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Information on EC 2.8.2.4 - estrone sulfotransferase and Organism(s) Bos taurus and UniProt Accession P19217

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EC Tree
     2 Transferases
         2.8 Transferring sulfur-containing groups
             2.8.2 Sulfotransferases
                2.8.2.4 estrone sulfotransferase
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This record set is specific for:
Bos taurus
UNIPROT: P19217 not found.
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Word Map
The taxonomic range for the selected organisms is: Bos taurus
The enzyme appears in selected viruses and cellular organisms
Synonyms
hsult1e1, oestrogen sulphotransferase, estrogen sulphotransferase, estrone sulfotransferase, sulfotransferase 1e1, oestrogen sulfotransferase, estrogen sult, estradiol sulfotransferase, rest-6, sult1e, more
SYNONYM
ORGANISM
UNIPROT
COMMENTARY hide
LITERATURE
estrogen sulfotransferase
-
estrogen-specific sulfotransferase
-
3'-phosphoadenylyl sulfate-estrone 3-sulfotransferase
-
-
-
-
3'-phosphoadenylyl sulfate:oestrone sulfotransferase
-
-
-
-
EST
-
-
estrogen sulfotransferase
estrogen sulphotransferase
-
-
-
-
oestrogen sulphotransferase
-
-
-
-
REACTION TYPE
ORGANISM
UNIPROT
COMMENTARY hide
LITERATURE
sulfate group transfer
-
-
-
-
PATHWAY SOURCE
PATHWAYS
SYSTEMATIC NAME
IUBMB Comments
3'-phosphoadenylyl-sulfate:estrone 3-sulfotransferase
-
CAS REGISTRY NUMBER
COMMENTARY hide
9026-06-6
-
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 + 17beta-estradiol
adenosine 3',5'-bisphosphate + 17beta-estradiol 3-sulfate
show the reaction diagram
-
-
-
?
3'-phosphoadenylyl sulfate + estrone
adenosine 3',5'-bisphosphate + estrone 3-sulfate
show the reaction diagram
3'-phosphoadenylyl sulfate + estradiol
adenosine 3',5'-bisphosphate + estradiol 3-sulfate
show the reaction diagram
-
-
-
-
?
3'-phosphoadenylylsulfate + 1,3,5(10)-estratrien-3,16alpha,17beta-triol
adenosine 3',5'-bisphosphate + 1,3,5(10)-estratrien-16alpha,17beta-diol 3-sulfate
show the reaction diagram
-
-
-
-
r
3'-phosphoadenylylsulfate + 1,3,5(10)-estratrien-3,17alpha-diol
adenosine 3',5'-bisphosphate + 1,3,5(10)-estratrien 17alpha-ol-3-sulfate
show the reaction diagram
-
-
-
-
r
3'-phosphoadenylylsulfate + 1,3,5(10)-estratrien-3,17beta-diol-17-monoacetate
adenosine 3',5'-bisphosphate + ?
show the reaction diagram
-
-
-
-
r
3'-phosphoadenylylsulfate + 1,3,5(10)-estratrien-3,17beta-diol-17-monoglucosiduronate
adenosine 3',5'-bisphosphate + ?
show the reaction diagram
-
very low sulfation rate
-
-
r
3'-phosphoadenylylsulfate + 1,3,5(10)-estratrien-3,17beta-diol-17-monovalerinate
adenosine 3',5'-bisphosphate + ?
show the reaction diagram
-
-
-
-
r
3'-phosphoadenylylsulfate + 1,3,5(10)-estratrien-3-ol
adenosine 3',5'-bisphosphate + 1,3,5(10)-estratrien 3-sulfate
show the reaction diagram
-
-
-
-
r
3'-phosphoadenylylsulfate + 11-hydroxy-1,3,5(10)-estratrien-17-one
adenosine 3',5'-bisphosphate + ?
