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Mutations in the proteins PKD1 and PKD2 are linked to the disease, but the function of these proteins remains unclear, both in physiology and disease. PKD1 has been implicated in the sensing of chemical and mechanical force stimuli, and PKD2 is proposed to be a calcium ion channel. Su\n                    <jats:italic>et al.<\/jats:italic>\n                    show that the transmembrane regions form a PKD1-PKD2 complex assembled in a 1:3 ratio. Their high-resolution cryo\u2013electron microscopy structure confirms that the complex adopts transient receptor potential channel architecture, with some distinctive features. Mapping disease-causing mutations onto the structure suggests that pathogenesis may come from incorrect folding or trafficking of the complex rather than from disruption of channel activity.\n                  <\/jats:p>\n                  <jats:p>\n                    <jats:italic>Science<\/jats:italic>\n                    , this issue p.\n                    <jats:related-article xmlns:xlink=\"http:\/\/www.w3.org\/1999\/xlink\" ext-link-type=\"doi\" related-article-type=\"in-this-issue\" xlink:href=\"10.1126\/science.aat9819\">eaat9819<\/jats:related-article>\n                  <\/jats:p>","DOI":"10.1126\/science.aat9819","type":"journal-article","created":{"date-parts":[[2018,8,9]],"date-time":"2018-08-09T13:56:21Z","timestamp":1533822981000},"source":"Crossref","is-referenced-by-count":270,"title":["Structure of the human PKD1-PKD2 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