8DKM
 
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8DYP
 
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5WCU
 
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8XI3
 
 | Structure of mouse SCMC-14-3-3gama complex | 分子名称: | 14-3-3 protein gamma, NACHT, LRR and PYD domains-containing protein 5, ... | 著者 | Chi, P, Han, Z, Jiao, H, Li, J, Wang, X, Hu, H, Deng, D. | 登録日 | 2023-12-19 | 公開日 | 2024-10-02 | 最終更新日 | 2025-06-18 | 実験手法 | ELECTRON MICROSCOPY (3 Å) | 主引用文献 | The subcortical maternal complex modulates the cell cycle during early mammalian embryogenesis via 14-3-3. Nat Commun, 15, 2024
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7FAF
 
 | S protein of SARS-CoV-2 in complex bound with P36-5D2 (state1) | 分子名称: | P36-5D2 heavy chain, P36-5D2 light chain, Spike glycoprotein | 著者 | Zhang, L, Wang, X, Zhang, S, Shan, S. | 登録日 | 2021-07-06 | 公開日 | 2021-12-22 | 最終更新日 | 2024-11-06 | 実験手法 | ELECTRON MICROSCOPY (3.69 Å) | 主引用文献 | A Potent and Protective Human Neutralizing Antibody Against SARS-CoV-2 Variants. Front Immunol, 12, 2021
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7FAE
 
 | S protein of SARS-CoV-2 in complex bound with P36-5D2(state2) | 分子名称: | 2-acetamido-2-deoxy-beta-D-glucopyranose, 2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose, P36-5D2 heavy chain, ... | 著者 | Zhang, L, Wang, X, Shan, S, Zhang, S. | 登録日 | 2021-07-06 | 公開日 | 2021-12-22 | 最終更新日 | 2024-11-06 | 実験手法 | ELECTRON MICROSCOPY (3.65 Å) | 主引用文献 | A Potent and Protective Human Neutralizing Antibody Against SARS-CoV-2 Variants. Front Immunol, 12, 2021
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1U3B
 
 | Auto-inhibition Mechanism of X11s/Mints Family Scaffold Proteins Revealed by the Closed Conformation of the Tandem PDZ Domains | 分子名称: | amyloid beta A4 precursor protein-binding, family A, member 1 | 著者 | Feng, W, Long, J.-F, Chan, L.-N, He, C, Fu, A, Xia, J, Ip, N.Y, Zhang, M. | 登録日 | 2004-07-21 | 公開日 | 2005-07-26 | 最終更新日 | 2024-05-29 | 実験手法 | SOLUTION NMR | 主引用文献 | Autoinhibition of X11/Mint scaffold proteins revealed by the closed conformation of the PDZ tandem Nat.Struct.Mol.Biol., 12, 2005
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1U38
 
 | Auto-inhibition Mechanism of X11s/Mints Family Scaffold Proteins Revealed by the Closed Conformation of the Tandem PDZ Domains | 分子名称: | PVYI, amyloid beta A4 precursor protein-binding, family A, ... | 著者 | Feng, W, Long, J.-F, Chan, L.-N, He, C, Fu, A, Xia, J, Ip, N.Y, Zhang, M. | 登録日 | 2004-07-21 | 公開日 | 2005-07-26 | 最終更新日 | 2024-05-29 | 実験手法 | SOLUTION NMR | 主引用文献 | Autoinhibition of X11/Mint scaffold proteins revealed by the closed conformation of the PDZ tandem Nat.Struct.Mol.Biol., 12, 2005
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3O8D
 