show the reaction diagram
-
-
-
-
r
3'-phosphoadenylylsulfate + 16-epiestriol
adenosine 3',5'-bisphosphate + 16-epiestriol 3-sulfate
show the reaction diagram
3'-phosphoadenylylsulfate + 17-deoxyestrone
adenosine 3',5'-bisphosphate + 17-deoxyestrone 3-sulfate
show the reaction diagram
-
-
-
r
3'-phosphoadenylylsulfate + 17-epiestriol
adenosine 3',5'-bisphosphate + 17-epiestriol 3-sulfate
show the reaction diagram
-
-
-
r
3'-phosphoadenylylsulfate + 17alpha-ethynyl-1,3,5(10)-estratrien-3,17beta-diol
adenosine 3',5'-bisphosphate + 17alpha-ethynyl-1,3,5(10)-estratrien-17beta-ol 3-sulfate
show the reaction diagram
-
-
-
-
r
3'-phosphoadenylylsulfate + 17beta-estradiol
adenosine 3',5'-bisphosphate + estradiol 3-sulfate
show the reaction diagram
3'-phosphoadenylylsulfate + 3,16alpha-dihydroxy-1,3,5(10)-estratrien-17-one
adenosine 3',5'-bisphosphate + 16-alpha-hydroxy-1,3,5(10)-estratrien-17-one 3-sulfate
show the reaction diagram
-
-
-
-
r
3'-phosphoadenylylsulfate + 3,17beta-dihydroxy-1,3,5(10),9-estratetraen-12-one
adenosine 3',5'-bisphosphate + ?
show the reaction diagram
-
-
-
-
r
3'-phosphoadenylylsulfate + 3,17beta-dihydroxy-1,3,5(10)-estratrien-6-one
adenosine 3',5'-bisphosphate + ?
show the reaction diagram
-
high sulfation rate
-
-
r
3'-phosphoadenylylsulfate + 3-hydroxy-1,3,5(10),6,8-estrapentaen-17-one
adenosine 3',5'-bisphosphate + 1,3,5(10),6,8-estrapentaen-17-one 3-sulfate
show the reaction diagram
-
-
-
-
r
3'-phosphoadenylylsulfate + 3-hydroxy-1,3,5(10),6-estratetraen-17-one
adenosine 3',5'-bisphosphate + 1,3,5(10),6-estratetraen-17-one 3-sulfate
show the reaction diagram
-
-
-
-
r
3'-phosphoadenylylsulfate + 3-hydroxy-1,3,5(10),7-estratetraen-17-one
adenosine 3',5'-bisphosphate + ?
show the reaction diagram
-
-
-
-
r
3'-phosphoadenylylsulfate + 3-hydroxy-1,3,5(10),9-estratetraen-12,17-dione
adenosine 3',5'-bisphosphate + 1,3,5(10),9-estratetraen-12,17-dione 3-sulfate
show the reaction diagram
-
-
-
-
r
3'-phosphoadenylylsulfate + 3-hydroxy-1,3,5(10)-estratrien-16-one
adenosine 3',5'-bisphosphate + 1,3,5(10)-estratriene-16-one 3-sulfate
show the reaction diagram
-
-
-
-
r
3'-phosphoadenylylsulfate + 4-nitro-1,3,5(10)estratrien-3,17beta-diol
adenosine 3',5'-bisphosphate + ?
show the reaction diagram
-
-
-
-
r
3'-phosphoadenylylsulfate + 7alpha-methyl-1,3,5(10)-estratrien-3,17beta-diol
adenosine 3',5'-bisphosphate + 7alpha-methyl-1,3,5(10)-estratrien 3-sulfate
show the reaction diagram
-
-
-
-
r
3'-phosphoadenylylsulfate + 7alpha-methyl-3-hydroxy-1,3,5(10)-estratrien-17-one
adenosine 3',5'-bisphosphate + ?
show the reaction diagram
-
-
-
-
r
3'-phosphoadenylylsulfate + estriol
adenosine 3',5'-bisphosphate + estriol 3-sulfate
show the reaction diagram
3'-phosphoadenylylsulfate + estrone
adenosine 3',5'-bisphosphate + estrone 3-sulfate
show the reaction diagram
3'-phosphoadenylylsulfate + hexestrol
adenosine 3',5'-bisphosphate + hexestrol 4-sulfate
show the reaction diagram
-
-
-
r
3'-phosphoadenylylsulfate + stilbestrol
adenosine 3',5'-bisphosphate + stilbestrol 4-sulfate
show the reaction diagram
-
-
-
r
8-bromoadenosine 3'-phosphate 5'-phosphosulfate + estrone
8-bromoadenosine 3',5'-bisphosphate + estrone sulfate
show the reaction diagram
-
-
-
-
r
adenosine 3'-phosphate 5'-phosphosulfate + estrone
adenosine 3',5'-bisphosphate + estrone sulfate
show the reaction diagram
-
-
-
-
r
formycin 3'-phosphate 5'-phosphosulfate + estrone
formycin 3',5'-bisphosphate + estrone sulfate
show the reaction diagram
-
-
-
-
r
tubercidin 3'-phosphate 5'-phosphosulfate + estrone
tubercidin 3',5'-bisphosphate + estrone sulfate
show the reaction diagram
-
-
-
-
r
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 + 17beta-estradiol
adenosine 3',5'-bisphosphate + 17beta-estradiol 3-sulfate
show the reaction diagram
-
-
-
?
