Molecular investigation of the dual inhibition mechanism for targeted P53 regulator MDM2/MDMX inhibitors

Author:

Zhao Xiaoyu1,Xiong Danyang1,Luo Song1,Duan Lili1ORCID

Affiliation:

1. School of Physics and Electronics, Shandong Normal University, Jinan, 250014, China

Abstract

Residues I61/60, M62/61, Y67/66, V93/92, and L54/M53 provide a vital condition for dual inhibition of MDM2/MDMX by inhibitors. Stronger attraction of H96/I99 in MDM2 to inhibitors leads to the ineffectiveness of targeted MDM2 inhibitors against MDMX.

Funder

National Natural Science Foundation of China

Publisher

Royal Society of Chemistry (RSC)

Subject

Physical and Theoretical Chemistry,General Physics and Astronomy

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