6cxi
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Cardiac thin filament decorated with C0C1 fragment of cardiac myosin binding protein C mode 1
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Structural highlights
DiseaseACTG_HUMAN Baraitser-Winter syndrome;Autosomal dominant non-syndromic sensorineural deafness type DFNA. The disease is caused by mutations affecting the gene represented in this entry. The disease is caused by mutations affecting the gene represented in this entry. FunctionACTG_HUMAN Actins are highly conserved proteins that are involved in various types of cell motility and are ubiquitously expressed in all eukaryotic cells. See Also | ||||||||||||||
This page was last modified 14:31, 13 March 2024.