EC Number   |
Substrates |
Organism |
Products |
Reversibility |
|---|
   1.13.11.17 | 5-bromoindole + O2 |
- |
Tecoma stans |
5-bromo-2-formylaminobenzaldehyde |
- |
? |
| 1.13.11.17 | 5-bromoindole + O2 |
- |
Jasminum grandiflorum |
5-bromo-2-formylaminobenzaldehyde |
- |
? |
| 1.13.11.17 | 5-bromoindole + O2 |
15% of the activity with indole |
Tecoma stans |
5-bromo-2-formylaminobenzaldehyde |
- |
? |
| 1.13.11.17 | 5-hydroxyindole + O2 |
- |
Tecoma stans |
2-formylamino-5-hydroxybenzaldehyde |
- |
? |
| 1.13.11.17 | 5-hydroxyindole + O2 |
- |
Jasminum grandiflorum |
2-formylamino-5-hydroxybenzaldehyde |
- |
? |
| 1.13.11.17 | 5-hydroxyindole + O2 |
20% of the activity with indole |
Tecoma stans |
2-formylamino-5-hydroxybenzaldehyde |
- |
? |
| 1.13.11.17 | 5-methylindole + O2 |
- |
Tecoma stans |
2-formylamino-5-methylbenzaldehyde |
- |
? |
| 1.13.11.17 | 5-methylindole + O2 |
26% of the activity with indole |
Tecoma stans |
2-formylamino-5-methylbenzaldehyde |
- |
? |
| 1.13.11.17 | indole + O2 |
- |
Tecoma stans |
anthranilic acid |
final product is anthranil, formylaminobenzaldehyde and o-aminobenzaldehyde are intermediates, 3 atoms of oxygen are consumed in the formation of anthranil from one molecule of indole |
? |
| 1.13.11.17 | indole + O2 |
4 atoms of oxygen utilized in disappearance of 1 mol of indole, 2 atoms of oxygen required for initial cleavage of indole and one each for the oxidation of o-aminobenzaldehyde to anthranil and anthranilic acid, simultaneously |
Zea mays |
anthranilic acid |
- |
? |
