3.1.6.19	(2R)-1-(4-chlorophenyl)propan-2-yl sulfate + H2O	enantiomeric excess of the product: 16%	Sulfolobus acidocaldarius	(2S)-1-(4-chlorophenyl)propan-2-ol + sulfate	-	?	419651	
3.1.6.19	(2R)-1-(4-chlorophenyl)propan-2-yl sulfate + H2O	enantiomeric excess of the product: 16%	Sulfolobus acidocaldarius DSM 639	(2S)-1-(4-chlorophenyl)propan-2-ol + sulfate	-	?	419651	
3.1.6.19	(2R)-1-(4-fluorophenyl)propan-2-yl sulfate + H2O	enantiomeric excess of the product: 16%	Sulfolobus acidocaldarius	(2S)-1-(4-chlorophenyl)propan-2-ol + sulfate	-	?	419652	
3.1.6.19	(2R)-1-(4-fluorophenyl)propan-2-yl sulfate + H2O	enantiomeric excess of the product: 16%	Sulfolobus acidocaldarius DSM 639	(2S)-1-(4-chlorophenyl)propan-2-ol + sulfate	-	?	419652	
3.1.6.19	(2R)-nonan-2-yl sulfate + H2O	enantiomeric excess of the product: 65%	Sulfolobus acidocaldarius	(2S)-nonan-2-ol + sulfate	-	?	419654	
3.1.6.19	(2R)-nonan-2-yl sulfate + H2O	enantiomeric excess of the product: 65%	Sulfolobus acidocaldarius DSM 639	(2S)-nonan-2-ol + sulfate	-	?	419654	
3.1.6.19	(2R)-octan-2-yl hydrogen sulfate + H2O	-	Pseudomonas sp. DSM 6611	(S)-2-octanol + sulfate	-	?	458746	
3.1.6.19	(2R)-octan-2-yl sulfate + H2O	-	Saccharolobus solfataricus	(2S)-octan-2-ol + sulfate	-	?	419655	
3.1.6.19	(2R)-octan-2-yl sulfate + H2O	-	Saccharolobus shibatae	(2S)-octan-2-ol + sulfate	-	?	419655	
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	-	?	419655