Anti-cooperative ligand binding and dimerisation in the glycopeptide antibiotic dalbavancin
Author:
Affiliation:
1. Division of Chemistry and Structural Biology
2. Institute for Molecular Bioscience
3. The University of Queensland
4. Brisbane, Australia
Abstract
Dalbavancin, a semi-synthetic glycopeptide with enhanced antibiotic activity compared to vancomycin and teicoplanin, dimerises strongly in an anti-cooperative manner with ligand binding.
Funder
National Health and Medical Research Council
Wellcome Trust
Publisher
Royal Society of Chemistry (RSC)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
http://pubs.rsc.org/en/content/articlepdf/2014/OB/C3OB42428F
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