8p76
From Proteopedia
(Difference between revisions)
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- | '''Unreleased structure''' | ||
- | + | ==Cryo-EM structure of CAK in complex with inhibitor ICEC0914== | |
- | + | <StructureSection load='8p76' size='340' side='right'caption='[[8p76]], [[Resolution|resolution]] 2.00Å' scene=''> | |
- | + | == Structural highlights == | |
- | + | <table><tr><td colspan='2'>[[8p76]] 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=8P76 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=8P76 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]] 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=X1W:N5-[(3S,4R)-4-phenylmethoxypyrrolidin-3-yl]-N7-(phenylmethyl)-3-propan-2-yl-pyrazolo[1,5-a]pyrimidine-5,7-diamine'>X1W</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=8p76 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=8p76 OCA], [https://pdbe.org/8p76 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=8p76 RCSB], [https://www.ebi.ac.uk/pdbsum/8p76 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=8p76 ProSAT]</span></td></tr> | ||
+ | </table> | ||
+ | == Function == | ||
+ | [https://www.uniprot.org/uniprot/MAT1_HUMAN MAT1_HUMAN] Stabilizes the cyclin H-CDK7 complex to form a functional 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.<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 ICEC0914
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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