Detailed Information on Publication Record
2016
Hammock: a hidden Markov model-based peptide clustering algorithm to identify protein-interaction consensus motifs in large datasets
KREJČÍ, Adam, TR HUPP, Matej LEXA, Bořivoj VOJTĚŠEK, Petr MÜLLER et. al.Basic information
Original name
Hammock: a hidden Markov model-based peptide clustering algorithm to identify protein-interaction consensus motifs in large datasets
Authors
KREJČÍ, Adam (203 Czech Republic), TR HUPP (826 United Kingdom of Great Britain and Northern Ireland), Matej LEXA (703 Slovakia, belonging to the institution), Bořivoj VOJTĚŠEK (203 Czech Republic) and Petr MÜLLER (203 Czech Republic)
Edition
Bioinformatics, Oxford, Oxford University Press, 2016, 1367-4803
Other information
Language
English
Type of outcome
Článek v odborném periodiku
Field of Study
10201 Computer sciences, information science, bioinformatics
Country of publisher
United Kingdom of Great Britain and Northern Ireland
Confidentiality degree
není předmětem státního či obchodního tajemství
Impact factor
Impact factor: 7.307
RIV identification code
RIV/00216224:14330/16:00089377
Organization unit
Faculty of Informatics
UT WoS
000368357800002
Keywords in English
phage display; sequence logo; clustering;
Tags
International impact, Reviewed
Změněno: 13/3/2018 14:02, doc. Ing. Matej Lexa, Ph.D.
Abstract
V originále
Motivation: Proteins often recognize their interaction partners on the basis of short linear motifs located in disordered regions on proteins' surface. Experimental techniques that study such motifs use short peptides to mimic the structural properties of interacting proteins. Continued development of these methods allows for large-scale screening, resulting in vast amounts of peptide sequences, potentially containing information on multiple protein-protein interactions. Processing of such datasets is a complex but essential task for large-scale studies investigating protein-protein interactions. Results: The software tool presented in this article is able to rapidly identify multiple clusters of sequences carrying shared specificity motifs in massive datasets from various sources and generate multiple sequence alignments of identified clusters. The method was applied on a previously published smaller dataset containing distinct classes of ligands for SH3 domains, as well as on a new, an order of magnitude larger dataset containing epitopes for several monoclonal antibodies. The software successfully identified clusters of sequences mimicking epitopes of antibody targets, as well as secondary clusters revealing that the antibodies accept some deviations from original epitope sequences. Another test indicates that processing of even much larger datasets is computationally feasible.