2kwf
From Proteopedia
(Difference between revisions)
(5 intermediate revisions not shown.) | |||
Line 1: | Line 1: | ||
- | {{STRUCTURE_2kwf| PDB=2kwf | SCENE= }} | ||
- | ===The structure of E-protein activation domain 1 bound to the KIX domain of CBP/p300 elucidates leukemia induction by E2A-PBX1=== | ||
- | == | + | ==The structure of E-protein activation domain 1 bound to the KIX domain of CBP/p300 elucidates leukemia induction by E2A-PBX1== |
- | [[http://www.uniprot.org/uniprot/CBP_HUMAN CBP_HUMAN | + | <StructureSection load='2kwf' size='340' side='right'caption='[[2kwf]]' scene=''> |
+ | == Structural highlights == | ||
+ | <table><tr><td colspan='2'>[[2kwf]] is a 2 chain structure with sequence from [https://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full experimental information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2KWF OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=2KWF FirstGlance]. <br> | ||
+ | </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='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=2kwf FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2kwf OCA], [https://pdbe.org/2kwf PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=2kwf RCSB], [https://www.ebi.ac.uk/pdbsum/2kwf PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=2kwf ProSAT]</span></td></tr> | ||
+ | </table> | ||
+ | == Disease == | ||
+ | [https://www.uniprot.org/uniprot/CBP_HUMAN CBP_HUMAN] Note=Chromosomal aberrations involving CREBBP may be a cause of acute myeloid leukemias. Translocation t(8;16)(p11;p13) with KAT6A; translocation t(11;16)(q23;p13.3) with MLL/HRX; translocation t(10;16)(q22;p13) with KAT6B. KAT6A-CREBBP may induce leukemia by inhibiting RUNX1-mediated transcription. Defects in CREBBP are a cause of Rubinstein-Taybi syndrome type 1 (RSTS1) [MIM:[https://omim.org/entry/180849 180849]. RSTS1 is an autosomal dominant disorder characterized by craniofacial abnormalities, broad thumbs, broad big toes, mental retardation and a propensity for development of malignancies.<ref>PMID:11331617</ref> <ref>PMID:12114483</ref> <ref>PMID:12566391</ref> <ref>PMID:15706485</ref> | ||
+ | == Function == | ||
+ | [https://www.uniprot.org/uniprot/CBP_HUMAN CBP_HUMAN] 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.<ref>PMID:9707565</ref> <ref>PMID:11154691</ref> <ref>PMID:12738767</ref> <ref>PMID:12929931</ref> | ||
- | == | + | ==See Also== |
- | [[ | + | *[[CREB-binding protein 3D structures|CREB-binding protein 3D structures]] |
- | + | == References == | |
- | + | <references/> | |
- | + | __TOC__ | |
- | + | </StructureSection> | |
- | == | + | |
- | <references | + | |
- | + | ||
[[Category: Homo sapiens]] | [[Category: Homo sapiens]] | ||
- | [[Category: Chitayat | + | [[Category: Large Structures]] |
- | [[Category: Denis | + | [[Category: Chitayat S]] |
- | [[Category: Ikura | + | [[Category: Denis CM]] |
- | [[Category: LeBrun | + | [[Category: Ikura M]] |
- | [[Category: Liu | + | [[Category: LeBrun DP]] |
- | [[Category: Plevin | + | [[Category: Liu S]] |
- | [[Category: Smith | + | [[Category: Plevin MJ]] |
- | [[Category: Spencer | + | [[Category: Smith SP]] |
- | + | [[Category: Spencer HL]] | |
- | + |
Current revision
The structure of E-protein activation domain 1 bound to the KIX domain of CBP/p300 elucidates leukemia induction by E2A-PBX1
|
Categories: Homo sapiens | Large Structures | Chitayat S | Denis CM | Ikura M | LeBrun DP | Liu S | Plevin MJ | Smith SP | Spencer HL