Abstract | ||
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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 similar to 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. |
Year | DOI | Venue |
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2021 | 10.1093/nar/gkaa857 | NUCLEIC ACIDS RESEARCH |
DocType | Volume | Issue |
Journal | 49 | D1 |
ISSN | Citations | PageRank |
0305-1048 | 0 | 0.34 |
References | Authors | |
0 | 9 |
Name | Order | Citations | PageRank |
---|---|---|---|
Le Huang | 1 | 2 | 1.73 |
Bowen Yang | 2 | 0 | 0.68 |
Haidong Yi | 3 | 3 | 3.17 |
Amina Asif | 4 | 5 | 5.51 |
jiawei wang | 5 | 37 | 11.22 |
Trevor Lithgow | 6 | 15 | 3.16 |
Han Zhang | 7 | 0 | 0.68 |
Fayyaz ul Amir Afsar Minhas | 8 | 27 | 9.37 |
Yanbin Yin | 9 | 31 | 7.75 |