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8P73

Cryo-EM structure of CAK in complex with inhibitor ICEC0829

Summary for 8P73
Entry DOI10.2210/pdb8p73/pdb
Related8ORM
EMDB information17129 17516
DescriptorCDK-activating kinase assembly factor MAT1, Cyclin-H, Cyclin-dependent kinase 7, ... (6 entities in total)
Functional Keywordskinase, inhibitor, transcription, cell cycle, transferase
Biological sourceHomo sapiens (human)
More
Total number of polymer chains3
Total formula weight88139.66
Authors
Cushing, V.I.,Koh, A.F.,Feng, J.,Jurgaityte, K.,Bahl, A.K.,Ali, S.,Kotecha, A.,Greber, B.J. (deposition date: 2023-05-30, release date: 2024-03-20, Last modification date: 2024-03-27)
Primary citationCushing, V.I.,Koh, A.F.,Feng, J.,Jurgaityte, K.,Bondke, A.,Kroll, S.H.B.,Barbazanges, M.,Scheiper, B.,Bahl, A.K.,Barrett, A.G.M.,Ali, S.,Kotecha, A.,Greber, B.J.
High-resolution cryo-EM of the human CDK-activating kinase for structure-based drug design.
Nat Commun, 15:2265-2265, 2024
Cited by
PubMed Abstract: Rational design of next-generation therapeutics can be facilitated by high-resolution structures of drug targets bound to small-molecule inhibitors. However, application of structure-based methods to macromolecules refractory to crystallization has been hampered by the often-limiting resolution and throughput of cryogenic electron microscopy (cryo-EM). Here, we use high-resolution cryo-EM to determine structures of the CDK-activating kinase, a master regulator of cell growth and division, in its free and nucleotide-bound states and in complex with 15 inhibitors at up to 1.8 Å resolution. Our structures provide detailed insight into inhibitor interactions and networks of water molecules in the active site of cyclin-dependent kinase 7 and provide insights into the mechanisms contributing to inhibitor selectivity, thereby providing the basis for rational design of next-generation therapeutics. These results establish a methodological framework for the use of high-resolution cryo-EM in structure-based drug design.
PubMed: 38480681
DOI: 10.1038/s41467-024-46375-9
PDB entries with the same primary citation
Experimental method
ELECTRON MICROSCOPY (2 Å)
Structure validation

226707

数据于2024-10-30公开中

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