2n3j | pdb_00002n3j
From Proteopedia
Solution Structure of the alpha-crystallin domain from the redox-sensitive chaperone, HSPB1
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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 21:29, 15 October 2015.