3EHN
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![BU of 3ehn by Molmil](/molmil-images/mine/3ehn) | BT1043 with N-acetyllactosamine | 分子名称: | SusD homolog, beta-D-galactopyranose-(1-4)-2-acetamido-2-deoxy-alpha-D-glucopyranose | 著者 | Smith, T.J, Koropatkin, N.M. | 登録日 | 2008-09-13 | 公開日 | 2009-05-12 | 最終更新日 | 2024-02-21 | 実験手法 | X-RAY DIFFRACTION (2.8 Å) | 主引用文献 | Structure of a SusD homologue, BT1043, involved in mucin O-glycan utilization in a prominent human gut symbiont. Biochemistry, 48, 2009
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6XDJ
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![BU of 6xdj by Molmil](/molmil-images/mine/6xdj) | Crystal Structure Analysis of MBP-SIN3 | 分子名称: | Maltodextrin-binding protein,Transcriptional regulatory protein SIN3, alpha-D-glucopyranose-(1-4)-alpha-D-glucopyranose, alpha-D-glucopyranose-(1-4)-alpha-D-glucopyranose-(1-4)-beta-D-glucopyranose | 著者 | Seo, H.-S, Dhe-Paganon, S. | 登録日 | 2020-06-10 | 公開日 | 2021-06-16 | 最終更新日 | 2023-10-18 | 実験手法 | X-RAY DIFFRACTION (2.2 Å) | 主引用文献 | Crystal Structure Analysis of MBP-SIN3 To be published
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3EKQ
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![BU of 3ekq by Molmil](/molmil-images/mine/3ekq) | Crystal structure of inhibitor saquinavir (SQV) in complex with multi-drug resistant HIV-1 protease (L63P/V82T/I84V) (referred to as ACT in paper) | 分子名称: | (2S)-N-[(2S,3R)-4-[(2S,3S,4aS,8aS)-3-(tert-butylcarbamoyl)-3,4,4a,5,6,7,8,8a-octahydro-1H-isoquinolin-2-yl]-3-hydroxy-1 -phenyl-butan-2-yl]-2-(quinolin-2-ylcarbonylamino)butanediamide, PHOSPHATE ION, Protease | 著者 | Prabu-Jeyabalan, M, King, N.M, Schiffer, C.A, Nalivaika, E. | 登録日 | 2008-09-19 | 公開日 | 2009-09-01 | 最終更新日 | 2023-08-30 | 実験手法 | X-RAY DIFFRACTION (2.2 Å) | 主引用文献 | Extreme Entropy-Enthalpy Compensation in a Drug-Resistant Variant of HIV-1 Protease. Acs Chem.Biol., 7, 2012
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6XFR
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3E64
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![BU of 3e64 by Molmil](/molmil-images/mine/3e64) | Fragment based discovery of JAK-2 inhibitors | 分子名称: | 4-(3-amino-1H-indazol-5-yl)-N-tert-butylbenzenesulfonamide, Tyrosine-protein kinase JAK2 | 著者 | Antonysamy, S, Fang, W, Hirst, G, Park, F, Russell, M, Smyth, L, Sprengeler, P, Stappenbeck, F, Steensma, R, Thompson, D.A, Wilson, M, Wong, M, Zhang, A, Zhang, F. | 登録日 | 2008-08-14 | 公開日 | 2008-10-14 | 最終更新日 | 2012-02-08 | 実験手法 | X-RAY DIFFRACTION (1.8 Å) | 主引用文献 | Fragment-based discovery of JAK-2 inhibitors. Bioorg.Med.Chem.Lett., 19, 2009
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3E3D
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![BU of 3e3d by Molmil](/molmil-images/mine/3e3d) | Structure of hen egg white lysozyme with the magic triangle I3C | 分子名称: | 4-(2-HYDROXYETHYL)-1-PIPERAZINE ETHANESULFONIC ACID, 5-amino-2,4,6-triiodobenzene-1,3-dicarboxylic acid, Lysozyme C | 著者 | Beck, T, Gruene, T, Sheldrick, G.M. | 登録日 | 2008-08-07 | 公開日 | 2008-10-28 | 最終更新日 | 2017-10-25 | 実験手法 | X-RAY DIFFRACTION (1.55 Å) | 主引用文献 | A magic triangle for experimental phasing of macromolecules Acta Crystallogr.,Sect.D, 64, 2008
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3E41
