BRENDA - Enzyme Database
show all sequences of 2.4.1.121

Enzymic synthesis of indole-3-acetyl-1-O-beta-D-glucose

Leznicki, A.J.; Bandurski, R.S.; Plant Physiol. 88, 1481-1485 (1988)

Data extracted from this reference:

Activating Compound
Activating Compound
Commentary
Organism
Structure
Calmodulin
stimulates
Zea mays
thiol compounds
stimulate
Zea mays
Inhibitors
Inhibitors
Commentary
Organism
Structure
2,4-dichlorophenoxy acetic acid
-
Zea mays
abscisic acid
weak
Zea mays
diphosphate
-
Zea mays
gibberellic acid
weak
Zea mays
indole-3-acetate glucan
-
Zea mays
indole-3-acetate-myo-inositol
-
Zea mays
kinetin
weak
Zea mays
naphthylphthalamic acid
-
Zea mays
phosphatidyl ethanolamine
-
Zea mays
zeatin
-
Zea mays
Metals/Ions
Metals/Ions
Commentary
Organism
Structure
Ca2+
stimulates
Zea mays
Molecular Weight [Da]
Molecular Weight [Da]
Molecular Weight Maximum [Da]
Commentary
Organism
52000
-
gel filtration
Zea mays
Organism
Organism
Primary Accession No. (UniProt)
Commentary
Textmining
Zea mays
-
-
-
Source Tissue
Source Tissue
Commentary
Organism
Textmining
embryo
-
Zea mays
-
endosperm
cultured
Zea mays
-
Substrates and Products (Substrate)
Substrates
Commentary Substrates
Literature (Substrates)
Organism
Products
Commentary (Products)
Literature (Products)
Organism (Products)
Reversibility
UDPglucose + indole-3-acetate
specific for UDPglucose
488523
Zea mays
UDP + indole-3-acetyl-beta-1-D-glucose
-
488523
Zea mays
r
UDPglucose + indole-3-acetate
equilibrium away from ester formation and towards formation of indole-3-acetate
488523
Zea mays
UDP + indole-3-acetyl-beta-1-D-glucose
-
488523
Zea mays
r
Activating Compound (protein specific)
Activating Compound
Commentary
Organism
Structure
Calmodulin
stimulates
Zea mays
thiol compounds
stimulate
Zea mays
Inhibitors (protein specific)
Inhibitors
Commentary
Organism
Structure
2,4-dichlorophenoxy acetic acid
-
Zea mays
abscisic acid
weak
Zea mays
diphosphate
-
Zea mays
gibberellic acid
weak
Zea mays
indole-3-acetate glucan
-
Zea mays
indole-3-acetate-myo-inositol
-
Zea mays
kinetin
weak
Zea mays
naphthylphthalamic acid
-
Zea mays
phosphatidyl ethanolamine
-
Zea mays
zeatin
-
Zea mays
Metals/Ions (protein specific)
Metals/Ions
Commentary
Organism
Structure
Ca2+
stimulates
Zea mays
Molecular Weight [Da] (protein specific)
Molecular Weight [Da]
Molecular Weight Maximum [Da]
Commentary
Organism
52000
-
gel filtration
Zea mays
Source Tissue (protein specific)
Source Tissue
Commentary
Organism
Textmining
embryo
-
Zea mays
-
endosperm
cultured
Zea mays
-
Substrates and Products (Substrate) (protein specific)
Substrates
Commentary Substrates
Literature (Substrates)
Organism
Products
Commentary (Products)
Literature (Products)
Organism (Products)
Reversibility
UDPglucose + indole-3-acetate
specific for UDPglucose
488523
Zea mays
UDP + indole-3-acetyl-beta-1-D-glucose
-
488523
Zea mays
r
UDPglucose + indole-3-acetate
equilibrium away from ester formation and towards formation of indole-3-acetate
488523
Zea mays
UDP + indole-3-acetyl-beta-1-D-glucose
-
488523
Zea mays
r
Other publictions for EC 2.4.1.121
No.
1st author
Pub Med
title
organims
journal
volume
pages
year
Activating Compound
Application
Cloned(Commentary)
Crystallization (Commentary)
Engineering
General Stability
Inhibitors
KM Value [mM]
Localization
Metals/Ions
Molecular Weight [Da]
Natural Substrates/ Products (Substrates)
Organic Solvent Stability
Organism
Oxidation Stability
Posttranslational Modification
Purification (Commentary)
Reaction
Renatured (Commentary)
Source Tissue
Specific Activity [micromol/min/mg]
Storage Stability
Substrates and Products (Substrate)
Subunits
Temperature Optimum [C]
Temperature Range [C]
Temperature Stability [C]
Turnover Number [1/s]
pH Optimum
pH Range
pH Stability
Cofactor
Ki Value [mM]
pI Value
IC50 Value
Activating Compound (protein specific)
Application (protein specific)
