Fragment-based drug discovery and mechanistic studies of human thymidylate synthase
Human thymidylate synthase (hTS) is the sole enzyme responsible for de novo biosynthesis of dTMP and is vital to cell proliferation and survival. Inhibition of hTS has been explored and found to be effective in cancer chemotherapy, while the efficacy is limited by drug resistance. Herein fragment sc...
Main Author: | Chen, Dan |
---|---|
Other Authors: | - |
Format: | Thesis-Doctor of Philosophy |
Language: | English |
Published: |
Nanyang Technological University
2016
|
Subjects: | |
Online Access: | https://hdl.handle.net/10356/65932 |
Similar Items
-
Structural analyses of human thymidylate synthase reveal a site that may control conformational switching between active and inactive states
by: Chen, Dan, et al.
Published: (2018) -
Unique structural and mechanistic properties of mycobacterial F-ATP synthases : implications for drug design
by: Kamariah, Neelagandan, et al.
Published: (2020) -
The molecular motor F-ATP synthase is targeted by the tumoricidal protein HAMLET
by: Ho, James, et al.
Published: (2015) -
Insights into the programmed ketoreduction of partially reducing polyketide synthases : stereo- and substrate-specificity of the ketoreductase domain
by: Soehano, Ishin, et al.
Published: (2015) -
Genes implicated in phorbol ester (PE) biosynthesis and interception through downregulation of casbene synthase genes
by: Ng, Ailing
Published: (2014)