Please wait a moment until all data is loaded. This message will disappear when all data is loaded.
Please wait a moment until the data is sorted. This message will disappear when the data is sorted.
(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 5Ā°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 EĆ, Bacillus megaterium NRS, Yersinia enterocolitica, Listeria monocytogenes scoot A, Bacillus megaterium EĆ, 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
-
-
?