| UPA00306 |
(S)-reticuline biosynthesis~Biosynthesis of (S)-reticuline, an important intermediate in synthesizing isoquinoline alkaloids. Reticuline is an important intermediate in the production of analgesic morphinan alkaloids (e.g. morphine), antimicrobial berberine alkaloids (e.g. berberine), and antimicrobial benzophenanthridine alkaloids (e.g. sanguinarine). |
None - {{∅}} |
None - {{∅}} |
Unexplained |
|
| UCR05123 |
(S)-norcoclaurine + S-adenosyl-L-methionine = (S)-coclaurine + S-adenosyl-L-homocysteine |
None - {{∅}} |
None - {{∅}} |
Unexplained |
|
| UER00444 |
(S)-reticuline from (S)-norcoclaurine: step 4/4~1 (S)-3'-hydroxy-N-methylcoclaurine + 1 S-adenosyl-L-methionine => 1 (S)-reticuline + 1 H(+) + 1 S-adenosyl-L-homocysteine. |
None - {{∅}} |
None - {{∅}} |
Unexplained |
|
| UER00443 |
(S)-reticuline from (S)-norcoclaurine: step 3/4~1 (S)-N-methylcoclaurine + 1 H(+) + 1 NADPH + 1 O(2) => 1 (S)-3'-hydroxy-N-methylcoclaurine + 1 H(2)O + 1 NADP(+). |
None - {{∅}} |
None - {{∅}} |
Unexplained |
|
| ULS00209 |
(S)-reticuline from (S)-norcoclaurine |
None - {{∅}} |
None - {{∅}} |
Unexplained |
|
| UCR04692 |
(S)-coclaurine + S-adenosyl-L-methionine = (S)-N-methylcoclaurine + H(+) + S-adenosyl-L-homocysteine |
None - {{∅}} |
None - {{∅}} |
Unexplained |
|
| UER00442 |
(S)-reticuline from (S)-norcoclaurine: step 2/4~1 (S)-coclaurine + 1 S-adenosyl-L-methionine => 1 (S)-N-methylcoclaurine + 1 H(+) + 1 S-adenosyl-L-homocysteine. |
None - {{∅}} |
None - {{∅}} |
Unexplained |
|
| UER00441 |
(S)-reticuline from (S)-norcoclaurine: step 1/4~1 (S)-norcoclaurine + 1 S-adenosyl-L-methionine => 1 (S)-coclaurine + 1 S-adenosyl-L-homocysteine. |
None - {{∅}} |
None - {{∅}} |
Unexplained |
|
| UCR05732 |
(S)-N-methylcoclaurine + H(+) + NADPH + O(2) = (S)-3'-hydroxy-N-methylcoclaurine + H(2)O + NADP(+) |
None - {{∅}} |
None - {{∅}} |
Unexplained |
|
| UCR03832 |
(S)-3'-hydroxy-N-methylcoclaurine + S-adenosyl-L-methionine = (S)-reticuline + H(+) + S-adenosyl-L-homocysteine |
None - {{∅}} |
None - {{∅}} |
Unexplained |
|