3'-phosphoadenylyl sulfate + estrone
adenosine 3',5'-bisphosphate + estrone 3-sulfate
show the reaction diagram
3'-phosphoadenylylsulfate + estrone
adenosine 3',5'-bisphosphate + estrone 3-sulfate
show the reaction diagram
additional information
?
-
excess SULT1E1 is the reason for perturbed low ratio of active to inactive estrogens and the resulting hormonal imbalance contributing to the lack of overt signs of readiness for partirition in cows pregnant with clones
-
-
?
METALS and IONS
ORGANISM
UNIPROT
COMMENTARY hide
LITERATURE
Ca2+
-
activated by, but no absolute requirement
Mg2+
-
activated by, but no absolute requirement
Mn2+
-
activated by, but no absolute requirement
INHIBITOR
ORGANISM
UNIPROT
COMMENTARY hide
LITERATURE
IMAGE
(17beta)-3,17-dihydroxy-1,3,5(10)estatriene-6-one
-
-
(17beta)-3-methoxyestra-1(10),2,4-trien-17-ol
-
-
(7-amino-3(beta-D-ribofuranosyl)-pyrazolo-[4,3-d]pyrimidine) 3',5'-diphosphate
-
-
1,3,5(10)estatriene-17beta-ol
-
-
1,3,5(10)estatriene-3,16alpha,17beta-triol
-
-
1,3,5(10)estatriene-3,16alpha-diol
-
-
1,3,5(10)estatriene-3,16beta,17beta-triol
-
-
1,3,5(10)estatriene-3,17beta-diol
-
-
1,3,5(10)estatriene-3,17beta-diol 17beta-phosphate
-
-
1,3,5(10)estatriene-3,17beta-diol 17beta-sulfate
-
-
1,3,5(10)estatriene-3,17beta-diol 3,17beta-diphosphate
-
-
1,3,5(10)estatriene-3,17beta-diol 3-phosphate
-
-
1,3,5(10)estatriene-3,17beta-diol-3-acetate
-
-
1,3,5(10)estatriene-3,17beta-diol-3-benzoate
-
-
1,3,5(10)estatriene-3-ol
-
-
1,3,5(10)estatriene-3-ol 17-one 3-sulfate
-
-
1-[2-(p-[3,4-dihydro-6-methoxy-2-phenyl-1-naphthyl]phenoxy)ethyl]-pyrrolidine hydrochloride
-
-
17beta-hydroxy-5alpha-androstane-3-one
-
-
17beta-hydroxy-5beta-androstane-3-one
-
-
2,4-dibromo-1,3,5(10)estatriene-3,17beta-diol
-
-
2,4-dinitro-1,3,5(10)estatriene-3,17beta-diol
-
-
2-amino-1,3,5(10)estatriene-3,17beta-diol
-
-
2-nitro-1,3,5(10)estatriene-3,17beta-diol
-
-
3'-phosphoadenylylsulfate
-
competitive inhibition
3-hydroxyestra-1(10),2,4-trien-17-one
-
-
3-methoxy-4-nitroestra-1(10),2,4-trien-17-one
-
-
3beta-hydroxy-5beta-androstane-17-one
-
-
3beta-hydroxy-androst-5-ene-17-one
-
-
4-amino-1,3,5(10)estatriene-3,17beta-diol
-
-
4-nitro-1,3,5(10)estatriene-3,17beta-diol
-
-
5-androstene-3beta,17beta-diol
-
-
5alpha-Androstane-3beta,17beta-diol
-
-
7-deazadenosine
-
tubercidin
8-bromoadenosine 3',5'-diphosphate
-
-
8-bromoadenosine 3'-phosphate 5'-phosphosulfate
-
-
adenosine 2',5'-diphosphate
-
noncompetitive inhibition
adenosine 3',5'-diphosphate
-
-
adenosine 3'-diphosphate 5'-phosphate
-
-
adenosine 3'-phosphate 5'-diphosphate
-
-
adenosine 5'-phosphosulfate
-
-
adenosine 5'-sulfate
