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 46 > >>
download as CSV
download all results as CSV
EC Number Substrates Commentary Substrates Organism Products Commentary (Products) Reversibility
Show all pathways known for 3.1.6.19Display the word mapDisplay the reaction diagram Show all sequences 3.1.6.19(3R)-pentan-3-yl sulfate + H2O low activity Pseudomonas sp. pentan-3-ol + sulfate - ?
Show all pathways known for 3.1.6.19Display the word mapDisplay the reaction diagram Show all sequences 3.1.6.19(4R)-heptan-4-yl sulfate + H2O the L-isomer is much more readily hydrolysed than the D-isomer. Enzymic hydrolysis of this group is accompanied by complete inversion of configuration at the asymmetric carbon atom Pseudomonas sp. (4S)-heptan-4-ol + sulfate - ?
Show all pathways known for 3.1.6.19Display the word mapDisplay the reaction diagram Show all sequences 3.1.6.19(5R)-nonan-5-yl sulfate + H2O the L-isomer is much more readily hydrolysed than the D-isomer. Enzymic hydrolysis of this group is accompanied by complete inversion of configuration at the asymmetric carbon atom Pseudomonas sp. nonan-5-ol + sulfate - ?
Show all pathways known for 3.1.6.19Display the word mapDisplay the reaction diagram Show all sequences 3.1.6.19(3R)-pentan-3-yl sulfate + H2O low activity Pseudomonas sp. C12B pentan-3-ol + sulfate - ?
Show all pathways known for 3.1.6.19Display the word mapDisplay the reaction diagram Show all sequences 3.1.6.19(4R)-heptan-4-yl sulfate + H2O the L-isomer is much more readily hydrolysed than the D-isomer. Enzymic hydrolysis of this group is accompanied by complete inversion of configuration at the asymmetric carbon atom Pseudomonas sp. C12B (4S)-heptan-4-ol + sulfate - ?
Show all pathways known for 3.1.6.19Display the word mapDisplay the reaction diagram Show all sequences 3.1.6.19(5R)-nonan-5-yl sulfate + H2O the L-isomer is much more readily hydrolysed than the D-isomer. Enzymic hydrolysis of this group is accompanied by complete inversion of configuration at the asymmetric carbon atom Pseudomonas sp. C12B nonan-5-ol + sulfate - ?
Show all pathways known for 3.1.6.19Display the word mapDisplay the reaction diagram Show all sequences 3.1.6.19(2R)-octan-2-yl hydrogen sulfate + H2O - Pseudomonas sp. DSM 6611 (S)-2-octanol + sulfate - ?
Show all pathways known for 3.1.6.19Display the word mapDisplay the reaction diagram Show all sequences 3.1.6.19octyl sulfate + H2O - Pseudomonas sp. DSM 6611 1-octanol + sulfate - ?
Show all pathways known for 3.1.6.19Display the word mapDisplay the reaction diagram Show all sequences 3.1.6.19(2R)-octan-2-yl sulfate + H2O enantioselectivity expressed by E-value is 21. The preferred substrates for the enzyme are linear sec-alkyl sulfate esters, particularly 2-, 3-, and 4-octyl sulfates. The enzymatic hydrolysis proceeds through inversion of the configuration at the stereogenic carbon atom Rhodococcus ruber (2S)-octan-2-ol + sulfate - ?
Show all pathways known for 3.1.6.19Display the word mapDisplay the reaction diagram Show all sequences 3.1.6.19(R)-2-octyl sulfate + H2O - Rhodococcus ruber (S)-2-octanol + sulfate - ?
Results 1 - 10 of 46 > >>
download as CSV
download all results as CSV