Structure of the <scp>d</scp>-Cycloserine-Resistant Variant D322N of Alanine Racemase from <i>Mycobacterium tuberculosis</i>-Reference-Cited by-同舟云学术

Structure of the d-Cycloserine-Resistant Variant D322N of Alanine Racemase from Mycobacterium tuberculosis

Published:2023-03-27 Issue:3 Volume:3 Page:233-239
ISSN:2694-2437
Container-title:ACS Bio & Med Chem Au
language:en
Short-container-title:ACS Bio Med Chem Au

Author:

de Chiara Cesira¹,Prosser Gareth A.¹,Ogrodowicz Roksana²,de Carvalho Luiz P. S.¹³^ORCID

Affiliation:

1. Mycobacterial Metabolism and Antibiotic Research Laboratory, The Francis Crick Institute, London, NW1 1AT, United Kingdom

2. Structural Biology Science Technology Platform, The Francis Crick Institute, London, NW1 1AT, United Kingdom

3. Department of Chemistry, The Herbert Wertheim UF Scripps Institute for Biomedical Innovation & Technology, Jupiter, Florida 33458, United States

Funder

Medical Research Council

Wellcome Trust

Cancer Research UK

Publisher

American Chemical Society (ACS)

Subject

Pharmaceutical Science,Drug Discovery,Molecular Biology,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acsbiomedchemau.2c00074

Reference17 articles.

1. Enzymes in the D-alanine branch of bacterial cell wall peptidoglycan assembly

2. Best drug treatment for multidrug-resistant and extensively drug-resistant tuberculosis

3. WHO. WHO consolidated guidelines on tuberculosis: Module 4: Treatment - Drug-resistant tuberculosis treatment. June 15, 2020. https://www.who.int/publications/i/item/9789240006997.

4. Comparative fitness analysis of D-cycloserine resistant mutants reveals both fitness-neutral and high-fitness cost genotypes

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