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Very fast empirical prediction and rationalization of protein pK a values
Author(s) -
Li Hui,
Robertson Andrew D.,
Jensen Jan H.
Publication year - 2005
Publication title -
proteins: structure, function, and bioinformatics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.699
H-Index - 191
eISSN - 1097-0134
pISSN - 0887-3585
DOI - 10.1002/prot.20660
Subject(s) - rationalization (economics) , histidine , chemistry , lysine , absolute deviation , enzyme , mathematics , amino acid , biochemistry , statistics , philosophy , epistemology
A very fast empirical method is presented for structure‐based protein pK a prediction and rationalization. The desolvation effects and intra‐protein interactions, which cause variations in pK a values of protein ionizable groups, are empirically related to the positions and chemical nature of the groups proximate to the pK a sites. A computer program is written to automatically predict pK a values based on these empirical relationships within a couple of seconds. Unusual pK a values at buried active sites, which are among the most interesting protein pK a values, are predicted very well with the empirical method. A test on 233 carboxyl, 12 cysteine, 45 histidine, and 24 lysine pK a values in various proteins shows a root‐mean‐square deviation (RMSD) of 0.89 from experimental values. Removal of the 29 pK a values that are upper or lower limits results in an RMSD = 0.79 for the remaining 285 pK a values. Proteins 2005. © 2005 Wiley‐Liss, Inc.