Cargando…
Computational Redesign of Bacterial Biotin Carboxylase Inhibitors Using Structure-Based Virtual Screening of Combinatorial Libraries
As the spread of antibiotic resistant bacteria steadily increases, there is an urgent need for new antibacterial agents. Because fatty acid synthesis is only used for membrane biogenesis in bacteria, the enzymes in this pathway are attractive targets for antibacterial agent development. Acetyl-CoA c...
Autores principales: | Brylinski, Michal, Waldrop, Grover L. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2014
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6271951/ https://www.ncbi.nlm.nih.gov/pubmed/24699146 http://dx.doi.org/10.3390/molecules19044021 |
Ejemplares similares
-
Mechanism of biotin carboxylase inhibition by ethyl 4-[[2-chloro-5-(phenylcarbamoyl)phenyl]sulphonylamino]benzoate
por: Craft, Matthew K., et al.
Publicado: (2021) -
Early evolution of the biotin-dependent carboxylase family
por: Lombard, Jonathan, et al.
Publicado: (2011) -
Correction: Early evolution of the biotin-dependent carboxylase family
por: Lombard, Jonathan, et al.
Publicado: (2012) -
Pyrrolocin C and equisetin inhibit bacterial acetyl-CoA carboxylase
por: Larson, Erica C., et al.
Publicado: (2020) -
A graph-based approach to construct target-focused libraries for virtual screening
por: Naderi, Misagh, et al.
Publicado: (2016)