EC Number   |
General Information  |
Reference |
|---|
    5.3.2.6 | evolution |
4-oxalocrotonate tautomerase is a member of the tautomerase superfamily |
720309 |
| 5.3.2.6 | evolution |
mechanism and the evolution of 4-oxalocrotonate tautomerase, and 5-(carboxymethyl)-2-hydroxymuconate isomerase, EC 5.3.3.10, and their respective pathways, overview |
-, 719634 |
| 5.3.2.6 | evolution |
mechanism and the evolution of 4-oxalocrotonate tautomerase, EC 5.3.2.6, and 5-(carboxymethyl)-2-hydroxymuconate isomerase and their respective pathways, overview |
-, 719634 |
| 5.3.2.6 | evolution |
the enzyme is a member of the tautomerase superfamily |
-, 718874 |
| 5.3.2.6 | malfunction |
covalent modification of Pro-1 by 3-bromopropiolate inactivates YwhB, implicating Pro-1 as a critical catalytic residue in the conversion of phenylenolpyruvate to phenylpyruvate |
718847 |
| 5.3.2.6 | malfunction |
introduction of polar residues into the active site produces significant decreases in kcat and Km |
-, 718844 |
| 5.3.2.6 | malfunction |
modification by 3-bromopyruvate of three active sites per hexamer abolishes essentially all activity of the hexamer, spectrocopic and sequence analysis of labeled peptides, overview |
-, 718826 |
| 5.3.2.6 | metabolism |
4-oxalocrotonate tautomerase is an essential enzyme in the degradative metabolism pathway occurring in the Krebs cycle |
720309 |
| 5.3.2.6 | metabolism |
4-oxalocrotonate tautomerase is part of a set of inducible enzymes that converts aromatic hydrocarbons to intermediates in the Krebs cycle |
-, 719636 |
| 5.3.2.6 | metabolism |
in the catechol meta-fission pathway elaborated by Pseudomonas putida mt-2 ketonization of 2-hydroxymuconate by 4-oxalocrotonate tautomerase generates the alpha,beta-unsaturated ketone 2-oxo-3-(E)-hexenedioate, which undergoes decarboxylation and further processing to intermediates in the Krebs cycle |
-, 719634 |
