EC Number   |
Title |
Organism |
|---|
   5.6.1.8 | Aberrant movement of beta-tropomyosin associated with congenital myopathy causes defective response of myosin heads and actin during the ATPase cycle |
Oryctolagus cuniculus |
| 5.6.1.8 | Alternative exon-encoding regions of Locusta migratoria muscle myosin modulate the pH dependence of ATPase activity |
Locusta migratoria |
| 5.6.1.8 | ATP-dependent interplay between local and global conformational changes in the myosin motor |
Homo sapiens |
| 5.6.1.8 | Cardiac leiomodin2 binds to the sides of actin filaments and regulates the ATPase activity of myosin |
Rattus norvegicus |
| 5.6.1.8 | Direct interaction between troponin and myosin enhances the ATPase activity of heavy meromyosin |
Oryctolagus cuniculus |
| 5.6.1.8 | Interplay of actin, ADP and Mg2+ interactions with striated muscle myosin Implications of their roles in ATPase |
Oryctolagus cuniculus |
| 5.6.1.8 | Myocyte contractility can be maintained by storing cells with the myosin ATPase inhibitor 2,3 butanedione monoxime |
Rattus norvegicus |
| 5.6.1.8 | Structure of actomyosin rigour complex at 5.2 A resolution and insights into the ATPase cycle mechanism |
Oryctolagus cuniculus |
| 5.6.1.8 | 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 |
Oryctolagus cuniculus |
| 5.6.1.8 | Thiacalix[4]arenes remove the inhibitory effects of Zn cations on the myosin ATPase activity |
Sus scrofa |
