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Mechanism of Inactivation of Neuronal Nitric Oxide Synthase by (S)-2-Amino-5-(2-(methylthio)acetimidamido)pentanoic Acid.
- Source :
-
Journal of the American Chemical Society [J Am Chem Soc] 2015 May 13; Vol. 137 (18), pp. 5980-9. Date of Electronic Publication: 2015 May 05. - Publication Year :
- 2015
-
Abstract
- Nitric oxide synthase (NOS) catalyzes the conversion of l-arginine to l-citrulline and the second messenger nitric oxide. Three mechanistic pathways are proposed for the inactivation of neuronal NOS (nNOS) by (S)-2-amino-5-(2-(methylthio)acetimidamido)pentanoic acid (1): sulfide oxidation, oxidative dethiolation, and oxidative demethylation. Four possible intermediates were synthesized. All compounds were assayed with nNOS, their IC50, KI, and kinact values were obtained, and their crystal structures were determined. The identification and characterization of the products formed during inactivation provide evidence for the details of the inactivation mechanism. On the basis of these studies, the most probable mechanism for the inactivation of nNOS involves oxidative demethylation with the resulting thiol coordinating to the cofactor heme iron. Although nNOS is a heme-containing enzyme, this is the first example of a NOS that catalyzes an S-demethylation reaction; the novel mechanism of inactivation described here could be applied to the design of inactivators of other heme-dependent enzymes.
- Subjects :
- Amino Acids metabolism
Formaldehyde metabolism
Kinetics
Models, Molecular
Molecular Structure
Nitric Oxide Synthase Type I chemistry
Nitric Oxide Synthase Type I metabolism
Pentanoic Acids chemical synthesis
Pentanoic Acids chemistry
Structure-Activity Relationship
Biocatalysis drug effects
Nitric Oxide Synthase Type I antagonists & inhibitors
Pentanoic Acids pharmacology
Subjects
Details
- Language :
- English
- ISSN :
- 1520-5126
- Volume :
- 137
- Issue :
- 18
- Database :
- MEDLINE
- Journal :
- Journal of the American Chemical Society
- Publication Type :
- Academic Journal
- Accession number :
- 25874809
- Full Text :
- https://doi.org/10.1021/jacs.5b01202