Glutamate receptor ionotropic, NMDA 2B
NMDA receptor subtype of glutamate-gated ion channels with high calcium permeability and voltage-dependent sensitivity to magnesium. Mediated by glycine. 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 (By similarity).
Database | Links |
---|---|
UniProt | Q13224 |
PDB | 1S11, 1S2S, 2IPV |
BioGrid | 109161 |
BindingDB | Q13224 |
DrugBank | DB00949, DB00502, DB00142, DB00836, DB01043 |
Guide to PHARMACOLOGY | 457 |
PharmGKB | PA28980 |
KEGG | hsa:2904 |
BioCyc | Not available |
Entrez Gene (GeneID) | 2904 |
Metric | Mean Value | Standard Deviation |
---|---|---|
AUC | 0.9637 | 0.0048 |
Accuracy | 0.9149 | 0.0082 |
Sensitivity | 0.9343 | 0.0084 |
Specificity | 0.8955 | 0.0134 |
BEDROC | 0.9543 | 0.0164 |
MCC Threshold | 0.492 | N/A |
MCC | 0.8312 | N/A |
F-score Threshold | 0.492 | N/A |
F-score | 0.9167 | N/A |