Cloned (Comment) | Organism |
---|---|
expressed in Escherichia coli as glutathione S-transferase fusion protein | Oryza sativa |
Protein Variants | Comment | Organism |
---|---|---|
D168L | mutation abolishes activity (with quercetin as substrate) | Oryza sativa |
D194L | mutation abolishes activity (with quercetin as substrate) | Oryza sativa |
D209L | mutation abolishes activity (with quercetin as substrate) | Oryza sativa |
D234L | mutation abolishes activity (with quercetin as substrate) | Oryza sativa |
E112L | mutation results in 40% loss of activity (with quercetin as substrate) | Oryza sativa |
E69L | mutation results in 14% loss of activity (with quercetin as substrate) | Oryza sativa |
N195I | mutation abolishes activity (with quercetin as substrate) | Oryza sativa |
N235I | mutation abolishes activity (with quercetin as substrate) | Oryza sativa |
KM Value [mM] | KM Value Maximum [mM] | Substrate | Comment | Organism | Structure |
---|---|---|---|---|---|
0.036 | - |
tricetin | pH 7.5, 37°C | Oryza sativa | |
0.072 | - |
tricetin | pH 7.5, 37°C | Oryza sativa |
Metals/Ions | Comment | Organism | Structure |
---|---|---|---|
Co2+ | the enzyme is metal-dependent, Mg2+ is the best cation for catalytic activity, Co2+ shows 41% of the activity with Mg2+ (with quercetin as substrate) | Oryza sativa | |
Co2+ | the enzyme is metal-dependent, Mg2+ is the best cation for catalytic activity, Co2+ shows 82% of the activity with Mg2+ (with quercetin as substrate) | Oryza sativa | |
Mg2+ | the enzyme is metal-dependent, Mg2+ is the best cation for catalytic activity (with quercetin as substrate) | Oryza sativa | |
Mn2+ | the enzyme is metal-dependent, Mg2+ is the best cation for catalytic activity, Mn2+ shows 69% of the activity with Mg2+ (with quercetin as substrate) | Oryza sativa | |
Mn2+ | the enzyme is metal-dependent, Mg2+ is the best cation for catalytic activity, Mn2+ shows 74% of the activity with Mg2+ (with quercetin as substrate) | Oryza sativa |
Molecular Weight [Da] | Molecular Weight Maximum [Da] | Comment | Organism |
---|---|---|---|
30600 | - |
x * 30600, SDS-PAGE, glutathione S-transferase fusion protein | Oryza sativa |
31100 | - |
x * 31100, SDS-PAGE, glutathione S-transferase fusion protein | Oryza sativa |
Organism | UniProt | Comment | Textmining |
---|---|---|---|
Oryza sativa | - |
- |
- |
Oryza sativa | Q9XGP7 | - |
- |
Source Tissue | Comment | Organism | Textmining |
---|---|---|---|
root | - |
Oryza sativa | - |
stem | - |
Oryza sativa | - |
stem | expressed in stems only | Oryza sativa | - |
Substrates | Comment Substrates | Organism | Products | Comment (Products) | Rev. | Reac. |
---|---|---|---|---|---|---|
2 S-adenosyl-L-methionine + tricetin | the enzyme catalyzes the stepwise methylation of tricetin to its 3'-mono- and 3',5'-dimethyl ethers. In contrast with the wheat enzyme, tricetin dimethyl ether is not converted to its 3',4',5'-trimethylated ester derivatives. The enzyme also catalyzes the methylation of luteolin, myricetin (formation of the 3',5'-dimethyl ether of myricetin, EC 2.1.1.149) and caffeoyl-CoA. ROMT-15 exhibits similar Kcat/Km values for the four substrates. ROMT-15 can not utilize naringenin, apigenin, or kaempferol. The 2,3-double bond and the O-dihydroxyl group are both required for catalytic activity | Oryza sativa | 2 S-adenosyl-L-homocysteine + 3',5'-O-dimethyltricetin | - |
? | |
2 S-adenosyl-L-methionine + tricetin | the enzyme catalyzes the stepwise methylation of tricetin to its 3'-mono- and 3',5'-dimethyl ethers. In contrast with the wheat enzyme, tricetin dimethyl ether is not converted to its 3',4',5'-trimethylated ester derivatives. The enzyme also catalyzes the methylation of luteolin, myricetin (formation of the 3',5'-dimethyl ether of myricetin, EC 2.1.1.149) and caffeoyl-CoA. ROMT-17 prefers tricetin. ROMT-15 can not utilize naringenin, apigenin, or kaempferol. The 2,3-double bond and the O-dihydroxyl group are both required for catalytic activity | Oryza sativa | 2 S-adenosyl-L-homocysteine + 3',5'-O-dimethyltricetin | - |
? | |
S-adenosyl-L-methionine + 3'-O-methyltricetin | the enzyme catalyzes the stepwise methylation of tricetin to its 3'-mono- and 3',5'-dimethyl ethers. In contrast with the wheat enzyme, tricetin dimethyl ether is not converted to its 3',4',5'-trimethylated ester derivatives | Oryza sativa | S-adenosyl-L-homocysteine + 3',5'-O-dimethyltricetin | - |
? | |
S-adenosyl-L-methionine + tricetin | the enzyme catalyzes the stepwise methylation of tricetin to its 3'-mono- and 3',5'-dimethyl ethers. In contrast with the wheat enzyme, tricetin dimethyl ether is not converted to its 3',4',5'-trimethylated ester derivatives | Oryza sativa | S-adenosyl-L-homocysteine + 3'-O-methyltricetin | - |
? |
Subunits | Comment | Organism |
---|---|---|
? | x * 30600, SDS-PAGE, glutathione S-transferase fusion protein | Oryza sativa |
? | x * 31100, SDS-PAGE, glutathione S-transferase fusion protein | Oryza sativa |
Synonyms | Comment | Organism |
---|---|---|
ROMT-15 | - |
Oryza sativa |
ROMT-17 | - |
Oryza sativa |
Temperature Optimum [°C] | Temperature Optimum Maximum [°C] | Comment | Organism |
---|---|---|---|
37 | - |
assay at | Oryza sativa |
pH Optimum Minimum | pH Optimum Maximum | Comment | Organism |
---|---|---|---|
7.5 | - |
assay at | Oryza sativa |
Cofactor | Comment | Organism | Structure |
---|---|---|---|
S-adenosyl-L-methionine | - |
Oryza sativa |
kcat/KM Value [1/mMs-1] | kcat/KM Value Maximum [1/mMs-1] | Substrate | Comment | Organism | Structure |
---|---|---|---|---|---|
0.949 | - |
tricetin | pH 7.5, 37°C | Oryza sativa | |
2.83 | - |
tricetin | pH 7.5, 37°C | Oryza sativa |