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M-Finder: Uncovering functionally associated proteins from interactome data integrated with GO annotations
BACKGROUND: Protein-protein interactions (PPIs) play a key role in understanding the mechanisms of cellular processes. The availability of interactome data has catalyzed the development of computational approaches to elucidate functional behaviors of proteins on a system level. Gene Ontology (GO) an...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3909039/ https://www.ncbi.nlm.nih.gov/pubmed/24565382 http://dx.doi.org/10.1186/1477-5956-11-S1-S3 |
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author | Cho, Young-Rae Mina, Marco Lu, Yanxin Kwon, Nayoung Guzzi, Pietro H |
author_facet | Cho, Young-Rae Mina, Marco Lu, Yanxin Kwon, Nayoung Guzzi, Pietro H |
author_sort | Cho, Young-Rae |
collection | PubMed |
description | BACKGROUND: Protein-protein interactions (PPIs) play a key role in understanding the mechanisms of cellular processes. The availability of interactome data has catalyzed the development of computational approaches to elucidate functional behaviors of proteins on a system level. Gene Ontology (GO) and its annotations are a significant resource for functional characterization of proteins. Because of wide coverage, GO data have often been adopted as a benchmark for protein function prediction on the genomic scale. RESULTS: We propose a computational approach, called M-Finder, for functional association pattern mining. This method employs semantic analytics to integrate the genome-wide PPIs with GO data. We also introduce an interactive web application tool that visualizes a functional association network linked to a protein specified by a user. The proposed approach comprises two major components. First, the PPIs that have been generated by high-throughput methods are weighted in terms of their functional consistency using GO and its annotations. We assess two advanced semantic similarity metrics which quantify the functional association level of each interacting protein pair. We demonstrate that these measures outperform the other existing methods by evaluating their agreement to other biological features, such as sequence similarity, the presence of common Pfam domains, and core PPIs. Second, the information flow-based algorithm is employed to discover a set of proteins functionally associated with the protein in a query and their links efficiently. This algorithm reconstructs a functional association network of the query protein. The output network size can be flexibly determined by parameters. CONCLUSIONS: M-Finder provides a useful framework to investigate functional association patterns with any protein. This software will also allow users to perform further systematic analysis of a set of proteins for any specific function. It is available online at http://bionet.ecs.baylor.edu/mfinder |
format | Online Article Text |
id | pubmed-3909039 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-39090392014-02-13 M-Finder: Uncovering functionally associated proteins from interactome data integrated with GO annotations Cho, Young-Rae Mina, Marco Lu, Yanxin Kwon, Nayoung Guzzi, Pietro H Proteome Sci Research BACKGROUND: Protein-protein interactions (PPIs) play a key role in understanding the mechanisms of cellular processes. The availability of interactome data has catalyzed the development of computational approaches to elucidate functional behaviors of proteins on a system level. Gene Ontology (GO) and its annotations are a significant resource for functional characterization of proteins. Because of wide coverage, GO data have often been adopted as a benchmark for protein function prediction on the genomic scale. RESULTS: We propose a computational approach, called M-Finder, for functional association pattern mining. This method employs semantic analytics to integrate the genome-wide PPIs with GO data. We also introduce an interactive web application tool that visualizes a functional association network linked to a protein specified by a user. The proposed approach comprises two major components. First, the PPIs that have been generated by high-throughput methods are weighted in terms of their functional consistency using GO and its annotations. We assess two advanced semantic similarity metrics which quantify the functional association level of each interacting protein pair. We demonstrate that these measures outperform the other existing methods by evaluating their agreement to other biological features, such as sequence similarity, the presence of common Pfam domains, and core PPIs. Second, the information flow-based algorithm is employed to discover a set of proteins functionally associated with the protein in a query and their links efficiently. This algorithm reconstructs a functional association network of the query protein. The output network size can be flexibly determined by parameters. CONCLUSIONS: M-Finder provides a useful framework to investigate functional association patterns with any protein. This software will also allow users to perform further systematic analysis of a set of proteins for any specific function. It is available online at http://bionet.ecs.baylor.edu/mfinder BioMed Central 2013-11-07 /pmc/articles/PMC3909039/ /pubmed/24565382 http://dx.doi.org/10.1186/1477-5956-11-S1-S3 Text en Copyright © 2013 Cho et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Cho, Young-Rae Mina, Marco Lu, Yanxin Kwon, Nayoung Guzzi, Pietro H M-Finder: Uncovering functionally associated proteins from interactome data integrated with GO annotations |
title | M-Finder: Uncovering functionally associated proteins from interactome data integrated with GO annotations |
title_full | M-Finder: Uncovering functionally associated proteins from interactome data integrated with GO annotations |
title_fullStr | M-Finder: Uncovering functionally associated proteins from interactome data integrated with GO annotations |
title_full_unstemmed | M-Finder: Uncovering functionally associated proteins from interactome data integrated with GO annotations |
title_short | M-Finder: Uncovering functionally associated proteins from interactome data integrated with GO annotations |
title_sort | m-finder: uncovering functionally associated proteins from interactome data integrated with go annotations |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3909039/ https://www.ncbi.nlm.nih.gov/pubmed/24565382 http://dx.doi.org/10.1186/1477-5956-11-S1-S3 |
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