Engelke J A, Hale J E, Suttie J W, Price P A
Department of Biochemistry, College of Agricultural and Life Sciences, University of Wisconsin-Madison 53706.
Biochim Biophys Acta. 1991 May 30;1078(1):31-4. doi: 10.1016/0167-4838(91)90088-h.
The ability of des-gamma-carboxy bone Gla protein (dBGP) and des-gamma-carboxy matrix Gla protein (dMGP) to act as substrates for the rat liver vitamin K-dependent carboxylase has been investigated. An amino-terminal 'propeptide' is present on the intracellular form of BGP and is thought to interact with a recognition site on the enzyme. dBGP, lacking this extension, is a poor, high apparent Km, carboxylase substrate, but is a much better substrate when free propeptide is added. MGP lacks an amino-terminal propeptide, but contains a a homologous region in the mature protein. dMGP is an excellent substrate for the carboxylase with a low apparent Km and its carboxylation is inhibited by free propeptide.
已对去γ-羧基骨钙素(dBGP)和去γ-羧基基质Gla蛋白(dMGP)作为大鼠肝脏维生素K依赖性羧化酶底物的能力进行了研究。BGP的细胞内形式存在一个氨基末端“前肽”,据认为它与该酶上的一个识别位点相互作用。缺乏这种延伸的dBGP是一种较差的、表观Km值高的羧化酶底物,但当添加游离前肽时,它是一种更好的底物。MGP缺乏氨基末端前肽,但在成熟蛋白中含有一个同源区域。dMGP是羧化酶的优良底物,表观Km值低,其羧化作用受到游离前肽的抑制。