5oc9 | pdb_00005oc9
From Proteopedia
Crystal Structure of human TMEM16K / Anoctamin 10
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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 06:05, 12 June 2019.