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Discover protein sequence signatures from protein-protein interaction data
BACKGROUND: The development of high-throughput technologies such as yeast two-hybrid systems and mass spectrometry technologies has made it possible to generate large protein-protein interaction (PPI) datasets. Mining these datasets for underlying biological knowledge has, however, remained a challe...
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/PMC1310605/ https://www.ncbi.nlm.nih.gov/pubmed/16305745 http://dx.doi.org/10.1186/1471-2105-6-277 |
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author | Fang, Jianwen Haasl, Ryan J Dong, Yinghua Lushington, Gerald H |
author_facet | Fang, Jianwen Haasl, Ryan J Dong, Yinghua Lushington, Gerald H |
author_sort | Fang, Jianwen |
collection | PubMed |
description | BACKGROUND: The development of high-throughput technologies such as yeast two-hybrid systems and mass spectrometry technologies has made it possible to generate large protein-protein interaction (PPI) datasets. Mining these datasets for underlying biological knowledge has, however, remained a challenge. RESULTS: A total of 3108 sequence signatures were found, each of which was shared by a set of guest proteins interacting with one of 944 host proteins in Saccharomyces cerevisiae genome. Approximately 94% of these sequence signatures matched entries in InterPro member databases. We identified 84 distinct sequence signatures from the remaining 172 unknown signatures. The signature sharing information was then applied in predicting sub-cellular localization of yeast proteins and the novel signatures were used in identifying possible interacting sites. CONCLUSION: We reported a method of PPI data mining that facilitated the discovery of novel sequence signatures using a large PPI dataset from S. cerevisiae genome as input. The fact that 94% of discovered signatures were known validated the ability of the approach to identify large numbers of signatures from PPI data. The significance of these discovered signatures was demonstrated by their application in predicting sub-cellular localizations and identifying potential interaction binding sites of yeast proteins. |
format | Text |
id | pubmed-1310605 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2005 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-13106052005-12-10 Discover protein sequence signatures from protein-protein interaction data Fang, Jianwen Haasl, Ryan J Dong, Yinghua Lushington, Gerald H BMC Bioinformatics Research Article BACKGROUND: The development of high-throughput technologies such as yeast two-hybrid systems and mass spectrometry technologies has made it possible to generate large protein-protein interaction (PPI) datasets. Mining these datasets for underlying biological knowledge has, however, remained a challenge. RESULTS: A total of 3108 sequence signatures were found, each of which was shared by a set of guest proteins interacting with one of 944 host proteins in Saccharomyces cerevisiae genome. Approximately 94% of these sequence signatures matched entries in InterPro member databases. We identified 84 distinct sequence signatures from the remaining 172 unknown signatures. The signature sharing information was then applied in predicting sub-cellular localization of yeast proteins and the novel signatures were used in identifying possible interacting sites. CONCLUSION: We reported a method of PPI data mining that facilitated the discovery of novel sequence signatures using a large PPI dataset from S. cerevisiae genome as input. The fact that 94% of discovered signatures were known validated the ability of the approach to identify large numbers of signatures from PPI data. The significance of these discovered signatures was demonstrated by their application in predicting sub-cellular localizations and identifying potential interaction binding sites of yeast proteins. BioMed Central 2005-11-23 /pmc/articles/PMC1310605/ /pubmed/16305745 http://dx.doi.org/10.1186/1471-2105-6-277 Text en Copyright © 2005 Fang 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 Fang, Jianwen Haasl, Ryan J Dong, Yinghua Lushington, Gerald H Discover protein sequence signatures from protein-protein interaction data |
title | Discover protein sequence signatures from protein-protein interaction data |
title_full | Discover protein sequence signatures from protein-protein interaction data |
title_fullStr | Discover protein sequence signatures from protein-protein interaction data |
title_full_unstemmed | Discover protein sequence signatures from protein-protein interaction data |
title_short | Discover protein sequence signatures from protein-protein interaction data |
title_sort | discover protein sequence signatures from protein-protein interaction data |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1310605/ https://www.ncbi.nlm.nih.gov/pubmed/16305745 http://dx.doi.org/10.1186/1471-2105-6-277 |
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