Cloned(Commentary) (protein specific)
Cofactor (protein specific)
Crystallization (Commentary) (protein specific)
Engineering (protein specific)
General Stability (protein specific)
IC50 Value (protein specific)
Inhibitors (protein specific)
Ki Value [mM] (protein specific)
KM Value [mM] (protein specific)
Localization (protein specific)
Metals/Ions (protein specific)
Molecular Weight [Da] (protein specific)
Natural Substrates/ Products (Substrates) (protein specific)
Organic Solvent Stability (protein specific)
Oxidation Stability (protein specific)
Posttranslational Modification (protein specific)
Purification (Commentary) (protein specific)
Renatured (Commentary) (protein specific)
Source Tissue (protein specific)
Specific Activity [micromol/min/mg] (protein specific)
Storage Stability (protein specific)
Substrates and Products (Substrate) (protein specific)
Subunits (protein specific)
Temperature Optimum [C] (protein specific)
Temperature Range [C] (protein specific)
Temperature Stability [C] (protein specific)
Turnover Number [1/s] (protein specific)
pH Optimum (protein specific)
pH Range (protein specific)
pH Stability (protein specific)
pI Value (protein specific)
Expression
General Information
General Information (protein specific)
Expression (protein specific)
KCat/KM [mM/s]
KCat/KM [mM/s] (protein specific)
736956
Ostrowski
Indole-3-acetic acid UDP-gluco ...
Pisum sativum
Phytochemistry
117
25-33
2015
1
-
-
-
-
-
3
4
-
1
-
1
-
5
-
-
1
-
-
2
4
-
5
-
1
-
-
4
1
-
-
-
3
-
-
1
-
-
-
-
-
-
-
3
3
4
-
1
-
1
-
-
-
1
-
2
4
-
5
-
1
-
-
4
1
-
-
-
-
3
3
-
4
4
659607
Jakubowska
The auxin conjugate 1-O-indole ...
Brassica napus, Pisum sativum
J. Exp. Bot.
55
791-801
2004
-
-
-
-
-
-
-
-
-
-
2
-
-
4
-
-
2
-
-
2
-
-
2
2
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
2
-
-
-
-
2
-
2
-
-
2
2
-
-
-
-
-
-
-
-
-
-
-
-
-
-
488525
Kowalczyk
-
1-Naphtalene acetic acid induc ...
Zea mays
Plant Growth Regul.
38
127-134
2002
-
-
-
-
-
-
-
-
-
-
-
1
-
1
-
-
-
-
-
3
-
-
3
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
1
-
-
-
-
-
3
-
-
3
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
488526
Jackson
Identification and biochemical ...
Arabidopsis sp.
J. Biol. Chem.
276
4350-4356
2001
-
-
-
-
-
-
1
5
-
3
-
-
-
1
-
-
1
-
-
-
-
-
2
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
1
-
5
-
3
-
-
-
-
-
1
-
-
-
-
2
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
488524
Kowalczyk
Enzymic synthesis of 1-O-(indo ...
Zea mays
Biochem. J.
279
509-514
1991
-
-
-
-
-
-
-
-
-
-
1
1
-
3
-
-
1
-
-
1
1
-
9
1
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
1
1
-
-
-
1
-
1
1
-
9
1
-
-
-
-
-
-
-
-
-
-
-
-
-
-
488521
Kowalczyk
Isomerization of 1-O-indol-3-y ...
Zea mays
Plant Physiol.
94
4-12
1990
-
-
-
-
-
-
-
-
-
-
-
1
-
3
-
-
-
-
-
1
-
-
2
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
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-
-
1
-
-
-
-
-
1
-
-
2
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
488522
Leznicki
Enzymic synthesis of indole-3- ...
Zea mays
Plant Physiol.
88
1474-1480
1988
-
-
-
-
-
3
1
-
-
-
1
1
-
3
-
-
1
-
-
2
1
1
2
-
-
-
-
-
1
1
-
-
-
-
-
-
-
-
-
-
-
3
-
1
-
-
-
-
1
1
-
-
-
1
-
2
1
1
2
-
-
-
-
-
1
1
-
-
-
-
-
-
-
-
488523
Leznicki
Enzymic synthesis of indole-3- ...
Zea mays
Plant Physiol.
88
1481-1485
1988
2
-
-
-
-
-
10
-
-
1
1
-
-
1
-
-
-
-
-
2
-
-
2
-
-
-
-
-
-
-
-
-
-
-
-
2
-
-
-
-
-
-
-
10
-
-
-
1
1
-
-
-
-
-
-
2
-
-
2
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
487444
Michalczuk
Enzymic synthesis of 1-O-indol ...
Zea mays
Biochem. J.
207
273-281
1982
-
-
-
-
-
-
-
2
-
-
-
-
-
2
-
-
-
-
-
1
1
-
2
-
-
-
-
-
1
-
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-
-
-
-
-
-
-
-
-
-
-
-
-
-
2
-
-
-
-
-
-
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-
-
1
1
-
2
-
-
-
-
-
1
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-
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-
-