Cargando…
Structural Basis for Inhibition of Human Primase by Arabinofuranosyl Nucleoside Analogues Fludarabine and Vidarabine
[Image: see text] Nucleoside analogues are widely used in clinical practice as chemotherapy drugs. Arabinose nucleoside derivatives such as fludarabine are effective in the treatment of patients with acute and chronic leukemias and non-Hodgkin’s lymphomas. Although nucleoside analogues are generally...
Autores principales: | Holzer, Sandro, Rzechorzek, Neil J., Short, Isobel R., Jenkyn-Bedford, Michael, Pellegrini, Luca, Kilkenny, Mairi L. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical
Society
2019
|
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6757278/ https://www.ncbi.nlm.nih.gov/pubmed/31479243 http://dx.doi.org/10.1021/acschembio.9b00367 |
Ejemplares similares
-
Structural basis for the interaction of SARS‐CoV‐2 virulence factor nsp1 with DNA polymerase α–primase
por: Kilkenny, Mairi L., et al.
Publicado: (2021) -
Primer synthesis by a eukaryotic-like archaeal primase is independent of its Fe-S cluster
por: Holzer, Sandro, et al.
Publicado: (2017) -
The human CTF4-orthologue AND-1 interacts with DNA polymerase α/primase via its unique C-terminal HMG box
por: Kilkenny, Mairi L., et al.
Publicado: (2017) -
A Conserved Motif in the C-terminal Tail of DNA Polymerase α Tethers Primase to the Eukaryotic Replisome
por: Kilkenny, Mairi L., et al.
Publicado: (2012) -
An Enzymatic Flow-Based Preparative Route to Vidarabine
por: Tamborini, Lucia, et al.
Publicado: (2020)