-
-
adenosine N1-oxide 3,5'-diphosphate
-
-
AMP
-
-
androst-5-ene-3beta-ol
-
-
ATP
-
mixed-type inhibition
cetyltrimethylammonium bromide
-
-
Co2+
-
strong inhibition
diethylstilbestrol
-
-
dithiothreitol
-
inhibition above 0.005 mM
fatty acid
-
unsaturated fatty acid of chain length C11-C14
formycin 3'-phosphate 5'-phosphosulfate
-
-
guanosine 2',3'-cyclic phosphate 5'-phosphate
-
-
inosine 3',5'-diphosphate
-
-
myristate
-
inhibition is non-competitive with respect to the substrate estrone
N6-dimethylaminoadenosine 3',5'-diphosphate
-
-
nebularine 3',5'-diphosphate
-
-
nebularine(9-beta-D-ribofuranosylpurine)adenosine 3',5'-diphosphate
-
-
Ni2+
-
strong inhibition
o-Iodosobenzoate
-
sensitive above 10 mM
p-chloromercuribenzoate
-
sensitive above 1 mM
p-hydroxymercuribenzoate
-
-
retinoic acid
-
-
Sodium dodecyl sulfate
-
-
tubercidin 2',5'-diphosphate
tubercidin 3',5'-bisphosphate
-
-
tubercidin 3'-phosphate 5'-phosphosulfate
-
-
Zn2+
-
strong inhibition
additional information
-
ACTIVATING COMPOUND
ORGANISM
UNIPROT
COMMENTARY hide
LITERATURE
IMAGE
2-mercaptoethanol
-
activation
cysteine
-
-
dithiothreitol
-
activation up to 0.005 mM
KM VALUE [mM]
SUBSTRATE
ORGANISM
UNIPROT
COMMENTARY hide
LITERATURE
IMAGE
0.014
16-epiestriol
-
pH 8.6, 37°C
0.014
17-deoxyestrone
-
pH 8.6, 37°C
0.008
17-epiestriol
-
pH 8.6, 37°C
0.014
17beta-estradiol
0.037
3'-phosphoadenylylsulfate
-
pH 8.1, 37°C
0.018
8-bromoadenosine 3'-phosphate 5'-phosphosulfate
-
pH 7.5, 37°C
0.07
adenosine 3',5'-bisphosphate
-
pH 8.1, 37°C
0.044
adenosine 3'-phosphate 5'-phosphosulfate
-
pH 7.5, 37°C
0.005
estriol
-
pH 8.6, 37°C
0.0027 - 0.015
estrone
0.13
formycin 3'-phosphate 5'-phosphosulfate
-
pH 7.5, 37°C
0.021
tubercidin 3'-phosphate 5'-phosphosulfate
-
pH 7.5, 37°C
Ki VALUE [mM]
INHIBITOR
ORGANISM
UNIPROT
COMMENTARY hide
LITERATURE
IMAGE
0.0055
(17beta)-3,17-dihydroxy-1,3,5(10)estatriene-6-one
-
pH 8.1, 37°C
0.0048
(17beta)-3-methoxyestra-1(10),2,4-trien-17-ol
-
pH 8.1, 37°C
0.043
(7-amino-3(beta-D-ribofuranosyl)-pyrazolo-[4,3-d]pyrimidine) 3,5''-diphosphate
-
pH 7.5, 37°C
0.016
1,3,5(10)estatriene-17beta-ol
-
pH 8.1, 37°C
0.0082
1,3,5(10)estatriene-3,16alpha,17beta-triol
-
pH 8.1, 37°C
0.0013
1,3,5(10)estatriene-3,16alpha-diol
-
pH 8.1, 37°C
0.0055
1,3,5(10)estatriene-3,16beta,17beta-triol
-
pH 8.1, 37°C
0.0061
1,3,5(10)estatriene-3,17beta-diol
-
pH 8.1, 37°C
0.021
1,3,5(10)estatriene-3,17beta-diol 17beta-phosphate
-
pH 8.1, 37°C
0.047
1,3,5(10)estatriene-3,17beta-diol 17beta-sulfate
-
pH 8.1, 37°C
0.333
1,3,5(10)estatriene-3,17beta-diol 3,17beta-diphosphate
-
pH 8.1, 37°C
0.024
1,3,5(10)estatriene-3,17beta-diol 3-phosphate
