Homo sapiens Protein: CSNK1D | |||||||||||||||||||||||||
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Summary | |||||||||||||||||||||||||
InnateDB Protein | IDBP-73383.5 | ||||||||||||||||||||||||
Last Modified | 2014-10-13 [Report errors or provide feedback] | ||||||||||||||||||||||||
Gene Symbol | CSNK1D | ||||||||||||||||||||||||
Protein Name | casein kinase 1, delta | ||||||||||||||||||||||||
Synonyms | ASPS; CKIdelta; FASPS2; HCKID; | ||||||||||||||||||||||||
Species | Homo sapiens | ||||||||||||||||||||||||
Ensembl Protein | ENSP00000324464 | ||||||||||||||||||||||||
InnateDB Gene | IDBG-73381 (CSNK1D) | ||||||||||||||||||||||||
Protein Structure |
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UniProt Annotation | |||||||||||||||||||||||||
Function | Essential serine/threonine-protein kinase that regulates diverse cellular growth and survival processes including Wnt signaling, DNA repair and circadian rhythms. It can phosphorylate a large number of proteins. Casein kinases are operationally defined by their preferential utilization of acidic proteins such as caseins as substrates. Phosphorylates connexin-43/GJA1, MAP1A, SNAPIN, MAPT/TAU, TOP2A, DCK, HIF1A, EIF6, p53/TP53, DVL2, DVL3, ESR1, AIB1/NCOA3, DNMT1, PKD2, YAP1, PER1 and PER2. Central component of the circadian clock. In balance with PP1, determines the circadian period length through the regulation of the speed and rhythmicity of PER1 and PER2 phospohorylation. Controls PER1 and PER2 nuclear transport and degradation. YAP1 phosphorylation promotes its SCF(beta-TRCP) E3 ubiquitin ligase-mediated ubiquitination and subsequent degradation. DNMT1 phosphorylation reduces its DNA-binding activity. Phosphorylation of ESR1 and AIB1/NCOA3 stimulates their activity and coactivation. Phosphorylation of DVL2 and DVL3 regulates WNT3A signaling pathway that controls neurite outgrowth. EIF6 phosphorylation promotes its nuclear export. Triggers down-regulation of dopamine receptors in the forebrain. Activates DCK in vitro by phosphorylation. TOP2A phosphorylation favors DNA cleavable complex formation. May regulate the formation of the mitotic spindle apparatus in extravillous trophoblast. Modulates connexin-43/GJA1 gap junction assembly by phosphorylation. Probably involved in lymphocyte physiology. Regulates fast synaptic transmission mediated by glutamate. {ECO:0000269PubMed:10606744, ECO:0000269PubMed:12270943, ECO:0000269PubMed:14761950, ECO:0000269PubMed:16027726, ECO:0000269PubMed:17562708, ECO:0000269PubMed:17962809, ECO:0000269PubMed:19043076, ECO:0000269PubMed:19339517, ECO:0000269PubMed:20041275, ECO:0000269PubMed:20048001, ECO:0000269PubMed:20407760, ECO:0000269PubMed:20637175, ECO:0000269PubMed:20696890, ECO:0000269PubMed:20699359, ECO:0000269PubMed:21084295, ECO:0000269PubMed:21422228, ECO:0000269PubMed:23636092}. | ||||||||||||||||||||||||
Subcellular Localization | Cytoplasm. Nucleus. Cytoplasm, cytoskeleton, microtubule organizing center, centrosome. Cytoplasm, perinuclear region. Cell membrane. Cytoplasm, cytoskeleton, spindle. Golgi apparatus. Note=Localized at mitotic spindle microtubules, and at the centrosomes and interphase in interphase cells. Recruited to the spindle apparatus and the centrosomes in response to DNA- damage. Correct subcellular localization requires kinase activity. | ||||||||||||||||||||||||
Disease Associations | Advanced sleep phase syndrome, familial, 2 (FASPS2) [MIM:615224]: A disorder characterized by very early sleep onset and offset. Individuals are 'morning larks' with a 4 hours advance of the sleep, temperature and melatonin rhythms. {ECO:0000269PubMed:15800623, ECO:0000269PubMed:23636092}. Note=The disease is caused by mutations affecting the gene represented in this entry. | ||||||||||||||||||||||||
Tissue Specificity | Expressed in all tissues examined, including brain, heart, lung, liver, pancreas, kidney, placenta and skeletal muscle. However, kinase activity is not uniform, with highest kinase activity in splenocytes. In blood, highly expressed in hemopoietic cells and mature granulocytes. Also found in monocytes and lymphocytes. {ECO:0000269PubMed:15070676, ECO:0000269PubMed:16027726}. | ||||||||||||||||||||||||
Comments | |||||||||||||||||||||||||
Interactions | |||||||||||||||||||||||||
Number of Interactions |
This gene and/or its encoded proteins are associated with 53 experimentally validated interaction(s) in this database.
They are also associated with 5 interaction(s) predicted by orthology.
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Gene Ontology | |||||||||||||||||||||||||
Molecular Function |
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Biological Process |
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Cellular Component |
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Protein Structure and Domains | |||||||||||||||||||||||||
PDB ID | |||||||||||||||||||||||||
InterPro |
IPR000719
Protein kinase domain IPR001245 Serine-threonine/tyrosine-protein kinase catalytic domain IPR002290 Serine/threonine/dual specificity protein kinase, catalytic domain IPR011009 Protein kinase-like domain IPR020635 Tyrosine-protein kinase, catalytic domain |
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PFAM |
PF00069
PF07714 |
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PRINTS |
PR00109
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PIRSF | |||||||||||||||||||||||||
SMART |
SM00220
SM00219 |
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TIGRFAMs | |||||||||||||||||||||||||
Post-translational Modifications | |||||||||||||||||||||||||
Modification | |||||||||||||||||||||||||
Cross-References | |||||||||||||||||||||||||
SwissProt | P48730 | ||||||||||||||||||||||||
PhosphoSite | PhosphoSite-P48730 | ||||||||||||||||||||||||
TrEMBL | A0A024R8X3 | ||||||||||||||||||||||||
UniProt Splice Variant | |||||||||||||||||||||||||
Entrez Gene | 1453 | ||||||||||||||||||||||||
UniGene | Hs.701266 | ||||||||||||||||||||||||
RefSeq | NP_001884 | ||||||||||||||||||||||||
HUGO | HGNC:2452 | ||||||||||||||||||||||||
OMIM | 600864 | ||||||||||||||||||||||||
CCDS | CCDS11805 | ||||||||||||||||||||||||
HPRD | 02920 | ||||||||||||||||||||||||
IMGT | |||||||||||||||||||||||||
EMBL | AB091044 AK291758 BC003558 BC015775 CH471099 EF015900 U29171 U31285 | ||||||||||||||||||||||||
GenPept | AAC50807 AAC50808 AAH03558 AAH15775 ABM64211 BAC10903 BAF84447 EAW89758 EAW89760 | ||||||||||||||||||||||||