Parker E J, González Bello C, Coggins J R, Hawkins A R, Abell C
University Chemical Laboratory, Cambridge, UK.
Bioorg Med Chem Lett. 2000 Feb 7;10(3):231-4. doi: 10.1016/s0960-894x(99)00660-5.
(6R)- and (6S)-6-Fluoro-3-dehydroquinic acids are shown to be substrates for type I and type II dehydroquinases. Their differential reactivity provides insight into details of the reaction mechanism and enables a novel enzyme-substrate imine to be trapped on the type I enzyme.
(6R)-和(6S)-6-氟-3-脱氢奎尼酸被证明是I型和II型脱氢奎尼酸酶的底物。它们的不同反应性有助于深入了解反应机制的细节,并能捕获一种新型的酶-底物亚胺到I型酶上。