EC Number | Activating Compound | Comment | Organism | Structure |
---|---|---|---|---|
1.11.1.13 | diphosphate | less activation than by lactate or malonate | Phanerodontia chrysosporium | |
1.11.1.13 | H2O2 | H2O2-dependent | Phanerodontia chrysosporium | |
1.11.1.13 | Lactate | activates, stabilizes Mn3+ in aqueous solution with a relatively high redox potential | Phanerodontia chrysosporium | |
1.11.1.13 | malonate | stabilizes Mn3+ at a relatively high redox potential and facilitate oxidation of organic substrates | Phanerodontia chrysosporium | |
1.11.1.13 | oxalate | activates by chelating and stabilizing Mn3+ | Phanerodontia chrysosporium | |
1.11.1.13 | oxalate | less activation than by lactate or malonate | Phanerodontia chrysosporium |
EC Number | Application | Comment | Organism |
---|---|---|---|
1.11.1.13 | environmental protection | thiol-mediated degradation of dimeric model compounds and of polymeric lignin by MnP has potential applications in the degradation of industrial lignins | Phanerodontia chrysosporium |
EC Number | Cloned (Comment) | Organism |
---|---|---|
1.11.1.13 | cDNA sequence encoding a MnP isoenzyme is determined | Phanerodontia chrysosporium |
EC Number | Inhibitors | Comment | Organism | Structure |
---|---|---|---|---|
1.11.1.13 | glutathione | - |
Phanerodontia chrysosporium |
EC Number | Localization | Comment | Organism | GeneOntology No. | Textmining |
---|---|---|---|---|---|
1.11.1.13 | extracellular | - |
Phanerodontia chrysosporium | - |
- |
EC Number | Molecular Weight [Da] | Molecular Weight Maximum [Da] | Comment | Organism |
---|---|---|---|---|
1.11.1.13 | 46000 | - |
- |
Phanerodontia chrysosporium |
EC Number | Natural Substrates | Organism | Comment (Nat. Sub.) | Natural Products | Comment (Nat. Pro.) | Rev. | Reac. |
---|---|---|---|---|---|---|---|
1.11.1.13 | Mn2+ + H+ + H2O2 | Phanerodontia chrysosporium | important component of lignin degradation system | Mn3+ + H2O | Mn3+ is produced under lignolytic conditions | ? | |
1.11.1.13 | Mn2+ + H+ + H2O2 | Phanerodontia chrysosporium OGC101 | important component of lignin degradation system | Mn3+ + H2O | Mn3+ is produced under lignolytic conditions | ? |
EC Number | Organism | UniProt | Comment | Textmining |
---|---|---|---|---|
1.11.1.13 | Phanerodontia chrysosporium | - |
- |
- |
1.11.1.13 | Phanerodontia chrysosporium | - |
white rot basidomycete | - |
1.11.1.13 | Phanerodontia chrysosporium OGC101 | - |
- |
- |
EC Number | Posttranslational Modification | Comment | Organism |
---|---|---|---|
1.11.1.13 | glycoprotein | - |
Phanerodontia chrysosporium |
EC Number | Purification (Comment) | Organism |
---|---|---|
1.11.1.13 | isoenzyme 1 | Phanerodontia chrysosporium |
EC Number | Substrates | Comment Substrates | Organism | Products | Comment (Products) | Rev. | Reac. |
---|---|---|---|---|---|---|---|
1.11.1.13 | Mn2+ + H+ + H2O2 | - |
Phanerodontia chrysosporium | Mn3+ + H2O | Mn3+ oxidizes phenolic lignin model compounds | ? | |
1.11.1.13 | Mn2+ + H+ + H2O2 | - |
Phanerodontia chrysosporium | Mn3+ + H2O | in presence of Mn2+, H2O2 and glutathione MnP oxidizes by Mn3+ nonphenolic beta-aryl ether lignin model compounds, veratryl alcohol, anisyl alcohol, benzyl alcohol and thiols to thiyl radicals which abstracts a hydrogen from the substrate forming a benzylic radical, mechanism, glutathione can be replaced by dithiothreitol, dithioerythritol or cysteine | ? | |
1.11.1.13 | Mn2+ + H+ + H2O2 | - |
Phanerodontia chrysosporium | Mn3+ + H2O | Mn3+ acts as obligatory redox coupler, oxidizing various phenols, dyes and amines | ? | |
1.11.1.13 | Mn2+ + H+ + H2O2 | important component of lignin degradation system | Phanerodontia chrysosporium | Mn3+ + H2O | Mn3+ is produced under lignolytic conditions | ? | |
1.11.1.13 | Mn2+ + H+ + H2O2 | - |
Phanerodontia chrysosporium OGC101 | Mn3+ + H2O | Mn3+ oxidizes phenolic lignin model compounds | ? | |
1.11.1.13 | Mn2+ + H+ + H2O2 | - |
Phanerodontia chrysosporium OGC101 | Mn3+ + H2O | in presence of Mn2+, H2O2 and glutathione MnP oxidizes by Mn3+ nonphenolic beta-aryl ether lignin model compounds, veratryl alcohol, anisyl alcohol, benzyl alcohol and thiols to thiyl radicals which abstracts a hydrogen from the substrate forming a benzylic radical, mechanism, glutathione can be replaced by dithiothreitol, dithioerythritol or cysteine | ? | |
1.11.1.13 | Mn2+ + H+ + H2O2 | - |
Phanerodontia chrysosporium OGC101 | Mn3+ + H2O | Mn3+ acts as obligatory redox coupler, oxidizing various phenols, dyes and amines | ? | |
1.11.1.13 | Mn2+ + H+ + H2O2 | important component of lignin degradation system | Phanerodontia chrysosporium OGC101 | Mn3+ + H2O | Mn3+ is produced under lignolytic conditions | ? |
EC Number | Temperature Optimum [°C] | Temperature Optimum Maximum [°C] | Comment | Organism |
---|---|---|---|---|
1.11.1.13 | 37 | - |
assay at | Phanerodontia chrysosporium |
EC Number | pH Optimum Minimum | pH Optimum Maximum | Comment | Organism |
---|---|---|---|---|
1.11.1.13 | additional information | - |
pI: 4.9 | Phanerodontia chrysosporium |
EC Number | pH Minimum | pH Maximum | Comment | Organism |
---|---|---|---|---|
1.11.1.13 | 3.1 | 6.1 | veratryl alcohol oxidation, activity increases with increasing pH | Phanerodontia chrysosporium |
EC Number | Cofactor | Comment | Organism | Structure |
---|---|---|---|---|
1.11.1.13 | heme | one iron protoporphyrin IX prosthetic group per enzyme molecule | Phanerodontia chrysosporium | |
1.11.1.13 | heme | heme protein | Phanerodontia chrysosporium |