| Literature DB >> 23914285 |
James D Patrone1, J Phillip Kennedy, Andreas O Frank, Michael D Feldkamp, Bhavatarini Vangamudi, Nicholas F Pelz, Olivia W Rossanese, Alex G Waterson, Walter J Chazin, Stephen W Fesik.
Abstract
Replication Protein A (RPA) is a ssDNA binding protein that is essential for DNA replication and repair. The initiation of the DNA damage response by RPA is mediated by protein-protein interactions involving the N-terminal domain of the 70 kDa subunit with partner proteins. Inhibition of these interactions increases sensitivity towards DNA damage and replication stress and may therefore be a potential strategy for cancer drug discovery. Towards this end, we have discovered two lead series of compounds, derived from hits obtained from a fragment-based screen, that bind to RPA70N with low micromolar affinity and inhibit the binding of an ATRIP-derived peptide to RPA. These compounds may offer a promising starting point for the discovery of clinically useful RPA inhibitors.Entities:
Keywords: DNA damage; Fragment-based discovery; Replication Protein A
Year: 2013 PMID: 23914285 PMCID: PMC3728914 DOI: 10.1021/ml400032y
Source DB: PubMed Journal: ACS Med Chem Lett ISSN: 1948-5875 Impact factor: 4.345