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Prior-Knowledge Description Expectation Prediction Conclusion Leaf Statistics
UCR06601 5-hydroxyisouric acid + H(2)O = 5-hydroxy-2-oxo-4-ureido-2,5-dihydro-1H-imidazole-5-carboxylic acid Both - {{t},{t,f}} True - {{t}} Ambiguous presence
UER00652 (S)-allantoin from urate: step 3/3~1 5-hydroxy-2-oxo-4-ureido-2,5-dihydro-1H-imidazole-5-carboxylic acid => 1 (S)-allantoin + 1 CO(2). Both - {{t,f}} True - {{t}} Ambiguous presence
UER00651 (S)-allantoin from urate: step 2/3~1 5-hydroxyisouric acid + 1 H(2)O => 1 5-hydroxy-2-oxo-4-ureido-2,5-dihydro-1H-imidazole-5-carboxylic acid. Both - {{t},{t,f}} True - {{t}} Ambiguous presence
UER00650 (S)-allantoin from urate: step 1/3~1 H(2)O + 1 O(2) + 1 urate => 1 5-hydroxyisouric acid + 1 H(2)O(2). Both - {{t},{t,f}} True - {{t}} Ambiguous presence
UCR06604 5-hydroxy-2-oxo-4-ureido-2,5-dihydro-1H-imidazole-5-carboxylic acid = (S)-allantoin + CO(2) Both - {{t},{t,f}} True - {{t}} Ambiguous presence
UCR02106 H(2)O + O(2) + urate = 5-hydroxyisouric acid + H(2)O(2) Both - {{t},{t,f}} True - {{t}} Ambiguous presence
UPA00394 urate degradation~Degradation of uric acid, a key compound in the degradation of purines. The ureide pathway, which mediates the oxidative degradation of uric acid to (S)-allantoin, represents the late stage of purine catabolism in most organisms. The metabolism of uric acid has a pivotal role in transforming the nitrogen that is fixed in leguminous plants and also plays a crucial role in some bacteria under nitrogen-limited conditions. Both - {{t,f}} True - {{t}} Ambiguous presence
ULS00313 (S)-allantoin from urate Both - {{t,f}} True - {{t}} Ambiguous presence