Conformational promiscuity in triazolamers derived from quaternary amino acids mimics peptide behaviour

descriptionPublicationkeyboard_double_arrow_right Article 01 Jan 2015 English Publisher:Royal Society of Chemistry (RSC)Journal:Organic & Biomolecular Chemistry, volume 13, pages 10,797-10,801 (issn: 1477-0520, eissn: 1477-0539,

Copyright policy )

Authors: Solà Oller, Jordi; Bolte, Michael; Alfonso, Ignacio;

doi: 10.1039/c5ob01461a

pmid: 26455861

handle: 10261/128330

Conformational promiscuity in triazolamers derived from quaternary amino acids mimics peptide behaviour

- Summary
- Subjects
- Metrics

Abstract

Oligomers made by click chemistry display a duality of secondary structures similar to natural peptides as inferred by NMR spectroscopy and X-ray diffraction experiments.

Related Organizations

Spanish National Research Council
Spain
Goethe University Frankfurt
Germany
Institute of Advanced Chemistry of Catalonia
Spain

Keywords

Models, Molecular, Amino acid derivatives, Crystal state, Triazoles, Crystallography, X-Ray, Protein Structure, Secondary, Zig-zag, Ordered structures, Natural peptide, Solvents, Amino Acid Sequence, Amino Acids, Peptides, Nuclear Magnetic Resonance, Biomolecular

Impact byBIP!

	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).	6
	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.	Average
	influence This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).	Average
	impulse This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.	Top 10%