2bim: Difference between revisions

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[[Image:2bim.gif|left|200px]]<br />
[[Image:2bim.gif|left|200px]]<br /><applet load="2bim" size="450" color="white" frame="true" align="right" spinBox="true"  
<applet load="2bim" size="450" color="white" frame="true" align="right" spinBox="true"  
caption="2bim, resolution 1.98&Aring;" />
caption="2bim, resolution 1.98&Aring;" />
'''HUMAN P53 CORE DOMAIN MUTANT M133L-V203A-N239Y-N268D-R273H'''<br />
'''HUMAN P53 CORE DOMAIN MUTANT M133L-V203A-N239Y-N268D-R273H'''<br />
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==About this Structure==
==About this Structure==
2BIM is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens] with ZN and SO4 as [http://en.wikipedia.org/wiki/ligands ligands]. Structure known Active Site: AC1. Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=2BIM OCA].  
2BIM is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens] with ZN and SO4 as [http://en.wikipedia.org/wiki/ligands ligands]. Known structural/functional Site: <scene name='pdbsite=AC1:So4 Binding Site For Chain B'>AC1</scene>. Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=2BIM OCA].  


==Reference==
==Reference==
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[[Category: tumor suppressor]]
[[Category: tumor suppressor]]


''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Mon Nov 12 21:02:58 2007''
''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Tue Dec 18 18:48:26 2007''

Revision as of 19:38, 18 December 2007

File:2bim.gif


2bim, resolution 1.98Å

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HUMAN P53 CORE DOMAIN MUTANT M133L-V203A-N239Y-N268D-R273H

OverviewOverview

We have solved the crystal structures of three oncogenic mutants of the, core domain of the human tumor suppressor p53. The mutations were, introduced into a stabilized variant. The cancer hot spot mutation R273H, simply removes an arginine involved in DNA binding without causing, structural distortions in neighboring residues. In contrast, the, "structural" oncogenic mutations H168R and R249S induce substantial, structural perturbation around the mutation site in the L2 and L3 loops, respectively. H168R is a specific intragenic suppressor mutation for, R249S. When both cancer mutations are combined in the same molecule, Arg(168) mimics the role of Arg(249) in wild type, and the wild type, conformation is largely restored in both loops. Our structural and, biophysical data provide compelling evidence for the mechanism of rescue, of mutant p53 by intragenic suppressor mutations and reveal features by, which proteins can adapt to deleterious mutations.

DiseaseDisease

Known diseases associated with this structure: Adrenal cortical carcinoma OMIM:[191170], Breast cancer OMIM:[191170], Colorectal cancer OMIM:[191170], Hepatocellular carcinoma OMIM:[191170], Histiocytoma OMIM:[191170], Li-Fraumeni syndrome OMIM:[191170], Multiple malignancy syndrome OMIM:[191170], Nasopharyngeal carcinoma OMIM:[191170], Osteosarcoma OMIM:[191170], Pancreatic cancer OMIM:[191170], Thyroid carcinoma OMIM:[191170]

About this StructureAbout this Structure

2BIM is a Single protein structure of sequence from Homo sapiens with ZN and SO4 as ligands. Known structural/functional Site: . Full crystallographic information is available from OCA.

ReferenceReference

Structures of p53 cancer mutants and mechanism of rescue by second-site suppressor mutations., Joerger AC, Ang HC, Veprintsev DB, Blair CM, Fersht AR, J Biol Chem. 2005 Apr 22;280(16):16030-7. Epub 2005 Feb 9. PMID:15703170

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