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Information on EC 2.8.2.15 - steroid sulfotransferase and Organism(s) Homo sapiens

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EC Tree
     2 Transferases
         2.8 Transferring sulfur-containing groups
             2.8.2 Sulfotransferases
                2.8.2.15 steroid sulfotransferase
IUBMB Comments
Broad specificity resembling EC 2.8.2.2 alcohol sulfotransferase, but also acts on estrone.
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This record set is specific for:
Homo sapiens
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Word Map
The taxonomic range for the selected organisms is: Homo sapiens
The enzyme appears in selected viruses and cellular organisms
Synonyms
sult2b1b, sult2b1, dhea-st, hsult2a1, cholesterol sulfotransferase, sult2a, steroid sulfotransferase, dhea sulfotransferase, st2b2, sulfotransferase ii, more
SYNONYM
ORGANISM
UNIPROT
COMMENTARY hide
LITERATURE
ADT sulfotransferase
-
-
cholesterol sulfotransferase
-
-
cytosolic sulfotransferase
dehydroepiandrosterone sulfotransferase
-
-
dehydroepiandrosterone sulfotransferase family 1A member 2
-
-
DHEA sulfotransferase
-
-
DHEA sulphotransferase
-
-
hEST1
-
-
human hydroxysteroid sulfotransferase 2A1
-
hydroxysteroid sulfotransferase
ST2A3
-
-
steroid alcohol sulfotransferase
-
-
-
-
steroid sulfatase
-
-
steroid-/bile acid-sulfotransferase
-
-
steroid/bile acid-sulfotransferase
-
-
steroid/sterol sulfotransferase
-
-
sulfotransferase 2A1
-
-
sulfotransferase 2B1
-
-
sulfotransferase 2B1b
-
-
SULT 1E1
-
-
SULT1B1
-
isoform
SULT1C2
-
isoform
SULT2A1
SULT2B1
additional information
REACTION TYPE
ORGANISM
UNIPROT
COMMENTARY hide
LITERATURE
sulfate group transfer
-
-
-
-
PATHWAY SOURCE
PATHWAYS
SYSTEMATIC NAME
IUBMB Comments
3'-phosphoadenylyl-sulfate:phenolic-steroid sulfotransferase
Broad specificity resembling EC 2.8.2.2 alcohol sulfotransferase, but also acts on estrone.
CAS REGISTRY NUMBER
COMMENTARY hide
9032-76-2
-
SUBSTRATE
PRODUCT                       
REACTION DIAGRAM
ORGANISM
UNIPROT
COMMENTARY
(Substrate) hide
LITERATURE
(Substrate)
COMMENTARY
(Product) hide
LITERATURE
(Product)
Reversibility
r=reversible
ir=irreversible
?=not specified
3'-phosphoadenylyl sulfate + 1-naphthol
adenosine 3',5'-bisphosphate + 1-naphthyl sulfate
show the reaction diagram
-
-
-
-
?
3'-phosphoadenylyl sulfate + 3,4-dihydroxyphenylacetic acid
adenosine 3',5'-bisphosphate + ?
show the reaction diagram
-
-
-
-
?
3'-phosphoadenylyl sulfate + 3alpha-hydroxytibolone
adenosine 3',5'-bisphosphate + 3alpha-hydroxytibolone 3-O-sulfate
show the reaction diagram
3'-phosphoadenylyl sulfate + 3beta-hydroxytibolone
adenosine 3',5'-bisphosphate + 3beta-hydroxytibolone 3-O-sulfate
show the reaction diagram
3'-phosphoadenylyl sulfate + 4'-hydroxy-2,3',4,5'-tetrachlorobiphenyl
adenosine 3',5'-bisphosphate + 4'-hydroxy-2,3',4,5'-tetrachlorobiphenyl 4'-O-sulfate
show the reaction diagram
-
i.e. 4'-OH PCB 68, substrate of SULT1A2
-
-
?
3'-phosphoadenylyl sulfate + 4-androstene-3,17-dione
adenosine 3',5'-bisphosphate + 3-O-sulfo-3,5-androstadien-3-ol-17-one
show the reaction diagram
-
-
-
?
3'-phosphoadenylyl sulfate + 4-hydroxy-2',3,5-trichlorobiphenyl
adenosine 3',5'-bisphosphate + 2',3,5-trichlorobiphenyl-4-yl hydrogen sulfate
show the reaction diagram
-
i.e. 4-OH PCB 34, substrate of SULT1A2
-
-
?
3'-phosphoadenylyl sulfate + 4-nitrophenol
adenosine 3',5'-bisphosphate + 4-nitrophenyl sulfate
show the reaction diagram
-
-
-
-
?
3'-phosphoadenylyl sulfate + 5alpha,6alpha-epoxycholesterol
adenosine 3',5'-bisphosphate + 5alpha,6alpha-epoxycholesteryl sulfate
show the reaction diagram
-
-
-
-
?
3'-phosphoadenylyl sulfate + 5beta,6beta-epoxycholesterol
adenosine 3',5'-bisphosphate + 5beta,6beta-epoxycholesteryl sulfate
show the reaction diagram
-
-
-
-
?
3'-phosphoadenylyl sulfate + 6beta-hydroxytestosterone
adenosine 3',5'-bisphosphate + ?
show the reaction diagram
-
-
-
?
3'-phosphoadenylyl sulfate + 7-oxo-cholesterol
adenosine 3',5'-bisphosphate + 7-oxo-cholesteryl sulfate
show the reaction diagram
-
-
-
-
?
3'-phosphoadenylyl sulfate + 7alpha-hydroxycholesterol
adenosine 3',5'-bisphosphate + 7alpha-hydroxycholesteryl sulfate
show the reaction diagram
-
-
-
-
?
3'-phosphoadenylyl sulfate + 7beta-hydroxycholesterol
adenosine 3',5'-bisphosphate + 7beta-hydroxycholesteryl sulfate
show the reaction diagram
-
-
-
-
?
3'-phosphoadenylyl sulfate + aldosterone
adenosine 3',5'-bisphosphate + ?
show the reaction diagram
-
-
-
?
3'-phosphoadenylyl sulfate + beta-estradiol
adenosine 3',5'-bisphosphate + beta-estradiol 3-sulfate
show the reaction diagram
-
-
-
-
?
3'-phosphoadenylyl sulfate + cholesterol
adenosine 3',5'-bisphosphate + cholesterol sulfate
show the reaction diagram
-
-
-
?
3'-phosphoadenylyl sulfate + cholesterol
adenosine 3',5'-bisphosphate + cholesteryl sulfate
show the reaction diagram
-
-
-
-
?
3'-phosphoadenylyl sulfate + cortisol
adenosine 3',5'-bisphosphate + ?
show the reaction diagram
-
-
-
?
3'-phosphoadenylyl sulfate + cortisone
adenosine 3',5'-bisphosphate + ?
show the reaction diagram
-
-
-
?
3'-phosphoadenylyl sulfate + dehydroepiandrosterone
adenosine 3',5'-bisphosphate + ?
show the reaction diagram
-
-
-
-
?
3'-phosphoadenylyl sulfate + dehydroepiandrosterone
adenosine 3',5'-bisphosphate + dehydroepiandrosterone 3-O-sulfate
show the reaction diagram
3'-phosphoadenylyl sulfate + dehydroepiandrosterone
adenosine 3',5'-bisphosphate + dehydroepiandrosterone O-sulfate
show the reaction diagram
-
-
-
-
?
