3WWI
 
 | | Crystal structure of the G136F mutant of the first R-stereoselective -transaminase identified from Arthrobacter sp. KNK168 (FERM-BP-5228) | | 分子名称: | (R)-amine transaminase, PYRIDOXAL-5'-PHOSPHATE | | 著者 | Guan, L.J, Ohtsuka, J, Miyakawa, T, Zhi, Y, Ito, N, Yasohara, Y, Tanokura, M. | | 登録日 | 2014-06-18 | | 公開日 | 2015-08-19 | | 最終更新日 | 2020-01-22 | | 実験手法 | X-RAY DIFFRACTION (2.27 Å) | | 主引用文献 | A new target region for changing the substrate specificity of amine transaminases.
Sci Rep, 5, 2015
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3WWJ
 | | Crystal structure of an engineered sitagliptin-producing transaminase, ATA-117-Rd11 | | 分子名称: | (R)-amine transaminase, PYRIDOXAL-5'-PHOSPHATE | | 著者 | Guan, L.J, Ohtsuka, J, Okai, M, Miyakawa, T, Mase, T, Zhi, Y, Hou, F, Ito, N, Yasohara, Y, Tanokura, M. | | 登録日 | 2014-06-18 | | 公開日 | 2015-08-12 | | 最終更新日 | 2018-11-21 | | 実験手法 | X-RAY DIFFRACTION (2.2 Å) | | 主引用文献 | A new target region for changing the substrate specificity of amine transaminases.
Sci Rep, 5, 2015
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3WWH
 | | Crystal structure of the first R-stereoselective -transaminase identified from Arthrobacter sp. KNK168 (FERM-BP-5228) | | 分子名称: | (R)-amine transaminase, GLYCEROL, PYRIDOXAL-5'-PHOSPHATE | | 著者 | Guan, L.J, Ohtsuka, J, Okai, M, Miyakawa, T, Mase, T, Zhi, Y, Ito, N, Yasohara, Y, Tanokura, M. | | 登録日 | 2014-06-18 | | 公開日 | 2015-08-12 | | 最終更新日 | 2018-11-21 | | 実験手法 | X-RAY DIFFRACTION (1.65 Å) | | 主引用文献 | A new target region for changing the substrate specificity of amine transaminases.
Sci Rep, 5, 2015
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6MPV
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8CYI
 | | Cryo-EM structures and computational analysis for enhanced potency in MTA-synergic inhibition of human protein arginine methyltransferase 5 | | 分子名称: | 5'-DEOXY-5'-METHYLTHIOADENOSINE, Methylosome protein 50, N-[(2-aminoquinolin-7-yl)methyl]-9-(2-hydroxyethyl)-2,3,4,9-tetrahydro-1H-carbazole-6-carboxamide, ... | | 著者 | Yadav, G.P, Wei, Z, Xiaozhi, Y, Chenglong, L, Jiang, Q. | | 登録日 | 2022-05-23 | | 公開日 | 2023-04-12 | | 最終更新日 | 2024-06-12 | | 実験手法 | ELECTRON MICROSCOPY (3.14 Å) | | 主引用文献 | Cryo-EM structure-based selection of computed ligand poses enables design of MTA-synergic PRMT5 inhibitors of better potency.
Commun Biol, 5, 2022
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