Insight into a novel p53 single point mutation (G389E) by Molecular Dynamics Simulations.

ABSTRACT: The majority of inactivating mutations of p53 reside in the central core DNA binding domain of the protein. In this computational study, we investigated the structural effects of a novel p53 mutation (G389E), identified in a patient with congenital adrenal hyperplasia, which is located within the extreme C-terminal domain (CTD) of p53, an unstructured, flexible region (residues 367-393) of major importance for the regulation of the protein. Based on the three-dimensional structure of a carboxyl-terminal peptide of p53 in complex with the S100B protein, which is involved in regulation of the tumor suppressor activity, a model of wild type (WT) and mutant extreme CTD was developed by molecular modeling and molecular dynamics simulation. It was found that the G389E amino acid replacement has

SUBMITTER: Pirolli D 

PROVIDER: S-EPMC3039947 | biostudies-literature | 2010 Dec

REPOSITORIES: biostudies-literature