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(2Z)-2-(4-aminophenyl)-3-(1H-indol-2-yl)prop-2-enenitrile + H2O2
?
-
-
-
-
?
(2Z)-2-(4-aminophenyl)-3-(4-hydroxyphenyl)prop-2-enenitrile + H2O2
?
-
-
-
-
?
(2Z)-2-(4-aminophenyl)-3-(9-ethyl-9H-carbazol-3-yl)prop-2-enenitrile + H2O2
?
-
-
-
-
?
(2Z)-2-(4-aminophenyl)-3-anthracen-9-ylprop-2-enenitrile + H2O2
?
-
-
-
-
?
(2Z)-2-(4-aminophenyl)-3-pyren-1-ylprop-2-enenitrile + H2O2
?
-
-
-
-
?
(2Z)-2-(4-aminophenyl)-3-thiophen-2-ylprop-2-enenitrile + H2O2
?
-
-
-
-
?
(2Z)-3-(1H-indol-3-yl)-2-(4-nitrophenyl)prop-2-enenitrile + H2O2
?
-
-
-
-
?
(2Z)-3-(4-hydroxyphenyl)-2-(4-nitrophenyl)prop-2-enenitrile + H2O2
?
-
-
-
-
?
(2Z)-3-[4-(dimethylamino)phenyl]-2-(4-nitrophenyl)prop-2-enenitrile + H2O2
?
-
-
-
-
?
(2Z,4E)-2-(4-aminophenyl)-5-[4-(dimethylamino)phenyl]penta-2,4-dienenitrile + H2O2
?
-
-
-
-
?
1-(1,3-dioxolan-2-ylmethyl)-4-[(E)-2-[4-[4-(2-hydroxyethyl)piperazin-1-yl]phenyl]ethenyl]pyridinium bromide + H2O2
?
-
-
-
-
?
1-(1,3-dioxolan-2-ylmethyl)-4-[(E)-2-[4-[4-(2-hydroxyethyl)piperazin-1-yl]phenyl]ethenyl]pyridinium perchlorate + H2O2
?
-
-
-
-
?
1-butyl-4-[(E)-2-(1H-indol-3-yl)ethenyl]quinolinium perchlorate + H2O2
?
-
-
-
-
?
1-ethyl-4-[(E)-2-(1H-indol-3-yl)ethenyl]quinolinium iodide + H2O2
?
-
-
-
-
?
1-ethyl-4-[(E)-2-(1H-pyrrol-2-yl)ethenyl]quinolinium iodide + H2O2
?
-
-
-
-
?
1-ethyl-4-[(E)-2-thiophen-2-ylethenyl]quinolinium iodide + H2O2
?
-
-
-
-
?
1-methyl-4-[(E)-2-(1H-pyrrol-2-yl)ethenyl]pyridinium iodide + H2O2
?
-
-
-
-
?
1-methyl-4-[(E)-2-thiophen-2-ylethenyl]pyridinium iodide + H2O2
?
-
-
-
-
?
1-naphthol + H2O2
? + H2O
-
peroxidase is inactived during oxidation
-
-
?
2 guaiacol + H2O2
3,3'-dimethoxy-4,4'-biphenylquinone + H2O
2 K4[Fe(CN)6] + H2O2
K3[Fe(CN)6] + H2O + K2O
2 Mn(II) + 2 H+ + H2O2
2 Mn(III) + 2 H2O
2 phenol + 2 nitrite + H2O2
2 nitrophenol + H2O
-
-
-
-
?
2 pyrogallol + H2O2
? + H2O
2 veratryl alcohol + H2O2
2 veratraldehyde + H2O
2,2'-azino-bis (3-ethylbenzthiazoline-6-sulphonic acid) + H2O2
? + H2O
2,2'-azino-bis(3-ethylbenzothiazoline-6-sulfonic acid) + H2O2
?
-
-
-
-
?
2,2'-azino-bis(3-ethylbenzthiazole-6-sulfonic acid) + H2O2
?
2,2'-azino-bis(3-ethylbenzthiazoline)-sulfonic acid + H2O2
?
2,2'-azino-bis-(3-ethyl-6-benzothiazolinsulfonate) + H2O2
?
100% activity
-
-
?
2,2'-azino-bis-(3-ethylbenzthiazole-6-sulfonic acid) + (13S)-hydroperoxylinoleic acid
?
-
-
-
-
?
2,2'-azino-bis-(3-ethylbenzthiazole-6-sulfonic acid) + (5S)-hydroperoxyarachidonic acid
?
-
-
-
-
?
2,2'-azino-bis-(3-ethylbenzthiazole-6-sulfonic acid) + (8R)-hydroperoxyarachidonic acid
?
-
-
-
-
?
2,2'-azino-bis-(3-ethylbenzthiazole-6-sulfonic acid) + (9S)-hydroperoxylinoleic acid
?
-
-
-
-
?
2,2'-azino-bis-(3-ethylbenzthiazole-6-sulfonic acid) + cumene hydroperoxide
?
-
-
-
-
?
2,2'-azino-bis-(3-ethylbenzthiazole-6-sulfonic acid) + H2O2
?
2,2'-azino-bis-(3-ethylbenzthiazole-6-sulfonic acid) + tert-butyl hydroperoxide
?
-
-
-
-
?
2,2'-azinobis(3-ethylbenzthiazoline-6-sulfonic acid) + H2O2
? + H2O
2,2'-methylene-bis[4-chlorophenol] + H2O2
4-chlorophenol-2,2'-methylene-1,4-benzoquinone + HCl
-
-
-
-
?
2,2-azino-bis(3-ethylbenzothiazoline-6-sulfonic acid)diammonium salt + H2O2
?
-
-
-
-
?
2,2-azino-bis-(3-ethylbenz-thiazoline-6-sulfonic acid) + H2O2
2,2-azino-bis-(3-ethylbenz-thiazoline-6-sulfonic acid) radical + H2O
-
-
-
-
?
2,2-azino-bis-(3-ethylbenz-thiazoline-6-sulfonic acid) + H2O2
? + H2O
2,3-dimethoxyphenol + H2O2
? + H2O
-
-
-
-
?
2,4,6-tribromophenol + H2O2
? + H2O
2,4,6-trichlorophenol + H2O2
?
-
-
-
-
?
2,4,6-trichlorophenol + H2O2
? + H2O
2,4-dibromophenol + H2O2
?
-
-
-
-
?
2,4-dichlorophenol + H2O2
?
2,6-dimethoxyphenol + 2 H+ + H2O2
oxidized 2,6-dimethoxyphenol + 2 H2O
2,6-dimethoxyphenol + H2O2
?
-
-
-
-
?
2,6-dimethoxyphenol + H2O2
? + H2O
-
lowest specific activity
-
-
?
2,6-dimethyloxyphenol + H2O2
? + H2O
2-(1,3-benzothiazol-2-yl)-5-(diethylamino)phenol + H2O2
?
-
-
-
-
?
2-(4-[4-[(E)-2-quinolin-2-ylethenyl]phenyl]piperazin-1-yl)ethanol perchlorate (salt) + H2O2
?
-
-
-
-
?
2-aminophenol + H2O2
2-amino-9,10a-dihydro-3H-phenoxazin-3-one
-
-
-
-
ir
2-chloro-4-methoxyphenol + H2O2
? + H2O
-
-
-
-
?
2-chlorophenol + H2O2
?
-
optimal concentrations of 2-chlorophenol and H2O2 are 0.2 mM and 0.3 mM, respectively
-
-
r
2-naphthol + H2O2
? + H2O
-
peroxidase is inactived during oxidation
-
-
?
2-[(1Z,3Z)-4-[4-(dimethylamino)phenyl]buta-1,3-dien-1-yl]-3-propyl-1,3-benzothiazol-3-ium iodide + H2O2
?
-
-
-
-
?
2-[(E)-2-[4-(diethylamino)phenyl]ethenyl]-3-propyl-1,3-benzothiazol-3-ium iodide + H2O2
?
-
-
-
-
?
2-[(E)-2-[4-(dimethylamino)naphthalen-1-yl]ethenyl]-3-ethyl-1,3-benzothiazol-3-ium iodide + H2O2
?
-
-
-
-
?
2-[(E)-2-[4-(dimethylamino)phenyl]ethenyl]-1-propylpyridinium iodide + H2O2
?
-
-
-
-
?
2-[(E)-2-[4-(dimethylamino)phenyl]ethenyl]-1-propylquinolinium iodide + H2O2
?
-
-
-
-
?
2-[(E)-2-[4-(dimethylamino)phenyl]ethenyl]-3-propyl-1,3-benzothiazol-3-ium iodide + H2O2
?
-
-
-
-
?
2-[(E)-2-[4-(diphenylamino)phenyl]ethenyl]-3-propyl-1,3-benzothiazol-3-ium iodide + H2O2
?
-
-
-
-
?
2-[(E)-2-[4-(diprop-2-en-1-ylamino)phenyl]ethenyl]-3-ethyl-1,3-benzothiazol-3-ium iodide + H2O2
?
-
-
-
-
?
2-[(E)-2-[4-[4-(2-hydroxyethyl)piperazin-1-yl]phenyl]ethenyl]-1-propylquinolinium iodide + H2O2
?
-
-
-
-
?
2-[(E)-2-[4-[4-(2-hydroxyethyl)piperazin-1-yl]phenyl]ethenyl]-3-propyl-1,3-benzothiazol-3-ium iodide + H2O2
?
-
-
-
-
?
2-[(E)-2-[4-[4-(2-hydroxyethyl)piperazin-1-yl]phenyl]ethenyl]-3-propyl-1,3-benzoxazol-3-ium iodide + H2O2
?
-
-
-
-
?
2-[(E)-2-[4-[bis(2-hydroxyethyl)amino]phenyl]ethenyl]-3-ethyl-1,3-benzothiazol-3-ium iodide + H2O2
?
-
-
-
-
?
2-[[4-(1,3-benzothiazol-2-yl)phenyl](ethyl)amino]ethanol + H2O2
?
-
-
-
-
?
3,3',5,5'-tetramethyl benzidine + H2O2
?
-
-
-
-
?
3,3',5,5'-tetramethylbenzidine + H2O2
?
3,3',5,5'-tetramethylbenzidine + H2O2
? + H2O
3,4-dihydroxyphenylacetic acid + H2O2
? + H2O
-
-
-
-
?
3,4-dimethoxyphenol + H2O2
? + H2O
-
-
-
-
?
3,5-dibromo-4-hydroxybenzonitrile + H2O2
? + HBr
-
-
a dimer and a trimer are the main products
-
?
3,5-dimethoxyphenol + H2O2
? + H2O
-
-
-
-
?
3,5-dimethyl-4-hydroxy-azobenzene-4'-sulfonic acid + H2O2
?
-
-
-
-
?
3-(4-carboxybutyl)-2-[(E)-2-[4-(dimethylamino)phenyl]ethenyl]-1,3-benzothiazol-3-ium iodide + H2O2
?
-
-
-
-
?
3-(4-hydroxyphenyl)propanoic acid + H2O2
? + H2O
-
-
-
-
?
3-(4-[(E)-2-[4-(dimethylamino)phenyl]ethenyl]quinolinium-1-yl)propanoate + H2O2
?
-
-
-
-
?
3-ethyl-2-[(E)-2-(9-ethyl-9H-carbazol-3-yl)ethenyl]-1,3-benzothiazol-3-ium iodide + H2O2
?
-
-
-
-
?
3-methyltyrosine + H2O2
3-hydroxy-5-methyltyrosine + H2O
-
-
-
-
?
3-[(E)-2-(4-nitrophenyl)ethenyl]-1H-indole + H2O2
?
-
-
-
-
?
4-(2-aminoethyl)phenol + H2O2
?
-
-
-
-
?
4-(4-[(E)-2-[4-(dimethylamino)phenyl]ethenyl]pyridinium-1-yl)butane-1-sulfonate + H2O2
?
-
-
-
-
?
4-(diethylamino)benzaldehyde + H2O2
?
-
-
-
-
?
4-(dimethylamino)benzaldehyde + H2O2
?
-
-
-
-
?
4-aminoantipyrin + H2O2
?
-
-
-
-
?
4-aminoantipyrine + H2O2
?
4-aminoantipyrine + phenol + H2O2
quinoneimine + H2O
-
-
-
-
?
4-aminophenazone + H2O2
?
-
-
-
-
r
4-aminophenol + H2O2
?
-
-
-
-
?
4-hydroxybenzaldehyde + H2O2
?
-
-
-
-
?
4-hydroxybenzoic acid + H2O2
?
-
-
-
-
?
4-hydroxybenzonitrile + H2O2
?
-
-
-
-
?
4-hydroxybiphenyl + H2O2
? + H2O
-
peroxidase is inactived during oxidation
-
-
?
4-methoxy-alpha-naphthol + H2O
? + H2O
-
-
-
-
?
4-methoxy-alpha-naphthol + H2O2
?
-
-
-
-
?
4-methoxy-alpha-naphthol + H2O2
? + H2O
-
-
-
-
?
4-methylcatechol + H2O2
?
4-methylphenol + H2O2
?
-
-
-
-
?
4-nitrophenol + H2O2
? + H2O
-
-
-
-
?
4-[(1E,3E)-4-[4-(dimethylamino)phenyl]buta-1,3-dien-1-yl]-1-methylpyridinium iodide + H2O2
?
-
-
-
-
?
4-[(1E,3E)-4-[4-(dimethylamino)phenyl]buta-1,3-dien-1-yl]-1-pentylpyridinium iodide + H2O2
?
-
-
-
-
?
4-[(1Z)-3-[4-(dimethylamino)phenyl]prop-1-en-1-yl]-1-(2-propoxyethyl)quinolinium perchlorate + H2O2
?
-
-
-
-
?
4-[(1Z,3Z)-4-[4-(dimethylamino)phenyl]buta-1,3-dien-1-yl]-1-(2-propoxyethyl)quinolinium perchlorate + H2O2
?
-
-
-
-
?
4-[(1Z,3Z)-4-[4-(dimethylamino)phenyl]buta-1,3-dien-1-yl]-1-methylquinolinium iodide + H2O2
?
-
-
-
-
?
4-[(1Z,3Z)-4-[4-(dimethylamino)phenyl]buta-1,3-dien-1-yl]-1-propylquinolinium iodide + H2O2
?
-
-
-
-
?
4-[(1Z,3Z)-4-[4-(dimethylamino)phenyl]buta-1,3-dien-1-yl]-1-[2-(2-hydroxyethoxy)ethyl]quinolinium iodide + H2O2
?
-
-
-
-
?
4-[(E)-2-(1,3-benzothiazol-2-yl)ethenyl]-N,N-dimethylaniline + H2O2
?
-
-
-
-
?
4-[(E)-2-(1H-indol-3-yl)ethenyl]-1-methylquinolinium iodide + H2O2
?
-
-
-
-
?
4-[(E)-2-(9-ethyl-9H-carbazol-3-yl)ethenyl]-1-methylpyridinium iodide + H2O2
?
-
-
-
-
?
4-[(E)-2-benzo[g]quinolin-4-ylethenyl]-N,N-dimethylaniline + H2O2
?
-
-
-
-
?
4-[(E)-2-[4-(acetylamino)phenyl]ethenyl]-1-methylpyridinium iodide + H2O2
?
-
-
-
-
?
4-[(E)-2-[4-(acetylamino)phenyl]ethenyl]-1-methylquinolinium iodide + H2O2
?
-
-
-
-
?
4-[(E)-2-[4-(dimethylamino)naphthalen-1-yl]ethenyl]-1-methylpyridinium iodide + H2O2
?
-
-
-
-
?
4-[(E)-2-[4-(dimethylamino)phenyl]ethenyl]-1-(1,3-dioxolan-2-ylmethyl)pyridinium + H2O2
?
-
-
-
-
?
4-[(E)-2-[4-(dimethylamino)phenyl]ethenyl]-1-(1,3-dioxolan-2-ylmethyl)pyridinium bromide + H2O2
?
-
-
-
-
?
4-[(E)-2-[4-(dimethylamino)phenyl]ethenyl]-1-(2-ethoxyethyl)pyridinium bromide + H2O2
?
-
-
-
-
?
4-[(E)-2-[4-(dimethylamino)phenyl]ethenyl]-1-(2-hydroxyethyl)pyridinium bromide + H2O2
?
-
-
-
-
?
4-[(E)-2-[4-(dimethylamino)phenyl]ethenyl]-1-(2-hydroxyethyl)pyridinium iodide + H2O2
?
-
-
-
-
?