3'-phosphoadenylyl sulfate + dehydroepiandrosterone
adenosine 3',5'-bisphosphate + dehydroepiandrosterone sulfate
show the reaction diagram
3'-phosphoadenylyl sulfate + desipramine
adenosine 3',5'-bisphosphate + ?
show the reaction diagram
-
-
-
-
?
3'-phosphoadenylyl sulfate + L-triiodothyronine
adenosine 3',5'-bisphosphate + ?
show the reaction diagram
-
-
-
-
?
3'-phosphoadenylyl sulfate + oxysterol
adenosine 3',5'-bisphosphate + oxysterol sulfate
show the reaction diagram
-
-
-
?
3'-phosphoadenylyl sulfate + pregnenolone
adenosine 3',5'-bisphosphate + pregnenolone sulfate
show the reaction diagram
3'-phosphoadenylyl sulfate + progesterone
adenosine 3',5'-bisphosphate + progesterone sulfate
show the reaction diagram
-
-
-
?
3'-phosphoadenylyl sulfate + testosterone
adenosine 3',5'-bisphosphate + ?
show the reaction diagram
-
-
-
?
3'-phosphoadenylyl sulfate + xanthurenic acid
adenosine 3',5'-bisphosphate + ?
show the reaction diagram
-
-
-
-
?
3'-phosphoadenylylsulfate + 11-deoxycorticosterone
adenosine 3',5'-bisphosphate + 11-deoxycorticosterone sulfate
show the reaction diagram
-
21-hydroxypregn-4-en-3,20-dione
pregn-4-en-3-one 21-sulfate
r
3'-phosphoadenylylsulfate + 16-hydroxy-estradiol
adenosine 3',5'-bisphosphate + ?
show the reaction diagram
-
-
-
-
r
3'-phosphoadenylylsulfate + 17alpha-estradiol
adenosine 3',5'-bisphosphate + ?
show the reaction diagram
-
estra-1,3,5(10)-triene-3,17alpha-diol
-
-
r
3'-phosphoadenylylsulfate + 17alpha-ethynylestradiol
adenosine 3',5'-bisphosphate + 17alpha-ethynylestradiol 3-sulfate
show the reaction diagram
-
celecoxib switches sulfation from the 3-O-position to the 17beta-O-position
-
-
?
3'-phosphoadenylylsulfate + 17beta-estradiol
adenosine 3',5'-bisphosphate + ?
show the reaction diagram
3'-phosphoadenylylsulfate + 2-hydroxy-estradiol
adenosine 3',5'-bisphosphate + ?
show the reaction diagram
-
-
-
-
r
3'-phosphoadenylylsulfate + 3alpha-hydroxy-5alpha-androstan-17-one
adenosine 3',5'-bisphosphate + 5alpha-androstan-17-one 3-sulfate
show the reaction diagram
3'-phosphoadenylylsulfate + 3beta-hydroxy-5alpha-androstan-17-one
adenosine 3',5'-bisphosphate + 5alpha-androstan-17-one 3-sulfate
show the reaction diagram
3'-phosphoadenylylsulfate + 4'-hydroxy-2',3,4-trichlorobiphenyl
adenosine 3',5'-bisphosphate + ?
show the reaction diagram
-
-
-
-
?
3'-phosphoadenylylsulfate + 4'-hydroxy-2,3',4-trichlorobiphenyl
adenosine 3',5'-bisphosphate + ?
show the reaction diagram
-
-
-
-
?
3'-phosphoadenylylsulfate + 4-hydroxy-2',3,5-trichlorobiphenyl
adenosine 3',5'-bisphosphate + ?
show the reaction diagram
-
-
-
-
?
3'-phosphoadenylylsulfate + 4-hydroxy-2,4'-dichlorobiphenyl
adenosine 3',5'-bisphosphate + ?
show the reaction diagram
-
-
-
-
?
3'-phosphoadenylylsulfate + 4-hydroxy-3,3',5-trichlorobiphenyl
adenosine 3',5'-bisphosphate + ?
show the reaction diagram
-
-
-
-
?
3'-phosphoadenylylsulfate + 4-hydroxy-3,3'-dichlorobiphenyl
adenosine 3',5'-bisphosphate + ?
show the reaction diagram
-
-
-
-
?
3'-phosphoadenylylsulfate + 4-hydroxy-3,5-dichlorobiphenyl
adenosine 3',5'-bisphosphate + ?
show the reaction diagram
-
-
-
-
?
3'-phosphoadenylylsulfate + 4-hydroxy-estradiol
adenosine 3',5'-bisphosphate + ?
show the reaction diagram
-
-
-
-
r
3'-phosphoadenylylsulfate + androst-5-ene-3beta,17beta-diol
adenosine 3',5'-bisphosphate + ?
show the reaction diagram
-
-
-
-
r
3'-phosphoadenylylsulfate + androst-5-ene-3beta17alpha-diol
adenosine 3',5'-bisphosphate + ?
show the reaction diagram
-
-
-
-
r
3'-phosphoadenylylsulfate + androstenediol
adenosine 3',5'-bisphosphate + ?
show the reaction diagram
SULT2B1 isoform
-
-
r
3'-phosphoadenylylsulfate + androsterone
adenosine 3',5'-bisphosphate + 5alpha-androstane-17-one 3-sulfate
show the reaction diagram
3'-phosphoadenylylsulfate + cholesterol
adenosine 3',5'-bisphosphate + cholesterol 3-sulfate
show the reaction diagram
3'-phosphoadenylylsulfate + cholesterol
adenosine 3',5'-bisphosphate + cholesterol sulfate
show the reaction diagram
-
sulfurylated at low rate
-
-
r
3'-phosphoadenylylsulfate + dehydroepiandrosterone
adenosine 3',5'-bisphosphate + androst-5-en-17-one 3-sulfate
show the reaction diagram
3'-phosphoadenylylsulfate + dehydroepiandrosterone
adenosine 3',5'-bisphosphate + dehydroepiandrosterone 3-sulfate
show the reaction diagram
3'-phosphoadenylylsulfate + epitestosterone
adenosine 3',5'-bisphosphate + epitestosterone sulfate
show the reaction diagram
-
17alpha-hydroxyandrost-4-en-3-one
androst-4-en-3-one 17-sulfate
r
3'-phosphoadenylylsulfate + estradiol
adenosine 3',5'-bisphosphate + ?
show the reaction diagram
-
-
-
-
?
3'-phosphoadenylylsulfate + estriol
adenosine 3',5'-bisphosphate + estriol sulfate
show the reaction diagram
-
-
-
r
3'-phosphoadenylylsulfate + estrone
adenosine 3',5'-bisphosphate + estrone sulfate
show the reaction diagram
3'-phosphoadenylylsulfate + etiocholanone
adenosine 3',5'-bisphosphate + etiocholanone sulfate
show the reaction diagram
3'-phosphoadenylylsulfate + genistein
adenosine 3',5'-bisphosphate + ?
show the reaction diagram
-
-
-
r
3'-phosphoadenylylsulfate + pregnenolone
adenosine 3',5'-bisphosphate + pregnenolone sulfate
show the reaction diagram
3'-phosphoadenylylsulfate + testosterone
adenosine 3',5'-bisphosphate + testosterone sulfate
show the reaction diagram
additional information
?
-
NATURAL SUBSTRATE
NATURAL PRODUCT
REACTION DIAGRAM
ORGANISM
UNIPROT
COMMENTARY
(Substrate) hide
LITERATURE
(Substrate)
COMMENTARY
(Product) hide
LITERATURE
(Product)
REVERSIBILITY
r=reversible
ir=irreversible
?=not specified
3'-phosphoadenylyl sulfate + 1-naphthol
adenosine 3',5'-bisphosphate + 1-naphthyl sulfate
show the reaction diagram
-
-
-
-
?