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3O8C
 
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3O8B
 
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3O8R
 
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8FSJ
 
 | Cryo-EM structure of engineered hepatitis C virus E1E2 ectodomain in complex with antibodies AR4A, HEPC74, and IGH520 | 分子名称: | 2-acetamido-2-deoxy-beta-D-glucopyranose, 2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose, AR4A heavy chain, ... | 著者 | Metcalf, M.C, Ofek, G. | 登録日 | 2023-01-10 | 公開日 | 2023-07-19 | 最終更新日 | 2024-10-23 | 実験手法 | ELECTRON MICROSCOPY (3.65 Å) | 主引用文献 | Structure of engineered hepatitis C virus E1E2 ectodomain in complex with neutralizing antibodies. Nat Commun, 14, 2023
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3HMM
 
 | Structure of Alk5 + GW855857 | 分子名称: | 2-(6-methylpyridin-2-yl)-N-pyridin-4-ylquinazolin-4-amine, TGF-beta receptor type-1 | 著者 | Smith, W, Janson, C. | 登録日 | 2009-05-29 | 公開日 | 2009-06-23 | 最終更新日 | 2023-11-01 | 実験手法 | X-RAY DIFFRACTION (1.7 Å) | 主引用文献 | Design of novel quinazoline derivatives and related analogues as potent and selective ALK5 inhibitors Bioorg.Med.Chem.Lett., 19, 2009
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8YBQ
 
 | Choline transporter BetT - CHT bound | 分子名称: | BCCT family transporter, CHOLINE ION | 著者 | Yang, T.J, Nian, Y.W, Lin, H.J, Li, J, Zhang, J.R, Fan, M.R. | 登録日 | 2024-02-16 | 公開日 | 2024-09-04 | 最終更新日 | 2025-06-18 | 実験手法 | ELECTRON MICROSCOPY (2.59 Å) | 主引用文献 | Structure and mechanism of the osmoregulated choline transporter BetT. Sci Adv, 10, 2024
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8YBR
 
 | Choline transporter BetT | 分子名称: | BCCT family transporter | 著者 | Yang, T.J, Nian, Y.W, Lin, H.J, Li, J, Zhang, J.R, Fan, M.R. | 登録日 | 2024-02-16 | 公開日 | 2024-09-04 | 最終更新日 | 2025-07-02 | 実験手法 | ELECTRON MICROSCOPY (2.57 Å) | 主引用文献 | Structure and mechanism of the osmoregulated choline transporter BetT. Sci Adv, 10, 2024
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8ZSB
 
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8ZSZ
 
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5TH6
 
 | Structure determination of a potent, selective antibody inhibitor of human MMP9 (apo MMP9) | 分子名称: | CALCIUM ION, Matrix metalloproteinase-9,Matrix metalloproteinase-9, ZINC ION | 著者 | Appleby, T.C, Greenstein, A.E, Kwon, H.J. | 登録日 | 2016-09-29 | 公開日 | 2017-03-01 | 最終更新日 | 2023-10-04 | 実験手法 | X-RAY DIFFRACTION (1.7 Å) | 主引用文献 | Biochemical characterization and structure determination of a potent, selective antibody inhibitor of human MMP9. J. Biol. Chem., 292, 2017
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8XYD
 
 | Structure of Platelet-activating factor receptor-G protein complex bound to platelet-activating factor | 分子名称: | (2R)-2-(acetyloxy)-3-(hexadecyloxy)propyl 2-(trimethylammonio)ethyl phosphate, Guanine nucleotide-binding protein G(I)/G(S)/G(O) subunit gamma-2, Guanine nucleotide-binding protein G(I)/G(S)/G(T) subunit beta-1, ... | 著者 | Fan, W, Xu, Y, Zhuang, Y, Xu, H.E. | 登録日 | 2024-01-19 | 公開日 | 2024-11-13 | 最終更新日 | 2024-11-27 | 実験手法 | ELECTRON MICROSCOPY (2.9 Å) | 主引用文献 | Molecular basis for the activation of PAF receptor by PAF. Cell Rep, 43, 2024
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8XLR
 
