Knaus U G, Bokoch G M
Department of Immunology, Scripps Research Institute, La Jolla, CA 92037, USA.
Int J Biochem Cell Biol. 1998 Aug;30(8):857-62. doi: 10.1016/s1357-2725(98)00059-4.
The p21-activated kinases (PAKs) are mammalian Rac/Cdc42-associated serine/threonine protein kinases. They contain diverse structural regulatory elements that allow them not only to participate as effectors in signaling processes initiated by activated GTPases but also in signal transduction events mediated by Src3 homology domains (SH3) or caspase-mediated proteolytic cleavage. The biological functions of PAK protein kinases result from the interplay of N- and C-terminal-mediated protein-protein interactions and signals derived from phosphorylation of downstream substrates. The potential regulation of microbial killing, stress responses, apoptosis, and cell motility by PAKs suggest it may be a therapeutically useful target in a number of disease states.
p21激活激酶(PAKs)是与哺乳动物Rac/Cdc42相关的丝氨酸/苏氨酸蛋白激酶。它们含有多种结构调节元件,这不仅使它们能够作为效应器参与由活化的GTP酶引发的信号传导过程,还能参与由Src3同源结构域(SH3)介导的信号转导事件或半胱天冬酶介导的蛋白水解切割。PAK蛋白激酶的生物学功能源于N端和C端介导的蛋白质-蛋白质相互作用以及下游底物磷酸化产生的信号之间的相互作用。PAKs对微生物杀伤、应激反应、细胞凋亡和细胞运动的潜在调节表明,它可能是多种疾病状态下具有治疗价值的靶点。