Get results CSV file
Prior-Knowledge Description Expectation Prediction Conclusion Leaf Statistics
UCR02715 D-arabinono-1,4-lactone + O(2) = H(2)O(2) + dehydro-D-arabinono-1,4-lactone None - {{∅}} None - {{∅}} Unexplained
VariantPath-2-UER00765 None - {{∅}} None - {{∅}} Unexplained
UER00977 None~1 D-arabinose + 1 NAD(+) => 1 D-arabinono-1,4-lactone + 1 H(+) + 1 NADH. None - {{∅}} None - {{∅}} Unexplained
UCR01574 D-arabinose + NAD(+) = D-arabinono-1,4-lactone + H(+) + NADH None - {{∅}} None - {{∅}} Unexplained
UER00766 dehydro-D-arabinono-1,4-lactone from D-arabinose: step 2/2~1 D-arabinono-1,4-lactone + 1 O(2) => 1 H(2)O(2) + 1 dehydro-D-arabinono-1,4-lactone. None - {{∅}} None - {{∅}} Unexplained
UPA00771 D-erythroascorbate biosynthesis~D-erythroascorbate (EASC), a five-carbon analog of L-ascorbate (ASC) is present in some eukaryotic microorganisms where ASC is rare or absent. In Candida albicans and Saccharomyces cerevisiae, the biosynthetic pathway of EASC from D-arabinose by D-arabinose dehydrogenase and D-arabinono-1,4-lactone oxidase has been established. EASC has biological properties similar to those of ASC. Considering that some eukaryotic microorganisms produce EASC instead of ASC, it is presumed that EASC may take the place of ASC in these microorganisms. EASC has been proved an important antioxidant molecule in S. cerevisiae, like ASC in animals and plants. None - {{∅}} None - {{∅}} Unexplained
ULS00375 dehydro-D-arabinono-1,4-lactone from D-arabinose None - {{∅}} None - {{∅}} Unexplained
UER00765 dehydro-D-arabinono-1,4-lactone from D-arabinose: step 1/2~D-arabinose + [NAD(+) or NADP(+)] => D-arabinono-1,4-lactone + H(+) + [NADH or NADPH]. None - {{∅}} None - {{∅}} Unexplained
UER00978 None~1 D-arabinose + 1 NADP(+) => 1 D-arabinono-1,4-lactone + 1 H(+) + 1 NADPH. None - {{∅}} None - {{∅}} Unexplained
VariantPath-1-UER00765 None - {{∅}} None - {{∅}} Unexplained
UCR01575 D-arabinose + NADP(+) = D-arabinono-1,4-lactone + H(+) + NADPH None - {{∅}} None - {{∅}} Unexplained