Any feedback?
Please rate this page
(search_result.php)
(0/150)

BRENDA support

Refine search

Search Substrates and Products (Substrate)

show results
Don't show organism specific information (fast!)
Search organism in taxonomic tree (slow, choose "exact" as search mode, e.g. "mammalia" for rat,human,monkey,...)
(Not possible to combine with the first option)
Refine your search

Search term:

Results 1 - 8 of 8
EC Number Substrates Commentary Substrates Organism Products Commentary (Products) Reversibility
Display the word mapDisplay the reaction diagram Show all sequences 1.14.14.39L-isoleucine + 2 O2 + 2 [reduced NADPH-hemoprotein reductase] - Lotus japonicus (1E,2S)-2-methylbutanal oxime + 2 [oxidized NADPH-hemoprotein reductase] + CO2 + 3 H2O overall reaction ?
Display the word mapDisplay the reaction diagram Show all sequences 1.14.14.39L-isoleucine + 2 O2 + 2 [reduced NADPH-hemoprotein reductase] - Manihot esculenta (1E,2S)-2-methylbutanal oxime + 2 [oxidized NADPH-hemoprotein reductase] + CO2 + 3 H2O overall reaction ?
Display the word mapDisplay the reaction diagram Show all sequences 1.14.14.39L-isoleucine + 2 [reduced NADPH-hemoprotein reductase] + 2 O2 higher catalytic efficiency with L-Ile as substrate than with L-Val, in agreement with lotaustralin and rhodiocyanoside A and D being the major cyanogenic and nitrile glucosides in Lotus japonicus Lotus japonicus (1E,2S)-2-methylbutanal oxime + 2 [oxidized NADPH-hemoprotein reductase] + CO2 + 3 H2O - ?
Display the word mapDisplay the reaction diagram Show all sequences 1.14.14.39L-valine + 2 [reduced NADPH-hemoprotein reductase] + 2 O2 higher catalytic efficiency with L-Ile as substrate than with L-Val, in agreement with lotaustralin and rhodiocyanoside A and D being the major cyanogenic and nitrile glucosides in Lotus japonicus Lotus japonicus (E)-2-methylpropanal oxime + 2 [oxidized NADPH-hemoprotein reductase] + CO2 + 3 H2O - ?
Display the word mapDisplay the reaction diagram Show all sequences 1.14.14.39more metabolism of L-Leu, L-Phe, or L-Tyr to the corresponding oximes is not detectable in consistence with the absence of cyanogenic glucosides derived from these amino acids. No substrate: L-Trp, L-Met, L-Pro Lotus japonicus ? - ?
Display the word mapDisplay the reaction diagram Show all sequences 1.14.14.39more enzyme additionally acts on L-valine, reaction of EC 1.14.14.38, the catalytic efficiency (Kcat/Km) being 6fold higher with L-Ile than with L-Val as substrate. No substrates: L-Tyr, L-Phe, L-Leu, L-Trp, L-Met, and L-Pro Lotus japonicus ? - ?
Display the word mapDisplay the reaction diagram Show all sequences 1.14.14.39more enzyme additionally acts on L-valine, reaction of EC 1.14.14.38. No substrates: D-valine, D-isoleucine, L-leucine, L-phenylalanine, or L-tyrosine Manihot esculenta ? - ?
Display the word mapDisplay the reaction diagram Show all sequences 1.14.14.39more enzyme additionally acts on L-valine, reaction of EC 1.14.14.38. The conversion rate of L-isoleucine is approximately 60% of that observed for L-valine. No substrates: D-valine, D-isoleucine, L-leucine, L-phenylalanine, or L-tyrosine Manihot esculenta ? - ?
Results 1 - 8 of 8