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FuzPred: a web server for the sequence-based prediction of the context-dependent binding modes of proteins.
Hatos, Andras; Teixeira, João M C; Barrera-Vilarmau, Susana; Horvath, Attila; Tosatto, Silvio C E; Vendruscolo, Michele; Fuxreiter, Monika.
Afiliação
  • Hatos A; Department of Biomedical Sciences, University of Padova, Padova, Italy.
  • Teixeira JMC; Department of Oncology, Lausanne University Hospital, Lausanne 1011, Switzerland.
  • Barrera-Vilarmau S; Department of Computational Biology, University of Lausanne, Lausanne 1015, Switzerland.
  • Horvath A; Swiss Institute of Bioinformatics, Lausanne1015, Switzerland.
  • Tosatto SCE; Swiss Cancer Center Leman, Lausanne 1011, Switzerland.
  • Vendruscolo M; Department of Biomedical Sciences, University of Padova, Padova, Italy.
  • Fuxreiter M; Department of Biomedical Sciences, University of Padova, Padova, Italy.
Nucleic Acids Res ; 51(W1): W198-W206, 2023 07 05.
Article em En | MEDLINE | ID: mdl-36987846
ABSTRACT
Proteins form complex interactions in the cellular environment to carry out their functions. They exhibit a wide range of binding modes depending on the cellular conditions, which result in a variety of ordered or disordered assemblies. To help rationalise the binding behavior of proteins, the FuzPred server predicts their sequence-based binding modes without specifying their binding partners. The binding mode defines whether the bound state is formed through a disorder-to-order transition resulting in a well-defined conformation, or through a disorder-to-disorder transition where the binding partners remain conformationally heterogeneous. To account for the context-dependent nature of the binding modes, the FuzPred method also estimates the multiplicity of binding modes, the likelihood of sampling multiple binding modes. Protein regions with a high multiplicity of binding modes may serve as regulatory sites or hot-spots for structural transitions in the assembly. To facilitate the interpretation of the predictions, protein regions with different interaction behaviors can be visualised on protein structures generated by AlphaFold. The FuzPred web server (https//fuzpred.bio.unipd.it) thus offers insights into the structural and dynamical changes of proteins upon interactions and contributes to development of structure-function relationships under a variety of cellular conditions.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Computadores / Proteínas Tipo de estudo: Prognostic_studies / Risk_factors_studies Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Computadores / Proteínas Tipo de estudo: Prognostic_studies / Risk_factors_studies Idioma: En Ano de publicação: 2023 Tipo de documento: Article