Jarabak R, Westley J
Department of Biochemistry and Molecular Biology, University of Chicago, Illinois 60637.
J Biochem Toxicol. 1991 Spring;6(1):65-70. doi: 10.1002/jbt.2570060109.
The results of kinetic experiments measuring the effects of a variety of ligands on the sulfur-cyanolysis reaction catalyzed by serum albumin point to the conclusion that the active site for cyanolysis is on subdomain 3-AB. Relationships among the inhibition by short-chain fatty acids, the activation by p-nitrophenyl acetate, and the influence of bilirubin and L-tryptophan on these effects indicate that the cyanolysis active site and the known primary binding site for indoles are both near, but on opposite sides of, tyrosine-409 of bovine albumin (tyrosine-411 of human albumin).
动力学实验测定了多种配体对血清白蛋白催化的硫氰解反应的影响,结果表明氰解的活性位点位于亚结构域3-AB上。短链脂肪酸的抑制作用、对硝基苯乙酸的激活作用以及胆红素和L-色氨酸对这些作用的影响之间的关系表明,氰解活性位点和已知的吲哚主要结合位点都靠近牛白蛋白的酪氨酸-409(人白蛋白的酪氨酸-411),但位于其两侧。