Structural Basis for Regulation of Phosphoinositide Kinases and Their Involvement in Human Disease

被引:201
作者
Burke, John E. [1 ]
机构
[1] Univ Victoria, Dept Biochem & Microbiol, Victoria, BC V8W 2Y2, Canada
基金
加拿大健康研究院; 加拿大自然科学与工程研究理事会;
关键词
PHOSPHATIDYLINOSITOL; 4-PHOSPHATE; 5-KINASE; SMALL-MOLECULE INHIBITOR; I PI3 KINASE; G-BETA-GAMMA; LIPID KINASE; CRYSTAL-STRUCTURE; PLASMA-MEMBRANE; 3-KINASE P110-ALPHA; PROTEIN-KINASE; HIGH-FREQUENCY;
D O I
10.1016/j.molcel.2018.08.005
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Lipid phosphoinositides play fundamental roles in virtually all pathways that control a cell's decision to grow, move, divide, and die. Because of this, kinases that phosphorylate phosphoinositide lipids are critically involved in myriad essential functions including growth, development, and membrane trafficking. The misregulation of phosphoinositide kinases is critical in human diseases, including cancer, primary immunodeficiencies, and developmental disorders. Phosphoinositide kinases also play a role in mediating bacterial and viral infections for many potent human pathogens. Furthermore, inhibitors of parasite phosphoinositide kinases are in development as therapies for both malaria and cryptosporidiosis. Therefore, understanding how phosphoinositide kinases are regulated has implications for the treatment of many devastating human diseases. Recent structures of phosphoinositide kinases have revealed unique molecular insight into their regulation. This review will summarize our current molecular knowledge on phosphoinositide kinase regulation, and how this information is being used to generate novel small molecule inhibitors as potential therapeutics.
引用
收藏
页码:653 / 673
页数:21
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