Prospects for pharmacological targeting of pseudokinases

被引:0
|
作者
Jennifer E. Kung
Natalia Jura
机构
[1] University of California,Cardiovascular Research Institute
[2] San Francisco,Department of Cellular and Molecular Pharmacology
[3] University of California,undefined
[4] San Francisco,undefined
来源
Nature Reviews Drug Discovery | 2019年 / 18卷
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摘要
Pseudokinases are members of the protein kinase superfamily but signal primarily through noncatalytic mechanisms. Many pseudokinases contribute to the pathologies of human diseases, yet they remain largely unexplored as drug targets owing to challenges associated with modulation of their biological functions. Our understanding of the structure and physiological roles of pseudokinases has improved substantially over the past decade, revealing intriguing similarities between pseudokinases and their catalytically active counterparts. Pseudokinases often adopt conformations that are analogous to those seen in catalytically active kinases and, in some cases, can also bind metal cations and/or nucleotides. Several clinically approved kinase inhibitors have been shown to influence the noncatalytic functions of active kinases, providing hope that similar properties in pseudokinases could be pharmacologically regulated. In this Review, we discuss known roles of pseudokinases in disease, their unique structural features and the progress that has been made towards developing pseudokinase-directed therapeutics.
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页码:501 / 526
页数:25
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