7XH8
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8TZO
| Structure of human Wnt7a bound to WLS and CALR | 分子名称: | (2S)-3-(hexadecanoyloxy)-2-[(9Z)-octadec-9-enoyloxy]propyl 2-(trimethylammonio)ethyl phosphate, CALCIUM ION, Calreticulin, ... | 著者 | Qi, X, Hu, Q, Li, X. | 登録日 | 2023-08-27 | 公開日 | 2023-10-18 | 最終更新日 | 2024-05-08 | 実験手法 | ELECTRON MICROSCOPY (3.1 Å) | 主引用文献 | Molecular basis of Wnt biogenesis, secretion, and Wnt7-specific signaling. Cell, 186, 2023
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8TZP
| Structure of human Wnt7a bound to WLS and RECK | 分子名称: | (2S)-3-(hexadecanoyloxy)-2-[(9Z)-octadec-9-enoyloxy]propyl 2-(trimethylammonio)ethyl phosphate, PALMITOLEIC ACID, Protein Wnt-7a, ... | 著者 | Qi, X, Hu, Q, Li, X. | 登録日 | 2023-08-27 | 公開日 | 2023-10-18 | 最終更新日 | 2024-05-08 | 実験手法 | ELECTRON MICROSCOPY (3.23 Å) | 主引用文献 | Molecular basis of Wnt biogenesis, secretion, and Wnt7-specific signaling. Cell, 186, 2023
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8TZS
| Structure of human WLS | 分子名称: | Protein wntless homolog | 著者 | Qi, X, Hu, Q, Li, X. | 登録日 | 2023-08-27 | 公開日 | 2023-10-18 | 最終更新日 | 2024-05-08 | 実験手法 | ELECTRON MICROSCOPY (3.84 Å) | 主引用文献 | Molecular basis of Wnt biogenesis, secretion, and Wnt7-specific signaling. Cell, 186, 2023
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8EDE
| Crystal structure of covalent inhibitor 2-chloro-N'-(N-(4-chlorophenyl)-N-methylglycyl)acetohydrazide bound to Ubiquitin C-terminal Hydrolase-L1 | 分子名称: | 2-[(4-chlorophenyl)-methyl-amino]-~{N}'-ethanoyl-ethanehydrazide, SULFATE ION, Ubiquitin carboxyl-terminal hydrolase isozyme L1 | 著者 | Patel, R, Imhoff, R, Flaherty, D, Das, C. | 登録日 | 2022-09-04 | 公開日 | 2023-09-20 | 最終更新日 | 2024-04-10 | 実験手法 | X-RAY DIFFRACTION (1.799 Å) | 主引用文献 | Covalent Fragment Screening and Optimization Identifies the Chloroacetohydrazide Scaffold as Inhibitors for Ubiquitin C-terminal Hydrolase L1. J.Med.Chem., 67, 2024
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4O6E
| Discovery of 5,6,7,8-tetrahydropyrido[3,4-d]pyrimidine Inhibitors of Erk2 | 分子名称: | Mitogen-activated protein kinase 1, N-[(1S)-1-(3-chloro-4-fluorophenyl)-2-hydroxyethyl]-2-(tetrahydro-2H-pyran-4-ylamino)-5,8-dihydropyrido[3,4-d]pyrimidine-7(6H)-carboxamide | 著者 | Yin, J, Wang, W. | 登録日 | 2013-12-20 | 公開日 | 2014-05-21 | 最終更新日 | 2024-02-28 | 実験手法 | X-RAY DIFFRACTION (1.95 Å) | 主引用文献 | Discovery of 5,6,7,8-tetrahydropyrido[3,4-d]pyrimidine inhibitors of Erk2. Bioorg.Med.Chem.Lett., 24, 2014
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8EYB
| Crystal structure of PTP1B D181A/Q262A/C215A phosphatase domain with JAK2 activation loop phosphopeptide | 分子名称: | 2-AMINO-2-HYDROXYMETHYL-PROPANE-1,3-DIOL, Tyrosine-protein kinase JAK2 activation loop phosphopeptide, Tyrosine-protein phosphatase non-receptor type 1 | 著者 | Morris, R, Kershaw, N.J, Babon, J.J. | 登録日 | 2022-10-26 | 公開日 | 2023-07-05 | 最終更新日 | 2023-11-15 | 実験手法 | X-RAY DIFFRACTION (2.349 Å) | 主引用文献 | Structure guided studies of the interaction between PTP1B and JAK. Commun Biol, 6, 2023
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8EXJ
| Crystal structure of PTP1B D181A/Q262A phosphatase domain in complex with a JAK1 activation loop phosphopeptide | 分子名称: | 2-AMINO-2-HYDROXYMETHYL-PROPANE-1,3-DIOL, PHOSPHATE ION, Tyrosine-protein kinase JAK1 activation loop peptide, ... | 著者 | Morris, R, Kershaw, N.J, Babon, J.J. | 登録日 | 2022-10-25 | 公開日 | 2023-07-05 | 最終更新日 | 2023-10-25 | 実験手法 | X-RAY DIFFRACTION (2.301 Å) | 主引用文献 | Structure guided studies of the interaction between PTP1B and JAK. Commun Biol, 6, 2023
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8EXI
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8EXM
| Crystal structure of PTP1B D181A/Q262A phosphatase domain with a JAK3 activation loop phosphopeptide | 分子名称: | 2-AMINO-2-HYDROXYMETHYL-PROPANE-1,3-DIOL, PHOSPHATE ION, Tyrosine-protein kinase JAK3 activation loop peptide, ... | 著者 | Morris, R, Kershaw, N.J, Babon, J.J. | 登録日 | 2022-10-25 | 公開日 | 2023-07-05 | 最終更新日 | 2023-10-25 | 実験手法 | X-RAY DIFFRACTION (2.349 Å) | 主引用文献 | Structure guided studies of the interaction between PTP1B and JAK. Commun Biol, 6, 2023
