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Prior-Knowledge Description Expectation Prediction Conclusion Leaf Statistics
UPA00067 ectoine biosynthesis~Biosynthesis of ectoine (1,4,5,6-tetrahydro-2-methyl-4-pyrimidine carboxylic acid), an excellent osmoprotectant. Since Galinski et al. (PMID:3838936) discovered ectoine as a compatible solute in Ectothiorhodospira halochloris, an extremely halophilic phototrophic eubacterium, it has been found to be distributed widely in nature, largely in moderately halophilic eubacteria. The biosynthetic pathway of ectoine from aspartic b-semialdehyde (ASA) was first elucidated in Halomonas elongata by purification and characterization of each enzyme involved. None - {{∅}} None - {{∅},{t}} Unexplained
UCR06979 N(4)-acetyl-L-2,4-diaminobutyric acid = H(2)O + L-ectoine None - {{∅}} None - {{∅}} Unexplained
UER00122 L-ectoine from L-aspartate 4-semialdehyde: step 2/3~1 L-2,4-diaminobutanoate + 1 acetyl-CoA => 1 CoA + 1 N(4)-acetyl-L-2,4-diaminobutyric acid. None - {{∅}} None - {{∅}} Unexplained
UCR06978 L-2,4-diaminobutanoate + acetyl-CoA = CoA + N(4)-acetyl-L-2,4-diaminobutyric acid None - {{∅}} None - {{∅}} Unexplained
UER00123 L-ectoine from L-aspartate 4-semialdehyde: step 3/3~1 N(4)-acetyl-L-2,4-diaminobutyric acid => 1 H(2)O + 1 L-ectoine. None - {{∅}} None - {{∅}} Unexplained
MUER1 Meta-UER 1~1 L-aspartate 4-semialdehyde + 1 L-glutamate => 1 2-oxoglutarate + 1 L-2,4-diaminobutanoate. None - {{∅}} True - {{t}} Unconfirmed presence
ULS00048 L-ectoine from L-aspartate 4-semialdehyde None - {{∅}} None - {{∅},{t}} Unexplained
UCR06977 L-aspartate 4-semialdehyde + L-glutamate = 2-oxoglutarate + L-2,4-diaminobutanoate None - {{∅}} True - {{t}} Unconfirmed presence