Down-Regulating Destruction: Phosphorylation Regulates the E3 Ubiquitin Ligase Nedd4-2

被引:52
|
作者
Snyder, Peter M. [1 ]
机构
[1] Univ Iowa, Dept Internal Med & Mol Physiol & Biophys, Iowa City, IA 52242 USA
关键词
EPITHELIAL NA+ CHANNEL; SODIUM-CHANNEL; FUNCTIONAL REGULATION; LIDDLES SYNDROME; WW DOMAINS; KINASE; ENAC; PROTEIN; SERUM; SGK;
D O I
10.1126/scisignal.279pe41
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
E3 ubiquitin ligases catalyze ubiquitination, which can target specific proteins for degradation. Although a growing number of E3 ubiquitin ligases and their targets have been identified, much less is known about the mechanisms that regulate their activity. A convergence of data indicate that phosphorylation regulates the binding of Nedd4-2, a HECT (homologous to the E6-AP C terminus) domain E3 ubiquitin ligase, to its target, the epithelial Na+ channel ENaC. Nedd4-2 phosphorylation is emerging as a central convergence point for the regulation of epithelial Na+ transport.
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页数:3
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