PDB: 66507 件ウェブページステータス検索Chemie searchBIRD

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3OVQ	Crystal Structure of hRPE and D-Ribulose-5-Phospate Complex 分子名称: 3,6,9,12,15,18,21,24,27-NONAOXANONACOSANE-1,29-DIOL, FE (II) ION, RIBULOSE-5-PHOSPHATE, ... 著者 Liang, W.G, Ouyang, S.Y, Shaw, N, Joachimiak, A, Zhang, R.G, Liu, Z.J. 登録日 2010-09-17 公開日 2011-03-09 最終更新日 2023-11-01 実験手法 X-RAY DIFFRACTION (1.999 Å) 主引用文献 Conversion of D-ribulose 5-phosphate to D-xylulose 5-phosphate: new insights from structural and biochemical studies on human RPE Faseb J., 25, 2011
3QQG	CDK2 in complex with inhibitor L2-5 分子名称: 1,2-ETHANEDIOL, 4-chloro-2-(4,6-diamino-1,3,5-triazin-2-yl)phenol, Cyclin-dependent kinase 2, ... 著者 Betzi, S, Alam, R, Han, H, Becker, A, Schonbrunn, E. 登録日 2011-02-15 公開日 2012-08-08 最終更新日 2023-09-13 実験手法 X-RAY DIFFRACTION (1.9 Å) 主引用文献 Structure-guided optimization of novel CDK2 inhibitors discovered by high-throughput screening To be Published
3R7I	CDK2 in complex with inhibitor KVR-1-74 分子名称: 1,2-ETHANEDIOL, 4-{[(2-carbamoyl-4-nitrophenyl)amino]methyl}benzoic acid, Cyclin-dependent kinase 2 著者 Betzi, S, Alam, R, Han, H, Becker, A, Schonbrunn, E. 登録日 2011-03-22 公開日 2012-08-08 最終更新日 2023-09-13 実験手法 X-RAY DIFFRACTION (1.85 Å) 主引用文献 Structure-guided optimization of novel CDK2 inhibitors discovered by high-throughput screening To be Published
3MH8	Crystal structure of LprG from Mycobacterium tuberculosis 分子名称: Lipoprotein lprG 著者 Tsai, H.-C, Sacchettini, J.C, TB Structural Genomics Consortium (TBSGC) 登録日 2010-04-07 公開日 2010-09-01 最終更新日 2024-02-21 実験手法 X-RAY DIFFRACTION (1.995 Å) 主引用文献 Mycobacterium tuberculosis lipoprotein LprG (Rv1411c) binds triacylated glycolipid agonists of Toll-like receptor 2. Nat.Struct.Mol.Biol., 17, 2010
3M8V	Crystal structure of the BTB domain from Kaiso/ZBTB33, form II 分子名称: Transcriptional regulator Kaiso 著者 Nielsen, T.K, Stogios, P.J, Prive, G.G. 登録日 2010-03-19 公開日 2011-03-02 最終更新日 2023-09-06 実験手法 X-RAY DIFFRACTION (2.7 Å) 主引用文献 Crystal structure of the BTB domain from Kaiso/ZBTB33, form II TO BE PUBLISHED
3MDC	DNA polymerase lambda in complex with dFdCTP 分子名称: 2'-deoxy-2',2'-difluorocytidine 5'-(tetrahydrogen triphosphate), DNA (5'-D(*CP*AP*GP*TP*AP*C)-3'), DNA (5'-D(*CP*GP*GP*CP*GP*GP*TP*AP*CP*TP*G)-3'), ... 著者 Garcia-Diaz, M, Murray, M, Kunkel, T, Chou, K.M. 登録日 2010-03-30 公開日 2010-04-28 最終更新日 2024-02-21 実験手法 X-RAY DIFFRACTION (1.999 Å) 主引用文献 Interaction between DNA Polymerase lambda and anticancer nucleoside analogs. J.Biol.Chem., 285, 2010
3RIR	Crystal Strucrture of Biotin Protein Ligase from S. aureus 分子名称: BIOTINYL-5-AMP, Biotin-[acetyl-CoA-carboxylase] ligase 著者 Wilce, M.C.J. 登録日 2011-04-14 公開日 2012-04-18 最終更新日 2023-11-01 実験手法 X-RAY DIFFRACTION (2.6 Å) 主引用文献 Crystal Strucrture of Biotin Protein Ligase from S. aureus To be published
3RPR	CDK2 in complex with inhibitor RC-2-49 分子名称: Cyclin-dependent kinase 2, [4-amino-2-(phenylamino)-1,3-thiazol-5-yl][3-(trifluoromethyl)phenyl]methanone 著者 Betzi, S, Alam, R, Han, H, Becker, A, Schonbrunn, E. 登録日 2011-04-27 公開日 2012-10-31 最終更新日 2023-09-13 実験手法 X-RAY DIFFRACTION (1.75 Å) 主引用文献 Development of highly potent and selective diaminothiazole inhibitors of cyclin-dependent kinases. J.Med.Chem., 56, 2013
