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 | Q00960 |
PDB | 3JPW, 3JPY, 3QEL, 3QEM |
BioGrid | 246575 |
BindingDB | Q00960 |
DrugBank | Not available |
Guide to PHARMACOLOGY | Not available |
PharmGKB | Not available |
KEGG | rno:24410 |
BioCyc | Not available |
Entrez Gene (GeneID) | 24410 |
Metric | Mean Value | Standard Deviation |
---|---|---|
AUC | 0.9576 | 0.0057 |
Accuracy | 0.9185 | 0.0058 |
Sensitivity | 0.9269 | 0.0034 |
Specificity | 0.9092 | 0.0101 |
BEDROC | 0.9867 | 0.0065 |
MCC Threshold | 0.512 | N/A |
MCC | 0.8381 | N/A |
F-score Threshold | 0.486 | N/A |
F-score | 0.9238 | N/A |