description
Ca2+ influx through the NMDA receptor initiates subsequent molecular pathways that have a defined role in establishing long-lasting synaptic changes. The molecular signaling initiated by a rise in Ca2+ within the spine leads to phosphorylation of Cyclic AMP Response Element binding protein (CREB) at serine 133 which is involved in the transcription of genes that results in long lasting changes in the synapse. The phosphorylation of CREB by increased Ca2+ can be brought about by distinct molecular pathways that may involve MAP kinase, activation of adenylate cyclase, activation of CaMKII and/or the activation of CaMKIV

external resources
NCBI:1268801
REACTOME:R-HSA-442742
PUBMED:12819448

genes
ACTN2 , BRAF , CALM1 , CALM2 , CALM3 , CAMK2A , CAMK2B , CAMK2D , CAMK2G , CREB1 , DLG4 , GRIN1 , GRIN2A , GRIN2B , GRIN2C , GRIN2D , HRAS , NEFL , PDPK1 , MAPK1 , RAF1 , RASGRF1 , RASGRF2 , RPS6KA1 , RPS6KA2 , RPS6KA3 , RRAS , AKAP9 , RPS6KA6 ,