4mjh
From Proteopedia
Contents |
Human Hsp27 core domain in complex with C-terminal peptide
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.
About this Structure
4mjh is a 4 chain structure. Full crystallographic information is available from OCA.
