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pubmed-article:21426012lifeskim:mentionsumls-concept:C0033684lld:lifeskim
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pubmed-article:21426012pubmed:issue4lld:pubmed
pubmed-article:21426012pubmed:dateCreated2011-3-23lld:pubmed
pubmed-article:21426012pubmed:abstractTextAccurate computational methods for predicting electrostatic energies are of major importance for our understanding of protein energetics in general for computer-aided drug design as well as for the design of novel biocatalysts and protein therapeutics. Electrostatic energies are of particular importance in such applications as virtual screening, drug design and protein-protein docking due to the high charge density of protein ligands and small-molecule drugs, and the frequent protonation state changes observed when drugs bind to their protein targets. Therefore, the development of a reliable and fast algorithm for the evaluation of electrostatic free energies, as an important contributor to the overall protein energy function, has been the focus for many scientists over the past three decades. In this review we describe the current state-of-the-art in modeling electrostatic effects in proteins and protein-ligand complexes. We focus mainly on the merits and drawbacks of the continuum methodology, and speculate on future directions in refining algorithms for calculating electrostatic energies in proteins using experimental data.lld:pubmed
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pubmed-article:21426012pubmed:issn1756-8927lld:pubmed
pubmed-article:21426012pubmed:authorpubmed-author:NielsenJens...lld:pubmed
pubmed-article:21426012pubmed:authorpubmed-author:Kuki?PredragPlld:pubmed
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pubmed-article:21426012pubmed:year2010lld:pubmed
pubmed-article:21426012pubmed:articleTitleElectrostatics in proteins and protein-ligand complexes.lld:pubmed
pubmed-article:21426012pubmed:affiliationSchool of Biomolecular and Biomedical Science, Centre for Synthesis and Chemical Biology, UCD Conway Institute, University College Dublin, Belfield, Dublin 4, Ireland.lld:pubmed
pubmed-article:21426012pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:21426012pubmed:publicationTypeReviewlld:pubmed
pubmed-article:21426012pubmed:publicationTypeResearch Support, Non-U.S. Gov'tlld:pubmed