激酶
生物
结合位点
计算生物学
c-Raf公司
G蛋白偶联受体激酶
蛋白激酶A
细胞生物学
遗传学
细胞周期蛋白依赖激酶2
信号转导
G蛋白偶联受体
作者
Georgi K. Kanev,Chris de Graaf,Iwan J. P. de Esch,Rob Leurs,Thomas Würdinger,Bart A. Westerman,Albert J. Kooistra
标识
DOI:10.1016/j.tips.2019.09.002
摘要
Kinases are attractive anticancer targets due to their central role in the growth, survival, and therapy resistance of tumor cells. This review explores the two primary kinase classes, the eukaryotic protein kinases (ePKs) and the atypical protein kinases (aPKs), and provides a structure-centered comparison of their sequences, structures, hydrophobic spines, mutation and SNP hotspots, and inhibitor interaction patterns. Despite the limited sequence similarity between these two classes, atypical kinases commonly share the archetypical kinase fold but lack conserved eukaryotic kinase motifs and possess altered hydrophobic spines. Furthermore, atypical kinase inhibitors explore only a limited number of binding modes both inside and outside the orthosteric binding site. The distribution of genetic variations in both classes shows multiple ways they can interfere with kinase inhibitor binding. This multilayered review provides a research framework bridging the eukaryotic and atypical kinase classes.
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