5f3a
From Proteopedia
(Difference between revisions)
| Line 1: | Line 1: | ||
| - | '''Unreleased structure''' | ||
| - | + | ==Crystal structure of the bromodomain of human ATAD2 in complex with Compound A14== | |
| - | + | <StructureSection load='5f3a' size='340' side='right' caption='[[5f3a]], [[Resolution|resolution]] 1.60Å' scene=''> | |
| - | + | == Structural highlights == | |
| - | + | <table><tr><td colspan='2'>[[5f3a]] is a 1 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=5F3A OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=5F3A FirstGlance]. <br> | |
| - | + | </td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=5U9:~{N}-(4-ETHANOYL-1,3-THIAZOL-2-YL)AZETIDIN-1-IUM-3-CARBOXAMIDE'>5U9</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=5f3a FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=5f3a OCA], [http://pdbe.org/5f3a PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=5f3a RCSB], [http://www.ebi.ac.uk/pdbsum/5f3a PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=5f3a 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 19:13, 15 December 2016
Crystal structure of the bromodomain of human ATAD2 in complex with Compound A14
| |||||||||||
