期刊
JOURNAL OF CHEMICAL THEORY AND COMPUTATION
卷 12, 期 2, 页码 714-727出版社
AMER CHEMICAL SOC
DOI: 10.1021/acs.jctc.5b01211
关键词
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资金
- Ministero dell'Universita e della Ricerca (PRIN) [2010NRREPL]
- Universita degli Studi di Milano
- CINECA
- Regione Lombardia award under LISA initiative
Replica exchange molecular dynamics simulations were performed to test the ability of six AMBER force fields and three implicit solvent models of predicting the native conformation of two helical peptides, three beta-hairpins, and three intrinsically disordered peptides. Although a combination of the force field and implicit solvation models able to accurately predict the native structure of all the considered peptides was not identified, we found that the GB-Neck2 model seems to well compensate for some of the conformational biases showed by ff96 and ff99SB/ildn/ildn-phi. Indeed, the force fields of the ff99SB series coupled with GB-Neck2 reasonably discriminated helices from disordered peptides, while a good prediction of beta-hairpin conformations was only achieved by performing two independent simulations: one with the ff96/GB-Neck2 combination and the other with GB-Neck2 coupled with any of the ff99SB/ildn/ildn-phi force fields.
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