タイトル | Development of Selective, Potent RabGGTase Inhibitors |
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ジャーナル・号・ページ | J. Med. Chem., Vol. 55, Page 8330-8340, Year 2012 |
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掲載日 | 2012年8月28日 (構造データの登録日) |
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著者 | Stigter, E.A. / Guo, Z. / Bon, R.S. / Wu, Y.W. / Choidas, A. / Wolf, A. / Menninger, S. / Waldmann, H. / Blankenfeldt, W. / Goody, R.S. |
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リンク | J. Med. Chem. / PubMed:22963166 |
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手法 | X線回折 |
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解像度 | 1.95 - 2.75 Å |
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構造データ | PDB-4gtm: FTase in complex with BMS analogue 11 手法: X-RAY DIFFRACTION / 解像度: 2.2 Å PDB-4gto: FTase in complex with BMS analogue 14 手法: X-RAY DIFFRACTION / 解像度: 2.15 Å PDB-4gtp: FTase in complex with BMS analogue 16 手法: X-RAY DIFFRACTION / 解像度: 2.75 Å PDB-4gtq: FTase in complex with BMS analogue 12 手法: X-RAY DIFFRACTION / 解像度: 2.6 Å PDB-4gtr: FTase in complex with BMS analogue 13 手法: X-RAY DIFFRACTION / 解像度: 2.2 Å PDB-4gts: Engineered RabGGTase in complex with BMS analogue 16 手法: X-RAY DIFFRACTION / 解像度: 2.45 Å PDB-4gtt: Engineered RabGGTase in complex with BMS analogue 12 手法: X-RAY DIFFRACTION / 解像度: 2.05 Å PDB-4gtv: Engineered RabGGTase in complex with BMS analogue 13 手法: X-RAY DIFFRACTION / 解像度: 1.95 Å |
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化合物 | ChemComp-7TM: 4-({(3R)-7-cyano-4-[(4-methoxyphenyl)sulfonyl]-1-[(1-methyl-1H-imidazol-5-yl)methyl]-2,3,4,5-tetrahydro-1H-1,4-benzodiazepin-3-yl}methyl)phenyl hexylcarbamate
ChemComp-7TO: 4-({(3R)-7-cyano-4-[(4-methoxyphenyl)sulfonyl]-1-[(1-methyl-1H-imidazol-5-yl)methyl]-2,3,4,5-tetrahydro-1H-1,4-benzodiazepin-3-yl}methyl)phenyl trifluoromethanesulfonate
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由来 | - rattus norvegicus (ドブネズミ)
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キーワード | TRANSFERASE/TRANSFERASE INHIBITOR / protein prenylation / inhibitor / TRANSFERASE-TRANSFERASE INHIBITOR complex |
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