“…Previous structural analyses by spectroscopic methods have been consistent with [4Fe-4S] (Evans et al, 1981) or [2Fe-2S] (Golbeck et al, 1987;McDermott et al, 1988;Bertrand et al, 1988) or a distorted [4Fe-4S] cluster (McDermott et al, 1988). Examination of the polypeptide sequences of psaA and psaB (Fish et al, 1985), which are the putative binding sites of Fx (Golbeck et al, 1988), reveals none of the characteristic sequence elements of or ferredoxins [reviewed in Stout (1982)]. A consideration of the stoichiometries of Fe, acid-labile sulfide, and cysteines per complex would argue against the presence of [2Fe-2S] clusters on the psaA and psaB polypeptides (Bruce & Malkin, 1988; 1 Abbreviations: EPR, electron paramagnetic resonance; EXAFS, extended X-ray absorption fine structure; FA, FB, and Fx, ferredoxins in photosystem I, alternatively referred to as centers A, B, and X; kDa, kilodaltons; PS I, photosystem I; psaA and psaB, reaction center polypeptides in PS I, also referred to as PSI-A1 and PSI-A2; P700, primary electron donor in PS I; Tirón, 4,5-dihydroxy-1,3-benzenedisulfonic acid; Tris, tris(hydroxymethyl)aminomethane.…”