PDB: 218820 件ウェブページステータス検索Chemie searchBIRD

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3VH8	KIR3DL1 in complex with HLA-B*5701 分子名称: 2-acetamido-2-deoxy-beta-D-glucopyranose, Beta-2-microglobulin, HLA class I histocompatibility antigen, ... 著者 Vivian, J.P, Rossjohn, J. 登録日 2011-08-24 公開日 2011-10-26 最終更新日 2023-11-08 実験手法 X-RAY DIFFRACTION (1.8 Å) 主引用文献 Killer cell immunoglobulin-like receptor 3DL1-mediated recognition of human leukocyte antigen B Nature, 479, 2011
2JUN	Structure of the MID1 tandem B-boxes reveals an interaction reminiscent of intermolecular RING heterodimers 分子名称: Midline-1, ZINC ION 著者 Tao, H, Singireddy, S, Jakkidi, M, Simmons, B.N, Short, K.M, Cox, T.C, Massiah, M.A. 登録日 2007-08-31 公開日 2008-03-04 最終更新日 2024-05-29 実験手法 SOLUTION NMR 主引用文献 Structure of the MID1 Tandem B-Boxes Reveals an Interaction Reminiscent of Intermolecular Ring Heterodimers Biochemistry, 47, 2008
4FN5	ELONGATION FACTOR G 1 (PSEUDOMONAS AERUGINOSA) IN COMPLEX WITH Argyrin B 分子名称: Argyrin B, Elongation factor G 1 著者 Kirby, C.A, Palestrant, D. 登録日 2012-06-19 公開日 2012-09-26 最終更新日 2024-07-10 実験手法 X-RAY DIFFRACTION (2.9 Å) 主引用文献 Identification of elongation factor g as the conserved cellular target of argyrin B. Plos One, 7, 2012
3BT6	Crystal Structure of Influenza B Virus Hemagglutinin 分子名称: 2-acetamido-2-deoxy-alpha-D-glucopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose, 2-acetamido-2-deoxy-beta-D-glucopyranose, 2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose, ... 著者 Wang, Q, Cheng, F, Lu, M, Tian, X, Ma, J. 登録日 2007-12-27 公開日 2008-05-27 最終更新日 2020-07-29 実験手法 X-RAY DIFFRACTION (2.8 Å) 主引用文献 Crystal structure of unliganded influenza B virus hemagglutinin. J.Virol., 82, 2008
3BVN	High resolution crystal structure of HLA-B*1402 in complex with the latent membrane protein 2 peptide (LMP2) of Epstein-Barr virus 分子名称: Beta-2-microglobulin, HLA class I histocompatibility antigen, B*1402 alpha chain, ... 著者 Kumar, P, Vahedi-Faridi, A, Saenger, W, Uchanska-Ziegler, B, Ziegler, A. 登録日 2008-01-07 公開日 2009-02-03 最終更新日 2023-08-30 実験手法 X-RAY DIFFRACTION (2.55 Å) 主引用文献 Structural basis for T cell alloreactivity among three HLA-B14 and HLA-B27 antigens J.Biol.Chem., 284, 2009
1D97	CHIRAL PHOSPHOROTHIOATE ANALOGUES OF B-DNA: THE CRYSTAL STRUCTURE OF RP-D(GP(S) CPGP(S)CPGP(S)C) 分子名称: DNA (5'-D(RP*GP*(SC)P*GP*(SC)P*GP*(SC))-3') 著者 Cruse, W.B.T, Salisbury, S.A, Brown, T, Cosstick, R, Eckstein, F, Kennard, O. 登録日 1992-10-17 公開日 1993-07-15 最終更新日 2024-02-07 実験手法 X-RAY DIFFRACTION (2.17 Å) 主引用文献 Chiral phosphorothioate analogues of B-DNA. The crystal structure of Rp-d[Gp(S)CpGp(S)CpGp(S)C]. J.Mol.Biol., 192, 1986
