6dv5 | pdb_00006dv5
From Proteopedia
Oligomeric complex of a Hsp27 24-mer at 3.6 A resolution
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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. Contents | ||||||||||||||||
This page was last modified 06:44, 26 June 2019.