1KEW
The crystal structure of dTDP-D-glucose 4,6-dehydratase (RmlB) from Salmonella enterica serovar Typhimurium with thymidine diphosphate bound
1KEW の概要
エントリーDOI | 10.2210/pdb1kew/pdb |
関連するPDBエントリー | 1G1A 1KEP 1KER 1KET 1KEU |
分子名称 | dTDP-D-glucose 4,6-dehydratase, THYMIDINE-5'-DIPHOSPHATE, NICOTINAMIDE-ADENINE-DINUCLEOTIDE, ... (5 entities in total) |
機能のキーワード | rossmann fold, lyase |
由来する生物種 | Salmonella enterica subsp. enterica serovar Typhimurium |
タンパク質・核酸の鎖数 | 2 |
化学式量合計 | 83942.54 |
構造登録者 | Allard, S.T.M.,Beis, K.,Giraud, M.-F.,Hegeman, A.D.,Gross, J.W.,Whitfield, C.,Graninger, M.,Messner, P.,Allen, A.G.,Naismith, J.H. (登録日: 2001-11-17, 公開日: 2002-01-25, 最終更新日: 2023-08-16) |
主引用文献 | Allard, S.T.,Beis, K.,Giraud, M.F.,Hegeman, A.D.,Gross, J.W.,Wilmouth, R.C.,Whitfield, C.,Graninger, M.,Messner, P.,Allen, A.G.,Maskell, D.J.,Naismith, J.H. Toward a structural understanding of the dehydratase mechanism. Structure, 10:81-92, 2002 Cited by PubMed Abstract: dTDP-D-glucose 4,6-dehydratase (RmlB) was first identified in the L-rhamnose biosynthetic pathway, where it catalyzes the conversion of dTDP-D-glucose into dTDP-4-keto-6-deoxy-D-glucose. The structures of RmlB from Salmonella enterica serovar Typhimurium in complex with substrate deoxythymidine 5'-diphospho-D-glucose (dTDP-D-glucose) and deoxythymidine 5'-diphosphate (dTDP), and RmlB from Streptococcus suis serotype 2 in complex with dTDP-D-glucose, dTDP, and deoxythymidine 5'-diphospho-D-pyrano-xylose (dTDP-xylose) have all been solved at resolutions between 1.8 A and 2.4 A. The structures show that the active sites are highly conserved. Importantly, the structures show that the active site tyrosine functions directly as the active site base, and an aspartic and glutamic acid pairing accomplishes the dehydration step of the enzyme mechanism. We conclude that the substrate is required to move within the active site to complete the catalytic cycle and that this movement is driven by the elimination of water. The results provide insight into members of the SDR superfamily. PubMed: 11796113DOI: 10.1016/S0969-2126(01)00694-3 主引用文献が同じPDBエントリー |
実験手法 | X-RAY DIFFRACTION (1.8 Å) |
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