5yx9
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proteopedia linkproteopedia linkCryo-EM structure of human TRPC6 at 3.8A resolution
Structural highlights
DiseaseTRPC6_HUMAN Familial idiopathic steroid-resistant nephrotic syndrome with focal segmental hyalinosis. The disease is caused by mutations affecting the gene represented in this entry. FunctionTRPC6_HUMAN Thought to form a receptor-activated non-selective calcium permeant cation channel (PubMed:19936226, PubMed:23291369). Probably is operated by a phosphatidylinositol second messenger system activated by receptor tyrosine kinases or G-protein coupled receptors. Activated by diacylglycerol (DAG) in a membrane-delimited fashion, independently of protein kinase C (PubMed:26892346). Seems not to be activated by intracellular calcium store depletion.[1] [2] [3] References
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Categories: Homo sapiens | Large Structures | Chen L | Guo W | Tang Q