8C5I
| Cyanide dihydratase from Bacillus pumilus C1 variant - Q86R,H305K,H308K,H323K | 分子名称: | Cyanide dihydratase | 著者 | Mulelu, A.E, Reitz, J, van Rooyen, J, Scheffer, M, Frangakis, A.S, Dlamini, L.S, Woodward, J.D, Benedik, M.J, Sewell, B.T. | 登録日 | 2023-01-09 | 公開日 | 2023-01-18 | 最終更新日 | 2024-07-24 | 実験手法 | ELECTRON MICROSCOPY (3.15 Å) | 主引用文献 | The Role of Histidine Residues in the Oligomerization of Cyanide Dihydratase from Bacillus pumilus C1 To Be Published
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8P4I
| Cyanide dihydratase from Bacillus pumilus C1 | 分子名称: | Cyanide dihydratase | 著者 | Mulelu, A.E, Reitz, J, van Rooyen, J.M, Scheffer, M, Frangakis, A.S, Dlamini, L.S, Woodward, J.D, Benedik, M.J, Sewell, B.T. | 登録日 | 2023-05-22 | 公開日 | 2023-08-16 | 実験手法 | ELECTRON MICROSCOPY (3.83 Å) | 主引用文献 | The Role of Histidine Residues in the Oligomerization of Cyanide Dihydratase from Bacillus pumilus C1 To Be Published
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2VN7
| Glycoside Hydrolase Family 15 Glucoamylase from Hypocrea jecorina | 分子名称: | 2-[BIS-(2-HYDROXY-ETHYL)-AMINO]-2-HYDROXYMETHYL-PROPANE-1,3-DIOL, 2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose, CALCIUM ION, ... | 著者 | Bott, R, Sandgren, M, Hansson, H. | 登録日 | 2008-01-31 | 公開日 | 2008-05-20 | 最終更新日 | 2024-10-09 | 実験手法 | X-RAY DIFFRACTION (1.9 Å) | 主引用文献 | Three-Dimensional Structure of an Intact Glycoside Hydrolase Family 15 Glucoamylase from Hypocrea Jecorina. Biochemistry, 47, 2008
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2VN4
| Glycoside Hydrolase Family 15 Glucoamylase from Hypocrea jecorina | 分子名称: | 2-[BIS-(2-HYDROXY-ETHYL)-AMINO]-2-HYDROXYMETHYL-PROPANE-1,3-DIOL, 2-acetamido-2-deoxy-beta-D-glucopyranose, 2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose, ... | 著者 | Bott, R, Sandgren, M, Hansson, H. | 登録日 | 2008-01-30 | 公開日 | 2008-05-20 | 最終更新日 | 2024-11-13 | 実験手法 | X-RAY DIFFRACTION (1.85 Å) | 主引用文献 | Three-Dimensional Structure of an Intact Glycoside Hydrolase Family 15 Glucoamylase from Hypocrea Jecorina. Biochemistry, 47, 2008
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3SHE
| Novel ATP-competitive MK2 inhibitors with potent biochemical and cell-based activity throughout the series | 分子名称: | MAP kinase-activated protein kinase 3, N-{4-[(3S)-4'-oxo-1',4',5',6'-tetrahydrospiro[piperidine-3,7'-pyrrolo[3,2-c]pyridin]-2'-yl]pyridin-2-yl}-3-(trifluoromethyl)benzamide | 著者 | Oubrie, A, Kazemier, B. | 登録日 | 2011-06-16 | 公開日 | 2011-12-14 | 最終更新日 | 2024-02-28 | 実験手法 | X-RAY DIFFRACTION (2.25 Å) | 主引用文献 | Novel ATP competitive MK2 inhibitors with potent biochemical and cell-based activity throughout the series. Bioorg.Med.Chem.Lett., 22, 2012
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