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8VQ3

CDK2-CyclinE1 in complex with allosteric inhibitor I-198.

This is a non-PDB format compatible entry.
Summary for 8VQ3
Entry DOI10.2210/pdb8vq3/pdb
Related8VQ4
DescriptorCyclin-dependent kinase 2, G1/S-specific cyclin-E1, (8R)-N-[(2S,3R)-3-(cyclohexylmethoxy)-1-(morpholin-4-yl)-1-oxobutan-2-yl]-2-[(1S)-2,2-dimethylcyclopropane-1-carbonyl]-6-(1,3-thiazole-5-carbonyl)-2,6-diazaspiro[3.4]octane-8-carboxamide, ... (4 entities in total)
Functional Keywordskinase, cell cycle-transferase-inhibitor complex, cell cycle/transferase/inhibitor
Biological sourceHomo sapiens (human)
More
Total number of polymer chains2
Total formula weight67739.78
Authors
Primary citationZhang, Y.,Liu, Z.,Hirschi, M.,Brodsky, O.,Johnson, E.,Won, S.J.,Nagata, A.,Petroski, M.D.,Majmudar, J.D.,Niessen, S.,VanArsdale, T.,Gilbert, A.M.,Hayward, M.M.,Stewart, A.E.,Nager, A.R.,Melillo, B.,Cravatt, B.
Expanding the ligandable proteome by paralog hopping with covalent probes.
Biorxiv, 2024
Cited by
PubMed: 38293178
DOI: 10.1101/2024.01.18.576274
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (1.84 Å)
Structure validation

218853

PDB entries from 2024-04-24

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