2C5C	Shiga-like toxin 1 B subunit complexed with a bivalent inhibitor 分子名称: DIETHYL PROPANE-1,3-DIYLBISCARBAMATE, SHIGA-LIKE TOXIN 1 B SUBUNIT, SULFATE ION, ... 著者 Dodd, R.B, Read, R.J. 登録日 2005-10-26 公開日 2006-11-27 最終更新日 2023-12-13 実験手法 X-RAY DIFFRACTION (2.94 Å) 主引用文献 Extensive Cross-Linking of the Shiga-Like Toxin 1 B Subunit by a Bivalent Ligand To be Published
4HY1	Pyrrolopyrimidine inhibitors of dna gyrase b and topoisomerase iv, part i: structure guided discovery and optimization of dual targeting agents with potent, broad-spectrum enzymatic activity. 分子名称: 6-({4-[(3R)-3-aminopyrrolidin-1-yl]-5-chloro-6-ethyl-7H-pyrrolo[2,3-d]pyrimidin-2-yl}sulfanyl)-1H-isoindol-1-one, Topoisomerase IV, subunit B 著者 Bensen, D.C, Creighton, C.J, Kwan, B, Tari, L.W. 登録日 2012-11-12 公開日 2013-02-13 最終更新日 2024-02-28 実験手法 X-RAY DIFFRACTION (1.9 Å) 主引用文献 Pyrrolopyrimidine inhibitors of DNA gyrase B (GyrB) and topoisomerase IV (ParE). Part I: Structure guided discovery and optimization of dual targeting agents with potent, broad-spectrum enzymatic activity. Bioorg.Med.Chem.Lett., 23, 2013
2DQ5	solution structure of the Mid1 B Box2 Chc(D/C)C2H2 Zinc-Binding Domain: insights into an evolutionary conserved ring fold 分子名称: Midline-1, ZINC ION 著者 Massiah, M.A, Matts, J.A.B, Short, K.M, Simmons, B.N, Singireddy, S, Zou, J, Cox, T.C. 登録日 2006-05-20 公開日 2007-04-03 最終更新日 2024-05-29 実験手法 SOLUTION NMR 主引用文献 Solution Structure of the MID1 B-box2 CHC(D/C)C(2)H(2) Zinc-binding Domain: Insights into an Evolutionarily Conserved RING Fold J.Mol.Biol., 369, 2007
4HXZ	Pyrrolopyrimidine inhibitors of dna gyrase b and topoisomerase iv, part i: structure guided discovery and optimization of dual targeting agents with potent, broad-spectrum enzymatic activity. 分子名称: 6-ethyl-4-methoxy-2-(pyridin-3-ylsulfanyl)-7H-pyrrolo[2,3-d]pyrimidine-5-carbaldehyde, Topoisomerase IV, subunit B 著者 Bensen, D.C, Creighton, C.J, Kwan, B, Tari, L.W. 登録日 2012-11-12 公開日 2013-02-13 最終更新日 2024-02-28 実験手法 X-RAY DIFFRACTION (2.7 Å) 主引用文献 Pyrrolopyrimidine inhibitors of DNA gyrase B (GyrB) and topoisomerase IV (ParE). Part I: Structure guided discovery and optimization of dual targeting agents with potent, broad-spectrum enzymatic activity. Bioorg.Med.Chem.Lett., 23, 2013
4IWD	Structure of dually phosphorylated c-MET receptor kinase in complex with an MK-8033 analog 分子名称: 1-{5-oxo-3-[1-(piperidin-4-yl)-1H-pyrazol-4-yl]-5H-benzo[4,5]cyclohepta[1,2-b]pyridin-7-yl}-N-(pyridin-2-ylmethyl)methanesulfonamide, Hepatocyte growth factor receptor 著者 Soisson, S.M, Northrup, A, Rickert, K, Patel, S, Allison, T. 登録日 2013-01-23 公開日 2013-12-11 最終更新日 2017-11-15 実験手法 X-RAY DIFFRACTION (1.99 Å) 主引用文献 Discovery of 1-[3-(1-methyl-1H-pyrazol-4-yl)-5-oxo-5H-benzo[4,5]cyclohepta[1,2-b]pyridin-7-yl]-N-(pyridin-2-ylmethyl)methanesulfonamide (MK-8033): A Specific c-Met/Ron dual kinase inhibitor with preferential affinity for the activated state of c-Met. J.Med.Chem., 56, 2013
