| pubmed-article:8804597 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:8804597 | lifeskim:mentions | umls-concept:C0026339 | lld:lifeskim |
| pubmed-article:8804597 | lifeskim:mentions | umls-concept:C0026336 | lld:lifeskim |
| pubmed-article:8804597 | lifeskim:mentions | umls-concept:C0033684 | lld:lifeskim |
| pubmed-article:8804597 | lifeskim:mentions | umls-concept:C0037638 | lld:lifeskim |
| pubmed-article:8804597 | lifeskim:mentions | umls-concept:C1441506 | lld:lifeskim |
| pubmed-article:8804597 | pubmed:issue | 1 | lld:pubmed |
| pubmed-article:8804597 | pubmed:dateCreated | 1996-12-18 | lld:pubmed |
| pubmed-article:8804597 | pubmed:abstractText | Continuum methods for calculation of protein electrostatics treat buried and ordered water molecules by one of two approximations; either the dielectric constant of regions containing ordered water molecules is equal to the bulk solvent dielectric constant, or it is equal to the protein dielectric constant though no fixed atoms are used to represent water molecules. A method for calculating the titration behavior of individual residues in proteins has been tested on models of hen egg white lysozyme containing various numbers of explicit water molecules. Water molecules were included based on hydrogen bonding, solvent accessibility, and/or proximity to titrating groups in the protein. Inclusion of water molecules significantly alters the calculated titration behavior of individual titrating sites, shifting calculated pKa values by up to 0.5 pH unit. Our results suggest that approximately one water molecule within hydrogen-bonding distance of each charged group should be included in protein electrostatics calculations. | lld:pubmed |
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| pubmed-article:8804597 | pubmed:language | eng | lld:pubmed |
| pubmed-article:8804597 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:8804597 | pubmed:citationSubset | IM | lld:pubmed |
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| pubmed-article:8804597 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:8804597 | pubmed:month | Jul | lld:pubmed |
| pubmed-article:8804597 | pubmed:issn | 0006-3495 | lld:pubmed |
| pubmed-article:8804597 | pubmed:author | pubmed-author:SubramanianRR | lld:pubmed |
| pubmed-article:8804597 | pubmed:author | pubmed-author:GhaeyKK | lld:pubmed |
| pubmed-article:8804597 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:8804597 | pubmed:volume | 71 | lld:pubmed |
| pubmed-article:8804597 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:8804597 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:8804597 | pubmed:pagination | 138-47 | lld:pubmed |
| pubmed-article:8804597 | pubmed:dateRevised | 2009-11-18 | lld:pubmed |
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| pubmed-article:8804597 | pubmed:year | 1996 | lld:pubmed |
| pubmed-article:8804597 | pubmed:articleTitle | Explicit solvent models in protein pKa calculations. | lld:pubmed |
| pubmed-article:8804597 | pubmed:affiliation | Department of Molecular and Integrative Physiology, University of Illinois at Urbana-Champaign 61801, USA. | lld:pubmed |
| pubmed-article:8804597 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:8804597 | pubmed:publicationType | Research Support, U.S. Gov't, Non-P.H.S. | lld:pubmed |
| pubmed-article:8804597 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
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