Title
Update On Phosphate And Charged Post-Translationally Modified Amino Acid Parameters In The Gromos Force Field
Abstract
In this study, we propose newly derived parameters for phosphate ions in the context of the GROMOS force field parameter sets. The non-bonded parameters used up to now lead to a hydration free energy, which renders the dihydrogen phosphate ion too hydrophobic when compared to experimentally derived values, making a reparametrization of the phosphate moiety necessary. Phosphate species are of great importance in biomolecular simulations not only because of their crucial role in the backbone of nucleic acids but also as they represent one of the most important types of post-translational modifications to protein side-chains and are an integral part in many lipids. Our re-parametrization of the free dihydrogen phosphate (H2PO4-) and three derivatives (methyl phosphate, dimethyl phosphate, and phenyl phosphate) leads, in conjunction with the previously updated charged side-chains in the GROMOS parameter set 54A8, to new nucleic acid backbone parameters and a 54A8 version of the widely used GROMOS protein post-translational modification parameter set. (C) 2017 Wiley Periodicals, Inc.
Year
DOI
Venue
2017
10.1002/jcc.24733
JOURNAL OF COMPUTATIONAL CHEMISTRY
Keywords
Field
DocType
parametrization, post-translational modifications, molecular dynamics, phosphates, force-field, solvation free energies
Force field (physics),Phosphate,Parametrization,Amino acid,Posttranslational modification,Computational chemistry,Chemistry,Molecular dynamics
Journal
Volume
Issue
ISSN
38
10
0192-8651
Citations 
PageRank 
References 
1
0.36
9
Authors
3
Name
Order
Citations
PageRank
Christian Margreitter192.37
Maria M Reif261.55
Chris Oostenbrink329738.41