The gas-phase acidity and proton affinity of nucleobases that are substrates for the enzyme hypoxanthine-guanine-(xanthine) phosphoribosyltransferase ( HG(X)PRT) have been examined using both computational and experimental methods. These thermochemical values have not heretofore been measured and provide experimental data to benchmark the theoretical results. HG(X)PRT is a target of interest in the development of antimalarials. We use our gas-phase results to lend insight into the HG(X)PRT mechanism, and also propose kinetic isotope studies that could potentially differentiate between possible mechanisms.
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http://dx.doi.org/10.1021/acs.joc.3c00115 | DOI Listing |
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