BRENDA - Enzyme Database

Synthesis and biological evaluation of guanidino compounds endowed with subnanomolar affinity as competitive inhibitors of maize polyamine oxidase

Manetti, F.; Cona, A.; Angeli, L.; Mugnaini, C.; Raffi, F.; Capone, C.; Dreassi, E.; Zizzari, A.T.; Tisi, A.; Federico, R.; Botta, M.; J. Med. Chem. 52, 4774-4785 (2009)

Data extracted from this reference:

Inhibitors
EC Number
Inhibitors
Commentary
Organism
Structure
1.5.3.14
(N1-5-aminopentyl)-N3-(cyclohexylethyl)-N1,N2,N3-tris(tert-butoxycarbonyl)guanidine
-
Zea mays
1.5.3.14
1,8-diaminooctane
-
Zea mays
1.5.3.14
1-(4-aminobutyl)-3-(4-fluorobenzyl)guanidine
competitive inhibition of spermidine oxidation
Zea mays
1.5.3.14
1-(4-aminobutyl)-3-but-3-en-1-ylguanidine
competitive inhibition of spermidine oxidation
Zea mays
1.5.3.14
1-(4-aminobutyl)-3-but-3-yn-1-ylguanidine
competitive inhibition of spermidine oxidation
Zea mays
1.5.3.14
1-(4-carbamimidamidobutyl)-3-(3-methylbut-2-en-1-yl)guanidine
-
Zea mays
1.5.3.14
1-(5-aminopentyl)-3-(2-cyclohexylethyl)guanidine
-
Zea mays
1.5.3.14
1-(5-aminopentyl)-3-(2-cyclopropylethyl)guanidine
-
Zea mays
1.5.3.14
1-(5-aminopentyl)-3-(3-methoxybenzyl)guanidine
-
Zea mays
1.5.3.14
1-(5-aminopentyl)-3-(4-methylpent-3-en-1-yl)guanidine
competitive inhibition of spermidine oxidation
Zea mays
1.5.3.14
1-(5-aminopentyl)-3-[(2E)-3-phenylprop-2-en-1-yl]guanidine
-
Zea mays
1.5.3.14
1-(6-aminohexyl)-3-(4-methylpent-3-en-1-yl)guanidine
competitive inhibition of spermidine oxidation
Zea mays
1.5.3.14
1-(guanidino)-17-(N1-(gamma,gamma-dimethylallyl)guanidino)-9-azaheptadecane tris(trifluoroacetate)
-
Zea mays
1.5.3.14
1-[3-[(3-aminopropyl)amino]propyl]-3-(3-methylbut-2-en-1-yl)guanidine
-
Zea mays
1.5.3.14
1-[7-[(9-carbamimidamidononyl)amino]heptyl]-3-(2-cyclopropylethyl)guanidine
-
Zea mays
1.5.3.14
1-[7-[(9-carbamimidamidononyl)amino]heptyl]-3-(2-phenylethyl)guanidine
-
Zea mays
1.5.3.14
1-[7-[(9-carbamimidamidononyl)amino]heptyl]-3-(3-methylbut-3-en-1-yl)guanidine
-
Zea mays
1.5.3.14
3-(4-methylpent-3-en-1-yl)-1-[9-([7-[(4-methylpent-3-en-1-yl)carbamimidamido]heptyl]amino)nonyl]guanidine
-
Zea mays
1.5.3.14
3-but-3-yn-1-yl-1-[7-[(9-carbamimidamidononyl)amino]heptyl]guanidine
-
Zea mays
1.5.3.14
3-[(2E)-but-2-en-1-yl]-1-[7-[(9-carbamimidamidononyl)amino]heptyl]guanidine
-
Zea mays
1.5.3.14
agmatine
competitive inhibition of spermidine oxidation
Zea mays
1.5.3.14
iminoctadine
-
Zea mays
1.5.3.14
additional information
computational structure-function analysis of inhibitors, overview
Zea mays
1.5.3.14
N,N'''-butane-1,4-diylbis[3-(3-methylbut-2-en-1-yl)guanidine]
competitive inhibition of spermidine oxidation
Zea mays
1.5.3.14
N-prenyl agmatine
-
Zea mays
1.5.3.14
N1,N2-bis(tert-butoxycarbonyl)-N1-(cyclohexylethyl)-S-methylisothiourea
