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KLHL3 is ubiquitously expressed and encodes a full-length protein which has an N-terminal BTB domain followed by a BACK domain and six kelch-like repeats in the C-terminus. Zusätzlich bieten wir Ihnen KLHL3 Proteine (5) und viele weitere Produktgruppen zu diesem Protein an.
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However, phosphorylation of SPAK (zeige STK39 Antikörper) and NCC (zeige SLC12A3 Antikörper) at distal convoluted tubules were almost completely absent even in WNK4 (zeige WNK4 Antikörper)(-/-)KLHL3(R528H/R528H) mice. In conclusion, increased WNK1 (zeige WNK1 Antikörper) was unable to compensate for WNK4 (zeige WNK4 Antikörper) deficiency and phosphorylate the NCC (zeige SLC12A3 Antikörper), indicating that WNK4 (zeige WNK4 Antikörper) is indispensable for the onset of PHAII.
the heterozygous deletion of KLHL3 was not sufficient to cause PHAII, indicating that autosomal dominant type pseudohypoaldosteronism type II (PHAII) is caused by the dominant negative effect of mutant KLHL3.
Potassium depletion stimulates NCC (zeige SLC12A3 Antikörper) via phosphorylation and inactivation of the KLHL3 and promoting increased blood pressure.
KLHL3 regulates paracellular chloride transport in the kidney by ubiquitination of claudin-8 (zeige CLDN8 Antikörper)
increased protein expression levels of WNK1 (zeige WNK1 Antikörper) and WNK4 (zeige WNK4 Antikörper) kinases cause PHAII by KLHL3 R528H mutation due to impaired KLHL3-Cullin3-mediated ubiquitination.
Mutation in the KLHL3 gene is associated with Gordon syndrome.
The results demonstrate that Hcy decreases the expression of cMyBP-C through a KLHL3-mediated ubiquitin-proteasome pathway, and thereby influences heart development.
This study provides substantial new insights into the role of phosphorylation of KLHL3 in regulating the interaction with WNK4 (zeige WNK4 Antikörper)
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.
Familial hyperkalemia and hypertension caused by KLHL3 mutations is accompanied by hypercalciuria as well as hyperkalemia and hypertension.
Akt (zeige AKT1 Antikörper) and PKA phosphorylated KLHL3 at S433, and phosphorylation of KLHL3 by PKA inhibited WNK4 (zeige WNK4 Antikörper) degradation.
KLHL3 is phosphorylated at serine 433 in the Kelch domain (a site frequently mutated in hypertension with hyperkalemia) by protein kinase C (zeige PKC Antikörper) in cultured cells and that this phosphorylation prevents WNK4 (zeige WNK4 Antikörper) binding and degradation.
Hyperkalemic hypertension-associated cul3 (zeige CUL3 Antikörper) mutations depletes KLHL3, preventing WNK degradation, despite increased CUL3 (zeige CUL3 Antikörper)-mediated WNK ubiquitylation.
CUL3 (zeige CUL3 Antikörper) and KLHL3 gene products are physiologically important regulators of thiazide-sensitive distal nephron sodium chloride reabsorption.
analysis of how mutations of KLHL3 show less ability to ubiquitinate WNK4 (zeige WNK4 Antikörper) because of KLHL3's low stability and/or decreased binding to CUL3 (zeige CUL3 Antikörper) or WNK4 (zeige WNK4 Antikörper)
This gene is ubiquitously expressed and encodes a full-length protein which has an N-terminal BTB domain followed by a BACK domain and six kelch-like repeats in the C-terminus. These kelch-like repeats promote substrate ubiquitination of bound proteins via interaction of the BTB domain with the CUL3 (cullin 3) component of a cullin-RING E3 ubiquitin ligase (CRL) complex. Muatations in this gene cause pseudohypoaldosteronism type IID (PHA2D)\; a rare Mendelian syndrome featuring hypertension, hyperkalaemia and metabolic acidosis. Alternative splicing results in multiple transcript variants encoding distinct isoforms.
kelch-like protein 3
, kelch-like 3