Structural highlights
Disease
[HSPB3_HUMAN] Distal hereditary motor neuropathy type 2. The disease is caused by mutations affecting the gene represented in this entry.
Function
[HSPB2_HUMAN] May regulate the kinase DMPK.[1] [HSPB3_HUMAN] Inhibitor of actin polymerization.
References
- ↑ Suzuki A, Sugiyama Y, Hayashi Y, Nyu-i N, Yoshida M, Nonaka I, Ishiura S, Arahata K, Ohno S. MKBP, a novel member of the small heat shock protein family, binds and activates the myotonic dystrophy protein kinase. J Cell Biol. 1998 Mar 9;140(5):1113-24. PMID:9490724
