4mjh

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.

See Also

• Heat Shock Protein structures