A new set of molecular mechanics parameters for hydroxyproline and its use in molecular dynamics simulations of collagen-like peptides

Copyright 2005 Wiley Periodicals, Inc.

Bibliographische Detailangaben
Veröffentlicht in:Journal of computational chemistry. - 1984. - 26(2005), 15 vom: 30. Nov., Seite 1612-6
1. Verfasser: Park, Sanghyun (VerfasserIn)
Weitere Verfasser: Radmer, Randall J, Klein, Teri E, Pande, Vijay S
Format: Aufsatz
Sprache:English
Veröffentlicht: 2005
Zugriff auf das übergeordnete Werk:Journal of computational chemistry
Schlagworte:Journal Article Research Support, N.I.H., Extramural Research Support, U.S. Gov't, P.H.S. Peptides Collagen 9007-34-5 Hydroxyproline RMB44WO89X
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245 1 2 |a A new set of molecular mechanics parameters for hydroxyproline and its use in molecular dynamics simulations of collagen-like peptides 
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520 |a Recently, the importance of proline ring pucker conformations in collagen has been suggested in the context of hydroxylation of prolines. The previous molecular mechanics parameters for hydroxyproline, however, do not reproduce the correct pucker preference. We have developed a new set of parameters that reproduces the correct pucker preference. Our molecular dynamics simulations of proline and hydroxyproline monomers as well as collagen-like peptides, using the new parameters, support the theory that the role of hydroxylation in collagen is to stabilize the triple helix by adjusting to the right pucker conformation (and thus the right phi angle) in the Y position 
650 4 |a Journal Article 
650 4 |a Research Support, N.I.H., Extramural 
650 4 |a Research Support, U.S. Gov't, P.H.S. 
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700 1 |a Radmer, Randall J  |e verfasserin  |4 aut 
700 1 |a Klein, Teri E  |e verfasserin  |4 aut 
700 1 |a Pande, Vijay S  |e verfasserin  |4 aut 
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