4-[(E)-2-[4-(dimethylamino)phenyl]ethenyl]-1-(3-methylbutyl)pyridinium bromide + H2O2
?
-
-
-
-
?
4-[(E)-2-[4-(dimethylamino)phenyl]ethenyl]-1-(5-ethoxy-5-oxopentyl)pyridinium perchlorate + H2O2
?
-
-
-
-
?
4-[(E)-2-[4-(dimethylamino)phenyl]ethenyl]-1-dodecylquinolinium bromide + H2O2
?
-
-
-
-
?
4-[(E)-2-[4-(dimethylamino)phenyl]ethenyl]-1-methylpyridinium iodide + H2O2
?
-
-
-
-
?
4-[(E)-2-[4-(dimethylamino)phenyl]ethenyl]-1-methylquinolinium iodide + H2O2
?
-
-
-
-
?
4-[(E)-2-[4-(dimethylamino)phenyl]ethenyl]-1-octylpyridinium bromide + H2O2
?
-
-
-
-
?
4-[(E)-2-[4-(dimethylamino)phenyl]ethenyl]-1-propylpyridinium iodide + H2O2
?
-
-
-
-
?
4-[(E)-2-[4-(dimethylamino)phenyl]ethenyl]-1-propylquinolinium iodide + H2O2
?
-
-
-
-
?
4-[(E)-2-[4-(diphenylamino)phenyl]ethenyl]-1-methylpyridinium iodide + H2O2
?
-
-
-
-
?
4-[(E)-2-[4-(diprop-2-en-1-ylamino)phenyl]ethenyl]-1-methylpyridinium iodide + H2O2
?
-
-
-
-
?
4-[(E)-2-[4-[4-(2-hydroxyethyl)piperazin-1-yl]phenyl]ethenyl]-1-propylpyridinium iodide + H2O2
?
-
-
-
-
?
4-[(E)-2-[4-[4-(2-hydroxyethyl)piperazin-1-yl]phenyl]ethenyl]-1-propylquinolinium iodide + H2O2
?
-
-
-
-
?
4-[(Z)-2-(4-aminophenyl)-2-cyanoethenyl]benzoic acid + H2O2
?
-
-
-
-
?
5-aminophthalhydrazide + H2O2
?
-
i.e. luminol, chemiluminescent substrate
-
-
?
5-aminosalicylic acid + H2O2
? + H2O
-
-
-
-
?
5-ethyl-6-phenyl-5,6-dihydrophenanthridine-3,8-diamine + H2O2
?
-
-
-
-
?
5-O-(trans-feruloyl)-L-arabinose + H2O2
?
-
-
-
-
?
7-nitropyren-1-amine + H2O2
?
-
-
-
-
?
8-nitropyren-1-amine + H2O2
?
-
-
-
-
?
9-ethyl-6-nitro-9H-carbazol-3-amine + H2O2
?
-
-
-
-
?
ABTS + H2O2
?
-
89% activity compared to guaiacol
-
-
?
acetaminophen + H2O2
?
-
-
-
-
?
Acid Blue 45 + H2O2
?
-
-
-
-
?
acrylonitrile + H2O2
cyanide + H2O
-
-
-
-
?
adlerol + H2O2
?
-
-
-
-
?
aminoantipyrine + H2O2
? + H2O
AmplexRed + cumene hydroperoxide
?
AmplexRed + tert-butyl hydroperoxide
?
aniline blue + H2O2
? + H2O
-
-
-
-
?
ascorbate + H2O2
dehydroascorbate + H2O
-
-
-
-
?
Azure B + H2O2
?
-
-
-
-
?
benzhydroxamic acid + H2O2
? + H2O
-
-
-
?
benzidine + H2O2
? + H2O
-
26% of the activity with tetramethylbenzidine
-
-
?
benzohydroxamic acid + H2O2
?
the estimated rate constant is approximately one-tenth of that of o-dianisidine
-
-
?
benzoic acid + H2O2
? + H2O
Br- + H2O2
hypobromous acid + H2O
caffeic acid + H2O2
? + H2O
capsaicin + H2O2
5,5'-dicapsaicin + 4'-O-5-dicapsaicin ether + capsaicin polymers
-
-
-
-
?
chlorogenic acid + H2O2
?
chlorogenic acid + H2O2
? + H2O
-
-
-
-
?
chlorophyll b + H2O2
?
-
-
-
-
?
chlorophyllide a + H2O2
?
-
-
-
-
?
chlorophyllide b + H2O2
?
-
-
-
-
?
cinnamic acid + H2O2
? + H2O
cis-beta-methylstyrene + H2O
cis-beta-methylstyrene epoxide + H2O
cis-beta-methylstyrene + H2O2
cis-beta-methylstyrene oxide + trans-beta-methylstyrene oxide + 1-phenyl-2-propanone + benzaldehyde + H2O
Armoracia sp.
-
only F41T-mutant
-
?
cis-stilbene + H2O
cis-stilbene epoxide + H2O
Cl- + H2O2
HOCl + H2O
-
-
-
-
?
coniferyl alcohol + H2O2
?
coniferyl alcohol + H2O2
? + H2O
D-iso-ascorbate + H2O2
?
-
134% activity compared to guaiacol
-
-
?
diaminobenzidine + H2O2
? + H2O
-
16% of the activity with tetramethylbenzidine
-
-
?
dihydrocapsaicin + H2O2
5,5-didihydrocapsaicin + 4'-O-5-didihydrocapsaicin ether + dihydrocapsaicin polymers
-
-
-
-
?
electron donor + H2O2
oxidized electron donor + H2O
estradiol + H2O2
?
-
-
-
-
?
estriol + H2O
?
-
-
-
-
?
estrone + H2O2
?
-
-
-
-
?
ethynylestradiol + H2O2
?
-
-
-
-
?
eugenol + H2O2
?
-
-
-
-
?
eugenol + H2O2
? + H2O
-
-
-
-
?
ferulic acid + H2O2
? + H2O
gallic acid + H2O2
? + H2O
-
-
-
-
?
guaiacol + H2O2
tetraguaiacol + H2O
guaicol + H2O2
tetraguaiacol + 2 H2O
-
-
-
-
?
hydroquinone + H2O2
? + H2O
-
-
-
-
?
indole-3-acetate + 2,4-dichlorophenolindophenol + H2O2
?
Elais guineensis
-
-
-
-
?
indole-3-acetic acid + H2O2
?
iodide + H2O2
?
15% activity compared to 2,2'-azino-bis-(3-ethyl-6-benzothiazolinsulfonate)
-
-
?
L-3,4-dihydroxyphenylalanine + H2O2
?
-
-
-
-
?
L-ascorbate + H2O2
?
-
126% activity compared to guaiacol
-
-
?
L-ascorbate + H2O2
dehydroascorbate + H2O
-
-
-
-
?
m-hydroxyanisol + H2O2
? + H2O
-
-
-
-
?
m-phenylenediamine + H2O2
? + H2O
malachite green + H2O2
?
-
-
-
-
?
mitoxanthrone + H2O2
?
-
-
-
?
N,N,N',N'-tetramethyl-p-phenyldiamine + H2O2
? + H2O
-
-
-
-
?
N,N-diethylaniline + H2O2
?
-
-
-
-
?
N,N-dimethyl-4-[(E)-2-(4-nitrophenyl)ethenyl]aniline + H2O2
?
-
-
-
-
?
N,N-dimethyl-4-[(E)-2-nitroethenyl]aniline + H2O2
?
-
-
-
-
?
N,N-dimethyl-4-[(E)-2-pyridin-4-ylethenyl]aniline + H2O2
?
-
-
-
-
?
N,N-dimethyl-4-[(E)-2-quinolin-2-ylethenyl]aniline + H2O2
?
-
-
-
-
?
N,N-dimethyl-4-[(E)-2-quinolin-2-ylethenyl]aniline perchlorate + H2O2
?
-
-
-
-
?
N,N-dimethyl-4-[(E)-2-quinolin-4-ylethenyl]aniline + H2O2
?
-
-
-
-
?
N,N-diphenyl-4-[(E)-2-pyridin-4-ylethenyl]aniline + H2O2
?
-
-
-
-
?
N-acetyl-L-tyrosine + H2O2
?
-
-
-
?
N-acetyl-L-tyrosine methyl ester + H2O2
?
-
-
-
?
N-ethyl-N-(2-hydroxy-3-sulfopropyl)-m-toluidine + H2O2
?
NADH + H2O2
NAD+ + H2O
-
-
-
?
NADPH + H2O2
?
-
134% activity compared to guaiacol
-
-
?
NADPH + H2O2
NADP+ + H2O
-
-
-
?
NO2- + H2O2
? + H2O
-
-
-
-
?
o-anisidine + H2O2
?
the peroxidase specific activities determined under comparable conditions (pH 8 and 5°C) reveal that of o-anisidine to be one-tenth of that of o-dianisidine
-
-
?
o-coumaric acid + H2O2
?
-
-
-
-
?
o-cresol + H2O2
?
-
-
-
-
?
o-dianisidine + H2O2
? + H2O
o-phenylenediamine + H2O2
?
o-phenylenediamine + H2O2
? + H2O
o-toluidine + H2O2
? + H2O
-
-
-
-
?
p-aminoantipyrine + H2O2
? + H2O
p-hydroxy-(beta-carboxymethyl)cinnamic acid + H2O2
?
-
-
-
-
?
p-hydroxybenzoic acid + H2O2
?
-
-
-
-
?
p-hydroxybenzoic acid + H2O2
? + H2O
p-hydroxyphenylacetamide + H2O2
? + H2O
-
a model compound of tyrosine residues in fibroins
-
-
?
p-phenylenediamine + H2O2
? + H2O
-
14% of the activity with tetramethylbenzidine
-
-
?
p-phenylenediamine + H2O2
benzene-1,4-diamine + H2O
-
-
-
-
?
p-phenylenediamine + H2O2
cyclohexa-2,5-diene-1,4-diimine + H2O
-
-
-
-
?
p-phenylenediamine hydrochloride + H2O2
?
-
-
-
-
?
pentachlorophenol + H2O2
2,3,5,6-tetrachloro-1,4-benzoquinone + HCl
-
-
-
-
?
phenyl cyclopropyl thioether + H2O2
?
Armoracia sp.
-
-
-
-
?
phenyl ethyl thioether + H2O2
?
Armoracia sp.
-
-
-
-
?
phenyl propyl thioether + H2O2
?
Armoracia sp.
-
-
-
-
?
pheophytin a + H2O2
?
-
-
-
-
?
promethazine + H2O2
promethazine sulfoxide + H2O
Armoracia sp.
-
-
-
?
pyrocatechol + H2O2
?
-
-
-
-
?
pyrogallol + H2O2
? + H2O
pyrogallol + H2O2
purpurogallin + H2O
Reactive Black 5 + H2O2
?
Reactive Black 5 + H2O2
? + H2O
-
-
-
-
?
Reactive Blue 114 + H2O2
?
-
-
-
-
?
Reactive Blue 119 + H2O2
?
-
-
-
-
?
reactive blue 19 + H2O2
? + H2O
Reactive Blue 4 + H2O2
?
-
-
-
-
?
reduced 2,2'-azino-bis-(3-ethylbenzthiazole-6-sulfonic acid) + H2O2
oxidized 2,2'-azino-bis-(3-ethylbenzthiazole-6-sulfonic acid) + H2O
reduced thioredoxin 1 + cumene hydroperoxide
oxidized thioredoxin 1 + cumene hydroxide
-
-
-
?
reduced thioredoxin 1 + H2O2
oxidized thioredoxin 1 + H2O
-
-
-
?
Remazol Brilliant Blue R + H2O2
?
rubredoxin + H2O2
? + H2O
-
-
-
-
?
sinapyl alcohol + H2O2
? + H2O
sodium 4-hydroxybenzoate + H2O2
?
-
-
-
-
?
styrene + H2O2
styrene epoxide + H2O
styrene + H2O2
styrene oxide + benzaldehyde + phenylacetaldehyde + H2O
Armoracia sp.
-
only F41L and F41T-mutant
-
?
syringaldehyde + H2O2
?
-
23% activity compared to guaiacol
-
-
?
tannic acid + H2O2
? + H2O
taurine + Cl- + H2O2
taurine chloramine + HOCl + H2O
-
-
-
-
?
tetramethylbenzidine + H2O2
?
tetramethylbenzidine + H2O2
? + H2O
-
-
-
-
?
thioanisole + H2O2
?
Armoracia sp.
-
-
-
-
?
thiocyanate + H2O2
?
-
-
-
-
?
thiocyanate + H2O2
hypothiocyanate + H2O
-
-
-
?
thiocyanate + H2O2
OSCN- + H2O
-
-
-
-
?
trans-beta-methylstyrene + H2O2
trans-beta-methylstyrene oxide + benzaldehyde + H2O
Armoracia sp.
-
-
-
?
tyrosine + H2O2
?
-
-
-
-
?
ubiquinol-1 + H2O2
? + H2O
ubiquinol-1 + H2O2
ubiquinone-1 + H2O
-
-
-
?
vanillic acid + H2O2
?
-
-
-
-
?
veratryl alcohol + H2O2
?
veratryl alcohol + H2O2
? + H2O
-
-
-
-
?
West Pico + H2O2
?
-
-
-
-
?
additional information
?
-
2 guaiacol + H2O2
3,3'-dimethoxy-4,4'-biphenylquinone + H2O
-
-
-
?
2 guaiacol + H2O2
3,3'-dimethoxy-4,4'-biphenylquinone + H2O
-
-
-
-
?
2 guaiacol + H2O2
3,3'-dimethoxy-4,4'-biphenylquinone + H2O
Brassica oleracea var. capitata f. rubra
-
-
-
-
?
2 guaiacol + H2O2
3,3'-dimethoxy-4,4'-biphenylquinone + H2O
-
-
-
-
?
2 guaiacol + H2O2
3,3'-dimethoxy-4,4'-biphenylquinone + H2O
-
-
-
-
?
2 guaiacol + H2O2
3,3'-dimethoxy-4,4'-biphenylquinone + H2O
-
-
-
-
?
2 guaiacol + H2O2
3,3'-dimethoxy-4,4'-biphenylquinone + H2O
-
27% of the activity with 2,4-dichlorophenol
-
-
?
2 guaiacol + H2O2
3,3'-dimethoxy-4,4'-biphenylquinone + H2O
-
27% of the activity with 2,4-dichlorophenol
-
-
?
2 guaiacol + H2O2
3,3'-dimethoxy-4,4'-biphenylquinone + H2O
-
-
-
-
?
2 guaiacol + H2O2
3,3'-dimethoxy-4,4'-biphenylquinone + H2O
-
-
-
-
?
2 guaiacol + H2O2
3,3'-dimethoxy-4,4'-biphenylquinone + H2O
-
-
-
-
?
2 K4[Fe(CN)6] + H2O2
K3[Fe(CN)6] + H2O + K2O
-
-
-
-
?
2 K4[Fe(CN)6] + H2O2
K3[Fe(CN)6] + H2O + K2O
-
-
-
-
?
2 Mn(II) + 2 H+ + H2O2
2 Mn(III) + 2 H2O
-
-
-
?
2 Mn(II) + 2 H+ + H2O2
2 Mn(III) + 2 H2O
-
-
-
?
2 pyrogallol + H2O2
? + H2O
-
-
-
?
2 pyrogallol + H2O2
? + H2O
-
-
-
?
2 veratryl alcohol + H2O2
2 veratraldehyde + H2O
-
-
-
-
?
2 veratryl alcohol + H2O2
2 veratraldehyde + H2O
-
-
-
-
?
2,2'-azino-bis (3-ethylbenzthiazoline-6-sulphonic acid) + H2O2
? + H2O
-
-
-
?
2,2'-azino-bis (3-ethylbenzthiazoline-6-sulphonic acid) + H2O2
? + H2O
-
-
-
-
?
2,2'-azino-bis(3-ethylbenzthiazole-6-sulfonic acid) + H2O2
?
-
-
-
-
?
2,2'-azino-bis(3-ethylbenzthiazole-6-sulfonic acid) + H2O2
?
Armoracia sp.
-
-
-
-
?
2,2'-azino-bis(3-ethylbenzthiazole-6-sulfonic acid) + H2O2
?
-
-
-
-
?
2,2'-azino-bis(3-ethylbenzthiazole-6-sulfonic acid) + H2O2
?
-
-
-
-
?
2,2'-azino-bis(3-ethylbenzthiazole-6-sulfonic acid) + H2O2
?
-
-
-
-
?
2,2'-azino-bis(3-ethylbenzthiazole-6-sulfonic acid) + H2O2
?