3'-phosphoadenylyl sulfate + 3,4-dihydroxyphenylacetic acid
adenosine 3',5'-bisphosphate + ?
show the reaction diagram
-
-
-
-
?
3'-phosphoadenylyl sulfate + 3alpha-hydroxytibolone
adenosine 3',5'-bisphosphate + 3alpha-hydroxytibolone 3-O-sulfate
show the reaction diagram
-
sulfation inactivates the hydroxylated metabolite of tibolone, a synthetic steroid used for the treatment for climacteric symptoms and postmenopausal osteoporosis
-
-
?
3'-phosphoadenylyl sulfate + 3beta-hydroxytibolone
adenosine 3',5'-bisphosphate + 3beta-hydroxytibolone 3-O-sulfate
show the reaction diagram
-
sulfation inactivates the hydroxylated metabolite of tibolone, a synthetic steroid used for the treatment for climacteric symptoms and postmenopausal osteoporosis
-
-
?
3'-phosphoadenylyl sulfate + 4-androstene-3,17-dione
adenosine 3',5'-bisphosphate + 3-O-sulfo-3,5-androstadien-3-ol-17-one
show the reaction diagram
-
-
-
?
3'-phosphoadenylyl sulfate + 4-nitrophenol
adenosine 3',5'-bisphosphate + 4-nitrophenyl sulfate
show the reaction diagram
-
-
-
-
?
3'-phosphoadenylyl sulfate + beta-estradiol
adenosine 3',5'-bisphosphate + beta-estradiol 3-sulfate
show the reaction diagram
-
-
-
-
?
3'-phosphoadenylyl sulfate + dehydroepiandrosterone
adenosine 3',5'-bisphosphate + ?
show the reaction diagram
-
-
-
-
?
3'-phosphoadenylyl sulfate + dehydroepiandrosterone
adenosine 3',5'-bisphosphate + dehydroepiandrosterone 3-O-sulfate
show the reaction diagram
3'-phosphoadenylyl sulfate + dehydroepiandrosterone
adenosine 3',5'-bisphosphate + dehydroepiandrosterone O-sulfate
show the reaction diagram
-
-
-
-
?
3'-phosphoadenylyl sulfate + dehydroepiandrosterone
adenosine 3',5'-bisphosphate + dehydroepiandrosterone sulfate
show the reaction diagram
-
-
-
?
3'-phosphoadenylyl sulfate + desipramine
adenosine 3',5'-bisphosphate + ?
show the reaction diagram
-
-
-
-
?
3'-phosphoadenylyl sulfate + L-triiodothyronine
adenosine 3',5'-bisphosphate + ?
show the reaction diagram
-
-
-
-
?
3'-phosphoadenylyl sulfate + pregnenolone
adenosine 3',5'-bisphosphate + pregnenolone sulfate
show the reaction diagram
-
-
-
?
3'-phosphoadenylyl sulfate + xanthurenic acid
adenosine 3',5'-bisphosphate + ?
show the reaction diagram
-
-
-
-
?
3'-phosphoadenylylsulfate + 4'-hydroxy-2',3,4-trichlorobiphenyl
adenosine 3',5'-bisphosphate + ?
show the reaction diagram
-
-
-
-
?
3'-phosphoadenylylsulfate + 4'-hydroxy-2,3',4-trichlorobiphenyl
adenosine 3',5'-bisphosphate + ?
show the reaction diagram
-
-
-
-
?
3'-phosphoadenylylsulfate + 4-hydroxy-2',3,5-trichlorobiphenyl
adenosine 3',5'-bisphosphate + ?
show the reaction diagram
-
-
-
-
?
3'-phosphoadenylylsulfate + 4-hydroxy-2,4'-dichlorobiphenyl
adenosine 3',5'-bisphosphate + ?
show the reaction diagram
-
-
-
-
?
3'-phosphoadenylylsulfate + 4-hydroxy-3,3',5-trichlorobiphenyl
adenosine 3',5'-bisphosphate + ?
show the reaction diagram
-
-
-
-
?
3'-phosphoadenylylsulfate + 4-hydroxy-3,3'-dichlorobiphenyl
adenosine 3',5'-bisphosphate + ?
show the reaction diagram
-
-
-
-
?
3'-phosphoadenylylsulfate + 4-hydroxy-3,5-dichlorobiphenyl
adenosine 3',5'-bisphosphate + ?
show the reaction diagram
-
-
-
-
?
3'-phosphoadenylylsulfate + androsterone
adenosine 3',5'-bisphosphate + 5alpha-androstane-17-one 3-sulfate
show the reaction diagram
-
enzyme is an androsterone sulfotransferase as well as a dehydroepiandrosterone sulfotransferase, implying an important role in steroid homeostasis for the adrenals and liver
-
-
?
3'-phosphoadenylylsulfate + cholesterol
adenosine 3',5'-bisphosphate + cholesterol 3-sulfate
show the reaction diagram
3'-phosphoadenylylsulfate + dehydroepiandrosterone
adenosine 3',5'-bisphosphate + androst-5-en-17-one 3-sulfate
show the reaction diagram
-
enzyme is an androsterone sulfotransferase as well as a dehydroepiandrosterone sulfotransferase, implying an important role in steroid homeostasis for the adrenals and liver
-
-
?
3'-phosphoadenylylsulfate + dehydroepiandrosterone
adenosine 3',5'-bisphosphate + dehydroepiandrosterone 3-sulfate
show the reaction diagram
additional information
?
