8HUI
Crystal structure of DFA I-forming Inulin Lyase from Streptomyces peucetius subsp. caesius ATCC 27952 in complex with GF4, DFA I, and fructose
8HUI の概要
エントリーDOI | 10.2210/pdb8hui/pdb |
分子名称 | Fructotransferase, beta-D-fructofuranose-(2-1)-alpha-D-fructofuranose, beta-D-fructofuranose-(2-1)-beta-D-fructofuranose-(2-1)-beta-D-fructofuranose-(2-1)-beta-D-fructofuranose-(2-1)-alpha-D-glucopyranose, ... (8 entities in total) |
機能のキーワード | right-handed beta-helix protein, dfa i-forming inulin lyase, complex, lyase |
由来する生物種 | Streptomyces peucetius subsp. caesius ATCC 27952 |
タンパク質・核酸の鎖数 | 3 |
化学式量合計 | 132800.60 |
構造登録者 | |
主引用文献 | Cheng, M.,Hou, X.,Huang, Z.,Chen, Z.,Ni, D.,Zhang, W.,Rao, Y.,Mu, W. Structural Insights into the Catalytic Cycle of Inulin Fructotransferase: From Substrate Anchoring to Product Releasing. J.Agric.Food Chem., 72:17030-17040, 2024 Cited by PubMed Abstract: Carbohydrate degradation is crucial for living organisms due to their essential functions in providing energy and composing various metabolic pathways. Nevertheless, in the catalytic cycle of polysaccharide degradation, the details of how the substrates bind and how the products release need more case studies. Here, we choose an inulin fructotransferase (IFTase) as a model system, which can degrade inulin into functionally difructose anhydride I. At first, the crystal structures of IFTase in the absence of carbohydrates and complex with fructosyl-nystose (GF4), difructose anhydride I, and fructose are obtained, giving the substrate trajectory and product path of IFTase, which are further supported by steered molecular dynamics simulations (MDSs) along with mutagenesis. Furthermore, structural topology variations at the active centers of inulin fructotransferases are suggested as the structural base for product release, subsequently proven by substitution mutagenesis and MDSs. Therefore, this study provides a case in point for a deep understanding of the catalytic cycle with substrate trajectory and product path. PubMed: 39034843DOI: 10.1021/acs.jafc.4c03615 主引用文献が同じPDBエントリー |
実験手法 | X-RAY DIFFRACTION (1.44 Å) |
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