2CNB
Trypanosoma brucei UDP-galactose-4-epimerase in ternary complex with NAD and the substrate analogue UDP-4-deoxy-4-fluoro-alpha-D-galactose
2CNB の概要
エントリーDOI | 10.2210/pdb2cnb/pdb |
関連するPDBエントリー | 1GY8 |
分子名称 | UDP-GALACTOSE-4-EPIMERASE, URIDINE-5'-DIPHOSPHATE-4-DEOXY-4-FLUORO-ALPHA-D-GALACTOSE, NICOTINAMIDE-ADENINE-DINUCLEOTIDE, ... (4 entities in total) |
機能のキーワード | epimerase, short-chain dehydrogenase/reductase, udp-galactose-4- epimerase, nad, isomerase, trypanosoma brucei, udp-4-deoxy- 4-fluoro-alpha-d-galactose |
由来する生物種 | TRYPANOSOMA BRUCEI |
タンパク質・核酸の鎖数 | 4 |
化学式量合計 | 180153.06 |
構造登録者 | |
主引用文献 | Alphey, M.S.,Burton, A.,Urbaniak, M.,Boons, G.J.,Ferguson, M.A.J.,Hunter, W.N. Trypanosoma Brucei Udp-Galactose-4-Epimerase in Ternary Complex with Nad+ and the Substrate Analogue Udp-4-Deoxy-4-Fluoro-Alpha-D-Galactose Acta Crystallogr.,Sect.F, 62:829-, 2006 Cited by PubMed Abstract: The structure of the NAD-dependent oxidoreductase UDP-galactose-4'-epimerase from Trypanosoma brucei in complex with cofactor and the substrate analogue UDP-4-deoxy-4-fluoro-alpha-D-galactose has been determined using diffraction data to 2.7 A resolution. Despite the high level of sequence and structure conservation between the trypanosomatid enzyme and those from humans, yeast and bacteria, the binding of the 4-fluoro-alpha-D-galactose moiety is distinct from previously reported structures. Of particular note is the observation that when bound to the T. brucei enzyme, the galactose moiety of this fluoro-derivative is rotated approximately 180 degrees with respect to the orientation of the hexose component of UDP-glucose when in complex with the human enzyme. The architecture of the catalytic centre is designed to effectively bind different orientations of the hexose, a finding that is consistent with a mechanism that requires the sugar to maintain a degree of flexibility within the active site. PubMed: 16946458DOI: 10.1107/S1744309106028740 主引用文献が同じPDBエントリー |
実験手法 | X-RAY DIFFRACTION (2.7 Å) |
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