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| Title | Structure-based design of high affinity peptides inhibiting the interaction of p53 with MDM2 and MDMX. |
|---|---|
| Journal, issue, pages | J. Biol. Chem., Vol. 285, Page 2174-2183, Year 2010 |
| Publish date | Sep 23, 2009 (structure data deposition date) |
Authors | Phan, J. / Li, Z. / Kasprzak, A. / Li, B. / Sebti, S. / Guida, W. / Schonbrunn, E. / Chen, J. |
External links | J. Biol. Chem. / PubMed:19910468 |
| Methods | X-ray diffraction |
| Resolution | 1.74 - 2.1 Å |
| Structure data | ![]() PDB-3jzo: ![]() PDB-3jzp: ![]() PDB-3jzq: ![]() PDB-3jzr: ![]() PDB-3jzs: |
| Chemicals | ![]() ChemComp-K: ![]() ChemComp-HOH: ![]() ChemComp-SO4: ![]() ChemComp-EDO: |
| Source |
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Keywords | CELL CYCLE / P53-BINDING PROTEIN MDM4 / DOUBLE MINUTE 4 PROTEIN / Alternative splicing / Metal-binding / Nucleus / Polymorphism / Zinc / Zinc-finger / LIGASE / P53-BINDING PROTEIN MDM2 / ONCOPROTEIN MDM2 / DOUBLE MINUTE 2 PROTEIN / HDM2 / Cytoplasm / Host-virus interaction / Phosphoprotein / Proto-oncogene / Ubl conjugation / Ubl conjugation pathway |
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homo sapiens (human)
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