5AR5

RIP2 Kinase Catalytic Domain (1 - 310) complex with Benzimidazole

5AR5 の概要

• エントリーDOI: 10.2210/pdb5ar5/pdb
• 関連するPDBエントリー: 5AR2 5AR3 5AR4 5AR7 5AR8
• 分子名称: RECEPTOR-INTERACTING SERINE/THREONINE-PROTEIN KINASE 2, CALCIUM ION, 2-(2-(4-CHLOROPHENYL)-1H-IMIDAZOL-5-YL)-N,1-BIS(2-METHOXYETHYL)-1H-BENZO[D]IMIDAZOLE-5-CARBOXAMIDE, ... (4 entities in total)
• 機能のキーワード: transferase, kinase domain, kinase inhibitor, structure-based drug design, inhibitor selectivity
• 由来する生物種: HOMO SAPIENS (HUMAN)
• 細胞内の位置: Cytoplasm : O43353
• タンパク質・核酸の鎖数: 2
• 化学式量合計: 76159.88

構造登録者

Charnley, A.K.,Convery, M.A.,Lakdawala Shah, A.,Jones, E.,Hardwicke, P.,Bridges, A.,Votta, B.J.,Gough, P.J.,Marquis, R.W.,Bertin, J.,Casillas, L. (登録日: 2015-09-24, 公開日: 2015-10-21, 最終更新日: 2024-01-10)

主引用文献

Charnley, A.K.,Convery, M.A.,Lakdawala Shah, A.,Jones, E.,Hardwicke, P.,Bridges, A.,Ouellette, M.,Totoritis, R.,Schwartz, B.,King, B.W.,Wisnoski, D.D.,Kang, J.,Eidam, P.M.,Votta, B.J.,Gough, P.J.,Marquis, R.W.,Bertin, J.,Casillas, L.
Crystal Structures of Human Rip2 Kinase Catalytic Domain Complexed with ATP-Competitive Inhibitors: Foundations for Understanding Inhibitor Selectivity.
Bioorg.Med.Chem., 23:7000-, 2015

PubMed Abstract: Receptor interacting protein 2 (RIP2) is an intracellular kinase and key signaling partner for the pattern recognition receptors NOD1 and NOD2 (nucleotide-binding oligomerization domain-containing proteins 1 and 2). As such, RIP2 represents an attractive target to probe the role of these pathways in disease. In an effort to design potent and selective inhibitors of RIP2 we established a crystallographic system and determined the structure of the RIP2 kinase domain in an apo form and also in complex with multiple inhibitors including AMP-PCP (β,γ-Methyleneadenosine 5'-triphosphate, a non-hydrolysable adenosine triphosphate mimic) and structurally diverse ATP competitive chemotypes identified via a high-throughput screening campaign. These structures represent the first set of diverse RIP2-inhibitor co-crystal structures and demonstrate that the protein possesses the ability to adopt multiple DFG-in as well as DFG-out and C-helix out conformations. These structures reveal key protein-inhibitor structural insights and serve as the foundation for establishing a robust structure-based drug design effort to identify both potent and highly selective inhibitors of RIP2 kinase.

PubMed: 26455654
DOI: 10.1016/J.BMC.2015.09.038

実験手法

X-RAY DIFFRACTION (2.66 Å)