7K89

Crystal structure of bovine RPE65 in complex with 4-fluoro-emixustat and palmitate

7K89 の概要

• エントリーDOI: 10.2210/pdb7k89/pdb
• 分子名称: Retinoid isomerohydrolase, FE (II) ION, PALMITIC ACID, ... (7 entities in total)
• 機能のキーワード: non-heme iron, isomerohydrolase, inhibitor, beta-propeller, isomerase, hydrolase-inhibitor complex, hydrolase/inhibitor
• 由来する生物種: Bos taurus (Bovine)
• タンパク質・核酸の鎖数: 2
• 化学式量合計: 123491.78

構造登録者

Kiser, P.D. (登録日: 2020-09-26, 公開日: 2021-06-02, 最終更新日: 2024-10-09)

主引用文献

Blum, E.,Zhang, J.,Zaluski, J.,Einstein, D.E.,Korshin, E.E.,Kubas, A.,Gruzman, A.,Tochtrop, G.P.,Kiser, P.D.,Palczewski, K.
Rational Alteration of Pharmacokinetics of Chiral Fluorinated and Deuterated Derivatives of Emixustat for Retinal Therapy.
J.Med.Chem., 64:8287-8302, 2021

PubMed Abstract: Recycling of all--retinal to 11--retinal through the visual cycle is a fundamental metabolic pathway in the eye. A potent retinoid isomerase (RPE65) inhibitor, ()-emixustat, has been developed and tested in several clinical trials; however, it has not received regulatory approval for use in any specific retinopathy. Rapid clearance of this drug presents challenges to maintaining concentrations in eyes within a therapeutic window. To address this pharmacokinetic inadequacy, we rationally designed and synthesized a series of emixustat derivatives with strategically placed fluorine and deuterium atoms to slow down the key metabolic transformations known for emixustat. Crystal structures and quantum chemical analysis of RPE65 in complex with the most potent emixustat derivatives revealed the structural and electronic bases for how fluoro substituents can be favorably accommodated within the active site pocket of RPE65. We found a close (∼3.0 Å) F-π interaction that is predicted to contribute ∼2.4 kcal/mol to the overall binding energy.

PubMed: 34081480
DOI: 10.1021/acs.jmedchem.1c00279

実験手法

X-RAY DIFFRACTION (2.15 Å)