1t4f: Difference between revisions
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|PDB= 1t4f |SIZE=350|CAPTION= <scene name='initialview01'>1t4f</scene>, resolution 1.90Å | |PDB= 1t4f |SIZE=350|CAPTION= <scene name='initialview01'>1t4f</scene>, resolution 1.90Å | ||
|SITE= | |SITE= | ||
|LIGAND= <scene name='pdbligand=SO4:SULFATE ION'>SO4</scene> | |LIGAND= <scene name='pdbligand=SO4:SULFATE+ION'>SO4</scene> | ||
|ACTIVITY= | |ACTIVITY= | ||
|GENE= MDM2 ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=9606 Homo sapiens]) | |GENE= MDM2 ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=9606 Homo sapiens]) | ||
|DOMAIN= | |||
|RELATEDENTRY=[[1t4e|1T4E]], [[1ycr|1YCR]], [[1rv1|1RV1]] | |||
|RESOURCES=<span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=1t4f FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1t4f OCA], [http://www.ebi.ac.uk/pdbsum/1t4f PDBsum], [http://www.rcsb.org/pdb/explore.do?structureId=1t4f RCSB]</span> | |||
}} | }} | ||
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[[Category: Schubert, C.]] | [[Category: Schubert, C.]] | ||
[[Category: Zhao, S Y.]] | [[Category: Zhao, S Y.]] | ||
[[Category: mdm2-p53 peptide complex]] | [[Category: mdm2-p53 peptide complex]] | ||
[[Category: p53-binding protein mdm2 oncoprotein mdm2 double minute 2 protein hdm2]] | [[Category: p53-binding protein mdm2 oncoprotein mdm2 double minute 2 protein hdm2]] | ||
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sun Mar 30 23:51:06 2008'' | ||
Revision as of 23:51, 30 March 2008
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| , resolution 1.90Å | |||||||
|---|---|---|---|---|---|---|---|
| Ligands: | |||||||
| Gene: | MDM2 (Homo sapiens) | ||||||
| Related: | 1T4E, 1YCR, 1RV1
| ||||||
| Resources: | FirstGlance, OCA, PDBsum, RCSB | ||||||
| Coordinates: | save as pdb, mmCIF, xml | ||||||
Structure of human MDM2 in complex with an optimized p53 peptide
OverviewOverview
HDM2 binds to an alpha-helical transactivation domain of p53, inhibiting its tumor suppressive functions. A miniaturized thermal denaturation assay was used to screen chemical libraries, resulting in the discovery of a novel series of benzodiazepinedione antagonists of the HDM2-p53 interaction. The X-ray crystal structure of improved antagonists bound to HDM2 reveals their alpha-helix mimetic properties. These optimized molecules increase the transcription of p53 target genes and decrease proliferation of tumor cells expressing wild-type p53.
About this StructureAbout this Structure
1T4F is a Single protein structure of sequence from Homo sapiens. Full crystallographic information is available from OCA.
ReferenceReference
Discovery and cocrystal structure of benzodiazepinedione HDM2 antagonists that activate p53 in cells., Grasberger BL, Lu T, Schubert C, Parks DJ, Carver TE, Koblish HK, Cummings MD, LaFrance LV, Milkiewicz KL, Calvo RR, Maguire D, Lattanze J, Franks CF, Zhao S, Ramachandren K, Bylebyl GR, Zhang M, Manthey CL, Petrella EC, Pantoliano MW, Deckman IC, Spurlino JC, Maroney AC, Tomczuk BE, Molloy CJ, Bone RF, J Med Chem. 2005 Feb 24;48(4):909-12. PMID:15715460
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