8p74
From Proteopedia
(Difference between revisions)
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- | '''Unreleased structure''' | ||
- | + | ==Cryo-EM structure of CAK in complex with inhibitor ICEC0880 (ring-up conformation)== | |
- | + | <StructureSection load='8p74' size='340' side='right'caption='[[8p74]], [[Resolution|resolution]] 2.20Å' scene=''> | |
- | + | == Structural highlights == | |
- | + | <table><tr><td colspan='2'>[[8p74]] is a 3 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=8P74 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=8P74 FirstGlance]. <br> | |
- | + | </td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">Electron Microscopy, [[Resolution|Resolution]] 2.2Å</td></tr> | |
- | [[Category: | + | <tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=ACE:ACETYL+GROUP'>ACE</scene>, <scene name='pdbligand=X3Z:(2S,3S)-3-[[7-[(2-bromophenyl)methylamino]-3-propan-2-yl-pyrazolo[1,5-a]pyrimidin-5-yl]amino]butane-1,2,4-triol'>X3Z</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=8p74 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=8p74 OCA], [https://pdbe.org/8p74 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=8p74 RCSB], [https://www.ebi.ac.uk/pdbsum/8p74 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=8p74 ProSAT]</span></td></tr> | ||
+ | </table> | ||
+ | == Function == | ||
+ | [https://www.uniprot.org/uniprot/CCNH_HUMAN CCNH_HUMAN] Regulates CDK7, the catalytic subunit of the CDK-activating kinase (CAK) enzymatic complex. CAK activates the cyclin-associated kinases CDK1, CDK2, CDK4 and CDK6 by threonine phosphorylation. CAK complexed to the core-TFIIH basal transcription factor activates RNA polymerase II by serine phosphorylation of the repetitive C-terminus domain (CTD) of its large subunit (POLR2A), allowing its escape from the promoter and elongation of the transcripts. Involved in cell cycle control and in RNA transcription by RNA polymerase II. Its expression and activity are constant throughout the cell cycle.<ref>PMID:7533895</ref> <ref>PMID:10024882</ref> | ||
+ | == References == | ||
+ | <references/> | ||
+ | __TOC__ | ||
+ | </StructureSection> | ||
+ | [[Category: Homo sapiens]] | ||
+ | [[Category: Large Structures]] | ||
+ | [[Category: Ali S]] | ||
+ | [[Category: Bahl AK]] | ||
+ | [[Category: Cushing VI]] | ||
+ | [[Category: Feng J]] | ||
+ | [[Category: Greber BJ]] | ||
+ | [[Category: Jurgaityte K]] | ||
+ | [[Category: Koh AF]] | ||
+ | [[Category: Kotecha A]] |
Revision as of 08:19, 20 March 2024
Cryo-EM structure of CAK in complex with inhibitor ICEC0880 (ring-up conformation)
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Categories: Homo sapiens | Large Structures | Ali S | Bahl AK | Cushing VI | Feng J | Greber BJ | Jurgaityte K | Koh AF | Kotecha A