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'''Unreleased structure'''
==Crystal structure of human PCAF bromodomain in complex with fragment BR013 (fragment 3)==
 
<StructureSection load='5fe2' size='340' side='right' caption='[[5fe2]], [[Resolution|resolution]] 2.25&Aring;' scene=''>
The entry 5fe2 is ON HOLD
== Structural highlights ==
 
<table><tr><td colspan='2'>[[5fe2]] is a 2 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=5FE2 OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=5FE2 FirstGlance]. <br>
Authors: Chaikuad, A., von Delft, F., Bountra, C., Arrowsmith, C.H., Edwards, A.M., Knapp, S., Structural Genomics Consortium (SGC)
</td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=5WV:2-METHYL-3~{H}-ISOINDOL-1-ONE'>5WV</scene>, <scene name='pdbligand=EDO:1,2-ETHANEDIOL'>EDO</scene></td></tr>
 
<tr id='activity'><td class="sblockLbl"><b>Activity:</b></td><td class="sblockDat"><span class='plainlinks'>[http://en.wikipedia.org/wiki/Histone_acetyltransferase Histone acetyltransferase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=2.3.1.48 2.3.1.48] </span></td></tr>
Description: Crystal structure of human PCAF bromodomain in complex with fragment BR013 (FR3)
<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=5fe2 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=5fe2 OCA], [http://pdbe.org/5fe2 PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=5fe2 RCSB], [http://www.ebi.ac.uk/pdbsum/5fe2 PDBsum]</span></td></tr>
[[Category: Unreleased Structures]]
</table>
== Function ==
[[http://www.uniprot.org/uniprot/KAT2B_HUMAN KAT2B_HUMAN]] Functions as a histone acetyltransferase (HAT) to promote transcriptional activation. Has significant histone acetyltransferase activity with core histones (H3 and H4), and also with nucleosome core particles. Also acetylates non-histone proteins, such as ACLY. Inhibits cell-cycle progression and counteracts the mitogenic activity of the adenoviral oncoprotein E1A. In case of HIV-1 infection, it is recruited by the viral protein Tat. Regulates Tat's transactivating activity and may help inducing chromatin remodeling of proviral genes.<ref>PMID:8684459</ref> <ref>PMID:9707565</ref> <ref>PMID:10675335</ref> <ref>PMID:23932781</ref> 
== References ==
<references/>
__TOC__
</StructureSection>
[[Category: Histone acetyltransferase]]
[[Category: Arrowsmith, C H]]
[[Category: Bountra, C]]
[[Category: Chaikuad, A]]
[[Category: Chaikuad, A]]
[[Category: Delft, F von]]
[[Category: Edwards, A M]]
[[Category: Knapp, S]]
[[Category: Knapp, S]]
[[Category: Bountra, C]]
[[Category: Structural genomic]]
[[Category: Arrowsmith, C.H]]
[[Category: Acetylation]]
[[Category: Von Delft, F]]
[[Category: Acetyllysine]]
[[Category: Edwards, A.M]]
[[Category: Bromodomain]]
[[Category: Structural Genomics Consortium (Sgc)]]
[[Category: Epigenetic]]
[[Category: Histone]]
[[Category: Histone acetyltransferase kat2b]]
[[Category: Signaling protein]]
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