The individual protein complexes of the oxidative phosphorylation system (OXPHOS complexes I to V) specifically interact and form defined supramolecular structures, the so-called "respiratory supercomplexes". Some supercomplexes appear to associate into larger structures, or megacomplexes, such as a string of dimeric ATP synthase (complex V(2)). A row-like organization of OXPHOS complexes I, III and IV into respiratory strings has also been proposed. These transient strings cannot be purified after detergent solubilization. Hence the shape and composition of the respiratory string was approached by an extensive structural characterization of all its possible building blocks, which are the supercomplexes. About 400,000 molecular projections of supercomplexes from potato mitochondria were processed by single particle electron microscopy. We obtained two-dimensional projection maps of at least five different supercomplexes, including the supercomplex I+III(2), III(2)+IV(1), V(2), I+III(2)+IV(1) and I(2)+III(2) in different types of position. From these maps the relative position of the individual complexes in the largest unit, the I(2)+III(2)+IV(2) supercomplex, could be determined in a coherent way. The maps also show that the I+III(2)+IV(1) supercomplex, or respirasome, differs from its counterpart in bovine mitochondria. The new structural features allow us to propose a consistent model of the respiratory string, composed of repeating I(2)+III(2)+IV(2) units, which is in agreement with dimensions observed in former freeze-fracture electron microscopy data.