6bdt | pdb_00006bdt
From Proteopedia
Crystal Structure of Human Calpain-3 Protease Core Mutant-C129S
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Structural highlights
Disease[CAN3_HUMAN] Autosomal recessive limb girdle muscular dystrophy type 2A. The disease is caused by mutations affecting the gene represented in this entry. Function[CAN3_HUMAN] Calcium-regulated non-lysosomal thiol-protease. Contents | ||||||||||||||||||||
This page was last modified 06:19, 7 February 2018.