2GQJ
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2H5G
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![BU of 2h5g by Molmil](/molmil-images/mine/2h5g) | Crystal structure of human pyrroline-5-carboxylate synthetase | 分子名称: | Delta 1-pyrroline-5-carboxylate synthetase, SULFATE ION | 著者 | Papagrigoriou, E, Shafqat, N, Turnbull, A.P, Berridge, G, Hozjan, V, Kavanagh, K, Gileadi, O, Smee, C, Bray, J, Gorrec, F, Sundstrom, M, Arrowsmith, C, Weigelt, J, Edwards, A, Oppermann, U, Structural Genomics Consortium (SGC) | 登録日 | 2006-05-26 | 公開日 | 2006-06-23 | 最終更新日 | 2017-10-18 | 実験手法 | X-RAY DIFFRACTION (2.25 Å) | 主引用文献 | Crystal structure of human pyrroline-5-carboxylate synthetase To be published
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4DAY
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4C0D
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![BU of 4c0d by Molmil](/molmil-images/mine/4c0d) | Structure of the NOT module of the human CCR4-NOT complex (CNOT1-CNOT2-CNOT3) | 分子名称: | CCR4-NOT TRANSCRIPTION COMPLEX SUBUNIT 1, CCR4-NOT TRANSCRIPTION COMPLEX SUBUNIT 2, CCR4-NOT TRANSCRIPTION COMPLEX SUBUNIT 3 | 著者 | Raisch, T, Jonas, S, Boland, A, Chen, Y, Izaurralde, E, Weichenrieder, O. | 登録日 | 2013-08-01 | 公開日 | 2013-10-09 | 最終更新日 | 2023-12-20 | 実験手法 | X-RAY DIFFRACTION (3.2 Å) | 主引用文献 | Structure and Assembly of the not Module of the Human Ccr4-not Complex Nat.Struct.Mol.Biol., 20, 2013
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4FTC
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![BU of 4ftc by Molmil](/molmil-images/mine/4ftc) | Crystal Structure of the CHK1 | 分子名称: | 1-(5-cyanopyrazin-2-yl)-3-(5-phenyl-1H-pyrazol-3-yl)urea, GLYCEROL, ISOPROPYL ALCOHOL, ... | 著者 | Kang, Y.N, Stuckey, J.A, Chang, P, Russell, A.J. | 登録日 | 2012-06-27 | 公開日 | 2012-08-22 | 最終更新日 | 2023-11-29 | 実験手法 | X-RAY DIFFRACTION (2 Å) | 主引用文献 | Crystal Structure of the CHK1 To be Published
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5L91
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4FTN
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![BU of 4ftn by Molmil](/molmil-images/mine/4ftn) | Crystal Structure of the CHK1 | 分子名称: | 4'-{6-methoxy-7-[2-(piperidin-1-yl)ethoxy]-1,2-dihydroindeno[1,2-c]pyrazol-3-yl}biphenyl-4-ol, GLYCEROL, ISOPROPYL ALCOHOL, ... | 著者 | Kang, Y.N, Stuckey, J.A, Chang, P, Russell, A.J. | 登録日 | 2012-06-27 | 公開日 | 2012-08-22 | 最終更新日 | 2023-11-29 | 実験手法 | X-RAY DIFFRACTION (2.02 Å) | 主引用文献 | Crystal Structure of the CHK1 To be Published
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4GA7
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![BU of 4ga7 by Molmil](/molmil-images/mine/4ga7) | Crystal structure of human serpinB1 mutant | 分子名称: | Leukocyte elastase inhibitor | 著者 | Wang, L, Li, Q, Wu, L, Zhang, K, Tong, L, Sun, F, Fan, Z. | 登録日 | 2012-07-25 | 公開日 | 2013-01-16 | 最終更新日 | 2023-11-08 | 実験手法 | X-RAY DIFFRACTION (2.9 Å) | 主引用文献 | Identification of SERPINB1 as a physiological inhibitor of human granzyme H J.Immunol., 190, 2013
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2RD8
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3CWW
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![BU of 3cww by Molmil](/molmil-images/mine/3cww) | Crystal Structure of IDE-bradykinin complex | 分子名称: | 1,4-DIETHYLENE DIOXIDE, ACETATE ION, Insulin-degrading enzyme, ... | 著者 | Malito, E, Tang, W.J. | 登録日 | 2008-04-23 | 公開日 | 2008-11-25 | 最終更新日 | 2023-08-30 | 実験手法 | X-RAY DIFFRACTION (1.96 Å) | 主引用文献 | Molecular Bases for the Recognition of Short Peptide Substrates and Cysteine-Directed Modifications of Human Insulin-Degrading Enzyme Biochemistry, 47, 2008
