Ca 2+ -ATPase inactivation in Ca-medium, which was well explained by the fast rod denaturation. In contrast, rod denaturation was slower than S-1 in EDTA-medium.Decrease in monomeric myosin content was explained by faster S-1 denaturation.Comparing the S-1 and rod denaturation rates at the fixed temperature, it was concluded that S-1 denaturation was suppressed by Ca 2+ whereas rod portion was not. Unfolding experiment with isolated myosin rod confirmed no stabilizing effect of Ca 2+ on rod. It was concluded that significant stabilization of S-1 portion by Ca 2+ generated apparently different myosin denaturation pattern in two media.