Taylor S S, Knighton D R, Zheng J, Sowadski J M, Gibbs C S, Zoller M J
Department of Chemistry, University of California, San Diego, La Jolla 92093-0654.
Trends Biochem Sci. 1993 Mar;18(3):84-9. doi: 10.1016/0968-0004(93)80001-r.
The crystal structure of the catalytic subunit of cAMP-dependent protein kinase, complexed with ATP and a 20-residue inhibitor peptide, is reviewed and correlated with chemical and genetic data. The striking convergence of the structure with the biochemistry and genetics provides for the first time a molecular basis for understanding how this enzyme functions, as well as an explanation for the highly conserved residues that are scattered throughout the molecule. Because these residues probably serve a common role in all eukaryotic protein kinases, this first protein kinase structure serves as a general template for the entire family of enzymes.
本文综述了与ATP及一个20个残基的抑制肽结合的环磷酸腺苷依赖性蛋白激酶催化亚基的晶体结构,并将其与化学和遗传学数据相关联。该结构与生物化学及遗传学惊人地趋同,首次为理解这种酶的作用方式提供了分子基础,同时也解释了遍布整个分子的高度保守残基。由于这些残基可能在所有真核蛋白激酶中发挥共同作用,因此首个蛋白激酶结构可作为整个酶家族的通用模板。