-
-
-
-
?
2,2'-azino-bis(3-ethylbenzthiazole-6-sulfonic acid) + H2O2
?
-
-
-
-
?
2,2'-azino-bis(3-ethylbenzthiazole-6-sulfonic acid) + H2O2
?
-
-
-
-
?
2,2'-azino-bis(3-ethylbenzthiazole-6-sulfonic acid) + H2O2
?
-
-
-
-
?
2,2'-azino-bis(3-ethylbenzthiazole-6-sulfonic acid) + H2O2
?
-
-
-
-
?
2,2'-azino-bis(3-ethylbenzthiazole-6-sulfonic acid) + H2O2
?
-
-
-
-
?
2,2'-azino-bis(3-ethylbenzthiazole-6-sulfonic acid) + H2O2
?
-
-
-
-
?
2,2'-azino-bis(3-ethylbenzthiazoline)-sulfonic acid + H2O2
?
-
-
-
-
?
2,2'-azino-bis(3-ethylbenzthiazoline)-sulfonic acid + H2O2
?
-
-
-
-
?
2,2'-azino-bis-(3-ethylbenzthiazole-6-sulfonic acid) + H2O2
?
-
-
-
-
?
2,2'-azino-bis-(3-ethylbenzthiazole-6-sulfonic acid) + H2O2
?
-
-
-
-
?
2,2'-azinobis(3-ethylbenzthiazoline-6-sulfonic acid) + H2O2
? + H2O
-
-
-
?
2,2'-azinobis(3-ethylbenzthiazoline-6-sulfonic acid) + H2O2
? + H2O
-
-
-
-
?
2,2'-azinobis(3-ethylbenzthiazoline-6-sulfonic acid) + H2O2
? + H2O
-
-
-
?
2,2'-azinobis(3-ethylbenzthiazoline-6-sulfonic acid) + H2O2
? + H2O
-
-
-
?
2,2'-azinobis(3-ethylbenzthiazoline-6-sulfonic acid) + H2O2
? + H2O
-
-
-
-
?
2,2'-azinobis(3-ethylbenzthiazoline-6-sulfonic acid) + H2O2
? + H2O
-
-
-
?
2,2'-azinobis(3-ethylbenzthiazoline-6-sulfonic acid) + H2O2
? + H2O
-
-
-
?
2,2'-azinobis(3-ethylbenzthiazoline-6-sulfonic acid) + H2O2
? + H2O
-
-
-
-
?
2,2'-azinobis(3-ethylbenzthiazoline-6-sulfonic acid) + H2O2
? + H2O
-
-
-
-
?
2,2'-azinobis(3-ethylbenzthiazoline-6-sulfonic acid) + H2O2
? + H2O
-
-
-
?
2,2-azino-bis-(3-ethylbenz-thiazoline-6-sulfonic acid) + H2O2
? + H2O
-
-
-
-
?
2,2-azino-bis-(3-ethylbenz-thiazoline-6-sulfonic acid) + H2O2
? + H2O
-
-
-
-
?
2,4,6-tribromophenol + H2O2
? + H2O
-
-
-
?
2,4,6-tribromophenol + H2O2
? + H2O
-
-
-
-
?
2,4,6-trichlorophenol + H2O2
? + H2O
-
-
-
?
2,4,6-trichlorophenol + H2O2
? + H2O
-
-
-
-
?
2,4-dichlorophenol + H2O2
?
-
-
-
-
?
2,4-dichlorophenol + H2O2
?
-
-
-
-
?
2,4-dichlorophenol + H2O2
?
-
-
-
-
?
2,4-dichlorophenol + H2O2
?
-
-
-
-
?
2,4-dichlorophenol + H2O2
?
-
-
-
-
?
2,6-dimethoxyphenol + 2 H+ + H2O2
oxidized 2,6-dimethoxyphenol + 2 H2O
Mn2+ is absolutely required for the activity
-
-
?
2,6-dimethoxyphenol + 2 H+ + H2O2
oxidized 2,6-dimethoxyphenol + 2 H2O
Mn2+ is absolutely required for the activity
-
-
?
2,6-dimethyloxyphenol + H2O2
? + H2O
-
-
-
-
?
2,6-dimethyloxyphenol + H2O2
? + H2O
-
-
-
-
?
3,3',5,5'-tetramethylbenzidine + H2O2
?
-
-
-
-
?
3,3',5,5'-tetramethylbenzidine + H2O2
?
-
-
-
?
3,3',5,5'-tetramethylbenzidine + H2O2
?
-
-
-
-
?
3,3',5,5'-tetramethylbenzidine + H2O2
? + H2O
-
-
-
-
?
3,3',5,5'-tetramethylbenzidine + H2O2
? + H2O
-
-
-
?
4-aminoantipyrine + H2O2
?
-
-
-
-
?
4-aminoantipyrine + H2O2
?
-
643% activity compared to guaiacol
-
-
?
4-aminoantipyrine + H2O2
?
-
-
-
-
?
4-aminoantipyrine + H2O2
?
-
-
-
-
?
4-aminoantipyrine + H2O2
?
-
-
-
-
?
4-aminoantipyrine + H2O2
?
-
-
-
-
?
4-chlorophenol + H2O2
?
-
-
-
-
?
4-chlorophenol + H2O2
?
-
in the absence of polyethylene glycol, pyromellitic dianhydride-modified peroxidase converts 100% 4-chlorophenol, while at the same time, native enzyme can convert only 85%. In the presence of polyethylene glycol, pyromellitic dianhydride-modified peroxidase converts 4-chlorophenol completely in 45 min, while native TP I requires 60 min for complete conversion
-
-
?
4-methylcatechol + H2O2
?
28% activity compared to guaiacol
-
-
?
4-methylcatechol + H2O2
?
47% activity compared to guaiacol
-
-
?
4-nitrophenol + H2O2
?
-
-
-
-
?
4-nitrophenol + H2O2
?
-
-
-
-
?
aminoantipyrine + H2O2
? + H2O
-
1.5% of the activity with o-phenylenediamine, isoenzyme FP2
-
-
?
aminoantipyrine + H2O2
? + H2O
-
2.5% of the activity with o-phenylenediamine, isoenzyme FP1
-
-
?
aminoantipyrine + H2O2
? + H2O
-
7.2% of the activity with o-phenylenediamine, isoenzyme FP3
-
-
?
Amplex Red + H2O2
?
-
-
-
-
?
Amplex Red + H2O2
?
-
-
-
-
?
AmplexRed + cumene hydroperoxide
?
the initial activity of CYP119 in the presence of cumene hydroperoxide is 5fold higher than that observed with H2O2
-
-
?
AmplexRed + cumene hydroperoxide
?
the initial activity of CYP119 in the presence of cumene hydroperoxide is 5fold higher than that observed with H2O2
-
-
?
AmplexRed + H2O2
? + H2O
-
-
-
?
AmplexRed + H2O2
? + H2O
-
-
-
?
AmplexRed + tert-butyl hydroperoxide
?
the initial activity of CYP119 in the presence of tert-butyl hydroperoxide is 2fold higher than that observed with H2O2
-
-
?
AmplexRed + tert-butyl hydroperoxide
?
the initial activity of CYP119 in the presence of tert-butyl hydroperoxide is 2fold higher than that observed with H2O2
-
-
?
ascorbic acid + H2O
?
-
isoenzyme POX I
-
-
?
ascorbic acid + H2O
?
-
isoenzyme POX II
-
-
?
benzoic acid + H2O2
?
10% activity compared to guaiacol
-
-
?
benzoic acid + H2O2
?
19% activity compared to guaiacol
-
-
?
benzoic acid + H2O2
? + H2O
-
27% compared to the activity with guaiacol, anionic peroxidase GCP2
-
-
?
benzoic acid + H2O2
? + H2O
-
activity is 2.13fold higher than activity with guaiacol, cationic peroxidase GCP1
-
-
?
Br- + H2O2
?
-
-
-
-
?
Br- + H2O2
hypobromous acid + H2O
-
-
-
-
?
Br- + H2O2
hypobromous acid + H2O
-
NO displays the potential capacity to promote substrate switching by modulating substrate selectivity of EPO. In the absence of NO, EPO-Fe(III) primarily converts to compound I and, upon H2O2 exhaustion, it decays rapidly to the ferric form. NO causes a significant increase in the accumulation of EPO compound II
-
-
?
caffeic acid + H2O2
?
-
-
-
-
?
caffeic acid + H2O2
?
-
-
-
-
?
caffeic acid + H2O2
? + H2O
-
-
-
-
?
caffeic acid + H2O2
? + H2O
-
-
-
-
?
catechin + H2O2
?
10% activity compared to guaiacol
-
-
?
catechin + H2O2
?
19% activity compared to guaiacol
-
-
?
catechin + H2O2
? + H2O
-
1.7% compared to the activity with guaiacol, cationic peroxidase GCP1
-
-
?
catechin + H2O2
? + H2O
-
3.5% compared to the activity with guaiacol, anionic peroxidase GCP2
-
-
?
catechol + H2O2
?
-
-
-
-
?
catechol + H2O2
?
-
4.0% activity compared to guaiacol
-
-
?
catechol + H2O2
?
30% activity compared to guaiacol
-
-
?
catechol + H2O2
?
36% activity compared to guaiacol
-
-
?
catechol + H2O2
?
-
-
-
-
?
catechol + H2O2
? + H2O
-
-
-
-
?
catechol + H2O2
? + H2O
-
4.5% compared to the activity with guaiacol, cationic peroxidase GCP1
-
-
?
catechol + H2O2
? + H2O
-
5.1% compared to the activity with guaiacol, anionic peroxidase GCP2
-
-
?
catechol + H2O2
? + H2O
-
-
-
-
?
catechol + H2O2
? + H2O
-
-
-
-
?
catechol + H2O2
? + H2O
-
-
-
?
catechol + H2O2
? + H2O
-
-
-
-
?
chlorogenic acid + H2O2
?
-
-
-
-
?
chlorogenic acid + H2O2
?
80% activity compared to guaiacol
-
-
?
chlorogenic acid + H2O2
?
95% activity compared to guaiacol
-
-
?
chlorogenic acid + H2O2
?
-
-
-
-
?
chlorogenic acid + H2O2
?
-
-
-
-
?
chlorophyll a + H2O2
?
-
in the active centre of the enzyme the imidazole nitrogen of His-42plays a crucial role in the C-132 deprotonation of chlorophyll a, which results in the chlorophyll a enolate ion resonance hybrid. The chlorophyll enolate is then oxidized to the chlorophyll 132-radical
-
-
?
chlorophyll a + H2O2
?
-
-
-
-
?
cinnamic acid + H2O2
? + H2O
-
15% compared to the activity with guaiacol, cationic peroxidase GCP1
-
-
?
cinnamic acid + H2O2
? + H2O
-
activity is 1.18fold higher than activity with guaiacol, anionic peroxidase GCP2
-
-
?
cis-beta-methylstyrene + H2O
cis-beta-methylstyrene epoxide + H2O
epoxidation takes place with complete retention of the olefin stereochemistry
-
-
?
cis-beta-methylstyrene + H2O
cis-beta-methylstyrene epoxide + H2O
epoxidation takes place with complete retention of the olefin stereochemistry
-
-
?
cis-stilbene + H2O
cis-stilbene epoxide + H2O
epoxidation takes place with complete retention of the olefin stereochemistry
-
-
?
cis-stilbene + H2O
cis-stilbene epoxide + H2O
epoxidation takes place with complete retention of the olefin stereochemistry
-
-
?
Cl- + H2O2
HClO + H2O
-
-
-
-
?
Cl- + H2O2
HClO + H2O
-
-
-
-
?
coniferyl alcohol + H2O2
?
-
-
-
-
?
coniferyl alcohol + H2O2
?
-
-
-
-
?
coniferyl alcohol + H2O2
? + H2O
-
18% compared to the activity with guaiacol, cationic peroxidase GCP1
-
-
?
coniferyl alcohol + H2O2
? + H2O
-
activity is 1.27fold higher than activity with guaiacol, anionic peroxidase GCP2
-
-
?
crystal violet + H2O2
?
-
-
-
-
?
crystal violet + H2O2
?
-
-
-
-
?
electron donor + H2O2
oxidized electron donor + H2O
-
-
-
-
?
electron donor + H2O2
oxidized electron donor + H2O
-
-
-
-
r
electron donor + H2O2
oxidized electron donor + H2O
-
LPO also has pseudo-catalase activity
-
-
r
esculetin + H2O2
?
-
-
-
-
?
esculetin + H2O2
?
-
demonstration, that esculetin is no inhibitor, but a substrate of mushroom polyphenol oxidase (PPO) and horseradish peroxidase (POD)
-
-
?
esculetin + H2O2
?
-
-
-
-
?
esculetin + H2O2
?
-
-
-
-
?
ferulic acid + H2O2
?
Armoracia sp.
-
-
-
-
?
ferulic acid + H2O2
?
-
major apparent catalytic efficiency towards ferulic acid
-
-
?
ferulic acid + H2O2
?
-
-
-
-
?
ferulic acid + H2O2
?
-
-
-
-
?
ferulic acid + H2O2
?
-
-
-
-
?
ferulic acid + H2O2
?
-
-
-
?
ferulic acid + H2O2
?
-
-
-
-
?
ferulic acid + H2O2
?
-
-
-
-
?
ferulic acid + H2O2
?
-
-
-
-
?
ferulic acid + H2O2
? + H2O
-
-
-
?
ferulic acid + H2O2
? + H2O
-
17% compared to the activity with guaiacol, cationic peroxidase GCP1
-
-
?
ferulic acid + H2O2
? + H2O
-
83.3% compared to the activity with guaiacol, anionic peroxidase GCP2
-
-
?
ferulic acid + H2O2
? + H2O
-
-
-
-
?
guaiacol + H2O2
?
-
100% activity
-
-
?
guaiacol + H2O2
?
-
-
-
-
?
guaiacol + H2O2
?
-
isoenzyme POX I
-
-
?
guaiacol + H2O2
?
-
isoenzyme POX II
-
-
?
guaiacol + H2O2
?
-
-
-
-
?
guaiacol + H2O2
? + H2O
-
-
-
-
?
guaiacol + H2O2
? + H2O
-
-
-
-
?
guaiacol + H2O2
? + H2O
-
-
-
-
?
guaiacol + H2O2
? + H2O
-
-
-
-
?
guaiacol + H2O2
? + H2O
Elais guineensis
-
-
-
-
?
guaiacol + H2O2
? + H2O
-
3.7% of the activity with o-phenylenediamine, isoenzyme FP2
-
-
?
guaiacol + H2O2
? + H2O
-
6.8% of the activity with o-phenylenediamine, isoenzyme FP3
-
-
?
guaiacol + H2O2
? + H2O
-
-
-
-
?
guaiacol + H2O2
? + H2O
-
-
-
?
guaiacol + H2O2
? + H2O
-
-
-
-
?
guaiacol + H2O2
tetraguaiacol + H2O
-
-
-
-
?
guaiacol + H2O2
tetraguaiacol + H2O
-
-
-
-
?
guaiacol + H2O2
tetraguaiacol + H2O
-
-
-
-
?
guaiacol + H2O2
tetraguaiacol + H2O
-
-
-
-
?
guaiacol + H2O2
tetraguaiacol + H2O
-
-
-
?
guaiacol + H2O2
tetraguaiacol + H2O
-
-
-
-
?
guaiacol + H2O2
tetraguaiacol + H2O
-
optimal concentrations of guaiacol and H2O2 are 0.5 mM and 0.3 mM, respectively
-
-
r
guaiacol + H2O2
tetraguaiacol + H2O
Armoracia sp.
-
-
-
?
guaiacol + H2O2
tetraguaiacol + H2O
Armoracia sp.
