| Literature DB >> 6316150 |
J A Tainer, E D Getzoff, J S Richardson, D C Richardson.
Abstract
Copper, zinc superoxide dismutase (SOD) catalyses the very rapid two-step dismutation of the toxic superoxide radical (O-2) to molecular oxygen and hydrogen peroxide through the alternate reduction and oxidation of the active-site copper. We report here that after refitting and further refinement of the previous 2 A structure of SOD2, analysis of the new model and its calculated molecular surface shows an extensive surface topography of sequence-conserved residues stabilized by underlying tight packing and H-bonding. There is a single, highly complementary position for O-2 to bind to both the Cu(II) and activity-important Arg 141 with correct geometry; two water molecules form a ghost of the superoxide in this position. The geometry and molecular surface of the active site, together with biochemical data, suggest a specific model for the enzyme mechanism.Entities:
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Year: 1983 PMID: 6316150 DOI: 10.1038/306284a0
Source DB: PubMed Journal: Nature ISSN: 0028-0836 Impact factor: 49.962