タイトル | Fragment-based design of ligands targeting a novel site on the integrase enzyme of human immunodeficiency virus 1 |
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ジャーナル・号・ページ | Chemmedchem, Vol. 6, Page 258-261, Year 2011 |
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掲載日 | 2010年9月17日 (構造データの登録日) |
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著者 | Wielens, J. / Headey, S.J. / Deadman, J.J. / Rhodes, D.I. / Parker, M.W. / Chalmers, D.K. / Scanlon, M.J. |
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リンク | Chemmedchem / PubMed:21275048 |
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手法 | X線回折 |
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解像度 | 1.8 - 1.95 Å |
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構造データ | PDB-3ao1: Fragment-based approach to the design of ligands targeting a novel site in HIV-1 integrase 手法: X-RAY DIFFRACTION / 解像度: 1.9 Å PDB-3ao2: Fragment-based approach to the design of ligands targeting a novel site on HIV-1 integrase 手法: X-RAY DIFFRACTION / 解像度: 1.8 Å PDB-3ao3: Fragment-based approach to the design of ligands targeting a novel site on HIV-1 integrase 手法: X-RAY DIFFRACTION / 解像度: 1.9 Å PDB-3ao4: Fragment-based approach to the design of ligands targeting a novel site on HIV-1 integrase 手法: X-RAY DIFFRACTION / 解像度: 1.95 Å PDB-3ao5: Fragment-based approach to the design of ligands targeting a novel site on HIV-1 integrase 手法: X-RAY DIFFRACTION / 解像度: 1.8 Å PDB-3ovn: Fragment-based approach to the design of ligands targeting a novel site on HIV-1 integrase 手法: X-RAY DIFFRACTION / 解像度: 1.95 Å |
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化合物 | ChemComp-AVX: 3-(7-bromo-1,3-benzodioxol-5-yl)-1-methyl-1H-pyrazol-5-amine
ChemComp-BMC: 3-(1,3-benzodioxol-5-yl)-1-methyl-1H-pyrazole-5-carboxylic acid
ChemComp-833: 3-(1,3-benzodioxol-5-yl)-1-methyl-1H-pyrazol-5-amine
ChemComp-BBY: 5-(7-bromo-1,3-benzodioxol-5-yl)-1-methyl-1H-pyrazol-3-amine
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由来 | ![](img/tx_virus.gif) human immunodeficiency virus 1 (ヒト免疫不全ウイルス)
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キーワード | VIRAL PROTEIN/TRANSFERASE INHIBITOR / DNA INTEGRATION / AIDS / INTEGRASE / ENDONUCLEASE / POLYNUCLEOTIDYL TRANSFERASE / DNA BINDING / VIRAL PROTEIN / RNaseH / Fragment binding / VIRAL PROTEIN-TRANSFERASE INHIBITOR complex |
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