-
-
-
-
?
guaiacol + H2O2
tetraguaiacol + H2O
-
-
-
-
?
guaiacol + H2O2
tetraguaiacol + H2O
-
-
-
-
?
guaiacol + H2O2
tetraguaiacol + H2O
-
-
-
-
?
guaiacol + H2O2
tetraguaiacol + H2O
-
-
-
-
?
guaiacol + H2O2
tetraguaiacol + H2O
-
-
-
-
?
guaiacol + H2O2
tetraguaiacol + H2O
-
-
-
-
?
guaiacol + H2O2
tetraguaiacol + H2O
-
-
-
-
?
guaiacol + H2O2
tetraguaiacol + H2O
-
-
-
-
?
guaiacol + H2O2
tetraguaiacol + H2O
-
-
-
?
guaiacol + H2O2
tetraguaiacol + H2O
-
-
-
-
?
guaiacol + H2O2
tetraguaiacol + H2O
-
100% activity
-
-
?
guaiacol + H2O2
tetraguaiacol + H2O
-
-
-
-
?
guaiacol + H2O2
tetraguaiacol + H2O
-
-
-
-
?
guaiacol + H2O2
tetraguaiacol + H2O
-
-
-
-
?
guaiacol + H2O2
tetraguaiacol + H2O
-
-
-
-
?
guaiacol + H2O2
tetraguaiacol + H2O
-
-
-
?
guaiacol + H2O2
tetraguaiacol + H2O
-
-
-
-
?
guaiacol + H2O2
tetraguaiacol + H2O
-
-
-
-
?
guaiacol + H2O2
tetraguaiacol + H2O
-
17% of the activity with o-phenylenediamine, isoenzyme FP1
-
-
?
guaiacol + H2O2
tetraguaiacol + H2O
-
-
-
-
?
guaiacol + H2O2
tetraguaiacol + H2O
-
-
-
-
?
guaiacol + H2O2
tetraguaiacol + H2O
-
-
-
?
guaiacol + H2O2
tetraguaiacol + H2O
100% activity with guaiacol at 25 mM
-
-
?
guaiacol + H2O2
tetraguaiacol + H2O
shows high efficiency of interaction with guaiacol at 25 mM
-
-
?
guaiacol + H2O2
tetraguaiacol + H2O
100% activity, high efficiency of interaction with guaiacol at 25 mM
-
-
?
guaiacol + H2O2
tetraguaiacol + H2O
-
-
-
-
?
guaiacol + H2O2
tetraguaiacol + H2O
-
-
-
-
?
guaiacol + H2O2
tetraguaiacol + H2O
-
-
-
-
?
guaiacol + H2O2
tetraguaiacol + H2O
74% activity compared to 2,2'-azino-bis-(3-ethyl-6-benzothiazolinsulfonate)
-
-
?
guaiacol + H2O2
tetraguaiacol + H2O
-
-
-
-
?
guaiacol + H2O2
tetraguaiacol + H2O
-
-
-
-
?
guaiacol + H2O2
tetraguaiacol + H2O
-
-
-
-
?
guaiacol + H2O2
tetraguaiacol + H2O
-
-
-
-
?
guaiacol + H2O2
tetraguaiacol + H2O
-
-
-
-
?
guaiacol + H2O2
tetraguaiacol + H2O
-
-
-
-
?
guaiacol + H2O2
tetraguaiacol + H2O
-
-
-
-
?
guaiacol + H2O2
tetraguaiacol + H2O
-
-
-
-
?
guaiacol + H2O2
tetraguaiacol + H2O
-
-
-
-
?
guaiacol + H2O2
tetraguaiacol + H2O
-
-
-
-
?
guaiacol + H2O2
tetraguaiacol + H2O
-
-
-
-
?
guaiacol + H2O2
tetraguaiacol + H2O
-
-
-
-
?
guaiacol + H2O2
tetraguaiacol + H2O
-
-
-
-
?
guaiacol + H2O2
tetraguaiacol + H2O
-
-
-
?
I- + H2O2
?
Armoracia sp.
-
-
-
-
?
indole-3-acetic acid + H2O2
?
-
-
-
?
indole-3-acetic acid + H2O2
?
-
-
-
-
?
L-tyrosine + H2O2
?
-
-
-
-
?
L-tyrosine + H2O2
?
-
-
-
-
?
luminol + H2O2
?
-
-
-
?
luminol + H2O2
?
-
-
-
-
?
m-phenylenediamine + H2O2
? + H2O
-
12% compared to the activity with guaiacol, cationic peroxidase GCP1
-
-
?
m-phenylenediamine + H2O2
? + H2O
-
13.5% compared to the activity with guaiacol, anionic peroxidase GCP2
-
-
?
N-ethyl-N-(2-hydroxy-3-sulfopropyl)-m-toluidine + H2O2
?
-
-
-
-
?
N-ethyl-N-(2-hydroxy-3-sulfopropyl)-m-toluidine + H2O2
?
-
-
-
-
?
NADH + H2O2
?
-
163% activity compared to guaiacol
-
-
?
o-dianisidine + H2O2
?
-
-
-
-
?
o-dianisidine + H2O2
?
best electron donor
-
-
?
o-dianisidine + H2O2
?
-
-
-
-
?
o-dianisidine + H2O2
?
-
93.7% activity compared to guaiacol
-
-
?
o-dianisidine + H2O2
?
-
isoenzyme POX I
-
-
?
o-dianisidine + H2O2
?
-
isoenzyme POX II
-
-
?
o-dianisidine + H2O2
?
-
-
-
-
?
o-dianisidine + H2O2
?
90% activity compared to 2,2'-azino-bis-(3-ethyl-6-benzothiazolinsulfonate)
-
-
?
o-dianisidine + H2O2
?
-
-
-
-
?
o-dianisidine + H2O2
?
-
-
-
-
?
o-dianisidine + H2O2
?
-
-
-
-
?
o-dianisidine + H2O2
?
-
-
-
-
?
o-dianisidine + H2O2
?
-
-
-
-
?
o-dianisidine + H2O2
? + H2O
-
most preferred substrate
-
-
?
o-dianisidine + H2O2
? + H2O
-
-
-
-
?
o-dianisidine + H2O2
? + H2O
-
10% of the activity with o-phenylenediamine, isoenzyme FP2
-
-
?
o-dianisidine + H2O2
? + H2O
-
11% of the activity with o-phenylenediamine, isoenzyme FP3
-
-
?
o-dianisidine + H2O2
? + H2O
-
30% of the activity with o-phenylenediamine, isoenzyme FP1
-
-
?
o-dianisidine + H2O2
? + H2O
-
25% compared to the activity with guaiacol, anionic peroxidase GCP2
-
-
?
o-dianisidine + H2O2
? + H2O
-
45% compared to the activity with guaiacol, cationic peroxidase GCP1
-
-
?
o-dianisidine + H2O2
? + H2O
-
-
-
-
?
o-dianisidine + H2O2
? + H2O
-
-
-
-
?
o-dianisidine + H2O2
? + H2O
-
-
-
-
?
o-dianisidine + H2O2
? + H2O
-
-
-
-
?
o-dianisidine + H2O2
? + H2O
-
-
-
?
o-dianisidine + H2O2
? + H2O
-
-
-
?
o-dianisidine + H2O2
? + H2O
-
-
-
-
?
o-dianisidine + H2O2
? + H2O
-
66% of the activity with tetramethylbenzidine
-
-
?
o-phenylenediamine + H2O2
?
-
isoenzyme E5
-
-
?
o-phenylenediamine + H2O2
?
-
171.7% activity compared to guaiacol
-
-
?
o-phenylenediamine + H2O2
?
-
-
-
-
?
o-phenylenediamine + H2O2
?
-
-
-
-
?
o-phenylenediamine + H2O2
?
-
-
-
-
?
o-phenylenediamine + H2O2
?
-
-
-
-
?
o-phenylenediamine + H2O2
? + H2O
-
-
-
-
?
o-phenylenediamine + H2O2
? + H2O
-
most suitable substrate
-
-
?
o-phenylenediamine + H2O2
? + H2O
-
-
-
-
?
o-phenylenediamine + H2O2
? + H2O
-
activity is 2.37fold higher than activity with guaiacol, anionic peroxidase GCP2
-
-
?
o-phenylenediamine + H2O2
? + H2O
-
activity is 3.14fold higher than activity with guaiacol, cationic peroxidase GCP1
-
-
?
o-phenylenediamine + H2O2
? + H2O
-
-
-
?
p-aminoantipyrine + H2O2
? + H2O
-
26.5% compared to the activity with guaiacol, cationic peroxidase GCP1
-
-
?
p-aminoantipyrine + H2O2
? + H2O
-
31% compared to the activity with guaiacol, anionic peroxidase GCP2
-
-
?
p-coumaric acid + H2O2
?
13% activity compared to guaiacol
-
-
?
p-coumaric acid + H2O2
?
15% activity compared to guaiacol
-
-
?
p-coumaric acid + H2O2
?
-
-
-
-
?
p-coumaric acid + H2O2
?
-
-
-
?
p-coumaric acid + H2O2
?
-
-
-
-
?
p-coumaric acid + H2O2
?
-
-
-
-
?
p-hydroxybenzoic acid + H2O2
? + H2O
-
5.0% compared to the activity with guaiacol, anionic peroxidase GCP2
-
-
?
p-hydroxybenzoic acid + H2O2
? + H2O
-
activity is 1.41fold higher than activity with guaiacol, cationic peroxidase GCP1
-
-
?
phenol + H2O2
?
-
-
-
-
?
phenol + H2O2
?
-
-
-
-
?
phenol + H2O2
?
-
optimal concentrations of phenol and H2O2 are 0.2 mM and 0.3 mM, respectively
-
-
r
phenol + H2O2
?
-
-
-
-
?
phenol + H2O2
?
-
-
-
-
?
phenol + H2O2
?
-
-
-
-
?
phenol + H2O2
? + H2O
-
-
-
?
phenol + H2O2
? + H2O
-
-
-
-
?
phenol red + H2O2
?
-
-
-
-
?
phenol red + H2O2
?
-
-
-
-
?
pyrogallol + H2O2
?
84% activity compared to guaiacol
-
-
?
pyrogallol + H2O2
?
90% activity compared to guaiacol
-
-
?
pyrogallol + H2O2
? + H2O
Elais guineensis
-
-
-
-
?
pyrogallol + H2O2
? + H2O
-
3.8% of the activity with o-phenylenediamine, isoenzyme FP2
-
-
?
pyrogallol + H2O2
? + H2O
-
4.5% of the activity with o-phenylenediamine, isoenzyme FP3
-
-
?
pyrogallol + H2O2
? + H2O
-
5.3% of the activity with o-phenylenediamine, isoenzyme FP1
-
-
?
pyrogallol + H2O2
? + H2O
-
7.4% compared to the activity with guaiacol, anionic peroxidase GCP2
-
-
?
pyrogallol + H2O2
? + H2O
-
88% compared to the activity with guaiacol, cationic peroxidase GCP1
-
-
?
pyrogallol + H2O2
? + H2O
-
-
-
-
?
pyrogallol + H2O2
? + H2O
-
-
-
-
?
pyrogallol + H2O2
? + H2O
-
-
-
-
?
pyrogallol + H2O2
? + H2O
-
-
-
?
pyrogallol + H2O2
purpurogallin + H2O
-
93% activity compared to guaiacol
-
-
?
pyrogallol + H2O2
purpurogallin + H2O
Armoracia sp.
-
-
-
?
pyrogallol + H2O2
purpurogallin + H2O
-
-
-
-
?
pyrogallol + H2O2
purpurogallin + H2O
-
isoenzyme E5
-
-
?
pyrogallol + H2O2
purpurogallin + H2O
-
6.2% activity compared to guaiacol
-
-
?
pyrogallol + H2O2
purpurogallin + H2O
84% activity compared to guaiacol
-
-
?
pyrogallol + H2O2
purpurogallin + H2O
90% activity compared to guaiacol
-
-
?
pyrogallol + H2O2
purpurogallin + H2O
-
-
-
-
?
pyrogallol + H2O2
purpurogallin + H2O
-
-
-
-
?
pyrogallol + H2O2
purpurogallin + H2O
-
-
-
?
pyrogallol + H2O2
purpurogallin + H2O
-
-
-
-
?
quercetin + H2O
?
-
isoenzyme POX I
-
-
?
quercetin + H2O
?
-
isoenzyme POX II
-
-
?
Reactive Black 5 + H2O2
?
-
-
-
-
?
Reactive Black 5 + H2O2
?
-
-
-
?
reactive blue 19 + H2O2
? + H2O
-
-
-
-
?
reactive blue 19 + H2O2
? + H2O
-
-
-
-
?
Reactive Blue 5 + H2O2
?
-
123% activity compared to guaiacol, the apparent optimum concentration of H2O2 required for the decolorization of Reactive Blue 5 by AnaPX is 0.4 mM
-
-
?
Reactive Blue 5 + H2O2
?
-
highest specific activity
-
-
?
reduced 2,2'-azino-bis-(3-ethylbenzthiazole-6-sulfonic acid) + H2O2
oxidized 2,2'-azino-bis-(3-ethylbenzthiazole-6-sulfonic acid) + H2O
-
-
-
-
?
reduced 2,2'-azino-bis-(3-ethylbenzthiazole-6-sulfonic acid) + H2O2
oxidized 2,2'-azino-bis-(3-ethylbenzthiazole-6-sulfonic acid) + H2O
-
-
-
?
reduced 2,2'-azino-bis-(3-ethylbenzthiazole-6-sulfonic acid) + H2O2
oxidized 2,2'-azino-bis-(3-ethylbenzthiazole-6-sulfonic acid) + H2O
-
the catalytic activity of peroxidase in the oxidation process of reduced 2,2'-azino-bis-(3-ethylbenzthiazole-6-sulfonic acid) is found to depend on the nature and the amount of added salt. The influence of the salt on the buffer pH can be identified as one of the major reasons
-
-
?
reduced 2,2'-azino-bis-(3-ethylbenzthiazole-6-sulfonic acid) + H2O2
oxidized 2,2'-azino-bis-(3-ethylbenzthiazole-6-sulfonic acid) + H2O
-
-
-
-
?
reduced 2,2'-azino-bis-(3-ethylbenzthiazole-6-sulfonic acid) + H2O2
oxidized 2,2'-azino-bis-(3-ethylbenzthiazole-6-sulfonic acid) + H2O
-
-
-
?
reduced 2,2'-azino-bis-(3-ethylbenzthiazole-6-sulfonic acid) + H2O2
oxidized 2,2'-azino-bis-(3-ethylbenzthiazole-6-sulfonic acid) + H2O
-
-
-
-
?
reduced 2,2'-azino-bis-(3-ethylbenzthiazole-6-sulfonic acid) + H2O2
oxidized 2,2'-azino-bis-(3-ethylbenzthiazole-6-sulfonic acid) + H2O
-
-
-
?
reduced 2,2'-azino-bis-(3-ethylbenzthiazole-6-sulfonic acid) + H2O2
oxidized 2,2'-azino-bis-(3-ethylbenzthiazole-6-sulfonic acid) + H2O
-
-
-
-
?
reduced 2,2'-azino-bis-(3-ethylbenzthiazole-6-sulfonic acid) + H2O2
oxidized 2,2'-azino-bis-(3-ethylbenzthiazole-6-sulfonic acid) + H2O
-
-
-
-
?
reduced 2,2'-azino-bis-(3-ethylbenzthiazole-6-sulfonic acid) + H2O2
oxidized 2,2'-azino-bis-(3-ethylbenzthiazole-6-sulfonic acid) + H2O
-
isoenzyme E5
-
-
?
reduced 2,2'-azino-bis-(3-ethylbenzthiazole-6-sulfonic acid) + H2O2
oxidized 2,2'-azino-bis-(3-ethylbenzthiazole-6-sulfonic acid) + H2O
-
-
-
-
?
reduced 2,2'-azino-bis-(3-ethylbenzthiazole-6-sulfonic acid) + H2O2
oxidized 2,2'-azino-bis-(3-ethylbenzthiazole-6-sulfonic acid) + H2O
Elais guineensis
-
-
-
-
?
reduced 2,2'-azino-bis-(3-ethylbenzthiazole-6-sulfonic acid) + H2O2
oxidized 2,2'-azino-bis-(3-ethylbenzthiazole-6-sulfonic acid) + H2O
-
isoenzyme POX II
-
-
?
reduced 2,2'-azino-bis-(3-ethylbenzthiazole-6-sulfonic acid) + H2O2
oxidized 2,2'-azino-bis-(3-ethylbenzthiazole-6-sulfonic acid) + H2O
-
-
-
-
?
reduced 2,2'-azino-bis-(3-ethylbenzthiazole-6-sulfonic acid) + H2O2
oxidized 2,2'-azino-bis-(3-ethylbenzthiazole-6-sulfonic acid) + H2O
-
-
-
-
?
reduced 2,2'-azino-bis-(3-ethylbenzthiazole-6-sulfonic acid) + H2O2
oxidized 2,2'-azino-bis-(3-ethylbenzthiazole-6-sulfonic acid) + H2O
-
-
-
-
?
reduced 2,2'-azino-bis-(3-ethylbenzthiazole-6-sulfonic acid) + H2O2
oxidized 2,2'-azino-bis-(3-ethylbenzthiazole-6-sulfonic acid) + H2O
-
trivial name ABTS, ping-pong mechanism
-
-
?
reduced 2,2'-azino-bis-(3-ethylbenzthiazole-6-sulfonic acid) + H2O2
oxidized 2,2'-azino-bis-(3-ethylbenzthiazole-6-sulfonic acid) + H2O
-
-
-
-
?
reduced 2,2'-azino-bis-(3-ethylbenzthiazole-6-sulfonic acid) + H2O2
oxidized 2,2'-azino-bis-(3-ethylbenzthiazole-6-sulfonic acid) + H2O
-
-
-
?
reduced 2,2'-azino-bis-(3-ethylbenzthiazole-6-sulfonic acid) + H2O2
oxidized 2,2'-azino-bis-(3-ethylbenzthiazole-6-sulfonic acid) + H2O
-
-
-
-
?
reduced 2,2'-azino-bis-(3-ethylbenzthiazole-6-sulfonic acid) + H2O2
oxidized 2,2'-azino-bis-(3-ethylbenzthiazole-6-sulfonic acid) + H2O
-
-
-
-
?
