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A high-resolution structure of the EF-hand domain of human polycystin-2
Autosomal dominant polycystic kidney disease (ADPKD) affects over 1:1000 of the worldwide population and is caused by mutations in two genes, PKD1 and PKD2. PKD2 encodes a 968-amino acid membrane spanning protein, Polycystin-2 (PC-2), which is a member of the TRP ion channel family. The C-terminal c...
Autores principales: | Allen, Mark D, Qamar, Seema, Vadivelu, Murali K, Sandford, Richard N, Bycroft, Mark |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Blackwell Publishing Ltd
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4244000/ https://www.ncbi.nlm.nih.gov/pubmed/24990821 http://dx.doi.org/10.1002/pro.2513 |
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