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| ==Structural diversity in CBP p160 complexes== | | ==Structural diversity in CBP p160 complexes== |
| <StructureSection load='2c52' size='340' side='right'caption='[[2c52]], [[NMR_Ensembles_of_Models | 37 NMR models]]' scene=''> | | <StructureSection load='2c52' size='340' side='right'caption='[[2c52]]' scene=''> |
| == Structural highlights == | | == Structural highlights == |
| <table><tr><td colspan='2'>[[2c52]] is a 2 chain structure with sequence from [https://en.wikipedia.org/wiki/Human Human] and [https://en.wikipedia.org/wiki/Lk3_transgenic_mice Lk3 transgenic mice]. Full experimental information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2C52 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=2C52 FirstGlance]. <br> | | <table><tr><td colspan='2'>[[2c52]] is a 2 chain structure with sequence from [https://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens] and [https://en.wikipedia.org/wiki/Mus_musculus Mus musculus]. Full experimental information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2C52 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=2C52 FirstGlance]. <br> |
| </td></tr><tr id='related'><td class="sblockLbl"><b>[[Related_structure|Related:]]</b></td><td class="sblockDat"><div style='overflow: auto; max-height: 3em;'>[[1f81|1f81]], [[1jjs|1jjs]], [[1kbh|1kbh]], [[1kdx|1kdx]], [[1l8c|1l8c]], [[1r8u|1r8u]], [[1sb0|1sb0]], [[1tot|1tot]], [[1u2n|1u2n]], [[1xiu|1xiu]], [[2a3i|2a3i]]</div></td></tr> | | </td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">Solution NMR</td></tr> |
| <tr id='activity'><td class="sblockLbl"><b>Activity:</b></td><td class="sblockDat"><span class='plainlinks'>[https://en.wikipedia.org/wiki/Histone_acetyltransferase Histone acetyltransferase], with EC number [https://www.brenda-enzymes.info/php/result_flat.php4?ecno=2.3.1.48 2.3.1.48] </span></td></tr>
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| <tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=2c52 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2c52 OCA], [https://pdbe.org/2c52 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=2c52 RCSB], [https://www.ebi.ac.uk/pdbsum/2c52 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=2c52 ProSAT]</span></td></tr> | | <tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=2c52 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2c52 OCA], [https://pdbe.org/2c52 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=2c52 RCSB], [https://www.ebi.ac.uk/pdbsum/2c52 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=2c52 ProSAT]</span></td></tr> |
| </table> | | </table> |
| == Disease ==
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| [[https://www.uniprot.org/uniprot/NCOA1_HUMAN NCOA1_HUMAN]] Note=A chromosomal aberration involving NCOA1 is a cause of rhabdomyosarcoma. Translocation t(2;2)(q35;p23) with PAX3 generates the NCOA1-PAX3 oncogene consisting of the N-terminus part of PAX3 and the C-terminus part of NCOA1. The fusion protein acts as a transcriptional activator. Rhabdomyosarcoma is the most common soft tissue carcinoma in childhood, representing 5-8% of all malignancies in children.
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| == Function == | | == Function == |
| [[https://www.uniprot.org/uniprot/CBP_MOUSE CBP_MOUSE]] Acetylates histones, giving a specific tag for transcriptional activation. Also acetylates non-histone proteins, like NCOA3 and FOXO1. Binds specifically to phosphorylated CREB and enhances its transcriptional activity toward cAMP-responsive genes. Acts as a coactivator of ALX1 in the presence of EP300 (By similarity).<ref>PMID:10207073</ref> <ref>PMID:11701890</ref> <ref>PMID:15220471</ref> <ref>PMID:16287980</ref> [[https://www.uniprot.org/uniprot/NCOA1_HUMAN NCOA1_HUMAN]] Nuclear receptor coactivator that directly binds nuclear receptors and stimulates the transcriptional activities in a hormone-dependent fashion. Involved in the coactivation of different nuclear receptors, such as for steroids (PGR, GR and ER), retinoids (RXRs), thyroid hormone (TRs) and prostanoids (PPARs). Also involved in coactivation mediated by STAT3, STAT5A, STAT5B and STAT6 transcription factors. Displays histone acetyltransferase activity toward H3 and H4; the relevance of such activity remains however unclear. Plays a central role in creating multisubunit coactivator complexes that act via remodeling of chromatin, and possibly acts by participating in both chromatin remodeling and recruitment of general transcription factors. Required with NCOA2 to control energy balance between white and brown adipose tissues. Required for mediating steroid hormone response. Isoform 2 has a higher thyroid hormone-dependent transactivation activity than isoform 1 and isoform 3.<ref>PMID:9427757</ref> <ref>PMID:7481822</ref> <ref>PMID:9223431</ref> <ref>PMID:9296499</ref> <ref>PMID:9223281</ref> <ref>PMID:10449719</ref> <ref>PMID:12954634</ref>
| | [https://www.uniprot.org/uniprot/CBP_MOUSE CBP_MOUSE] Acetylates histones, giving a specific tag for transcriptional activation. Also acetylates non-histone proteins, like NCOA3 and FOXO1. Binds specifically to phosphorylated CREB and enhances its transcriptional activity toward cAMP-responsive genes. Acts as a coactivator of ALX1 in the presence of EP300 (By similarity).<ref>PMID:10207073</ref> <ref>PMID:11701890</ref> <ref>PMID:15220471</ref> <ref>PMID:16287980</ref> |
| == Evolutionary Conservation == | | == Evolutionary Conservation == |
| [[Image:Consurf_key_small.gif|200px|right]] | | [[Image:Consurf_key_small.gif|200px|right]] |
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| __TOC__ | | __TOC__ |
| </StructureSection> | | </StructureSection> |
| [[Category: Histone acetyltransferase]] | | [[Category: Homo sapiens]] |
| [[Category: Human]]
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| [[Category: Large Structures]] | | [[Category: Large Structures]] |
| [[Category: Lk3 transgenic mice]] | | [[Category: Mus musculus]] |
| [[Category: Bramham, J]] | | [[Category: Bramham J]] |
| [[Category: Carr, M D]] | | [[Category: Carr MD]] |
| [[Category: Frenkiel, T]] | | [[Category: Frenkiel T]] |
| [[Category: Heery, D M]] | | [[Category: Heery DM]] |
| [[Category: Kelly, G]] | | [[Category: Kelly G]] |
| [[Category: Matsuda, S]] | | [[Category: Matsuda S]] |
| [[Category: Muskett, F W]] | | [[Category: Muskett FW]] |
| [[Category: Renshaw, P S]] | | [[Category: Renshaw PS]] |
| [[Category: Veverka, V]] | | [[Category: Veverka V]] |
| [[Category: Waters, L C]] | | [[Category: Waters LC]] |
| [[Category: Yue, B]] | | [[Category: Yue B]] |
| [[Category: Activator]]
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| [[Category: Acyltransferase]]
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| [[Category: Alternative splicing]]
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| [[Category: Bromodomain]]
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| [[Category: Chromosomal translocation]]
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| [[Category: Metal-binding]]
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| [[Category: Methylation]]
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| [[Category: Nuclear protein]]
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| [[Category: Polymorphism]]
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| [[Category: Proto-oncogene]]
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| [[Category: Transcription]]
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| [[Category: Transcription regulation]]
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| [[Category: Transferase]]
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| [[Category: Ubl conjugation]]
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| [[Category: Zinc]]
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| [[Category: Zinc-finger]]
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