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 11 - 18 of 18
EC Number Substrates Commentary Substrates Organism Products Commentary (Products) Reversibility
Display the word mapDisplay the reaction diagram Show all sequences 1.7.1.B1cyclohexenone + NADPH + H+ - Pseudomonas putida KT 2240 ? - ?
Display the word mapDisplay the reaction diagram Show all sequences 1.7.1.B1glycerol trinitrate + NADPH + H+ - Pseudomonas putida ? - ?
Display the word mapDisplay the reaction diagram Show all sequences 1.7.1.B1glycerol trinitrate + NADPH + H+ - Pseudomonas putida KT 2240 ? - ?
Display the word mapDisplay the reaction diagram Show all sequences 1.7.1.B1more ability to reduce nitroaromatic compounds, enzyme demonstrates type I and type II hydride transferase activity and reduced the nitro groups of 2,4,6-trinitrotoluene to hydroxylaminodinitrotoluene derivatives. The condensations of the primary products of type I and type II hydride transferases react with each other to yield diarylamines and nitrite, the latter can be further reduced to ammonium and serves as a nitrogen source for microorganisms in vivo Pseudomonas putida ? - ?
Display the word mapDisplay the reaction diagram Show all sequences 1.7.1.B1more enzyme additionally catalyzes reduction of nitrobenzene, reaction of EC 1.7.1.16 Pseudomonas sp. ? - ?
Display the word mapDisplay the reaction diagram Show all sequences 1.7.1.B1more the enzyme shows no reactivity with CB1954 Pseudomonas putida ? - -
Display the word mapDisplay the reaction diagram Show all sequences 1.7.1.B1more ability to reduce nitroaromatic compounds, enzyme demonstrates type I and type II hydride transferase activity and reduced the nitro groups of 2,4,6-trinitrotoluene to hydroxylaminodinitrotoluene derivatives. The condensations of the primary products of type I and type II hydride transferases react with each other to yield diarylamines and nitrite, the latter can be further reduced to ammonium and serves as a nitrogen source for microorganisms in vivo Pseudomonas putida KT 2240 ? - ?
Display the word mapDisplay the reaction diagram Show all sequences 1.7.1.B1N-ethylmaleimide + NADPH + H+ - Pseudomonas putida ? - ?
<< < Results 11 - 18 of 18