The mechanism of orotidine 5′-monophosphate decarboxylase:: Catalysis by destabilization of the substrate
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Feng, WY
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San Francisco State Univ, Dept Chem & Biochem, San Francisco, CA 94132 USASan Francisco State Univ, Dept Chem & Biochem, San Francisco, CA 94132 USA
Feng, WY
[1
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Austin, TJ
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San Francisco State Univ, Dept Chem & Biochem, San Francisco, CA 94132 USASan Francisco State Univ, Dept Chem & Biochem, San Francisco, CA 94132 USA
Austin, TJ
[1
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Chew, F
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San Francisco State Univ, Dept Chem & Biochem, San Francisco, CA 94132 USASan Francisco State Univ, Dept Chem & Biochem, San Francisco, CA 94132 USA
Chew, F
[1
]
Gronert, S
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San Francisco State Univ, Dept Chem & Biochem, San Francisco, CA 94132 USASan Francisco State Univ, Dept Chem & Biochem, San Francisco, CA 94132 USA
Gronert, S
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Wu, WM
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San Francisco State Univ, Dept Chem & Biochem, San Francisco, CA 94132 USASan Francisco State Univ, Dept Chem & Biochem, San Francisco, CA 94132 USA
Wu, WM
[1
]
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[1] San Francisco State Univ, Dept Chem & Biochem, San Francisco, CA 94132 USA
The mechanism of orotidine 5'-monophosphate decarboxylase (OMP decarboxylase, ODCase) was studied using the decarboxylation of orotic acid analogues as a model system, The rate of decarboxylation of 1,3-dimethylorotic acid and its analogues as well as the stability of their corresponding carbanion intermediates was determined. The results have shown that the stability of the carbanion intermediate is not a critical factor in the rate of decarboxylation. On the other hand, the reaction rate is largely dependent on the equilibrium constant for the formation of a zwitterion. Based on these results, we have proposed a new mechanism in which ODCase catalyzes the decarboxylation of OMP by binding the substrate in a zwitterionic form and providing a destabilizing environment for the carboxylate group of OMP.