6NZF

CRYSTAL STRUCTURE OF TYROSINE KINASE 2 JH2 (PSEUDO KINASE DOMAIN) COMPLEXED WITH Compound_5 AKA 4-[(2-CARBAMOYLPHEN YL)AMINO]-6-[(5-FLUOROPYRIDIN-2-YL)AMINO]-N-METHYLPYRIDINE -3-CARBOXAMIDE

6NZF の概要

• エントリーDOI: 10.2210/pdb6nzf/pdb
• 分子名称: Non-receptor tyrosine-protein kinase TYK2, 6-[(5-fluoropyridin-2-yl)amino]-N-methyl-4-{[2-(methylsulfonyl)phenyl]amino}pyridine-3-carboxamide, SULFATE ION, ... (4 entities in total)
• 機能のキーワード: jtk1, 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: 72117.38

構造登録者

Muckelbauer, J.M. (登録日: 2019-02-13, 公開日: 2019-07-24, 最終更新日: 2023-10-11)

主引用文献

Moslin, R.,Zhang, Y.,Wrobleski, S.T.,Lin, S.,Mertzman, M.,Spergel, S.,Tokarski, J.S.,Strnad, J.,Gillooly, K.,McIntyre, K.W.,Zupa-Fernandez, A.,Cheng, L.,Sun, H.,Chaudhry, C.,Huang, C.,D'Arienzo, C.,Heimrich, E.,Yang, X.,Muckelbauer, J.K.,Chang, C.,Tredup, J.,Mulligan, D.,Xie, D.,Aranibar, N.,Chiney, M.,Burke, J.R.,Lombardo, L.,Carter, P.H.,Weinstein, D.S.
Identification ofN-Methyl Nicotinamide andN-Methyl Pyridazine-3-Carboxamide Pseudokinase Domain Ligands as Highly Selective Allosteric Inhibitors of Tyrosine Kinase 2 (TYK2).
J.Med.Chem., 62:8953-8972, 2019

PubMed Abstract: As a member of the Janus (JAK) family of nonreceptor tyrosine kinases, TYK2 plays an important role in mediating the signaling of pro-inflammatory cytokines including IL-12, IL-23, and type 1 interferons. The nicotinamide , identified by a SPA-based high-throughput screen targeting the TYK2 pseudokinase domain, potently inhibits IL-23 and IFNα signaling in cellular assays. The described work details the optimization of this poorly selective hit () to potent and selective molecules such as and . The discoveries described herein were critical to the eventual identification of the clinical TYK2 JH2 inhibitor (see following report in this issue). Compound provided robust inhibition in a mouse IL-12-induced IFNγ pharmacodynamic model as well as efficacy in an IL-23 and IL-12-dependent mouse colitis model. These results demonstrate the ability of TYK2 JH2 domain binders to provide a highly selective alternative to conventional TYK2 orthosteric inhibitors.

PubMed: 31314518
DOI: 10.1021/acs.jmedchem.9b00443

実験手法

X-RAY DIFFRACTION (2.39 Å)