Protein-coding gene in the species Homo sapiens
Serine/threonine-protein kinase WNK3 , also known as protein kinase lysine-deficient 3 , is a protein that in humans is encoded by the WNK3 gene .[ 5]
Function WNK3 is a protein belonging to the 'with no lysine' family of serine-threonine protein kinases . These family members lack the catalytic lysine in subdomain II, and instead have a conserved lysine in subdomain I. This family member functions as a positive regulator of the transcellular Ca2+ transport pathway, and it plays a role in the increase of cell survival in a caspase 3 dependent pathway.[ 5]
References
Further reading
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Veríssimo F, Silva E, Morris JD, et al. (2006). "Protein kinase WNK3 increases cell survival in a caspase-3-dependent pathway". Oncogene . 25 (30): 4172–82. doi :10.1038/sj.onc.1209449 . PMID 16501604 . S2CID 20133914 .
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Qiao Y, Liu X, Harvard C, et al. (2008). "Autism-associated familial microdeletion of Xp11.22". Clin. Genet . 74 (2): 134–44. doi :10.1111/j.1399-0004.2008.01028.x . PMID 18498374 . S2CID 22008997 .
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Heise CJ, Xu BE, Deaton SL, et al. (2010). "Serum and glucocorticoid-induced kinase (SGK) 1 and the epithelial sodium channel are regulated by multiple with no lysine (WNK) family members" . J. Biol. Chem . 285 (33): 25161–7. doi :10.1074/jbc.M110.103432 . PMC 2919078 . PMID 20525693 .
Holden S, Cox J, Raymond FL (2004). "Cloning, genomic organization, alternative splicing and expression analysis of the human gene WNK3 (PRKWNK3)". Gene . 335 : 109–19. doi :10.1016/j.gene.2004.03.009 . PMID 15194194 .
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This article incorporates text from the United States National Library of Medicine , which is in the public domain .
Activity Regulation Classification Kinetics Types