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. 2020 Aug 11;295(41):14100–14110. doi: 10.1074/jbc.RA120.014445

Figure 1.

Figure 1.

Schematic representation of thin (actin, tropomyosin, and troponins) and thick filaments (myosin and MyBP-C) substructures, key participants in Ca2+-dependent muscle contraction and relaxation. Actin-binding compounds can affect interaction between actin and these actin-binding partners and play a crucial role in regulation of these processes.