3RPY	CDK2 in complex with inhibitor RC-2-40 分子名称: 4-amino-2-[(4-sulfamoylphenyl)amino]-1,3-thiazole-5-carboxamide, Cyclin-dependent kinase 2 著者 Betzi, S, Alam, R, Han, H, Becker, A, Schonbrunn, E. 登録日 2011-04-27 公開日 2012-10-31 最終更新日 2023-09-13 実験手法 X-RAY DIFFRACTION (1.9 Å) 主引用文献 Development of highly potent and selective diaminothiazole inhibitors of cyclin-dependent kinases. J.Med.Chem., 56, 2013
3RK5	CDK2 in complex with inhibitor RC-2-72 分子名称: 4-{[4-amino-5-(pyridin-3-ylcarbonyl)-1,3-thiazol-2-yl]amino}benzoic acid, Cyclin-dependent kinase 2 著者 Betzi, S, Alam, R, Han, H, Becker, A, Schonbrunn, E. 登録日 2011-04-17 公開日 2012-10-31 最終更新日 2023-09-13 実験手法 X-RAY DIFFRACTION (2 Å) 主引用文献 Development of highly potent and selective diaminothiazole inhibitors of cyclin-dependent kinases. J.Med.Chem., 56, 2013
3RAK	CDK2 in complex with inhibitor RC-2-32 分子名称: 4-[(4-amino-5-benzoyl-1,3-thiazol-2-yl)amino]benzenesulfonamide, Cyclin-dependent kinase 2 著者 Betzi, S, Alam, R, Han, H, Becker, A, Schonbrunn, E. 登録日 2011-03-28 公開日 2012-10-31 最終更新日 2023-09-13 実験手法 X-RAY DIFFRACTION (1.75 Å) 主引用文献 Development of highly potent and selective diaminothiazole inhibitors of cyclin-dependent kinases. J.Med.Chem., 56, 2013
3U9M	Structure of reduced human FBXL5 hemerythrin like domain 分子名称: F-box/LRR-repeat protein 5, FE (III) ION 著者 Li, P. 登録日 2011-10-19 公開日 2012-02-22 最終更新日 2024-02-28 実験手法 X-RAY DIFFRACTION (1.95 Å) 主引用文献 The Structural Basis of Iron Sensing by the Human F-box Protein FBXL5. Chembiochem, 13, 2012
3NZ3	Crystal structure of the mucin-binding domain of Spr1345 from Streptococcus pneumoniae 分子名称: Putative uncharacterized protein, SULFATE ION, TRIETHYLENE GLYCOL 著者 Du, Y, He, Y.-X, Zhang, Z.-Y, Yang, Y.-H, Shi, W.-W, Frolet, C, Guilmi, A.M, Vernet, T, Zhou, C.-Z, Chen, Y. 登録日 2010-07-15 公開日 2011-04-20 最終更新日 2024-03-20 実験手法 X-RAY DIFFRACTION (2 Å) 主引用文献 Crystal structure of the mucin-binding domain of Spr1345 from Streptococcus pneumoniae J.Struct.Biol., 174, 2011
3TIZ	CDK2 in complex with NSC 111848 分子名称: 1,2-ETHANEDIOL, 1-{(E)-[(4-hydroxyphenyl)imino]methyl}naphthalen-2-ol, Cyclin-dependent kinase 2 著者 Alam, R, Schonbrunn, E. 登録日 2011-08-22 公開日 2012-08-22 最終更新日 2023-09-13 実験手法 X-RAY DIFFRACTION (2.02 Å) 主引用文献 A Novel Approach to the Discovery of Small-Molecule Ligands of CDK2. Chembiochem, 13, 2012
3TVD	Crystal Structure of Mouse RhoA-GTP complex 分子名称: 5'-GUANOSINE-DIPHOSPHATE-MONOTHIOPHOSPHATE, MAGNESIUM ION, Transforming protein RhoA 著者 Swaminathan, K, Pal, K, Jobichen, C. 登録日 2011-09-20 公開日 2012-10-10 最終更新日 2023-11-01 実験手法 X-RAY DIFFRACTION (2.989 Å) 主引用文献 Crystal structure of mouse RhoA:GTPgammaS complex in a centered lattice. J.Struct.Funct.Genom., 13, 2012
3NOR	Crystal Structure of T102S Isocyanide Hydratase from Pseudomonas fluorescens 分子名称: CITRIC ACID, ThiJ/PfpI family protein 著者 Lakshminarasimhan, M, Madzelan, P, Nan, R, Milkovic, N.M, Wilson, M.A. 登録日 2010-06-25 公開日 2010-07-07 最終更新日 2023-09-06 実験手法 X-RAY DIFFRACTION (1.9 Å) 主引用文献 Evolution of New Enzymatic Function by Structural Modulation of Cysteine Reactivity in Pseudomonas fluorescens Isocyanide Hydratase. J.Biol.Chem., 285, 2010
