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3.1.6.1: arylsulfatase (type I)

This is an abbreviated version!
For detailed information about arylsulfatase (type I), go to the full flat file.

Word Map on EC 3.1.6.1

Reaction

an aryl sulfate
+
H2O
=
a phenol
+
sulfate

Synonyms

4-methylumbelliferyl sulfatase, ARS, ARS-A, ARS-B, ARSA, ARSB, ARSE, ARSK, ary 423, Aryl-sulfate sulphohydrolase, arylsufatase B, arylsulfatase, arylsulfatase A, arylsulfatase B, arylsulfatase E, arylsulfatase Es-2, arylsulfatase G, arylsulfatase gene, arylsulfatase III, arylsulfatase J, arylsulfatase K, arylsulfatase type VI, arylsulfate sulfohydrolase II, arylsulfohydrolase, arylsulphatase, arylsulphatase A, AS-A, ASG, AstA, AtsA, estrogen sulfatase, KIAA1001, nitrocatechol sulfatase, p-nitrophenyl sulfatase, P70, PAS, phenolsulfatase, phenylsulfatase, sulfatase, sulfatase, aryl-

ECTree

     3 Hydrolases
         3.1 Acting on ester bonds
             3.1.6 Sulfuric-ester hydrolases
                3.1.6.1 arylsulfatase (type I)

Inhibitors

Inhibitors on EC 3.1.6.1 - arylsulfatase (type I)

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INHIBITOR
ORGANISM
UNIPROT
COMMENTARY hide
LITERATURE
IMAGE
(NH4)2SO4
1,10-phenanthroline
-
-
1,2,3-benzoxathiazine 2,2-dioxide
-
irreversible
1,3-phenanthroline
-
-
2-(difluoromethyl)phenyl hydrogen sulfate
-
competitive
2-hydroxy-4-methyl-5-nitrophenyl sulfate
-
substrate inhibition
2-mercaptoethanol
3,4-dihydro-1,2,3-benzoxathiazine 2,2-dioxide
-
irreversible
3-(alpha-acetonylbenzyl)-4-hydroxycoumarin
-
2.5 mM results in 50% reduced activity of arylsulfatase
3H-1,2,3-benzoxathiazole 2,2-dioxide
-
irreversible
4-(difluoromethyl)phenyl hydrogen sulfate
-
competitive
4-nitrophenyl phosphate
4-nitrophenyl sulfate
5-sulfosalicylic acid
-
strong
AgNO3
-
0.2 mM, 20-30% inhibition
Al3+
1 mM, less than 20% residual activity, both free and immobilized enzyme
AlCl3
BaCl2
Borate
CdCl2
citrate
CoCl2
CuCl2
dithiothreitol
dopamine
Estrone 3-sulfate
-
-
Fe2+
1 mM, less than 20% residual activity, both free and immobilized enzyme
FeCl2
FeSO4
guanidine hydrochloride
1 mM, 69.5% of initial activity, mutant H260L
heparin
-
-
hydroxylamine
imidazole
-
-
iodoacetate
iodoacetic acid
-
10 mM, 48% residual activity
IPTG
-
at concentrations from 50 micromolar up to 5000 micromolar of IPTG the activity decreases by more than 50%
K2HPO4
K2SO3
KCN
-
10 mM, 23% residual activity
Mg2+
1 mM, 88% of initial activity, mutant H260L
Mn2+
10 mM, 69% residual activity
MnCl2
N-benzyloxycarbonyl-L-Phe-L-Tyr-O-sulfate methyl ester
-
hydrolysis of 4-nitrophenyl sulfate
Na2B4O7
-
10 mM, 12% residual activity
Na2SO3
Na3PO4
NiCl2
octopamine
p-(amidinophenyl)methanesulfonyl fluoride
-
-
p-(amidinophenyl)methanesulfonyl fluoride HCl
-
-
Phenolphthalein disulfate
-
hydrolysis of 4-nitrophenyl sulfate
phenyl sulfamate
-
irreversible
phosphate
PO43-
praziquantel
-
schistosomical drug, inhibitory to enzyme. No effect on immunological properties of enzyme
SO32-
sodium dodecyl sulfonate
-
-
sodium dodecylsulfate
-
1 mM, 4% residual activity
sodium phenylmethane sulfonate
-
-
sulfate
Triton X-100
1 mM, 15% residual activity, free enzyme, 35% residual activity, immobilized enzyme, respectively
Tween 80
1 mM, 10% residual activity, free enzyme, 60% residual activity, immobilized enzyme, respectively
tyramine
warfarin
-
-
ZnCl2
-
10 mM, 10% residual activity
additional information
-