Cargando…
Enduracididine, a rare amino acid component of peptide antibiotics: Natural products and synthesis
Rising resistance to current clinical antibacterial agents is an imminent threat to global public health and highlights the demand for new lead compounds for drug discovery. One such potential lead compound, the peptide antibiotic teixobactin, was recently isolated from an uncultured bacterial sourc...
Autores principales: | Atkinson, Darcy J, Naysmith, Briar J, Furkert, Daniel P, Brimble, Margaret A |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Beilstein-Institut
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5238550/ https://www.ncbi.nlm.nih.gov/pubmed/28144300 http://dx.doi.org/10.3762/bjoc.12.226 |
Ejemplares similares
-
Teixobactin analogues reveal enduracididine to be non-essential for highly potent antibacterial activity and lipid II binding
por: Parmar, Anish, et al.
Publicado: (2017) -
Screening a Natural Product-Inspired Library for Anti-Phytophthora Activities
por: Lawrence, Scott A., et al.
Publicado: (2021) -
Mechanistic and structural insights into a divergent PLP-dependent L-enduracididine cyclase from a toxic cyanobacterium
por: Cordoza, Jennifer L., et al.
Publicado: (2023) -
Mechanistic and
Structural Insights into a Divergent
PLP-Dependent l-Enduracididine Cyclase from a Toxic
Cyanobacterium
por: Cordoza, Jennifer L., et al.
Publicado: (2023) -
Halogenation of glycopeptide antibiotics occurs at the amino acid level during non-ribosomal peptide synthesis
por: Kittilä, Tiia, et al.
Publicado: (2017)