PDB ID 8g4l
MYL3_HUMAN Familial isolated hypertrophic cardiomyopathy. The disease is caused by mutations affecting the gene represented in this entry.
MYL3_HUMAN Regulatory light chain of myosin. Does not bind calcium.
OCA
Categories: Homo sapiens | Large Structures | Craig R | Dutta D | Nguyen V | Padron R