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Literature summary extracted from

  • Khalil, E.M.; De Angelis, J.; Cole, P.A.
    Indoleamine analogs as probes of the substrate selectivity and catalytic mechanism of serotonin N-acetyltransferase (1998), J. Biol. Chem., 273, 30321-30327.
    View publication on PubMed

Inhibitors

EC Number Inhibitors Comment Organism Structure
2.3.1.87 alpha-trifluoromethyltryptamine modest, competitive Ovis aries

Organism

EC Number Organism UniProt Comment Textmining
2.3.1.87 Ovis aries
-
-
-

Reaction

EC Number Reaction Comment Organism Reaction ID
2.3.1.87 acetyl-CoA + a 2-arylethylamine = CoA + an N-acetyl-2-arylethylamine mechanism Ovis aries
a

Substrates and Products (Substrate)

EC Number Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
2.3.1.87 acetyl-CoA + 3-indolebutylamine 60-fold less efficiently than serotonin Ovis aries CoA + N-acetyl-(3-indol-3-yl-butyl)-amine
-
 ?
2.3.1.87 acetyl-CoA + 3-indolepropylamine 20-fold less efficiently than serotonin Ovis aries CoA + N-acetyl-(3-indol-3-yl-propyl)-amine
-
 ?
2.3.1.87 acetyl-CoA + alpha-methyltryptamine racemic, 9:1 stereoselectivity for R-enantiomer, less efficiently than serotonin Ovis aries CoA + N-acetyl-alpha-methyltryptamine
-
 ?
2.3.1.87 acetyl-CoA + Nomega-methyltryptamine less efficiently than serotonin Ovis aries CoA + ?
-
 ?