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ABSTRACT: Motivation
Many intracellular signaling processes are mediated by interactions involving peptide recognition modules such as SH3 domains. These domains bind to small, linear protein sequence motifs which can be identified using high-throughput experimental screens such as phage display. Binding motif patterns can then be used to computationally predict protein interactions mediated by these domains. While many protein-protein interaction prediction methods exist, most do not work with peptide recognition module mediated interactions or do not consider many of the known constraints governing physiologically relevant interactions between two proteins.Results
A novel method for predicting physiologically relevant SH3 domain-peptide mediated protein-protein interactions in S. c
SUBMITTER: Jain S
PROVIDER: S-EPMC4908317 | biostudies-literature | 2016 Jun
REPOSITORIES: biostudies-literature