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2WB5

GlcNAcstatins are nanomolar inhibitors of human O-GlcNAcase inducing cellular hyper-O-GlcNAcylation

2WB5 の概要
エントリーDOI10.2210/pdb2wb5/pdb
関連するPDBエントリー2J62 2JH2 2V5C 2V5D 2VUR
分子名称O-GLCNACASE NAGJ, CHLORIDE ION, SODIUM ION, ... (5 entities in total)
機能のキーワードhydrolase, glycosidase
由来する生物種CLOSTRIDIUM PERFRINGENS
タンパク質・核酸の鎖数2
化学式量合計134300.50
構造登録者
Dorfmueller, H.C.,Borodkin, V.S.,Schimpl, M.,van Aalten, D.M.F. (登録日: 2009-02-20, 公開日: 2009-03-31, 最終更新日: 2023-12-13)
主引用文献Dorfmueller, H.C.,Borodkin, V.S.,Schimpl, M.,Van Aalten, D.M.F.
Glcnacstatins are Nanomolar Inhibitors of Human O-Glcnacase Inducing Cellular Hyper-O-Glcnacylation
Biochem.J., 420:221-, 2009
Cited by
PubMed Abstract: O-GlcNAcylation is an essential, dynamic and inducible post-translational glycosylation of cytosolic proteins in metazoa and can show interplay with protein phosphorylation. Inhibition of OGA (O-GlcNAcase), the enzyme that removes O-GlcNAc from O-GlcNAcylated proteins, is a useful strategy to probe the role of this modification in a range of cellular processes. In the present study, we report the rational design and evaluation of GlcNAcstatins, a family of potent, competitive and selective inhibitors of human OGA. Kinetic experiments with recombinant human OGA reveal that the GlcNAcstatins are the most potent human OGA inhibitors reported to date, inhibiting the enzyme in the sub-nanomolar to nanomolar range. Modification of the GlcNAcstatin N-acetyl group leads to up to 160-fold selectivity against the human lysosomal hexosaminidases which employ a similar substrate-assisted catalytic mechanism. Mutagenesis studies in a bacterial OGA, guided by the structure of a GlcNAcstatin complex, provides insight into the role of conserved residues in the human OGA active site. GlcNAcstatins are cell-permeant and, at low nanomolar concentrations, effectively modulate intracellular O-GlcNAc levels through inhibition of OGA, in a range of human cell lines. Thus these compounds are potent selective tools to study the cell biology of O-GlcNAc.
PubMed: 19275764
DOI: 10.1042/BJ20090110
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (2.31 Å)
構造検証レポート
Validation report summary of 2wb5
検証レポート(詳細版)ダウンロードをダウンロード

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件を2024-10-30に公開中

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