Remazol Brilliant Blue R + H2O2
?
-
-
-
-
?
Remazol Brilliant Blue R + H2O2
?
-
-
-
-
?
SCN- + H2O2
OSCN- + H2O
-
preferred substrate
-
-
?
SCN- + H2O2
OSCN- + H2O
-
-
-
-
?
SCN- + H2O2
OSCN- + H2O
-
-
-
-
?
scopoletin + H2O2
?
-
-
-
-
?
scopoletin + H2O2
?
-
-
-
-
?
scopoletin + H2O2
?
-
-
-
-
?
sinapic acid + H2O2
?
-
-
-
-
?
sinapic acid + H2O2
?
-
-
-
-
?
sinapyl alcohol + H2O2
? + H2O
-
30% compared to the activity with guaiacol, cationic peroxidase GCP1
-
-
?
sinapyl alcohol + H2O2
? + H2O
-
activity is 1.32fold higher than activity with guaiacol, anionic peroxidase GCP2
-
-
?
styrene + H2O2
styrene epoxide + H2O
endogenous electron transfer partners for CYP119 remain unknown, highly unlikely that styrene is the natural substrate for CYP119. Catalytic activity can be assayed in the absence of electron donor proteins using H2O2 as the source of oxidizing equivalents. The enzyme is not able to support styrene epoxidation by putidaredoxin/putidaredoxin reductase
-
-
?
styrene + H2O2
styrene epoxide + H2O
endogenous electron transfer partners for CYP119 remain unknown, highly unlikely that styrene is the natural substrate for CYP119. Catalytic activity can be assayed in the absence of electron donor proteins using H2O2 as the source of oxidizing equivalents. The enzyme is not able to support styrene epoxidation by putidaredoxin/putidaredoxin reductase
-
-
?
syringic acid + H2O2
?
-
-
-
-
?
syringic acid + H2O2
?
-
-
-
-
?
tannic acid + H2O2
? + H2O
-
3.8% compared to the activity with guaiacol, cationic peroxidase GCP1
-
-
?
tannic acid + H2O2
? + H2O
-
78% compared to the activity with guaiacol, anionic peroxidase GCP2
-
-
?
tetramethylbenzidine + H2O2
?
206% activity compared to guaiacol
-
-
?
tetramethylbenzidine + H2O2
?
215% activity compared to guaiacol
-
-
?
ubiquinol-1 + H2O2
? + H2O
-
-
-
?
ubiquinol-1 + H2O2
? + H2O
-
-
-
?
veratryl alcohol + H2O2
?
-
-
-
-
?
veratryl alcohol + H2O2
?
-
-
-
?
additional information
?
-
-
is capable of catalyzing polypeptide and chorion protein crosslinking through dityrosine formation during in vitro assays
-
-
?
additional information
?
-
QPO catalyzes the reduction of H2O2 but not tert-butyl hydroperoxide and cumene hydroperoxide
-
-
?
additional information
?
-
-
QPO catalyzes the reduction of H2O2 but not tert-butyl hydroperoxide and cumene hydroperoxide
-
-
?
additional information
?
-
in the reaction sequence, the first substrate (quinol) combines with the enzyme to form a substituted enzyme intermediate, with the concomitant release of the first product. The second substrate, H2O2, then interacts with the substituted enzyme intermediate to form the second product, thereby regenerating the native enzyme
-
-
?
additional information
?
-
-
in the reaction sequence, the first substrate (quinol) combines with the enzyme to form a substituted enzyme intermediate, with the concomitant release of the first product. The second substrate, H2O2, then interacts with the substituted enzyme intermediate to form the second product, thereby regenerating the native enzyme
-
-
?
additional information
?
-
QPO catalyzes the reduction of H2O2 but not tert-butyl hydroperoxide and cumene hydroperoxide
-
-
?
additional information
?
-
-
no activity with Mn2+ and veratryl alcohol as electron donors
-
-
?
additional information
?
-
-
class III peroxidases are involved in cell wall metabolism, lignification, wound healing, auxin catabolism, removal of H2O2, oxidation of toxic reductants, defence against pathogen or insect attack, as well as symbiosis and normal cell growth, and can generate highly reactive reactive oxygen species
-
-
?
additional information
?
-
-
direct electron transfer kinetics in horseradish peroxidase electrocatalysis
-
-
?
additional information
?
-
-
HRP in colloidal carbon microspheres/chitosan hybrid keeps its native bioactivity and has high affinity for H2O2
-
-
?
additional information
?
-
Armoracia sp.
-
proposed mechanism for substrate oxidation in plant oxidases of small phenolic substrates via compound I and compound II
-
-
?
additional information
?
-
Armoracia sp.
-
can also catalyze a reaction that results in the production of hydroxyl radicals from H2O2 in the presence of (O2)- radicals
-
-
?
additional information
?
-
Armoracia sp.
-
methyl and ethyl hydrogen peroxide can also act as substrates
-
-
?
additional information
?
-
Armoracia sp.
-
when the enzyme is immobilized on a graphite electrode, the electrode can substitute the electron donor substrates
-
-
?
additional information
?
-
-
methyl and ethyl hydrogen peroxide can also act as substrates
-
-
?
additional information
?
-
-
the enzyme shows high antibacterial activity in 100 mM thiocyanate 100 mM H2O2 medium for some pathogenic bacteria, such as Aeromonas hydrophila ATCC 79666, Micrococcus luteus LA 2971, Mycobacterium smegmatis RUT, Bacillus subtilis IMG22, Pseudomonas pyocyanea, Bacillus subtilis var. niger ATCC 10, Pseudomonas aeruginosa ATCC 27853, Enterococcus faecalis ATCC 15753, Bacillus brevis FMC3, Klebsiella pneumoniae FMC5, Corynebacterium xerosis UC9165, Bacillus cereus EÜ, Bacillus megaterium NRS, Yersinia enterocolitica, Listeria monocytogenes scoot A, Bacillus megaterium EÜ, Bacillus megaterium DSM32, Klebsiella oxytoca, Staphylococcus aerogenes, Streptococcus faecalis, Mycobacterium smegmatis CCM 2067
-
-
?
additional information
?
-
-
no activity with pregnenolone and mestranol
-
-
?
additional information
?
-
-
lactoperoxidase can effectively and selectively iodinate the tyrosyl residues in angiotensin peptides
-
-
?
additional information
?
-
-
no substrate: Congo red
-
-
?
additional information
?
-
-
the enzyme catalyzes the decolourization of Reactive Blue 19 and Acid Blue 25
-
-
-
additional information
?
-
-
class III peroxidases are involved in cell wall metabolism, lignification, wound healing, auxin catabolism, removal of H2O2, oxidation of toxic reductants, defence against pathogen or insect attack, as well as symbiosis and normal cell growth, and can generate highly reactive reactive oxygen species
-
-
?
additional information
?
-
-
class III peroxidases are involved in cell wall metabolism, lignification, wound healing, auxin catabolism, removal of H2O2, oxidation of toxic reductants, defence against pathogen or insect attack, as well as symbiosis and normal cell growth, and can generate highly reactive reactive oxygen species
-
-
?
additional information
?
-
-
negligible activity with guaiacol, isoenzyme E5
-
-
?
additional information
?
-
-
not active towards L-tyrosine, ascorbic acid, alpha-naphthylamine, p-aminoantipyrine, potassium ferrocyanide, potassium iodide, and NADH
-
-
?
additional information
?
-
-
shows no detectable activity with ascorbic acid or veratryl alcohol
-
-
?
additional information
?
-
shows no detectable activity with ascorbic acid or veratryl alcohol
-
-
?
additional information
?
-
-
class III peroxidases are involved in cell wall metabolism, lignification, wound healing, auxin catabolism, removal of H2O2, oxidation of toxic reductants, defence against pathogen or insect attack, as well as symbiosis and normal cell growth, and can generate highly reactive reactive oxygen species
-
-
?
additional information
?
-
-
isoenzyme POX I shows no activity with reduced 2,2'-azino-bis-(3-ethylbenzthiazole-6-sulfonic acid)
-
-
?
additional information
?
-
-
overview of different dyes that are oxidated by this enzyme
-
-
?
additional information
?
-
-
not active on iodoacetic acid
-
-
?
additional information
?
-
-
under conditions of severe inflammation and oxidative stress, peroxidase activity of hemoglobin-haptoglobin covalent aggregates may cause macrophage dysfunction and microvascular vasoconstriction
-
-
?
additional information
?
-
-
transient-state kinetic analysis
-
-
?
additional information
?
-
-
class III peroxidases are involved in cell wall metabolism, lignification, wound healing, auxin catabolism, removal of H2O2, oxidation of toxic reductants, defence against pathogen or insect attack, as well as symbiosis and normal cell growth, and can generate highly reactive reactive oxygen species
-
-
?
additional information
?
-
-
no activity with Mn2+ at pH 4.5 and with H2O2 at pH 3.0
-
-
?
additional information
?
-
-
MAP-2744c exhibits strong peroxidase activity using fatty acid hydroperoxides
-
-
?
additional information
?
-
the rate-limiting step in the catalytic cycle is the electron transfer between the two hemes
-
-
?
additional information
?
-
the rate-limiting step in the catalytic cycle is the electron transfer between the two hemes
-
-
?
additional information
?
-
-
is likely to be an important component of the defense arsenal against reactive oxygen species generated during hyperthermia and oxidative stress
-
-
?
additional information
?
-
-
class III peroxidases are involved in cell wall metabolism, lignification, wound healing, auxin catabolism, removal of H2O2, oxidation of toxic reductants, defence against pathogen or insect attack, as well as symbiosis and normal cell growth, and can generate highly reactive reactive oxygen species
-
-
?
additional information
?
-
-
class III peroxidases are involved in cell wall metabolism, lignification, wound healing, auxin catabolism, removal of H2O2, oxidation of toxic reductants, defence against pathogen or insect attack, as well as symbiosis and normal cell growth, and can generate highly reactive reactive oxygen species
-
-
?
additional information
?
-
-
hemoglobin 1 does not function in vivo as a peroxidase
-
-
?
additional information
?
-
-
the system is proposed to operate in vivo for the efficient elimination of endogeneous H2O2
-
-
?
additional information
?
-
-
as the parasite is susceptible to oxidative stress, this peroxidase may offer antioxidant role by scavenging endogenous H2O2
-
-
?
additional information
?
-
-
cationic peroxidase Cs plays an important role in plant cell wall formation during seed germination
-
-
?
additional information
?
-
no peroxidase activity is observed with ascorbate as substrate
-
-
?
additional information
?
-
-
class III peroxidases are involved in cell wall metabolism, lignification, wound healing, auxin catabolism, removal of H2O2, oxidation of toxic reductants, defence against pathogen or insect attack, as well as symbiosis and normal cell growth, and can generate highly reactive reactive oxygen species
-
-
?
additional information
?
-
-
in vitro, sigma-specific peroxidase does not show enzyme activity with the monophenolic substrates phenol and catechol, or any detectable indole-3-acetic acid oxidase activity
-
-
?
additional information
?
-
-
class III peroxidases are involved in cell wall metabolism, lignification, wound healing, auxin catabolism, removal of H2O2, oxidation of toxic reductants, defence against pathogen or insect attack, as well as symbiosis and normal cell growth, and can generate highly reactive reactive oxygen species
-
-
?
additional information
?
-
-
substrate specificity, overview, the enzyme shows broad substrate specificity and exhibits also acid phosphatase, EC 3.1.3.2
-
-
?
additional information
?
-
-
class III peroxidases are involved in cell wall metabolism, lignification, wound healing, auxin catabolism, removal of H2O2, oxidation of toxic reductants, defence against pathogen or insect attack, as well as symbiosis and normal cell growth, and can generate highly reactive reactive oxygen species
-
-
?
additional information
?
-
-
for most substrates, the value of kcat/Km measured by steady-state kinetics is equal to the slowest step in catalysis measured by stopped-flow spectroscopy, namely the decay of the ferryl FeIV=O species (compound II) to form the ferric species
-
-
?
additional information
?
-
-
for most substrates, the value of kcat/Km measured by steady-state kinetics is equal to the slowest step in catalysis measured by stopped-flow spectroscopy, namely the decay of the ferryl FeIV=O species (compound II) to form the ferric species
-
-
?
additional information
?
-
catalytic mechanism: Thr213 is catalytically important and Thr214 helps to control the iron spin state
-
-
?
additional information
?
-
catalytic mechanism: Thr213 is catalytically important and Thr214 helps to control the iron spin state
-
-
?
additional information
?
-
-
no substrates: veratryl alcohol, reactive black 5, Mn2+
-
-
?
additional information
?
-
no substrate: ferulic acid
-
-
?
additional information
?
-
-
class III peroxidases are involved in cell wall metabolism, lignification, wound healing, auxin catabolism, removal of H2O2, oxidation of toxic reductants, defence against pathogen or insect attack, as well as symbiosis and normal cell growth, and can generate highly reactive reactive oxygen species
-
-
?
