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6UL8

RIP2 kinase catalytic domain complex with (5S,6S,8R)-2-(benzo[d]thiazol-5-yl)-6-hydroxy-4,5,6,7,8,9-hexahydro-5,8-methanopyrazolo[1,5-a][1,3]diazocine-3-carboxamide

6UL8 の概要
エントリーDOI10.2210/pdb6ul8/pdb
分子名称Receptor-interacting serine/threonine-protein kinase 2, (5S,6S,8R)-2-(1,3-benzothiazol-5-yl)-6-hydroxy-4,5,6,7,8,9-hexahydro-5,8-methanopyrazolo[1,5-a][1,3]diazocine-3-carboxamide, CALCIUM ION, ... (4 entities in total)
機能のキーワードkinase, transferase
由来する生物種Homo sapiens (Human)
タンパク質・核酸の鎖数2
化学式量合計71139.84
構造登録者
Shewchuk, L.M.,Convery, M.A. (登録日: 2019-10-07, 公開日: 2019-12-04, 最終更新日: 2023-10-11)
主引用文献Haffner, C.D.,Charnley, A.K.,Aquino, C.J.,Casillas, L.,Convery, M.A.,Cox, J.A.,Elban, M.A.,Goodwin, N.C.,Gough, P.J.,Haile, P.A.,Hughes, T.V.,Knapp-Reed, B.,Kreatsoulas, C.,Lakdawala, A.S.,Li, H.,Lian, Y.,Lipshutz, D.,Mehlmann, J.F.,Ouellette, M.,Romano, J.,Shewchuk, L.,Shu, A.,Votta, B.J.,Zhou, H.,Bertin, J.,Marquis, R.W.
Discovery of Pyrazolocarboxamides as Potent and Selective Receptor Interacting Protein 2 (RIP2) Kinase Inhibitors.
Acs Med.Chem.Lett., 10:1518-1523, 2019
Cited by
PubMed: 31749904
DOI: 10.1021/acsmedchemlett.9b00141
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (2.68 Å)
構造検証レポート
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2024-06-12に公開中

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