Evidence map›Paper›PMID 41854513›Full record

ArticleFASEB journal : official publication of the Federation of American Societies for Experimental Biology2026

AcrVA3 Is a Double Strand DNA-Cleaving Anti-CRISPR That Indirectly Inhibits Cas12.

Ju Hee Han, Young Jun Kang, So Yeon Lee, Hyo Been Jin, Chang Sup Lee, Hyun Ho Park

Abstract read
In one paragraph

Article in FASEB journal : official publication of the Federation of American Societies for Experimental Biology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Ju Hee HanCollege of Pharmacy, Chung-Ang University, Seoul, Republic of Korea.
Young Jun KangCollege of Pharmacy, Chung-Ang University, Seoul, Republic of Korea.
So Yeon LeeCollege of Pharmacy, Chung-Ang University, Seoul, Republic of Korea.
Hyo Been JinCollege of Pharmacy, Chung-Ang University, Seoul, Republic of Korea.
Chang Sup LeeCollege of Pharmacy and Research Institute of Pharmaceutical Science, Gyeongsang National University, Jinju, Republic of Korea.
Hyun Ho ParkCollege of Pharmacy, Chung-Ang University, Seoul, Republic of Korea.ORCID https://orcid.org/0000-0001-9928-0847

Funding

National Research Foundation of Korea (NRF) RS-2025-02316334National Research Foundation of Korea (NRF) RS-2026-25470081
6 · The paper itself

Abstract

CRISPR-Cas12 systems protect bacteria from foreign DNA, but are themselves targeted by anti-CRISPR (Acr) proteins evolved by phages. Among the eight known AcrV proteins that inhibit Cas12-based type V CRISPR-Cas systems, the mechanisms of all except AcrVA3 have been structurally and biochemically characterized. Here, we report the high-resolution structure of AcrVA3 and examine its inhibitory function in vitro. Unexpectedly, AcrVA3 does not directly work on Cas12. Instead, it exhibits double-stranded DNA (dsDNA) cleavage activity, suggesting an indirect mechanism of CRISPR inhibition through DNA degradation. This unique DNA-centric strategy contrasts with previously known Acr mechanisms and expands our understanding of how mobile genetic elements evade CRISPR immunity.

Indexed as

Bacterial ProteinsClustered Regularly Interspaced Short Palindromic RepeatsCRISPR-Associated ProteinsCRISPR-Cas SystemsDNAViral ProteinsDNA CleavageModels, MolecularBacterial ProteinsCRISPR-Associated ProteinsDNAViral Proteins

Identifiers

PMID41854513
PMCPMC13001698

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.