4J6K	Crystal structure of calcium2+-free wild-type CD23 lectin domain (crystal form B) 分子名称: Low affinity immunoglobulin epsilon Fc receptor, SULFATE ION 著者 Dhaliwal, B, Pang, M.O.Y, Sutton, B.J. 登録日 2013-02-11 公開日 2013-08-28 実験手法 X-RAY DIFFRACTION (2.3 Å) 主引用文献 Conformational plasticity at the IgE-binding site of the B-cell receptor CD23. Mol.Immunol., 56, 2013
1XH7	Crystal Structures of Protein Kinase B Selective Inhibitors in Complex with Protein Kinase A and Mutants 分子名称: N-[4-({4-[5-(3,3-DIMETHYLPIPERIDIN-1-YL)-2-HYDROXYBENZOYL]BENZOYL}AMINO)AZEPAN-3-YL]ISONICOTINAMIDE, cAMP-dependent protein kinase inhibitor, alpha form, ... 著者 Breitenlechner, C.B, Friebe, W.-G, Brunet, E, Werner, G, Graul, K, Thomas, U, Kuenkele, K.-P, Schaefer, W, Gassel, M, Bossemeyer, D, Huber, R, Engh, R.A, Masjost, B. 登録日 2004-09-17 公開日 2005-09-17 最終更新日 2024-06-26 実験手法 X-RAY DIFFRACTION (2.47 Å) 主引用文献 Design and crystal structures of protein kinase B-selective inhibitors in complex with protein kinase A and mutants J.Med.Chem., 48, 2005
3DZL	Crystal structure of PhzA/B from Burkholderia cepacia R18194 in complex with (R)-3-oxocyclohexanecarboxylic acid 分子名称: (1R)-3-oxocyclohexanecarboxylic acid, Phenazine biosynthesis protein A/B 著者 Ahuja, E.G, Mentel, M, Graebsch, A, Breinbauer, R, Blankenfeldt, W. 登録日 2008-07-30 公開日 2008-12-30 最終更新日 2024-03-20 実験手法 X-RAY DIFFRACTION (1.75 Å) 主引用文献 PhzA/B Catalyzes the Formation of the Tricycle in Phenazine Biosynthesis. J.Am.Chem.Soc., 130, 2008
3CNM	Crystal Structure of Phenazine Biosynthesis Protein PhzA/B from Burkholderia cepacia R18194, DHHA complex 分子名称: (2S,3S)-TRANS-2,3-DIHYDRO-3-HYDROXYANTHRANILIC ACID, ACETATE ION, Phenazine biosynthesis protein A/B 著者 Ahuja, E.G, Blankenfeldt, W. 登録日 2008-03-26 公開日 2008-12-30 最終更新日 2023-08-30 実験手法 X-RAY DIFFRACTION (1.65 Å) 主引用文献 PhzA/B catalyzes the formation of the tricycle in phenazine biosynthesis. J.Am.Chem.Soc., 130, 2008
3EXV	Crystal structure of the human Adenovirus type 11 fiber knob 分子名称: Fiber protein 著者 Persson, B.D, Reiter, D.M, Arnberg, N, Stehle, T. 登録日 2008-10-17 公開日 2008-11-25 最終更新日 2024-04-03 実験手法 X-RAY DIFFRACTION (1.45 Å) 主引用文献 An arginine switch in the species B adenovirus knob determines high-affinity engagement of cellular receptor CD46 J.Virol., 83, 2009
