NMDAR2B: an NMDA receptor subtype of glutamate-gated ion channels with high calcium permeability and voltage-dependent sensitivity to magnesium. Mediated by glycine. Plays a key role in synaptic plasticity, synaptogenesis, excitotoxicity, memory acquisition and learning. Mediates neuronal functions in glutamate neurotransmission. In concert with DAPK1 at extrasynaptic sites, acts as a central mediator for stroke damage. Its phosphorylation at Ser-1303 by DAPK1 enhances synaptic NMDA receptor channel activity inducing injurious Ca2+ influx through them, resulting in an irreversible neuronal death.
Protein type: Channel, ligand-gated; Channel, calcium; Membrane protein, multi-pass; Membrane protein, integral
Chromosomal Location of Human Ortholog: 12p12
Cellular Component: cell junction; cell surface; integral to plasma membrane; N-methyl-D-aspartate selective glutamate receptor complex; neuron projection; plasma membrane; postsynaptic membrane; synaptic vesicle
Molecular Function: calcium channel activity; extracellular-glutamate-gated ion channel activity; glycine binding; N-methyl-D-aspartate selective glutamate receptor activity; protein binding; zinc ion binding
Biological Process: activation of MAPKK activity; axon guidance; behavioral fear response; behavioral response to pain; detection of mechanical stimulus involved in sensory perception of pain; ephrin receptor signaling pathway; epidermal growth factor receptor signaling pathway; fibroblast growth factor receptor signaling pathway; glutamate signaling pathway; in utero embryonic development; innate immune response; insulin receptor signaling pathway; ionotropic glutamate receptor signaling pathway; learning; learning and/or memory; MAPKKK cascade; memory; nerve growth factor receptor signaling pathway; Ras protein signal transduction; regulation of excitatory postsynaptic membrane potential; response to ethanol; sensory organ development; small GTPase mediated signal transduction; startle response; suckling behavior; synaptic transmission; transport; vascular endothelial growth factor receptor signaling pathway
Disease: Epileptic Encephalopathy, Early Infantile, 27; Mental Retardation, Autosomal Dominant 6
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