PDB: 105044 件ウェブページステータス検索Chemie searchBIRD

---

3AUA	Crystal structure of the quaternary complex-2 of an isomerase 分子名称: 1-deoxy-D-xylulose 5-phosphate reductoisomerase, 3-[ethanoyl(hydroxy)amino]propylphosphonic acid, CALCIUM ION, ... 著者 Umeda, T, Tanaka, N, Kusakabe, Y, Nakanishi, M, Kitade, Y, Nakamura, K.T. 登録日 2011-02-01 公開日 2011-08-10 最終更新日 2024-03-13 実験手法 X-RAY DIFFRACTION (2.15 Å) 主引用文献 Molecular basis of fosmidomycin's action on the human malaria parasite Plasmodium falciparum Sci Rep, 1, 2011
3V13	Bovine trypsin variant X(tripleGlu217Phe227) in complex with small molecule inhibitor 分子名称: 3-(3-carbamimidoylphenyl)-N-(2'-sulfamoylbiphenyl-4-yl)-1,2-oxazole-4-carboxamide, CALCIUM ION, CHLORIDE ION, ... 著者 Tziridis, A, Neumann, P, Kolenko, P, Stubbs, M.T. 登録日 2011-12-09 公開日 2012-12-12 最終更新日 2024-10-30 実験手法 X-RAY DIFFRACTION (1.63 Å) 主引用文献 Correlating structure and ligand affinity in drug discovery: a cautionary tale involving second shell residues. Biol.Chem., 395, 2014
3ARV	Crystal Structure Analysis of Chitinase A from Vibrio harveyi with novel inhibitors - complex structure with Sanguinarine 分子名称: 13-methyl[1,3]benzodioxolo[5,6-c][1,3]dioxolo[4,5-i]phenanthridin-13-ium, Chitinase A, GLYCEROL 著者 Pantoom, S, Vetter, I.R, Prinz, H, Suginta, W. 登録日 2010-12-09 公開日 2011-04-20 最終更新日 2024-11-06 実験手法 X-RAY DIFFRACTION (1.5 Å) 主引用文献 Potent family-18 chitinase inhibitors: x-ray structures, affinities, and binding mechanisms J.Biol.Chem., 286, 2011
4BKR	Enoyl-ACP reductase from Yersinia pestis (wildtype, removed Histag) with cofactor NADH 分子名称: 1,4-DIHYDRONICOTINAMIDE ADENINE DINUCLEOTIDE, DIMETHYL SULFOXIDE, GLYCEROL, ... 著者 Hirschbeck, M.W, Neckles, C, Tonge, P.J, Kisker, C. 登録日 2013-04-29 公開日 2014-05-14 最終更新日 2023-12-20 実験手法 X-RAY DIFFRACTION (1.798 Å) 主引用文献 Selectivity of Pyridone- and Diphenyl Ether-Based Inhibitors for the Yersinia Pestis Fabv Enoyl-Acp Reductase. Biochemistry, 55, 2016
3ARZ	Crystal Structure Analysis of Chitinase A from Vibrio harveyi with novel inhibitors - complex structure with 2-(imidazolin-2-yl)-5-isothiocyanatobenzofuran 分子名称: 2-(5-isothiocyanato-1-benzofuran-2-yl)-4,5-dihydro-1H-imidazole, Chitinase A, GLYCEROL 著者 Pantoom, S, Vetter, I.R, Prinz, H, Suginta, W. 登録日 2010-12-09 公開日 2011-04-20 最終更新日 2024-10-16 実験手法 X-RAY DIFFRACTION (1.82 Å) 主引用文献 Potent family-18 chitinase inhibitors: x-ray structures, affinities, and binding mechanisms J.Biol.Chem., 286, 2011
3AS0	Crystal Structure Analysis of Chitinase A from Vibrio harveyi with novel inhibitors - W275G mutant complex structure with Sanguinarine 分子名称: 13-methyl[1,3]benzodioxolo[5,6-c][1,3]dioxolo[4,5-i]phenanthridin-13-ium, Chitinase A, GLYCEROL 著者 Pantoom, S, Vetter, I.R, Prinz, H, Suginta, W. 登録日 2010-12-09 公開日 2011-04-20 最終更新日 2024-10-23 実験手法 X-RAY DIFFRACTION (2 Å) 主引用文献 Potent family-18 chitinase inhibitors: x-ray structures, affinities, and binding mechanisms J.Biol.Chem., 286, 2011
