Affiliation:
1. School of Computational Sciences
2. Center for Advanced Computation, Korea Institute for Advanced Study, Korea
Abstract
AbstractMotivationDomain boundary prediction is one of the most important problems in the study of protein structure and function. Many sequence-based domain boundary prediction methods are either template-based or machine learning (ML) based. ML-based methods often perform poorly due to their use of only local (i.e. short-range) features. These conventional features such as sequence profiles, secondary structures and solvent accessibilities are typically restricted to be within 20 residues of the domain boundary candidate.ResultsTo address the performance of ML-based methods, we developed a new protein domain boundary prediction method (ConDo) that utilizes novel long-range features such as coevolutionary information in addition to the aforementioned local window features as inputs for ML. Toward this purpose, two types of coevolutionary information were extracted from multiple sequence alignment using direct coupling analysis: (i) partially aligned sequences, and (ii) correlated mutation information. Both the partially aligned sequence information and the modularity of residue–residue couplings possess long-range correlation information.Availability and implementationhttps://github.com/gicsaw/ConDo.gitSupplementary informationSupplementary data are available at Bioinformatics online.
Funder
Basic Science Research Program
National Research Foundation of Korea
NRF
Ministry of Science
ICT
Publisher
Oxford University Press (OUP)
Subject
Computational Mathematics,Computational Theory and Mathematics,Computer Science Applications,Molecular Biology,Biochemistry,Statistics and Probability
Cited by
20 articles.
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