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K336I mutant actin alters the structure of neighbouring protomers in filaments and reduces affinity for actin-binding proteins

Mutation of the Lys-336 residue of actin to Ile (K336I) or Asp (K336E) causes congenital myopathy. To understand the effect of this mutation on the function of actin filaments and gain insight into the mechanism of disease onset, we prepared and biochemically characterised K336I mutant actin from Di...

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Detaylı Bibliyografya
Yayımlandı:Sci Rep
Asıl Yazarlar: Umeki, Nobuhisa, Shibata, Keitaro, Noguchi, Taro Q. P., Hirose, Keiko, Sako, Yasushi, Uyeda, Taro Q. P.
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Nature Publishing Group UK 2019
Konular:
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC6441083/
https://ncbi.nlm.nih.gov/pubmed/30926871
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41598-019-41795-w
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