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4nyv
From Proteopedia
(Difference between revisions)
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| - | + | ==Crystal Structure of the Bromodomain of human CREBBP in complex with a quinazolin-one ligand== | |
| - | + | <StructureSection load='4nyv' size='340' side='right' caption='[[4nyv]], [[Resolution|resolution]] 1.83Å' scene=''> | |
| - | + | == Structural highlights == | |
| - | ==Disease== | + | <table><tr><td colspan='2'>[[4nyv]] is a 4 chain structure with sequence from [http://en.wikipedia.org/wiki/Human Human]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=4NYV OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=4NYV FirstGlance]. <br> |
| + | </td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=15E:6-BROMO-3-METHYL-3,4-DIHYDROQUINAZOLIN-2(1H)-ONE'>15E</scene></td></tr> | ||
| + | <tr id='related'><td class="sblockLbl"><b>[[Related_structure|Related:]]</b></td><td class="sblockDat">[[4nyw|4nyw]], [[4nyx|4nyx]]</td></tr> | ||
| + | <tr id='gene'><td class="sblockLbl"><b>[[Gene|Gene:]]</b></td><td class="sblockDat">CBP, CREBBP ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=9606 HUMAN])</td></tr> | ||
| + | <tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=4nyv FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4nyv OCA], [http://www.rcsb.org/pdb/explore.do?structureId=4nyv RCSB], [http://www.ebi.ac.uk/pdbsum/4nyv PDBsum]</span></td></tr> | ||
| + | </table> | ||
| + | == Disease == | ||
[[http://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:[http://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> | [[http://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:[http://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 == | |
| - | ==Function== | + | |
[[http://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> | [[http://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|CREB-binding protein]] |
| - | + | == References == | |
| - | == | + | <references/> |
| - | <references | + | __TOC__ |
| - | [[Category: Arrowsmith, C H | + | </StructureSection> |
| - | [[Category: Bountra, C | + | [[Category: Human]] |
| - | [[Category: Brennan, P | + | [[Category: Arrowsmith, C H]] |
| - | [[Category: Delft, F Von | + | [[Category: Bountra, C]] |
| - | [[Category: Edwards, A M | + | [[Category: Brennan, P]] |
| - | [[Category: Fedorov, O | + | [[Category: Delft, F Von]] |
| - | [[Category: Felletar, I | + | [[Category: Edwards, A M]] |
| - | [[Category: Filippakopoulos, P | + | [[Category: Fedorov, O]] |
| - | [[Category: Knapp, S | + | [[Category: Felletar, I]] |
| - | [[Category: Martin, S | + | [[Category: Filippakopoulos, P]] |
| - | [[Category: Monteiro, O P | + | [[Category: Knapp, S]] |
| - | [[Category: Picaud, S | + | [[Category: Martin, S]] |
| - | [[Category: | + | [[Category: Monteiro, O P]] |
| + | [[Category: Picaud, S]] | ||
| + | [[Category: Structural genomic]] | ||
[[Category: Bromodomain]] | [[Category: Bromodomain]] | ||
[[Category: Creb binding]] | [[Category: Creb binding]] | ||
[[Category: Crebbp]] | [[Category: Crebbp]] | ||
[[Category: Kat3a]] | [[Category: Kat3a]] | ||
| - | [[Category: Rst]] | ||
[[Category: Rst]] | [[Category: Rst]] | ||
[[Category: Sgc]] | [[Category: Sgc]] | ||
| - | [[Category: Structural genomics consortium]] | ||
[[Category: Transcription]] | [[Category: Transcription]] | ||
Revision as of 09:15, 15 February 2015
Crystal Structure of the Bromodomain of human CREBBP in complex with a quinazolin-one ligand
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Categories: Human | Arrowsmith, C H | Bountra, C | Brennan, P | Delft, F Von | Edwards, A M | Fedorov, O | Felletar, I | Filippakopoulos, P | Knapp, S | Martin, S | Monteiro, O P | Picaud, S | Structural genomic | Bromodomain | Creb binding | Crebbp | Kat3a | Rst | Sgc | Transcription
