Dataset Information
PROSPERous: high-throughput prediction of substrate cleavage sites for 90 proteases with improved accuracy.
Ontology highlight
ABSTRACT: Summary
Proteases are enzymes that specifically cleave the peptide backbone of their target proteins. As an important type of irreversible post-translational modification, protein cleavage underlies many key physiological processes. When dysregulated, proteases' actions are associated with numerous diseases. Many proteases are highly specific, cleaving only those target substrates that present certain particular amino acid sequence patterns. Therefore, tools that successfully identify potential target substrates for proteases may also identify previously unknown, physiologically relevant cleavage sites, thus providing insights into biological processes and guiding hypothesis-driven experiments aimed at verifying protease-substrate interaction. In this work, we present PROSPERous, a tool for rapid in silico prediction of protease-specific cleavage sites in substrate sequences. Our tool is based on logistic regression models and uses different scoring functions and their pairwise combinations to subsequently predict potential cleavage sites. PROSPERous represents a state-of-the-art tool that enables fast, accurate and high-throughput prediction of substrate cleavage sites for 90 proteases.Availability and implementation
http://prosperous.erc.monash.edu/.Contact
jiangning.song@monash.edu or geoff.webb@monash.edu or r.pike@latrobe.edu.au.Supplementary information
Supplementary data are available at Bioinformatics online.
SUBMITTER: Song J
PROVIDER: S-EPMC5860617 | biostudies-literature | 2018 Feb
REPOSITORIES: biostudies-literature
Publications
PROSPERous: high-throughput prediction of substrate cleavage sites for 90 proteases with improved accuracy.
Bioinformatics (Oxford, England) 20180201 4
<h4>Summary</h4>Proteases are enzymes that specifically cleave the peptide backbone of their target proteins. As an important type of irreversible post-translational modification, protein cleavage underlies many key physiological processes. When dysregulated, proteases' actions are associated with numerous diseases. Many proteases are highly specific, cleaving only those target substrates that present certain particular amino acid sequence patterns. Therefore, tools that successfully identify po ...[more]