Welburn Julie P I, Jeyaprakash A Arockia
Wellcome Trust Centre for Cell Biology, School of Biological Sciences, University of Edinburgh, Scotland, United Kingdom.
Front Cell Dev Biol. 2018 Feb 5;6:6. doi: 10.3389/fcell.2018.00006. eCollection 2018.
Protein kinases are major regulators of mitosis, with over 30% of the mitotic proteome phosphorylated on serines, threonines and tyrosines. The human genome encodes for 518 kinases that have a structurally conserved catalytic domain and includes about a dozen of cell division specific ones. Yet each kinase has unique structural features that allow their distinct substrate recognition and modes of regulation. These unique regulatory features determine their accurate spatio-temporal activation critical for correct progression through mitosis and are exploited for therapeutic purposes. In this review, we will discuss the principles of mitotic kinase activation and the structural determinants that underlie functional specificity.
蛋白激酶是有丝分裂的主要调节因子,超过30%的有丝分裂蛋白质组在丝氨酸、苏氨酸和酪氨酸上发生磷酸化。人类基因组编码518种激酶,它们具有结构保守的催化结构域,其中包括约12种细胞分裂特异性激酶。然而,每种激酶都有独特的结构特征,使其能够识别不同的底物并采用不同的调节方式。这些独特的调节特征决定了它们精确的时空激活,这对于有丝分裂的正确进行至关重要,并且被用于治疗目的。在这篇综述中,我们将讨论有丝分裂激酶激活的原理以及功能特异性背后的结构决定因素。