The Binding Mode of N-Hydroxyamidines to Indoleamine 2,3-Dioxygenase 1 (IDO1).

Détails

ID Serval
serval:BIB_B02CF9601B42
Type
Article: article d'un périodique ou d'un magazine.
Sous-type
Lettre (letter): communication adressée à l'éditeur.
Collection
Publications
Institution
Titre
The Binding Mode of N-Hydroxyamidines to Indoleamine 2,3-Dioxygenase 1 (IDO1).
Périodique
Biochemistry
Auteur⸱e⸱s
Röhrig U.F., Zoete V., Michielin O.
ISSN
1520-4995 (Electronic)
ISSN-L
0006-2960
Statut éditorial
Publié
Date de publication
2017
Peer-reviewed
Oui
Volume
56
Numéro
33
Pages
4323-4325
Langue
anglais
Résumé
Indoleamine 2,3-dioxygenase 1 (IDO1) is an important target in cancer immunotherapy. The most advanced clinical compound, epacadostat (INCB024360), binds to the heme cofactor of IDO1 through an N-hydroxyamidine function. Conflicting binding modes have recently been proposed, reporting iron binding either through the hydroxyamidine oxygen or through the hydroxyamidine nitrogen atom. Here, we use quantum chemical calculations, docking, and quantum mechanics/molecular mechanics calculations based on available X-ray data to resolve this issue and to propose a physically meaningful binding mode. Our findings will aid the design of novel IDO1 ligands based on this pharmacophore.

Mots-clé
Crystallography, X-Ray, Heme/chemistry, Heme/metabolism, Humans, Indoleamine-Pyrrole 2,3,-Dioxygenase/chemistry, Indoleamine-Pyrrole 2,3,-Dioxygenase/metabolism, Molecular Docking Simulation, Oximes/chemistry, Oximes/metabolism, Protein Binding, Sulfonamides/chemistry, Sulfonamides/metabolism
Pubmed
Web of science
Création de la notice
28/08/2017 11:36
Dernière modification de la notice
20/08/2019 16:19
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