4XUF

Crystal structure of the FLT3 kinase domain bound to the inhibitor quizartinib (AC220)

4XUF の概要

• エントリーDOI: 10.2210/pdb4xuf/pdb
• 分子名称: Receptor-type tyrosine-protein kinase FLT3, 1-(5-tert-butyl-1,2-oxazol-3-yl)-3-(4-{7-[2-(morpholin-4-yl)ethoxy]imidazo[2,1-b][1,3]benzothiazol-2-yl}phenyl)urea (3 entities in total)
• 機能のキーワード: flt3, receptor tyrosine kinase, ac220, quizartinib, transferase-transferase inhibitor complex, transferase/transferase inhibitor
• 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: 69085.44

構造登録者

Zorn, J.A.,Wang, Q.,Fujimura, E.,Barros, T.,Kuriyan, J. (登録日: 2015-01-25, 公開日: 2015-04-15, 最終更新日: 2023-09-27)

主引用文献

Zorn, J.A.,Wang, Q.,Fujimura, E.,Barros, T.,Kuriyan, J.
Crystal Structure of the FLT3 Kinase Domain Bound to the Inhibitor Quizartinib (AC220).
Plos One, 10:e0121177-e0121177, 2015

PubMed Abstract: More than 30% of acute myeloid leukemia (AML) patients possess activating mutations in the receptor tyrosine kinase FMS-like tyrosine kinase 3 or FLT3. A small-molecule inhibitor of FLT3 (known as quizartinib or AC220) that is currently in clinical trials appears promising for the treatment of AML. Here, we report the co-crystal structure of the kinase domain of FLT3 in complex with quizartinib. FLT3 with quizartinib bound adopts an "Abl-like" inactive conformation with the activation loop stabilized in the "DFG-out" orientation and folded back onto the kinase domain. This conformation is similar to that observed for the uncomplexed intracellular domain of FLT3 as well as for related receptor tyrosine kinases, except for a localized induced fit in the activation loop. The co-crystal structure reveals the interactions between quizartinib and the active site of FLT3 that are key for achieving its high potency against both wild-type FLT3 as well as a FLT3 variant observed in many AML patients. This co-complex further provides a structural rationale for quizartinib-resistance mutations.

PubMed: 25837374
DOI: 10.1371/journal.pone.0121177

実験手法

X-RAY DIFFRACTION (3.2 Å)