Ann K. Daly

Timothy J. Mantle

The steady-state kinetics of the major form of ox kidney aldehyde reductase with d-glucuronic acid have been determined at pH7. Initial rate and product inhibition studies performed in both directions are consistent with a Di-Iso Ordered Bi Bi mechanism. The mechanism of inhibition by sodium valproate and benzoic acid is shown to involve flux through an alternative pathway.</jats:p

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Biochemical Journal

The kinetic mechanism of the major form of ox kidney aldehyde reductase with <scp>d</scp>-glucuronic acid

http://www.biochemj.org/content/ppbiochemj/205/2/381.full.pdf

The kinetic mechanism of the major form of ox kidney aldehyde reductase with d-glucuronic acid

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