6dv5

Structural highlights

Disease

[HSPB1_HUMAN] Autosomal dominant Charcot-Marie-Tooth disease type 2F;Distal hereditary motor neuropathy type 2. 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.

Function

[HSPB1_HUMAN] Involved in stress resistance and actin organization.