-
METALS and IONS
ORGANISM
UNIPROT
COMMENTARY hide
LITERATURE
NaCl
-
activates
INHIBITOR
ORGANISM
UNIPROT
COMMENTARY hide
LITERATURE
IMAGE
2,3-dichlorophenol
-
IC50: 0.0007 mM, vs. 10 nM estradiol
2,4-Dichlorophenol
-
IC50: 0.0007 mM, vs. 10 nM estradiol
2,5-dichlorophenol
-
IC50: 0.0022 mM, vs. 10 nM estradiol
2,6-Dichloro-4-nitrophenol
-
non-specific SULT inhibitor
2,6-dichlorophenol
-
IC50: 0.0016 mM, vs. 10 nM estradiol
2-chlorophenol
-
IC50: 0.02 mM, vs. 10 nM estradiol
2-phenylphenol
-
IC50: 0.0052 mM, vs. 10 nM estradiol
3',4'-dihydroxy-2,3-dichlorobiphenyl
-
-
3',4'-dihydroxy-4-monochlorobiphenyl
-
-
3,4-dichlorophenol
-
IC50: 0.013 mM, vs. 10 nM estradiol
3,5-dichlorophenol
-
IC50: 0.017 mM, vs. 10 nM estradiol
3-chlorophenol
-
IC50: 0.13 mM, vs. 10 nM estradiol
4'-hydroxy-2',3,4-trichlorobiphenyl
-
-
4'-hydroxy-2,3',4,5'-tetrachlorobiphenyl
-
-
4'-hydroxy-2,3',4-trichlorobiphenyl
-
-
4'-hydroxy-2,3'-dichlorobiphenyl
-
-
4'-hydroxy-2,5-dichlorobiphenyl
4'-hydroxy-3,4-dichlorobiphenyl
-
-
4'-hydroxy-4-monochlorobiphenyl
-
-
4-chloro-3-methylphenol
-
IC50: 0.024 mM, vs. 10 nM estradiol
4-Chlorophenol
-
IC50: 0.11 mM, vs. 10 nM estradiol
4-hydroxy-2',3,5-trichlorobiphenyl
4-hydroxy-2,4'-dichlorobiphenyl
-
-
4-hydroxy-3,3',5-trichlorobiphenyl
-
-
4-hydroxy-3,3'-dichlorobiphenyl
-
-
4-hydroxy-3,5-dichlorobiphenyl
-
-
4-hydroxytamoxifen
noncompetitive inhibition
5,7-dichlorokynurenic acid
-
-
6'-hydroxy-3,3'-4-trichlorobiphenyl
-
-
adenosine 3',5'-bisphosphate
-
-
androsterone
-
stronger substrate inhibition than dehydroepiandrosterone adenosine
celecoxib
-
heterotrophic modulator, 3-O-sulfation is inhibited by celecoxib to the same extent, independent of the concentration of 17alpha-ethynylestradiol, switches sulfation from the 3-O-position to the 17beta-O-position
DCNP
-
-
dehydroepiandrosterone
endoxifen
i.e. 4-hydroxy-N-desmethyltamoxifen, potent noncompetitive inhibition
gavestinel
-
i.e. 4,6-dichloro-3-[(1E)-3-oxo-3-(phenylamino)-1-propenyl]-1H-indole-2-carboxylic acid sodium salt
Kynurenic acid
-
exhibits selective inhibitory effects on Sult1b1-mediated sulfation of various compounds with IC50 values in the low micromolar range
L689,560
-
i.e. trans-2-carboxy-5,7-dichloro-4-phenylaminocarboxylamino-1,2,3,4-tetrahydroquinoline
L701,324
-
i.e. 7-chloro-4-hydroxy-3(3-phenoxy)phenyl-2(H)-quinolinone
Mefenamic acid
-
-
N-demethyltamoxifen
competitive inhibition
pregnenolone
-
substrate inhibition
tamoxifen N-oxide
noncompetitive inhibition
additional information
-
ACTIVATING COMPOUND
ORGANISM
UNIPROT
COMMENTARY hide
LITERATURE
IMAGE
celecoxib
-
heterotrophic modulator, switches sulfation from the 3-O-position to the 17beta-O-position and activates such that the total sulfated product exceed product formation by the native enzyme, 3fold to 4fold at 0.25 mM celecoxib
additional information
-
KM VALUE [mM]
SUBSTRATE
ORGANISM
UNIPROT
COMMENTARY hide
LITERATURE
IMAGE
0.0012
1-naphthol
-
isoform SULT1B1, in 50 mM Tris/HCl buffer, pH 7.4, 1 mM dithiothreitol, 5 mM MgCl2, and 1 mg/ml bovine serum albumin, at 37°C
0.191
17alpha-ethynylestradiol
-
-
0.00001
17beta-estradiol
-
pH 7.4, 37°C
0.0003 - 0.0096
3'-phosphoadenylylsulfate
0.00079
3alpha-tibolone
-
pH 6.0, 37°C, recombinant SULT1A1
0.0016 - 0.0185
3beta-hydroxyandrost-5-ene-17-one
0.00056
3beta-tibolone
-
pH 7.0, 37°C, recombinant SULT1A1
0.0262
4'-hydroxy-2',3,4-trichlorobiphenyl
-
in 0.25 M potassium phosphate at pH 7.0, and 7.5 mM 2-mercaptoethanol, at 37°C
0.0086
4'-hydroxy-2,3',4-trichlorobiphenyl
-
in 0.25 M potassium phosphate at pH 7.0, and 7.5 mM 2-mercaptoethanol, at 37°C
0.0081 - 0.046
4-hydroxy-2',3,5-trichlorobiphenyl
0.0568
4-hydroxy-2,4'-dichlorobiphenyl
-
in 0.25 M potassium phosphate at pH 7.0, and 7.5 mM 2-mercaptoethanol, at 37°C
0.0136
4-hydroxy-3,3',5-trichlorobiphenyl
-
in 0.25 M potassium phosphate at pH 7.0, and 7.5 mM 2-mercaptoethanol, at 37°C
0.0366
4-hydroxy-3,3'-dichlorobiphenyl
-
in 0.25 M potassium phosphate at pH 7.0, and 7.5 mM 2-mercaptoethanol, at 37°C
0.0085
4-hydroxy-3,5-dichlorobiphenyl
-
in 0.25 M potassium phosphate at pH 7.0, and 7.5 mM 2-mercaptoethanol, at 37°C
0.0399
4-nitrophenol
-
isoform SULT1B1, in 50 mM Tris/HCl buffer, pH 7.4, 1 mM dithiothreitol, 5 mM MgCl2, and 1 mg/ml bovine serum albumin, at 37°C
0.0021
androsterone
-
pH 7.5, 37°C
0.0006 - 0.025
dehydroepiandrosterone
0.0000105
estrone
-
pH 7.4, 37°C
0.145
L-triiodothyronine
-
isoform SULT1B1, in 50 mM Tris/HCl buffer, pH 7.4, 1 mM dithiothreitol, 5 mM MgCl2, and 1 mg/ml bovine serum albumin, at 37°C
0.0018 - 0.0072
pregnenolone
0.0063 - 0.206
xanthurenic acid
additional information
additional information
-
TURNOVER NUMBER [1/s]
SUBSTRATE
ORGANISM
UNIPROT
COMMENTARY hide
LITERATURE
IMAGE
0.13
androsterone
-
pH 7.5, 37°C
0.1
dehydroepiandrosterone
-
pH 7.5, 37°C
Ki VALUE [mM]
INHIBITOR
ORGANISM
UNIPROT
COMMENTARY hide
LITERATURE
IMAGE
0.253
4-hydroxy-2',3,5-trichlorobiphenyl
-
pH 7.0, 37°C, recombinant SULT1A2
0.0127 - 0.0194
4-hydroxytamoxifen
0.0016
adenosine 3',5'-bisphosphate
-
pH 7.5
0.0038
androsterone
-
pH 7.5, 37°C
0.008 - 0.112
dehydroepiandrosterone
0.0028 - 0.0035
endoxifen
0.0098 - 0.0172
N-demethyltamoxifen
0.0096 - 0.0169
tamoxifen N-oxide
IC50 VALUE [mM]
INHIBITOR
ORGANISM
UNIPROT
COMMENTARY hide
LITERATURE
IMAGE
0.0007
2,3-dichlorophenol
Homo sapiens
-
IC50: 0.0007 mM, vs. 10 nM estradiol
0.0007
2,4-Dichlorophenol
Homo sapiens
-
IC50: 0.0007 mM, vs. 10 nM estradiol
0.0022
2,5-dichlorophenol
Homo sapiens
-
IC50: 0.0022 mM, vs. 10 nM estradiol
0.0342 - 24
