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 - 10 of 24 > >>
download as CSV
download all results as CSV
EC Number Substrates Commentary Substrates Organism Products Commentary (Products) Reversibility
Display the reaction diagram Show all sequences 2.2.1.122-oxobutanoate + (3E)-4-(4-chlorophenyl)but-3-en-2-one - Serratia marcescens ? - ?
Display the reaction diagram Show all sequences 2.2.1.12more PigD catalyzes 1,2-additions using 2-oxoacids as donor substrates and aldehydes as acceptors. In the case of ketones as acceptors PigD catalyzes the 1,4-addition. Although pyruvate is the preferred donor substrate, 2-oxobutanoate is also employed using (E)-4-(4-chlorophenyl)-but-3-en-2-one as an acceptor Serratia marcescens ? - ?
Display the reaction diagram Show all sequences 2.2.1.12pyruvate + (2E)-1,3-diphenylprop-2-en-1-one the PigD-catalyzed reaction yields 3% 1,4-carboligation product, with an enantiomeric excess above 99% Serratia marcescens (3R)-1,3-diphenylpentane-1,4-dione + CO2 - ?
Display the reaction diagram Show all sequences 2.2.1.12pyruvate + (2E)-3-(2-hydroxyphenyl)-1-phenylprop-2-en-1-one the PigD-catalyzed reaction yields 39% 1,4-carboligation product, with an enantiomeric excess above 99% Serratia marcescens (3R)-3-(2-hydroxyphenyl)-1-phenylpentane-1,4-dione + CO2 - ?
Display the reaction diagram Show all sequences 2.2.1.12pyruvate + (2E)-3-(4-methoxyphenyl)-1-phenylprop-2-en-1-one - Serratia marcescens (3R)-3-(4-methoxyphenyl)-1-phenylpentane-1,4-dione + CO2 - ?
Display the reaction diagram Show all sequences 2.2.1.12pyruvate + (3E)-4-(4-chlorophenyl)but-3-en-2-one 39% conversion. (3R)-3-(4-Chlorophenyl)hexane-2,5-dione is produced with 75% enantiomeric excess Serratia marcescens (3R)-3-(4-chlorophenyl)hexane-2,5-dione + CO2 - ?
Display the reaction diagram Show all sequences 2.2.1.12pyruvate + (3E)-4-(4-chlorophenyl)but-3-en-2-one the PigD-catalyzed reaction yields 13% 1,4-carboligation product, with an enantiomeric excess above 99% Serratia marcescens (3R)-3-(4-chlorophenyl)hexane-2,5-dione + CO2 - ?
Display the reaction diagram Show all sequences 2.2.1.12pyruvate + (3E)-4-(4-hydroxy-3-methoxyphenyl)but-3-en-2-one - Serratia marcescens (3R)-3-(4-hydroxy-3-methoxyphenyl)hexane-2,5-dione + CO2 - ?
Display the reaction diagram Show all sequences 2.2.1.12pyruvate + (3E)-4-(furan-2-yl)but-3-en-2-one 11% conversion Serratia marcescens 3-(furan-2-yl)hexane-2,5-dione + CO2 - ?
Display the reaction diagram Show all sequences 2.2.1.12pyruvate + (3E)-4-(furan-2-yl)but-3-en-2-one 10% conversion Serratia marcescens (3R)-3-(furan-2-yl)hexane-2,5-dione + CO2 - ?
Results 1 - 10 of 24 > >>
download as CSV
download all results as CSV