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EC Number General Information Commentary Reference
Show all pathways known for 5.3.2.6Display the word mapDisplay the reaction diagram Show all sequences 5.3.2.6metabolism in the homoprotocatechuate pathway elaborated by Escherichia coli C ketonization of 5-(carboxymethyl)-2-hydroxymuconate by 5-(carboxymethyl)-2-hydroxymuconate isomerase generates the alpha,beta-unsaturated ketone, which undergoes decarboxylation and further processing to intermediates in the Krebs cycle -, 719634
Show all pathways known for 5.3.2.6Display the word mapDisplay the reaction diagram Show all sequences 5.3.2.6metabolism the enzyme is involved in the degradation of 4-hydroxybenzoate via the protocatechuate 2,3-cleavage pathway, overview 704310
Show all pathways known for 5.3.2.6Display the word mapDisplay the reaction diagram Show all sequences 5.3.2.6metabolism the enzyme is part of a degradative pathway that converts various aromatic hydrocarbons to intermediates in the Krebs cycle -, 718830
Show all pathways known for 5.3.2.6Display the word mapDisplay the reaction diagram Show all sequences 5.3.2.6more immediate nonenzymatic conversion of 2-oxo-3-hexenedioate to 2-hydroxy-3-trans-hexenedioate with NaBH4. Rate constants for the nonenzymatic phosphate-catalyzed ketonization of 2-hydroxymuconate, overview -, 719633
Show all pathways known for 5.3.2.6Display the word mapDisplay the reaction diagram Show all sequences 5.3.2.6more structure-function relationship and kinetic analysis, detailed overview 718840
Show all pathways known for 5.3.2.6Display the word mapDisplay the reaction diagram Show all sequences 5.3.2.6more structure-function relationship, spectroscopic NMR analysis, detailed overview. Three arginine residues, Arg11, Arg39, and Arg61, are localized in the active site of 4-oxalocrotonate tautomerase. Importance of Arg11 in properly orienting the dicarboxylate substrate by interacting with the charged 6-carboxylate group. Arg39 interacts with the 1-carboxylate and the 2-keto group of the substrate to promote carbonyl polarization and catalysis, while Pro-1 transfers protons from C-3 to C-5. Arg61 does not play a significant role in either substrate binding or catalysis -, 718830
Show all pathways known for 5.3.2.6Display the word mapDisplay the reaction diagram Show all sequences 5.3.2.6more the fully functional enzyme requires both subunits, active site structure and function of hh4-OT, overview. Three type II sites are formed at the other end of the heterodimeric unit interface around betaPro-1. As with the type I sites, two of the type II active site sides are composed of loops, but these loops are contributed from different subunits, that is, the alphaA'beta2' loop in the beta-subunit and the beta1alphaA loop in the alpha-subunit. The third side of the type II active site is composed of the intramonomeric alpha-subunit beta2-beta3 loop instead of a 310 helix -, 718874
Show all pathways known for 5.3.2.6Display the word mapDisplay the reaction diagram Show all sequences 5.3.2.6physiological function 4-OT catalyzes the ketonization process of 2-oxo-4-hexenedioate to its conjugated isomer, 2-oxo-3-hexadienedioate, through the dienol intermediate 2-hydroxymuconate. This proton transfer process is an essential part of degradative metabolism pathway to convert various aromatic hydrocarbons into their corresponding intermediates in the Krebs cycle 720309
Show all pathways known for 5.3.2.6Display the word mapDisplay the reaction diagram Show all sequences 5.3.2.6physiological function 4-oxalocrotonate tautomerase is an extremely efficient catalyst apparently processing either isomer near the diffusion control limit of a small molecule and an enzyme -, 719633
Show all pathways known for 5.3.2.6Display the word mapDisplay the reaction diagram Show all sequences 5.3.2.6physiological function 4-oxalocrotonate tautomerase isozymes play prominent roles in the bacterial utilization of aromatic hydrocarbons as sole carbon sources -, 718874
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