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Identification and Analysis of Natural Building Blocks for Evolution-Guided Fragment-Based Protein Design.
Ferruz, Noelia; Lobos, Francisco; Lemm, Dominik; Toledo-Patino, Saacnicteh; Farías-Rico, José Arcadio; Schmidt, Steffen; Höcker, Birte.
Afiliação
  • Ferruz N; Department of Biochemistry, University of Bayreuth, Bayreuth, Germany.
  • Lobos F; Department of Biochemistry, University of Bayreuth, Bayreuth, Germany; Max Planck Institute for Developmental Biology, Tübingen, Germany.
  • Lemm D; Department of Biochemistry, University of Bayreuth, Bayreuth, Germany.
  • Toledo-Patino S; Department of Biochemistry, University of Bayreuth, Bayreuth, Germany; Max Planck Institute for Developmental Biology, Tübingen, Germany.
  • Farías-Rico JA; Max Planck Institute for Developmental Biology, Tübingen, Germany.
  • Schmidt S; Max Planck Institute for Developmental Biology, Tübingen, Germany; Computational Biochemistry, University of Bayreuth, Bayreuth, Germany. Electronic address: steffen.schmidt@uni-bayreuth.de.
  • Höcker B; Department of Biochemistry, University of Bayreuth, Bayreuth, Germany; Max Planck Institute for Developmental Biology, Tübingen, Germany. Electronic address: birte.hoecker@uni-bayreuth.de.
J Mol Biol ; 432(13): 3898-3914, 2020 06 12.
Article em En | MEDLINE | ID: mdl-32330481
Natural evolution has generated an impressively diverse protein universe via duplication and recombination from a set of protein fragments that served as building blocks. The application of these concepts to the design of new proteins using subdomain-sized fragments from different folds has proven to be experimentally successful. To better understand how evolution has shaped our protein universe, we performed an all-against-all comparison of protein domains representing all naturally existing folds and identified conserved homologous protein fragments. Overall, we found more than 1000 protein fragments of various lengths among different folds through similarity network analysis. These fragments are present in very different protein environments and represent versatile building blocks for protein design. These data are available in our web server called F(old P)uzzle (fuzzle.uni-bayreuth.de), which allows to individually filter the dataset and create customized networks for folds of interest. We believe that our results serve as an invaluable resource for structural and evolutionary biologists and as raw material for the design of custom-made proteins.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Proteínas / Dobramento de Proteína / Evolução Molecular Tipo de estudo: Diagnostic_studies Idioma: En Revista: J Mol Biol Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Alemanha

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Proteínas / Dobramento de Proteína / Evolução Molecular Tipo de estudo: Diagnostic_studies Idioma: En Revista: J Mol Biol Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Alemanha