3VCI	Thaumatin by Classical Hanging Drop Vapour Diffusion after 9.05 MGy X-Ray dose at ESRF ID29 beamline (Worst Case) 分子名称: GLYCEROL, Thaumatin I 著者 Belmonte, L, Pechkova, E, Scudieri, D, Nicolini, C. 登録日 2012-01-04 公開日 2012-11-21 最終更新日 2024-11-06 実験手法 X-RAY DIFFRACTION (2.3 Å) 主引用文献 Langmuir-blodgett nanotemplate and radiation resistance in protein crystals: state of the art. Crit Rev Eukaryot Gene Expr, 22, 2012
3ARS	Crystal Structure Analysis of Chitinase A from Vibrio harveyi with novel inhibitors - apo structure of mutant W275G 分子名称: Chitinase A 著者 Pantoom, S, Vetter, I.R, Prinz, H, Suginta, W. 登録日 2010-12-09 公開日 2011-04-20 最終更新日 2024-10-16 実験手法 X-RAY DIFFRACTION (2.45 Å) 主引用文献 Potent family-18 chitinase inhibitors: x-ray structures, affinities, and binding mechanisms J.Biol.Chem., 286, 2011
2Y6Y	Crystal structure of TtrD from Archaeoglobus fulgidus 分子名称: CHAPERONE PROTEIN TTRD, CHLORIDE ION 著者 Dawson, A, Coulthurst, S.J, Sargent, F, Hunter, W.N. 登録日 2011-01-27 公開日 2012-02-15 最終更新日 2023-12-20 実験手法 X-RAY DIFFRACTION (2.2 Å) 主引用文献 Conserved Signal Peptide Recognition Systems Across the Prokaryotic Domains. Biochemistry, 51, 2012
4AQK	Inositol 1,3,4,5,6-pentakisphosphate 2-kinase in complex with ADP and IP6 分子名称: ADENOSINE-5'-DIPHOSPHATE, INOSITOL HEXAKISPHOSPHATE, INOSITOL-PENTAKISPHOSPHATE 2-KINASE, ... 著者 I Banos-Sanz, J, Sanz-Aparicio, J, Gonzalez, B. 登録日 2012-04-18 公開日 2012-05-02 最終更新日 2023-12-20 実験手法 X-RAY DIFFRACTION (2.4 Å) 主引用文献 Expression, Purification, Crystallization and Preliminary X-Ray Diffraction Analysis of the Apo Form of Insp5 2-K from Arabidopsis Thaliana. Acta Crystallogr.,Sect.F, 68, 2012
2NTH	Structure of Spin-labeled T4 Lysozyme Mutant L118R1 分子名称: Lysozyme, S-[(1-oxyl-2,2,5,5-tetramethyl-2,5-dihydro-1H-pyrrol-3-yl)methyl] methanesulfonothioate 著者 Guo, Z, Cascio, D, Hideg, K, Hubbell, W.L. 登録日 2006-11-07 公開日 2007-06-12 最終更新日 2024-11-06 実験手法 X-RAY DIFFRACTION (1.8 Å) 主引用文献 Structural determinants of nitroxide motion in spin-labeled proteins: Tertiary contact and solvent-inaccessible sites in helix G of T4 lysozyme. Protein Sci., 16, 2007
4AKN	N-Terminal Bromodomain of Human BRD2 With tbutyl-phenyl-amino- dimethyl-oxazolyl-quinoline-carboxylic acid 分子名称: 1,2-ETHANEDIOL, 4-[(2-tert-butylphenyl)amino]-7-(3,5-dimethyl-1,2-oxazol-4-yl)quinoline-3-carboxylic acid, BROMODOMAIN-CONTAINING PROTEIN 2, ... 著者 Chung, C, Lamotte, Y, Donche, F, Bouillot, A, Mirguet, O. 登録日 2012-02-26 公開日 2012-07-04 最終更新日 2024-05-08 実験手法 X-RAY DIFFRACTION (1.82 Å) 主引用文献 Identification of a Novel Series of Bet Family Bromodomain Inhibitors: Binding Mode and Profile of I-Bet151 (Gsk1210151A). Bioorg.Med.Chem.Lett., 22, 2012
