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AtPID: the overall hierarchical functional protein interaction network interface and analytic platform for Arabidopsis
Protein interactions are involved in important cellular functions and biological processes that are the fundamentals of all life activities. With improvements in experimental techniques and progress in research, the overall protein interaction network frameworks of several model organisms have been...
Autores principales: | , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3013798/ https://www.ncbi.nlm.nih.gov/pubmed/21036873 http://dx.doi.org/10.1093/nar/gkq959 |
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author | Li, Peng Zang, Weidong Li, Yuhua Xu, Feng Wang, Jigang Shi, Tieliu |
author_facet | Li, Peng Zang, Weidong Li, Yuhua Xu, Feng Wang, Jigang Shi, Tieliu |
author_sort | Li, Peng |
collection | PubMed |
description | Protein interactions are involved in important cellular functions and biological processes that are the fundamentals of all life activities. With improvements in experimental techniques and progress in research, the overall protein interaction network frameworks of several model organisms have been created through data collection and integration. However, most of the networks processed only show simple relationships without boundary, weight or direction, which do not truly reflect the biological reality. In vivo, different types of protein interactions, such as the assembly of protein complexes or phosphorylation, often have their specific functions and qualifications. Ignorance of these features will bring much bias to the network analysis and application. Therefore, we annotate the Arabidopsis proteins in the AtPID database with further information (e.g. functional annotation, subcellular localization, tissue-specific expression, phosphorylation information, SNP phenotype and mutant phenotype, etc.) and interaction qualifications (e.g. transcriptional regulation, complex assembly, functional collaboration, etc.) via further literature text mining and integration of other resources. Meanwhile, the related information is vividly displayed to users through a comprehensive and newly developed display and analytical tools. The system allows the construction of tissue-specific interaction networks with display of canonical pathways. The latest updated AtPID database is available at http://www.megabionet.org/atpid/. |
format | Text |
id | pubmed-3013798 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-30137982011-01-03 AtPID: the overall hierarchical functional protein interaction network interface and analytic platform for Arabidopsis Li, Peng Zang, Weidong Li, Yuhua Xu, Feng Wang, Jigang Shi, Tieliu Nucleic Acids Res Articles Protein interactions are involved in important cellular functions and biological processes that are the fundamentals of all life activities. With improvements in experimental techniques and progress in research, the overall protein interaction network frameworks of several model organisms have been created through data collection and integration. However, most of the networks processed only show simple relationships without boundary, weight or direction, which do not truly reflect the biological reality. In vivo, different types of protein interactions, such as the assembly of protein complexes or phosphorylation, often have their specific functions and qualifications. Ignorance of these features will bring much bias to the network analysis and application. Therefore, we annotate the Arabidopsis proteins in the AtPID database with further information (e.g. functional annotation, subcellular localization, tissue-specific expression, phosphorylation information, SNP phenotype and mutant phenotype, etc.) and interaction qualifications (e.g. transcriptional regulation, complex assembly, functional collaboration, etc.) via further literature text mining and integration of other resources. Meanwhile, the related information is vividly displayed to users through a comprehensive and newly developed display and analytical tools. The system allows the construction of tissue-specific interaction networks with display of canonical pathways. The latest updated AtPID database is available at http://www.megabionet.org/atpid/. Oxford University Press 2011-01 2010-10-29 /pmc/articles/PMC3013798/ /pubmed/21036873 http://dx.doi.org/10.1093/nar/gkq959 Text en © The Author(s) 2010. Published by Oxford University Press. http://creativecommons.org/licenses/by-nc/2.5 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/2.5), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Articles Li, Peng Zang, Weidong Li, Yuhua Xu, Feng Wang, Jigang Shi, Tieliu AtPID: the overall hierarchical functional protein interaction network interface and analytic platform for Arabidopsis |
title | AtPID: the overall hierarchical functional protein interaction network interface and analytic platform for Arabidopsis |
title_full | AtPID: the overall hierarchical functional protein interaction network interface and analytic platform for Arabidopsis |
title_fullStr | AtPID: the overall hierarchical functional protein interaction network interface and analytic platform for Arabidopsis |
title_full_unstemmed | AtPID: the overall hierarchical functional protein interaction network interface and analytic platform for Arabidopsis |
title_short | AtPID: the overall hierarchical functional protein interaction network interface and analytic platform for Arabidopsis |
title_sort | atpid: the overall hierarchical functional protein interaction network interface and analytic platform for arabidopsis |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3013798/ https://www.ncbi.nlm.nih.gov/pubmed/21036873 http://dx.doi.org/10.1093/nar/gkq959 |
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