-
Zea mays
1.5.3.14
N1,N2-bis(tert-butoxycarbonyl)-N1-(gamma,gamma-dimethylallyl)-S-methylisothiourea
-
Zea mays
1.5.3.14
N1,N2-bis(tert-butoxycarbonyl)-N1-(gamma,gamma-methylallyl)-S-methylisothiourea
-
Zea mays
1.5.3.14
N1-(3-methoxybenzyl)-N3-(5-aminopentyl)-N2,N3,N4-tris(tertbutoxycarbonyl)guanidine
-
Zea mays
1.5.3.14
N1-benzylamine-N3-(gamma,gamma-dimethyallyl)-N2,N3,N4-tris(tert-butoxycarbonyl)guanidine
-
Zea mays
1.5.3.14
N1-benzylamine-N3-(gamma,gamma-dimethylallyl)guanidine bis-(trifluoroacetate)
-
Zea mays
1.5.3.14
N1-[(30-aminopropyl)-3-aminopropyl]-N3-(gamma,gamma-dimethylallyl)-N2,N3-bis(tert-butoxycarbonyl)guanidine
-
Zea mays
1.5.3.14
tert-butyl (2E)-but-2-en-1-yl[(E)-[(tert-butoxycarbonyl)imino](methylsulfanyl)methyl]carbamate
-
Zea mays
1.5.3.14
tert-butyl (4-[(tert-butoxycarbonyl)[(E)-[(tert-butoxycarbonyl)imino](methylsulfanyl)methyl]amino]butyl)methylcarbamate
-
Zea mays
1.5.3.14
tert-butyl (6-aminohexyl)[(tert-butoxycarbonyl)(cyclopropylmethyl)carbamimidoyl]carbamate
-
Zea mays
1.5.3.14
tert-butyl (6-aminohexyl)[(tert-butoxycarbonyl)[(3E)-4-phenylbut-3-en-1-yl]carbamimidoyl]carbamate
-
Zea mays
1.5.3.14
tert-butyl benzyl[(E)-[(tert-butoxycarbonyl)imino](methylsulfanyl)methyl]carbamate
-
Zea mays
1.5.3.14
tert-butyl [(1E)-[(tert-butoxycarbonyl)(cyclopropylmethyl)amino](methylsulfanyl)methylidene]carbamate
-
Zea mays
1.5.3.14
tert-butyl [(E)-[(tert-butoxycarbonyl)imino](methylsulfanyl)methyl]prop-2-yn-1-ylcarbamate
-
Zea mays
1.5.3.14
tert-butyl [(E)-[(tert-butoxycarbonyl)imino](methylsulfanyl)methyl][(2E)-3-phenylprop-2-en-1-yl]carbamate
-
Zea mays
Natural Substrates/ Products (Substrates)
EC Number
Natural Substrates
Organism
Commentary (Nat. Sub.)
Natural Products
Commentary (Nat. Pro.)
Organism (Nat. Pro.)
Reversibility
1.5.3.14
spermidine + O2 + H2O
Zea mays
-
propane-1,3-diamine + 4-aminobutanal + H2O2
-
-
?
Organism
EC Number
Organism
Primary Accession No. (UniProt)
Commentary
Textmining
1.5.3.14
Zea mays
O64411
-
-
Source Tissue
EC Number
Source Tissue
Commentary
Organism
Textmining
1.5.3.14
leaf
-
Zea mays
-
Substrates and Products (Substrate)
EC Number
Substrates
Commentary Substrates
Literature (Substrates)
Organism
Products
Commentary (Products)
Literature (Products)
Organism (Products)
Reversibility
1.5.3.14
spermidine + O2 + H2O
-
705043
Zea mays
propane-1,3-diamine + 4-aminobutanal + H2O2
-
-
-
?
1.5.3.14
spermidine + O2 + H2O
enzyme activity is measured spectrophotometrically by following the formation of a pink adduct resulting from the H2O2-dependent oxidation of 4-aminoantipyrine catalyzed by horseradish peroxidase and the subsequent condensation of oxidized 4-aminoantipyrine with 3,5-dichloro-2-hydroxybenzenesulfonic acid
705043
Zea mays
propane-1,3-diamine + 4-aminobutanal + H2O2
-
-
-
?
