8AJ5
X-ray structure of lysozyme obtained upon reaction with [VIVO(malt)2] (Structure B)
これはPDB形式変換不可エントリーです。
8AJ5 の概要
| エントリーDOI | 10.2210/pdb8aj5/pdb |
| 分子名称 | Lysozyme, SODIUM ION, VANADATE ION, ... (8 entities in total) |
| 機能のキーワード | metallodrug, vanadium, oxidovanadium, covalent binding, non-covalent binding, protein-metal interaction, hydrolase |
| 由来する生物種 | Gallus gallus (chicken) |
| タンパク質・核酸の鎖数 | 1 |
| 化学式量合計 | 15464.99 |
| 構造登録者 | |
| 主引用文献 | Ferraro, G.,Paolillo, M.,Sciortino, G.,Garribba, E.,Merlino, A. Multiple and Variable Binding of Pharmacologically Active Bis(maltolato)oxidovanadium(IV) to Lysozyme. Inorg.Chem., 61:16458-16467, 2022 Cited by PubMed Abstract: The interaction with proteins of metal-based drugs plays a crucial role in their transport, mechanism, and activity. For an active ML complex, where L is the organic carrier, various binding modes (covalent and non-covalent, single or multiple) may occur and several metal moieties (M, ML, ML, etc.) may interact with proteins. In this study, we have evaluated the interaction of [VO(malt)] (bis(maltolato)oxidovanadium(IV) or BMOV, where malt = maltolato, i.e., the common name for 3-hydroxy-2-methyl-4-pyran-4-onato) with the model protein hen egg white lysozyme (HEWL) by electrospray ionization mass spectrometry, electron paramagnetic resonance, and X-ray crystallography. The multiple binding of different V-containing isomers and enantiomers to different sites of HEWL is observed. The data indicate both non-covalent binding of -[VO(malt)(HO)] and [VO(malt)(HO)] and covalent binding of [VO(HO)] and -[VO(malt)] and other V-containing fragments to the side chains of Glu35, Asp48, Asn65, Asp87, and Asp119 and to the C-terminal carboxylate. Our results suggest that the multiple and variable interactions of potential VOL drugs with proteins can help to better understand their solution chemistry and contribute to define the molecular basis of the mechanism of action of these intriguing molecules. PubMed: 36205235DOI: 10.1021/acs.inorgchem.2c02690 主引用文献が同じPDBエントリー |
| 実験手法 | X-RAY DIFFRACTION (1.31 Å) |
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