Sodium cotransporters

被引:55
作者
Wright, EM
Loo, DDF
Turk, E
Hirayama, BA
机构
[1] Department of Physiology, School of Medicine, University of California, Los Angeles
关键词
D O I
10.1016/S0955-0674(96)80022-6
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Recent studies of cloned mammalian sodium cotransporters in heterologous systems have revealed that these integral membrane proteins serve multiple functions as cotransporters, uniporters, channels and water transporters. Some progress has been gained in understanding their secondary structure, but information on helical bundling and tertiary structure is lacking. Site-directed mutagenesis and the construction of chimeras have resulted in the identification of residues and domains involved in ligand binding, and natural mutations have also been round that are responsible for human genetic diseases. Major factors in the short-term regulation of cotransporter function by protein kinases are exocytosis and endocytosis.
引用
收藏
页码:468 / 473
页数:6
相关论文
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