6BJW

Eubacterium eligens Beta-glucuronidase

6BJW の概要

• エントリーDOI: 10.2210/pdb6bjw/pdb
• 分子名称: Glycoside Hydrolase Family 2 candidate b-glucuronidase (1 entity in total)
• 機能のキーワード: glycosyl hydrolase, beta-glucuronidase, hydrolase
• 由来する生物種: Eubacterium eligens (strain ATCC 27750 / VPI C15-48)
• タンパク質・核酸の鎖数: 1
• 化学式量合計: 72349.87

構造登録者

Pellock, S.J.,Walton, W.G.,Redinbo, M.R. (登録日: 2017-11-07, 公開日: 2018-07-25, 最終更新日: 2024-05-22)

主引用文献

Pellock, S.J.,Creekmore, B.C.,Walton, W.G.,Mehta, N.,Biernat, K.A.,Cesmat, A.P.,Ariyarathna, Y.,Dunn, Z.D.,Li, B.,Jin, J.,James, L.I.,Redinbo, M.R.
Gut Microbial beta-Glucuronidase Inhibition via Catalytic Cycle Interception.
ACS Cent Sci, 4:868-879, 2018

PubMed Abstract: Microbial β-glucuronidases (GUSs) cause severe gut toxicities that limit the efficacy of cancer drugs and other therapeutics. Selective inhibitors of bacterial GUS have been shown to alleviate these side effects. Using structural and chemical biology, mass spectrometry, and cell-based assays, we establish that piperazine-containing GUS inhibitors intercept the glycosyl-enzyme catalytic intermediate of these retaining glycosyl hydrolases. We demonstrate that piperazine-based compounds are substrate-dependent GUS inhibitors that bind to the GUS-GlcA catalytic intermediate as a piperazine-linked glucuronide (GlcA, glucuronic acid). We confirm the GUS-dependent formation of inhibitor-glucuronide conjugates by LC-MS and show that methylated piperazine analogs display significantly reduced potencies. We further demonstrate that a range of approved piperazine- and piperidine-containing drugs from many classes, including those for the treatment of depression, infection, and cancer, function by the same mechanism, and we confirm through gene editing that these compounds selectively inhibit GUS in living bacterial cells. Together, these data reveal a unique mechanism of GUS inhibition and show that a range of therapeutics may impact GUS activities in the human gut.

PubMed: 30062115
DOI: 10.1021/acscentsci.8b00239

実験手法

X-RAY DIFFRACTION (3 Å)