| ULS00217 |
indole and pyruvate from L-tryptophan |
None - {{∅}} |
None - {{∅}} |
Unexplained |
|
| UPA00846 |
serotonin biosynthesis~Biosynthesis of serotonin (5-hydroxytryptamine, or 5-HT), a monoamine neurotransmitter. Serotonin is synthesized in serotonergic neurons in the central nervous system (CNS) and enterochromaffin cells in the gastrointestinal tract of animals including humans. Serotonin is also found in many mushrooms and plants, including fruits and vegetables. In plants, serotonin is implicated in several physiological roles such as flowering, morphogenesis, and adaptation to environmental changes. |
Both - {{∅},{t,f}} |
True - {{t}} |
Ambiguous presence |
|
| ULS00218 |
L-kynurenine from L-tryptophan |
None - {{∅}} |
None - {{∅}} |
Unexplained |
|
| UCR00678 |
L-tryptophan + O(2) = N-formyl-N-kynurenine |
None - {{∅}} |
None - {{∅}} |
Unexplained |
|
| UCR07213 |
L-tryptophan + O(2) + tetrahydrobiopterin = 4a-hydroxytetrahydrobiopterin + 5-hydroxy-L-tryptophan |
Both - {{∅},{t,f}} |
None - {{∅}} |
Ambiguous |
|
| UER00453 |
L-kynurenine from L-tryptophan: step 1/2~1 L-tryptophan + 1 O(2) => 1 N-formyl-N-kynurenine. |
None - {{∅}} |
None - {{∅}} |
Unexplained |
|
| UER00814 |
serotonin from L-tryptophan: step 2/2~1 5-hydroxy-L-tryptophan => 1 CO(2) + 1 serotonin. |
Both - {{∅},{t,f}} |
True - {{t}} |
Ambiguous presence |
|
| ULS00398 |
serotonin from L-tryptophan |
Both - {{∅},{t,f}} |
True - {{t}} |
Ambiguous presence |
|
| UER00454 |
L-kynurenine from L-tryptophan: step 2/2~1 H(2)O + 1 N-formyl-N-kynurenine => 1 L-kynurenine + 1 formate. |
None - {{∅}} |
None - {{∅}} |
Unexplained |
|
| UCR02701 |
5-hydroxy-L-tryptophan = CO(2) + serotonin |
Both - {{∅},{t,f}} |
True - {{t}} |
Ambiguous presence |
|
| UPA00526 |
L-tryptophan degradation~Degradation of amino-acid L-tryptophan. |
Both - {{t,f}} |
True - {{t}} |
Ambiguous presence |
|
| UCR00673 |
H(2)O + L-tryptophan = NH(3) + indole + pyruvate |
None - {{∅}} |
None - {{∅}} |
Unexplained |
|
| UER00452 |
indole and pyruvate from L-tryptophan: step 1/1~1 H(2)O + 1 L-tryptophan => 1 NH(3) + 1 indole + 1 pyruvate. |
None - {{∅}} |
None - {{∅}} |
Unexplained |
|
| UPA00333 |
L-tryptophan degradation via kynurenine pathway~Degradation of amino-acid L-tryptophan into L-kynurenine. |
None - {{∅}} |
None - {{∅}} |
Unexplained |
|
| UCR01959 |
H(2)O + N-formyl-N-kynurenine = L-kynurenine + formate |
None - {{∅}} |
None - {{∅}} |
Unexplained |
|
| UPA00332 |
L-tryptophan degradation via pyruvate pathway~Degradation of amino-acid L-tryptophan into pyruvate and indole. Among the multiple products of tryptophan catabolism, indole is suspected to be responsible for the cell-cycle arrest and to add a role in stationary-phase signalling [PMID:17163965]. |
None - {{∅}} |
None - {{∅}} |
Unexplained |
|
| UER00799 |
serotonin from L-tryptophan: step 1/2~1 L-tryptophan + 1 O(2) + 1 tetrahydrobiopterin => 1 4a-hydroxytetrahydrobiopterin + 1 5-hydroxy-L-tryptophan. |
Both - {{∅},{t,f}} |
None - {{∅}} |
Ambiguous |
|