IMP dehydrogenase (EC 1.1.1.205) (IMPDH) catalyzes the rate-limiting reaction
of de novo GTP biosynthesis, the NAD-dependent reduction of IMP into XMP [1].
Inhibition of IMP dehydrogenase activity results in the cessation of DNA
synthesis. As IMP dehydrogenase is associated with cell proliferation, it is a
possible target for cancer chemotherapy. Mammalian and bacterial IMPDHs are
tetramers of identical chains. There are two IMP dehydrogenase isozymes in
humans [2].
GMP reductase (EC 1.7.1.7) catalyzes the irreversible and NADPH-dependent
reductive deamination of GMP into IMP [3]. It converts nucleobase, nucleoside
and nucleotide derivatives of G to A nucleotides, and maintains intracellular
balance of A and G nucleotides.
IMP dehydrogenase and GMP reductase share many regions of sequence similarity.
One of these regions is centered on a cysteine residue thought [3] to be
involved in binding IMP. We have used this region as a signature pattern.
December 2004 / Pattern and text revised.
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