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Results 1 - 10 of 17 > >>
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EC Number Substrates Commentary Substrates Organism Products Commentary (Products) Reversibility
Show all pathways known for 1.14.13.243Display the word mapDisplay the reaction diagram Show all sequences 1.14.13.2432-methylphenol + NADH + H+ + O2 - Burkholderia cepacia 3-methylcatechol + NAD+ + H2O - ?
Show all pathways known for 1.14.13.243Display the word mapDisplay the reaction diagram Show all sequences 1.14.13.2432-methylphenol + NADH + H+ + O2 - Burkholderia cepacia G4 3-methylcatechol + NAD+ + H2O - ?
Show all pathways known for 1.14.13.243Display the word mapDisplay the reaction diagram Show all sequences 1.14.13.243indole + NADH + H+ + O2 - Burkholderia cepacia isoindigo + NAD+ + H2O - ?
Show all pathways known for 1.14.13.243Display the word mapDisplay the reaction diagram Show all sequences 1.14.13.243indole + NADH + H+ + O2 - Burkholderia cepacia G4 isoindigo + NAD+ + H2O - ?
Show all pathways known for 1.14.13.243Display the word mapDisplay the reaction diagram Show all sequences 1.14.13.243methyl p-tolyl sulfide + NADH + H+ + O2 - Burkholderia cepacia methyl p-tolyl sulfoxide + NAD+ + H2O - ?
Show all pathways known for 1.14.13.243Display the word mapDisplay the reaction diagram Show all sequences 1.14.13.243methyl p-tolyl sulfide + NADH + H+ + O2 - Burkholderia cepacia G4 methyl p-tolyl sulfoxide + NAD+ + H2O - ?
Show all pathways known for 1.14.13.243Display the word mapDisplay the reaction diagram Show all sequences 1.14.13.243more enzyme additionally oxidizes trichloroethylene, reaction of EC 1.14.13.243. All three purified toluene 2-monooxygenase protein components and NADH are required to reconstitute full trichloroethylene oxidation activity in vitro. Trichloroethylene-dependent inactivation of toluene 2-monooxygenase activity is observed Burkholderia cepacia ? - ?
Show all pathways known for 1.14.13.243Display the word mapDisplay the reaction diagram Show all sequences 1.14.13.243more wild-type forms isoindigo via C-2 hydroxylation of the indole pyrrole. Mutant TomA3 A113G produces 4-hydroxyindole. TomA3 V106/A113 mutants with hydrophobic, polar, or charged amino acids hydroxylate indole at the C-3 and C-2 positions, forming isatin, indigo, and indirubin in a variety of distributions Burkholderia cepacia ? - ?
Show all pathways known for 1.14.13.243Display the word mapDisplay the reaction diagram Show all sequences 1.14.13.243more wild-type forms isoindigo via C-2 hydroxylation of the indole pyrrole. Mutant TomA3 A113G produces 4-hydroxyindole. TomA3 V106/A113 mutants with hydrophobic, polar, or charged amino acids hydroxylate indole at the C-3 and C-2 positions, forming isatin, indigo, and indirubin in a variety of distributions Burkholderia cepacia G4 ? - ?
Show all pathways known for 1.14.13.243Display the word mapDisplay the reaction diagram Show all sequences 1.14.13.243more enzyme additionally oxidizes trichloroethylene, reaction of EC 1.14.13.243. All three purified toluene 2-monooxygenase protein components and NADH are required to reconstitute full trichloroethylene oxidation activity in vitro. Trichloroethylene-dependent inactivation of toluene 2-monooxygenase activity is observed Burkholderia cepacia G4 ? - ?
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