Temperature Optimum [C]
EC Number
Temperature Optimum [C]
Temperature Optimum Maximum [C]
Commentary
Organism
1.5.3.14
25
-
assay at
Zea mays
pH Optimum
EC Number
pH Optimum Minimum
pH Optimum Maximum
Commentary
Organism
1.5.3.14
6.5
-
assay at
Zea mays
Ki Value [mM]
EC Number
Ki Value [mM]
Ki Value maximum [mM]
Inhibitor
Commentary
Organism
Structure
1.5.3.14
0.00000008
-
1-[7-[(9-carbamimidamidononyl)amino]heptyl]-3-(2-cyclopropylethyl)guanidine
pH 6.5, 25C
Zea mays
1.5.3.14
0.0000005
-
1-[7-[(9-carbamimidamidononyl)amino]heptyl]-3-(3-methylbut-3-en-1-yl)guanidine
pH 6.5, 25C
Zea mays
1.5.3.14
0.0000007
-
3-but-3-yn-1-yl-1-[7-[(9-carbamimidamidononyl)amino]heptyl]guanidine
pH 6.5, 25C
Zea mays
1.5.3.14
0.000001
-
1-[7-[(9-carbamimidamidononyl)amino]heptyl]-3-(2-phenylethyl)guanidine
pH 6.5, 25C
Zea mays
1.5.3.14
0.0000011
-
3-[(2E)-but-2-en-1-yl]-1-[7-[(9-carbamimidamidononyl)amino]heptyl]guanidine
pH 6.5, 25C
Zea mays
1.5.3.14
0.0000017
-
3-(4-methylpent-3-en-1-yl)-1-[9-([7-[(4-methylpent-3-en-1-yl)carbamimidamido]heptyl]amino)nonyl]guanidine
pH 6.5, 25C
Zea mays
1.5.3.14
0.000003
-
1-(guanidino)-17-(N1-(gamma,gamma-dimethylallyl)guanidino)-9-azaheptadecane tris(trifluoroacetate)
pH 6.5, 25C
Zea mays
1.5.3.14
0.0000075
-
iminoctadine
pH 6.5, 25C
Zea mays
1.5.3.14
0.00001
-
1-(5-aminopentyl)-3-(4-methylpent-3-en-1-yl)guanidine
pH 6.5, 25C
Zea mays
1.5.3.14
0.000015
-
N-prenylagmatine
pH 6.5, 25C
Zea mays
1.5.3.14
0.000022
-
1-(6-aminohexyl)-3-(4-methylpent-3-en-1-yl)guanidine
pH 6.5, 25C
Zea mays
1.5.3.14
0.00013
-
1-(4-aminobutyl)-3-but-3-en-1-ylguanidine
pH 6.5, 25C
Zea mays
1.5.3.14
0.00025
-
1-(4-aminobutyl)-3-but-3-yn-1-ylguanidine
pH 6.5, 25C
Zea mays
1.5.3.14
0.0003
-
1,8-diaminooctane
pH 6.5, 25C
Zea mays
1.5.3.14
0.00063
-
1-(4-aminobutyl)-3-(4-fluorobenzyl)guanidine
pH 6.5, 25C
Zea mays
1.5.3.14
0.0007
-
1-(4-carbamimidamidobutyl)-3-(3-methylbut-2-en-1-yl)guanidine
pH 6.5, 25C
Zea mays
1.5.3.14
0.00115
-
1-(5-aminopentyl)-3-(3-methoxybenzyl)guanidine
pH 6.5, 25C
Zea mays
1.5.3.14
0.00121
-
1-[3-[(3-aminopropyl)amino]propyl]-3-(3-methylbut-2-en-1-yl)guanidine
pH 6.5, 25C
Zea mays
1.5.3.14
0.0015
-
N,N'''-butane-1,4-diylbis[3-(3-methylbut-2-en-1-yl)guanidine]
pH 6.5, 25C
Zea mays
1.5.3.14
0.00153
-
1-(5-aminopentyl)-3-[(2E)-3-phenylprop-2-en-1-yl]guanidine
pH 6.5, 25C
Zea mays
1.5.3.14
0.00172
-
1-(5-aminopentyl)-3-(2-cyclohexylethyl)guanidine
pH 6.5, 25C
Zea mays
1.5.3.14
0.00258
-
1-(5-aminopentyl)-3-(2-cyclopropylethyl)guanidine
pH 6.5, 25C
Zea mays
1.5.3.14
0.003
-
agmatine
pH 6.5, 25C
Zea mays
1.5.3.14
0.018
-
N1-benzylamine-N3-(gamma,gamma-dimethylallyl)guanidine bis-(trifluoroacetate)
