1F8C
Native Influenza Neuraminidase in Complex with 4-amino-2-deoxy-2,3-dehydro-N-neuraminic Acid
1F8C の概要
エントリーDOI | 10.2210/pdb1f8c/pdb |
関連するPDBエントリー | 7NN9 |
分子名称 | NEURAMINIDASE, alpha-D-mannopyranose-(1-2)-alpha-D-mannopyranose-(1-2)-alpha-D-mannopyranose-(1-3)-[alpha-D-mannopyranose-(1-6)]alpha-D-mannopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose, 2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose, ... (7 entities in total) |
機能のキーワード | neuraminidase, hydrolase, influenza protein, glycosylated protein, 4-amino-dana, hydrolase-hydrolase inhibitor complex, hydrolase/hydrolase inhibitor |
由来する生物種 | Influenza A virus (A/tern/Australia/G70C/1975(H11N9)) |
タンパク質・核酸の鎖数 | 1 |
化学式量合計 | 45974.91 |
構造登録者 | Smith, B.J.,Colman, P.M.,Von Itzstein, M.,Danylec, B.,Varghese, J.N. (登録日: 2000-06-30, 公開日: 2001-04-11, 最終更新日: 2024-10-09) |
主引用文献 | Smith, B.J.,Colman, P.M.,Von Itzstein, M.,Danylec, B.,Varghese, J.N. Analysis of inhibitor binding in influenza virus neuraminidase. Protein Sci., 10:689-696, 2001 Cited by PubMed Abstract: 2,3-didehydro-2-deoxy-N:-acetylneuraminic acid (DANA) is a transition state analog inhibitor of influenza virus neuraminidase (NA). Replacement of the hydroxyl at the C9 position in DANA and 4-amino-DANA with an amine group, with the intention of taking advantage of an increased electrostatic interaction with a conserved acidic group in the active site to improve inhibitor binding, significantly reduces the inhibitor activity of both compounds. The three-dimensional X-ray structure of the complexes of these ligands and NA was obtained to 1.4 A resolution and showed that both ligands bind isosterically to DANA. Analysis of the geometry of the ammonium at the C4 position indicates that Glu119 may be neutral when these ligands bind. A computational analysis of the binding energies indicates that the substitution is successful in increasing the energy of interaction; however, the gains that are made are not sufficient to overcome the energy that is required to desolvate that part of the ligand that comes in contact with the protein. PubMed: 11274459DOI: 10.1110/ps.41801 主引用文献が同じPDBエントリー |
実験手法 | X-RAY DIFFRACTION (1.7 Å) |
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