3V12	Bovine trypsin variant X(tripleGlu217Phe227) in complex with small molecule inhibitor 分子名称: CALCIUM ION, Cationic trypsin, GLYCEROL, ... 著者 Tziridis, A, Neumann, P, Kolenko, P, Stubbs, M.T. 登録日 2011-12-09 公開日 2012-12-12 最終更新日 2024-11-06 実験手法 X-RAY DIFFRACTION (1.8 Å) 主引用文献 Correlating structure and ligand affinity in drug discovery: a cautionary tale involving second shell residues. Biol.Chem., 395, 2014
2G87	Crystallographic model of bathorhodopsin 分子名称: 2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose, HEPTANE-1,2,3-TRIOL, MERCURY (II) ION, ... 著者 Nakamichi, H, Okada, T. 登録日 2006-03-02 公開日 2006-09-02 最終更新日 2024-10-23 実験手法 X-RAY DIFFRACTION (2.6 Å) 主引用文献 Crystallographic analysis of primary visual photochemistry Angew.Chem.Int.Ed.Engl., 45, 2006
3T47	Crystal Structure of truncated form of Staphylococcal Complement Inhibitor D (SCIN-D) at 1.3 Angstrom 分子名称: SCIN-D 著者 Garcia, B.L, Geisbrecht, B.V, Summers, B.J. 登録日 2011-07-25 公開日 2011-11-23 最終更新日 2023-09-13 実験手法 X-RAY DIFFRACTION (1.301 Å) 主引用文献 Diversity in the C3b Convertase Contact Residues and Tertiary Structures of the Staphylococcal Complement Inhibitor (SCIN) Protein Family. J.Biol.Chem., 287, 2012
4ACO	Structure of the budding yeast Ndc10 N-terminal domain 分子名称: CENTROMERE DNA-BINDING PROTEIN COMPLEX CBF3 SUBUNIT A 著者 Perriches, T, Singleton, M.R. 登録日 2011-12-16 公開日 2012-01-11 最終更新日 2024-05-08 実験手法 X-RAY DIFFRACTION (1.89 Å) 主引用文献 The Structure of the Yeast Kinetochore Ndc10 DNA-Binding Domain Reveals an Unexpected Evolutionary Relationship to Tyrosine Recombinases. J.Biol.Chem., 287, 2012
2OGG	Structure of B. subtilis trehalose repressor (TreR) effector binding domain 分子名称: GLYCEROL, SODIUM ION, SULFATE ION, ... 著者 Rezacova, P, Krejcirikova, V, Borek, D, Moy, S.F, Joachimiak, A, Otwinowski, Z, Midwest Center for Structural Genomics (MCSG) 登録日 2007-01-05 公開日 2007-02-06 最終更新日 2024-10-09 実験手法 X-RAY DIFFRACTION (2.5 Å) 主引用文献 The crystal structure of the effector-binding domain of the trehalose repressor TreR from Bacillus subtilis 168 reveals a unique quarternary assembly. Proteins, 69, 2007
2NZ0	Crystal structure of potassium channel Kv4.3 in complex with its regulatory subunit KChIP1 分子名称: CALCIUM ION, Kv channel-interacting protein 1, Potassium voltage-gated channel subfamily D member 3, ... 著者 Wang, H, Yan, Y, Shen, Y, Chen, L, Wang, K. 登録日 2006-11-22 公開日 2006-12-26 最終更新日 2023-12-27 実験手法 X-RAY DIFFRACTION (3.2 Å) 主引用文献 Structural basis for modulation of Kv4 K(+) channels by auxiliary KChIP subunits. Nat.Neurosci., 10, 2007
3VCG	Thaumatin by LB based Hanging Drop Vapour Diffusion after 18.1 MGy X-Ray dose at ESRF ID29 beamline (Worst Case) 分子名称: GLYCEROL, Thaumatin I 著者 Belmonte, L, Pechkova, E, Scudieri, D, Nicolini, C. 登録日 2012-01-04 公開日 2012-11-21 最終更新日 2024-11-20 実験手法 X-RAY DIFFRACTION (2.3 Å) 主引用文献 Langmuir-blodgett nanotemplate and radiation resistance in protein crystals: state of the art. Crit Rev Eukaryot Gene Expr, 22, 2012