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![BU of 3e41 by Molmil](/molmil-images/mine/3e41) | Q138F HincII bound to GTCGAC and 5 mM Ca2+ | 分子名称: | 5'-D(*DGP*DCP*DCP*DGP*DGP*DTP*DCP*DGP*DAP*DCP*DCP*DGP*DGP*DC)-3', CALCIUM ION, SODIUM ION, ... | 著者 | Horton, N.C, Babic, A.C, Little, E.J, Manohar, V.M. | 登録日 | 2008-08-08 | 公開日 | 2008-08-26 | 最終更新日 | 2024-02-21 | 実験手法 | X-RAY DIFFRACTION (2.73 Å) | 主引用文献 | DNA distortion and specificity in a sequence-specific endonuclease. J.Mol.Biol., 383, 2008
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6OHE
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3E7L
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![BU of 3e7l by Molmil](/molmil-images/mine/3e7l) | Crystal structure of sigma54 activator NtrC4's DNA binding domain | 分子名称: | Transcriptional regulator (NtrC family), ZINC ION | 著者 | Batchelor, J.D, Doucleff, M, Lee, C.-J, Matsubara, K, De Carlo, S, Heideker, J, Lamers, M.M, Pelton, J.G, Wemmer, D.E. | 登録日 | 2008-08-18 | 公開日 | 2008-11-25 | 最終更新日 | 2024-02-21 | 実験手法 | X-RAY DIFFRACTION (2.252 Å) | 主引用文献 | Structure and regulatory mechanism of Aquifex aeolicus NtrC4: variability and evolution in bacterial transcriptional regulation. J.Mol.Biol., 384, 2008
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7Q4R
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![BU of 7q4r by Molmil](/molmil-images/mine/7q4r) | Crystal structure of human HSP72-NBD in complex with fragment 1 | 分子名称: | 4-(4-phenyl-1,3-thiazol-2-yl)piperazine-1-carboxamide, Heat shock 70 kDa protein 1A, MAGNESIUM ION, ... | 著者 | Le Bihan, Y.V, Westwood, I.M, van Montfort, R.L.M. | 登録日 | 2021-11-02 | 公開日 | 2022-02-02 | 最終更新日 | 2024-01-31 | 実験手法 | X-RAY DIFFRACTION (1.79 Å) | 主引用文献 | Discovery and Characterization of a Cryptic Secondary Binding Site in the Molecular Chaperone HSP70. Molecules, 27, 2022
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6OH8
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3EIK
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6OJR
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![BU of 6ojr by Molmil](/molmil-images/mine/6ojr) | Crystal structure of Sphingomonas paucimobilis TMY1009 apo-LsdA | 分子名称: | GLYCEROL, Lignostilbene-alpha,beta-dioxygenase isozyme I, MAGNESIUM ION | 著者 | Kuatsjah, E, Verstraete, M.M, Kobylarz, M.J, Liu, A.K.N, Murphy, M.E.P, Eltis, L.D. | 登録日 | 2019-04-12 | 公開日 | 2019-07-24 | 最終更新日 | 2023-10-11 | 実験手法 | X-RAY DIFFRACTION (2.3 Å) | 主引用文献 | Identification of functionally important residues and structural features in a bacterial lignostilbene dioxygenase. J.Biol.Chem., 294, 2019
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3EDK
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3NFS
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![BU of 3nfs by Molmil](/molmil-images/mine/3nfs) | Crystal structure the Fab fragment of therapeutic antibody daclizumab | 分子名称: | Heavy chain of Fab fragment of daclizumab, Light chain of Fab fragment of daclizumab | 著者 | Yang, H, Wang, J, Du, J, Zhong, C, Guo, Y, Ding, J. | 登録日 | 2010-06-10 | 公開日 | 2010-09-15 | 最終更新日 | 2023-11-01 | 実験手法 | X-RAY DIFFRACTION (2.6 Å) | 主引用文献 | Structural basis of immunosuppression by the therapeutic antibody daclizumab Cell Res., 20, 2010
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3EE8
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3EEE
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![BU of 3eee by Molmil](/molmil-images/mine/3eee) | Probing the function of heme distortion in the H-NOX family | 分子名称: | CHLORIDE ION, Methyl-accepting chemotaxis protein, OXYGEN MOLECULE, ... | 著者 | Olea Jr, C, Boon, E.M, Pellicena, P, Kuriyan, J, Marletta, M.A. | 登録日 | 2008-09-04 | 公開日 | 2008-11-25 | 最終更新日 | 2023-08-30 | 実験手法 | X-RAY DIFFRACTION (2.12 Å) | 主引用文献 | Probing the function of heme distortion in the H-NOX family. Acs Chem.Biol., 3, 2008
