Common folding processes of mini‐proteins: Partial formations of secondary structures initiate the immediate protein folding. Issue 11 (13th February 2017)
- Record Type:
- Journal Article
- Title:
- Common folding processes of mini‐proteins: Partial formations of secondary structures initiate the immediate protein folding. Issue 11 (13th February 2017)
- Main Title:
- Common folding processes of mini‐proteins: Partial formations of secondary structures initiate the immediate protein folding
- Authors:
- Harada, Ryuhei
Takano, Yu
Shigeta, Yasuteru - Abstract:
- Abstract : The folding processes of mini‐proteins (FSD‐EY/FBPWW28 domain) were computationally investigated by an enhanced conformational sampling method. Through the analyses of trajectories, these mini‐proteins had multiple folding pathways different from a simple two‐state folding, and the multiple folding processes were initiated by partial formations of secondary structures. These findings can be used to understand the folding of large proteins, that is, which secondary structures are partially folded in the early process, and how the remaining parts are sequentially folded. It is found that FSD‐EY (α/β topology) folds by a simple diffusion‐collision mechanism, while the folding process of the FBPWW28 domain (all‐β topology) requires a modification of the diffusion‐collision theory to adequately treat the coil‐sheet transition for the β sheet formation. © 2017 Wiley Periodicals, Inc. Abstract : The folding processes of mini‐proteins (FSD‐EY/FBPWW28 domain) were computationally investigated. Through the analyses of trajectories, these mini‐proteins had multiple folding pathways, and their folding processes were initiated by partial formations of secondary structures, that is, FSD‐EY (α/β topology) folds by a simple diffusion‐collision mechanism, while the folding process of the FBPWW28 domain (all‐β topology) requires a modification of the diffusion‐collision theory to adequately treat the coil‐sheet transition for the β sheet formation.
- Is Part Of:
- Journal of computational chemistry. Volume 38:Issue 11(2017)
- Journal:
- Journal of computational chemistry
- Issue:
- Volume 38:Issue 11(2017)
- Issue Display:
- Volume 38, Issue 11 (2017)
- Year:
- 2017
- Volume:
- 38
- Issue:
- 11
- Issue Sort Value:
- 2017-0038-0011-0000
- Page Start:
- 790
- Page End:
- 797
- Publication Date:
- 2017-02-13
- Subjects:
- protein folding -- molecular dynamics simulation -- enhanced conformational sampling -- folding pathway
Chemistry -- Data processing -- Periodicals
542.85 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1096-987X ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/jcc.24748 ↗
- Languages:
- English
- ISSNs:
- 0192-8651
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 4963.460000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 382.xml