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Mu-8: visualizing differences between proteins and their families
BACKGROUND: A complete understanding of the relationship between the amino acid sequence and resulting protein function remains an open problem in the biophysical sciences. Current approaches often rely on diagnosing functionally relevant mutations by determining whether an amino acid frequently occ...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4155612/ https://www.ncbi.nlm.nih.gov/pubmed/25237392 http://dx.doi.org/10.1186/1753-6561-8-S2-S5 |
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author | Mercer, Johnathan D Pandian, Balaji Lex, Alexander Bonneel, Nicolas Pfister, Hanspeter |
author_facet | Mercer, Johnathan D Pandian, Balaji Lex, Alexander Bonneel, Nicolas Pfister, Hanspeter |
author_sort | Mercer, Johnathan D |
collection | PubMed |
description | BACKGROUND: A complete understanding of the relationship between the amino acid sequence and resulting protein function remains an open problem in the biophysical sciences. Current approaches often rely on diagnosing functionally relevant mutations by determining whether an amino acid frequently occurs at a specific position within the protein family. However, these methods do not account for the biophysical properties and the 3D structure of the protein. We have developed an interactive visualization technique, Mu-8, that provides researchers with a holistic view of the differences of a selected protein with respect to a family of homologous proteins. Mu-8 helps to identify areas of the protein that exhibit: (1) significantly different bio-chemical characteristics, (2) relative conservation in the family, and (3) proximity to other regions that have suspect behavior in the folded protein. METHODS: Our approach quantifies and communicates the difference between a reference protein and its family based on amino acid indices or principal components of amino acid index classes, while accounting for conservation, proximity amongst residues, and overall 3D structure. RESULTS: We demonstrate Mu-8 in a case study with data provided by the 2013 BioVis contest. When comparing the sequence of a dysfunctional protein to its functional family, Mu-8 reveals several candidate regions that may cause function to break down. |
format | Online Article Text |
id | pubmed-4155612 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-41556122014-09-18 Mu-8: visualizing differences between proteins and their families Mercer, Johnathan D Pandian, Balaji Lex, Alexander Bonneel, Nicolas Pfister, Hanspeter BMC Proc Research BACKGROUND: A complete understanding of the relationship between the amino acid sequence and resulting protein function remains an open problem in the biophysical sciences. Current approaches often rely on diagnosing functionally relevant mutations by determining whether an amino acid frequently occurs at a specific position within the protein family. However, these methods do not account for the biophysical properties and the 3D structure of the protein. We have developed an interactive visualization technique, Mu-8, that provides researchers with a holistic view of the differences of a selected protein with respect to a family of homologous proteins. Mu-8 helps to identify areas of the protein that exhibit: (1) significantly different bio-chemical characteristics, (2) relative conservation in the family, and (3) proximity to other regions that have suspect behavior in the folded protein. METHODS: Our approach quantifies and communicates the difference between a reference protein and its family based on amino acid indices or principal components of amino acid index classes, while accounting for conservation, proximity amongst residues, and overall 3D structure. RESULTS: We demonstrate Mu-8 in a case study with data provided by the 2013 BioVis contest. When comparing the sequence of a dysfunctional protein to its functional family, Mu-8 reveals several candidate regions that may cause function to break down. BioMed Central 2014-08-28 /pmc/articles/PMC4155612/ /pubmed/25237392 http://dx.doi.org/10.1186/1753-6561-8-S2-S5 Text en Copyright © 2014 Mercer et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/4.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Mercer, Johnathan D Pandian, Balaji Lex, Alexander Bonneel, Nicolas Pfister, Hanspeter Mu-8: visualizing differences between proteins and their families |
title | Mu-8: visualizing differences between proteins and their families |
title_full | Mu-8: visualizing differences between proteins and their families |
title_fullStr | Mu-8: visualizing differences between proteins and their families |
title_full_unstemmed | Mu-8: visualizing differences between proteins and their families |
title_short | Mu-8: visualizing differences between proteins and their families |
title_sort | mu-8: visualizing differences between proteins and their families |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4155612/ https://www.ncbi.nlm.nih.gov/pubmed/25237392 http://dx.doi.org/10.1186/1753-6561-8-S2-S5 |
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