1cok
From Proteopedia
(New page: 200px<br /> <applet load="1cok" size="450" color="white" frame="true" align="right" spinBox="true" caption="1cok" /> '''STRUCTURE OF THE C-TERMINAL DOMAIN OF P73''...) |
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'''STRUCTURE OF THE C-TERMINAL DOMAIN OF P73'''<br /> | '''STRUCTURE OF THE C-TERMINAL DOMAIN OF P73'''<br /> | ||
==Overview== | ==Overview== | ||
- | p73 and p63 are two recently cloned genes with homology to the tumor | + | p73 and p63 are two recently cloned genes with homology to the tumor suppressor p53, whose protein product is a key transcriptional regulator of genes involved in cell cycle arrest and apoptosis. While all three proteins share conserved transcriptional activation, DNA-binding and oligomerization domains, p73 and p63 have an additional conserved C-terminal region. We have determined the three-dimensional solution structure of this conserved C-terminal domain of human p73. The structure reveals a small five-helix bundle with striking similarity to the SAM (sterile alpha motif) domains of two ephrin receptor tyrosine kinases. The SAM domain is a putative protein-protein interaction domain found in a variety of cytoplasmic signaling proteins and has been shown to form both homo- and hetero-oligomers. However, the SAM-like C-terminal domains of p73 and p63 are monomeric and do not interact with one another, suggesting that this domain may interact with additional, as yet uncharacterized proteins in a signaling and/or regulatory role. |
==Disease== | ==Disease== | ||
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==About this Structure== | ==About this Structure== | ||
- | 1COK is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http:// | + | 1COK is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1COK OCA]. |
==Reference== | ==Reference== | ||
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[[Category: Homo sapiens]] | [[Category: Homo sapiens]] | ||
[[Category: Single protein]] | [[Category: Single protein]] | ||
- | [[Category: Arrowsmith, C | + | [[Category: Arrowsmith, C H.]] |
[[Category: Ayed, A.]] | [[Category: Ayed, A.]] | ||
- | [[Category: Chi, S | + | [[Category: Chi, S W.]] |
[[Category: gene regulation]] | [[Category: gene regulation]] | ||
[[Category: p73 sam-like domain]] | [[Category: p73 sam-like domain]] | ||
- | ''Page seeded by [http:// | + | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 12:08:05 2008'' |
Revision as of 10:08, 21 February 2008
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STRUCTURE OF THE C-TERMINAL DOMAIN OF P73
Contents |
Overview
p73 and p63 are two recently cloned genes with homology to the tumor suppressor p53, whose protein product is a key transcriptional regulator of genes involved in cell cycle arrest and apoptosis. While all three proteins share conserved transcriptional activation, DNA-binding and oligomerization domains, p73 and p63 have an additional conserved C-terminal region. We have determined the three-dimensional solution structure of this conserved C-terminal domain of human p73. The structure reveals a small five-helix bundle with striking similarity to the SAM (sterile alpha motif) domains of two ephrin receptor tyrosine kinases. The SAM domain is a putative protein-protein interaction domain found in a variety of cytoplasmic signaling proteins and has been shown to form both homo- and hetero-oligomers. However, the SAM-like C-terminal domains of p73 and p63 are monomeric and do not interact with one another, suggesting that this domain may interact with additional, as yet uncharacterized proteins in a signaling and/or regulatory role.
Disease
Known disease associated with this structure: Neuroblastoma (1) OMIM:[601990]
About this Structure
1COK is a Single protein structure of sequence from Homo sapiens. Full crystallographic information is available from OCA.
Reference
Solution structure of a conserved C-terminal domain of p73 with structural homology to the SAM domain., Chi SW, Ayed A, Arrowsmith CH, EMBO J. 1999 Aug 16;18(16):4438-45. PMID:10449409
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