Cargando…
Use of Broken-Symmetry Density Functional Theory To Characterize the IspH Oxidized State: Implications for IspH Mechanism and Inhibition
[Image: see text] With current therapies becoming less efficacious due to increased drug resistance, new inhibitors of both bacterial and malarial targets are desperately needed. The recently discovered methylerythritol phosphate (MEP) pathway for isoprenoid synthesis provides novel targets for the...
Autores principales: | Blachly, Patrick G., Sandala, Gregory M., Giammona, Debra Ann, Liu, Tiqing, Bashford, Donald, McCammon, J. Andrew, Noodleman, Louis |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American
Chemical Society
2014
|
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4159220/ https://www.ncbi.nlm.nih.gov/pubmed/25221444 http://dx.doi.org/10.1021/ct5005214 |
Ejemplares similares
-
Broken-Symmetry DFT Computations for the Reaction
Pathway of IspH, an Iron–Sulfur Enzyme in Pathogenic Bacteria
por: Blachly, Patrick G., et al.
Publicado: (2015) -
IspH–RPS1 and IspH–UbiA: “Rosetta stone” proteins
por: Rao, Guodong, et al.
Publicado: (2015) -
Utilizing a Dynamical Description of IspH to Aid in the Development of Novel Antimicrobial Drugs
por: Blachly, Patrick G., et al.
Publicado: (2013) -
Insights
into the Binding of Pyridines to the Iron–Sulfur
Enzyme IspH
por: Span, Ingrid, et al.
Publicado: (2014) -
IspH inhibitors kill Gram-negative bacteria and mobilize immune clearance
por: Singh, Kumar Sachin, et al.
Publicado: (2021)