Robust Chemoenzymatic Synthesis of Keratinimicin Aglycone Analogues Facilitated by the Structure and Selectivity of OxyB-Reference-Cited by-同舟云学术

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Robust Chemoenzymatic Synthesis of Keratinimicin Aglycone Analogues Facilitated by the Structure and Selectivity of OxyB

Published:2023-07-05 Issue:7 Volume:18 Page:1473-1479
ISSN:1554-8929
Container-title:ACS Chemical Biology
language:en
Short-container-title:ACS Chem. Biol.

Author:

Hauser Nicole¹^ORCID,Ireland Kendra A.²^ORCID,Chioti Vasiliki T.¹,Forneris Clarissa C.¹,Davis Katherine M.²^ORCID,Seyedsayamdost Mohammad R.¹³^ORCID

Affiliation:

1. Department of Chemistry, Princeton University, Princeton, New Jersey 08544, United States

2. Department of Chemistry, Emory University, Atlanta, Georgia 30322, United States

3. Department of Molecular Biology, Princeton University, Princeton, New Jersey 08544, United States

Funder

Division of Chemistry

Schweizerischer Nationalfonds zur F?rderung der Wissenschaftlichen Forschung

National Institute of General Medical Sciences

Publisher

American Chemical Society (ACS)

Subject

Molecular Medicine,General Medicine,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acschembio.3c00192

Reference40 articles.

1. Specificity of combination between mucopeptide precursors and vancomycin or ristocetin

2. Modifications of the acyl-d-alanyl-d-alanine terminus affecting complex-formation with vancomycin

3. Molecular basis of the activity of antibiotics of the vancomycin group

4. Crystal structure of vancomycin

5. Glycopeptide and Lipoglycopeptide Antibiotics

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