Interaction of the high-affinity inhibitor tetrahydro-dUMP with the allosteric enzyme deoxycytidylate aminohydrolase.

Abstract:

:Tetrahydro-dUMP, an analog of the putative transition state in aminohydrolysis of deoxycytidine monophosphate (dCMP) inhibits the allosteric enzyme deoxycytidylate aminohydrolase with high affinity. The inhibition is reversible, and its kinetics is consistent with the analog binding at the substrate site only to one and the same conformation that binds the substrate dCMP. Such kinetics is what would be expected for a transition state analog interacting in an allosteric "K system."

journal_name

Arch Biochem Biophys

authors

Nucci R,Febbraio F,Piccialli G,de Napoli L,Vaccaro C,Rossi M,Whitehead EP

doi

10.1006/abbi.1994.1138

subject

Has Abstract

pub_date

1994-04-01 00:00:00

pages

49-53

issue

1

eissn

0003-9861

issn

1096-0384

pii

S0003986184711386

journal_volume

310

pub_type

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