Investigation of the mycobacterial enzyme HsaD as a potential novel target for anti-tubercular agents using a fragment-based drug design approach

Author:

Ryan Ali1ORCID,Polycarpou Elena1,Lack Nathan A23,Evangelopoulos Dimitrios456ORCID,Sieg Christian1,Halman Alice1,Bhakta Sanjib4,Eleftheriadou Olga1,McHugh Timothy D5ORCID,Keany Sebastian2,Lowe Edward D7,Ballet Romain2,Abuhammad Areej8,Jacobs William R9,Ciulli Alessio1011ORCID,Sim Edith12ORCID

Affiliation:

1. Faculty of Science, Engineering and Computing; Kingston University London; Kingston upon Thames UK

2. Department of Pharmacology; University of Oxford; Oxford UK

3. School of Medicine; Koç University; Istanbul Turkey

4. Mycobacteria Research Laboratory, Institute of Structural and Molecular Biology, Department of Biological Sciences; Birkbeck, University of London; London UK

5. Centre for Clinical Microbiology; University College London, Royal Free Campus; London UK

6. Mycobacterial Metabolism and Antibiotic Research Laboratory; The Francis Crick Institute, Mill Hill Laboratory; London UK

7. Department of Biochemistry; University of Oxford; Oxford UK

8. School of Pharmacy; University of Jordan; Amman Jordan

9. Department of Microbiology and Immunology; Howard Hughes Medical Institute, Albert Einstein College of Medicine; Bronx New York USA

10. Department of Chemistry; University of Cambridge; Cambridge UK

11. Division of Biological Chemistry & Drug Discovery, School of Life Sciences; University of Dundee, James Black Centre; Dundee UK

Publisher

Wiley

Subject

Pharmacology

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3. Recent advances in Fragment-based strategies against tuberculosis;European Journal of Medicinal Chemistry;2023-10

4. Direct capture, inhibition and crystal structure of HsaD (Rv3569c) from M. tuberculosis;The FEBS Journal;2022-10-13

5. The unusual convergence of steroid catabolic pathways in Mycobacterium abscessus;Proceedings of the National Academy of Sciences;2022-09-26

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