ArticleProceedings of the National Academy of Sciences of the United States of America2015
Using homology relations within a database markedly boosts protein sequence similarity search.
Article in Proceedings of the National Academy of Sciences of the United States of America, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.
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4 citing papers in PubMed.
- Identification of Two Flip-Over Genes in Grass Family as Potential Signature of C4 Photosynthesis Evolution.International journal of molecular sciences · 2023Article
- UBTOR/KIAA1024 regulates neurite outgrowth and neoplasia through mTOR signaling.PLoS genetics · 2018Article
- ECOD: new developments in the evolutionary classification of domains.Nucleic acids research · 2017Article
- AnABlast: a new in silico strategy for the genome-wide search of novel genes and fossil regions.DNA research : an international journal for rapid publication of reports on genes and genomes · 2015Article
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5 authors.
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Abstract
Inference of homology from protein sequences provides an essential tool for analyzing protein structure, function, and evolution. Current sequence-based homology search methods are still unable to detect many similarities evident from protein spatial structures. In computer science a search engine can be improved by considering networks of known relationships within the search database. Here, we apply this idea to protein-sequence-based homology search and show that it dramatically enhances the search accuracy. Our new method, COMPADRE (COmparison of Multiple Protein sequence Alignments using Database RElationships) assesses the relationship between the query sequence and a hit in the database by considering the similarity between the query and hit's known homologs. This approach increases detection quality, boosting the precision rate from 18% to 83% at half-coverage of all database homologs. The increased precision rate allows detection of a large fraction of protein structural relationships, thus providing structure and function predictions for previously uncharacterized proteins. Our results suggest that this general approach is applicable to a wide variety of methods for detection of biological similarities. The web server is available at prodata.swmed.edu/compadre.
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