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Model of a complex between the tetrahemic cytochrome c3 and the ferredoxin I from Desulfovibrio desulfuricans (Norway strain)
Author(s) -
Cambillau C.,
Frey M.,
Mossé J.,
Guerlesquin F.,
Bruschi M.
Publication year - 1988
Publication title -
proteins: structure, function, and bioinformatics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.699
H-Index - 191
eISSN - 1097-0134
pISSN - 0887-3585
DOI - 10.1002/prot.340040109
Subject(s) - ferredoxin , crystallography , molecular graphics , chemistry , redox , electron transfer , cytochrome , cytochrome c , molecule , strain (injury) , chemical physics , stereochemistry , photochemistry , inorganic chemistry , computer graphics , biology , biochemistry , computer science , organic chemistry , artificial intelligence , mitochondrion , enzyme , anatomy
A three‐dimensional model of an electron‐transfer complex between the tetrahemic cytochrome c3 and the ferredoxin I from the sulfatereducing bacterium Desulfovibrio desulfuricans (Norway strain) has been generated through computer graphics methods. The model is based on the known X‐ray structure of the cytochrome and on a model of the ferredoxin that has been derived through computer graphics modeling and energy minimization methods, from the X‐ray structure of the homologous ferredoxin from Peptococcus aerogenes . Four possible models of interaction between the two molecules were examined by bringing in close proximity each of the four hemes and the redox center (4Fe‐4S) of the ferredoxin and by optimizing the ion pairs interactions. One of these models shows by far the “best” structure in terms of charges, interactions, and complementary f the topology of the contact surfaces. In this complex, the distance between the iron atoms of the ferredoxin redox center and the hemic iron atom is 11.8 Å, which compares well with those found between redox centers in other complexes. The contact surface area between the two molecules is 170 Å 2 .

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