4D9T

Rsk2 C-terminal Kinase Domain with inhibitor (E)-methyl 3-(4-amino-7-(3-hydroxypropyl)-5-p-tolyl-7H-pyrrolo[2,3-d]pyrimidin-6-yl)-2-cyanoacrylate

4D9T の概要

• エントリーDOI: 10.2210/pdb4d9t/pdb
• 関連するPDBエントリー: 4D9U
• 分子名称: Ribosomal protein S6 kinase alpha-3, methyl (2S)-3-{4-amino-7-[(1E)-3-hydroxyprop-1-en-1-yl]-5-(4-methylphenyl)-7H-pyrrolo[2,3-d]pyrimidin-6-yl}-2-cyanopropanoate, SODIUM ION, ... (4 entities in total)
• 機能のキーワード: kinase, inhibitor, reversible, thiol, phosphorylation, migration, transferase-transferase inhibitor complex, transferase/transferase inhibitor
• 由来する生物種: Homo sapiens (human)
• 細胞内の位置: Nucleus (By similarity): P51812
• タンパク質・核酸の鎖数: 1
• 化学式量合計: 38893.34

構造登録者

Serafimova, I.M.,Pufall, M.A.,Krishnan, S.,Duda, K.,Cohen, M.S.,Maglathlin, R.L.,McFarland, J.M.,Miller, R.M.,Frodin, M.,Taunton, J. (登録日: 2012-01-12, 公開日: 2012-04-25, 最終更新日: 2024-11-20)

主引用文献

Serafimova, I.M.,Pufall, M.A.,Krishnan, S.,Duda, K.,Cohen, M.S.,Maglathlin, R.L.,McFarland, J.M.,Miller, R.M.,Frodin, M.,Taunton, J.
Reversible targeting of noncatalytic cysteines with chemically tuned electrophiles.
Nat.Chem.Biol., 8:471-476, 2012

PubMed Abstract: Targeting noncatalytic cysteine residues with irreversible acrylamide-based inhibitors is a powerful approach for enhancing pharmacological potency and selectivity. Nevertheless, concerns about off-target modification motivate the development of reversible cysteine-targeting strategies. Here we show that electron-deficient olefins, including acrylamides, can be tuned to react with cysteine thiols in a rapidly reversible manner. Installation of a nitrile group increased the olefins' intrinsic reactivity, but, paradoxically, eliminated the formation of irreversible adducts. Incorporation of these electrophiles into a noncovalent kinase-recognition scaffold produced slowly dissociating, covalent inhibitors of the p90 ribosomal protein S6 kinase RSK2. A cocrystal structure revealed specific noncovalent interactions that stabilize the complex by positioning the electrophilic carbon near the targeted cysteine. Disruption of these interactions by protein unfolding or proteolysis promoted instantaneous cleavage of the covalent bond. Our results establish a chemistry-based framework for engineering sustained covalent inhibition without accumulating permanently modified proteins and peptides.

PubMed: 22466421
DOI: 10.1038/nchembio.925

実験手法

X-RAY DIFFRACTION (2.4 Å)