The heteromeric PC-1/PC-2 polycystin complex is activated by the PC-1 N-terminus
Mutations in the polycystin proteins, PC-1 and PC-2, result in autosomal dominant polycystic kidney disease (ADPKD) and ultimately renal failure. PC-1 and PC-2 enrich on primary cilia, where they are thought to form a heteromeric ion channel complex. However, a functional understanding of the putati...
Main Authors: | Kotdaji Ha, Mai Nobuhara, Qinzhe Wang, Rebecca V Walker, Feng Qian, Christoph Schartner, Erhu Cao, Markus Delling |
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Format: | Article |
Language: | English |
Published: |
eLife Sciences Publications Ltd
2020-11-01
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Series: | eLife |
Subjects: | |
Online Access: | https://elifesciences.org/articles/60684 |
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