6ZGC

Crystal structure of the ACVR1 (ALK2) kinase in complex with the compound Saracatinib (AZD0530)

6ZGC の概要

• エントリーDOI: 10.2210/pdb6zgc/pdb
• 分子名称: Activin receptor type I, N-(5-CHLORO-1,3-BENZODIOXOL-4-YL)-7-[2-(4-METHYLPIPERAZIN-1-YL)ETHOXY]-5-(TETRAHYDRO-2H-PYRAN-4-YLOXY)QUINAZOLIN-4-AMINE, POTASSIUM ION, ... (5 entities in total)
• 機能のキーワード: inhibitor complex. kinase. type i receptor, bmp, signalling., signaling protein
• 由来する生物種: Homo sapiens (Human)
• タンパク質・核酸の鎖数: 4
• 化学式量合計: 141994.56

構造登録者

Williams, E.P.,Galan Bartual, S.,Burgess-Brown, N.,von Delft, F.,Arrowsmith, C.H.,Edwards, A.M.,Bountra, C.,Bullock, A.N. (登録日: 2020-06-18, 公開日: 2020-07-29, 最終更新日: 2024-10-16)

主引用文献

Williams, E.,Bagarova, J.,Kerr, G.,Xia, D.D.,Place, E.S.,Dey, D.,Shen, Y.,Bocobo, G.A.,Mohedas, A.H.,Huang, X.,Sanderson, P.E.,Lee, A.,Zheng, W.,Economides, A.N.,Smith, J.C.,Yu, P.B.,Bullock, A.N.
Saracatinib is an efficacious clinical candidate for fibrodysplasia ossificans progressiva.
JCI Insight, 6:-, 2021

PubMed Abstract: Currently, no effective therapies exist for fibrodysplasia ossificans progressiva (FOP), a rare congenital syndrome in which heterotopic bone is formed in soft tissues owing to dysregulated activity of the bone morphogenetic protein (BMP) receptor kinase ALK2 (also known as ACVR1). From a screen of known biologically active compounds, we identified saracatinib as a potent ALK2 kinase inhibitor. In enzymatic and cell-based assays, saracatinib preferentially inhibited ALK2, compared with other receptors of the BMP/TGF-β signaling pathway, and induced dorsalization in zebrafish embryos consistent with BMP antagonism. We further tested the efficacy of saracatinib using an inducible ACVR1Q207D-transgenic mouse line, which provides a model of heterotopic ossification (HO), as well as an inducible ACVR1R206H-knockin mouse, which serves as a genetically and physiologically faithful FOP model. In both models, saracatinib was well tolerated and potently inhibited the development of HO, even when administered transiently following soft tissue injury. Together, these data suggest that saracatinib is an efficacious clinical candidate for repositioning in FOP treatment, offering an accelerated path to clinical proof-of-efficacy studies and potentially significant benefits to individuals with this devastating condition.

PubMed: 33705358
DOI: 10.1172/jci.insight.95042

実験手法

X-RAY DIFFRACTION (2.67 Å)