3SDL	Crystal structure of human ISG15 in complex with NS1 N-terminal region from influenza B virus, Northeast Structural Genomics Consortium Target IDs HX6481, HR2873, and OR2 分子名称: Non-structural protein 1, Ubiquitin-like protein ISG15 著者 Guan, R, Ma, L.-C, Krug, R.M, Montelione, G.T, Northeast Structural Genomics Consortium (NESG) 登録日 2011-06-09 公開日 2011-07-20 最終更新日 2023-11-29 実験手法 X-RAY DIFFRACTION (2.29 Å) 主引用文献 Structural basis for the sequence-specific recognition of human ISG15 by the NS1 protein of influenza B virus. Proc.Natl.Acad.Sci.USA, 108, 2011
3D18	Crystal structure of HLA-B*2709 complexed with a variant of the latent membrane protein 2 peptide (LMP2(L)) of epstein-barr virus 分子名称: 2-(N-MORPHOLINO)-ETHANESULFONIC ACID, 2-AMINO-2-HYDROXYMETHYL-PROPANE-1,3-DIOL, Beta-2-microglobulin, ... 著者 Beltrami, A, Gabdulkhakov, A, Rossmann, M, Ziegler, A, Uchanska-Ziegler, B, Saenger, W. 登録日 2008-05-05 公開日 2009-05-05 最終更新日 2023-08-30 実験手法 X-RAY DIFFRACTION (1.74 Å) 主引用文献 Crystal structure of HLA-B*2709 complexed with a variant of the latent membrane protein 2 peptide (LMP2(L)) of epstein-barr virus To be Published
1JO2	Crystal Structure of the B-DNA Hexamer (CgATCG).Daunomycin Complex Containing a Ribose at the Intercalation Site 分子名称: 5'-D(*C)-R(P*G)-D(P*AP*TP*CP*G)-3', DAUNOMYCIN 著者 Shi, K, Pan, B, Sundaralingam, M. 登録日 2001-07-26 公開日 2003-07-29 最終更新日 2024-02-07 実験手法 X-RAY DIFFRACTION (1.5 Å) 主引用文献 Structure of a B-form DNA/RNA chimera (dC)(rG)d(ATCG) complexed with daunomycin at 1.5 A resolution. Acta Crystallogr.,Sect.D, 59, 2003
1K06	Crystallographic Binding Study of 100 mM N-benzoyl-N'-beta-D-glucopyranosyl urea to glycogen phosphorylase b 分子名称: Glycogen Phosphorylase, N-[(phenylcarbonyl)carbamoyl]-beta-D-glucopyranosylamine, PYRIDOXAL-5'-PHOSPHATE 著者 Oikonomakos, N.G, Kosmopoulou, M, Zographos, S.E, Leonidas, D.D, Chrysina, E.D, Somsak, L, Nagy, V, Praly, J.P, Docsa, T, Toth, B, Gergely, P. 登録日 2001-09-18 公開日 2001-10-03 最終更新日 2023-08-16 実験手法 X-RAY DIFFRACTION (1.8 Å) 主引用文献 Binding of N-acetyl-N '-beta-D-glucopyranosyl urea and N-benzoyl-N '-beta-D-glucopyranosyl urea to glycogen phosphorylase b: kinetic and crystallographic studies. Eur.J.Biochem., 269, 2002
1XHA	Crystal Structures of Protein Kinase B Selective Inhibitors in Complex with Protein Kinase A and Mutants 分子名称: N-{4-[(4-{3-[(2R)-3,3-DIMETHYLPIPERIDIN-2-YL]-2-FLUORO-6-HYDROXYBENZOYL}BENZOYL)AMINO]AZEPAN-3-YL}ISONICOTINAMIDE, cAMP-dependent protein kinase inhibitor, alpha form, ... 著者 Breitenlechner, C.B, Friebe, W.-G, Brunet, E, Werner, G, Graul, K, Thomas, U, Kuenkele, K.-P, Schaefer, W, Gassel, M, Bossemeyer, D, Huber, R, Engh, R.A, Masjost, B. 登録日 2004-09-17 公開日 2005-09-17 最終更新日 2024-06-26 実験手法 X-RAY DIFFRACTION (2.46 Å) 主引用文献 Design and crystal structures of protein kinase B-selective inhibitors in complex with protein kinase A and mutants J.Med.Chem., 48, 2005