pH 6.5, 25C
Zea mays
Inhibitors (protein specific)
EC Number
Inhibitors
Commentary
Organism
Structure
1.5.3.14
(N1-5-aminopentyl)-N3-(cyclohexylethyl)-N1,N2,N3-tris(tert-butoxycarbonyl)guanidine
-
Zea mays
1.5.3.14
1,8-diaminooctane
-
Zea mays
1.5.3.14
1-(4-aminobutyl)-3-(4-fluorobenzyl)guanidine
competitive inhibition of spermidine oxidation
Zea mays
1.5.3.14
1-(4-aminobutyl)-3-but-3-en-1-ylguanidine
competitive inhibition of spermidine oxidation
Zea mays
1.5.3.14
1-(4-aminobutyl)-3-but-3-yn-1-ylguanidine
competitive inhibition of spermidine oxidation
Zea mays
1.5.3.14
1-(4-carbamimidamidobutyl)-3-(3-methylbut-2-en-1-yl)guanidine
-
Zea mays
1.5.3.14
1-(5-aminopentyl)-3-(2-cyclohexylethyl)guanidine
-
Zea mays
1.5.3.14
1-(5-aminopentyl)-3-(2-cyclopropylethyl)guanidine
-
Zea mays
1.5.3.14
1-(5-aminopentyl)-3-(3-methoxybenzyl)guanidine
-
Zea mays
1.5.3.14
1-(5-aminopentyl)-3-(4-methylpent-3-en-1-yl)guanidine
competitive inhibition of spermidine oxidation
Zea mays
1.5.3.14
1-(5-aminopentyl)-3-[(2E)-3-phenylprop-2-en-1-yl]guanidine
-
Zea mays
1.5.3.14
1-(6-aminohexyl)-3-(4-methylpent-3-en-1-yl)guanidine
competitive inhibition of spermidine oxidation
Zea mays
1.5.3.14
1-(guanidino)-17-(N1-(gamma,gamma-dimethylallyl)guanidino)-9-azaheptadecane tris(trifluoroacetate)
-
Zea mays
1.5.3.14
1-[3-[(3-aminopropyl)amino]propyl]-3-(3-methylbut-2-en-1-yl)guanidine
-
Zea mays
1.5.3.14
1-[7-[(9-carbamimidamidononyl)amino]heptyl]-3-(2-cyclopropylethyl)guanidine
-
Zea mays
1.5.3.14
1-[7-[(9-carbamimidamidononyl)amino]heptyl]-3-(2-phenylethyl)guanidine
-
Zea mays
1.5.3.14
1-[7-[(9-carbamimidamidononyl)amino]heptyl]-3-(3-methylbut-3-en-1-yl)guanidine
-
Zea mays
1.5.3.14
3-(4-methylpent-3-en-1-yl)-1-[9-([7-[(4-methylpent-3-en-1-yl)carbamimidamido]heptyl]amino)nonyl]guanidine
-
Zea mays
1.5.3.14
3-but-3-yn-1-yl-1-[7-[(9-carbamimidamidononyl)amino]heptyl]guanidine
-
Zea mays
1.5.3.14
3-[(2E)-but-2-en-1-yl]-1-[7-[(9-carbamimidamidononyl)amino]heptyl]guanidine
-
Zea mays
1.5.3.14
agmatine
competitive inhibition of spermidine oxidation
Zea mays
1.5.3.14
iminoctadine
-
Zea mays
1.5.3.14
additional information
computational structure-function analysis of inhibitors, overview
Zea mays
1.5.3.14
N,N'''-butane-1,4-diylbis[3-(3-methylbut-2-en-1-yl)guanidine]
competitive inhibition of spermidine oxidation
Zea mays
1.5.3.14
N-prenyl agmatine
-
Zea mays
1.5.3.14
N1,N2-bis(tert-butoxycarbonyl)-N1-(cyclohexylethyl)-S-methylisothiourea
-
Zea mays
1.5.3.14
N1,N2-bis(tert-butoxycarbonyl)-N1-(gamma,gamma-dimethylallyl)-S-methylisothiourea
-
Zea mays
1.5.3.14
N1,N2-bis(tert-butoxycarbonyl)-N1-(gamma,gamma-methylallyl)-S-methylisothiourea
