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Literature summary for 1.5.3.7 extracted from

  • Zabriskie, T.M.; Kelly, W.L.; Liang, X.
    Stereochemical course of the oxidation of L-pipecolic acid by the flavoenzyme L-pipecolate oxidase (1997), J. Am. Chem. Soc., 119, 6446-6447.
No PubMed abstract available

KM Value [mM]

KM Value [mM] KM Value Maximum [mM] Substrate Comment Organism Structure
6
-
L-pipecolic acid
-
Macaca mulatta

Natural Substrates/ Products (Substrates)

Natural Substrates Organism Comment (Nat. Sub.) Natural Products Comment (Nat. Pro.) Rev. Reac.
L-pipecolate + O2 Macaca mulatta
-
2,3,4,5-tetrahydropyridine-2-carboxylate + H2O2 the product reacts with water to form 2-aminoadipate 6-semialdehyde ?

Organism

Organism UniProt Comment Textmining
Macaca mulatta
-
-
-

Substrates and Products (Substrate)

Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
L-pipecolate + O2
-
Macaca mulatta 2,3,4,5-tetrahydropyridine-2-carboxylate + H2O2 the product reacts with water to form 2-aminoadipate 6-semialdehyde ?
L-pipecolate + O2 the pro-6(R)-hydrogen of pipecolic acid is removed stereospecifically Macaca mulatta 2,3,4,5-tetrahydropyridine-2-carboxylate + H2O2 the product reacts with water to form 2-aminoadipate 6-semialdehyde ?