7P4C
Crystal Structure of Agd31B, alpha-transglucosylase in Glycoside Hydrolase Family 31, in complex with noncovalent Cyclophellitol Sulfamidate probe KK131
これはPDB形式変換不可エントリーです。
7P4C の概要
| エントリーDOI | 10.2210/pdb7p4c/pdb |
| 関連するPDBエントリー | 7P2Z 7P32 7P4D |
| 分子名称 | Oligosaccharide 4-alpha-D-glucosyltransferase, 1,2-ETHANEDIOL, OXALATE ION, ... (6 entities in total) |
| 機能のキーワード | glycoside hydrolase, gh31, inhibitor, carbohydrate, hydrolase |
| 由来する生物種 | Cellvibrio japonicus (strain Ueda107) (Pseudomonas fluorescens subsp. cellulosa) |
| タンパク質・核酸の鎖数 | 1 |
| 化学式量合計 | 96048.81 |
| 構造登録者 | |
| 主引用文献 | Kok, K.,Kuo, C.L.,Katzy, R.E.,Lelieveld, L.T.,Wu, L.,Roig-Zamboni, V.,van der Marel, G.A.,Codee, J.D.C.,Sulzenbacher, G.,Davies, G.J.,Overkleeft, H.S.,Aerts, J.M.F.G.,Artola, M. 1,6- epi-Cyclophellitol Cyclosulfamidate Is a Bona Fide Lysosomal alpha-Glucosidase Stabilizer for the Treatment of Pompe Disease. J.Am.Chem.Soc., 144:14819-14827, 2022 Cited by PubMed Abstract: α-Glucosidase inhibitors are potential therapeutics for the treatment of diabetes, viral infections, and Pompe disease. Herein, we report a 1,6--cyclophellitol cyclosulfamidate as a new class of reversible α-glucosidase inhibitors that displays enzyme inhibitory activity by virtue of its conformational mimicry of the substrate when bound in the Michaelis complex. The α-d-configured cyclophellitol cyclosulfamidate binds in a competitive manner the human lysosomal acid α-glucosidase (GAA), ER α-glucosidases, and, at higher concentrations, intestinal α-glucosidases, displaying an excellent selectivity over the human β-glucosidases GBA and GBA2 and glucosylceramide synthase (GCS). Cyclosulfamidate stabilizes recombinant human GAA (rhGAA, alglucosidase alfa, Myozyme) in cell medium and plasma and facilitates enzyme trafficking to lysosomes. It stabilizes rhGAA more effectively than existing small-molecule chaperones and does so , , and in zebrafish, thus representing a promising therapeutic alternative to Miglustat for Pompe disease. PubMed: 35917590DOI: 10.1021/jacs.2c05666 主引用文献が同じPDBエントリー |
| 実験手法 | X-RAY DIFFRACTION (1.86 Å) |
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