3.1.6.19: (R)-specific secondary-alkylsulfatase (type III)

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For detailed information about (R)-specific secondary-alkylsulfatase (type III), go to the full flat file.

Word Map on EC 3.1.6.19

3.1.6.19

enantioselective

sec-alcohols

r-enantiomer

sulfur

stereoselective

synthesis

homochiral

deracemization

furnish

Reaction

Synonyms

(R)-specific sec-alkylsulfatase, Pisa1, S3 secondary alkylsulphohydrolase, sec-alkylsulfatase, sulfatase RS2

ECTree

3 Hydrolases

3.1 Acting on ester bonds

3.1.6 Sulfuric-ester hydrolases

3.1.6.19 (R)-specific secondary-alkylsulfatase (type III)

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Results	in table
1	AA Sequence
4	Application
1	Cloned(Commentary)
1	Crystallization (Commentary)
1	General Information
3	Inhibitors
8	kcat/KM [mM/s]
2	Ki Value [mM]
10	KM Value [mM]
1	Metals/Ions
4	Molecular Weight [Da]
81	Organism
2	Pathway
7	pH Optimum
2	pH Range
1	pI Value
9	Protein Variants
2	Purification (Commentary)
1	Reaction
17	Reference
2	Specific Activity [micromol/min/mg]
46	Substrates and Products (Substrate)
2	Subunits
10	Synonyms
1	Systematic Name
3	Temperature Optimum [°C]
1	Temperature Range [°C]
9	Turnover Number [1/s]

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Reference on EC 3.1.6.19 - (R)-specific secondary-alkylsulfatase (type III)

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718578

Pogorevc, M.; Kroutil, W.; Wallner, S.R.; Faber, K.

Enantioselective stereoinversion in the kinetic resolution of rac-sec-alkyl sulfate esters by hydrolysis with an alkylsulfatase from Rhodococcus ruber DSM 44541 furnishes homochiral products

Angew. Chem. Int. Ed. Engl.

4052-4954

2002

Rhodococcus ruber, Rhodococcus ruber DSM 44541

12412078

718622

Pogorevc, M.; Faber, K.

Purification and characterization of an inverting stereo- and enantioselective sec-alkylsulfatase from the gram-positive bacterium Rhodococcus ruber DSM 44541

Appl. Environ. Microbiol.

2810-2815

2003

Rhodococcus ruber, Rhodococcus ruber DSM 44541

12732552

718768

Shaw, D.J.; Dodgson, K.S.; White, G.F.

Substrate specificity and other properties of the inducible S3 secondary alkylsulphohydrolase purified from the detergent-degrading bacterium Pseudomonas C12B

Biochem. J.

187

181-190

1980

Pseudomonas sp., Pseudomonas sp. C12B

7406859

718808

Gadler, P.; Glueck, S.M.; Kroutil, W.; Nestl, B.M.;, Larissegger-Schnell, B.; Ueberbacher, B.T.; Wallner, S.R.; Faber, K.

Biocatalytic approaches for the quantitative production of single stereoisomers from racemates

Biochem. Soc. Trans.

296-300

2006

Sulfolobus acidocaldarius, Sulfolobus acidocaldarius DSM 639

16545098

720613

Wallner, S.R.; Nestl, B.M.; Faber, K.

Highly enantioselective stereo-inverting sec-alkylsulfatase activity of hyperthermophilic Archaea

Org. Biomol. Chem.

2652-2656

2005

Sulfolobus acidocaldarius, Saccharolobus shibatae, Saccharolobus solfataricus, Sulfolobus acidocaldarius DSM 639, Saccharolobus shibatae DSM 5389, Saccharolobus solfataricus DSM 1617

15999201

720621

Wallner, S.R.; Nestl, B.M.; Faber, K.

Highly enantioselective sec-alkyl sulfatase activity of Sulfolobus acidocaldarius DSM 639

Org. Lett.

5009-5010

2004

Sulfolobus acidocaldarius, Sulfolobus acidocaldarius DSM 639

15606122

761062

Knaus, T.; Schober, M.; Kepplinger, B.; Faccinelli, M.; Pitzer, J.; Faber, K.; Macheroux, P.; Wagner, U.

Structure and mechanism of an inverting alkylsulfatase from Pseudomonas sp. DSM6611 specific for secondary alkyl sulfates

FEBS J.

279

4374-4384

2012

Pseudomonas sp. DSM 6611 (F8KAY7)

23061549