Binding and Dynamics Demonstrate the Destabilization of Ligand Binding for the S688Y Mutation in the NMDA Receptor GluN1 Subunit
Encephalopathies are brain dysfunctions that lead to cognitive, sensory, and motor development impairments. Recently, the identification of several mutations within the <i>N</i>-methyl-D-aspartate receptor (NMDAR) have been identified as significant in the etiology of this group of condi...
Main Authors: | Jake Zheng Chen, William Bret Church, Karine Bastard, Anthony P. Duff, Thomas Balle |
---|---|
Format: | Article |
Language: | English |
Published: |
MDPI AG
2023-05-01
|
Series: | Molecules |
Subjects: | |
Online Access: | https://www.mdpi.com/1420-3049/28/10/4108 |
Similar Items
-
Potential Roles for the GluN2D NMDA Receptor Subunit in Schizophrenia
by: Chitra Vinnakota, et al.
Published: (2023-07-01) -
GluN2 Subunit-Dependent Redox Modulation of NMDA Receptor Activation by Homocysteine
by: Dmitry A. Sibarov, et al.
Published: (2020-10-01) -
GluN2A subunit-containing NMDA receptors are the preferential neuronal targets of homocysteine
by: Dmitry A Sibarov, et al.
Published: (2016-11-01) -
NMDA receptor GluN2D subunit participates to levodopa-induced dyskinesia pathophysiology
by: Manuela Mellone, et al.
Published: (2019-01-01) -
NMDA receptor GluN2A/GluN2B subunit ratio as synaptic trait of levodopa-induced dyskinesias: from experimental models to patients
by: Manuela eMellone, et al.
Published: (2015-07-01)