 | Cryo-EM structure of Ca2+-bound TMEM16A in complex with Tamsulosin | 分子名称: | 2-acetamido-2-deoxy-beta-D-glucopyranose, Anoctamin-1, CALCIUM ION, ... | 著者 | Li, H.L, Li, S.L, Li, S. | 登録日 | 2023-12-26 | 公開日 | 2024-12-18 | 最終更新日 | 2025-02-05 | 実験手法 | ELECTRON MICROSCOPY (2.93 Å) | 主引用文献 | Tamsulosin ameliorates bone loss by inhibiting the release of Cl - through wedging into an allosteric site of TMEM16A. Proc.Natl.Acad.Sci.USA, 122, 2025
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8JGD
 
 | GDP-bound KRAS G12C in complex with YK-8S | 分子名称: | (2~{S})-1-[4-[7-(8-ethynyl-7-fluoranyl-naphthalen-1-yl)-8-fluoranyl-2-[[(2~{R},8~{S})-2-fluoranyl-1,2,3,5,6,7-hexahydropyrrolizin-8-yl]methoxy]pyrido[4,3-d]pyrimidin-4-yl]piperazin-1-yl]-2-oxidanyl-propan-1-one, GTPase KRas, GUANOSINE-5'-DIPHOSPHATE, ... | 著者 | Zhang, Z.M, Wang, R.L. | 登録日 | 2023-05-20 | 公開日 | 2024-01-31 | 最終更新日 | 2024-11-13 | 実験手法 | X-RAY DIFFRACTION (1.60037053 Å) | 主引用文献 | Simultaneous Covalent Modification of K-Ras(G12D) and K-Ras(G12C) with Tunable Oxirane Electrophiles. J.Am.Chem.Soc., 145, 2023
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8JHL
 
 | GDP-bound KRAS G12D in complex with YK-8S | 分子名称: | 1-[4-[7-(8-ethynyl-7-fluoranyl-naphthalen-1-yl)-8-fluoranyl-2-[[(2~{R},8~{S})-2-fluoranyl-1,2,3,5,6,7-hexahydropyrrolizin-8-yl]methoxy]pyrido[4,3-d]pyrimidin-4-yl]piperazin-1-yl]-3-oxidanyl-propan-1-one, GTPase KRas, N-terminally processed, ... | 著者 | Zhang, Z.M, Wang, R.L. | 登録日 | 2023-05-23 | 公開日 | 2024-01-31 | 実験手法 | X-RAY DIFFRACTION (2.10004044 Å) | 主引用文献 | Simultaneous Covalent Modification of K-Ras(G12D) and K-Ras(G12C) with Tunable Oxirane Electrophiles. J.Am.Chem.Soc., 145, 2023
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5TH9
 
 | Structure determination of a potent, selective antibody inhibitor of human MMP9 (GS-5745 bound to MMP-9) | 分子名称: | CALCIUM ION, COBALT HEXAMMINE(III), GS-5745 Fab heavy chain, ... | 著者 | Appleby, T.C, Greenstein, A.E, Kwon, H.J. | 登録日 | 2016-09-29 | 公開日 | 2017-03-15 | 最終更新日 | 2024-11-20 | 実験手法 | X-RAY DIFFRACTION (2.999 Å) | 主引用文献 | Biochemical characterization and structure determination of a potent, selective antibody inhibitor of human MMP9. J. Biol. Chem., 292, 2017
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3GXL
 
 | ALK-5 kinase complex with GW857175 | 分子名称: | N-1H-indazol-5-yl-2-(6-methylpyridin-2-yl)quinazolin-4-amine, TGF-beta receptor type-1 | 著者 | Smith, W, Janson, C. | 登録日 | 2009-04-02 | 公開日 | 2009-04-21 | 最終更新日 | 2023-11-01 | 実験手法 | X-RAY DIFFRACTION (1.8 Å) | 主引用文献 | Design of novel quinazoline derivatives and related analogues as potent and selective ALK5 inhibitors Bioorg.Med.Chem.Lett., 19, 2009
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