2,6-Dichloro-4-nitrophenol
0.0016
2,6-dichlorophenol
Homo sapiens
-
IC50: 0.0016 mM, vs. 10 nM estradiol
0.02
2-chlorophenol
Homo sapiens
-
IC50: 0.02 mM, vs. 10 nM estradiol
0.0052
2-phenylphenol
Homo sapiens
-
IC50: 0.0052 mM, vs. 10 nM estradiol
0.016
3',4'-dihydroxy-2,3-dichlorobiphenyl
Homo sapiens
-
in 0.25 M potassium phosphate at pH 7.0, and 7.5 mM 2-mercaptoethanol, at 37°C
0.096
3',4'-dihydroxy-4-monochlorobiphenyl
Homo sapiens
-
in 0.25 M potassium phosphate at pH 7.0, and 7.5 mM 2-mercaptoethanol, at 37°C
0.013
3,4-dichlorophenol
Homo sapiens
-
IC50: 0.013 mM, vs. 10 nM estradiol
0.017
3,5-dichlorophenol
Homo sapiens
-
IC50: 0.017 mM, vs. 10 nM estradiol
0.13
3-chlorophenol
Homo sapiens
-
IC50: 0.13 mM, vs. 10 nM estradiol
0.0025
4'-hydroxy-2',3,4-trichlorobiphenyl
Homo sapiens
-
in 0.25 M potassium phosphate at pH 7.0, and 7.5 mM 2-mercaptoethanol, at 37°C
0.0008
4'-hydroxy-2,3',4,5'-tetrachlorobiphenyl
Homo sapiens
-
in 0.25 M potassium phosphate at pH 7.0, and 7.5 mM 2-mercaptoethanol, at 37°C
0.0044
4'-hydroxy-2,3',4-trichlorobiphenyl
Homo sapiens
-
in 0.25 M potassium phosphate at pH 7.0, and 7.5 mM 2-mercaptoethanol, at 37°C
0.0098
4'-hydroxy-2,3'-dichlorobiphenyl
Homo sapiens
-
in 0.25 M potassium phosphate at pH 7.0, and 7.5 mM 2-mercaptoethanol, at 37°C
0.0039 - 0.0075
4'-hydroxy-2,5-dichlorobiphenyl
0.016
4'-hydroxy-3,4-dichlorobiphenyl
Homo sapiens
-
in 0.25 M potassium phosphate at pH 7.0, and 7.5 mM 2-mercaptoethanol, at 37°C
0.028
4'-hydroxy-4-monochlorobiphenyl
Homo sapiens
-
in 0.25 M potassium phosphate at pH 7.0, and 7.5 mM 2-mercaptoethanol, at 37°C
0.024
4-chloro-3-methylphenol
Homo sapiens
-
IC50: 0.024 mM, vs. 10 nM estradiol
0.11
4-Chlorophenol
Homo sapiens
-
IC50: 0.11 mM, vs. 10 nM estradiol
0.0006
4-hydroxy-2',3,5-trichlorobiphenyl
Homo sapiens
-
in 0.25 M potassium phosphate at pH 7.0, and 7.5 mM 2-mercaptoethanol, at 37°C
0.01
4-hydroxy-2,4'-dichlorobiphenyl
Homo sapiens
-
in 0.25 M potassium phosphate at pH 7.0, and 7.5 mM 2-mercaptoethanol, at 37°C
0.0044
4-hydroxy-3,3',5-trichlorobiphenyl
Homo sapiens
-
in 0.25 M potassium phosphate at pH 7.0, and 7.5 mM 2-mercaptoethanol, at 37°C
0.014
4-hydroxy-3,3'-dichlorobiphenyl
Homo sapiens
-
in 0.25 M potassium phosphate at pH 7.0, and 7.5 mM 2-mercaptoethanol, at 37°C
0.013
4-hydroxy-3,5-dichlorobiphenyl
Homo sapiens
-
in 0.25 M potassium phosphate at pH 7.0, and 7.5 mM 2-mercaptoethanol, at 37°C
0.01 - 0.0167
4-hydroxytamoxifen
0.1642 - 0.2536
5,7-dichlorokynurenic acid
0.016
6'-hydroxy-3,3'-4-trichlorobiphenyl
Homo sapiens
-
in 0.25 M potassium phosphate at pH 7.0, and 7.5 mM 2-mercaptoethanol, at 37°C
0.0017 - 0.0027
endoxifen
0.0012 - 0.0017
gavestinel
0.0337 - 9
Kynurenic acid
0.0473 - 0.0536
L689,560
0.005
Mefenamic acid
0.0083 - 0.015
N-demethyltamoxifen
0.0111 - 0.0161
tamoxifen N-oxide
SPECIFIC ACTIVITY [µmol/min/mg]
ORGANISM
UNIPROT
COMMENTARY hide
LITERATURE
0.0073
-
-
0.0175
-
purified recombinant SULT1A2, substrate 4'-hydroxy-2,3',4,5'-tetrachlorobiphenyl
0.0201
-
-
0.027
-
purified recombinant SULT1A2, substrate 4-hydroxy-2',3,5-trichlorobiphenyl
0.133
-
-
pH OPTIMUM
ORGANISM
UNIPROT
COMMENTARY hide
LITERATURE
6 - 7
-
assay at
7
-
assay at
7.5
-
assay at
TEMPERATURE OPTIMUM
ORGANISM
UNIPROT
COMMENTARY hide
LITERATURE
37
-
assay at
ORGANISM
COMMENTARY hide
LITERATURE
UNIPROT
SEQUENCE DB
SOURCE
SOURCE TISSUE
ORGANISM
UNIPROT
COMMENTARY hide
LITERATURE
SOURCE
-
aortic smooth muscle cell line CRL-1999
Manually annotated by BRENDA team
-
Ishikawa adenocarcinoma
Manually annotated by BRENDA team
-
foetal tissue is a much richer source of enzyme than adult
Manually annotated by BRENDA team
-
aortic smooth muscle cell line CRL-1999
Manually annotated by BRENDA team
-
postmenopausal, SULT2A1
Manually annotated by BRENDA team
-
highest expression
Manually annotated by BRENDA team
additional information
LOCALIZATION
ORGANISM
UNIPROT
COMMENTARY hide
GeneOntology No.
LITERATURE
SOURCE
GENERAL INFORMATION
ORGANISM
UNIPROT
COMMENTARY hide
LITERATURE
malfunction
-
knockdown of SULT2B1 in Hepa1-6 cells induces cell-cycle arrest and apoptosis and suppresses tumorigenesis in vivo
metabolism
enzyme SULT1E1 cannot catalyze the sulfation of either of these two DELTA4-3-ketosteroids, whereas SULT2B1b exhibits weak activity toward only 4-androstene-3,17-dione (7.1 pmol/min/mg enzyme), but not progesterone. Thus, SULT2A1 may be the only major human SULT that is capable of sulfating DELTA4-3-ketosteroids, particularly 4-androstene-3,17-dione
physiological function
additional information
modeling of the binding of hSULT2A1 with substrate 4-androstene-3,17-dione using the crystal structure of 3-ketosteroid-DELTA4-(5alpha)-dehydrogenase from Rhodococcus jostii RHA1 in complex with 4-androstene-3,17-dione (PDB ID 4AT2) and two crystal structures of human SULT2A1 in complex with DHEA and lithocholic acid (PDB IDs 1J99 and 3F3Y) as templates. The intact steroid nucleus is important for the binding of DELTA4-3-keto steroids by SULT2A1. Proposed mechanism of DELTA4-3-ketosteroid sulfation by SULT2A1, overview. Enzyme residues W77 and H99 are likely involved in the catalysis, possibly in the deprotonation of C-6. The sulfation of 4-androstene-3,17-dione might progress through the formation of a hydroxyl group which is a typical target for sulfation, it would require the isomerization of 4-androstene-3,17-dione from a keto form to an enol form
UNIPROT
ENTRY NAME
ORGANISM
NO. OF AA
NO. OF TRANSM. HELICES
MOLECULAR WEIGHT[Da]
SOURCE
SEQUENCE
LOCALIZATION PREDICTION?
