The reason for a high Ca2+-sensitivity associated with Arg91Gly substitution in TPM2 gene is the abnormal behavior and high flexibility of tropomyosin during the ATPase cycle

Podobne zapisy

• Gly126Arg substitution causes anomalous behaviour of α-skeletal and β-smooth tropomyosins during the ATPase cycle.
  od: Rysev, N, i wsp.
  Wydane: (2014)
• The effect of the arthrogryposis-causing Arg91Gly mutation in beta-skeletal tropomyosin on its position on the thin filament and flexibility during the ATPase cycle
  od: Simonyan, A, i wsp.
  Wydane: (2013)
• Hypertrophic cardiomyopathy-causing Asp175asn and Glu180gly Tpm1 mutations shift tropomyosin strands further towards the open position during the ATPase cycle
  od: Borovikov, Y, i wsp.
  Wydane: (2011)
• Hypertrophic cardiomyopathy-causing Asp175asn and Glu180gly Tpm1 mutations shift tropomyosin strands further towards the open position during the ATPase cycle.
  od: Borovikov, Y, i wsp.
  Wydane: (2011)
• Molecular mechanisms of dysfunction of muscle fibres associated with Glu139 deletion in TPM2 gene
  od: Borovikov, Y, i wsp.
  Wydane: (2017)