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

Details

Serval ID
serval:BIB_B02CF9601B42
Type
Article: article from journal or magazin.
Publication sub-type
Letter (letter): Communication to the publisher.
Collection
Publications
Institution
Title
The Binding Mode of N-Hydroxyamidines to Indoleamine 2,3-Dioxygenase 1 (IDO1).
Journal
Biochemistry
Author(s)
Röhrig U.F., Zoete V., Michielin O.
ISSN
1520-4995 (Electronic)
ISSN-L
0006-2960
Publication state
Published
Issued date
2017
Peer-reviewed
Oui
Volume
56
Number
33
Pages
4323-4325
Language
english
Abstract
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.

Keywords
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
Create date
28/08/2017 11:36
Last modification date
20/08/2019 16:19
Usage data