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Literature summary extracted from

  • Kinne, M.; Ullrich, R.; Hammel, K.E.; Scheibner, K.; Hofrichter, M.
    Regioselective preparation of (R)-2-(4-hydroxyphenoxy)propionic acid with a fungal peroxygenase (2008), Tetrahedron Lett., 49, 5950-5953.
No PubMed abstract available

Localization

EC Number Localization Comment Organism GeneOntology No. Textmining
1.11.2.1 extracellular
-
 Cyclocybe aegerita
-
-

Organism

EC Number Organism UniProt Comment Textmining
1.11.2.1 Cyclocybe aegerita
-
-
-

Substrates and Products (Substrate)

EC Number Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
1.11.2.1 2-phenoxypropionic acid + H2O2 the enzyme hydroxylates 2-phenoxypropionic acid regioselectively at the para-position Cyclocybe aegerita (R)-2-(4-hydroxyphenoxy)propionic acid + H2O the reaction yields the R-isomer of 2-(4-hydroxyphenoxy)propionic acid with an enantiomeric excess of 60% ?

Cofactor

EC Number Cofactor Comment Organism Structure
1.11.2.1 heme
-
 Cyclocybe aegerita