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Bioorg Med Chem Lett ; 10(3): 231-4, 2000 Feb 07.
Article in English | MEDLINE | ID: mdl-10698442

ABSTRACT

(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.


Subject(s)
Cyclohexanecarboxylic Acids/metabolism , Cyclohexanones/metabolism , Hydro-Lyases/metabolism , Isoenzymes/metabolism , Magnetic Resonance Spectroscopy , Mass Spectrometry , Mycobacterium tuberculosis/enzymology , Stereoisomerism
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