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Published February 25, 2022 | Version 1
Dataset Open

Dipeptidyl peptidase 11 (PgDPP11); A Target Enabling Package

  • 1. Centre for Medicines Discovery, Nuffield Department of Medicine, University of Oxford
  • 2. Department of Oral Molecular Biology, Nagasaki University

Description

Porphyromonas gingivalis (P. gingivalis) is the main causative agent of Periodontitis, the most widespread inflammatory condition world-wide. Recently this organism has been implicated in several systemic conditions, such as Alzheimer’s disease and type 2 diabetes. P. gingivalis does not ferment carbohydrates, instead it uses proteases to generate energy and carbon source. Dipeptidyl peptidase 11 plays a central role in the energy metabolism of this bacterium and has been proposed as an attractive drug target. This TEP provide early tools to develop inhibitors of PgDPP11, including purification protocols of recombinant proteins, a crystal structure of the protein in complex with a dipeptide, crystallisation conditions suitable for crystallography-based fragment screening, an inhibition assay and fragment hits in the active site and an allosteric site. These molecules provide a promising starting point for the development of more specific and potent PgDPP11 inhibitors.

Notes

This document represents version 1 of the TEP. For more information about TEPs and the TEP Programme, please visit https://www.cmd.ox.ac.uk/resources/teps

Files

TEP_PgDPP11_v1.pdf

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Additional details

Funding

A UK Hub to Catalyse Open Target Discovery. 106169
Wellcome Trust