1LES
LENTIL LECTIN COMPLEXED WITH SUCROSE
1LES の概要
| エントリーDOI | 10.2210/pdb1les/pdb |
| 関連するBIRD辞書のPRD_ID | PRD_900003 |
| 分子名称 | LENTIL LECTIN, beta-D-fructofuranose-(2-1)-alpha-D-glucopyranose, CALCIUM ION, ... (6 entities in total) |
| 機能のキーワード | protein-sugar interactions, lectin |
| 由来する生物種 | Lens culinaris (lentil) 詳細 |
| タンパク質・核酸の鎖数 | 4 |
| 化学式量合計 | 52185.29 |
| 構造登録者 | |
| 主引用文献 | Casset, F.,Hamelryck, T.,Loris, R.,Brisson, J.R.,Tellier, C.,Dao-Thi, M.H.,Wyns, L.,Poortmans, F.,Perez, S.,Imberty, A. NMR, molecular modeling, and crystallographic studies of lentil lectin-sucrose interaction. J.Biol.Chem., 270:25619-25628, 1995 Cited by PubMed Abstract: The conformational features of sucrose in the combining site of lentil lectin have been characterized through elucidation of a crystalline complex at 1.9-A resolution, transferred nuclear Overhauser effect experiments performed at 600 Mhz, and molecular modeling. In the crystal, the lentil lectin dimer binds one sucrose molecule per monomer. The locations of 229 water molecules have been identified. NMR experiments have provided 11 transferred NOEs. In parallel, the docking study and conformational analysis of sucrose in the combining site of lentil lectin indicate that three different conformations can be accommodated. Of these, the orientation with lowest energy is identical with the one observed in the crystalline complex and provides good agreement with the observed transferred NOEs. These structural investigations indicate that the bound sucrose has a unique conformation for the glycosidic linkage, close to the one observed in crystalline sucrose, whereas the fructofuranose ring remains relatively flexible and does not exhibit any strong interaction with the protein. Major differences in the hydrogen bonding network of sucrose are found. None of the two inter-residue hydrogen bonds in crystalline sucrose are conserved in the complex with the lectin. Instead, a water molecule bridges hydroxyl groups O2-g and O3-f of sucrose. PubMed: 7592736DOI: 10.1074/jbc.270.43.25619 主引用文献が同じPDBエントリー |
| 実験手法 | X-RAY DIFFRACTION (1.9 Å) |
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