4ADG	Crystal structure of the Rubella virus envelope Glycoprotein E1 in post-fusion form (crystal form II) 分子名称: 2-acetamido-2-deoxy-beta-D-galactopyranose, 2-acetamido-2-deoxy-beta-D-glucopyranose, ACETATE ION, ... 著者 DuBois, R.M, Vaney, M.C, Tortorici, M.A, Al Kurdi, R, Barba-Spaeth, G, Rey, F.A. 登録日 2011-12-26 公開日 2013-01-09 最終更新日 2024-10-16 実験手法 X-RAY DIFFRACTION (2.18 Å) 主引用文献 Functional and Evolutionary Insight from the Crystal Structure of Rubella Virus Protein E1. Nature, 493, 2013
2ZQQ	Crystal structure of human AUH (3-methylglutaconyl-coa hydratase) mixed with (AUUU)24A RNA 分子名称: Methylglutaconyl-CoA hydratase 著者 Kurimoto, K, Kuwasako, K, Muto, Y, Nureki, O, Yokoyama, S, RIKEN Structural Genomics/Proteomics Initiative (RSGI) 登録日 2008-08-16 公開日 2009-06-30 最終更新日 2023-11-01 実験手法 X-RAY DIFFRACTION (2.2 Å) 主引用文献 AU-rich RNA-binding induces changes in the quaternary structure of AUH Proteins, 75, 2009
4AYV	Human thrombin - inhibitor complex 分子名称: 2-acetamido-2-deoxy-beta-D-glucopyranose, HIRUDIN-3A', SODIUM ION, ... 著者 Banner, D.W, D'Arcy, A, Winkler, F.K, Hilpert, K. 登録日 2012-06-22 公開日 2012-08-15 最終更新日 2024-10-23 実験手法 X-RAY DIFFRACTION (2.8 Å) 主引用文献 Design and Synthesis of Potent and Highly Selective Thrombin Inhibitors. J.Med.Chem., 37, 1994
4AZ2	Human thrombin - inhibitor complex 分子名称: (R)-N-((S)-1-CARBAMIMIDOYL-PIPERIDIN-3-YLMETHYL)-2-(NAPHTHALENE-2-SULFONYLAMINO)-3-PHENYL-PROPIONAMIDE, 2-acetamido-2-deoxy-beta-D-glucopyranose, HIRUDIN-3A', ... 著者 Banner, D.W, D'Arcy, A, Winkler, F.K, Hilpert, K. 登録日 2012-06-22 公開日 2012-08-15 最終更新日 2024-10-16 実験手法 X-RAY DIFFRACTION (2.6 Å) 主引用文献 Design and Synthesis of Potent and Highly Selective Thrombin Inhibitors. J.Med.Chem., 37, 1994
4AYY	Human thrombin - inhibitor complex 分子名称: (R)-1-[(S)-3-[((S)-1-Carbamimidoyl-piperidin-3-ylmethyl)-carbamoyl]-2-(naphthalene-2-sulfonylamino)-propionyl]-4-methyl-piperidine-2-carboxylic acid, 2-acetamido-2-deoxy-beta-D-glucopyranose, HIRUDIN-3A', ... 著者 Banner, D.W, D'Arcy, A, Winkler, F.K, Hilpert, K. 登録日 2012-06-22 公開日 2012-08-15 最終更新日 2024-11-06 実験手法 X-RAY DIFFRACTION (2.6 Å) 主引用文献 Design and Synthesis of Potent and Highly Selective Thrombin Inhibitors. J.Med.Chem., 37, 1994
1E79	Bovine F1-ATPase inhibited by DCCD (dicyclohexylcarbodiimide) 分子名称: ADENOSINE-5'-DIPHOSPHATE, ADENOSINE-5'-TRIPHOSPHATE, ATP SYNTHASE ALPHA CHAIN HEART ISOFORM, ... 著者 Gibbons, C, Montgomery, M.G, Leslie, A.G.W, Walker, J.E. 登録日 2000-08-25 公開日 2000-11-03 最終更新日 2024-10-09 実験手法 X-RAY DIFFRACTION (2.4 Å) 主引用文献 The Structure of the Central Stalk in Bovine F(1)-ATPase at 2.4 A Resolution. Nat.Struct.Biol., 7, 2000

<468469470471472473474475476477478479480481482483>