EC Number |
Substrates |
Organism |
Products |
Reversibility |
---|
1.5.1.27 | 1,2-dehydroreticuline + NADPH + H+ |
- |
Papaver somniferum |
(R)-reticuline + NADP+ |
- |
? |
1.5.1.27 | 1,2-dehydroreticuline + NADPH + H+ |
- |
Papaver bracteatum |
(R)-reticuline + NADP+ |
- |
? |
1.5.1.27 | 1,2-dehydroreticulinium + NADPH + H+ |
- |
Papaver somniferum |
(R)-reticuline + NADP+ |
- |
r |
1.5.1.27 | 1,2-dehydroreticulinium + NADPH + H+ |
- |
Papaver rhoeas |
(R)-reticuline + NADP+ |
- |
r |
1.5.1.27 | 1,2-dehydroreticulinium + NADPH + H+ |
- |
Papaver somniferum |
(R)-reticuline + NADP+ |
- |
? |
1.5.1.27 | 1,2-dehydroreticulinium + NADPH + H+ |
- |
Papaver somniferum |
(R)-reticuline + NADP+ |
- |
ir |
1.5.1.27 | more |
enzyme PsREPI also catalyzes the stereochemical inversion of (S)-N-methylcoclaurine |
Papaver somniferum |
? |
- |
? |
1.5.1.27 | 1,2-Dehydroreticuline + NADPH |
formation of the precursor of morphinan alkaloids |
Papaver somniferum |
? |
- |
? |
1.5.1.27 | 1,2-dehydroreticulinium + NADPH + H+ |
no activity in the back reaction |
Papaver somniferum |
(R)-reticuline + NADP+ |
- |
ir |
1.5.1.27 | 1,2-dehydro-N-methylcoclaurine + NADPH + H+ |
PrDRR reduces 1,2-dehydro-N-methylcoclaurine to N-methylcoclaurine, although the low product yield precludes determination of the enantiomer |
Papaver rhoeas |
N-methylcoclaurine + NADP+ |
- |
? |