| EC Number | Natural Substrates | Organism | Comment (Nat. Sub.) | Natural Products | Comment (Nat. Pro.) | Rev. | Reac. |
|---|---|---|---|---|---|---|---|
| 2.1.1.4 | S-adenosyl-L-methionine + N-acetylserotonin | Oryza sativa Japonica Group | - |
S-adenosyl-L-homocysteine + melatonin | - |
? |
| EC Number | Organism | UniProt | Comment | Textmining |
|---|---|---|---|---|
| 2.1.1.4 | Arabidopsis thaliana | Q9FK25 | cf. EC 2.1.1.68, EC 2.1.1.42 | - |
| 2.1.1.4 | Oryza sativa Japonica Group | Q6EPG8 | - |
- |
| 2.1.1.42 | Arabidopsis thaliana | Q9FK25 | cf. EC 2.1.1.68, Ec 2.1.1.4 | - |
| 2.1.1.68 | Arabidopsis thaliana | Q9FK25 | cf. EC 2.1.1.4, Ec 2.1.1.42 | - |
| EC Number | Substrates | Comment Substrates | Organism | Products | Comment (Products) | Rev. | Reac. |
|---|---|---|---|---|---|---|---|
| 2.1.1.4 | S-adenosyl-L-methionine + N-acetylserotonin | - |
Oryza sativa Japonica Group | S-adenosyl-L-homocysteine + melatonin | - |
? |
| EC Number | Synonyms | Comment | Organism |
|---|---|---|---|
| 2.1.1.4 | ASMT1 | - |
Oryza sativa Japonica Group |
| 2.1.1.4 | At5g54160 | - |
Arabidopsis thaliana |
| 2.1.1.4 | N-acetylserotonin methyltransferase | - |
Oryza sativa Japonica Group |
| 2.1.1.42 | At5g54160 | - |
Arabidopsis thaliana |
| 2.1.1.68 | At5g54160 | - |
Arabidopsis thaliana |
| EC Number | Cofactor | Comment | Organism | Structure |
|---|---|---|---|---|
| 2.1.1.4 | S-adenosyl-L-methionine | - |
Oryza sativa Japonica Group |
| EC Number | General Information | Comment | Organism |
|---|---|---|---|
| 2.1.1.4 | evolution | caffeic acid O-methyltransferase likely evolved from N-acetylserotonin methyltransferase by gene duplication and subsequent divergence. Caffeic acid O-methyltransferase gained a significantly higher N-acetylserotonin methyltransferase activity to produce greater amounts of melatonin for immobile plants to acclimate to the land environments. The caffeic acid O-methyltransferase genes possess more conserved substrate-binding sites at the amino acid level and more open protein conformation compared to N-acetylserotonin methyltransferase genes | Arabidopsis thaliana |
| 2.1.1.42 | evolution | caffeic acid O-methyltransferase likely evolved from N-acetylserotonin methyltransferase by gene duplication and subsequent divergence. Caffeic acid O-methyltransferase gained a significantly higher N-acetylserotonin methyltransferase activity to produce greater amounts of melatonin for immobile plants to acclimate to the land environments. The caffeic acid O-methyltransferase genes possess more conserved substrate-binding sites at the amino acid level and more open protein conformation compared to N-acetylserotonin methyltransferase genes | Arabidopsis thaliana |
| 2.1.1.68 | evolution | caffeic acid O-methyltransferase likely evolved from N-acetylserotonin methyltransferase by gene duplication and subsequent divergence. Caffeic acid O-methyltransferase gained a significantly higher N-acetylserotonin methyltransferase activity to produce greater amounts of melatonin for immobile plants to acclimate to the land environments. The caffeic acid O-methyltransferase genes possess more conserved substrate-binding sites at the amino acid level and more open protein conformation compared to N-acetylserotonin methyltransferase genes | Arabidopsis thaliana |