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1,10-phenanthroline
-
69% inhibition at 5 mM
1-(5-fluoro-1H-indol-3-yl)methanamine
-
-
1-butyl-3-methylimidazolium tetrafluoroborate
-
weak, non-competitive inhibitor
1-methyl-L-tryptophan
-
-
2,2'-bipyridyl
-
25% inhibition at 5 mM
2,4,6-tribromophenol
substrate inhibition at high concentration due to the internal binding at the distal pocket of DHP; substrate inhibition at high concentration due to the internal binding at the distal pocket of DHP
2,4,6-Trichlorophenol
substrate inhibition at high concentration due to the internal binding at the distal pocket of DHP; substrate inhibition at high concentration due to the internal binding at the distal pocket of DHP
2,4-dinitroresorcinol
-
competitive inhibition of 3,3',5,5'-tetramethylbenzidine oxidation
2-(5-fluoro-1H-indol-3-yl)-N,N-dimethylethanamine
-
-
2-(5-fluoro-1H-indol-3-yl)-N-methylethanamine
-
-
2-amino-4-nitrophenol
-
competitive inhibition of 3,3',5,5'-tetramethylbenzidine oxidation
2-mercaptoethanol
-
97% inhibition
3-(5-fluoro-1H-indol-3-yl)-N,N-dimethylpropan-1-amine
-
-
3-(5-fluoro-1H-indol-3-yl)-N-methylpropan-1-amine
-
-
3-(5-fluoro-1H-indol-3-yl)-N-propylpropan-1-amine
-
-
3-(5-fluoro-1H-indol-3-yl)propan-1-amine
-
-
4-(5-fluoro-1H-indol-3-yl)butan-1-amine
-
-
4-aminobenzenesulfanilamide
-
competitive inhibition
4-aminobenzohydrazide
Brassica oleracea var. capitata f. rubra
-
-
5-(5-fluoro-1H-indol-3-yl)pentan-1-amine
-
-
5-fluoro-3-[(4-methylpiperazin-1-yl)methyl]-1H-indole
-
-
5-fluoro-3-[2-(4-methylpiperazin-1-yl)ethyl]-1H-indole
-
-
5-fluoro-3-[2-(pyrrolidin-1-yl)ethyl]-1H-indole
-
-
5-fluoro-3-[3-(4-methylpiperazin-1-yl)propyl]-1H-indole
-
-
5-fluoro-3-[3-(pyrrolidin-1-yl)propyl]-1H-indol
-
-
5-fluoro-3-[3-(pyrrolidin-1-yl)propyl]-1H-indole
-
-
5-fluoro-L-tryptophan
-
-
5-methyl-2-thiouracil
-
-
5-n-propyl-2-thiouracil
-
-
6-(5-fluoro-1H-indol-3-yl)hexan-1-amine
-
-
9-methylanthracene
-
strong inhibitor of native HRP
AgNO3
-
0.25 mM, 31% loss of activity
AlCl3
-
84% inhibition at 1 mM
alpha-tocopherol
-
58% inhibition at 0.1 mM
astilbin
-
efficient inhibitor
benzohydroxyamic acid
-
-
beta-cyclodextrin
-
1 mM, 16% inhibition
butanol
-
81.0% residual activity at 30% (v/v)
butyl-3-methylimidazolium tetrafluoroborate
-
significantly weakens the binding affinity of guaiacol to HRP
Cs+
-
86.3% relative activity at 10 mM
Cu+
-
1 mM, 70% residual activity
diethyldithiocarbamate
-
87% inhibition at 1 mM
dioxane
-
82.0% residual activity at 50% (v/v)
DMSO
-
76.0% residual activity at 30% (v/v)
ethylene diamine tetraacetic acid
fluoranthene
-
strong inhibitor of native HRP
gallic acid
-
competetive inhibition of 3,3',5,5'-tetramethylbenzidine oxidation
guanidine isothiocyanate
-
82.4% residual activity at 1.5 mM
Haptoglobin
-
mixed type of inhibition, haptoglobin binds with hemoglobin and weakens hemoglobin peroxidase activity
-
HgCl2
-
84% inhibition at 1 mM
histidine
-
0.18 mM, 43% inhibition of the activity with quercetin, 13% inhibition of the activity with o-dianisidine, isoenzyme POX II; 0.18 mM, 71% inhibition of the activity with quercetin, 95% inhibition of the activity with o-dianisidine, isoenzyme POX I
hydrazine
-
5 mM, 45% residual activity
hydroquinone
-
98% inhibition at 1 mM
imidazole
-
0.18 mM, 24% inhibition of the activity with quercetin, 81% inhibition of the activity with o-dianisidine, isoenzyme POX II; 0.18 mM, 72% inhibition of the activity with quercetin, 97% inhibition of the activity with o-dianisidine, isoenzyme POX I
indomethacin
-
the presence of indomethacin in the LPO/H2O2/acetonitrile system leads to a modest, yet significant decline in the rate of cyanide formation of only 84.1% of the control
KI
30% inhibition at 1 mM; 30% inhibition at 1 mM; 36% inhibition at 1 mM; 36% inhibition at 1 mM
L-tryptophan benzyl ester
-
-
La3+
-
the formation of the La3+-HRP complex causes the destruction of the native structure of HRP molecule, leading to the decrease in the non-planarity of the porphyrin ring in the heme group of HRP molecule, and then in the exposure extent of active center, Fe(III) of the porphyrin ring of HRP molecule. Thus, the direct electrochemical and catalytic activities of HRP are decreased. When the molar ratio of La3+ and HRP is 10, the catalytic activity of HRP is decreased by 12% comparing with that of HRP in the absence of La3+
Li+
-
22% inhibition at 5 mM, at 37°C
linoleic acid
-
3.6 mM, 76% inhibition of the activity with quercetin, 48% inhibition of the activity with o-dianisidine, isoenzyme POX II; 3.6 mM, no inhibition of the activity with quercetin, 32% inhibition of the activity with o-dianisidine, isoenzyme POX I
linolenic acid
-
3.6 mM, 16% inhibition of the activity with quercetin, 21% inhibition of the activity with o-dianisidine, isoenzyme POX I; 3.6 mM, 35% inhibition of the activity with quercetin, 37% inhibition of the activity with o-dianisidine, isoenzyme POX II
menadione sodium bisulfate
-
-
methanol
-
85.0% residual activity at 70% (v/v)
MgSO4
-
5 mM, 23% inhibition
N,N-diethyl-2-(5-fluoro-1H-indol-3-yl)ethanamine
-
-
N,N-diethyl-3-(5-fluoro-1H-indol-3-yl)propan-1-amine
-
-
N-bromosuccinimide
-
5 mM, 16% inhibition
N-ethyl-2-(5-fluoro-1H-indol-3-yl)ethanamine
-
-
N-ethyl-3-(5-fluoro-1H-indol-3-yl)propan-1-amine
-
-
N-ethyl-N-[(5-fluoro-1H-indol-3-yl)methyl]ethanamine
-
-
N-ethylmaleimide
-
18% inhibition at 5 mM
n-Hexanol
-
the enzymatic activity of horseradish peroxidase decreases upon addition of n-hexanol
N-[2-(5-fluoro-1H-indol-3-yl)ethyl]butan-1-amine
-
-
N-[2-(5-fluoro-1H-indol-3-yl)ethyl]propan-1-amine
-
-
N-[3-(5-fluoro-1H-indol-3-yl)propyl]butan-1-amine
-
-
Na2S2O5
-
100% inhibition at 0.1 mM
NaCl
44% inhibition at 1 mM
Nalpha-methoxycarbonyl-L-tryptophan methyl ester
-
-
Nalpha-methyl-L-tryptophan
-
-
NH4+
-
0.18 mM, 6% inhibition of the activity with quercetin; 0.18 mM, no inhibition of the activity with quercetin, 27% inhibition of the activity with o-dianisidine, isoenzyme POX I
oleic acid
-
3.6 mM, isoenzyme POX I, 62% inhibition of the activity with quercetin, 19% inhibition of the activity with o-dianisidine, isoenzyme POX I; 3.6 mM, isoenzyme POX II, 72% inhibition of the activity with quercetin, 41% inhibition of the activity with o-dianisidine, isoenzyme POX II
Pb2+
-
91.8% relative activity at 10 mM
PCMB
-
4 mM, 78% without substrate, 75% inhibition in presence of substrate
Periodate
-
completely and competitively inhibited by periodate
phenoxy radical
phenylalanine residues are vulnerable to modification by phenoxyl radicals. Radical coupling does not change the secondary structure or the active site of HRP isoform C
phenyl hydrazine
-
competitive
promethazine sulfoxide
Armoracia sp.
-
-
quercetin
-
incubation of the LPO/H2O2/acetonitrile system with 0.1 mM quercetin is associated with the highest rate of inhibition amounting to 40.2% of the control
salicylhydroxyamic acid
-
-
Semicarbazide
-
32% inhibition at 1 mM
Sodium metabisulfite
complete inhibition at 1 mM; complete inhibition at 1 mM; complete inhibition at 1 mM
Tb3+
-
after treatment with 0.2 mM Tb3+, the HRP bioactivity in horseradish leaf is inhibited by 27.2% compared to the sample without Tb3+treatment
Tiron
-
100% inhibition at 1 mM
trolox C
-
incubation of the LPO/H2O2/acetonitrile system with 0.1 mM trolox C is associated with the highest rate of inhibition amounting to 47.8% of the control
Tween 80
30% inhibition at 1 mM; 38% inhibition at 1 mM; 45% inhibition at 1 mM; 45% inhibition at 1 mM
ubiquinone-1
product inhibition, mixed-type
Urea
-
loss of more than 50% of its activity at 1M urea
acetone
-
25%, 62% inhibition
acetone
-
5 mM, 21% inhibition
acetonitrile
-
about 98% activity is lost for native HRP after incubation in 50% (v/v) acetonitrile at 35°C for 3 h, native HRP only possess less than 20% activity in 30% (v/v) acetonitrile
acetonitrile
-
88.0% residual activity at 60% (v/v)
Al3+
-
1 mM, slight inhibition
Al3+
-
5 mM, 56% residual activity
ascorbate
-
0.1 mM, complete inhibition of membrane-bound isoform, 0.2 mM, complete inhibition of soluble isoform
ascorbate
-
99% inhibition
ascorbic acid
Armoracia sp.
-
-
ascorbic acid
-
1 mM, 82% inhibition
ascorbic acid
-
strong inhibitor, complete inhibition at 0.06 mM
ascorbic acid
-
95% inhibition at 1 mM
ascorbic acid
complete inhibition at 1 mM; complete inhibition at 1 mM; complete inhibition at 1 mM
azide
-
-
benzhydroxamic acid
-
50% activity at 0.004 mM
benzhydroxamic acid
-
50% activity at 0.0004 mM
beta-mercaptoethanol
-
4 mM, 80% without substrate, 78% inhibition in presence of substrate
beta-mercaptoethanol
94% inhibition at 1 mM; 94% inhibition at 1 mM; 96% inhibition at 1 mM; 96% inhibition at 1 mM
Ca2+
-
5mM, 79% inhibition
Ca2+
-
5 mM, 17% inhibition
Ca2+
-
61.8% relative activity at 10 mM
Ca2+
-
5 mM, 47% residual activity
Co2+
-
1 mM, slight inhibition
Co2+
-
10 mM, 17% loss of activity, isoenzyme FP2; 10 mM, 42% loss of activity, isoenzyme FP1; 10 mM, 53% loss of activity, isoenzyme FP3
Co2+
-
51.9% relative activity at 10 mM
Co2+
-
5 mM, 79% inhibition of cationic peroxidase GCP1. 5 mM, 20% inhibition of anionic peroxidase GCP2
Cu2+
-
61% inhibition
Cu2+
-
4% inhibition at 5 mM, at 37°C
Cu2+
-
10 mM, 67% loss of activity, isoenzyme FP3; 10 mM, complete loss of activity, isoenzyme FP1
Cu2+
-
80.8% relative activity at 10 mM
Cu2+
-
5 mM, 85% inhibition of cationic peroxidase GCP1. 5 mM, 26% inhibition of anionic peroxidase GCP2
cysteine
-
1 mM, 28% inhibition
cysteine
73% inhibition at 1 mM; 73% inhibition at 1 mM; 78% inhibition at 1 mM; 78% inhibition at 1 mM
D-fructose
-
D-fructose at different concentrations, POD activities are measured at 25°C and pH 7.0 to determine inhibitor effects of sugars on enzymatic activities. POD activities from both cultivars show a decreasing pattern as sugar concentration in the assay medium increased, except in POD extract from Charentais, which maintained its activity in the presence of high D-glucose concentration (up to 5 M)
D-glucose
-
D-glucose at different concentrations, POD activities are measured at 25°C and pH 7.0 to determine inhibitor effects of sugars on enzymatic activities. POD activities from both cultivars show a decreasing pattern as sugar concentration in the assay medium increased, except in POD extract from Charentais, which maintained its activity in the presence of high D-glucose concentration (up to 5 M)
D-glucose
-
87% loss of activity in presence of 1 M D-glucose
diethyl dicarbonate
-
less than 50% inhibition at 50 mM
diethyl dicarbonate
-
4 mM, 50% without substrate, 21% inhibition in presence of substrate
dithiothreitol
-
79% inhibition at 1 mM
dithiothreitol
98% inhibition at 1 mM; 98% inhibition at 1 mM; complete inhibition at 1 mM; complete inhibition at 1 mM
dithiothreitol
-
complete inhibition
dithiothreitol
-
5 mM, complete loss of activity
EDTA
-
5 mM, 26% inhibition
EDTA
-
10 mM, 14% loss of activity, isoenzyme FP2; 10 mM, 36% loss of activity, isoenzyme FP1; 10 mM, 88% loss of activity, isoenzyme FP3
EDTA
24% inhibition at 1 mM; 28% inhibition at 1 mM; 28% inhibition at 1 mM; 28% inhibition at 1 mM
EDTA
-
87.3% relative activity at 10 mM
EDTA
-
5 mM, 59% inhibition
ethanol
-
25%, 72% inhibition
ethanol
-
82.0% residual activity at 65% (v/v)
ethylene diamine tetraacetic acid
-
-
ethylene diamine tetraacetic acid
-
17% inhibition at 10 mM
Fe2+
-
5mM, 75% inhibition
Fe2+
-
98.8% inhibition at 5 mM
Fe2+
-
1 mM, 72% residual activity
Fe2+
5 mM, 13% residual activity
glutathione
Armoracia sp.
-
-
glutathione
-
1 mM, 79% inhibition
glutathione
-
56% inhibition at 1 mM
guanidine hydrochloride
-
84.2% residual activity at 3 mM
guanidine hydrochloride
-
less than 10% activity at 1M guanidine hydrochloride
H2O2
inactivation by H2O2 is expressed by pseudofirst order kinetics and is an irreversible process
H2O2
-
3 mM, suicide inactivation. Addition of SDS to the reaction mixture intensifies the inactivation process; 3 mM, suicide inactivation through a steady-state mechanism
H2O2
-
suicide substrate inhibition in absence of reductant
H2O2
-
at concentrations higher than 1 mM
H2O2
-
peroxidase isozyme A1 activity is decreased by 30% already at 20 mM H2O2
H2O2
-
at 40 mM, 50% inactivation within 30 min at 25°C
H2O2
-
enzyme retains more than 80% of its initial activity after 24 h incubation in 5000fold molar excess of H2O2
Hg2+
-
5 mM, 47% inhibition
Hg2+
-
1 mM, slight inhibition
Hg2+
-
80% inhibition at 5 mM, at 37°C
Hg2+
-
10 mM, 54% loss of activity, isoenzyme FP2; 10 mM, 82% loss of activity, isoenzyme FP3; 10 mM, 91% loss of activity, isoenzyme FP1
Hg2+
41% relative activity at 1 mM; 50% inhibition at 1 mM; 50% relative activity at 1 mM; 59% inhibition at 1 mM
Hg2+
-
complete inhibition at 10 mM
Hg2+
-
5 mM, 93% inhibition of cationic peroxidase GCP1. 5 mM, 33% inhibition of anionic peroxidase GCP2
Hg2+
-
5 mM, 17% residual activity
hydroxylamine
-
85% inhibition at 1 mM
hydroxylamine
Armoracia sp.
-
50% inhibition at 1 mM
hydroxylamine
-
79% inhibition at 1 mM
hydroxylamine
-
84% inhibition at 1 mM
Isopropanol
-
25%, 78% inhibition
Isopropanol
-
80.0% residual activity at 45% (v/v)
K+
-
5 mM, 8% inhibition
K+
26% inhibition at 1 mM; 27% inhibition at 1 mM; 74% relative activity at 1 mM; 77% relative activity at 1 mM
K+
-
92.6% relative activity at 10 mM
K+
-
5 mM, 41% residual activity
KCN
-
very low sensitivity, causes only 9% and 14% inhibition of the activity at 1 and 10 mM, respectively
KCN
-
76% inhibition at 0.1 mM
KCN
-
isozyme ECPOX 1 shows 1% residual activity, isozyme ECPOX 2 shows complete inhibition, and isozyme ECPOX 3 shows 3% residual activity at 0.1 mM
L-cysteine
-
0.15 mM, complete inhibition of membrane-bound isoform, 2 mM, complete inhibition of soluble isoform
L-cysteine
-
71% inhibition at 1 mM
L-cysteine
-
93% inhibition
L-cysteine
-
94% inhibition at 0.1 mM
L-cysteine
-
10 mM, complete loss of activity
Metabisulfite
-
3 mM, complete inhibition of membrane-bound isoform, 3.5 mM, complete inhibition of soluble isoform
Mg2+
-
5 mM, 7% inhibition
Mg2+
-
83.5% relative activity at 10 mM
Mg2+
-
5 mM, 46% residual activity
Mn2+
-
5mM, 55% inhibition
Mn2+
-
57.1% inhibition at 5 mM
Mn2+
-
noncompetitive inhibition
Mn2+
-
1 mM, slight inhibition
Mn2+
-
10 mM, 19% loss of activity, isoenzyme FP1; 10 mM, 2% loss of activity, isoenzyme FP2; 10 mM, 75% loss of activity, isoenzyme FP3
Mn2+
-
9% inhibition at 1 mM
Mn2+
30% inhibition at 1 mM; 30% inhibition at 1 mM; 70% relative activity at 1 mM; 73% relative activity at 1 mM
Mn2+
-
93.2% relative activity at 10 mM
Mn2+
-
5 mM, 41% inhibition of cationic peroxidase GCP1
Mn2+
-
1 mM, 73% residual activity
Mn2+
5 mM, 10% residual activity
Mn2+
-
isozyme ECPOX 2 shows 69% residual activity at 0.5 mM
n-propyl gallate
-
95% inhibition at 1 mM
Na+
44% inhibition at 1 mM; 49% inhibition at 1 mM; 49% inhibition at 1 mM
Na+
-
94.8% relative activity at 10 mM
Na+
-
5 mM, 53% residual activity
NaCN
-
100% inhibition at 10 mM
NaCN
Armoracia sp.
