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Prediction of allosteric druggable pockets of cyclin-dependent kinases.
Ning, Shangbo; Wang, Huiwen; Zeng, Chen; Zhao, Yunjie.
Afiliação
  • Ning S; Institute of Biophysics and Department of Physics, Central China Normal University, Wuhan, 430079, China.
  • Wang H; School of Physics and Engineering, Henan University of Science and Technology, Luoyang 471023, China.
  • Zeng C; Department of Physics, The George Washington University, Washington, DC 20052, USA.
  • Zhao Y; Institute of Biophysics and Department of Physics, Central China Normal University, Wuhan, 430079, China.
Brief Bioinform ; 23(4)2022 07 18.
Article em En | MEDLINE | ID: mdl-35830869
Cyclin-dependent kinase (Cdk) proteins play crucial roles in the cell cycle progression and are thus attractive drug targets for therapy against such aberrant cell cycle processes as cancer. Since most of the available Cdk inhibitors target the highly conserved catalytic ATP pocket and their lack of specificity often lead to side effects, it is imperative to identify and characterize less conserved non-catalytic pockets capable of interfering with the kinase activity allosterically. However, a systematic analysis of these allosteric druggable pockets is still in its infancy. Here, we summarize the existing Cdk pockets and their selectivity. Then, we outline a network-based pocket prediction approach (NetPocket) and illustrate its utility for systematically identifying the allosteric druggable pockets with case studies. Finally, we discuss potential future directions and their challenges.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Prognostic_studies / Risk_factors_studies Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Prognostic_studies / Risk_factors_studies Idioma: En Ano de publicação: 2022 Tipo de documento: Article