Title : Structural basis of ketamine action on human NMDA receptors.

Pub. Date : 2021 Aug

PMID : 34321660






1 Functional Relationships(s)
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Protein Name
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1 Two amino acids-leucine 642 on GluN2A (homologous to leucine 643 on GluN2B) and asparagine 616 on GluN1-were identified as key residues that form hydrophobic and hydrogen-bond interactions with ketamine, and mutations at these residues reduced the potency of ketamine in blocking NMDA receptor channel activity. Asparagine glutamate ionotropic receptor NMDA type subunit 1 Homo sapiens