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Results 1 - 10 of 11 > >>
EC Number Natural Substrates Commentary (Nat. Sub.)
Show all pathways known for 3.5.2.2Display the word mapDisplay the reaction diagram Show all sequences 3.5.2.25,6-dihydropyrimidine + H2O -
Show all pathways known for 3.5.2.2Display the word mapDisplay the reaction diagram Show all sequences 3.5.2.25,6-dihydrothymine + H2O -
Show all pathways known for 3.5.2.2Display the word mapDisplay the reaction diagram Show all sequences 3.5.2.25,6-dihydrouracil + H2O -
Show all pathways known for 3.5.2.2Display the word mapDisplay the reaction diagram Show all sequences 3.5.2.25,6-dihydrouracil + H2O purified preparation demonstrates no activity on this substrate
Show all pathways known for 3.5.2.2Display the word mapDisplay the reaction diagram Show all sequences 3.5.2.25-(4-hydroxyphenyl) hydantoin + H2O -
Show all pathways known for 3.5.2.2Display the word mapDisplay the reaction diagram Show all sequences 3.5.2.2dihydrothymidine + H2O -
Show all pathways known for 3.5.2.2Display the word mapDisplay the reaction diagram Show all sequences 3.5.2.2DL-4-hydroxyphenylhydantoin + H2O -
Show all pathways known for 3.5.2.2Display the word mapDisplay the reaction diagram Show all sequences 3.5.2.2hydantoin + H2O -
Show all pathways known for 3.5.2.2Display the word mapDisplay the reaction diagram Show all sequences 3.5.2.2isobutylhydantoin + H2O 98.7 % enantiomeric excess (ee), isolation yield of 78.3%, and substrate to biocatalyst ratio of 15.6 in recombinant Escherichia coli
Show all pathways known for 3.5.2.2Display the word mapDisplay the reaction diagram Show all sequences 3.5.2.2more catalyzes the hydrolysis of 5-monosubstituted hydantoin to enantionmeric N-carbamoyl-amino acids
Results 1 - 10 of 11 > >>