Skip to Main content Skip to Navigation
Journal articles

Binding evaluation of fragment-based scaffolds for probing allosteric enzymes.

Abstract : Fragment-based drug discovery has become a powerful method for the generation of drug leads against therapeutic targets. Beyond the identification of novel and effective starting points for drug design, fragments have emerged as reliable tools for assessing protein druggability and identifying protein hot spots. Here, we have examined fragments resulting from the deconstruction of known inhibitors from the glycogen phosphorylase enzyme, a therapeutic target against type 2 diabetes, with two motivations. First, we have analyzed the fragment binding to the multiple binding sites of the glycogen phosphorylase, and then we have investigated the use of fragments to study allosteric enzymes. The work we report illustrates the power of fragmentlike ligands not only for probing the various binding pockets of proteins, but also for uncovering cooperativity between these various binding sites.
Complete list of metadatas

https://hal.archives-ouvertes.fr/hal-00691495
Contributor : Frédérique Depierre <>
Submitted on : Thursday, April 26, 2012 - 1:50:00 PM
Last modification on : Friday, April 17, 2020 - 10:46:09 AM

Identifiers

Citation

Isabelle Krimm, Jean-Marc Lancelin, Jean-Pierre Praly. Binding evaluation of fragment-based scaffolds for probing allosteric enzymes.. Journal of Medicinal Chemistry, American Chemical Society, 2012, 55 (3), pp.1287-95. ⟨10.1021/jm201439b⟩. ⟨hal-00691495⟩

Share

Metrics

Record views

273