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WNK4 encodes a member of the WNK family of serine-threonine protein kinases. Additionally we are shipping WNK4 Proteins (4) and many more products for this protein.
Showing 10 out of 65 products:
Human Polyclonal WNK4 Primary Antibody for EM, IHC - ABIN153223
Wilson, Disse-Nicodème, Choate, Ishikawa, Nelson-Williams, Desitter, Gunel, Milford, Lipkin, Achard, Feely, Dussol, Berland, Unwin, Mayan, Simon, Farfel, Jeunemaitre, Lifton: Human hypertension caused by mutations in WNK kinases. in Science (New York, N.Y.) 2001
Show all 7 references for ABIN153223
Data indicate that WNK lysine deficient protein kinase 4 protein (WNK4) was degraded not only by proteasomes but also by atypical protein kinase C scaffold protein p62 (p62)-kelch-like 3 protein (KLHL3)-mediated selective autophagy.
this meta-analysis suggested that WNK4 G1155942T and C6749T gene polymorphisms may contribute to the susceptibility and development of hypertension.
Akt (show AKT1 Antibodies) and PKA phosphorylated KLHL3 (show KLHL3 Antibodies) at S433, and phosphorylation of KLHL3 (show KLHL3 Antibodies) by PKA inhibited WNK4 degradation.
WNK4 is a substrate of SFKs and the association of c-Src (show SRC Antibodies) and PTP-1D (show PTPN11 Antibodies) with WNK4 at Tyr (show TYR Antibodies)(1092) and Tyr (show TYR Antibodies)(1143) plays an important role in modulating the inhibitory effect of WNK4 on ROMK (show KCNJ1 Antibodies)
WNK4 inhibits SNARE (show NAPA Antibodies) formation of syntaxin 13 (show STX12 Antibodies) with VAMP2 (show VAMP2 Antibodies).
Regulation of WNK4 by CUL3 (show CUL3 Antibodies) and its relationship to blood pressure regulation and electrolyte homeostasis. [Review]
WNK4 inhibits Large-conductance, Ca(2 )-activated K( ) channel activity, in part, by increasing channel degradation through an ubiquitin-dependent pathway.
analysis of how mutations of KLHL3 (show KLHL3 Antibodies) show less ability to ubiquitinate WNK4 because of KLHL3 (show KLHL3 Antibodies)'s low stability and/or decreased binding to CUL3 (show CUL3 Antibodies) or WNK4
WNK4 inhibits ENaC (show SCNN1A Antibodies) channel activity independently of Nedd4-2 (show NEDD4L Antibodies)-mediated ENaC (show SCNN1A Antibodies) ubiquitination.
KLHL3 is a substrate adaptor for WNK4 in a ubiquitin E3 ligase complex
increased protein expression levels of WNK1 (show WNK1 Antibodies) and WNK4 kinases cause PHAII by KLHL3 (show KLHL3 Antibodies) R528H mutation due to impaired KLHL3 (show KLHL3 Antibodies)-Cullin3-mediated ubiquitination.
KLHL3 (show KLHL3 Antibodies) is phosphorylated at serine 433 in the Kelch domain (a site frequently mutated in hypertension with hyperkalemia) by protein kinase C (show PKC Antibodies) in cultured cells and that this phosphorylation prevents WNK4 binding and degradation.
WNK4 is the major positive regulator of NCC (show SLC12A3 Antibodies) in the kidneys.
WNK1 (show WNK1 Antibodies) stimulates the activity of the Na-Cl cotransporter (show SLC12A3 Antibodies) via SPAK (show STK39 Antibodies), an effect antagonized by WNK4.
in addition to SPAK (show STK39 Antibodies) and OSR1 (show OSR1 Antibodies), WNK4 is able to anchor itself to the N-terminal domain of NKCC1 (show SLC12A2 Antibodies) and to promote cotransporter activation.
SPAK (show STK39 Antibodies) deficiency corrects pseudohypoaldosteronism II caused by WNK4 mutation.
Activation of the renal Na+:Cl- cotransporter by angiotensin II is a WNK4-dependent process.
data suggest that WNK4 inhibits NCC (show SLC12A3 Antibodies) protein through activating the MAPK (show MAPK1 Antibodies) ERK1/2 (show MAPK1/3 Antibodies) signaling pathway.
these results suggest that these PHAII-causing mutations disrupt a Ca(2 (show CA2 Antibodies)+)-sensing mechanism around the acidic motif necessary for the regulation of WNK4 kinase activity by Ca(2 (show CA2 Antibodies)+) ions.
Immunolocalization of WNK4 in mouse kidney.
This gene encodes a member of the WNK family of serine-threonine protein kinases. The kinase is part of the tight junction complex in kidney cells, and regulates the balance between NaCl reabsorption and K(+) secretion. The kinase regulates the activities of several types of ion channels, cotransporters, and exchangers involved in electrolyte flux in epithelial cells. Mutations in this gene result in pseudohypoaldosteronism type IIB.
WNK lysine deficient protein kinase 4
, protein kinase lysine-deficient 4
, protein kinase with no lysine 4
, serine/threonine-protein kinase WNK4
, protein kinase, lysine deficient 4
, WNK4 Ser/Thr kinase
, protein kinase, lysine-deficient 4