| Literature DB >> 16599535 |
Andrea Amadei1, Maira D'Alessandro, Maurizio Paci, Alfredo Di Nola, Massimiliano Aschi.
Abstract
In this paper, we investigate the effects of a point mutation on the enzymatic activity of copper-zinc superoxide dismutase, which we recently studied in detail by means of a theoretical-computational procedure. Comparison of the reactivity of the initial catalytic steps in this mutant (G93A mutation far from the active site) with our previous data, reveals the beautiful mechanical-dynamical architecture of the enzyme, altered by such an apparently irrelevant mutation. Finally, our results suggest a possible atomic-molecular-based explanation for the mutant-pathology correlation, in line with the most recent experimental data.Entities:
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Year: 2006 PMID: 16599535 DOI: 10.1021/jp057095h
Source DB: PubMed Journal: J Phys Chem B ISSN: 1520-5207 Impact factor: 2.991