activity. We also revealed that AcrIF24 directly bound to type I-F Cascade, specifically to Cas7 via its head domain as part of its Acr mechanism. Our results provide new molecular insights into the mechanism of a dual functional Acr-Aca protein.
PubMed: 36243977
DOI: 10.1093/nar/gkac880
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.53 Å)
Structure validation

227111

數據於2024-11-06公開中

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