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Protein electrostatics and pKa blind predictions; contribution from empirical predictions of internal ionizable residues

Authors

  • Mats H. M. Olsson

    Corresponding author
    1. Department of Chemistry, University of Copenhagen, Universitetsparken 5, 2100 Copenhagen, Denmark
    • Department of Chemistry, University of Copenhagen, Universitetsparken 5, 2100 Copenhagen, Denmark
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  • The authors state no conflict of interest.

Abstract

In this study, we validate and probe the description of electrostatic interactions within proteins by predicting and comparing pKa values of ionizable groups in a series of mutated staphylococcal nuclease variants with experiments. This set of pKa values is found to be the most challenging pKa data to date, because ionizable residues have been introduced in hydrophobic patches in the protein interior and are therefore significantly shifted from their reference solvated values. We find that using PROPKA2 (Li et al., Proteins 2005;61:704–721) results in an rmsd value close to 2 for true blind predictions (1.6 if we reassign the tightly coupled Asp19/21 pair) and close to 1 for postpredictions with the newly developed PROPKA3 (Olsson et al., J. Chem. Theor. Comp. 2011;7:525–537). We also use the performance of the Null-model, predictions made with the reference value only, to provide a better description of the expected errors in pKa predictions and to compare submissions made using different subsets of the pKa data more consistently. Proteins 2011; © 2011 Wiley-Liss, Inc.

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