The Hypertrophic Cardiomyopathy Myosin Mutation R453C Alters ATP Binding and Hydrolysis of Human Cardiac β-Myosin

Benzer Materyaller

• Myosin motor domains carrying mutations implicated in early or late onset hypertrophic cardiomyopathy have similar properties
  Yazar:: Vera, Carlos D., ve diğerleri
  Baskı/Yayın Bilgisi: (2019)
• The Most Prevalent Freeman-Sheldon Syndrome Mutations in the Embryonic Myosin Motor Share Functional Defects
  Yazar:: Walklate, Jonathan, ve diğerleri
  Baskı/Yayın Bilgisi: (2016)
• Molecular consequences of the R453C hypertrophic cardiomyopathy mutation on human β-cardiac myosin motor function
  Yazar:: Sommese, Ruth F., ve diğerleri
  Baskı/Yayın Bilgisi: (2013)
• The Relay/Converter Interface Influences Hydrolysis of ATP by Skeletal Muscle Myosin II
  Yazar:: Bloemink, Marieke J., ve diğerleri
  Baskı/Yayın Bilgisi: (2016)
• Contractility parameters of human β-cardiac myosin with the hypertrophic cardiomyopathy mutation R403Q show loss of motor function
  Yazar:: Nag, Suman, ve diğerleri
  Baskı/Yayın Bilgisi: (2015)