EC Number | Cloned (Comment) | Organism |
---|---|---|
1.11.1.10 | expression in Aspergillus niger | Leptoxyphium fumago |
EC Number | Molecular Weight [Da] | Molecular Weight Maximum [Da] | Comment | Organism |
---|---|---|---|---|
1.11.1.10 | 42000 | - |
- |
Leptoxyphium fumago |
1.11.2.1 | 46000 | - |
gel filtration | Cyclocybe aegerita |
EC Number | Organism | UniProt | Comment | Textmining |
---|---|---|---|---|
1.11.1.10 | Leptoxyphium fumago | - |
- |
- |
1.11.1.18 | Cyclocybe aegerita | - |
- |
- |
1.11.2.1 | Cyclocybe aegerita | - |
- |
- |
EC Number | Posttranslational Modification | Comment | Organism |
---|---|---|---|
1.11.1.10 | glycoprotein | heavily glycosylated protein (2530% carbohydrates, two high-mannose N-glycosylation sites) | Leptoxyphium fumago |
1.11.2.1 | glycoprotein | - |
Cyclocybe aegerita |
EC Number | Purification (Comment) | Organism |
---|---|---|
1.11.2.1 | - |
Cyclocybe aegerita |
EC Number | Substrates | Comment Substrates | Organism | Products | Comment (Products) | Rev. | Reac. |
---|---|---|---|---|---|---|---|
1.11.1.10 | additional information | catalyzes the unspecific chlorination, bromination, and iodation (but no fluorination) of a variety of electrophilic organic substrates via hypohalous acid as actual halogenating agent. In the absence of halide, CPO resembles cytochrome P450s and epoxidizes and hydroxylates activated substrates such as organic sulfides and olefins. Aromatic rings are not susceptible to CPO-catalyzed oxygen-transfer | Leptoxyphium fumago | ? | - |
? | |
1.11.1.18 | additional information | strong brominating aactivity, weak chlorinating and iodating activities, catalyzes both benzylic and aromatic hydroxylations (e.g., of toluene and naphthalene) | Cyclocybe aegerita | ? | - |
? | |
1.11.1.18 | phenol + H2O2 + Br- | - |
Cyclocybe aegerita | 4-bromophenol + 2-bromophenol + H2O | 4-bromophenol + 2-bromophenol at the ratio of 4:1 | ? | |
1.11.2.1 | 4-ethoxy-3-methoxybenzyl alcohol + H2O2 | - |
Cyclocybe aegerita | 4-ethoxy-3-methoxybenzaldehyde + H2O | - |
? | |
1.11.2.1 | anisyl alcohol + H2O2 | - |
Cyclocybe aegerita | anisaldehyde + H2O | - |
? | |
1.11.2.1 | benzyl alcohol + H2O2 | - |
Cyclocybe aegerita | benzaldehyde + H2O | - |
? | |
1.11.2.1 | additional information | the Agrocybe aegerita peroxidase has strong brominating as well as weak chlorinating and iodating activities, and catalyzes both benzylic and aromatic hydroxylations | Cyclocybe aegerita | ? | - |
? | |
1.11.2.1 | naphthalene + H2O2 | - |
Cyclocybe aegerita | ? | - |
? | |
1.11.2.1 | phenol + KBr | the Agrocybe aegerita peroxidase has also strong brominating activity | Cyclocybe aegerita | 4-bromophenol + 2-bromophenol | - |
? | |
1.11.2.1 | toluene + H2O2 | - |
Cyclocybe aegerita | 4-cresol + 2-cresol + methyl-4-benzoquinone + H2O | - |
? | |
1.11.2.1 | vanillyl alcohol + H2O2 | - |
Cyclocybe aegerita | vanillaldehyde + H2O | - |
? |
EC Number | Synonyms | Comment | Organism |
---|---|---|---|
1.11.1.10 | CPO | - |
Leptoxyphium fumago |
1.11.1.10 | heme-thiolate chloroperoxidase | - |
Leptoxyphium fumago |
1.11.2.1 | Agrocybe aegerita peroxidase | - |
Cyclocybe aegerita |
EC Number | Cofactor | Comment | Organism | Structure |
---|---|---|---|---|
1.11.1.10 | heme | - |
Leptoxyphium fumago | |
1.11.2.1 | heme | - |
Cyclocybe aegerita |
EC Number | Organism | Comment | pI Value Maximum | pI Value |
---|---|---|---|---|
1.11.1.10 | Leptoxyphium fumago | - |
- |
4 |
1.11.2.1 | Cyclocybe aegerita | there are six isoforms with different isoelectric points between pH 4.6 and 5.4, isoelectric focusing | 5.4 | 4.6 |
EC Number | Organism | Comment | Expression |
---|---|---|---|
1.11.2.1 | Cyclocybe aegerita | Agrocybe aegerita produces relatively high and stable peroxidase levels in complex liquid media based on soybeans | up |