8p6v
From Proteopedia
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m (Protected "8p6v" [edit=sysop:move=sysop]) |
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- | '''Unreleased structure''' | ||
- | + | ==Cryo-EM structure of CAK in complex with inhibitor ICEC0942== | |
- | + | <StructureSection load='8p6v' size='340' side='right'caption='[[8p6v]], [[Resolution|resolution]] 1.90Å' scene=''> | |
- | + | == Structural highlights == | |
- | + | <table><tr><td colspan='2'>[[8p6v]] 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=8P6V OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=8P6V 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]] 1.9Å</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=I74:(3R,4R)-4-[[[7-[(PHENYLMETHYL)AMINO]-3-PROPAN-2-YL-PYRAZOLO[1,5-A]PYRIMIDIN-5-YL]AMINO]METHYL]PIPERIDIN-3-OL'>I74</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=8p6v FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=8p6v OCA], [https://pdbe.org/8p6v PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=8p6v RCSB], [https://www.ebi.ac.uk/pdbsum/8p6v PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=8p6v 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 09:18, 30 August 2023
Cryo-EM structure of CAK in complex with inhibitor ICEC0942
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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