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SAFlex: A structural alphabet extension to integrate protein structural flexibility and missing data information
In this paper, we describe SAFlex (Structural Alphabet Flexibility), an extension of an existing structural alphabet (HMM-SA), to better explore increasing protein three dimensional structure information by encoding conformations of proteins in case of missing residues or uncertainties. An SA aims t...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6033379/ https://www.ncbi.nlm.nih.gov/pubmed/29975698 http://dx.doi.org/10.1371/journal.pone.0198854 |
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author | Allam, Ikram Flatters, Delphine Caumes, Géraldine Regad, Leslie Delos, Vincent Nuel, Gregory Camproux, Anne-Claude |
author_facet | Allam, Ikram Flatters, Delphine Caumes, Géraldine Regad, Leslie Delos, Vincent Nuel, Gregory Camproux, Anne-Claude |
author_sort | Allam, Ikram |
collection | PubMed |
description | In this paper, we describe SAFlex (Structural Alphabet Flexibility), an extension of an existing structural alphabet (HMM-SA), to better explore increasing protein three dimensional structure information by encoding conformations of proteins in case of missing residues or uncertainties. An SA aims to reduce three dimensional conformations of proteins as well as their analysis and comparison complexity by simplifying any conformation in a series of structural letters. Our methodology presents several novelties. Firstly, it can account for the encoding uncertainty by providing a wide range of encoding options: the maximum a posteriori, the marginal posterior distribution, and the effective number of letters at each given position. Secondly, our new algorithm deals with the missing data in the protein structure files (concerning more than 75% of the proteins from the Protein Data Bank) in a rigorous probabilistic framework. Thirdly, SAFlex is able to encode and to build a consensus encoding from different replicates of a single protein such as several homomer chains. This allows localizing structural differences between different chains and detecting structural variability, which is essential for protein flexibility identification. These improvements are illustrated on different proteins, such as the crystal structure of an eukaryotic small heat shock protein. They are promising to explore increasing protein redundancy data and obtain useful quantification of their flexibility. |
format | Online Article Text |
id | pubmed-6033379 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-60333792018-07-19 SAFlex: A structural alphabet extension to integrate protein structural flexibility and missing data information Allam, Ikram Flatters, Delphine Caumes, Géraldine Regad, Leslie Delos, Vincent Nuel, Gregory Camproux, Anne-Claude PLoS One Research Article In this paper, we describe SAFlex (Structural Alphabet Flexibility), an extension of an existing structural alphabet (HMM-SA), to better explore increasing protein three dimensional structure information by encoding conformations of proteins in case of missing residues or uncertainties. An SA aims to reduce three dimensional conformations of proteins as well as their analysis and comparison complexity by simplifying any conformation in a series of structural letters. Our methodology presents several novelties. Firstly, it can account for the encoding uncertainty by providing a wide range of encoding options: the maximum a posteriori, the marginal posterior distribution, and the effective number of letters at each given position. Secondly, our new algorithm deals with the missing data in the protein structure files (concerning more than 75% of the proteins from the Protein Data Bank) in a rigorous probabilistic framework. Thirdly, SAFlex is able to encode and to build a consensus encoding from different replicates of a single protein such as several homomer chains. This allows localizing structural differences between different chains and detecting structural variability, which is essential for protein flexibility identification. These improvements are illustrated on different proteins, such as the crystal structure of an eukaryotic small heat shock protein. They are promising to explore increasing protein redundancy data and obtain useful quantification of their flexibility. Public Library of Science 2018-07-05 /pmc/articles/PMC6033379/ /pubmed/29975698 http://dx.doi.org/10.1371/journal.pone.0198854 Text en © 2018 Allam et al 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 author and source are credited. |
spellingShingle | Research Article Allam, Ikram Flatters, Delphine Caumes, Géraldine Regad, Leslie Delos, Vincent Nuel, Gregory Camproux, Anne-Claude SAFlex: A structural alphabet extension to integrate protein structural flexibility and missing data information |
title | SAFlex: A structural alphabet extension to integrate protein structural flexibility and missing data information |
title_full | SAFlex: A structural alphabet extension to integrate protein structural flexibility and missing data information |
title_fullStr | SAFlex: A structural alphabet extension to integrate protein structural flexibility and missing data information |
title_full_unstemmed | SAFlex: A structural alphabet extension to integrate protein structural flexibility and missing data information |
title_short | SAFlex: A structural alphabet extension to integrate protein structural flexibility and missing data information |
title_sort | saflex: a structural alphabet extension to integrate protein structural flexibility and missing data information |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6033379/ https://www.ncbi.nlm.nih.gov/pubmed/29975698 http://dx.doi.org/10.1371/journal.pone.0198854 |
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