Mycobacterium tuberculosis PanD structure-function analysis and identification of a potent pyrazinoic acid-derived enzyme inhibitor
A common strategy employed in antibacterial drug discovery is targeting of biosynthetic processes which are essential and specific for the pathogen. Specificity in particular avoids undesirable interactions with potential enzymatic counterparts in the human host, and ensures on-target toxicity. S...
Main Authors: | Ragunathan, Priya, Cole, Malcolm, Latka, Chitra, Aragaw, Wassihun Wedajo, Hegde, Pooja, Shin, Joon, Manimekalai, Malathy Sony Subramanian, Rishikesan, Sankaranarayanan, Aldrich, Courtney C., Dick, Thomas, Grüber, Gerhard |
---|---|
其他作者: | School of Biological Sciences |
格式: | Journal Article |
語言: | English |
出版: |
2022
|
主題: | |
在線閱讀: | https://hdl.handle.net/10356/155645 |
相似書籍
-
Structural and mechanistic insights into Mycobacterium abscessus as-partate decarboxylase PanD and a pyrazinoic acid-derived inhibitor
由: Saw, Wuan Geok, et al.
出版: (2022) -
Structure activity relationship of pyrazinoic acid analogs as potential antimycobacterial agents
由: Hegde, Pooja V., et al.
出版: (2023) -
Quantitative MODS-Wayne assay for rapid detection of pyrazinamide resistance in Mycobacterium tuberculosis from sputum samples
由: Emily Toscano-Guerra, et al.
出版: (2024-12-01) -
A conserved oxalyl-coenzyme A decarboxylase in oxalate catabolism
由: Ninghui Cheng, et al.
出版: (2022-12-01) -
Crystallization and preliminary X-ray crystallographic analysis of subunit F (F1-94), an essential coupling subunit of the eukaryotic V1VO-ATPase from Saccharomyces cerevisiae
由: Basak, Sandip, et al.
出版: (2013)