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Results 1 - 10 of 20 > >>
EC Number Natural Substrates Commentary (Nat. Sub.)
Display the word mapDisplay the reaction diagram Show all sequences 1.2.3.113-cis-retinal + O2 + H2O -
Display the word mapDisplay the reaction diagram Show all sequences 1.2.3.13 brimonidine + 4 H2O + 4 O2 -
Display the word mapDisplay the reaction diagram Show all sequences 1.2.3.14-hydroxypyrazolo(3,4-d)pyrimidine + O2 + H2O 12-13% of the activity compared to purine
Display the word mapDisplay the reaction diagram Show all sequences 1.2.3.14-hydroxypyrazolo(3,4-d)pyrimidine + O2 + H2O i.e. allopurinol
Display the word mapDisplay the reaction diagram Show all sequences 1.2.3.19-cis-retinal + O2 + H2O -
Display the word mapDisplay the reaction diagram Show all sequences 1.2.3.1abscisic aldehyde + H2O + O2 four aldehyde oxidases are known that have varying affinities to abscisic aldehyde. AOdelta, endcoded by AAO3 specifically catalyses this step in rosette leaves
Display the word mapDisplay the reaction diagram Show all sequences 1.2.3.1all-trans-retinal + O2 + H2O -
Display the word mapDisplay the reaction diagram Show all sequences 1.2.3.1hypoxanthine + O2 + H2O 22-26% of the activity compared to purine
Display the word mapDisplay the reaction diagram Show all sequences 1.2.3.1more enzyme plays an important role in the biotransformation of drugs and xenobiotics, e.g. antiviral, antimalarial and antitumour compounds and nicotine
Display the word mapDisplay the reaction diagram Show all sequences 1.2.3.1more enzyme plays an important role in detoxification of the toxic heterocycles synthesized by certain plants
Results 1 - 10 of 20 > >>