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Prior-Knowledge Description Expectation Prediction Conclusion Leaf Statistics
UCR00678 L-tryptophan + O(2) = N-formyl-N-kynurenine True - {{t}} None - {{∅}} Missing
ULS00398 serotonin from L-tryptophan 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
ULS00217 indole and pyruvate from L-tryptophan 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. None - {{∅}} None - {{∅}} Unexplained
ULS00218 L-kynurenine from L-tryptophan True - {{t}} None - {{∅},{t}} Missing
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. True - {{t}} None - {{∅},{t}} Missing
UCR01959 H(2)O + N-formyl-N-kynurenine = L-kynurenine + formate True - {{t}} True - {{t}} Confirmed presence
UER00454 L-kynurenine from L-tryptophan: step 2/2~1 H(2)O + 1 N-formyl-N-kynurenine => 1 L-kynurenine + 1 formate. True - {{t}} True - {{t}} Confirmed presence
UCR02701 5-hydroxy-L-tryptophan = CO(2) + serotonin 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. None - {{∅}} None - {{∅}} Unexplained
UCR07213 L-tryptophan + O(2) + tetrahydrobiopterin = 4a-hydroxytetrahydrobiopterin + 5-hydroxy-L-tryptophan None - {{∅}} None - {{∅}} Unexplained
UER00814 serotonin from L-tryptophan: step 2/2~1 5-hydroxy-L-tryptophan => 1 CO(2) + 1 serotonin. None - {{∅}} None - {{∅}} Unexplained
UCR00673 H(2)O + L-tryptophan = NH(3) + indole + pyruvate None - {{∅}} None - {{∅}} Unexplained
UER00453 L-kynurenine from L-tryptophan: step 1/2~1 L-tryptophan + 1 O(2) => 1 N-formyl-N-kynurenine. True - {{t}} None - {{∅}} Missing
UPA00526 L-tryptophan degradation~Degradation of amino-acid L-tryptophan. True - {{t}} None - {{∅},{t}} Missing