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Literature summary extracted from

  • Aburto, J.; Correa-Basurto, J.; Torres, E.
    Atypical kinetic behavior of chloroperoxidase-mediated oxidative halogenation of polycyclic aromatic hydrocarbons (2008), Arch. Biochem. Biophys., 480, 33-40.
    View publication on PubMed

Organism

EC Number Organism UniProt Comment Textmining
1.11.1.10 Leptoxyphium fumago
-
-
-

Purification (Commentary)

EC Number Purification (Comment) Organism
1.11.1.10
-
 Leptoxyphium fumago

Substrates and Products (Substrate)

EC Number Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
1.11.1.10 2 pyrene + 3 KCl + 3 H2O2
-
 Leptoxyphium fumago chloropyrene + dichloropyrene + 3 KOH + 3 H2O
-
 ?
1.11.1.10 anthracene + 2 KCl + 2 H2O2
-
 Leptoxyphium fumago 9,10-dichloroanthracene + 2 KOH + 2 H2O
-
 ?
1.11.1.10 naphthalene + KCl + H2O2
-
 Leptoxyphium fumago chloronaphthalene + KOH + H2O
-
 ?

Synonyms

EC Number Synonyms Comment Organism
1.11.1.10 chloroperoxidase
-
 Leptoxyphium fumago

Turnover Number [1/s]

EC Number Turnover Number Minimum [1/s] Turnover Number Maximum [1/s] Substrate Comment Organism Structure
1.11.1.10 3.6
-
 Naphthalene from Hill equation Leptoxyphium fumago
1.11.1.10 4.5
-
 Naphthalene from the dimer model Leptoxyphium fumago
1.11.1.10 7.2
-
 anthracene from Hill equation Leptoxyphium fumago
1.11.1.10 8
-
 anthracene from the dimer model Leptoxyphium fumago
1.11.1.10 46
-
 pyrene from Hill equation Leptoxyphium fumago
1.11.1.10 56.6
-
 pyrene from the dimer model Leptoxyphium fumago

Cofactor

EC Number Cofactor Comment Organism Structure
1.11.1.10 heme
-
 Leptoxyphium fumago