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

BRENDA support

Refine search

Search General Information

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 - 3 of 3
EC Number General Information Commentary Reference
Display the reaction diagram Show all sequences 2.3.1.288physiological function acyltransferases PapA2 and PapA1 are responsible for the sequential acylation of trehalose-2-sulfate to form diacetylated intermediate SL1278 and are essential for sulfolipid SL-1 biosynthesis. In vitro, recombinant PapA2 converts T2S to 2'-palmitoyl T2S, and PapA1 further elaborates this SL-1 intermediate to an analog of SL1278. Disruption of PapA2 and PapA1 genes results in loss of SL-1 (and SL1278). The deletions do not appear to affect bacterial replication, trafficking or virulence -, 752027
Display the reaction diagram Show all sequences 2.3.1.288physiological function deletion of PapA2 gene abolishes sulfolipid-I production. Both acyltransferases PapA1 and PapA2 are required for all acylation steps of sulfolipid-I assembly -, 751497
Display the reaction diagram Show all sequences 2.3.1.288physiological function sulfolipid SL-1 biosynthesis is initiated by sulfotransferase by sulfating the abundant disaccharide trehalose to form T2S. The acyltransferase PapA2 then catalyzes the esterification of T2S at the 2'-position to generate a monoacylated intermediate. The polyketide synthase Pks2 synthesizes methyl-branched (hydroxy)phthioceranoyl chains. PapA1 transfers the product of Pks2 to the 3'-position of the monoacylated intermediate, yielding adiacylated species. Additional acylations at the 6- and 6'-positions produce fully elaborated SL-1 -, 751035
Results 1 - 3 of 3