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TopFIND 2.0—linking protein termini with proteolytic processing and modifications altering protein function
Protein termini provide critical insights into the functional state of individual proteins. With recent advances in specific proteomics approaches to enrich for N- and C-terminomes, the global analysis of whole terminomes at a proteome-wide scale is now possible. Information on the actual N- and C-t...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3244998/ https://www.ncbi.nlm.nih.gov/pubmed/22102574 http://dx.doi.org/10.1093/nar/gkr1025 |
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author | Lange, Philipp F. Huesgen, Pitter F. Overall, Christopher M. |
author_facet | Lange, Philipp F. Huesgen, Pitter F. Overall, Christopher M. |
author_sort | Lange, Philipp F. |
collection | PubMed |
description | Protein termini provide critical insights into the functional state of individual proteins. With recent advances in specific proteomics approaches to enrich for N- and C-terminomes, the global analysis of whole terminomes at a proteome-wide scale is now possible. Information on the actual N- and C-termini of proteins in vivo and any post-translational modifications, including their generation by proteolytic processing, is rapidly accumulating. To access this information we present version 2.0 of TopFIND (http://clipserve.clip.ubc.ca/topfind), a knowledgebase for protein termini, terminus modifications and underlying proteolytic processing. Built on a protein-centric framework TopFIND covers five species: Homo sapiens, Mus musculus, Arabidopsis thaliana, Saccharomyces cerevisiae and Escherichia coli and incorporates information from curated community submissions, publications, UniProtKB and MEROPS. Emphasis is placed on the detailed description and classification of evidence supporting the reported identification of each cleavage site, terminus and modification. A suite of filters can be applied to select supporting evidence. A dynamic network representation of the relationship between proteases, their substrates and inhibitors as well as visualization of protease cleavage site specificities complements the information displayed. Hence, TopFIND supports in depth investigation of protein termini information to spark new hypotheses on protein function by correlating cleavage events and termini with protein domains and mutations. |
format | Online Article Text |
id | pubmed-3244998 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-32449982012-01-10 TopFIND 2.0—linking protein termini with proteolytic processing and modifications altering protein function Lange, Philipp F. Huesgen, Pitter F. Overall, Christopher M. Nucleic Acids Res Articles Protein termini provide critical insights into the functional state of individual proteins. With recent advances in specific proteomics approaches to enrich for N- and C-terminomes, the global analysis of whole terminomes at a proteome-wide scale is now possible. Information on the actual N- and C-termini of proteins in vivo and any post-translational modifications, including their generation by proteolytic processing, is rapidly accumulating. To access this information we present version 2.0 of TopFIND (http://clipserve.clip.ubc.ca/topfind), a knowledgebase for protein termini, terminus modifications and underlying proteolytic processing. Built on a protein-centric framework TopFIND covers five species: Homo sapiens, Mus musculus, Arabidopsis thaliana, Saccharomyces cerevisiae and Escherichia coli and incorporates information from curated community submissions, publications, UniProtKB and MEROPS. Emphasis is placed on the detailed description and classification of evidence supporting the reported identification of each cleavage site, terminus and modification. A suite of filters can be applied to select supporting evidence. A dynamic network representation of the relationship between proteases, their substrates and inhibitors as well as visualization of protease cleavage site specificities complements the information displayed. Hence, TopFIND supports in depth investigation of protein termini information to spark new hypotheses on protein function by correlating cleavage events and termini with protein domains and mutations. Oxford University Press 2012-01 2011-11-17 /pmc/articles/PMC3244998/ /pubmed/22102574 http://dx.doi.org/10.1093/nar/gkr1025 Text en © The Author(s) 2011. Published by Oxford University Press. http://creativecommons.org/licenses/by-nc/3.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Articles Lange, Philipp F. Huesgen, Pitter F. Overall, Christopher M. TopFIND 2.0—linking protein termini with proteolytic processing and modifications altering protein function |
title | TopFIND 2.0—linking protein termini with proteolytic processing and modifications altering protein function |
title_full | TopFIND 2.0—linking protein termini with proteolytic processing and modifications altering protein function |
title_fullStr | TopFIND 2.0—linking protein termini with proteolytic processing and modifications altering protein function |
title_full_unstemmed | TopFIND 2.0—linking protein termini with proteolytic processing and modifications altering protein function |
title_short | TopFIND 2.0—linking protein termini with proteolytic processing and modifications altering protein function |
title_sort | topfind 2.0—linking protein termini with proteolytic processing and modifications altering protein function |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3244998/ https://www.ncbi.nlm.nih.gov/pubmed/22102574 http://dx.doi.org/10.1093/nar/gkr1025 |
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