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WNK1 information


WNK1
Available structures
PDBOrtholog search: PDBe RCSB
Identifiers
AliasesWNK1, HSAN2, HSN2, KDP, PPP1R167, PRKPSK, p65, WNK lysine deficient protein kinase 1
External IDsOMIM: 605232; MGI: 2442092; HomoloGene: 14253; GeneCards: WNK1; OMA:WNK1 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_001184985
NM_014823
NM_018979
NM_213655

RefSeq (protein)

NP_001171914
NP_055638
NP_061852
NP_998820

NP_001171949
NP_001171950
NP_001186012
NP_001186013
NP_941992

Location (UCSC)Chr 12: 0.75 – 0.91 MbChr 6: 119.92 – 120.04 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

WNK (lysine deficient protein kinase 1), also known as WNK1, is an enzyme that is encoded by the WNK1 gene.[5][6][7][8][9] WNK1 is serine-threonine protein kinase and part of the "with no lysine/K" kinase WNK family.[5][6][7][9] The predominant role of WNK1 is the regulation of cation-Cl cotransporters (CCCs) such as the sodium chloride cotransporter (NCC), basolateral Na-K-Cl symporter (NKCC1), and potassium chloride cotransporter (KCC1) located within the kidney.[5][6][9] CCCs mediate ion homeostasis and modulate blood pressure by transporting ions in and out of the cell.[5] WNK1 mutations as a result have been implicated in blood pressure disorders/diseases; a prime example being familial hyperkalemic hypertension (FHHt).[5][6][7][8][9]

  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000060237 – Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000045962 – Ensembl, May 2017
  3. ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. ^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. ^ a b c d e Shekarabi M, Zhang J, Khanna AR, Ellison DH, Delpire E, Kahle KT (February 2017). "WNK Kinase Signaling in Ion Homeostasis and Human Disease". Cell Metabolism. 25 (2): 285–299. doi:10.1016/j.cmet.2017.01.007. hdl:10871/33390. PMID 28178566.
  6. ^ a b c d Hadchouel J, Ellison DH, Gamba G (2016). "Regulation of Renal Electrolyte Transport by WNK and SPAK-OSR1 Kinases". Annual Review of Physiology. 78: 367–89. doi:10.1146/annurev-physiol-021115-105431. PMID 26863326.
  7. ^ a b c Bazúa-Valenti S, Gamba G (May 2015). "Revisiting the NaCl cotransporter regulation by with-no-lysine kinases". American Journal of Physiology. Cell Physiology. 308 (10): C779-91. doi:10.1152/ajpcell.00065.2015. PMC 4436992. PMID 25788573.
  8. ^ a b Cite error: The named reference Xu_2005 was invoked but never defined (see the help page).
  9. ^ a b c d Huang CL, Cheng CJ (November 2015). "A unifying mechanism for WNK kinase regulation of sodium-chloride cotransporter". Pflügers Archiv. 467 (11): 2235–41. doi:10.1007/s00424-015-1708-2. PMC 4601926. PMID 25904388.

and 19 Related for: WNK1 information

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WNK1

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(lysine deficient protein kinase 1), also known as WNK1, is an enzyme that is encoded by the WNK1 gene. WNK1 is serine-threonine protein kinase and part of...

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Distal convoluted tubule

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group of kinases called WNK kinases. There are 4 different WNK kinases, WNK1, WNK2, WNK3, and WNK4. It also participates in calcium regulation by reabsorbing...

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HSN2

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parent protein which in humans is encoded by the WNK1 gene. It is a transcript variant of the WNK1 gene that is selectively expressed in nervous system...

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WNK4

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regions within WNK1. The kinase domain of WNK4 has an 83% sequence identity with that of WNK1. The overall fold of the kinase domain of WNK1 resembles those...

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Hereditary sensory and autonomic neuropathy

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HSAN2A and HSAN2B are the same. The WNK1 gene provides instructions for making multiple versions (isoforms) of the WNK1 protein. HSAN2A is caused by mutations...

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ROMK

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hdl:2066/70313. PMID 18211905. Wang HR, Liu Z, Huang CL (August 2008). "Domains of WNK1 kinase in the regulation of ROMK1". American Journal of Physiology. Renal...

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Pseudohypoaldosteronism

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transporters in the kidney. PHA2 is associated with mutations in the WNK4, WNK1, KLHL3 and CUL3 genes. These genes regulate the Sodium-chloride symporter...

Word Count : 1581

WNK

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639-3 code wnk WNK, one of the STADAN stations A group of kinases called WNK WNK1 WNK2 WNK3 WNK4 This disambiguation page lists articles associated with the...

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OXSR1

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S2CID 39457788. Moriguchi T, Urushiyama S, Hisamoto N, et al. (2006). "WNK1 regulates phosphorylation of cation-chloride-coupled cotransporters via the...

Word Count : 774

Human accelerated regions

Last Update:

HAR02: CENTG2 including the HACNS1 module HAR03: MAD1L1 HAR04: ? HAR05: WNK1 HAR06: WWOX HAR07:  ? HAR08: POU6F2 HAR09: PTPRT HAR10: FHIT HAR11: DMD HAR12: ...

Word Count : 634

STK39

Last Update:

1038/ng1285. PMID 14702039. Moriguchi T, Urushiyama S, Hisamoto N, et al. (2006). "WNK1 regulates phosphorylation of cation-chloride-coupled cotransporters via the...

Word Count : 605

Minor histocompatibility antigen

Last Update:

chr6 7310026 rs10004 SSR1 ENSG00000124783 LB-WNK1-1I RTLSPE[I/M]ITV A*02:01 chr12 889199 rs12828016 WNK1 ENSG00000060237 T4A GLYTYWSAG[A/E] A*02:01 chr3...

Word Count : 1681

Protein kinase domain

Last Update:

TYRO3 ; UHMK1 ; ULK1 ; ULK2 ; ULK3 ; ULK4 ; VRK1 ; VRK2 ; VRK3 ; WEE1 ; WEE2 ; WNK1 ; WNK2 ; WNK3 ; WNK4 ; YES1 ; ZAP70 Knighton DR, Bell SM, Zheng J, et al...

Word Count : 1559

Gene trapping

Last Update:

Ramirez-Solis R, Richter LJ, Piggott J, BeltrandelRio H, et al. (November 2003). "Wnk1 kinase deficiency lowers blood pressure in mice: a gene-trap screen to identify...

Word Count : 786

CUL3

Last Update:

by regulating the proteasomal degradation of With-no-lysine [K] kinases WNK1 and WNK4. It was shown that mutations in CUL3 gene lead to WNKs accumulation...

Word Count : 2387

Chloride potassium symporter 5

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different sites on the KCC2 protein determines different regulational outcomes: Wnk1/Wnk3 and tyrosine kinase (i.e. TrkB) phosphorylation downregulates KCC2 activity...

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LINGO1

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neurological and psychiatric disorders: WNK lysine deficient protein in kinase 1 (WNK1), mitogen activated protein kinase 2/3 (MEK 2/3), extracellular signal reduced...

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SYT2

Last Update:

Chen S, Shu H, Luby-Phelps K, Goldsmith EJ, Cobb MH (September 2004). "WNK1 phosphorylates synaptotagmin 2 and modulates its membrane binding". Molecular...

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List of OMIM disorder codes

Last Update:

162400; SPTLC1 Neuropathy, hereditary sensory and autonomic, type II; 201300; WNK1 Neuropathy, hereditary sensory and autonomic, type IIB; 613115; FAM134B Neuropathy...

Word Count : 18877

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