Inhibitors Incorporating Zinc‐Binding Groups Target the GlcNAc‐PI de‐N‐acetylase inTrypanosoma brucei, the Causative Agent of African Sleeping Sickness
Author:
Affiliation:
1. Division of Biological Chemistry and Drug Discovery, College of Life Sciences, University of Dundee, Dundee DD1 5EH, UK
Publisher
Wiley
Subject
Molecular Medicine,Biochemistry,Drug Discovery,Pharmacology,Organic Chemistry
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1111/j.1747-0285.2011.01300.x
Reference36 articles.
1. The structure, biosynthesis and function of glycosylphosphatidyl inositol anchors, and the contributions of trypanosome research;Ferguson M.A.J.;J Cell Sci,1999
2. Critical roles of glycosylphosphatidylinositol for Trypanosoma brucei
3. Cloning of Trypanosoma brucei and Leishmania major Genes Encoding the GlcNAc-Phosphatidylinositol De-N-acetylase of Glycosylphosphatidylinositol Biosynthesis That Is Essential to the African Sleeping Sickness Parasite
4. Essential Roles for GPI-anchored Proteins in African Trypanosomes Revealed Using Mutants Deficient in GPI8
5. Chemical validation of GPI biosynthesis as a drug target against African sleeping sickness
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2. Bioisosteres of Carbohydrate Functional Groups in Glycomimetic Design;Biomimetics;2019-07-28
3. Targeting the GPI biosynthetic pathway;Pathogens and Global Health;2018-02-27
4. In silico drug re-purposing against African sleeping sickness using GlcNAc-PI de- N -acetylase as an experimental target;Computational Biology and Chemistry;2015-12
5. Fragment screening reveals salicylic hydroxamic acid as an inhibitor of Trypanosoma brucei GPI GlcNAc-PI de-N-acetylase;Carbohydrate Research;2014-03
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