Rapid Calculation of Accurate Atomic Charges for Proteins via the Electronegativity Equalization Method
| Autoři | |
|---|---|
| Rok publikování | 2013 |
| Druh | Článek v odborném periodiku |
| Časopis / Zdroj | Journal of Chemichal Information a Modeling |
| Fakulta / Pracoviště MU | |
| Citace | |
| www | http://pubs.acs.org/doi/pdf/10.1021/ci400448n |
| Doi | http://dx.doi.org/10.1021/ci400448n |
| Obor | Biochemie |
| Klíčová slova | MOLECULAR ELECTROSTATIC POTENTIALS; PREDICTING PK(A) VALUES; DYNAMICS SIMULATIONS; POPULATION ANALYSIS; ORGANIC-MOLECULES; DIPOLE-MOMENTS; METHOD EEM; BASIS-SET; VALIDATION; SCHEMES |
| Přiložené soubory | |
| Popis | We focused on the parametrization and evaluation of empirical models for fast and accurate calculation of conformationally dependent atomic charges in proteins. The models were based on the electronegativity equalization method (EEM), and the parametrization procedure was tailored to proteins. We used large protein fragments as reference structures and fitted the EEM model parameters using atomic charges computed by three population analyses (Mulliken, Natural, iterative Hirshfeld), at the Hartre-Fock level with two basis sets (6-31G*, 6-31G**) and in two environments (gas phase, implicit solvation). We parametrized and successfully validated 24 EEM models. When tested on insulin and ubiquitin, all models reproduced quantum mechanics level charges well and were consistent with respect to population analysis and basis set. Specifically, the models showed on average a correlation of 0.961, RMSD 0.097 e, and average absolute error per atom 0.072 e. The EEM models can be used with the freely available EEM implementation EEM_SOLVER. |
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