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Literature summary extracted from

  • Thatcher, D.R.; Cain, R.B.
    The kinetic properties of 3-carboxy-cis-cis-muconate cycloisomerase (1972), Biochem. J., 127, 33P-34P.
    View publication on PubMedView publication on EuropePMC

Inhibitors

EC Number Inhibitors Comment Organism Structure
5.5.1.2 Dicarboxylic acids saturated dicarboxylic acids with the exception of oxalate, are less inhibitory as the molecular weight increases. Compounds with two cis-carboxyl groups are much more inhibitory than the corresponding trans-isomers Aspergillus niger
5.5.1.2 Tricarboxylic acids
-
Aspergillus niger

KM Value [mM]

EC Number KM Value [mM] KM Value Maximum [mM] Substrate Comment Organism Structure
5.5.1.2 0.052
-
2-carboxy-2,5-dihydro-5-oxofuran-2-acetate
-
Aspergillus niger

Organism

EC Number Organism UniProt Comment Textmining
5.5.1.2 Aspergillus niger
-
-
-

Substrates and Products (Substrate)

EC Number Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
5.5.1.2 2-Carboxy-2,5-dihydro-5-oxofuran-2-acetate i.e. beta-carboxy-cis,cis-muconate Aspergillus niger cis-Butadiene-1,2,4-tricarboxylate i.e. gamma-carboxymuconolactone ?