6r65 | pdb_00006r65
From Proteopedia
Crystal Structure of human TMEM16K / Anoctamin 10 (Form 2)
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Structural highlights
Disease[ANO10_HUMAN] Adult-onset autosomal recessive cerebellar ataxia. The disease is caused by mutations affecting the gene represented in this entry. Function[ANO10_HUMAN] Does not exhibit calcium-activated chloride channel (CaCC) activity. Can inhibit the activity of ANO1.[1] [2] References
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This page was last modified 08:58, 1 May 2019.