5epb: Difference between revisions
Jump to navigation
Jump to search
m Protected "5epb" [edit=sysop:move=sysop] |
No edit summary |
||
Line 1: | Line 1: | ||
==Crystal structure of the bromodomain of human ATAD2 in complex with Compound 49== | |||
<StructureSection load='5epb' size='340' side='right' caption='[[5epb]], [[Resolution|resolution]] 1.50Å' scene=''> | |||
== Structural highlights == | |||
<table><tr><td colspan='2'>[[5epb]] is a 1 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=5EPB OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=5EPB FirstGlance]. <br> | |||
</td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=5QW:~{N}-[(2~{S})-2-MORPHOLIN-4-YLPROPYL]-4-OXIDANYLIDENE-3,5-DIHYDRO-2~{H}-1,5-BENZOTHIAZEPINE-7-CARBOXAMIDE'>5QW</scene>, <scene name='pdbligand=SO4:SULFATE+ION'>SO4</scene></td></tr> | |||
[[Category: | <tr id='activity'><td class="sblockLbl"><b>Activity:</b></td><td class="sblockDat"><span class='plainlinks'>[http://en.wikipedia.org/wiki/Adenosinetriphosphatase Adenosinetriphosphatase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=3.6.1.3 3.6.1.3] </span></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=5epb FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=5epb OCA], [http://pdbe.org/5epb PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=5epb RCSB], [http://www.ebi.ac.uk/pdbsum/5epb PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=5epb ProSAT]</span></td></tr> | |||
</table> | |||
== Function == | |||
[[http://www.uniprot.org/uniprot/ATAD2_HUMAN ATAD2_HUMAN]] May be a transcriptional coactivator of the nuclear receptor ESR1 required to induce the expression of a subset of estradiol target genes, such as CCND1, MYC and E2F1. May play a role in the recruitment or occupancy of CREBBP at some ESR1 target gene promoters. May be required for histone hyperacetylation. Involved in the estrogen-induced cell proliferation and cell cycle progression of breast cancer cells.<ref>PMID:17998543</ref> | |||
== References == | |||
<references/> | |||
__TOC__ | |||
</StructureSection> | |||
[[Category: Adenosinetriphosphatase]] | |||
[[Category: Caflisch, A]] | |||
[[Category: Dong, J]] | [[Category: Dong, J]] | ||
[[Category: | [[Category: Hydrolase inhibitor complex]] | ||
[[Category: Transferase]] |
Revision as of 13:48, 10 December 2016
Crystal structure of the bromodomain of human ATAD2 in complex with Compound 49Crystal structure of the bromodomain of human ATAD2 in complex with Compound 49
Structural highlights
Function[ATAD2_HUMAN] May be a transcriptional coactivator of the nuclear receptor ESR1 required to induce the expression of a subset of estradiol target genes, such as CCND1, MYC and E2F1. May play a role in the recruitment or occupancy of CREBBP at some ESR1 target gene promoters. May be required for histone hyperacetylation. Involved in the estrogen-induced cell proliferation and cell cycle progression of breast cancer cells.[1] References
|
|