8VQ4

CDK2-CyclinE1 in complex with allosteric inhibitor I-125A.

これはPDB形式変換不可エントリーです。

8VQ4 の概要

• エントリーDOI: 10.2210/pdb8vq4/pdb
• 関連するPDBエントリー: 8VQ3
• 分子名称: Cyclin-dependent kinase 2, G1/S-specific cyclin-E1, (8R)-6-(1-benzyl-1H-pyrazole-4-carbonyl)-N-[(2S,3R)-3-(2-cyclohexylethoxy)-1-(methylamino)-1-oxobutan-2-yl]-2-[(1S)-2,2-dimethylcyclopropane-1-carbonyl]-2,6-diazaspiro[3.4]octane-8-carboxamide, ... (4 entities in total)
• 機能のキーワード: kinase, cell cycle-transferase-inhibitor complex, cell cycle/transferase/inhibitor
• 由来する生物種: Homo sapiens (human); 詳細
• タンパク質・核酸の鎖数: 2
• 化学式量合計: 67770.82

構造登録者

Hirschi, M.,Johnson, E.,Zhang, Y.,Liu, Z.,Brodsky, O.,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. (登録日: 2024-01-17, 公開日: 2024-01-31, 最終更新日: 2025-03-12)

主引用文献

Zhang, Y.,Liu, Z.,Hirschi, M.,Brodsky, O.,Johnson, E.,Won, S.J.,Nagata, A.,Bezwada, D.,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.F.
An allosteric cyclin E-CDK2 site mapped by paralog hopping with covalent probes.
Nat.Chem.Biol., 21:420-431, 2025

PubMed Abstract: More than half of the ~20,000 protein-encoding human genes have paralogs. Chemical proteomics has uncovered many electrophile-sensitive cysteines that are exclusive to subsets of paralogous proteins. Here we explore whether such covalent compound-cysteine interactions can be used to discover ligandable pockets in paralogs lacking the cysteine. Leveraging the covalent ligandability of C109 in the cyclin CCNE2, we substituted the corresponding residue in paralog CCNE1 to cysteine (N112C) and found through activity-based protein profiling that this mutant reacts stereoselectively and site-specifically with tryptoline acrylamides. We then converted the tryptoline acrylamide-CCNE1-N112C interaction into in vitro NanoBRET (bioluminescence resonance energy transfer) and in cellulo activity-based protein profiling assays capable of identifying compounds that reversibly inhibit both the N112C mutant and wild-type CCNE1:CDK2 (cyclin-dependent kinase 2) complexes. X-ray crystallography revealed a cryptic allosteric pocket at the CCNE1:CDK2 interface adjacent to N112 that binds the reversible inhibitors. Our findings, thus, show how electrophile-cysteine interactions mapped by chemical proteomics can extend the understanding of protein ligandability beyond covalent chemistry.

PubMed: 39294320
DOI: 10.1038/s41589-024-01738-7

実験手法

X-RAY DIFFRACTION (1.9 Å)