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Prior-Knowledge Description Expectation Prediction Conclusion Leaf Statistics
UER00777 2-hydroxy-2,4-pentadienoate and salicylate from dibenzofuran: step 2/3~1 O(2) + 1 biphenyl-2,2',3-triol => 1 2-hydroxy-6-(2-hydroxyphenyl)-6-oxo-cis,cis-hexa-2,4-dienoic acid. None - {{∅}} None - {{∅}} Unexplained
UER00776 2-hydroxy-2,4-pentadienoate and salicylate from dibenzofuran: step 1/3~1 H(+) + 1 NADH + 1 O(2) + 1 dibenzofuran => 1 NAD(+) + 1 biphenyl-2,2',3-triol. None - {{∅}} None - {{∅}} Unexplained
ULS00383 2-hydroxy-2,4-pentadienoate and salicylate from dibenzofuran None - {{∅}} None - {{∅}} Unexplained
UPA00808 dibenzofuran degradation~Degradation of dibenzofuran. Dibenzofuran is created as by-products during industrial processes such as incineration, paper bleaching, and chemical synthesis. It has also been used as an insecticide, and is formed from the photolysis of chlorinated biphenyl ethers. Several species of bacteria capable degrading dibenzofuran have been identified, including Pseudomonas, Xanthomonas, Terrabacter, Microbacterium, and Rhodococcus. None - {{∅}} None - {{∅}} Unexplained
UER00778 2-hydroxy-2,4-pentadienoate and salicylate from dibenzofuran: step 3/3~1 2-hydroxy-6-(2-hydroxyphenyl)-6-oxo-cis,cis-hexa-2,4-dienoic acid + 1 H(2)O => 1 2-hydroxy-2,4-pentadienoate + 1 salicylate. None - {{∅}} None - {{∅}} Unexplained