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- W2003804150 abstract "We recently reported that chloroperoxidase (CPO) from Caldariomyces fumago showed atypical kinetic behavior for the oxidation of 4,6 dimethyl dibenzothiophene (DMDBT). In this work, we undertake the theoretical study of DMDBT docking into CPO's active site, in order to clarify its binding capacity and affinity using molecular interaction fields and quantum mechanical procedure. The results revealed that CPO has two substrate binding sites with similar affinities for DMDBT. This finding suggests that the atypical kinetic behavior of CPO for the oxidation of DMDBT might be due to the simultaneous binding of two DMDBT molecules during its reaction cycle. Finally, we extend these results to carbazole, a nitrogen-containing PAH, through experimental and theoretical studies." @default.
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- W2003804150 date "2007-07-01" @default.
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- W2003804150 title "Ligand recognition by chloroperoxidase using molecular interaction fields and quantum chemistry calculations" @default.
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- W2003804150 doi "https://doi.org/10.1080/08927020701342041" @default.
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