Institut für Pharmazeutische Wissenschaften, Albert-Ludwigs-Universität Freiburg, Germany.
Angew Chem Int Ed Engl. 2012 Mar 12;51(11):2643-6. doi: 10.1002/anie.201107695. Epub 2012 Feb 3.
In reduced circumstances: tetrahydroxynaphthalene reductase shows a broad substrate range including alternate phenolic compounds and cyclic ketones. Structural modeling reveals major enzyme-substrate interactions; C-terminal truncation of the enzyme causes an altered substrate preference, in accordance with stabilization of the substrate by the C-terminal carboxylate. This effect allows the identification of a homologous enzyme.
四氢萘醌还原酶表现出广泛的底物范围,包括替代酚类化合物和环状酮类。结构建模揭示了主要的酶-底物相互作用;酶的 C 端截断导致底物偏好的改变,这与 C 端羧酸盐稳定底物的作用一致。这种效应允许鉴定同源酶。