Cargando…
Structural basis for exploring the allosteric inhibition of human kidney type glutaminase
Cancer cells employ glutaminolysis to provide a source of intermediates for their upregulated biosynthetic needs. Glutaminase, which catalyzes the conversion of glutamine to glutamate, is gaining increasing attention as a potential drug target. Small-molecule inhibitors such as BPTES and CB-839, whi...
Autores principales: | Ramachandran, Sarath, Pan, Catherine Qiurong, Zimmermann, Sarah C., Duvall, Bridget, Tsukamoto, Takashi, Low, Boon Chuan, Sivaraman, J. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5295402/ https://www.ncbi.nlm.nih.gov/pubmed/27462863 http://dx.doi.org/10.18632/oncotarget.10791 |
Ejemplares similares
-
Structural Basis for the Active Site Inhibition Mechanism of Human Kidney-Type Glutaminase (KGA)
por: Thangavelu, K., et al.
Publicado: (2014) -
Allosteric Glutaminase Inhibitors Based on a 1,4-Di(5-amino-1,3,4-thiadiazol-2-yl)butane
Scaffold
por: Zimmermann, Sarah C., et al.
Publicado: (2016) -
Self-Assembled Micellar Glutaminase Allosteric Inhibitor for Effective Therapeutic Intervention
por: Fang, Jinzhang, et al.
Publicado: (2022) -
Upregulation of the Glutaminase II Pathway Contributes to Glutamate Production upon Glutaminase 1 Inhibition in Pancreatic Cancer
por: Udupa, Sunag, et al.
Publicado: (2019) -
Dendrimer-conjugated glutaminase inhibitor selectively targets microglial glutaminase in a mouse model of Rett syndrome
por: Khoury, Elizabeth Smith, et al.
Publicado: (2020)