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3N3A
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![BU of 3n3a by Molmil](/molmil-images/mine/3n3a) | Ribonucleotide Reductase Dimanganese(II)-NrdF from Escherichia coli in Complex with Reduced NrdI | 分子名称: | FLAVIN MONONUCLEOTIDE, MANGANESE (II) ION, Protein nrdI, ... | 著者 | Boal, A.K, Cotruvo Jr, J.A, Stubbe, J, Rosenzweig, A.C. | 登録日 | 2010-05-19 | 公開日 | 2010-08-18 | 最終更新日 | 2023-09-06 | 実験手法 | X-RAY DIFFRACTION (1.99 Å) | 主引用文献 | Structural basis for activation of class Ib ribonucleotide reductase. Science, 329, 2010
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6OOX
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3ENQ
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3N39
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![BU of 3n39 by Molmil](/molmil-images/mine/3n39) | Ribonucleotide Reductase Dimanganese(II)-NrdF from Escherichia coli in Complex with NrdI | 分子名称: | FLAVIN MONONUCLEOTIDE, MANGANESE (II) ION, Protein nrdI, ... | 著者 | Boal, A.K, Cotruvo Jr, J.A, Stubbe, J, Rosenzweig, A.C. | 登録日 | 2010-05-19 | 公開日 | 2010-08-18 | 最終更新日 | 2023-09-06 | 実験手法 | X-RAY DIFFRACTION (2.5 Å) | 主引用文献 | Structural basis for activation of class Ib ribonucleotide reductase. Science, 329, 2010
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3N96
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3E2M
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![BU of 3e2m by Molmil](/molmil-images/mine/3e2m) | LFA-1 I domain bound to inhibitors | 分子名称: | Integrin alpha-L, cis-4-{[2-({4-[(1E)-3-morpholin-4-yl-3-oxoprop-1-en-1-yl]-2,3-bis(trifluoromethyl)phenyl}sulfanyl)phenoxy]methyl}cyclohexanecarboxylic acid | 著者 | Silvian, L.F. | 登録日 | 2008-08-05 | 公開日 | 2008-08-19 | 最終更新日 | 2023-08-30 | 実験手法 | X-RAY DIFFRACTION (2 Å) | 主引用文献 | Structure-activity relationship of ortho- and meta-phenol based LFA-1 ICAM inhibitors Bioorg.Med.Chem.Lett., 18, 2008
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3N7C
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![BU of 3n7c by Molmil](/molmil-images/mine/3n7c) | Crystal structure of the RAN binding domain from the nuclear pore complex component NUP2 from Ashbya gossypii | 分子名称: | ABR034Wp | 著者 | Sampathkumar, P, Manglicmot, D, Gilmore, J, Bain, K, Gheyi, T, Atwell, S, Thompson, D.A, Emtage, J.S, Wasserman, S, Sauder, J.M, Burley, S.K, New York SGX Research Center for Structural Genomics (NYSGXRC) | 登録日 | 2010-05-26 | 公開日 | 2010-06-16 | 最終更新日 | 2021-02-10 | 実験手法 | X-RAY DIFFRACTION (2.26 Å) | 主引用文献 | Crystal structure of the RAN binding domain from the nuclear pore complex component NUP2 from Ashbya gossypii To be Published
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6O9H
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![BU of 6o9h by Molmil](/molmil-images/mine/6o9h) | Mouse ECD with Fab1 | 分子名称: | Gastric inhibitory polypeptide receptor, Heavy chain, Light chain, ... | 著者 | Min, X, Wang, Z. | 登録日 | 2019-03-13 | 公開日 | 2020-01-22 | 最終更新日 | 2020-04-01 | 実験手法 | X-RAY DIFFRACTION (2.1 Å) | 主引用文献 | Molecular mechanism of an antagonistic antibody against glucose-dependent insulinotropic polypeptide receptor. Mabs, 12, 2020
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