1XH8	Crystal Structures of Protein Kinase B Selective Inhibitors in Complex with Protein Kinase A and Mutants 分子名称: N-[4-({4-[5-(4,4-DIMETHYLPIPERIDIN-1-YL)-2-HYDROXYBENZOYL]BENZOYL}AMINO)AZEPAN-3-YL]ISONICOTINAMIDE, cAMP-dependent protein kinase inhibitor, alpha form, ... 著者 Breitenlechner, C.B, Friebe, W.-G, Brunet, E, Werner, G, Graul, K, Thomas, U, Kuenkele, K.-P, Schaefer, W, Gassel, M, Bossemeyer, D, Huber, R, Engh, R.A, Masjost, B. 登録日 2004-09-17 公開日 2005-09-17 最終更新日 2024-06-26 実験手法 X-RAY DIFFRACTION (1.6 Å) 主引用文献 Design and crystal structures of protein kinase B-selective inhibitors in complex with protein kinase A and mutants J.Med.Chem., 48, 2005
1XH6	Crystal Structures of Protein Kinase B Selective Inhibitors in Complex with Protein Kinase A and Mutants 分子名称: N-(4-{[4-(2-HYDROXY-5-PIPERIDIN-1-YLBENZOYL)BENZOYL]AMINO}AZEPAN-3-YL)ISONICOTINAMIDE, cAMP-dependent protein kinase inhibitor, alpha form, ... 著者 Breitenlechner, C.B, Friebe, W.-G, Brunet, E, Werner, G, Graul, K, Thomas, U, Kuenkele, K.-P, Schaefer, W, Gassel, M, Bossemeyer, D, Huber, R, Engh, R.A, Masjost, B. 登録日 2004-09-17 公開日 2005-09-17 最終更新日 2024-06-26 実験手法 X-RAY DIFFRACTION (1.9 Å) 主引用文献 Design and crystal structures of protein kinase B-selective inhibitors in complex with protein kinase A and mutants J.Med.Chem., 48, 2005
1XH9	Crystal Structures of Protein Kinase B Selective Inhibitors in Complex with Protein Kinase A and Mutants 分子名称: (R,R)-2,3-BUTANEDIOL, N-[4-({4-[5-(DIMETHYLAMINO)-2-HYDROXYBENZOYL]BENZOYL}AMINO)AZEPAN-3-YL]ISONICOTINAMIDE, cAMP-dependent protein kinase inhibitor, ... 著者 Breitenlechner, C.B, Friebe, W.-G, Brunet, E, Werner, G, Graul, K, Thomas, U, Kuenkele, K.-P, Schaefer, W, Gassel, M, Bossemeyer, D, Huber, R, Engh, R.A, Masjost, B. 登録日 2004-09-17 公開日 2005-09-17 最終更新日 2024-06-26 実験手法 X-RAY DIFFRACTION (1.64 Å) 主引用文献 Design and crystal structures of protein kinase B-selective inhibitors in complex with protein kinase A and mutants J.Med.Chem., 48, 2005
1XH5	Crystal Structures of Protein Kinase B Selective Inhibitors in Complex with Protein Kinase A and Mutants 分子名称: (R,R)-2,3-BUTANEDIOL, N-{4-[(4-{3-[(2R)-3,3-DIMETHYLPIPERIDIN-2-YL]-2-FLUORO-6-HYDROXYBENZOYL}BENZOYL)AMINO]AZEPAN-3-YL}ISONICOTINAMIDE, cAMP-dependent protein kinase inhibitor, ... 著者 Breitenlechner, C.B, Friebe, W.-G, Brunet, E, Werner, G, Graul, K, Thomas, U, Kuenkele, K.-P, Schaefer, W, Gassel, M, Bossemeyer, D, Huber, R, Engh, R.A, Masjost, B. 登録日 2004-09-17 公開日 2005-09-17 最終更新日 2024-06-26 実験手法 X-RAY DIFFRACTION (2.05 Å) 主引用文献 Design and crystal structures of protein kinase B-selective inhibitors in complex with protein kinase A and mutants J.Med.Chem., 48, 2005

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