4mjh
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Human Hsp27 core domain in complex with C-terminal peptideHuman Hsp27 core domain in complex with C-terminal peptide
Structural highlights
DiseaseHSPB1_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. FunctionHSPB1_HUMAN Involved in stress resistance and actin organization. See Also |
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