2GIZ
| Structural and functional analysis of Natrin, a member of crisp-3 family blocks a variety of ion channels | 分子名称: | Natrin-1 | 著者 | Jiang, T, Wang, F, Li, H, Yin, C, Zhou, Y, Shu, Y, Qi, Z, Lin, Z. | 登録日 | 2006-03-30 | 公開日 | 2006-11-28 | 最終更新日 | 2024-10-30 | 実験手法 | X-RAY DIFFRACTION (1.68 Å) | 主引用文献 | Structural and functional analysis of natrin, a venom protein that targets various ion channels Biochem.Biophys.Res.Commun., 351, 2006
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5HU9
| Crystal structure of ABL1 in complex with CHMFL-074 | 分子名称: | 1,2-ETHANEDIOL, 4-[(4-methylpiperazin-1-yl)methyl]-N-(4-methyl-3-{[1-(pyridin-3-ylcarbonyl)piperidin-4-yl]oxy}phenyl)-3-(trifluoromethyl)benzamide, CHLORIDE ION, ... | 著者 | Kong, L.L, Yun, C.H. | 登録日 | 2016-01-27 | 公開日 | 2016-07-13 | 最終更新日 | 2023-11-08 | 実験手法 | X-RAY DIFFRACTION (1.529 Å) | 主引用文献 | Discovery and characterization of a novel potent type II native and mutant BCR-ABL inhibitor (CHMFL-074) for Chronic Myeloid Leukemia (CML) Oncotarget, 7, 2016
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8TG8
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8TFU
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8TGC
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8TG7
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7VO5
| Pimaricin type I PKS thioesterase domain (holo Pim TE) | 分子名称: | (1R,3S,5E,7S,11R,13E,15E,17E,19E,21R,23S,24R,25S)-11,24-dimethyl-1,3,7,21,25-pentakis(oxidanyl)-10,27-dioxabicyclo[21.3.1]heptacosa-5,13,15,17,19-pentaen-9-one, ScnS4 | 著者 | Bai, L, Zhou, Y. | 登録日 | 2021-10-12 | 公開日 | 2022-01-19 | 最終更新日 | 2023-11-29 | 実験手法 | X-RAY DIFFRACTION (2.4 Å) | 主引用文献 | Structural and Mechanistic Insights into Chain Release of the Polyene PKS Thioesterase Domain Acs Catalysis, 12, 2022
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7VO4
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5GNK
| Crystal structure of EGFR 696-988 T790M in complex with LXX-6-34 | 分子名称: | 1,2-ETHANEDIOL, 1-[(3R)-3-[4-azanyl-3-[3-chloranyl-4-[(1-methylimidazol-2-yl)methoxy]phenyl]pyrazolo[3,4-d]pyrimidin-1-yl]piperidin-1-yl]prop-2-en-1-one, CHLORIDE ION, ... | 著者 | Yan, X.E, Yun, C.H. | 登録日 | 2016-07-21 | 公開日 | 2017-04-05 | 最終更新日 | 2024-10-23 | 実験手法 | X-RAY DIFFRACTION (1.796 Å) | 主引用文献 | Discovery of (R)-1-(3-(4-Amino-3-(3-chloro-4-(pyridin-2-ylmethoxy)phenyl)-1H-pyrazolo[3,4-d]pyrimidin-1-yl)piperidin-1-yl)prop-2-en-1-one (CHMFL-EGFR-202) as a Novel Irreversible EGFR Mutant Kinase Inhibitor with a Distinct Binding Mode. J. Med. Chem., 60, 2017
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8K5N
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5GTY
| Crystal structure of EGFR 696-1022 T790M in complex with LXX-6-26 | 分子名称: | 1,2-ETHANEDIOL, 1-[(3R)-3-[4-azanyl-3-[3-chloranyl-4-[(6-methylpyridin-2-yl)methoxy]phenyl]pyrazolo[3,4-d]pyrimidin-1-yl]piperidin-1-yl]prop-2-en-1-one, Epidermal growth factor receptor | 著者 | Yan, X.E, Yun, C.H. | 登録日 | 2016-08-23 | 公開日 | 2017-09-06 | 最終更新日 | 2024-10-09 | 実験手法 | X-RAY DIFFRACTION (3.14 Å) | 主引用文献 | Discovery and characterization of a novel irreversible EGFR mutants selective and potent kinase inhibitor CHMFL-EGFR-26 with a distinct binding mode. Oncotarget, 8, 2017
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