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1 via the intermediates 2-aminomuconate and 4-oxalocrotonate.
3 tive as a complex with the metal-dependent 4-oxalocrotonate decarboxylase (4-OD), the enzyme followin
4 zyme converted 2-aminomuconate directly to 4-oxalocrotonate, rather than 2-hydroxymuconate, which sug
5 al homology with two bacterial isomerases, 4-oxalocrotonate tautomerase (4-OT) and 5-(carboxymethyl)-
6 urally homologous to the bacterial enzymes 4-oxalocrotonate tautomerase (4-OT) and 5-carboxymethyl-2-
8 as potential inhibitors of three enzymes: 4-oxalocrotonate tautomerase (4-OT) and vinylpyruvate hydr
10 echanism for the reaction catalyzed by the 4-oxalocrotonate tautomerase (4-OT) enzyme has been studie
11 ns, SAR1376, a 62 amino acid member of the 4-oxalocrotonate tautomerase (4-OT) family, was pro-immuno
14 neral base catalyst Pro-1 (pK(a) = 6.4) in 4-oxalocrotonate tautomerase (4-OT) has been ascribed to b
15 ate profiles for the kinetic parameters of 4-oxalocrotonate tautomerase (4-OT) have been measured usi
21 sts of three major families represented by 4-oxalocrotonate tautomerase (4-OT), 5-(carboxymethyl)-2-h
24 terohexamer (molecular weight 47,547), and 4-oxalocrotonate tautomerase (4-OT), an (alpha)(6) homohex
25 exameric CaaD and the bacterial isomerase, 4-oxalocrotonate tautomerase (4-OT), thereby distinguishin
26 ant systems, including carbonic anhydrase, 4-oxalocrotonate tautomerase (4OT) analogue, and SecB, a c
27 le of polypeptide backbone interactions in 4-oxalocrotonate tautomerase (4OT) catalysis has been inve
30 used to study the quaternary structure of 4-oxalocrotonate tautomerase (EC 5.3.2; 4OT), and four ana
31 ucture and active site similar to those of 4-oxalocrotonate tautomerase and 5-carboxymethyl-2-hydroxy
32 similar to that of two microbial enzymes (4-oxalocrotonate tautomerase and 5-carboxymethyl-2-hydroxy
33 talytic general base, Pro-1, of the enzyme 4-oxalocrotonate tautomerase has been mutated to Gly, Ala,
34 9, Arg-61) are found at the active site of 4-oxalocrotonate tautomerase in the X-ray structure of the
35 is a more potent irreversible inhibitor of 4-oxalocrotonate tautomerase than is 2-OP suggest that Arg
37 TSF members may have evolved from a short 4-oxalocrotonate tautomerase-like ancestor followed by gen
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