SCUBA

DAPK1 — Death associated protein kinase 1

DAPK1 belongs to a gene co-expression module in 3 of 28 SCUBA cell types. Each module groups genes that rise and fall together in that cell type; the genes it shares a module with are its closest co-expression partners there.

DAPK1's module in each cell type

Cell typeModuleShares the module with
EndothelialVenous EC Identity
Endothelial cell development
ACTN1, AK4, CCL14, CTTNBP2, EPB41L3, FAM171A1, IL1R1, LRRC1 +18 moreView in SCUBA
MacrophagesER Stress Response
Stress
ARHGEF12, ATXN7, BTBD7, CD2AP, CLIP2, DST, ERN1, ERO1B +14 moreView in SCUBA
MonocytesNon-classical Monocyte
Lysosomal & pahgocytosis
ABI3, CAMK1, CD300A, CHCHD10, FCGR3A, GNGT2, ICAM2, ITM2B +5 moreView in SCUBA

About the gene

SynonymsDAPK
Chromosome9: 87497228-87708634
Predicted locationMembrane
Essential geneNo
Protein classCancer-related genes, Enzymes, Human disease related genes, Predicted membrane proteins
Molecular functionCalmodulin-binding, Kinase, Serine/threonine-protein kinase, Transferase
Biological processApoptosis, Translation regulation

Function

Calcium/calmodulin-dependent serine/threonine kinase involved in multiple cellular signaling pathways that trigger cell survival, apoptosis, and autophagy. Regulates both type I apoptotic and type II autophagic cell deaths signal, depending on the cellular setting. The former is caspase-dependent, while the latter is caspase-independent and is characterized by the accumulation of autophagic vesicles. Phosphorylates PIN1 resulting in inhibition of its catalytic activity, nuclear localization, and cellular function. Phosphorylates TPM1, enhancing stress fiber formation in endothelial cells. Phosphorylates STX1A and significantly decreases its binding to STXBP1. Phosphorylates PRKD1 and regulates JNK signaling by binding and activating PRKD1 under oxidative stress. Phosphorylates BECN1, reducing its interaction with BCL2 and BCL2L1 and promoting the induction of autophagy. Phosphorylates TSC2, disrupting the TSC1-TSC2 complex and stimulating mTORC1 activity in a growth factor-dependent pathway. Phosphorylates RPS6, MYL9 and DAPK3. Acts as a signaling amplifier of NMDA receptors at extrasynaptic sites for mediating brain damage in stroke. Cerebral ischemia recruits DAPK1 into the NMDA receptor complex and it phosphorylates GRINB at Ser-1303 inducing injurious Ca(2+) influx through NMDA receptor channels, resulting in an irreversible neuronal death. Required together with DAPK3 for phosphorylation of RPL13A upon interferon-gamma activation which is causing RPL13A involvement in transcript-selective translation inhibition. Isoform 2 cannot induce apoptosis but can induce membrane blebbing

Human Protein Atlas · Open Targets · UniProt

Gene annotation from the Human Protein Atlas and UniProt; see sources & licences.