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Literature summary extracted from

  • Huppatz, J.L.; Casida, J.E.
    Acetohydroxyacid synthase inhibitors N-phthalyl-L-valine anilide and related compounds (1985), Z. Naturforsch. C, 40, 652-656 .
    View publication on PubMed

Inhibitors

EC Number Inhibitors Comment Organism Structure
2.2.1.6 L-valine 50% inhibition at 20 mM, crude enzyme preparation Zea mays
2.2.1.6 additional information no inhibition by N-phthalyl-L-leucine, N-phthalyl-L-norleucine, N-phthalyl-L-phenylglycine, N-phthalyl-L-norvaline, N-phthalyl-L-glycine, N-phthalyl-L-alanine, crude enzyme preparation Zea mays
2.2.1.6 N-phthalyl-L-isoleucine anilide 50% inhibition at 0.1 mM, crude enzyme preparation Zea mays
2.2.1.6 N-phthalyl-L-phenylalanine anilide 50% inhibition at 0.047 mM, crude enzyme preparation Zea mays
2.2.1.6 N-phthalyl-L-valine anilide 50% inhibition at 0.0023 mM, crude enzyme preparation Zea mays

Natural Substrates/ Products (Substrates)

EC Number Natural Substrates Organism Comment (Nat. Sub.) Natural Products Comment (Nat. Pro.) Rev. Reac.
2.2.1.6 2 pyruvate Zea mays
-
 2-acetolactate + CO2
-
 ?

Organism

EC Number Organism UniProt Comment Textmining
2.2.1.6 Zea mays K7TWQ8
-
-

Substrates and Products (Substrate)

EC Number Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
2.2.1.6 2 pyruvate
-
 Zea mays 2-acetolactate + CO2
-
 ?

Synonyms

EC Number Synonyms Comment Organism
2.2.1.6 acetohydroxyacid synthase
-
 Zea mays
2.2.1.6 AHAS
-
 Zea mays