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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 Journal of Peptide S...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
Journal of Peptide Science
Article . 2021 . Peer-reviewed
License: Wiley Online Library User Agreement
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The first non‐helical Aib‐containing hexapeptide: The crystal structure of Z‐Gly‐Aib‐Gly‐Aib‐Gly‐Aib‐OtBu

Authors: Renate Gessmann; Hans Brückner; Kyriacos Petratos;

The first non‐helical Aib‐containing hexapeptide: The crystal structure of Z‐Gly‐Aib‐Gly‐Aib‐Gly‐Aib‐OtBu

Abstract

The synthetic peptide Z‐Gly‐Aib‐Gly‐Aib‐Gly‐Aib‐OtBu was crystallized from a mixture of ethyl acetate and n‐hexane. The crystals belong to the centrosymmetric space group Pbca. There are three molecules in the asymmetric unit. The three molecules differ mainly in the Z‐group conformation. The first Gly residue adopts a fully extended conformation, residues 2 and 3 lie in the left‐handed helical region, residues 4 and 5 in the right‐handed helical region, and residue 6 again in the left‐handed helical region of the Ramachandran plot. There are only two of four possible intramolecular hydrogen bonds formed, namely, between Aib4 and Gly1 forming a β‐turn of type III′ and between Aib6 and Gly3 forming a β‐turn of type I. The inverted molecules (by space group symmetry) lie in the regions with opposite handedness and form β‐turns of type III and I′. In contrast to all known long synthetic and naturally occurring Aib‐containing peptides that fold as 310‐ or α‐helix, Z‐(Gly‐Aib)3‐OtBu folds in a quite flat structure from which only the protecting groups bulge out.

Keywords

Models, Molecular, Aminoisobutyric Acids, Crystallography, X-Ray, Oligopeptides

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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!
2
Average
Average
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