ST2B1_HUMAN
365
0
41308
Swiss-Prot
Mitochondrion (Reliability: 1)
ST2A1_HUMAN
285
0
33780
Swiss-Prot
-
MOLECULAR WEIGHT
ORGANISM
UNIPROT
COMMENTARY hide
LITERATURE
33000
-
immunoblot analysis, antibodies against rat liver sulfotransferases
33785
-
x * 33785, calculated from amino acid sequence
34000
34500
-
2 * 34500, SDS-PAGE
35000
39620
isoform SULT2B1a
41000
-
x * 41000, SDS-PAGE
41300
isoform SULT2B1b
68000
-
sucrose density gradient ultracentrifugation
68000 - 70000
-
gel filtration
SUBUNIT
ORGANISM
UNIPROT
COMMENTARY hide
LITERATURE
dimer
additional information
-
isozyme SULT2B1b has an extension at the proline- and serine-rich carboxyl end of about 53 amino acids
POSTTRANSLATIONAL MODIFICATION
ORGANISM
UNIPROT
COMMENTARY hide
LITERATURE
phosphoprotein
CRYSTALLIZATION (Commentary)
ORGANISM
UNIPROT
LITERATURE
hanging drop vapor diffusion technique, structure of human dehydroepiandrosterone adenosine sulfotransferase in complex with androsterone has been solved at 2.7 A resolution
-
PROTEIN VARIANTS
ORGANISM
UNIPROT
COMMENTARY hide
LITERATURE
A679G
-
naturally occuring polymorphisms of SULT2A1, genotyping, SULT2A1 variant allele frequencies in African-American populations, overview
G187C
-
naturally occuring polymorphisms of SULT2A1, genotyping, SULT2A1 variant allele frequencies in African-American populations, overview
G781A
-
naturally occuring polymorphisms of SULT2A1, genotyping, SULT2A1 variant allele frequencies in African-American populations, overview
H99A
site-directed mutagenesis, 50% reduced sulfating activity toward 4-androstene-3,17-dione compared to wild-type
H99S
site-directed mutagenesis, mutant H99S shows complete loss of the sulfating activity toward 4-androstene-3,17-dione
W77A
site-directed mutagenesis, 50% reduced sulfating activity toward 4-androstene-3,17-dione compared to wild-type
Y160F
site-directed mutagenesis, unaltered sulfating activity toward 4-androstene-3,17-dione compared to wild-type
Y231F
site-directed mutagenesis, unaltered sulfating activity toward 4-androstene-3,17-dione compared to wild-type
additional information
TEMPERATURE STABILITY
ORGANISM
UNIPROT
COMMENTARY hide
LITERATURE
42
-
after 30 min, dehydroepiandrosterone sulfation activity with recombinant truncated SULT2B1b is decreased 3.5fold more than that of recombinant full-length SULT2B1b, after 45 min,the truncated SULT2B1b activity is completely eliminated, whereas full-length SULT2B1b still maintains about 70% of its original activity
42 - 45
-
truncated SULT2B1b is more sensitive to thermal inactivation than the full-length enzyme. After incubation at 42°C for 30 min, dehydroepiandrosterone sulfation activity with truncated SULT2B1b is decreased 3.5fold more than that of full-length enzyme. After 45 min of incubation at 42°C, truncated SULT2B1b activity is completely eliminated, whereas full-length SULT2B1b still maintains about 70% of its original activity
additional information
-
the proline- and serine-rich carboxyl end is an important site in the immunogenicity, nuclear translocation, kinetic activity, and thermostability of SULT2B1b
GENERAL STABILITY
ORGANISM
UNIPROT
LITERATURE
removal of the extension at the proline- and serine-rich carboxyl end of about 53 amino acids significantly decreases the thermostability of the expressed enzyme as well as decreasing the rate of dehydroepiandrosterone sulfation
-
STORAGE STABILITY
ORGANISM
UNIPROT
LITERATURE
-70°C, stored in glass ampoules , 0.05 M Tris-HCl buffer, pH 7.5, 0.1 mM DTT, 2% propylene glycol, 1 mg/ml protein, no significant difference in activity observed after storage for 3.5 months
-
0°C, redialyzed againstTris/thiol buffer, stored under N2, activity retains for at least 4 weeks
-
PURIFICATION (Commentary)
ORGANISM
UNIPROT
LITERATURE
DE-52 column chromatography and hydroxyapatite column chromatography
DE52 anion exchange column chromatography and hydroxyapatite column chromatography
-
Ni-NTA agarose column chromatography
-
Ni-NTA column chromatography and Protein A-Sepharose column chromatography
-
recombinant enzyme, expressed in Escherichia coli
-
recombinant His-tagged full-length SULT2B1b as well as truncated SULT2B1b without the PSC extension from Escherichia coli strain DH5alpha by nickel affinity chromatography
-
CLONED (Commentary)
ORGANISM
UNIPROT
LITERATURE
baculovirus expression-system, expression in Sf9 cells
-
cDNA for isozymes STS and EST cloned
-
cloning of 5'-flanking region of SULT2A1 and expression of a SULT2A1-reporter construct in Caco-2 cells, transcriptional regulation mechanism analysis, co-expression of human nuclear receptors constitutive androstane receptor CAR and retinoid X receptor alpha RXRalpha which are involved in the regulation, electrophoretic mobility shift assay for interaction study, overview
-
DHEA-ST cDNA cloned and sequenced from human adrenal cDNA library, expression vectors transfected into 293 cells, gene hEST, Hugo nomenclature named it STM gene, because it also codes for monoamine-sulfating phenolsulfotransferase M-PST
-
enzyme expression induction by 1alpha,25-dihydroxyvitamin D3 via the vitamin D responsive element C/ERB-alpha, but not C/ERB-beta, coactivators p300, steroid receptor coactivator 1 and 2, SRC-1 and SRC-2, but not SRC-3, are also required, regulation of transcription and translation, overview, co-expression of SULT2A1 with C/ERB-alpha and 1alpha,25-dihydroxyvitamin D3 in murine NIH3T3 cells
-
expressed in Escherichia coli BL21(DE3) cells
expressed in livers from Rattus norvegicus and Mus musculus by using a recombinant adenovirus
-
expression and expression analysis of wild-type and mutant SULT2A1
-
expression of His-tagged full-length SULT2B1b and truncated SULT2B1b without the PSC extension in Escherichia coli strain DH5alpha and in human BeWo choriocarcinoma cells, translocation of the wild-type enzyme to nuclei, but not of the truncation mutant
-
expression of SULT1A2 in Escherichia coli strain BL21 (DE3)
-
expression of SULT2B1b eliminates the cytotoxic effect of 7-oxo-cholesterol on 293T cells, which are normally devoid of SULT2B1b
-
full-length isoform SULT2B1b as well as truncated SULT2B1b without the PS proline- and serine-rich carboxyl extension are expressed in Escherichia coli XL1-Blue cells
-
gene SULT2A1, expression and regulation analysis, the enzyme promoter contains composite elements inducible by nuclear receptors pregnane X receptor, PXR, and constitutive androstane receptor, CAR, synergizing effects by HNF4alpha binding at a site near the promoter, overview
-
gene SULT2A1, recombinant expression of wild-type and mutant enzymes in Escherichia coli strain BL21
hEST1 and hEST2 cloned and overexpressed in Escherichia coli in fusion with GST
-
SULT2A1 is a target gene for metabolic regulation/induction by thyroid hormone T3, T3 overexpressing Hep-G2 cells, with co-expression of the T3-receptor-alpha, show increased SULT2A1 expression in a DNA microarray analysis, 5fold at protein level and 9fold at mRNA level, which is inhibited by cycloheximide indicating an indirect regulation mechanism via the transcription factor steroidogenic factor 1, SF1, SULT2A1 contains seven SF1 binding sites, analysis of promoter activity in wild-type and truncation mutants of the enzyme, overview
-
SULT2A1, determination of the promoter sequence, SULT2A1-reporter gene expression in Hep-G2 cells and expression analysis, the constitutive active receptor, CAR, mediates the methotrexate induction of SULT2A1 in both Caco-2 andHep G2 cells, vitamin D receptor, VDR, also upregulates SULT2A1 gene expression, while human pregnane X receptor, PXR, downregulates it
-
SULT2B1 gene encodes 2 isoforms, SULT2B1a and SULT2B1b, generated by alternate splicing of the first exon, cloned and expressed in Escherichia coli
EXPRESSION
ORGANISM
UNIPROT
LITERATURE
activation of liver X receptor alpha as well as liver X receptor synthetic ligands like TO901317 and GW3965 induce the expression of isoform SULT2A1 at mRNA, protein, and enzymatic levels
-
down-regulation of RORalpha and/or RORgamma by small interfering RNA inhibits the expression of endogenous SULT2A1
-
estrogen-related receptor alpha upregulates SULT2A1 transcription in Caco-2 cells
inhibition of SULT2B1b expression induces cell-cycle arrest and apoptosis in Hepa1-6 cells by upregulating the expression of FAS, downregulating the expression of cyclinB1, BCL2 and MYC in vitro and in vivo at both the transcript and protein levels. Knock-down of SULT2B1b expression significantly suppresses tumor growth in nude mouse xenografts
-
retinoid-related orphan receptor (ROR)alpha and RORgamma transactivate the SULT2A1 gene promoter through their binding to a ROR response element found in the SULT2A1 gene promoter
-
SULT2B1 is comparatively higher in the human hepatocarcinoma tumorous tissues than their adjacent tissues
-
the amount of SULT2B1b mRNA in human endometrial tissues is significantly higher during the midluteal phase than during other phases of the menstrual cycle. Expression of SULT2B1b mRNA is induced by cAMP or phosphate in human endometrial stromal cells, whereas it is induced by cAMP or relaxin in endometrial epithelial cells
-
APPLICATION
ORGANISM
UNIPROT
COMMENTARY hide
LITERATURE
medicine
REF.