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4FZS
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![BU of 4fzs by Molmil](/molmil-images/mine/4fzs) | Structure of human SNX1 BAR domain | 分子名称: | Sorting nexin-1 | 著者 | van Weering, J.R.T, Sessions, R.B, Traer, C.J, Kloer, D.P, Bhatia, V.K, Stamou, D, Hurley, J.H, Cullen, P.J. | 登録日 | 2012-07-07 | 公開日 | 2013-07-10 | 最終更新日 | 2024-02-28 | 実験手法 | X-RAY DIFFRACTION (2.8 Å) | 主引用文献 | Molecular insight into vesicle-to-tubule membrane remodeling by SNX-BAR proteins To be Published
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2RFI
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![BU of 2rfi by Molmil](/molmil-images/mine/2rfi) | Crystal structure of catalytic domain of human euchromatic histone methyltransferase 1 in complex with SAH and dimethylated H3K9 peptide | 分子名称: | Histone H3, Histone-lysine N-methyltransferase, H3 lysine-9 specific 5, ... | 著者 | Min, J, Wu, H, Loppnau, P, Weigelt, J, Sundstrom, M, Arrowsmith, C.H, Edwards, A.M, Bochkarev, A, Plotnikov, A.N, Structural Genomics Consortium (SGC) | 登録日 | 2007-09-30 | 公開日 | 2007-10-23 | 最終更新日 | 2023-08-30 | 実験手法 | X-RAY DIFFRACTION (1.59 Å) | 主引用文献 | Structural biology of human H3K9 methyltransferases Plos One, 5, 2010
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4FSW
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![BU of 4fsw by Molmil](/molmil-images/mine/4fsw) | Crystal Structure of the CHK1 | 分子名称: | 8-chloro-5,10-dihydro-11H-dibenzo[b,e][1,4]diazepin-11-one, ISOPROPYL ALCOHOL, SULFATE ION, ... | 著者 | Kang, Y.N, Stuckey, J.A, Chang, P, Russell, A.J. | 登録日 | 2012-06-27 | 公開日 | 2012-08-22 | 最終更新日 | 2023-11-29 | 実験手法 | X-RAY DIFFRACTION (2.3 Å) | 主引用文献 | Crystal Structure of the CHK1 To be Published
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2RGZ
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![BU of 2rgz by Molmil](/molmil-images/mine/2rgz) | Ensemble refinement of the protein crystal structure of human heme oxygenase-2 C127A (HO-2) with bound heme | 分子名称: | Heme oxygenase 2, PROTOPORPHYRIN IX CONTAINING FE | 著者 | Bianchetti, C.M, Bingman, C.A, Bitto, E, Wesenberg, G.E, Phillips Jr, G.N, Center for Eukaryotic Structural Genomics (CESG) | 登録日 | 2007-10-05 | 公開日 | 2007-10-23 | 最終更新日 | 2023-08-30 | 実験手法 | X-RAY DIFFRACTION (2.61 Å) | 主引用文献 | Comparison of Apo- and Heme-bound Crystal Structures of a Truncated Human Heme Oxygenase-2. J.Biol.Chem., 282, 2007
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3D45
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![BU of 3d45 by Molmil](/molmil-images/mine/3d45) | Crystal structure of mouse PARN in complex with m7GpppG | 分子名称: | 7N-METHYL-8-HYDROGUANOSINE-5'-MONOPHOSPHATE, GUANOSINE-5'-DIPHOSPHATE, Poly(A)-specific ribonuclease PARN | 著者 | Wu, M, Song, H. | 登録日 | 2008-05-13 | 公開日 | 2009-03-17 | 最終更新日 | 2023-08-30 | 実験手法 | X-RAY DIFFRACTION (3 Å) | 主引用文献 | Structural basis of m(7)GpppG binding to poly(A)-specific ribonuclease. Structure, 17, 2009
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3D4Q
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![BU of 3d4q by Molmil](/molmil-images/mine/3d4q) | Pyrazole-based inhibitors of B-Raf kinase | 分子名称: | (1E)-5-(1-piperidin-4-yl-3-pyridin-4-yl-1H-pyrazol-4-yl)-2,3-dihydro-1H-inden-1-one oxime, B-Raf proto-oncogene serine/threonine-protein kinase | 著者 | Morales, T, Vigers, G.P.A, Brandhuber, B.J. | 登録日 | 2008-05-14 | 公開日 | 2008-08-19 | 最終更新日 | 2024-02-21 | 実験手法 | X-RAY DIFFRACTION (2.8 Å) | 主引用文献 | Potent and selective pyrazole-based inhibitors of B-Raf kinase. Bioorg.Med.Chem.Lett., 18, 2008
