Desleucyl-Oritavancin with a Damaged d-Ala-d-Ala Binding Site Inhibits the Transpeptidation Step of Cell-Wall Biosynthesis in Whole Cells of Staphylococcus aureus-Reference-Cited by-同舟云学术

Desleucyl-Oritavancin with a Damaged d-Ala-d-Ala Binding Site Inhibits the Transpeptidation Step of Cell-Wall Biosynthesis in Whole Cells of Staphylococcus aureus

Published:2017-03-03 Issue:10 Volume:56 Page:1529-1535
ISSN:0006-2960
Container-title:Biochemistry
language:en
Short-container-title:Biochemistry

Author:

Kim Sung Joon¹^ORCID,Singh Manmilan²,Sharif Shasad²,Schaefer Jacob²^ORCID

Affiliation:

1. Department of Chemistry and Biochemistry, Baylor University, 101 Bagby Avenue, Waco, Texas 76798, United States

2. Department of Chemistry, Washington University, One Brookings Drive, St. Louis, Missouri 63130, United States

Funder

National Institute of General Medical Sciences

Publisher

American Chemical Society (ACS)

Subject

Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.biochem.6b01125

Reference24 articles.

1. Synthesis and Mode of Action of Hydrophobic Derivatives of the Glycopeptide Antibiotic Eremomycin and Des-(N-methyl-d-leucyl)eremomycin against Glycopeptide-Sensitive and -Resistant Bacteria

2. Reductive Alkylation of Glycopeptide Antibiotics: Synthesis and Antibacterial Activity.

3. Activity of Oritavancin (LY333328), an Investigational Glycopeptide, Compared to That of Vancomycin against Multidrug-Resistant Streptococcus pneumoniae in an In Vitro Pharmacodynamic Model

4. Cooperativity in ligand binding expressed at a model cell membrane by the vancomycin group antibiotics

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