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Prior-Knowledge Description Expectation Prediction Conclusion Leaf Statistics
UCR00226 (S)-2-acetolactate + CO(2) = 2 pyruvate None - {{∅}} True - {{t}} Unconfirmed presence
UCR02948 (S)-2-acetolactate = (R)-acetoin + CO(2) None - {{∅}} None - {{∅}} Unexplained
UER00679 (R,R)-butane-2,3-diol from pyruvate: step 3/3~1 (R)-acetoin + 1 H(+) + 1 NADH => 1 (R,R)-butane-2,3-diol + 1 NAD(+). None - {{∅}} True - {{t}} Unconfirmed presence
ULS00333 (R,R)-butane-2,3-diol from pyruvate None - {{∅}} True - {{t}} Unconfirmed presence
UCR02946 (R,R)-butane-2,3-diol + NAD(+) = (R)-acetoin + H(+) + NADH None - {{∅}} True - {{t}} Unconfirmed presence
UER00678 (R,R)-butane-2,3-diol from pyruvate: step 2/3~1 (S)-2-acetolactate => 1 (R)-acetoin + 1 CO(2). None - {{∅}} None - {{∅}} Unexplained
UER00677 (R,R)-butane-2,3-diol from pyruvate: step 1/3~2 pyruvate => 1 (S)-2-acetolactate + 1 CO(2). None - {{∅}} True - {{t}} Unconfirmed presence
UPA00626 (R,R)-butane-2,3-diol biosynthesis~In some bacteria, pyruvate can be channeled via alpha-acetolactate into neutral compound 2,3-butanediol. The production of (R,R)-2,3-butanediol is enhanced when oxygen is limited and the pH is lowered. None - {{∅}} True - {{t}} Unconfirmed presence