-
pH 8.1, 37°C
0.017
1,3,5(10)estatriene-3,17beta-diol-3-acetate
-
pH 8.1, 37°C
0.09
1,3,5(10)estatriene-3,17beta-diol-3-benzoate
-
pH 8.1, 37°C
0.0035
1,3,5(10)estatriene-3-ol
-
pH 8.1, 37°C
0.128
1,3,5(10)estatriene-3-ol-17-one 3-sulfate
-
pH 8.1, 37°C
0.074
1-[2-(p-[3,4-dihydro-6-methoxy-2-phenyl-1-naphthyl]phenoxy)ethyl]-pyrrolidine hydrochloride
-
pH 8.1, 37°C
0.038
17beta-hydroxy-5alpha-androstane-3-one
-
pH 8.1, 37°C
0.074
17beta-hydroxy-5beta-androstane-3-one
-
pH 8.1, 37°C
0.00011
2,4-dibromo-1,3,5(10)estatriene-3,17beta-diol
-
pH 8.1, 37°C
0.0043
2,4-dinitro-1,3,5(10)estatriene-3,17beta-diol
-
pH 8.1, 37°C
0.0035
2-amino-1,3,5(10)estatriene-3,17beta-diol
-
pH 8.1, 37°C
0.0024
2-nitro-1,3,5(10)estatriene-3,17beta-diol
-
pH 8.1, 37°C
1.9 - 5
3'-AMP
0.056
3'-phosphoadenylylsulfate
-
pH 8.1, 37°C
0.0049
3-hydroxyestra-1(10),2,4-trien-17-one
-
pH 8.1, 37°C
0.0043
3-methoxy-4-nitroestra-1(10),2,4-trien-17-one
-
pH 8.1, 37°C
0.17
3beta-hydroxy-5-androstene-17-one
-
pH 8.1, 37°C
0.302
3beta-hydroxy-5beta-androstane-17-one
-
pH 8.1, 37°C
0.0035
4-amino-1,3,5(10)estatriene-3,17beta-diol
-
pH 8.1, 37°C
0.00015
4-nitro-1,3,5(10)estatriene-3,17beta-diol
-
pH 8.1, 37°C
0.035
5-androstene-3beta,17beta-diol
-
pH 8.1, 37°C
0.047
5alpha-Androstane-3beta,17beta-diol
-
pH 8.1, 37°C
0.0017
8-bromoadenosine 3',5'-diphosphate
-
pH 7.5, 37°C
0.0017
8-bromoadenosine 3'-phosphate 5'-phosphosulfate
-
pH 7.5, 37°C, competitive inhibition
12.9
adenosine 2',5'-diphosphate
-
pH 7.5, 37°C, noncompetitive inhibition
0.007
adenosine 3',5'-diphosphate
-
pH 7.5, 37°C
0.046
adenosine 3'-diphosphate 5'-phosphate
-
pH 7.5, 37°C
0.116
adenosine 3'-phosphate 5'-diphosphate
-
pH 7.5, 37°C
1.49
adenosine 5'-phosphosulfate
-
pH 7.5, 37°C
5
adenosine 5'-sulfate
-
pH 7.5, 37°C
0.35
adenosine N1-oxide 3,5'-diphosphate
-
pH 7.5, 37°C
1.1 - 2.8
ADP
0.05
androst-5-ene-3beta-ol
-
pH 8.1, 37°C
0.12
diethylstilbestrol
-
pH 8.1, 37°C
0.043
formycin 3'-phosphate 5'-phosphosulfate
-
pH 7.5, 37°C, noncompetitive inhibition
0.084
guanosine 2',3'-cyclic phosphate 5'-phosphate
-
pH 7.5, 37°C
0.8
inosine 3',5'-diphosphate
-
pH 7.5, 37°C
0.125
N6-dimethylaminoadenosine 3',5'-diphosphate
-
pH 7.5, 37°C
0.068
nebularine 3',5'-diphosphate
-
pH 7.5, 37°C
0.068
nebularine(9-beta-D-ribofuranosylpurine)adenosine 3',5'-diphosphate
-
pH 7.5, 37°C
0.005 - 0.0053
tubercidin 2',5'-diphosphate
0.0006
tubercidin 3',5'-bisphosphate
-
pH 7.5, 37°C
0.0006
tubercidin 3'-phosphate 5'-phosphosulfate
-
pH 7.5, 37°C, competitive inhibition
SPECIFIC ACTIVITY [µmol/min/mg]
ORGANISM
UNIPROT
COMMENTARY hide
LITERATURE
0.01
-
-
pH OPTIMUM
ORGANISM
UNIPROT