-
100% inhibition at 10 mM
NaCN
-
50% inhibition at 10 mM
NaCN
-
99% inhibition at 0.1 mM
NaCN
-
0.5 mM, 93% inhibition
NaN3
-
82% inhibition 10 mM
NaN3
-
10 mM, 98% loss of activity, isoenzyme FP2; 10 mM, 99% loss of activity, isoenzyme FP1; 10 mM, complete loss of activity, isoenzyme FP3
NaN3
-
71% inhibition at 1 mM
NaN3
-
99% inhibition at 20 mM
NaN3
-
95% inhibition at 0.1 mM
NaN3
-
isozyme ECPOX 1 shows 4% residual activity, isozyme ECPOX 2 shows complete inhibition, and isozyme ECPOX 3 shows 11% residual activity at 1 mM
Ni2+
-
5mM, 57% inhibition
Ni2+
-
10% inhibition at 5 mM, at 37°C
Ni2+
-
10 mM, 14% loss of activity, isoenzyme FP1; 10 mM, 27% loss of activity, isoenzyme FP2; 10 mM, 55% loss of activity, isoenzyme FP3
Ni2+
-
90.6% relative activity at 10 mM
phenylhydrazine
-
complete inhibition at 1 mM
phenylhydrazine
-
100% inhibition at 1 mM
propofol
-
i.e. 2,6-diisopropylphenol, competitive inhibitor
resorcinol
-
competitive inhibition of 3,3',5,5'-tetramethylbenzidine oxidation
resorcinol
-
incubation of the LPO/H2O2/acetonitrile system with resorcinol is associated with amoderate decline in the rate of cyanide production which is 64.8% of the control
SDS
-
81.7% residual activity at 10 mM
SDS
-
about 75% loss of activity at 2% W/V SDS
Sodium azide
-
non-competitive inhibitor
Sodium azide
-
incubation of the LPO/H2O2/acetonitrile system with sodium azide is associated with amoderate decline in the rate of cyanide production which is 61.6% of the control
Sodium azide
-
0.187 mM, more than 75% inhibition, 0.5 mM, complete inhibition, heme-containing enzyme
Sodium azide
-
99% inhibition
Sodium azide
-
competitive
Zn2+
-
5mM, 53% inhibition
Zn2+
-
1 mM, slight inhibition
Zn2+
-
13% inhibition at 5 mM, at 37°C
Zn2+
38% relative activity at 1 mM; 46% relative activity at 1 mM; 54% inhibition at 1 mM; 62% inhibition at 1 mM
Zn2+
-
95.0% relative activity at 10 mM
additional information
-
no substrate inhibition by 2,2'-azinobis(3-ethylbenzthiazoline-6-sulfonic acid); no substrate inhibition by 2,2'-azinobis(3-ethylbenzthiazoline-6-sulfonic acid)
-
additional information
no substrate inhibition by 2,2'-azinobis(3-ethylbenzthiazoline-6-sulfonic acid); no substrate inhibition by 2,2'-azinobis(3-ethylbenzthiazoline-6-sulfonic acid)
-
additional information
-
the enzyme is not sensitive to the prototypical catalase inhibitor 3-amino-1, 2, 4,-triazole in presence of ascorbic acid (1.0 mM)
-
additional information
-
HRP-DNA conjugates reveal a reduced peroxidase activity
-
additional information
-
incorporation of an iron corrole into the apo-form of horseradish peroxidase leads to decreased catalytic activity as a result of the iron attaining the +4 oxidation state which causes poor binding and/or activation of H2O2 on the iron
-
additional information
-
no inhibition of enzyme activity when the concentrations of phenol and H2O2 are at or below 10 mM and 0.1 mM, respectively
-
additional information
-
enzyme does not exhibit any measurable substrate inhibition
-
additional information
-
the enzyme keeps its activity in the presence of high D-glucose concentrations (up to 5 M)
-
additional information
-
the enzyme keeps its activity in the presence of high D-glucose concentrations (up to 5 M)
-
additional information
-
not inhibited by Cu2+ and Mg2+
-
additional information
not inhibited by Cu2+ and Mg2+
-
additional information
not inhibited by Cu2+ and Mg2+
-
additional information
-
inhibition is not observed with ethylmaleinimide and urea
-
additional information
peroxidase activity is not inhibited by 3-amino-1,2,4-triazole concentrations up to 20 mM
-
additional information
presence of Mg2+, Cu2+, Fe3+, Ni2+, citric acid, and urea has no effect on the peroxidase activity
-
Please wait a moment until the data is sorted. This message will disappear when the data is sorted.
Please wait a moment until the data is sorted. This message will disappear when the data is sorted.
0.75
1-naphthol
-
25°C, pH 5.5
0.65
2,2'-azino-bis (3-ethylbenzthiazoline-6-sulphonic acid)
-
pH 3.5, 25°C
0.036 - 10.4
2,2'-azino-bis(3-ethylbenzthiazole-6-sulfonic acid)
0.000358
2,2'-azino-bis(3-ethylbenzthiazoline)-sulfonic acid
-
at 25°C, pH 6.0
0.023 - 1.6
2,2'-azino-bis-(3-ethylbenzthiazole-6-sulfonic acid)
0.16 - 5.4
2,2'-azinobis(3-ethylbenzthiazoline-6-sulfonic acid)
4.9
2,2-azino-bis-(3-ethylbenz-thiazoline)-6-sulfonic acid
-
-
0.495
2,2-azino-bis-(3-ethylbenz-thiazoline-6-sulfonic acid)
-
in 50 mM sodium citrate buffer (pH 5.0), at 25°C
5
2,3-dimethoxyphenol
-
pH 7.0
0.312 - 4.53
2,4,6-tribromophenol
0.229 - 5.1
2,4,6-Trichlorophenol
5.6 - 15.3
2,6-dimethyloxyphenol
0.4
2-chloro-4-methoxyphenol
-
pH 7.0
0.18
2-naphthol
-
25°C, pH 5.5
0.045 - 0.2
3,3',5,5'-tetramethylbenzidine
5.05 - 24
3,4-dihydroxyphenylacetic acid
1.4
3,4-dimethoxyphenol
-
pH 7.0
0.031
3,5-dibromo-4-hydroxybenzonitrile
-
pH 4.0
3.7
3,5-dimethoxyphenol
-
pH 7.0
9.7
3-(4-hydroxyphenyl)propanoic acid
-
pH 7.0
0.64
3-methyltyrosine
-
in 100 mM Tris-HCl, pH 9.0, at 25°C
0.12 - 15.38
4-aminoantipyrine
83.33
4-aminophenazone
-
-
2.36
4-Aminophenol
-
native enzyme, at 30°C
0.03
4-Hydroxybiphenyl
-
25°C, pH 5.5
0.1 - 0.39
4-methoxy-alpha-naphthol
0.25 - 0.5
5-O-(trans-feruloyl)-L-arabinose
0.081
amplex red
-
native HRP
0.029 - 0.043
ascorbic acid
0.15 - 0.64
chlorogenic acid
0.009 - 3
cumene hydroperoxide
0.092
ethynylestradiol
-
-
4.53
eugenol
-
pH 5.0, 16°C
5.05
fructosyl-6-phosphate alpha-Boc-L-lysine
-
at 25°C in 0.2 M sodium phosphate buffer (pH 6.0)
-
1.3
gallic acid
-
pH 6.0, temperature not specified in the publication
1
L-tyrosine
-
in 100 mM Tris-HCl, pH 9.0, at 25°C
3.5
m-hydroxyanisol
-
pH 7.0
0.029
malachite green
-
-
0.025
N,N,N,N-tetramethyl-p-phenyldiamine
-
pH 7.0
0.137 - 12.56
o-Dianisidine
0.38 - 9
o-phenylenediamine
18.76
p-hydroxybenzoic acid
-
native enzyme, at 30°C
0.032
Pentachlorophenol
-
pH 4.0
0.11
Promethazine
Armoracia sp.
-
promethazine oxidation
0.0028 - 0.0036
Reactive Black 5
0.0036
Reactive Blue 5
-
at pH 4.8
0.016 - 607
reduced 2,2'-azino-bis-(3-ethylbenzthiazole-6-sulfonic acid)
0.011
Remazol Brilliant Blue R
-
-
0.07
rubredoxin
-
85°C, pH 7.5
-
22
tert-butyl hydroperoxide
-
in 50 mM potassium phosphate buffer, pH 7.0
0.023
thioredoxin 1
25°C, pH 7.0
0.111
ubiquinol-1
pH 7.5, temperature not specified in the publication
2.41 - 16
veratryl alcohol
additional information
additional information
-
0.036
2,2'-azino-bis(3-ethylbenzthiazole-6-sulfonic acid)
-
-
0.21
2,2'-azino-bis(3-ethylbenzthiazole-6-sulfonic acid)
-
-
0.73
2,2'-azino-bis(3-ethylbenzthiazole-6-sulfonic acid)
-
pH 7.0, 25°C
10.4
2,2'-azino-bis(3-ethylbenzthiazole-6-sulfonic acid)
-
pH 5.0, 25°C
0.023
2,2'-azino-bis-(3-ethylbenzthiazole-6-sulfonic acid)
-
25°C, pH 3.5
0.045
2,2'-azino-bis-(3-ethylbenzthiazole-6-sulfonic acid)
-
25°C, pH 5.0
0.17
2,2'-azino-bis-(3-ethylbenzthiazole-6-sulfonic acid)
-
25°C, pH 6.8
0.18
2,2'-azino-bis-(3-ethylbenzthiazole-6-sulfonic acid)
-
25°C, pH 6.8
0.18
2,2'-azino-bis-(3-ethylbenzthiazole-6-sulfonic acid)
-
pyromellitic dianhydride-modified enzyme, in 0.01 M phosphate buffer at pH 7.5 and 25°C
0.19
2,2'-azino-bis-(3-ethylbenzthiazole-6-sulfonic acid)
-
native enzyme, in 0.01 M phosphate buffer at pH 7.5 and 25°C
0.27
2,2'-azino-bis-(3-ethylbenzthiazole-6-sulfonic acid)
-
25°C, pH 5.0
0.9
2,2'-azino-bis-(3-ethylbenzthiazole-6-sulfonic acid)
-
25°C, pH 6.0, partially deglycosylated enzyme
1.1
2,2'-azino-bis-(3-ethylbenzthiazole-6-sulfonic acid)
-
25°C, pH 6.0, native enzyme
1.6
2,2'-azino-bis-(3-ethylbenzthiazole-6-sulfonic acid)
Elais guineensis
-
-
0.16
2,2'-azinobis(3-ethylbenzthiazoline-6-sulfonic acid)
pH 3.0, 23°C
0.296
2,2'-azinobis(3-ethylbenzthiazoline-6-sulfonic acid)
-
pH 5.0, 16°C
0.43
2,2'-azinobis(3-ethylbenzthiazoline-6-sulfonic acid)
-
membrane-bound isoform, pH not specified in the publication, temperature not specified in the publication
0.685
2,2'-azinobis(3-ethylbenzthiazoline-6-sulfonic acid)
pH 7.0, temperature not specified in the publication
0.92
2,2'-azinobis(3-ethylbenzthiazoline-6-sulfonic acid)
-
soluble isoform, pH not specified in the publication, temperature not specified in the publication
0.99
2,2'-azinobis(3-ethylbenzthiazoline-6-sulfonic acid)
mutant N13D/N57S/N255D/N268D, pH 6.5, 30°C
1.01
2,2'-azinobis(3-ethylbenzthiazoline-6-sulfonic acid)
pH 6.5, 37°C
1.5
2,2'-azinobis(3-ethylbenzthiazoline-6-sulfonic acid)
wild-type, pH 6.5, 30°C
1.95
2,2'-azinobis(3-ethylbenzthiazoline-6-sulfonic acid)
pH 6.5, 37°C
2.07
2,2'-azinobis(3-ethylbenzthiazoline-6-sulfonic acid)
pH 7.0, temperature not specified in the publication
3.5
2,2'-azinobis(3-ethylbenzthiazoline-6-sulfonic acid)
pH 6.5, 37°C
5.4
2,2'-azinobis(3-ethylbenzthiazoline-6-sulfonic acid)
-
pH 7.0, temperature not specified in the publication
0.312
2,4,6-tribromophenol
pH 7.0, temperature not specified in the publication
1.02
2,4,6-tribromophenol
pH 7.0, temperature not specified in the publication
4.53
2,4,6-tribromophenol
-
pH 7.0, temperature not specified in the publication
0.229
2,4,6-Trichlorophenol
pH 7.0, temperature not specified in the publication
0.448
2,4,6-Trichlorophenol
pH 7.0, temperature not specified in the publication
5.1
2,4,6-Trichlorophenol
-
pH 7.0, temperature not specified in the publication
5.6
2,6-dimethyloxyphenol
-
pH 9.0, 25°C
15.3
2,6-dimethyloxyphenol
-
pH 7.0, 25°C
0.045
3,3',5,5'-tetramethylbenzidine
-
native enzyme, in 0.01 M phosphate buffer at pH 7.5 and 25°C
0.045
3,3',5,5'-tetramethylbenzidine
-
pyromellitic dianhydride-modified enzyme, in 0.01 M phosphate buffer at pH 7.5 and 25°C
0.09
3,3',5,5'-tetramethylbenzidine
-
20°C, pH 7.4
0.09
3,3',5,5'-tetramethylbenzidine
-
20°C, pH 6.8
0.09
3,3',5,5'-tetramethylbenzidine
pH 6.5, 30°C, 600 mM sorbotol
0.11
3,3',5,5'-tetramethylbenzidine
pH 6.5, 30°C, 300 mM glycine
0.15
3,3',5,5'-tetramethylbenzidine
-
20°C, pH 6.4
0.2
3,3',5,5'-tetramethylbenzidine
pH 6.5, 30°C
5.05
3,4-dihydroxyphenylacetic acid
-
for Cucumis melo L. inodorus cv. Amarillo
24
3,4-dihydroxyphenylacetic acid
-
for Cucumis melo L. cantalupensis cv. Charentais
0.12
4-aminoantipyrine
-
at pH 7.0
10.63
4-aminoantipyrine
-
isoform PRB-A, pH 7, pH 7, 23°C
15.38
4-aminoantipyrine
-
isoform PRB-B, pH 7, pH 7, 23°C
1.1
4-Chlorophenol
-
pyromellitic dianhydride-modified enzyme, in 0.01 M phosphate buffer at pH 7.5 and 25°C
1.5
4-Chlorophenol
-
native enzyme, in 0.01 M phosphate buffer at pH 7.5 and 25°C
0.1
4-methoxy-alpha-naphthol
-
25°C, pH 5.5
0.39
4-methoxy-alpha-naphthol
-
in 50 mM sodium acetate buffer (pH 5.0), at 25°C
0.25
5-O-(trans-feruloyl)-L-arabinose
-
without CaCl2
0.5
5-O-(trans-feruloyl)-L-arabinose
-
with 20 mM CaCl2
0.029
ascorbic acid
-
isoenzyme POX II
0.043
ascorbic acid
-
isoenzyme POX I
1.3
Br-
-
20°C, pH 6.5
0.08
caffeic acid
-
covalently bound POD from artichoke leaves, apparent Km value
0.1
caffeic acid
-
covalently bound POD from artichoke heads, apparent Km value
0.167
caffeic acid
-
pH 5.0, 16°C
0.19
caffeic acid
-
ionically bound POD from artichoke heads, apparent Km value
0.59
caffeic acid
-
soluble POD from artichoke heads, apparent Km value
1.59
caffeic acid
-
soluble POD from artichoke leaves, apparent Km value
1.9
caffeic acid
-
ionically bound POD from artichoke leaves, apparent Km value
18.2
catechol
-
30°C, pH 5.0
125
catechol
-
in 50 mM sodium acetate buffer, at pH 5.5
0.15
chlorogenic acid
-
soluble POD from artichoke heads, apparent Km value
0.17
chlorogenic acid
-
covalently bound POD from artichoke heads, apparent Km value
0.23
chlorogenic acid
-
covalently bound POD from artichoke leaves, apparent Km value
0.28
chlorogenic acid
-
ionically bound POD from artichoke leaves, apparent Km value
0.36
chlorogenic acid
-
in 50 mM sodium acetate buffer (pH 5.0), at 25°C
0.55
chlorogenic acid
-
soluble POD from artichoke leaves, apparent Km value
0.64
chlorogenic acid
-
ionically bound POD from artichoke heads, apparent Km value
0.009
cumene hydroperoxide
25°C, pH 7.0
3
