Scott J D
Vollum Institute for Advanced Biomedical Research L-474, Portland, OR 97201-3098.
Pharmacol Ther. 1991;50(1):123-45. doi: 10.1016/0163-7258(91)90075-w.
The actions of several hormones and neurotransmitters evoke signal transduction pathways which rapidly elevate the cytosolic concentrations of the intracellular messengers, cAMP and cGMP. The cyclic-nucleotide dependent protein kinases, cAMP-dependent protein kinase (PKA) and cGMP-dependent protein kinase (PKG), are the major intracellular receptors of cAMP and cGMP. These enzymes become active upon binding respective cyclic nucleotides and modulate a diverse array of biochemical events through the phosphorylation of specific substrate proteins. The focus of this review is to describe the progress made in understanding the structure and function of both PKA and PKG.
几种激素和神经递质的作用可引发信号转导途径,迅速提高细胞内信使环磷酸腺苷(cAMP)和环磷酸鸟苷(cGMP)的胞质浓度。环核苷酸依赖性蛋白激酶,即cAMP依赖性蛋白激酶(PKA)和cGMP依赖性蛋白激酶(PKG),是cAMP和cGMP的主要细胞内受体。这些酶在结合各自的环核苷酸后变得活跃,并通过特定底物蛋白的磷酸化来调节各种生化事件。本综述的重点是描述在理解PKA和PKG的结构与功能方面所取得的进展。