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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.
Afiliação
  • Allam I; Molécules thérapeutiques in silico (MTi), INSERM UMR-S973, University Paris Diderot, Paris 7, France.
  • Flatters D; Probability Statistique and Biology (PSB), LPMA laboratory, CNRS INSMI UMR 7599, University Pierre et Marie Curie, Paris 6, France.
  • Caumes G; Mathématiques Appliquées, MAP5 laboratory, CNRS UMR 8145, University Paris Descartes, Paris 5, France.
  • Regad L; Sorbonne Paris Cité, Paris, France.
  • Delos V; Molécules thérapeutiques in silico (MTi), INSERM UMR-S973, University Paris Diderot, Paris 7, France.
  • Nuel G; Sorbonne Paris Cité, Paris, France.
  • Camproux AC; Molécules thérapeutiques in silico (MTi), INSERM UMR-S973, University Paris Diderot, Paris 7, France.
PLoS One ; 13(7): e0198854, 2018.
Article em En | MEDLINE | ID: mdl-29975698
ABSTRACT
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.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Conformação Proteica / Proteínas / Modelos Moleculares / Sequência de Aminoácidos Idioma: En Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Conformação Proteica / Proteínas / Modelos Moleculares / Sequência de Aminoácidos Idioma: En Ano de publicação: 2018 Tipo de documento: Article