2kwf: Difference between revisions

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-[[Image:2kwf.png|left|200px]]
-<!--
+==The structure of E-protein activation domain 1 bound to the KIX domain of CBP/p300 elucidates leukemia induction by E2A-PBX1==
-The line below this paragraph, containing "STRUCTURE_2kwf", creates the "Structure Box" on the page.
+<StructureSection load='2kwf' size='340' side='right'caption='[[2kwf]]' scene=''>
-You may change the PDB parameter (which sets the PDB file loaded into the applet)
+== Structural highlights ==
-or the SCENE parameter (which sets the initial scene displayed when the page is loaded),
+<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>
-or leave the SCENE parameter empty for the default display.
+</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>
-{{STRUCTURE_2kwf|  PDB=2kwf  |  SCENE=  }}
+</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>
-===The structure of E-protein activation domain 1 bound to the KIX domain of CBP/p300 elucidates leukemia induction by E2A-PBX1===
+==See Also==
+*[[CREB-binding protein 3D structures|CREB-binding protein 3D structures]]
+== References ==
-==About this Structure==
+<references/>
-[[2kwf]] is a 2 chain structure with sequence from [http://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].
+__TOC__
-[[Category: Histone acetyltransferase]]
+</StructureSection>
 [[Category: Homo sapiens]]
-[[Category: Chitayat, S.]]
+[[Category: Large Structures]]
-[[Category: Denis, C M.]]
+[[Category: Chitayat S]]
-[[Category: Ikura, M.]]
+[[Category: Denis CM]]
-[[Category: LeBrun, D P.]]
+[[Category: Ikura M]]
-[[Category: Liu, S.]]
+[[Category: LeBrun DP]]
-[[Category: Plevin, M J.]]
+[[Category: Liu S]]
-[[Category: Smith, S P.]]
+[[Category: Plevin MJ]]
-[[Category: Spencer, H L.]]
+[[Category: Smith SP]]
-[[Category: Transcription]]
+[[Category: Spencer HL]]
-[[Category: Transferase]]