3KTX
Crystal structure of Leishmania mexicana pyruvate kinase (LmPYK)in complex with 1,3,6,8-pyrenetetrasulfonic acid
3KTX の概要
| エントリーDOI | 10.2210/pdb3ktx/pdb |
| 関連するPDBエントリー | 1PKL |
| 分子名称 | Pyruvate kinase, GLYCEROL, pyrene-1,3,6,8-tetrasulfonic acid, ... (4 entities in total) |
| 機能のキーワード | transferase, allosteric enzyme, atp-binding, glycolysis, kinase, magnesium, metal-binding, nucleotide-binding, pyruvate |
| 由来する生物種 | Leishmania mexicana |
| タンパク質・核酸の鎖数 | 2 |
| 化学式量合計 | 110010.93 |
| 構造登録者 | |
| 主引用文献 | Morgan, H.P.,McNae, I.W.,Hsin, K.Y.,Michels, P.A.,Fothergill-Gilmore, L.A.,Walkinshaw, M.D. An improved strategy for the crystallization of Leishmania mexicana pyruvate kinase. Acta Crystallogr.,Sect.F, 66:215-218, 2010 Cited by PubMed Abstract: The inclusion of novel small molecules in crystallization experiments has provided very encouraging results and this method is now emerging as a promising alternative strategy for crystallizing 'problematic' biological macromolecules. These small molecules have the ability to promote lattice formation through stabilizing intermolecular interactions in protein crystals. Here, the use of 1,3,6,8-pyrenetetrasulfonic acid (PTS), which provides a helpful intermolecular bridge between Leishmania mexicana PYK (LmPYK) macromolecules in the crystal, is reported, resulting in the rapid formation of a more stable crystal lattice at neutral pH and greatly improved X-ray diffraction results. The refined structure of the LmPYK-PTS complex revealed the negatively charged PTS molecule to be stacked between positively charged (surface-exposed) arginine side chains from neighbouring LmPYK molecules in the crystal lattice. PubMed: 20208146DOI: 10.1107/S1744309109053494 主引用文献が同じPDBエントリー |
| 実験手法 | X-RAY DIFFRACTION (2.1 Å) |
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