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5f3a
From Proteopedia
(Difference between revisions)
(New page: '''Unreleased structure''' The entry 5f3a is ON HOLD Authors: Dong, J., Caflisch, A. Description: Crystal structure of the bromodomain of human ATAD2 in complex with Compound A14 [[Cat...) |
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| - | '''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 with sequence from [https://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. 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 [https://proteopedia.org/fgij/fg.htm?mol=5F3A FirstGlance]. <br> | ||
| + | </td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 1.599Å</td></tr> | ||
| + | <tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><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> | ||
| + | <tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=5f3a FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=5f3a OCA], [https://pdbe.org/5f3a PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=5f3a RCSB], [https://www.ebi.ac.uk/pdbsum/5f3a PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=5f3a ProSAT]</span></td></tr> | ||
| + | </table> | ||
| + | == Function == | ||
| + | [https://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> | ||
| - | + | ==See Also== | |
| - | + | *[[ATPase family AAA domain-containing protein|ATPase family AAA domain-containing protein]] | |
| - | + | == References == | |
| - | [[Category: | + | <references/> |
| - | [[Category: | + | __TOC__ |
| - | [[Category: Caflisch | + | </StructureSection> |
| + | [[Category: Homo sapiens]] | ||
| + | [[Category: Large Structures]] | ||
| + | [[Category: Caflisch A]] | ||
| + | [[Category: Dong J]] | ||
Current revision
Crystal structure of the bromodomain of human ATAD2 in complex with Compound A14
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