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EC Number General Information Commentary Reference
Show all pathways known for 3.1.6.19Display the word mapDisplay the reaction diagram Show all sequences 3.1.6.19metabolism Pisa1 shows a preference for secondary rather than primary alkyl sulfates, and enantioselectively hydrolyzes the (R)-enantiomer of rac-2-octyl sulfate, yielding (S)-2-octanol with inversion of absolute configuration as a result of C-O bond cleavage. An invariant histidine (His317) near the sulfate-binding site acts as general acid for crucial protonation of the sulfate leaving group 761062
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