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Mutationmapper: A Tool to Aid the Mapping of Protein Mutation Data

There has been a rapid increase in the amount of mutational data due to, amongst other things, an increase in single nucleotide polymorphism (SNP) data and the use of site-directed mutagenesis as a tool to help dissect out functional properties of proteins. Many manually curated databases have been...

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Autores principales: Vohra, Shabana, Biggin, Philip C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3739722/
https://www.ncbi.nlm.nih.gov/pubmed/23951226
http://dx.doi.org/10.1371/journal.pone.0071711
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author Vohra, Shabana
Biggin, Philip C.
author_facet Vohra, Shabana
Biggin, Philip C.
author_sort Vohra, Shabana
collection PubMed
description There has been a rapid increase in the amount of mutational data due to, amongst other things, an increase in single nucleotide polymorphism (SNP) data and the use of site-directed mutagenesis as a tool to help dissect out functional properties of proteins. Many manually curated databases have been developed to index point mutations but they are not sustainable with the ever-increasing volume of scientific literature. There have been considerable efforts in the automatic extraction of mutation specific information from raw text involving use of various text-mining approaches. However, one of the key problems is to link these mutations with its associated protein and to present this data in such a way that researchers can immediately contextualize it within a structurally related family of proteins. To aid this process, we have developed an application called MutationMapper. Point mutations are extracted from abstracts and are validated against protein sequences in Uniprot as far as possible. Our methodology differs in a fundamental way from the usual text-mining approach. Rather than start with abstracts, we start with protein sequences, which facilitates greatly the process of validating a potential point mutation identified in an abstract. The results are displayed as mutations mapped on to the protein sequence or a multiple sequence alignment. The latter enables one to readily pick up mutations performed at equivalent positions in related proteins. We demonstrate the use of MutationMapper against several examples including a single sequence and multiple sequence alignments. The application is available as a web-service at http://mutationmapper.bioch.ox.ac.uk.
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spelling pubmed-37397222013-08-15 Mutationmapper: A Tool to Aid the Mapping of Protein Mutation Data Vohra, Shabana Biggin, Philip C. PLoS One Research Article There has been a rapid increase in the amount of mutational data due to, amongst other things, an increase in single nucleotide polymorphism (SNP) data and the use of site-directed mutagenesis as a tool to help dissect out functional properties of proteins. Many manually curated databases have been developed to index point mutations but they are not sustainable with the ever-increasing volume of scientific literature. There have been considerable efforts in the automatic extraction of mutation specific information from raw text involving use of various text-mining approaches. However, one of the key problems is to link these mutations with its associated protein and to present this data in such a way that researchers can immediately contextualize it within a structurally related family of proteins. To aid this process, we have developed an application called MutationMapper. Point mutations are extracted from abstracts and are validated against protein sequences in Uniprot as far as possible. Our methodology differs in a fundamental way from the usual text-mining approach. Rather than start with abstracts, we start with protein sequences, which facilitates greatly the process of validating a potential point mutation identified in an abstract. The results are displayed as mutations mapped on to the protein sequence or a multiple sequence alignment. The latter enables one to readily pick up mutations performed at equivalent positions in related proteins. We demonstrate the use of MutationMapper against several examples including a single sequence and multiple sequence alignments. The application is available as a web-service at http://mutationmapper.bioch.ox.ac.uk. Public Library of Science 2013-08-09 /pmc/articles/PMC3739722/ /pubmed/23951226 http://dx.doi.org/10.1371/journal.pone.0071711 Text en © 2013 Vohra, Biggin http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Vohra, Shabana
Biggin, Philip C.
Mutationmapper: A Tool to Aid the Mapping of Protein Mutation Data
title Mutationmapper: A Tool to Aid the Mapping of Protein Mutation Data
title_full Mutationmapper: A Tool to Aid the Mapping of Protein Mutation Data
title_fullStr Mutationmapper: A Tool to Aid the Mapping of Protein Mutation Data
title_full_unstemmed Mutationmapper: A Tool to Aid the Mapping of Protein Mutation Data
title_short Mutationmapper: A Tool to Aid the Mapping of Protein Mutation Data
title_sort mutationmapper: a tool to aid the mapping of protein mutation data
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3739722/
https://www.ncbi.nlm.nih.gov/pubmed/23951226
http://dx.doi.org/10.1371/journal.pone.0071711
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