AUTHORS
TITLE
JOURNAL
VOL.
PAGES
YEAR
ORGANISM (UNIPROT)
PUBMED ID
SOURCE
Adams, J.B.; McDonald, D.
Enzymic synthesis of steroid sulphates. XII. Isolation of dehydroepiandrosterone sulphotransferase from human adrenals by affinity chromatography
Biochim. Biophys. Acta
567
144-153
1979
Homo sapiens
Manually annotated by BRENDA team
Adams, J.B.; McDonald, D.
Enzymic synthesis of steroid sulphates. XIII. Isolation and properties of dehydroepiandrosterone sulphotransferase from human foetal adrenals
Biochim. Biophys. Acta
615
275-278
1980
Homo sapiens
Manually annotated by BRENDA team
Falany, C.N.; Vasquez, M.E.; Kalb, J.M.
Purification and characterization of human liver dehydroepiandrosterone sulphotransferase
Biochem. J.
260
641-646
1989
Homo sapiens
Manually annotated by BRENDA team
Forbes-Bamforth, K.J.; Coughtrie, M.W.H.
Identification of a new adult human liver sulfotransferase with specificity for endogenous and xenobiotic estrogens
Biochem. Biophys. Res. Commun.
198
707-711
1994
Homo sapiens
Manually annotated by BRENDA team
Luu-The, V.; Bernier, F.; Dufort, I.
Steroid sulfotransferases
J. Endocrinol.
150
87-97
1996
Bos taurus, Cavia porcellus, Homo sapiens, Rattus norvegicus
Manually annotated by BRENDA team
Chetrite, G.; Pasqualini, J.R.
Steroid sulphotransferase and 17beta-hydroxysteroid dehydrogenase activities in Ishikawa human endometrial adenocarcinoma cells
J. Steroid Biochem. Mol. Biol.
61
27-34
1997
Homo sapiens
Manually annotated by BRENDA team
Faucher, F.; Lacoste, L.; Dufort, I.; Luu-The, V.
High metabolization of catecholestrogens by type 1 estrogen sulfotransferase (hEST1)
J. Steroid Biochem. Mol. Biol.
77
83-86
2001
Homo sapiens
Manually annotated by BRENDA team
Meloche, C.A.; Falany, C.N.
Expression and characterization of the human 3b-hydroxysteroid sulfotransferases (SULT2B1alpha and SULT2B1beta)
J. Steroid Biochem. Mol. Biol.
77
261-269
2001
Homo sapiens, Homo sapiens (O00204), Homo sapiens (Q06520)
Manually annotated by BRENDA team
Nakamura, Y.; Miki, Y.; Suzuki, T.; Nakata, T.; Darnel, A.D.; Moriya, T.; Tazawa, C.; Saito, H.; Ishibashi, T.; Takahashi, S.; Yamada, S.; Sasano, H.
Steroid sulfatase and estrogen sulfotransferase in the atherosclerotic human aorta
Am. J. Pathol.
163
1329-1339
2003
Homo sapiens
Manually annotated by BRENDA team
Suzuki, T.; Nakata, T.; Miki, Y.; Kaneko, C.; Moriya, T.; Ishida, T.; Akinaga, S.; Hirakawa, H.; Kimura, M.; Sasano, H.
Estrogen sulfotransferase and steroid sulfatase in human breast carcinoma
Cancer Res.
63
2762-2770
2003
Homo sapiens
Manually annotated by BRENDA team
He, D.; Meloche, C.A.; Dumas, N.A.; Frost, A.R.; Falany, C.N.
Different subcellular localization of sulfotransferase 2B1b in human placenta and prostate
Biochem. J.
379
533-540
2004
Homo sapiens
Manually annotated by BRENDA team
He, D.; Frost, A.R.; Falany, C.N.
Identification and immunohistochemical localization of sulfotransferase 2B1b (SULT2B1b) in human lung
Biochim. Biophys. Acta
1724
119-126
2005
Homo sapiens
Manually annotated by BRENDA team
Cui, D.; Booth-Genthe, C.L.; Carlini, E.; Carr, B.; Schrag, M.L.
Heterotropic modulation of sulfotransferase 2A1 activity by celecoxib: product ratio switching of ethynylestradiol sulfation
Drug Metab. Dispos.
32
1260-1264
2004
Homo sapiens
Manually annotated by BRENDA team
Chang, H.J.; Shi, R.; Rehse, P.; Lin, S.X.
Identifying androsterone (ADT) as a cognate substrate for human dehydroepiandrosterone sulfotransferase (DHEA-ST) important for steroid homeostasis: structure of the enzyme-ADT complex
J. Biol. Chem.
279
2689-2696
2004
Homo sapiens
Manually annotated by BRENDA team
Higashi, Y.; Fuda, H.; Yanai, H.; Lee, Y.; Fukushige, T.; Kanzaki, T.; Strott, C.A.
Expression of cholesterol sulfotransferase (SULT2B1b) in human skin and primary cultures of human epidermal keratinocytes
J. Invest. Dermatol.
122
1207-1213
2004
Homo sapiens
Manually annotated by BRENDA team
Harris, R.M.; Kirk, C.J.; Waring, R.H.
Non-genomic effects of endocrine disrupters: inhibition of estrogen sulfotransferase by phenols and chlorinated phenols
Mol. Cell. Endocrinol.
244
72-74
2005
Homo sapiens
Manually annotated by BRENDA team
Liu, Y.; Apak, T.I.; Lehmler, H.J.; Robertson, L.W.; Duffel, M.W.
Hydroxylated polychlorinated biphenyls are substrates and inhibitors of human hydroxysteroid sulfotransferase SULT2A1
Chem. Res. Toxicol.
19
1420-1425
2006
Homo sapiens
Manually annotated by BRENDA team
He, D.; Falany, C.N.