-
Zea mays
1.5.3.14
N1-(3-methoxybenzyl)-N3-(5-aminopentyl)-N2,N3,N4-tris(tertbutoxycarbonyl)guanidine
-
Zea mays
1.5.3.14
N1-benzylamine-N3-(gamma,gamma-dimethyallyl)-N2,N3,N4-tris(tert-butoxycarbonyl)guanidine
-
Zea mays
1.5.3.14
N1-benzylamine-N3-(gamma,gamma-dimethylallyl)guanidine bis-(trifluoroacetate)
-
Zea mays
1.5.3.14
N1-[(30-aminopropyl)-3-aminopropyl]-N3-(gamma,gamma-dimethylallyl)-N2,N3-bis(tert-butoxycarbonyl)guanidine
-
Zea mays
1.5.3.14
tert-butyl (2E)-but-2-en-1-yl[(E)-[(tert-butoxycarbonyl)imino](methylsulfanyl)methyl]carbamate
-
Zea mays
1.5.3.14
tert-butyl (4-[(tert-butoxycarbonyl)[(E)-[(tert-butoxycarbonyl)imino](methylsulfanyl)methyl]amino]butyl)methylcarbamate
-
Zea mays
1.5.3.14
tert-butyl (6-aminohexyl)[(tert-butoxycarbonyl)(cyclopropylmethyl)carbamimidoyl]carbamate
-
Zea mays
1.5.3.14
tert-butyl (6-aminohexyl)[(tert-butoxycarbonyl)[(3E)-4-phenylbut-3-en-1-yl]carbamimidoyl]carbamate
-
Zea mays
1.5.3.14
tert-butyl benzyl[(E)-[(tert-butoxycarbonyl)imino](methylsulfanyl)methyl]carbamate
-
Zea mays
1.5.3.14
tert-butyl [(1E)-[(tert-butoxycarbonyl)(cyclopropylmethyl)amino](methylsulfanyl)methylidene]carbamate
-
Zea mays
1.5.3.14
tert-butyl [(E)-[(tert-butoxycarbonyl)imino](methylsulfanyl)methyl]prop-2-yn-1-ylcarbamate
-
Zea mays
1.5.3.14
tert-butyl [(E)-[(tert-butoxycarbonyl)imino](methylsulfanyl)methyl][(2E)-3-phenylprop-2-en-1-yl]carbamate
-
Zea mays
Ki Value [mM] (protein specific)
EC Number
Ki Value [mM]
Ki Value maximum [mM]
Inhibitor
Commentary
Organism
Structure
1.5.3.14
0.00000008
-
1-[7-[(9-carbamimidamidononyl)amino]heptyl]-3-(2-cyclopropylethyl)guanidine
pH 6.5, 25C
Zea mays
1.5.3.14
0.0000005
-
1-[7-[(9-carbamimidamidononyl)amino]heptyl]-3-(3-methylbut-3-en-1-yl)guanidine
pH 6.5, 25C
Zea mays
1.5.3.14
0.0000007
-
3-but-3-yn-1-yl-1-[7-[(9-carbamimidamidononyl)amino]heptyl]guanidine
pH 6.5, 25C
Zea mays
1.5.3.14
0.000001
-
1-[7-[(9-carbamimidamidononyl)amino]heptyl]-3-(2-phenylethyl)guanidine
pH 6.5, 25C
Zea mays
1.5.3.14
0.0000011
-
3-[(2E)-but-2-en-1-yl]-1-[7-[(9-carbamimidamidononyl)amino]heptyl]guanidine
pH 6.5, 25C
Zea mays
1.5.3.14
0.0000017
-
3-(4-methylpent-3-en-1-yl)-1-[9-([7-[(4-methylpent-3-en-1-yl)carbamimidamido]heptyl]amino)nonyl]guanidine
pH 6.5, 25C
Zea mays
1.5.3.14
0.000003
-
1-(guanidino)-17-(N1-(gamma,gamma-dimethylallyl)guanidino)-9-azaheptadecane tris(trifluoroacetate)
pH 6.5, 25C
Zea mays
1.5.3.14
0.0000075
-
iminoctadine
pH 6.5, 25C
Zea mays
1.5.3.14
0.00001
-
1-(5-aminopentyl)-3-(4-methylpent-3-en-1-yl)guanidine
pH 6.5, 25C
Zea mays
1.5.3.14
0.000015
-
N-prenylagmatine
pH 6.5, 25C
Zea mays
1.5.3.14
0.000022
-
