1ow1

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[[Image:1ow1.gif|left|200px]]<br /><applet load="1ow1" size="350" color="white" frame="true" align="right" spinBox="true"
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[[Image:1ow1.gif|left|200px]]
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caption="1ow1, resolution 1.80&Aring;" />
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'''Crystal structure of the SPOC domain of the human transcriptional corepressor, SHARP.'''<br />
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{{Structure
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|PDB= 1ow1 |SIZE=350|CAPTION= <scene name='initialview01'>1ow1</scene>, resolution 1.80&Aring;
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|SITE=
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|LIGAND=
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|ACTIVITY=
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'''Crystal structure of the SPOC domain of the human transcriptional corepressor, SHARP.'''
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==Overview==
==Overview==
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==About this Structure==
==About this Structure==
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1OW1 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=1OW1 OCA].
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1OW1 is a [[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=1OW1 OCA].
==Reference==
==Reference==
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A conserved structural motif reveals the essential transcriptional repression function of Spen proteins and their role in developmental signaling., Ariyoshi M, Schwabe JW, Genes Dev. 2003 Aug 1;17(15):1909-20. PMID:[http://ispc.weizmann.ac.il//pmbin/getpm?pmid=12897056 12897056]
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A conserved structural motif reveals the essential transcriptional repression function of Spen proteins and their role in developmental signaling., Ariyoshi M, Schwabe JW, Genes Dev. 2003 Aug 1;17(15):1909-20. PMID:[http://www.ncbi.nlm.nih.gov/pubmed/12897056 12897056]
[[Category: Homo sapiens]]
[[Category: Homo sapiens]]
[[Category: Single protein]]
[[Category: Single protein]]
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[[Category: spoc domain]]
[[Category: spoc domain]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 14:22:14 2008''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Mar 20 13:16:21 2008''

Revision as of 11:16, 20 March 2008


PDB ID 1ow1

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, resolution 1.80Å
Coordinates: save as pdb, mmCIF, xml



Crystal structure of the SPOC domain of the human transcriptional corepressor, SHARP.


Contents

Overview

Spen proteins regulate the expression of key transcriptional effectors in diverse signaling pathways. They are large proteins characterized by N-terminal RNA-binding motifs and a highly conserved C-terminal SPOC domain. The specific biological role of the SPOC domain (Spen paralog and ortholog C-terminal domain), and hence, the common function of Spen proteins, has been unclear to date. The Spen protein, SHARP (SMRT/HDAC1-associated repressor protein), was identified as a component of transcriptional repression complexes in both nuclear receptor and Notch/RBP-Jkappa signaling pathways. We have determined the 1.8 A crystal structure of the SPOC domain from SHARP. This structure shows that essentially all of the conserved surface residues map to a positively charged patch. Structure-based mutational analysis indicates that this conserved region is responsible for the interaction between SHARP and the universal transcriptional corepressor SMRT/NCoR (silencing mediator for retinoid and thyroid receptors/nuclear receptor corepressor. We demonstrate that this interaction involves a highly conserved acidic motif at the C terminus of SMRT/NCoR. These findings suggest that the conserved function of the SPOC domain is to mediate interaction with SMRT/NCoR corepressors, and that Spen proteins play an essential role in the repression complex.

Disease

Known disease associated with this structure: Megakaryoblastic leukemia, acute OMIM:[606077]

About this Structure

1OW1 is a Single protein structure of sequence from Homo sapiens. Full crystallographic information is available from OCA.

Reference

A conserved structural motif reveals the essential transcriptional repression function of Spen proteins and their role in developmental signaling., Ariyoshi M, Schwabe JW, Genes Dev. 2003 Aug 1;17(15):1909-20. PMID:12897056

Page seeded by OCA on Thu Mar 20 13:16:21 2008

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