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5T8Q

Crystal structure of murine NF-kappaB inducing kinase (NIK) bound to aryl pyrrole fragment 17

5T8Q の概要
エントリーDOI10.2210/pdb5t8q/pdb
分子名称Mitogen-activated protein kinase kinase kinase 14, SULFATE ION, 1-[(2-chlorophenyl)methyl]pyrrole-2-carboxamide, ... (4 entities in total)
機能のキーワードprotein serine/threonine kinase, nf-kappab, map3k14, transferase
由来する生物種Mus musculus (House Mouse)
細胞内の位置Cytoplasm: Q9WUL6
タンパク質・核酸の鎖数2
化学式量合計78612.96
構造登録者
Smith, M.A.,McEwan, P.A.,Hymowitz, S.G. (登録日: 2016-09-08, 公開日: 2017-01-11, 最終更新日: 2024-05-08)
主引用文献Castanedo, G.M.,Blaquiere, N.,Beresini, M.,Bravo, B.,Brightbill, H.,Chen, J.,Cui, H.F.,Eigenbrot, C.,Everett, C.,Feng, J.,Godemann, R.,Gogol, E.,Hymowitz, S.,Johnson, A.,Kayagaki, N.,Kohli, P.B.,Knuppel, K.,Kraemer, J.,Kruger, S.,Loke, P.,McEwan, P.,Montalbetti, C.,Roberts, D.A.,Smith, M.,Steinbacher, S.,Sujatha-Bhaskar, S.,Takahashi, R.,Wang, X.,Wu, L.C.,Zhang, Y.,Staben, S.T.
Structure-Based Design of Tricyclic NF-kappa B Inducing Kinase (NIK) Inhibitors That Have High Selectivity over Phosphoinositide-3-kinase (PI3K).
J. Med. Chem., 60:627-640, 2017
Cited by
PubMed Abstract: We report here structure-guided optimization of a novel series of NF-κB inducing kinase (NIK) inhibitors. Starting from a modestly potent, low molecular weight lead, activity was improved by designing a type 11/2 binding mode that accessed a back pocket past the methionine-471 gatekeeper. Divergent binding modes in NIK and PI3K were exploited to dampen PI3K inhibition while maintaining NIK inhibition within these series. Potent compounds were discovered that selectively inhibit the nuclear translocation of NF-κB2 (p52/REL-B) but not canonical NF-κB1 (REL-A/p50).
PubMed: 28005357
DOI: 10.1021/acs.jmedchem.6b01363
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (2.63 Å)
構造検証レポート
Validation report summary of 5t8q
検証レポート(詳細版)ダウンロードをダウンロード

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件を2026-04-29に公開中

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