5D61
MOA-Z-VAD-fmk complex, direct orientation
5D61 の概要
エントリーDOI | 10.2210/pdb5d61/pdb |
関連するPDBエントリー | 2IHO 3EF2 |
関連するBIRD辞書のPRD_ID | PRD_000338 |
分子名称 | Agglutinin, Z-VAD-fmk, alpha-L-fucopyranose-(1-2)-[alpha-D-galactopyranose-(1-3)]beta-D-galactopyranose, ... (10 entities in total) |
機能のキーワード | hydrolase, papain-like, inhibitor, protease, fungal |
由来する生物種 | Marasmius oreades 詳細 |
タンパク質・核酸の鎖数 | 2 |
化学式量合計 | 34668.86 |
構造登録者 | Cordara, G.,van Eerde, A.,Grahn, E.M.,Goldstein, I.J.,Krengel, U. (登録日: 2015-08-11, 公開日: 2016-03-02, 最終更新日: 2024-10-23) |
主引用文献 | Cordara, G.,van Eerde, A.,Grahn, E.M.,Winter, H.C.,Goldstein, I.J.,Krengel, U. An Unusual Member of the Papain Superfamily: Mapping the Catalytic Cleft of the Marasmius oreades agglutinin (MOA) with a Caspase Inhibitor. Plos One, 11:e0149407-e0149407, 2016 Cited by PubMed Abstract: Papain-like cysteine proteases (PLCPs) constitute the largest group of thiol-based protein degrading enzymes and are characterized by a highly conserved fold. They are found in bacteria, viruses, plants and animals and involved in a number of physiological and pathological processes, parasitic infections and host defense, making them interesting targets for drug design. The Marasmius oreades agglutinin (MOA) is a blood group B-specific fungal chimerolectin with calcium-dependent proteolytic activity. The proteolytic domain of MOA presents a unique structural arrangement, yet mimicking the main structural elements in known PLCPs. Here we present the X-ray crystal structure of MOA in complex with Z-VAD-fmk, an irreversible caspase inhibitor known to cross-react with PLCPs. The structural data allow modeling of the substrate binding geometry and mapping of the fundamental enzyme-substrate interactions. The new information consolidates MOA as a new, yet strongly atypical member of the papain superfamily. The reported complex is the first published structure of a PLCP in complex with the well characterized caspase inhibitor Z-VAD-fmk. PubMed: 26901797DOI: 10.1371/journal.pone.0149407 主引用文献が同じPDBエントリー |
実験手法 | X-RAY DIFFRACTION (1.6 Å) |
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