8qjh
Connexin-32 gap junction channel in complex with mefloquineConnexin-32 gap junction channel in complex with mefloquine
Structural highlights
DiseaseCXB1_HUMAN X-linked Charcot-Marie-Tooth disease type 1;X-linked progressive cerebellar ataxia. The disease is caused by mutations affecting the gene represented in this entry. The gene represented in this entry may act as a disease modifier. FunctionCXB1_HUMAN One gap junction consists of a cluster of closely packed pairs of transmembrane channels, the connexons, through which materials of low MW diffuse from one cell to a neighboring cell. |
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