1.11.2.1: unspecific peroxygenase

This is an abbreviated version!
For detailed information about unspecific peroxygenase, go to the full flat file.

Reaction

Synonyms

45 kDa peroxygenase/peroxidase, Agrocybe aegerita peroxidase, Agrocybe aegerita peroxidase/peroxygenase, Agrocybe aegerita peroxygenase, APO, aromatic peroxygenase, extracellular peroxygenase, haloperoxidase, haloperoxidase-peroxygenase, heme-thiolate peroxygenase, mushroom peroxygenase, P450st, PaDa-I, PII, unspecific heme peroxygenase, UPO, UPO-I, UPO-II, UPO1

ECTree

     1 Oxidoreductases

         1.11 Acting on a peroxide as acceptor

             1.11.2 Peroxygenases

                1.11.2.1 unspecific peroxygenase

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Results	in table
3	Activating Compound
173	AA Sequence
2	Application
1	CAS Registry Number
26	Cloned(Commentary)
38	Cofactor
2	Crystallization (Commentary)
3	Expression
9	General Information
1	General Stability
11	Inhibitors
138	kcat/KM [mM/s]
4	Ki Value [mM]
139	KM Value [mM]
32	Localization
3	Metals/Ions
15	Molecular Weight [Da]
2	Natural Substrates/ Products (Substrates)
131	Organism
1	Oxidation Stability
27	PDB ID
32	pH Optimum
12	pH Range
2	pH Stability
21	pI Value
18	Posttranslational Modification
26	Protein Variants
38	Purification (Commentary)
3	Reaction
7	Reaction Type
113	Reference
1	Source Tissue
28	Specific Activity [micromol/min/mg]
651	Substrates and Products (Substrate)
36	Subunits
133	Synonyms
1	Systematic Name
2	Temperature Optimum [°C]
4	Temperature Stability [°C]
142	Turnover Number [1/s]

Systematic Name

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Systematic Name on EC 1.11.2.1 - unspecific peroxygenase

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SYSTEMATIC NAME

IUBMB Comments

substrate:hydrogen peroxide oxidoreductase (RH-hydroxylating or -epoxidising)

A heme-thiolate protein (P-450). Enzymes of this type include glycoproteins secreted by agaric basidiomycetes. They catalyse the insertion of an oxygen atom from H2O2 into a wide variety of substrates, including aromatic rings such as naphthalene, toluene, phenanthrene, pyrene and p-nitrophenol, recalcitrant heterocycles such as pyridine, dibenzofuran, various ethers (resulting in O-dealkylation) and alkanes such as propane, hexane and cyclohexane. Reactions catalysed include hydroxylation, epoxidation, N-oxidation, sulfooxidation, O- and N-dealkylation, bromination and one-electron oxidations. They have little or no activity toward chloride. Mechanistically, the catalytic cycle of unspecific (mono)-peroxygenases combines elements of the "shunt" pathway of cytochrome P-450s (a side activity that utilizes a peroxide in place of dioxygen and NAD[P]H) and the classic heme peroxidase cycle.