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HomoMINT: an inferred human network based on orthology mapping of protein interactions discovered in model organisms
BACKGROUND: The application of high throughput approaches to the identification of protein interactions has offered for the first time a glimpse of the global interactome of some model organisms. Until now, however, such genome-wide approaches have not been applied to the human proteome. RESULTS: In...
Autores principales: | , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2005
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1866386/ https://www.ncbi.nlm.nih.gov/pubmed/16351748 http://dx.doi.org/10.1186/1471-2105-6-S4-S21 |
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author | Persico, Maria Ceol, Arnaud Gavrila, Caius Hoffmann, Robert Florio, Arnaldo Cesareni, Gianni |
author_facet | Persico, Maria Ceol, Arnaud Gavrila, Caius Hoffmann, Robert Florio, Arnaldo Cesareni, Gianni |
author_sort | Persico, Maria |
collection | PubMed |
description | BACKGROUND: The application of high throughput approaches to the identification of protein interactions has offered for the first time a glimpse of the global interactome of some model organisms. Until now, however, such genome-wide approaches have not been applied to the human proteome. RESULTS: In order to fill this gap we have assembled an inferred human protein interaction network where interactions discovered in model organisms are mapped onto the corresponding human orthologs. In addition to a stringent assignment to orthology classes based on the InParanoid algorithm, we have implemented a string matching algorithm to filter out orthology assignments of proteins whose global domain organization is not conserved. Finally, we have assessed the accuracy of our own, and related, inferred networks by benchmarking them against i) an assembled experimental interactome, ii) a network derived by mining of the scientific literature and iii) by measuring the enrichment of interacting protein pairs sharing common Gene Ontology annotation. CONCLUSION: The resulting networks are named HomoMINT and HomoMINT_filtered, the latter being based on the orthology table filtered by the domain architecture matching algorithm. They contains 9749 and 5203 interactions respectively and can be analyzed and viewed in the context of the experimentally verified interactions between human proteins stored in the MINT database. HomoMINT is constantly updated to take into account the growing information in the MINT database. |
format | Text |
id | pubmed-1866386 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2005 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-18663862007-05-11 HomoMINT: an inferred human network based on orthology mapping of protein interactions discovered in model organisms Persico, Maria Ceol, Arnaud Gavrila, Caius Hoffmann, Robert Florio, Arnaldo Cesareni, Gianni BMC Bioinformatics Research Article BACKGROUND: The application of high throughput approaches to the identification of protein interactions has offered for the first time a glimpse of the global interactome of some model organisms. Until now, however, such genome-wide approaches have not been applied to the human proteome. RESULTS: In order to fill this gap we have assembled an inferred human protein interaction network where interactions discovered in model organisms are mapped onto the corresponding human orthologs. In addition to a stringent assignment to orthology classes based on the InParanoid algorithm, we have implemented a string matching algorithm to filter out orthology assignments of proteins whose global domain organization is not conserved. Finally, we have assessed the accuracy of our own, and related, inferred networks by benchmarking them against i) an assembled experimental interactome, ii) a network derived by mining of the scientific literature and iii) by measuring the enrichment of interacting protein pairs sharing common Gene Ontology annotation. CONCLUSION: The resulting networks are named HomoMINT and HomoMINT_filtered, the latter being based on the orthology table filtered by the domain architecture matching algorithm. They contains 9749 and 5203 interactions respectively and can be analyzed and viewed in the context of the experimentally verified interactions between human proteins stored in the MINT database. HomoMINT is constantly updated to take into account the growing information in the MINT database. BioMed Central 2005-12-01 /pmc/articles/PMC1866386/ /pubmed/16351748 http://dx.doi.org/10.1186/1471-2105-6-S4-S21 Text en Copyright © 2005 Persico 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. |
spellingShingle | Research Article Persico, Maria Ceol, Arnaud Gavrila, Caius Hoffmann, Robert Florio, Arnaldo Cesareni, Gianni HomoMINT: an inferred human network based on orthology mapping of protein interactions discovered in model organisms |
title | HomoMINT: an inferred human network based on orthology mapping of protein interactions discovered in model organisms |
title_full | HomoMINT: an inferred human network based on orthology mapping of protein interactions discovered in model organisms |
title_fullStr | HomoMINT: an inferred human network based on orthology mapping of protein interactions discovered in model organisms |
title_full_unstemmed | HomoMINT: an inferred human network based on orthology mapping of protein interactions discovered in model organisms |
title_short | HomoMINT: an inferred human network based on orthology mapping of protein interactions discovered in model organisms |
title_sort | homomint: an inferred human network based on orthology mapping of protein interactions discovered in model organisms |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1866386/ https://www.ncbi.nlm.nih.gov/pubmed/16351748 http://dx.doi.org/10.1186/1471-2105-6-S4-S21 |
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