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Literature summary extracted from

  • Leznicki, A.J.; Bandurski, R.S.
    Enzymic synthesis of indole-3-acetyl-1-O-beta-D-glucose (1988), Plant Physiol., 88, 1481-1485.
    View publication on PubMedView publication on EuropePMC

Activating Compound

EC Number Activating Compound Comment Organism Structure
2.4.1.121 Calmodulin stimulates Zea mays
2.4.1.121 thiol compounds stimulate Zea mays

Inhibitors

EC Number Inhibitors Comment Organism Structure
2.4.1.121 2,4-dichlorophenoxy acetic acid
-
 Zea mays
2.4.1.121 abscisic acid weak Zea mays
2.4.1.121 diphosphate
-
 Zea mays
2.4.1.121 gibberellic acid weak Zea mays
2.4.1.121 indole-3-acetate glucan
-
 Zea mays
2.4.1.121 indole-3-acetate-myo-inositol
-
 Zea mays
2.4.1.121 kinetin weak Zea mays
2.4.1.121 naphthylphthalamic acid
-
 Zea mays
2.4.1.121 phosphatidyl ethanolamine
-
 Zea mays
2.4.1.121 zeatin
-
 Zea mays

Metals/Ions

EC Number Metals/Ions Comment Organism Structure
2.4.1.121 Ca2+ stimulates Zea mays

Molecular Weight [Da]

EC Number Molecular Weight [Da] Molecular Weight Maximum [Da] Comment Organism
2.4.1.121 52000
-
 gel filtration Zea mays

Organism

EC Number Organism UniProt Comment Textmining
2.4.1.121 Zea mays
-
-
-

Source Tissue

EC Number Source Tissue Comment Organism Textmining
2.4.1.121 embryo
-
 Zea mays
-
2.4.1.121 endosperm cultured Zea mays
-

Substrates and Products (Substrate)

EC Number Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
2.4.1.121 UDPglucose + indole-3-acetate specific for UDPglucose Zea mays UDP + indole-3-acetyl-beta-1-D-glucose
-
 r
2.4.1.121 UDPglucose + indole-3-acetate equilibrium away from ester formation and towards formation of indole-3-acetate Zea mays UDP + indole-3-acetyl-beta-1-D-glucose
-
 r