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TRIP Database: a manually curated database of protein–protein interactions for mammalian TRP channels

Transient receptor potential (TRP) channels are a superfamily of Ca(2+)-permeable cation channels that translate cellular stimuli into electrochemical signals. Aberrant activity of TRP channels has been implicated in a variety of human diseases, such as neurological disorders, cardiovascular disease...

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Autores principales: Shin, Young-Cheul, Shin, Soo-Yong, So, Insuk, Kwon, Dongseop, Jeon, Ju-Hong
Formato: Texto
Lenguaje:English
Publicado: Oxford University Press 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3013757/
https://www.ncbi.nlm.nih.gov/pubmed/20851834
http://dx.doi.org/10.1093/nar/gkq814
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author Shin, Young-Cheul
Shin, Soo-Yong
So, Insuk
Kwon, Dongseop
Jeon, Ju-Hong
author_facet Shin, Young-Cheul
Shin, Soo-Yong
So, Insuk
Kwon, Dongseop
Jeon, Ju-Hong
author_sort Shin, Young-Cheul
collection PubMed
description Transient receptor potential (TRP) channels are a superfamily of Ca(2+)-permeable cation channels that translate cellular stimuli into electrochemical signals. Aberrant activity of TRP channels has been implicated in a variety of human diseases, such as neurological disorders, cardiovascular disease and cancer. To facilitate the understanding of the molecular network by which TRP channels are associated with biological and disease processes, we have developed the TRIP (TRansient receptor potential channel-Interacting Protein) Database (http://www.trpchannel.org), a manually curated database that aims to offer comprehensive information on protein–protein interactions (PPIs) of mammalian TRP channels. The TRIP Database was created by systematically curating 277 peer-reviewed literature; the current version documents 490 PPI pairs, 28 TRP channels and 297 cellular proteins. The TRIP Database provides a detailed summary of PPI data that fit into four categories: screening, validation, characterization and functional consequence. Users can find in-depth information specified in the literature on relevant analytical methods and experimental resources, such as gene constructs and cell/tissue types. The TRIP Database has user-friendly web interfaces with helpful features, including a search engine, an interaction map and a function for cross-referencing useful external databases. Our TRIP Database will provide a valuable tool to assist in understanding the molecular regulatory network of TRP channels.
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spelling pubmed-30137572011-01-03 TRIP Database: a manually curated database of protein–protein interactions for mammalian TRP channels Shin, Young-Cheul Shin, Soo-Yong So, Insuk Kwon, Dongseop Jeon, Ju-Hong Nucleic Acids Res Articles Transient receptor potential (TRP) channels are a superfamily of Ca(2+)-permeable cation channels that translate cellular stimuli into electrochemical signals. Aberrant activity of TRP channels has been implicated in a variety of human diseases, such as neurological disorders, cardiovascular disease and cancer. To facilitate the understanding of the molecular network by which TRP channels are associated with biological and disease processes, we have developed the TRIP (TRansient receptor potential channel-Interacting Protein) Database (http://www.trpchannel.org), a manually curated database that aims to offer comprehensive information on protein–protein interactions (PPIs) of mammalian TRP channels. The TRIP Database was created by systematically curating 277 peer-reviewed literature; the current version documents 490 PPI pairs, 28 TRP channels and 297 cellular proteins. The TRIP Database provides a detailed summary of PPI data that fit into four categories: screening, validation, characterization and functional consequence. Users can find in-depth information specified in the literature on relevant analytical methods and experimental resources, such as gene constructs and cell/tissue types. The TRIP Database has user-friendly web interfaces with helpful features, including a search engine, an interaction map and a function for cross-referencing useful external databases. Our TRIP Database will provide a valuable tool to assist in understanding the molecular regulatory network of TRP channels. Oxford University Press 2011-01 2010-09-17 /pmc/articles/PMC3013757/ /pubmed/20851834 http://dx.doi.org/10.1093/nar/gkq814 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
Shin, Young-Cheul
Shin, Soo-Yong
So, Insuk
Kwon, Dongseop
Jeon, Ju-Hong
TRIP Database: a manually curated database of protein–protein interactions for mammalian TRP channels
title TRIP Database: a manually curated database of protein–protein interactions for mammalian TRP channels
title_full TRIP Database: a manually curated database of protein–protein interactions for mammalian TRP channels
title_fullStr TRIP Database: a manually curated database of protein–protein interactions for mammalian TRP channels
title_full_unstemmed TRIP Database: a manually curated database of protein–protein interactions for mammalian TRP channels
title_short TRIP Database: a manually curated database of protein–protein interactions for mammalian TRP channels
title_sort trip database: a manually curated database of protein–protein interactions for mammalian trp channels
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3013757/
https://www.ncbi.nlm.nih.gov/pubmed/20851834
http://dx.doi.org/10.1093/nar/gkq814
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