cumene hydroperoxide
-
in 50 mM potassium phosphate buffer, pH 7.0
0.0052
esculetin
-
at pH 7
1.4
esculetin
-
KM as a kinetic constant of the POD/H2O2/ESC system at pH 7
2
esculetin
-
KM as a kinetic constant of the POD/H2O2/ESC system at pH 4.5
0.01
ferulic acid
-
covalently bound POD from artichoke heads, apparent Km value
0.06
ferulic acid
-
covalently bound POD from artichoke leaves, apparent Km value
0.11
ferulic acid
-
soluble POD from artichoke leaves, apparent Km value
0.21
ferulic acid
-
ionically bound POD from artichoke leaves, apparent Km value
0.29
ferulic acid
-
ionically bound POD from artichoke heads, apparent Km value
0.58
ferulic acid
-
without CaCl2
0.72
ferulic acid
-
soluble POD from artichoke heads, apparent Km value
1.5
ferulic acid
-
with 20 mM CaCl2
0.00063
guaiacol
-
pH 7.0, 25°C
0.036
guaiacol
-
pH 6.0, 30°C
0.048
guaiacol
Brassica oleracea var. capitata f. rubra
-
pH 6.0, 25°C
0.14
guaiacol
-
native enzyme, in 0.01 M phosphate buffer at pH 7.5 and 25°C
0.14
guaiacol
-
pyromellitic dianhydride-modified enzyme, in 0.01 M phosphate buffer at pH 7.5 and 25°C
0.202
guaiacol
-
isoenzyme POX II
0.288
guaiacol
-
isoenzyme POX I
0.3
guaiacol
-
25°C, pH 6.0
0.7
guaiacol
-
25°C, pH 6.0
0.966
guaiacol
mutant F130A, pH 5, temperature not specified in the publication
0.966
guaiacol
wild-type isoform C, pH 5, temperature not specified in the publication
1.06
guaiacol
mutant F68A, pH 5, temperature not specified in the publication
1.2
guaiacol
-
pH 6.0-7.5, 30°C, cationic peroxidase GCP1
1.72
guaiacol
mutant F143A, pH 5, temperature not specified in the publication
1.82
guaiacol
mutant F179A, pH 5, temperature not specified in the publication
2
guaiacol
Elais guineensis
-
-
2.04
guaiacol
mutant F142A, pH 5, temperature not specified in the publication
2.16
guaiacol
mutant F130A/F142A/ F143A/F179A, pH 5, temperature not specified in the publication
2.69
guaiacol
mutant F68A/F142A/ F143A/F179A, pH 5, temperature not specified in the publication
2.8
guaiacol
-
in the absence of 1-butyl-3-methylimidazolium tetrafluoroborate, in potassium phosphate buffer (20 mM, pH 7.0) at 25°C
2.8
guaiacol
-
in the absence of butyl-3-methylimidazolium tetrafluoroborate, at 25°C
3.6
guaiacol
-
pH 7.0, 40°C, anionic peroxidase GCP2
3.7
guaiacol
-
pH 6.0, temperature not specified in the publication
3.755
guaiacol
-
pH 6.0, temperature not specified in the publication
3.8
guaiacol
-
30°C, pH 5.0
4.1
guaiacol
-
in the presence of 5% (v/v) 1-butyl-3-methylimidazolium tetrafluoroborate, in potassium phosphate buffer (20 mM, pH 7.0) at 25°C
4.64
guaiacol
-
pH 5.0, 16°C
5
guaiacol
-
in 50 mM sodium acetate buffer, at pH 5.5
5.05
guaiacol
-
at pH 7.0 and 25°C
5.68
guaiacol
-
pH 5.5, temperature not specified in the publication, isoenzyme FP1
6.8
guaiacol
-
in the presence of 10% (v/v) 1-butyl-3-methylimidazolium tetrafluoroborate, in potassium phosphate buffer (20 mM, pH 7.0) at 25°C
6.89
guaiacol
-
pH 5.5, temperature not specified in the publication, isoenzyme FP2
7.5
guaiacol
-
pH 6.0, 25°C
7.8
guaiacol
-
in the presence of 15% (v/v) 1-butyl-3-methylimidazolium tetrafluoroborate, in potassium phosphate buffer (20 mM, pH 7.0) at 25°C
8.8
guaiacol
-
25°C, pH 6.0
9.5
guaiacol
-
25°C, pH 5.0
13.3
guaiacol
-
isozyme Cn
15.1
guaiacol
-
in the presence of 20% (v/v) 1-butyl-3-methylimidazolium tetrafluoroborate, in potassium phosphate buffer (20 mM, pH 7.0) at 25°C
15.94
guaiacol
-
pH 5.5, temperature not specified in the publication, isoenzyme FP3
17.5
guaiacol
-
pH 7.0, 25°C
18.18
guaiacol
-
in 0.01 M citrate phosphate buffer (pH 7.0), at 25°C
22.5
guaiacol
-
in 25% (v/v) butyl-3-methylimidazolium tetrafluoroborate, at 25°C
22.5
guaiacol
-
in the presence of 25% (v/v) 1-butyl-3-methylimidazolium tetrafluoroborate, in potassium phosphate buffer (20 mM, pH 7.0) at 25°C
24
guaiacol
-
at pH 7.0 and 25°C
28.1
guaiacol
-
pH 10.5, 25°C
46.5
guaiacol
-
pH 7.0, temperature not specified in the publication, soluble enzyme
50.68
guaiacol
-
in 0.01 M citrate phosphate buffer (pH 7.0), at 25°C
64.5
guaiacol
-
pH 7.0, temperature not specified in the publication, immobilized enzyme (entrapped onto a carboxymethyl cellulose/Fe3O4 magnetic hybrid material)
98.61
guaiacol
-
at 25°C in 0.2 M sodium phosphate buffer (pH 6.0)
0.004
H2O2
pH 7.0, 25°C
0.005
H2O2
-
oxidation of 3,5-dimethoxyphenol, pH 7.0
0.0052
H2O2
-
KM as a kinetic constant of the POD/H2O2/ESC system at pH 7
0.006
H2O2
-
oxidation of 2,3-dimethoxyphenol, pH 7.0
0.0084
H2O2
-
pH 6.0, 30°C
0.009
H2O2
wild-type, pH 6.5, 30°C
0.012
H2O2
-
2,4,6-trichlorophenol, pH 7.0, temperature not specified in the publication
0.015
H2O2
mutant N13D/N57S/N255D/N268D, pH 6.5, 30°C
0.016
H2O2
-
oxidation of o-toluidine, pH 7.0
0.016
H2O2
-
30°C, pH 5.5, cosubstrate: pyrogallol, isoenzyme E5
0.017
H2O2
-
oxidation of 3-p-hydroxyphenyl propionic acid, pH 7.0
0.019
H2O2
-
pH 4, oxidative dehalogenation of 3,5-dibromo-4-hydroxybenzonitrile
0.025
H2O2
-
25°C, pH 6.0, partially deglycosylated enzyme
0.025
H2O2
-
oxidation of m-hydroxyanisole, pH 7.0
0.025
H2O2
2,4,6-trichlorophenol, pH 7.0, temperature not specified in the publication
0.026
H2O2
-
pH 4, oxidative dehalogenation of pentachlorophenol
0.029
H2O2
2,4,6-trichlorophenol, pH 7.0, temperature not specified in the publication
0.035
H2O2
-
85°C, pH 7.5
0.038
H2O2
-
oxidation of N,N,N,N-tetramethyl-p-phenyldiamine, pH 7.0
0.039
H2O2
pH 7.5, temperature not specified in the publication
0.042
H2O2
-
25°C, pH 6.0
0.043
H2O2
-
isoform PRB-A, pH 7, pH 7, 23°C
0.045
H2O2
-
pH 5.5, temperature not specified in the publication
0.05
H2O2
-
cosubstrate 2,2'-azinobis(3-ethylbenzthiazoline-6-sulfonic acid), pH 7.0, temperature not specified in the publication
0.052
H2O2
-
KM as a kinetic constant of the POD/H2O2/ESC system at pH 4.5
0.055
H2O2
-
25°C, pH 3.5
0.055
H2O2
-
25°C, pH 6.0, native enzyme
0.058
H2O2
-
oxidation of guaiacol, pH 7.0
0.067
H2O2
-
isoform PRB-B, pH 7, pH 7, 23°C
0.093
H2O2
-
cosubstrate 2,4,6-tribromophenol, pH 7.0, temperature not specified in the publication
0.1
H2O2
-
pH 6.0, temperature not specified in the publication, cosubstrate: gallic acid
0.11
H2O2
Armoracia sp.
-
promethazine oxidation
0.11
H2O2
-
oxidation of 2-chloro-4-methoxyphenol, pH 7.0
0.11
H2O2
-
oxidation of 3,4-dimethoxyphenol, pH 7.0
0.113
H2O2
-
at 25°C in 0.2 M sodium phosphate buffer (pH 6.0)
0.12
H2O2
-
30°C, pH 5.0, reaction with o-phenylenediamine
0.141
H2O2
cosubstrate 2,4,6-tribromophenol, pH 7.0, temperature not specified in the publication
0.165
H2O2
cosubstrate 2,2'-azinobis(3-ethylbenzthiazoline-6-sulfonic acid), pH 7.0, temperature not specified in the publication
0.17
H2O2
-
in the presence of chlorogenic acid, in 50 mM sodium acetate buffer (pH 5.0), at 25°C
0.2
H2O2
-
pH 6.0, temperature not specified in the publication, cosubstrate: guaiacol
0.21
H2O2
-
pH 5.5, temperature not specified in the publication, isoenzyme FP3
0.212
H2O2
cosubstrate 2,4,6-tribromophenol, pH 7.0, temperature not specified in the publication
0.25
H2O2
-
pH 5.5, temperature not specified in the publication, isoenzyme FP2
0.28
H2O2
-
30°C, pH 5.5, cosubstrate: o-phenylenediamine, isoenzyme E5
0.31
H2O2
-
30°C, pH 5.0, reaction with o-phenylenediamine
0.335
H2O2
cosubstrate 2,2'-azinobis(3-ethylbenzthiazoline-6-sulfonic acid), pH 7.0, temperature not specified in the publication
0.34
H2O2
-
pH 5.5, temperature not specified in the publication, isoenzyme FP1
0.35
H2O2
-
30°C, pH 5.5, cosubstrate: reduced 2,2'-azino-bis-(3-ethylbenzthiazole-6-sulfonic acid), isoenzyme E5
0.48
H2O2
-
in the presence of 4-methoxy-alpha-naphthol, in 50 mM sodium acetate buffer (pH 5.0), at 25°C
0.5
H2O2
-
pH 6.0, temperature not specified in the publication, cosubstrate: o-phenylenediamine
0.54
H2O2
-
in 50 mM sodium acetate buffer, at pH 5.5
0.62
H2O2
-
soluble isoform, pH not specified in the publication, temperature not specified in the publication
0.73
H2O2
-
without CaCl2
0.93
H2O2
-
30°C, pH 5.0, reaction with o-phenylenediamine
1.1
H2O2
-
membrane-bound isoform, pH not specified in the publication, temperature not specified in the publication
1.1
H2O2
-
pH 6.0-7.5, 30°C, cationic peroxidase GCP1
1.2
H2O2
-
with 20 mM CaCl2
1.32
H2O2
-
in 50 mM sodium citrate buffer (pH 5.0), at 25°C
1.6
H2O2
-
presence of Ca2+, pH 5.5, 25°C
1.6
H2O2
-
pH 7.0, 40°C, anionic peroxidase GCP2
2.33
H2O2
-
HRP in colloidal carbon microspheres/chitosan hybrid, apparent Km value
2.36
H2O2
-
30°C, pH 5.0, reaction with o-phenylenediamine
4.5
H2O2
pH 6.5, 30°C, 600 mM sorbitol
4.81
H2O2
-
pH 7.0, temperature not specified in the publication, soluble enzyme
5.1
H2O2
pH 6.5, 30°C, 300 mM glycine
5.71
H2O2
-
pH 7.0, temperature not specified in the publication, immobilized enzyme (entrapped onto a carboxymethyl cellulose/Fe3O4 magnetic hybrid material)
30
H2O2
-
in 50 mM potassium phosphate buffer, pH 7.0
3.1
K4[Fe(CN)6]
-
pH 5.0, 25°C
16.3
K4[Fe(CN)6]
-
pH 7.0, 25°C
0.11
Mn2+
24°C, pH 5, mutant enzyme W164S
0.126
Mn2+
24°C, pH 5, mutant enzyme W164H
0.189
Mn2+
24°C, pH 5, wild-type enzyme
0.218
Mn2+
24°C, pH 5, mutant enzyme H232F
0.262
Mn2+
24°C, pH 5, mutant enzyme P76H
0.351
Mn2+
24°C, pH 5, mutant enzyme W164S/P76H
9.1
o-Cresol
-
pyromellitic dianhydride-modified enzyme, in 0.01 M phosphate buffer at pH 7.5 and 25°C
16.7
o-Cresol
-
native enzyme, in 0.01 M phosphate buffer at pH 7.5 and 25°C
0.137
o-Dianisidine
-
isoenzyme POX II
0.2
o-Dianisidine
-
pH 5.0, 16°C
0.229
o-Dianisidine
-
isoenzyme POX I
0.5
o-Dianisidine
-
at pH 8.0
1.28
o-Dianisidine
-
pH 5.5, temperature not specified in the publication
2.134
o-Dianisidine
-
at 25°C in 0.2 M sodium phosphate buffer (pH 6.0)
11
o-Dianisidine
-
in 50 mM sodium acetate buffer, at pH 5.5
12.56
o-Dianisidine
-
pH 6.0, temperature not specified in the publication
0.38
o-phenylenediamine
-
20°, pH 6.2
2.02
o-phenylenediamine
-
at pH 5.5
2.85
o-phenylenediamine
-
in 50 mM sodium acetate buffer, at pH 5.5
2.9
o-phenylenediamine
-
30°C, pH 5.0
3.33
o-phenylenediamine
-
pH 5.5, temperature not specified in the publication, isoenzyme FP3
3.64
o-phenylenediamine
-
pH 5.5, temperature not specified in the publication, isoenzyme FP2
3.87
o-phenylenediamine
-
pH 5.5, temperature not specified in the publication, isoenzyme FP1
5.9
o-phenylenediamine
-
pH 6.0, temperature not specified in the publication
9
o-phenylenediamine
-
30°C, pH 5.5, isoenzyme E5
1.12
phenol
-
pyromellitic dianhydride-modified enzyme, in 0.01 M phosphate buffer at pH 7.5 and 25°C
1.17
phenol
-
native enzyme, in 0.01 M phosphate buffer at pH 7.5 and 25°C
3.59
phenol
-
native enzyme, at 30°C
9.45
phenol
-
pH 7.0, 25°C
0.29
pyrogallol
-
at pH 5.5
0.449
pyrogallol
-
pH 5.0, 16°C
1.2
pyrogallol
Elais guineensis
-
-
1.63
pyrogallol
-
at pH 6.0
2 - 3
pyrogallol
-
in 50 mM sodium acetate buffer, at pH 5.5
2.5
pyrogallol
-
30°C, pH 5.0
55.4
pyrogallol
-
30°C, pH 5.5, isoenzyme E5
0.028
quercetin
-
isoenzyme POX II
0.071
quercetin
-
isoenzyme POX I
0.0028
Reactive Black 5
24°C, pH 3.5, wild-type enzyme
0.0031
Reactive Black 5
24°C, pH 3.5, mutant enzyme P76H
0.0036
Reactive Black 5
24°C, pH 3.5, mutant enzyme H232F
0.016
reduced 2,2'-azino-bis-(3-ethylbenzthiazole-6-sulfonic acid)
-
isoenzyme POX II
0.21
reduced 2,2'-azino-bis-(3-ethylbenzthiazole-6-sulfonic acid)
-
30°C, pH 5.5, isoenzyme E5
9.56
reduced 2,2'-azino-bis-(3-ethylbenzthiazole-6-sulfonic acid)
-
-
607
reduced 2,2'-azino-bis-(3-ethylbenzthiazole-6-sulfonic acid)
25°C, pH 5.0, mutant enzyme
0.076
SCN-
-
20°C, pH 6.5
2.41
veratryl alcohol
24°C, pH 3, mutant enzyme P76H
2.75
veratryl alcohol
24°C, pH 3, wild-type enzyme
3.58
veratryl alcohol
24°C, pH 3, mutant enzyme H232F
16
veratryl alcohol
-
pH 5.0, 25°C
additional information
additional information
-
Hofmeister specific-ion effects
-
additional information
additional information
the activity of MnP124076 toward Mn2+ is too low to obtain reliable kinetic parameters
-
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