| Literature DB >> 24466404 |
Kareem Khoury1, Grzegorz M Popowicz2, Tad A Holak2, Alexander Dömling1.
Abstract
The protein-protein interaction (PPI) of the tumor suppressor p53 and its negative regulator MDM2 consists of the most intense studied PPI with a group of small molecular weight antagonists described and many more disclosed in patent literature. Due to the Å-level structural insight into p53 interaction with MDM2 there is a reasonable understanding of the requirements of the molecules to bind. In contrast and despite the very close homology and 3-D similarity no potent MDMX antagonist has been disclosed up to date. The current review summarizes the different disclosed chemotypes for MDM2 including a discussion of the cocrystal structures. Structures and approaches to reconstitute functional p53 from mutated p53 are presented. Finally new screening methods and recent biotech deals based on p53 are discussed.Entities:
Year: 2011 PMID: 24466404 PMCID: PMC3898590 DOI: 10.1039/C0MD00248H
Source DB: PubMed Journal: Medchemcomm ISSN: 2040-2503 Impact factor: 3.597