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4G21
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![BU of 4g21 by Molmil](/molmil-images/mine/4g21) | Structural basis for the accommodation of bis- and tris-aromatic derivatives in Vitamin D Nuclear Receptor | 分子名称: | 3-(5'-{[3,4-bis(hydroxymethyl)benzyl]oxy}-2'-ethyl-2-propylbiphenyl-4-yl)pentan-3-ol, Nuclear receptor coactivator 1, Vitamin D3 receptor A | 著者 | Ciesielski, F, Sato, Y, Moras, D, Rochel, N. | 登録日 | 2012-07-11 | 公開日 | 2012-09-26 | 最終更新日 | 2024-02-28 | 実験手法 | X-RAY DIFFRACTION (2.9 Å) | 主引用文献 | Structural basis for the accommodation of bis- and tris-aromatic derivatives in vitamin d nuclear receptor. J.Med.Chem., 55, 2012
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3CZF
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![BU of 3czf by Molmil](/molmil-images/mine/3czf) | Crystal structure of HLA-B*2709 complexed with the glucagon receptor (GR) peptide (residues 412-420) | 分子名称: | BETA-2-MICROGLOBULIN, GLUCAGON RECEPTOR PEPTIDE, GLYCEROL, ... | 著者 | Loll, B, Fiorillo, M.T, Rueckert, C, Saenger, W, Sorrentino, R, Ziegler, A, Uchanska-Ziegler, B. | 登録日 | 2008-04-29 | 公開日 | 2009-04-07 | 最終更新日 | 2023-08-30 | 実験手法 | X-RAY DIFFRACTION (1.2 Å) | 主引用文献 | Conformational Plasticity of HLA-B27 Molecules Correlates Inversely With Efficiency of Negative T Cell Selection. Front Immunol, 11, 2020
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4FTL
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![BU of 4ftl by Molmil](/molmil-images/mine/4ftl) | Crystal Structure of the CHK1 | 分子名称: | 4'-[7-(hydroxymethyl)-2,4-dihydroindeno[1,2-c]pyrazol-3-yl]biphenyl-4-ol, ISOPROPYL ALCOHOL, SULFATE ION, ... | 著者 | Kang, Y.N, Stuckey, J.A, Chang, P, Russell, A.J. | 登録日 | 2012-06-27 | 公開日 | 2012-08-22 | 最終更新日 | 2023-11-29 | 実験手法 | X-RAY DIFFRACTION (2.5 Å) | 主引用文献 | Crystal Structure of the CHK1 To be Published
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4FTU
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![BU of 4ftu by Molmil](/molmil-images/mine/4ftu) | Crystal Structure of the CHK1 | 分子名称: | GLYCEROL, ISOPROPYL ALCOHOL, SULFATE ION, ... | 著者 | Kang, Y.N, Stuckey, J.A, Chang, P, Russell, A.J. | 登録日 | 2012-06-28 | 公開日 | 2012-08-22 | 最終更新日 | 2024-02-28 | 実験手法 | X-RAY DIFFRACTION (2.1 Å) | 主引用文献 | Crystal Structure of the CHK1 To be Published
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2RF9
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![BU of 2rf9 by Molmil](/molmil-images/mine/2rf9) | Crystal structure of the complex between the EGFR kinase domain and a Mig6 peptide | 分子名称: | ERBB receptor feedback inhibitor 1, Epidermal growth factor receptor | 著者 | Zhang, X, Pickin, K.A, Bose, R, Jura, N, Cole, P.A, Kuriyan, J. | 登録日 | 2007-09-28 | 公開日 | 2007-12-04 | 最終更新日 | 2023-08-30 | 実験手法 | X-RAY DIFFRACTION (3.5 Å) | 主引用文献 | Inhibition of the EGF receptor by binding of MIG6 to an activating kinase domain interface. Nature, 450, 2007
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3CH6
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5L92
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3D6M
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3D7H
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