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A PKD1L3 splicing variant in taste buds is not cleaved at the G protein-coupled receptor proteolytic site

Mutations in polycystin proteins PKD1 and TRPP2 lead to autosomal dominant polycystic kidney disease. These two proteins form a receptor-ion channel complex on primary cilia. PKD1 undergoes an autoproteolysis at the N terminal G-protein-coupled receptor proteolytic site (GPS), which is essential for...

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Detalhes bibliográficos
Publicado no:Biochem Biophys Res Commun
Main Authors: Kashyap, Parul, Ng, Courtney, Wang, Zhifei, Li, Bin, Arif Pavel, Mahmud, Martin, Hannah, Yu, Yong
Formato: Artigo
Idioma:Inglês
Publicado em: 2019
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC6467730/
https://ncbi.nlm.nih.gov/pubmed/30928102
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.bbrc.2019.03.099
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