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image/svg+xml Jakob Voss, based on art designer at PLoS, modified by Wikipedia users Nina and Beao Closed Access logo, derived from PLoS Open Access logo. This version with transparent background. http://commons.wikimedia.org/wiki/File:Closed_Access_logo_transparent.svg Jakob Voss, based on art designer at PLoS, modified by Wikipedia users Nina and Beao Proteins Structure F...arrow_drop_down
image/svg+xml Jakob Voss, based on art designer at PLoS, modified by Wikipedia users Nina and Beao Closed Access logo, derived from PLoS Open Access logo. This version with transparent background. http://commons.wikimedia.org/wiki/File:Closed_Access_logo_transparent.svg Jakob Voss, based on art designer at PLoS, modified by Wikipedia users Nina and Beao
Proteins Structure Function and Bioinformatics
Article . 2008 . Peer-reviewed
License: Wiley Online Library User Agreement
Data sources: Crossref
UQ eSpace
Article . 2009
Data sources: UQ eSpace
UQ eSpace
Article . 2009
Data sources: UQ eSpace
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Calcium binding to the purple membrane: A molecular dynamics study

A molecular dynamics study
Authors: Wassenaar, Tsjerk A.; Daura, Xavier; Padros, Esteve; Mark, Alan E.;

Calcium binding to the purple membrane: A molecular dynamics study

Abstract

AbstractThe purple membrane (PM) is a specialized membrane patch found in halophilic archaea, containing the photoreceptor bacteriorhodopsin (bR). It is long known that calcium ions bind to the PM, but their position and role remain elusive to date. Molecular dynamics simulations in conjunction with a highly detailed model of the PM have been used to investigate the stability of calcium ions placed at three proposed cation binding sites within bR, one near the Schiff base, one in the region of the proton release group, and one near Glu9. The simulations suggest that, of the sites investigated, the binding of calcium ions was most likely at the proton release group. Binding in the region of the Schiff base, while possible, was associated with significant changes in local geometry. Calcium ions placed near Glu9 in the interior of bR (simultaneously to a Ca2+ near the Schiff base and another one near the Glu194–Glu204 site) were not stable. The results obtained are discussed in relation to recent experimental observations and theoretical considerations. Proteins 2009. © 2008 Wiley‐Liss, Inc.

Countries
Australia, Netherlands
Keywords

Models, Molecular, RETINAL POCKET, CATION-BINDING, ANGSTROM RESOLUTION, Glutamic Acid, Crystallography, X-Ray, C1, WATER-MOLECULES, Purple Membrane, PROTON-TRANSFER, Computer Simulation, cation binding, Schiff Bases, model, TO-BLUE TRANSITION, Binding Sites, bacteriorhodopsin, 540, simulation, M-INTERMEDIATE, bond valence sum, ELECTRON CRYSTALLOGRAPHY, 970106 Expanding Knowledge in the Biological Sciences, FORCE-FIELD, 060112 Structural Biology (incl. Macromolecular Modelling), Calcium, STRUCTURAL-CHANGES

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selected citations
These citations are derived from selected sources.
This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Citations provided by BIP!
popularity
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
BIP!Popularity provided by BIP!
influence
This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Influence provided by BIP!
impulse
This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
BIP!Impulse provided by BIP!
5
Average
Average
Average
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