(2R)-butane-2-sulfonate
General
Type : Transition state analogue,Sulfur Compound
Chemical_Nomenclature : (2R)-butane-2-sulfonic acid
Canonical SMILES : CCC(C)S(=O)(=O)O
InChI : InChI=1S\/C4H10O3S\/c1-3-4(2)8(5,6)7\/h4H,3H2,1-2H3,(H,5,6,7)\/t4-\/m1\/s1
InChIKey : BRXCDHOLJPJLLT-SCSAIBSYSA-N
Other name(s) : 2-Butanesulfonic acid, (2R)-,(2r)-Butane-2-Sulfonate,SCHEMBL4253570,CTK0C6378,[R,(+)]-2-Butanesulfonic acid
MW : 138.18
Formula : C4H10O3S
CAS_number : 115555-41-4
PubChem : 46398806
UniChem : BRXCDHOLJPJLLT-SCSAIBSYSA-N
IUPHAR :
Wikipedia :
-butane-2-sulfonate.gif)
Target
Families : (2R)-butane-2-sulfonate ligand of proteins in family: Haloperoxidase
Stucture : 3IA2 Pseudomonas fluorescens esterase complexed to the R-enantiomer of a sulfonate transition state analog
Protein : psefl-este
References (1)
| Title : Different active-site loop orientation in serine hydrolases versus acyltransferases - Jiang_2011_Chembiochem_12_768 |
| Author(s) : Jiang Y , Morley KL , Schrag JD , Kazlauskas RJ |
| Ref : Chembiochem , 12 :768 , 2011 |
| Abstract : Jiang_2011_Chembiochem_12_768 |
| ESTHER : Jiang_2011_Chembiochem_12_768 |
| PubMedSearch : Jiang_2011_Chembiochem_12_768 |
| PubMedID: 21351219 |
| Gene_locus related to this paper: psefl-este |