Allosteric Targeting of the Fanconi Anemia Ubiquitin-Conjugating Enzyme Ube2T by Fragment Screening
Author(s) -
Francesca Morreale,
Alessio Bortoluzzi,
Viduth K. Chaugule,
Connor Arkinson,
Helen Walden,
Alessio Ciulli
Publication year - 2017
Publication title -
journal of medicinal chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.01
H-Index - 261
eISSN - 1520-4804
pISSN - 0022-2623
DOI - 10.1021/acs.jmedchem.7b00147
Subject(s) - ubiquitin conjugating enzyme , ubiquitin , fanconi anemia , chemistry , allosteric regulation , enzyme , dna , in vitro , biochemistry , ubiquitin ligase , dna repair , gene
Ube2T is the E2 ubiquitin-conjugating enzyme of the Fanconi anemia DNA repair pathway and it is overexpressed in several cancers, representing an attractive target for the development of inhibitors. Despite the extensive efforts in targeting the ubiquitin system, very few E2 binders have currently been discovered. Herein we report the identification of a new allosteric pocket on Ube2T through a fragment screening using biophysical methods. Several fragments binding to this site inhibit ubiquitin conjugation in vitro.
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