COMMENTARY hide
LITERATURE
6.2
-
placental enzyme
8.1
-
-
pH RANGE
ORGANISM
UNIPROT
COMMENTARY hide
LITERATURE
5.5 - 8.5
-
-
pI VALUE
ORGANISM
UNIPROT
COMMENTARY hide
LITERATURE
5.3
-
isoelectric focusing, active enzyme exists in polymorphic forms
5.7
-
isoelectric focusing, active enzyme exists in polymorphic forms
5.9
-
isoelectric focusing, active enzyme exists in polymorphic forms
ORGANISM
COMMENTARY hide
LITERATURE
UNIPROT
SEQUENCE DB
SOURCE
-
Uniprot
Manually annotated by BRENDA team
SOURCE TISSUE
ORGANISM
UNIPROT
COMMENTARY hide
LITERATURE
SOURCE
-
EST is localized all along the excurrent duct with a higher signal in the caput and corpus epididymis
Manually annotated by BRENDA team
-
-
Manually annotated by BRENDA team
-
-
Manually annotated by BRENDA team
LOCALIZATION
ORGANISM
UNIPROT
COMMENTARY hide
GeneOntology No.
LITERATURE
SOURCE
UNIPROT
ENTRY NAME
ORGANISM
NO. OF AA
NO. OF TRANSM. HELICES
MOLECULAR WEIGHT[Da]
SOURCE
SEQUENCE
LOCALIZATION PREDICTION?
ST1E1_BOVIN
295
0
34640
Swiss-Prot
other Location (Reliability: 2)
MOLECULAR WEIGHT
ORGANISM
UNIPROT
COMMENTARY hide
LITERATURE
35000
x * 35000, SDS-PAGE
35000
37000
-
recombinant enzyme, SDS-PAGE
67000
-
enzyme form B, gel filtration
70000
-
PAGE
73800
-
sedimentation equilibrium centrifugation
74000
-
sucrose density gradient, pH 5.8
74000 - 76000
-
SDS-PAGE
74800
-
meniscus depletion method, sucrose density gradient centrifugation, pH 7.0
76000
-
sucrose density gradient centrifugation, pH 9.0
SUBUNIT
ORGANISM
UNIPROT
COMMENTARY hide
LITERATURE
dimer
-
2 * 35000, SDS-PAGE
monomer
-
1 * 74000, SDS-PAGE
STORAGE STABILITY
ORGANISM
UNIPROT
LITERATURE
0°C, partially purified A form of enzyme loses only a small percentage of its activity on standing in ice for a period of 2 weeks, B form loses 50% of its initial activity in this time
-
PURIFICATION (Commentary)
ORGANISM
UNIPROT
LITERATURE
adrenal enzyme
-
isoforms A and B highly purified
-
placental enzyme
-
Sephacryl S-500 gel filtration
-
CLONED (Commentary)
ORGANISM
UNIPROT
LITERATURE
cDNA cloned
-
expressed in Escherichia coli BL21(DE3) cells
-
REF.
AUTHORS
TITLE
JOURNAL
VOL.
PAGES
YEAR
ORGANISM (UNIPROT)
PUBMED ID
SOURCE
Adams, J.B.
Enzymic synthesis of steroid sulphates. V. On the binding of estrogens to estrogen sulphotransferase
Biochim. Biophys. Acta
146
522-528
1967
Bos taurus
Manually annotated by BRENDA team
Adams, J.B.; Chulavatnatol, M.
Enzymic synthesis of steroid sulphates. IV. The nature of the two forms of estrogen sulphotransferase of bovine adrenals
Biochim. Biophys. Acta
146
509-521
1967
Bos taurus
Manually annotated by BRENDA team
Adams, J.B.; Poulos, A.
