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Ligand migration in human indoleamine-2,3 dioxygenase.
Nienhaus, Karin; Nickel, Elena; Lu, Changyuan; Yeh, Syun-Ru; Nienhaus, G Ulrich.
Afiliação
  • Nienhaus K; Karlsruhe Institute of Technology (KIT), Institute of Applied Physics and Center for Functional Nanostructures, Karlsruhe, Germany. Karin.nienhaus@kit.edu
IUBMB Life ; 63(3): 153-9, 2011 Mar.
Article em En | MEDLINE | ID: mdl-21445845
ABSTRACT
Human indoleamine 2,3-dioxygenase (hIDO), a monomeric heme enzyme, catalyzes the oxidative degradation of L-tryptophan (L-Trp) and other indoleamine derivatives. Its activity follows typical Michaelis-Menten behavior only for L-Trp concentrations up to 50 µM; a further increase in the concentration of L-Trp causes a decrease in the activity. This substrate inhibition of hIDO is a result of the binding of a second L-Trp molecule in an inhibitory substrate binding site of the enzyme. The molecular details of the reaction and the inhibition are not yet known. In the following, we summarize the present knowledge about this heme enzyme.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Indolamina-Pirrol 2,3,-Dioxigenase Limite: Humans Idioma: En Ano de publicação: 2011 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Indolamina-Pirrol 2,3,-Dioxigenase Limite: Humans Idioma: En Ano de publicação: 2011 Tipo de documento: Article