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6VRC

Cryo-EM structure of Cas13(crRNA)

Summary for 6VRC
Entry DOI10.2210/pdb6vrc/pdb
EMDB information21366 21367
DescriptorCRISPR-associated endoribonuclease Cas13a, RNA (51-MER) (2 entities in total)
Functional Keywordscrispr-cas system, cas13, immune system, typevi
Biological sourceListeria seeligeri serovar 1/2b (strain ATCC 35967 / DSM 20751 / CIP 100100 / SLCC 3954)
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Total number of polymer chains2
Total formula weight152344.68
Authors
Jia, N.,Meeske, A.J.,Marraffini, L.A.,Patel, D.J. (deposition date: 2020-02-07, release date: 2020-06-10, Last modification date: 2024-03-06)
Primary citationMeeske, A.J.,Jia, N.,Cassel, A.K.,Kozlova, A.,Liao, J.,Wiedmann, M.,Patel, D.J.,Marraffini, L.A.
A phage-encoded anti-CRISPR enables complete evasion of type VI-A CRISPR-Cas immunity.
Science, 369:54-59, 2020
Cited by
PubMed Abstract: The CRISPR RNA (crRNA)-guided nuclease Cas13 recognizes complementary viral transcripts to trigger the degradation of both host and viral RNA during the type VI CRISPR-Cas antiviral response. However, how viruses can counteract this immunity is not known. We describe a listeriaphage (ϕLS46) encoding an anti-CRISPR protein (AcrVIA1) that inactivates the type VI-A CRISPR system of Using genetics, biochemistry, and structural biology, we found that AcrVIA1 interacts with the guide-exposed face of Cas13a, preventing access to the target RNA and the conformational changes required for nuclease activation. Unlike inhibitors of DNA-cleaving Cas nucleases, which cause limited immunosuppression and require multiple infections to bypass CRISPR defenses, a single dose of AcrVIA1 delivered by an individual virion completely dismantles type VI-A CRISPR-mediated immunity.
PubMed: 32467331
DOI: 10.1126/science.abb6151
PDB entries with the same primary citation
Experimental method
ELECTRON MICROSCOPY (3.2 Å)
Structure validation

240971

数据于2025-08-27公开中

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