2lsp: Difference between revisions
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==solution structures of BRD4 second bromodomain with NF-kB-K310ac peptide== | ==solution structures of BRD4 second bromodomain with NF-kB-K310ac peptide== | ||
<StructureSection load='2lsp' size='340' side='right'caption='[[2lsp | <StructureSection load='2lsp' size='340' side='right'caption='[[2lsp]]' scene=''> | ||
== Structural highlights == | == Structural highlights == | ||
<table><tr><td colspan='2'>[[2lsp]] is a 2 chain structure with sequence from [https://en.wikipedia.org/wiki/ | <table><tr><td colspan='2'>[[2lsp]] is a 2 chain structure with sequence from [https://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full experimental information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2LSP OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=2LSP FirstGlance]. <br> | ||
</td></tr><tr id=' | </td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=ALY:N(6)-ACETYLLYSINE'>ALY</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=2lsp FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2lsp OCA], [https://pdbe.org/2lsp PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=2lsp RCSB], [https://www.ebi.ac.uk/pdbsum/2lsp PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=2lsp ProSAT]</span></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=2lsp FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2lsp OCA], [https://pdbe.org/2lsp PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=2lsp RCSB], [https://www.ebi.ac.uk/pdbsum/2lsp PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=2lsp ProSAT]</span></td></tr> | ||
</table> | </table> | ||
== Function == | == Function == | ||
[https://www.uniprot.org/uniprot/TF65_HUMAN TF65_HUMAN] NF-kappa-B is a pleiotropic transcription factor present in almost all cell types and is the endpoint of a series of signal transduction events that are initiated by a vast array of stimuli related to many biological processes such as inflammation, immunity, differentiation, cell growth, tumorigenesis and apoptosis. NF-kappa-B is a homo- or heterodimeric complex formed by the Rel-like domain-containing proteins RELA/p65, RELB, NFKB1/p105, NFKB1/p50, REL and NFKB2/p52 and the heterodimeric p65-p50 complex appears to be most abundant one. The dimers bind at kappa-B sites in the DNA of their target genes and the individual dimers have distinct preferences for different kappa-B sites that they can bind with distinguishable affinity and specificity. Different dimer combinations act as transcriptional activators or repressors, respectively. NF-kappa-B is controlled by various mechanisms of post-translational modification and subcellular compartmentalization as well as by interactions with other cofactors or corepressors. NF-kappa-B complexes are held in the cytoplasm in an inactive state complexed with members of the NF-kappa-B inhibitor (I-kappa-B) family. In a conventional activation pathway, I-kappa-B is phosphorylated by I-kappa-B kinases (IKKs) in response to different activators, subsequently degraded thus liberating the active NF-kappa-B complex which translocates to the nucleus. NF-kappa-B heterodimeric p65-p50 and p65-c-Rel complexes are transcriptional activators. The NF-kappa-B p65-p65 complex appears to be involved in invasin-mediated activation of IL-8 expression. The inhibitory effect of I-kappa-B upon NF-kappa-B the cytoplasm is exerted primarily through the interaction with p65. p65 shows a weak DNA-binding site which could contribute directly to DNA binding in the NF-kappa-B complex. Associates with chromatin at the NF-kappa-B promoter region via association with DDX1.<ref>PMID:10928981</ref> <ref>PMID:12748188</ref> <ref>PMID:17000776</ref> <ref>PMID:17620405</ref> <ref>PMID:19058135</ref> <ref>PMID:20547752</ref> | |||
<div style="background-color:#fffaf0;"> | <div style="background-color:#fffaf0;"> | ||
== Publication Abstract from PubMed == | == Publication Abstract from PubMed == | ||
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__TOC__ | __TOC__ | ||
</StructureSection> | </StructureSection> | ||
[[Category: | [[Category: Homo sapiens]] | ||
[[Category: Large Structures]] | [[Category: Large Structures]] | ||
[[Category: Chuang | [[Category: Chuang PY]] | ||
[[Category: Gerona-Nevarro | [[Category: Gerona-Nevarro G]] | ||
[[Category: He | [[Category: He J]] | ||
[[Category: Joshua | [[Category: Joshua J]] | ||
[[Category: Liu | [[Category: Liu R]] | ||
[[Category: Moshkina | [[Category: Moshkina N]] | ||
[[Category: Ohlmeyer | [[Category: Ohlmeyer M]] | ||
[[Category: Plotnikov | [[Category: Plotnikov AN]] | ||
[[Category: Rusinova | [[Category: Rusinova E]] | ||
[[Category: Zhang | [[Category: Zhang G]] | ||
[[Category: Zhang | [[Category: Zhang W]] | ||
[[Category: Zhong | [[Category: Zhong Y]] | ||
[[Category: Zhou | [[Category: Zhou M-M]] | ||