Characterization of proline-serine-rich carboxyl terminus in human sulfotransferase 2B1b: immunogenicity, subcellular localization, kinetic properties, and phosphorylation
Drug Metab. Dispos.
34
1749-1755
2006
Homo sapiens
Manually annotated by BRENDA team
Huang, Y.H.; Lee, C.Y.; Tai, P.J.; Yen, C.C.; Liao, C.Y.; Chen, W.J.; Liao, C.J.; Cheng, W.L.; Chen, R.N.; Wu, S.M.; Wang, C.S.; Lin, K.H.
Indirect regulation of human dehydroepiandrosterone sulfotransferase family 1A member 2 by thyroid hormones
Endocrinology
147
2481-2489
2006
Homo sapiens
Manually annotated by BRENDA team
Chen, X.; Maiti, S.; Zhang, J.; Chen, G.
Nuclear receptor interactions in methotrexate induction of human dehydroepiandrosterone sulfotransferase (hSULT2A1)
J. Biochem. Mol. Toxicol.
20
309-317
2006
Homo sapiens
Manually annotated by BRENDA team
Fuda, H.; Javitt, N.B.; Mitamura, K.; Ikegawa, S.; Strott, C.A.
Oxysterols are substrates for cholesterol sulfotransferase
J. Lipid Res.
48
1343-1352
2007
Homo sapiens
Manually annotated by BRENDA team
Song, C.S.; Echchgadda, I.; Seo, Y.; Oh, T.; Kim, S.; Kim, S.; Cho, S.; Shi, L.; Chatterjee, B.
An essential role of the CAAT/enhancer binding protein-alpha in the vitamin D-induced expression of the human steroid/bile acid-sulfotransferase (SULT2A1)
Mol. Endocrinol.
20
1286
2006
Homo sapiens
Manually annotated by BRENDA team
Echchgadda, I.; Song, C.S.; Oh, T.; Ahmed, M.; De La Cruz, I.J.; Chatterjee, B.
The xenobiotic-sensing nuclear receptors pregnane X receptor, constitutive androstane receptor, and orphan nuclear receptor hepatocyte nuclear factor 4alpha in the regulation of human steroid-/bile acid-sulfotransferase
Mol. Endocrinol.
21
2099-2111
2007
Homo sapiens
Manually annotated by BRENDA team
Nowell, S.; Falany, C.N.
Pharmacogenetics of human cytosolic sulfotransferases
Oncogene
25
1673-1678
2006
Homo sapiens
Manually annotated by BRENDA team
Wang, M.; Ebmeier, C.C.; Olin, J.R.; Anderson, R.J.
Sulfation of tibolone metabolites by human postmenopausal liver and small intestinal sulfotransferases (SULTs)
Steroids
71
343-351
2006
Homo sapiens
Manually annotated by BRENDA team
Chen, X.; Zhang, J.; Baker, S.M.; Chen, G.
Human constitutive androstane receptor mediated methotrexate induction of human dehydroepiandrosterone sulfotransferase (hSULT2A1)
Toxicology
231
224-233
2007
Homo sapiens
Manually annotated by BRENDA team
Senggunprai, L.; Yoshinari, K.; Yamazoe, Y.
Inhibitory effects of kynurenic acid, a tryptophan metabolite, and its derivatives on cytosolic sulfotransferases
Biochem. J.
422
455-462
2009
Homo sapiens, Mus musculus
Manually annotated by BRENDA team
Zhang, X.; Bai, Q.; Xu, L.; Kakiyama, G.; Pandak, W.M.; Zhang, Z.; Ren, S.
Cytosolic sulfotransferase 2B1b promotes hepatocyte proliferation gene expression in vivo and in vitro
Am. J. Physiol. Gastrointest. Liver Physiol.
303
G344-G355
2012
Homo sapiens
Manually annotated by BRENDA team
Gulcan, H.O.; Duffel, M.W.
Substrate inhibition in human hydroxysteroid sulfotransferase SULT2A1: studies on the formation of catalytically non-productive enzyme complexes
Arch. Biochem. Biophys.
507
232-240
2011
Homo sapiens
Manually annotated by BRENDA team
Ekuase, E.J.; Liu, Y.; Lehmler, H.J.; Robertson, L.W.; Duffel, M.W.
Structure-activity relationships for hydroxylated polychlorinated biphenyls as inhibitors of the sulfation of dehydroepiandrosterone catalyzed by human hydroxysteroid sulfotransferase SULT2A1
Chem. Res. Toxicol.
24
1720-1728
2011
Homo sapiens
Manually annotated by BRENDA team
Koizumi, M.
Momoeda, M.; Hiroi, H.; Hosokawa, Y.; Tsutsumi, R.; Osuga, Y.; Yano, T.; Taketani, Y.: Expression and regulation of cholesterol sulfotransferase (SULT2B1b) in human endometrium
Fertil. Steril.
93
1538-1544
2010
Homo sapiens
Manually annotated by BRENDA team
Ou, Z.; Shi, X.; Gilroy, R.K.; Kirisci, L.; Romkes, M.; Lynch, C.; Wang, H.; Xu, M.; Jiang, M.; Ren, S.; Gramignoli, R.; Strom, S.C.; Huang, M.; Xie, W.
Regulation of the human hydroxysteroid sulfotransferase (SULT2A1) by RORalpha and RORgamma and its potential relevance to human liver diseases
Mol. Endocrinol.
27
106-115
2013
Homo sapiens
Manually annotated by BRENDA team
Yang, X.; Xu, Y.; Guo, F.; Ning, Y.; Zhi, X.; Yin, L.; Li, X.
Hydroxysteroid sulfotransferase SULT2B1b promotes hepatocellular carcinoma cells proliferation in vitro and in vivo
PLoS ONE
8
e60853
2013
Homo sapiens
Manually annotated by BRENDA team
Ou, Z.; Jiang, M.; Hu, B.; Huang, Y.; Xu, M.; Ren, S.; Li, S.; Liu, S.; Xie, W.; Huang, M.
Transcriptional regulation of human hydroxysteroid sulfotransferase SULT2A1 by LXR?
Drug Metab. Dispos.
42
1684-1689
2014
Homo sapiens
Manually annotated by BRENDA team
Squirewell, E.J.; Qin, X.; Duffel, M.W.
Endoxifen and other metabolites of tamoxifen inhibit human hydroxysteroid sulfotransferase 2A1 (hSULT2A1)
Drug Metab. Dispos.
42
1843-1850
2014
Homo sapiens (Q06520), Homo sapiens
Manually annotated by BRENDA team
Falany, C.N.; Rohn-Glowacki, K.J.
SULT2B1: unique properties and characteristics of a hydroxysteroid sulfotransferase family
Drug Metab. Rev.
45
388-400
2013
Homo sapiens (O00204), Homo sapiens
Manually annotated by BRENDA team
Huang, C.; Zhou, T.; Chen, Y.; Sun, T.; Zhang, S.; Chen, G.
Estrogen-related receptor ERRalpha regulation of human hydroxysteroid sulfotransferase (SULT2A1) gene expression in human Caco-2 cells
J. Biochem. Mol. Toxicol.
28
32-38
2014
Homo sapiens (Q06520)
Manually annotated by BRENDA team
Hashiguchi, T.; Kurogi, K.; Shimohira, T.; Teramoto, T.; Liu, M.C.; Suiko, M.; Sakakibara, Y.
DELTA4-3-ketosteroids as a new class of substrates for the cytosolic sulfotransferases
Biochim. Biophys. Acta
1861
2883-2890
2017
Homo sapiens (Q06520)
Manually annotated by BRENDA team