8OHV

Crystal structure of Beta-glucuronidase from Acidobacterium capsulatum in complex with glucuronic acid configured 3-geminal diol iminosugar inhibitor

これはPDB形式変換不可エントリーです。

8OHV の概要

• エントリーDOI: 10.2210/pdb8ohv/pdb
• 分子名称: beta-glucuronidase from Acidobacterium capsulatum, (3~{S},4~{R})-4,5,5-tris(oxidanyl)piperidine-3-carboxylic acid, SULFATE ION, ... (4 entities in total)
• 機能のキーワード: inhibitor, complex, hydrolase
• 由来する生物種: Acidobacterium capsulatum
• タンパク質・核酸の鎖数: 1
• 化学式量合計: 51087.78

構造登録者

Armstrong, Z.,Yurong, C.,Wu, L.,Overkleeft, H.S.,Davies, G.J. (登録日: 2023-03-21, 公開日: 2024-01-10, 最終更新日: 2024-01-24)

主引用文献

Chen, Y.,van den Nieuwendijk, A.M.C.H.,Wu, L.,Moran, E.,Skoulikopoulou, F.,van Riet, V.,Overkleeft, H.S.,Davies, G.J.,Armstrong, Z.
Molecular Basis for Inhibition of Heparanases and beta-Glucuronidases by Siastatin B.
J.Am.Chem.Soc., 146:125-133, 2024

PubMed Abstract: Siastatin B is a potent and effective iminosugar inhibitor of three diverse glycosidase classes, namely, sialidases, β--glucuronidases, and -acetyl-glucosaminidases. The mode of inhibition of glucuronidases, in contrast to sialidases, has long been enigmatic as siastatin B appears too bulky and incorrectly substituted to be accommodated within a β--glucuronidase active site pocket. Herein, we show through crystallographic analysis of protein-inhibitor complexes that siastatin B generates both a hemiaminal and a 3-geminal diol iminosugar (3-GDI) that are, rather than the parent compound, directly responsible for enzyme inhibition. The hemiaminal product is the first observation of a natural product that belongs to the noeuromycin class of inhibitors. Additionally, the 3-GDI represents a new and potent class of the iminosugar glycosidase inhibitor. To substantiate our findings, we synthesized both the - and -configured 3-GDIs and characterized their binding both structurally and kinetically to exo-β--glucuronidases and the anticancer target human heparanase. This revealed submicromolar inhibition of exo-β--glucuronidases and an unprecedented binding mode by this new class of inhibitor. Our results reveal the mechanism by which siastatin B acts as a broad-spectrum glycosidase inhibitor, identify a new class of glycosidase inhibitor, and suggest new functionalities that can be incorporated into future generations of glycosidase inhibitors.

PubMed: 38118176
DOI: 10.1021/jacs.3c04162

実験手法

X-RAY DIFFRACTION (1.5 Å)