| 1 |
34958576 | Grafting Hydrophobic Amino Acids Critical for Inhibition of Protein-Protein Interactions on a Cell-Penetrating Peptide Scaffold. | 2022 Feb 7 |
1 |
| 2 |
34977581 | Discovery, X-ray structure and CPP-conjugation enabled uptake of p53/MDM2 macrocyclic peptide inhibitors. | 2021 Dec 2 |
1 |
| 3 |
31226791 | Incorporation of Putative Helix-Breaking Amino Acids in the Design of Novel Stapled Peptides: Exploring Biophysical and Cellular Permeability Properties. | 2019 Jun 20 |
1 |
| 4 |
19153082 | Crystal Structures of Human MdmX (HdmX) in Complex with p53 Peptide Analogues Reveal Surprising Conformational Changes. | 2009 Mar 27 |
1 |
| 5 |
18707164 | Quantum mechanical studies of residue-specific hydrophobic interactions in p53-MDM2 binding. | 2008 Sep 11 |
3 |
| 6 |
17002294 | Determinants of specificity of MDM2 for the activation domains of p53 and p65: proline27 disrupts the MDM2-binding motif of p53. | 2006 Oct 3 |
1 |
| 7 |
15600307 | Use of a retroinverso p53 peptide as an inhibitor of MDM2. | 2004 Dec 22 |
1 |
| 8 |
11925449 | The conformationally flexible S9-S10 linker region in the core domain of p53 contains a novel MDM2 binding site whose mutation increases ubiquitination of p53 in vivo. | 2002 Aug 9 |
1 |
| 9 |
7926727 | Several hydrophobic amino acids in the p53 amino-terminal domain are required for transcriptional activation, binding to mdm-2 and the adenovirus 5 E1B 55-kD protein. | 1994 May 15 |
3 |