“…Extension to larger systems was, however, hampered by the computational expense of the method. More recently, thanks to both advances in computer equipment as well as new methods based on simpler models, it has become possible to examine larger structures, including the skeletal ryanodine receptor [42], virus capsids [43,44,45], Ca-ATPase [46], Myosin-II [46,47,48], F1-ATPase [49], GroEL [50,51,52], the ribosome [53,54,55], the C-ring of the bacterial flagellar motor [56], and the yeast nuclear pore complex [57].…”