8s7a

Structural highlights

Disease

HSPB8_HUMAN Autosomal dominant distal axonal motor neuropathy-myofibrillar myopathy syndrome;Autosomal dominant Charcot-Marie-Tooth disease type 2L;Distal hereditary motor neuropathy type 2. The disease is caused by variants affecting the gene represented in this entry. The disease is caused by variants affecting the gene represented in this entry.

Function

HSPB8_HUMAN Displays temperature-dependent chaperone activity.