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Protein structural motifs in prediction and design.
Mackenzie, Craig O; Grigoryan, Gevorg.
Afiliação
  • Mackenzie CO; Institute for Quantitative Biomedical Sciences, Dartmouth College, Hanover, NH 03755, United States.
  • Grigoryan G; Institute for Quantitative Biomedical Sciences, Dartmouth College, Hanover, NH 03755, United States; Department of Computer Science, Dartmouth College, Hanover, NH 03755, United States. Electronic address: gevorg.grigoryan@dartmouth.edu.
Curr Opin Struct Biol ; 44: 161-167, 2017 06.
Article em En | MEDLINE | ID: mdl-28460216
ABSTRACT
The Protein Data Bank (PDB) has been an integral resource for shaping our fundamental understanding of protein structure and for the advancement of such applications as protein design and structure prediction. Over the years, information from the PDB has been used to generate models ranging from specific structural mechanisms to general statistical potentials. With accumulating structural data, it has become possible to mine for more complete and complex structural observations, deducing more accurate generalizations. Motif libraries, which capture recurring structural features along with their sequence preferences, have exposed modularity in the structural universe and found successful application in various problems of structural biology. Here we summarize recent achievements in this arena, focusing on subdomain level structural patterns and their applications to protein design and structure prediction, and suggest promising future directions as the structural database continues to grow.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Desenho de Fármacos / Proteínas / Biologia Computacional Tipo de estudo: Prognostic_studies / Risk_factors_studies Idioma: En Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Desenho de Fármacos / Proteínas / Biologia Computacional Tipo de estudo: Prognostic_studies / Risk_factors_studies Idioma: En Ano de publicação: 2017 Tipo de documento: Article