Enzymic synthesis of steroid sulphates. III. Isolation and properties of estrogen sulphotransferase of bovine adrenal glands
Biochim. Biophys. Acta
146
493-508
1967
Bos taurus
Manually annotated by BRENDA team
Adams, J.B.; Ellyard, R.K.
Enzymic synthesis of steroid sulphates. VIII. Inhibition of estrogen sulphotransferase by retinoic acid and free fatty acids
Biochim. Biophys. Acta
260
724-730
1972
Bos taurus
Manually annotated by BRENDA team
Adams, J.B.; Ellyard, R.K.; Low, J.
Enzymic synthesis of steroid sulphates. IX. Physical and chemical properties of purified oestrogen sulphotransferase from bovine adrenal glands, the nature of its isoenzymic forms and a proposed model to explain its wave-like kinetics
Biochim. Biophys. Acta
370
160-188
1974
Bos taurus
Manually annotated by BRENDA team
Adams, J.B.; Low, J.
Enzymic synthesis of steroid sulphates. X. Isolation of oestrogen sulphotransferase from bovine placenta and comparison of its properties with adrenal oestrogen sulphotransferase
Biochim. Biophys. Acta
370
189-196
1974
Bos taurus
Manually annotated by BRENDA team
Rozhin, J.; Soderstrom, R.L.; Brooks, S.C.
Specificity studies on bovine adrenal estrogen sulfotransferase
J. Biol. Chem.
249
2079-2087
1974
Bos taurus
Manually annotated by BRENDA team
Rozhin, J.; Huo, A.; Zemlicka, J.; Brooks, S.C.
Studies on bovine adrenal estrogen sulfotransferase. Inhibition and possible involvement of adenine-estrogen stacking
J. Biol. Chem.
252
7214-7220
1977
Bos taurus
Manually annotated by BRENDA team
Horwitz, J.P.; Misra, R.S.; Rozhin, J.; Neenan, J.P.; Huo, A.; Godefroi, V.E.; Philips, K.D.; Chung, H.L.; Butke, G.; Brooks, S.C.
IV. Synthesis and assay of analogs of adenosine 3,5-diphosphate as inhibitors of bovine adrenal estrogen sulfotranferase
Biochim. Biophys. Acta
525
364-372
1978
Bos taurus
Manually annotated by BRENDA team
Horwitz, J.P.; Misra, R.S.; Rozhin, J.; Helmer, S.; Bhuta, A.; Brooks, S.C.
Studies on bovine adrenal estrogen sulfotransferase. V. Synthesis and assay of analogs of 3-phosphoadenosine 5-phosphosulfate as cosubstrates for estrogen sulfurylation
Biochim. Biophys. Acta
613
85-94
1980
Bos taurus
Manually annotated by BRENDA team
Adams, J.B.
Enzymic synthesis of steroid sulphates. XVII. On the structure of bovine estrogen sulphotransferase
Biochim. Biophys. Acta
1076
282-288
1991
Bos taurus
Manually annotated by BRENDA team
Song, W.C.
Biochemistry and reproductive endocrinology of estrogen sulfotransferase
Ann. N. Y. Acad. Sci.
948
43-50
2001
Bos taurus, Cavia porcellus, Homo sapiens, Mus musculus, Rattus norvegicus
Manually annotated by BRENDA team
Hirayama, H.; Sawai, K.; Moriyasu, S.; Hirayama, M.; Goto, Y.; Kaneko, E.; Miyamoto, A.; Ushizawa, K.; Takahashi, T.; Minamihashi, A.
Excess estrogen sulfoconjugation as the possible cause for a poor sign of parturition in pregnant cows carrying somatic cell clone fetuses
Reproduction
136
639-647
2008
Bos taurus (P19217)
Manually annotated by BRENDA team
Frenette, G.; Leclerc, P.; Damours, O.; Sullivan, R.
Estrogen sulfotransferase is highly expressed along the bovine epididymis and is secreted into the intraluminal environment
J. Androl.
30
580-589
2009
Bos taurus
Manually annotated by BRENDA team
Polei, M.; Viergutz, T.; Tomek, W.; Schuler, G.; Fuerbass, R.
Estrogen-specific sulfotransferase (SULT1E1) in bovine placentomes: inverse levels of mRNA and protein in uninucleated trophoblast cells and trophoblast giant cells
Biol. Reprod.
91
48
2014
Bos taurus (P19217), Bos taurus
Manually annotated by BRENDA team