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8EXK
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8EXN
| Crystal structure of PTP1B D181A/Q262A phosphatase domain with TYK2 activation loop phosphopeptide | 分子名称: | 2-AMINO-2-HYDROXYMETHYL-PROPANE-1,3-DIOL, Non-receptor tyrosine-protein kinase TYK2 activation loop peptide, PHOSPHATE ION, ... | 著者 | Morris, R, Kershaw, N.J, Babon, J.J. | 登録日 | 2022-10-25 | 公開日 | 2023-07-05 | 最終更新日 | 2023-10-25 | 実験手法 | X-RAY DIFFRACTION (2.151 Å) | 主引用文献 | Structure guided studies of the interaction between PTP1B and JAK. Commun Biol, 6, 2023
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8EYA
| Crystal structure of PTP1B D181A/Q262A/C215A phosphatase domain with a JAK2 activation loop phosphopeptide | 分子名称: | 1,2-ETHANEDIOL, 2-AMINO-2-HYDROXYMETHYL-PROPANE-1,3-DIOL, CHLORIDE ION, ... | 著者 | Morris, R, Kershaw, N.J, Babon, J.J. | 登録日 | 2022-10-26 | 公開日 | 2023-07-05 | 最終更新日 | 2023-11-15 | 実験手法 | X-RAY DIFFRACTION (2.099 Å) | 主引用文献 | Structure guided studies of the interaction between PTP1B and JAK. Commun Biol, 6, 2023
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8F88
| Crystal structure of PTP1B D181A/Q262A/C215A phosphatase domain with monophosphorylated JAK2 activation loop phosphopeptide | 分子名称: | 2-AMINO-2-HYDROXYMETHYL-PROPANE-1,3-DIOL, Tyrosine-protein kinase JAK2, Tyrosine-protein phosphatase non-receptor type 1 | 著者 | Morris, R, Kershaw, N.J, Babon, J.J. | 登録日 | 2022-11-21 | 公開日 | 2023-07-05 | 最終更新日 | 2023-11-15 | 実験手法 | X-RAY DIFFRACTION (3.1 Å) | 主引用文献 | Structure guided studies of the interaction between PTP1B and JAK. Commun Biol, 6, 2023
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8SLY
| Rat TRPV2 bound with 2 CBD ligands in nanodiscs | 分子名称: | (2S)-3-(hexadecanoyloxy)-2-[(9Z)-octadec-9-enoyloxy]propyl 2-(trimethylammonio)ethyl phosphate, SODIUM ION, Transient receptor potential cation channel subfamily V member 2, ... | 著者 | Tan, X, Swartz, K.J. | 登録日 | 2023-04-24 | 公開日 | 2023-05-31 | 最終更新日 | 2023-07-05 | 実験手法 | ELECTRON MICROSCOPY (3.32 Å) | 主引用文献 | Cannabidiol sensitizes TRPV2 channels to activation by 2-APB. Elife, 12, 2023
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8SLX
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8U8J
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8EXF
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8EXE
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8TGH
| VMAT1 dimer with amphetamine and reserpine | 分子名称: | (2S)-1-phenylpropan-2-amine, Chromaffin granule amine transporter, reserpine | 著者 | Ye, J, Liu, B, Li, W. | 登録日 | 2023-07-12 | 公開日 | 2024-03-20 | 最終更新日 | 2024-05-15 | 実験手法 | ELECTRON MICROSCOPY (3.5 Å) | 主引用文献 | Structural insights into vesicular monoamine storage and drug interactions. Nature, 629, 2024
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8U8K
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8TGJ
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8TGG
| VMAT1 dimer with MPP+ and reserpine | 分子名称: | 1-methyl-4-phenylpyridin-1-ium, Chromaffin granule amine transporter, reserpine | 著者 | Ye, J, Liu, B, Li, W. | 登録日 | 2023-07-12 | 公開日 | 2024-03-20 | 最終更新日 | 2024-05-15 | 実験手法 | ELECTRON MICROSCOPY (3.6 Å) | 主引用文献 | Structural insights into vesicular monoamine storage and drug interactions. Nature, 629, 2024
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8TGI
| VMAT1 dimer with dopamine and reserpine | 分子名称: | Chromaffin granule amine transporter, L-DOPAMINE, reserpine | 著者 | Ye, J, Liu, B, Li, W. | 登録日 | 2023-07-12 | 公開日 | 2024-03-20 | 最終更新日 | 2024-05-15 | 実験手法 | ELECTRON MICROSCOPY (3.4 Å) | 主引用文献 | Structural insights into vesicular monoamine storage and drug interactions. Nature, 629, 2024
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8TGL
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