FigureĀ 5.
(A) cryo-EM structure of cyt b6f complex (pdb 6rqf) from spinach [51]. (B) X-ray structure of cyt bc1 complex (pdb 2qjy) from Rhodobacter sphaeroides [69]; (C) cryo-EM structure of cyt bc1 complex (pdb 6kls) from Aquifex aeolicus [72]; (D) X-ray structure of cyt bc1 complex (pdb 2ibz) from baker's yeast [67]. The deposited structure contains only one protomer which belongs to the crystallographic asymmetric unit. Here the dimeric structure shown was generated by applying symmetry operation; (E) cryo-EM structure of a supercomplex containing a dimeric cyt bc1 complex and a monomeric cyt c oxidase (supercomplex III2/IV, pdb 6giq) from baker's yeast [47]; (F) cryo-EM structure of a supercomplex containing a dimeric cyt bc1 complex and a dimeric cyt c oxidase (supercomplex III2/IV2, pdb 6hu9) from baker's yeast [46].
Positions of natural quinone molecules resolved in cyt b6f and bc1 complexes.

(A) cryo-EM structure of cyt b6f complex (pdb 6rqf) from spinach [51]. (B) X-ray structure of cyt bc1 complex (pdb 2qjy) from Rhodobacter sphaeroides [69]; (C) cryo-EM structure of cyt bc1 complex (pdb 6kls) from Aquifex aeolicus [72]; (D) X-ray structure of cyt bc1 complex (pdb 2ibz) from baker's yeast [67]. The deposited structure contains only one protomer which belongs to the crystallographic asymmetric unit. Here the dimeric structure shown was generated by applying symmetry operation; (E) cryo-EM structure of a supercomplex containing a dimeric cyt bc1 complex and a monomeric cyt c oxidase (supercomplex III2/IV, pdb 6giq) from baker's yeast [47]; (F) cryo-EM structure of a supercomplex containing a dimeric cyt bc1 complex and a dimeric cyt c oxidase (supercomplex III2/IV2, pdb 6hu9) from baker's yeast [46].

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