7KBJ

Co-crystal structure of alpha glucosidase with compound 9

7KBJ の概要

• エントリーDOI: 10.2210/pdb7kbj/pdb
• 分子名称: Neutral alpha-glucosidase AB Trypsin-cleaved Fragment #1, DI(HYDROXYETHYL)ETHER, CALCIUM ION, ... (12 entities in total)
• 機能のキーワード: alpha glucosidase ii, endoplasmic reticulum, hydrolase, inhibitor complex
• 由来する生物種: Mus musculus (Mouse); 詳細
• タンパク質・核酸の鎖数: 8
• 化学式量合計: 239800.63

構造登録者

Karade, S.S.,Mariuzza, R.A. (登録日: 2020-10-02, 公開日: 2021-10-06, 最終更新日: 2024-12-25)

主引用文献

Karade, S.S.,Hill, M.L.,Kiappes, J.L.,Manne, R.,Aakula, B.,Zitzmann, N.,Warfield, K.L.,Treston, A.M.,Mariuzza, R.A.
N-Substituted Valiolamine Derivatives as Potent Inhibitors of Endoplasmic Reticulum alpha-Glucosidases I and II with Antiviral Activity.
J.Med.Chem., 64:18010-18024, 2021

PubMed Abstract: Most enveloped viruses rely on the host cell endoplasmic reticulum (ER) quality control (QC) machinery for proper folding of glycoproteins. The key ER α-glucosidases (α-Glu) I and II of the ERQC machinery are attractive targets for developing broad-spectrum antivirals. Iminosugars based on deoxynojirimycin have been extensively studied as ER α-glucosidase inhibitors; however, other glycomimetic compounds are less established. Accordingly, we synthesized a series of N-substituted derivatives of valiolamine, the iminosugar scaffold of type 2 diabetes drug voglibose. To understand the basis for up to 100,000-fold improved inhibitory potency, we determined high-resolution crystal structures of mouse ER α-GluII in complex with valiolamine and 10 derivatives. The structures revealed extensive interactions with all four α-GluII subsites. We further showed that N-substituted valiolamines were active against dengue virus and SARS-CoV-2 . This study introduces valiolamine-based inhibitors of the ERQC machinery as candidates for developing potential broad-spectrum therapeutics against the existing and emerging viruses.

PubMed: 34870992
DOI: 10.1021/acs.jmedchem.1c01377

実験手法

X-RAY DIFFRACTION (2.21 Å)