The microtubule-based kinesin motors and actin-based myosin motors generate
motions associated with intracellular trafficking, cell division, and musc
le contraction. Early studies suggested that these molecular motors work by
very different mechanisms. Recently, however, it has become clear that kin
esin and myosin share a common core structure and convert energy from adeno
sine triphosphate into protein motion using a similar conformational change
strategy. Many different types of mechanical amplifiers have evolved that
operate in conjunction with the conserved core. This modular design has giv
en rise to a remarkable diversity of kinesin and myosin motors whose motile
properties are optimized for performing distinct biological functions.