1-(6-aminohexyl)-3-(4-methylpent-3-en-1-yl)guanidine
pH 6.5, 25C
Zea mays
1.5.3.14
0.00013
-
1-(4-aminobutyl)-3-but-3-en-1-ylguanidine
pH 6.5, 25C
Zea mays
1.5.3.14
0.00025
-
1-(4-aminobutyl)-3-but-3-yn-1-ylguanidine
pH 6.5, 25C
Zea mays
1.5.3.14
0.0003
-
1,8-diaminooctane
pH 6.5, 25C
Zea mays
1.5.3.14
0.00063
-
1-(4-aminobutyl)-3-(4-fluorobenzyl)guanidine
pH 6.5, 25C
Zea mays
1.5.3.14
0.0007
-
1-(4-carbamimidamidobutyl)-3-(3-methylbut-2-en-1-yl)guanidine
pH 6.5, 25C
Zea mays
1.5.3.14
0.00115
-
1-(5-aminopentyl)-3-(3-methoxybenzyl)guanidine
pH 6.5, 25C
Zea mays
1.5.3.14
0.00121
-
1-[3-[(3-aminopropyl)amino]propyl]-3-(3-methylbut-2-en-1-yl)guanidine
pH 6.5, 25C
Zea mays
1.5.3.14
0.0015
-
N,N'''-butane-1,4-diylbis[3-(3-methylbut-2-en-1-yl)guanidine]
pH 6.5, 25C
Zea mays
1.5.3.14
0.00153
-
1-(5-aminopentyl)-3-[(2E)-3-phenylprop-2-en-1-yl]guanidine
pH 6.5, 25C
Zea mays
1.5.3.14
0.00172
-
1-(5-aminopentyl)-3-(2-cyclohexylethyl)guanidine
pH 6.5, 25C
Zea mays
1.5.3.14
0.00258
-
1-(5-aminopentyl)-3-(2-cyclopropylethyl)guanidine
pH 6.5, 25C
Zea mays
1.5.3.14
0.003
-
agmatine
pH 6.5, 25C
Zea mays
1.5.3.14
0.018
-
N1-benzylamine-N3-(gamma,gamma-dimethylallyl)guanidine bis-(trifluoroacetate)
pH 6.5, 25C
Zea mays
Natural Substrates/ Products (Substrates) (protein specific)
EC Number
Natural Substrates
Organism
Commentary (Nat. Sub.)
Natural Products
Commentary (Nat. Pro.)
Organism (Nat. Pro.)
Reversibility
1.5.3.14
spermidine + O2 + H2O
Zea mays
-
propane-1,3-diamine + 4-aminobutanal + H2O2
-
-
?
Source Tissue (protein specific)
EC Number
Source Tissue
Commentary
Organism
Textmining
1.5.3.14
leaf
-
Zea mays
-
Substrates and Products (Substrate) (protein specific)
EC Number
Substrates
Commentary Substrates
Literature (Substrates)
Organism
Products
Commentary (Products)
Literature (Products)
Organism (Products)
Reversibility
1.5.3.14
spermidine + O2 + H2O
-
705043
Zea mays
propane-1,3-diamine + 4-aminobutanal + H2O2
-
-
-
?
1.5.3.14
spermidine + O2 + H2O
enzyme activity is measured spectrophotometrically by following the formation of a pink adduct resulting from the H2O2-dependent oxidation of 4-aminoantipyrine catalyzed by horseradish peroxidase and the subsequent condensation of oxidized 4-aminoantipyrine with 3,5-dichloro-2-hydroxybenzenesulfonic acid
705043
Zea mays
propane-1,3-diamine + 4-aminobutanal + H2O2
-
-
-
?
Temperature Optimum [C] (protein specific)
EC Number
Temperature Optimum [C]
Temperature Optimum Maximum [C]
Commentary
Organism
1.5.3.14
25
-
assay at
Zea mays
pH Optimum (protein specific)
EC Number
pH Optimum Minimum
pH Optimum Maximum
Commentary
Organism
1.5.3.14
6.5
-
assay at
Zea mays