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Results 1 - 6 of 6
EC Number Substrates Commentary Substrates Organism Products Commentary (Products) Reversibility
Display the reaction diagram Show all sequences 1.14.99.46more the pyrimidine ring is cleaved directly by adding a pair of oxygen atoms and producing ureidoacrylate peracid. This odd metabolite, a strong and highly toxic oxidizing agent, is reduced spontaneously, albeit slowly, to ureidoacrylate Escherichia coli ? - ?
Display the reaction diagram Show all sequences 1.14.99.46more (Z)-3-ureidoacrylic peracid decomposes nonenzymatically to form primarily (Z)-3-ureidoacrylic acid and uracil, half life of (Z)-3-ureidoacrylic peracid is 3 hours at pH 10.0 at 25°C and much less at lower pH Escherichia coli ? - ?
Display the reaction diagram Show all sequences 1.14.99.46more (Z)-3-ureidoacrylic peracid is not stable and decomposes nonenzymatically to give (Z)-3-ureidoacrylate Escherichia coli ? - ?
Display the reaction diagram Show all sequences 1.14.99.46thymine + FMNH2 + O2 - Escherichia coli (Z)-2-methylureidoacrylate peracid + FMN - ?
Display the reaction diagram Show all sequences 1.14.99.46uracil + FMNH2 + O2 - Escherichia coli (Z)-3-ureidoacrylate peracid + FMN - ?
Display the reaction diagram Show all sequences 1.14.99.46uracil + FMNH2 + O2 RutA directly cleaves the uracil ring between N-3 and C-4 to yield ureidoacrylate Escherichia coli (Z)-3-ureidoacrylate peracid + FMN product analysis by both NMR spectroscopy and mass spectrometry, overview ?
Results 1 - 6 of 6