Temperature-pressure shuffling outlier flooding method enhances the conformational sampling of proteins

© 2019 Wiley Periodicals, Inc.

Bibliographische Detailangaben
Veröffentlicht in:Journal of computational chemistry. - 1984. - 40(2019), 15 vom: 05. Juni, Seite 1530-1537
1. Verfasser: Harada, Ryuhei (VerfasserIn)
Weitere Verfasser: Yoshino, Ryunosuke, Nishizawa, Hiroaki, Shigeta, Yasuteru
Format: Online-Aufsatz
Sprache:English
Veröffentlicht: 2019
Zugriff auf das übergeordnete Werk:Journal of computational chemistry
Schlagworte:Journal Article Research Support, Non-U.S. Gov't Enhanced Sampling of Proteins Extended OFLOOD Molecular Dynamics Protein Folding Trp-Cage Proteins
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245 1 0 |a Temperature-pressure shuffling outlier flooding method enhances the conformational sampling of proteins 
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520 |a Outlier flooding method (OFLOOD) is an efficient conformational sampling method developed by the authors. In the present study, to further enhance the conformational sampling efficiency, a set of parameters (temperatures and pressures) specified as inputs in the original OFLOOD were shuffled before restarting the short-time molecular dynamics (MD) simulations. Because of the diversity of these parameters, it was confirmed that the extended OFLOOD becomes superior to the original one in finding the folding pathways of Trp-cage. © 2019 Wiley Periodicals, Inc 
650 4 |a Journal Article 
650 4 |a Research Support, Non-U.S. Gov't 
650 4 |a Enhanced Sampling of Proteins 
650 4 |a Extended OFLOOD 
650 4 |a Molecular Dynamics 
650 4 |a Protein Folding 
650 4 |a Trp-Cage 
650 7 |a Proteins  |2 NLM 
700 1 |a Yoshino, Ryunosuke  |e verfasserin  |4 aut 
700 1 |a Nishizawa, Hiroaki  |e verfasserin  |4 aut 
700 1 |a Shigeta, Yasuteru  |e verfasserin  |4 aut 
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