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Strategies for Engineering and Rewiring Kinase Regulation.
McCormick, James W; Pincus, David; Resnekov, Orna; Reynolds, Kimberly A.
  • McCormick JW; The Green Center for Systems Biology, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA; Department of Biophysics, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA.
  • Pincus D; Department of Molecular Genetics and Cell Biology, University of Chicago, Chicago, IL 60637, USA; Center for Physics of Evolving Systems, University of Chicago, Chicago, IL 60637, USA.
  • Resnekov O; Currently unaffiliated independent scientist.
  • Reynolds KA; The Green Center for Systems Biology, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA; Department of Biophysics, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA. Electronic address: kimberly.reynolds@utsouthwestern.edu.
Trends Biochem Sci ; 45(3): 259-271, 2020 03.
Article en En | MEDLINE | ID: mdl-31866305
ABSTRACT
Eukaryotic protein kinases (EPKs) catalyze the transfer of a phosphate group onto another protein in response to appropriate regulatory cues. In doing so, they provide a primary means for cellular information transfer. Consequently, EPKs play crucial roles in cell differentiation and cell-cycle progression, and kinase dysregulation is associated with numerous disease phenotypes including cancer. Nonnative cues for synthetically regulating kinases are thus much sought after, both for dissecting cell signaling pathways and for pharmaceutical development. In recent years advances in protein engineering and sequence analysis have led to new approaches for manipulating kinase activity, localization, and in some instances specificity. These tools have revealed fundamental principles of intracellular signaling and suggest paths forward for the design of therapeutic allosteric kinase regulators.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Proteínas Quinasas / Ingeniería de Proteínas / Neoplasias Límite: Humans Idioma: En Año: 2020 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Proteínas Quinasas / Ingeniería de Proteínas / Neoplasias Límite: Humans Idioma: En Año: 2020 Tipo del documento: Article