AcrDB: a database of anti-CRISPR operons in prokaryotes and viruses release_62ro3r7sfnea5kqwz22bzy5f3u

by Le Huang, Bowen Yang, Haidong Yi, Amina Asif, Jiawei Wang, Trevor James Lithgow, Han Zhang, Fayyaz ul Amir Afsar Minhas, Yanbin Yin

Published in Nucleic Acids Research by Oxford University Press (OUP).

2020  

Abstract

<jats:title>Abstract</jats:title> CRISPR–Cas is an anti-viral mechanism of prokaryotes that has been widely adopted for genome editing. To make CRISPR–Cas genome editing more controllable and safer to use, anti-CRISPR proteins have been recently exploited to prevent excessive/prolonged Cas nuclease cleavage. Anti-CRISPR (Acr) proteins are encoded by (pro)phages/(pro)viruses, and have the ability to inhibit their host's CRISPR–Cas systems. We have built an online database AcrDB (http://bcb.unl.edu/AcrDB) by scanning ∼19 000 genomes of prokaryotes and viruses with AcrFinder, a recently developed Acr-Aca (Acr-associated regulator) operon prediction program. Proteins in Acr-Aca operons were further processed by two machine learning-based programs (AcRanker and PaCRISPR) to obtain numerical scores/ranks. Compared to other anti-CRISPR databases, AcrDB has the following unique features: (i) It is a genome-scale database with the largest collection of data (39 799 Acr-Aca operons containing Aca or Acr homologs); (ii) It offers a user-friendly web interface with various functions for browsing, graphically viewing, searching, and batch downloading Acr-Aca operons; (iii) It focuses on the genomic context of Acr and Aca candidates instead of individual Acr protein family and (iv) It collects data with three independent programs each having a unique data mining algorithm for cross validation. AcrDB will be a valuable resource to the anti-CRISPR research community.
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Type  article-journal
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Date   2020-10-17
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DOI  10.1093/nar/gkaa857
PubMed  33068435
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