3QA9	Crystal Structure of Prb (PH1109 protein redesigned for binding) 分子名称: CoA binding domain protein 著者 Spiegel, P.C. 登録日 2011-01-10 公開日 2011-04-20 最終更新日 2024-02-21 実験手法 X-RAY DIFFRACTION (1.9 Å) 主引用文献 A de novo protein binding pair by computational design and directed evolution. Mol.Cell, 42, 2011
3ONN	Crystal structure of 5'-nucleotidase SDT1 from saccharomyces cerevisiae 分子名称: ACETATE ION, GLYCEROL, IODIDE ION, ... 著者 Teng, M.K, Niu, L.W, Shi, N. 登録日 2010-08-30 公開日 2011-03-02 最終更新日 2024-03-20 実験手法 X-RAY DIFFRACTION (1.87 Å) 主引用文献 Crystal structure of the first pyrimidine 5'-nucleotidase SDT1 from saccharomyces cerevisiae To be Published
3OD7	Haemophilus influenzae ferric binding protein A -Iron Loaded 分子名称: FE (III) ION, Iron-utilization periplasmic protein, PHOSPHATE ION 著者 Khambati, H.K, Moraes, T.F, Singh, J, Shouldice, S.R, Yu, R.H, Schryvers, A.B. 登録日 2010-08-11 公開日 2010-09-15 最終更新日 2023-11-01 実験手法 X-RAY DIFFRACTION (1.801 Å) 主引用文献 The role of vicinal tyrosine residues in the function of Haemophilus influenzae ferric binding protein A. Biochem.J., 2010
3OG8	Crystal structure of human RIG-I CTD bound to a 14-bp blunt-ended dsRNA 分子名称: Antiviral innate immune response receptor RIG-I, RNA (5'-R(*GP*GP*CP*GP*CP*GP*CP*GP*CP*GP*CP*GP*CP*C)-3'), ZINC ION 著者 Li, P. 登録日 2010-08-16 公開日 2010-11-03 最終更新日 2024-02-21 実験手法 X-RAY DIFFRACTION (2.4 Å) 主引用文献 Crystal structure of RIG-I C-terminal domain bound to blunt-ended double-strand RNA without 5' triphosphate. Nucleic Acids Res., 39, 2011
3QXO	CDK2 in complex with inhibitor KVR-1-84 分子名称: 1,2-ETHANEDIOL, 5-nitro-2-[(4-sulfamoylbenzyl)amino]benzamide, Cyclin-dependent kinase 2 著者 Betzi, S, Alam, R, Han, H, Becker, A, Schonbrunn, E. 登録日 2011-03-02 公開日 2012-08-08 最終更新日 2023-09-13 実験手法 X-RAY DIFFRACTION (1.75 Å) 主引用文献 Structure-guided optimization of novel CDK2 inhibitors discovered by high-throughput screening To be Published
3QQ4	Crystal structure of swine major histocompatibility complex class I SLA-1 0401 and identification of 2009 pandemic swine-origin influenza A H1N1 virus cytotoxic T lymphocyte epitope peptides 分子名称: Beta-2-microglobulin, MHC class I antigen, VP35 著者 Zhang, N, Qi, J, Gao, F, Pan, X, Chen, R, Li, Q, Chen, Z, Li, X, Xia, C, Gao, G.F. 登録日 2011-02-15 公開日 2011-12-28 最終更新日 2023-11-01 実験手法 X-RAY DIFFRACTION (2.097 Å) 主引用文献 Crystal structure of swine major histocompatibility complex class I SLA-1 0401 and identification of 2009 pandemic swine-origin influenza A H1N1 virus cytotoxic T lymphocyte epitope peptides. J.Virol., 85, 2011
3QRU	CDK2 in complex with inhibitor NSK-MC1-12 分子名称: (5S)-N-methyl-5-(2-methylbutan-2-yl)-4,5,6,7-tetrahydro-2H-indazole-3-carboxamide, 1,2-ETHANEDIOL, Cyclin-dependent kinase 2 著者 Betzi, S, Alam, R, Han, H, Becker, A, Schonbrunn, E. 登録日 2011-02-18 公開日 2012-08-08 最終更新日 2023-09-13 実験手法 X-RAY DIFFRACTION (1.95 Å) 主引用文献 Structure-guided optimization of novel CDK2 inhibitors discovered by high-throughput screening To be Published
3QTU	CDK2 in complex with inhibitor RC-2-132 分子名称: 4-{[4-amino-5-(4-sulfamoylbenzoyl)-1,3-thiazol-2-yl]amino}benzenesulfonamide, Cyclin-dependent kinase 2 著者 Betzi, S, Alam, R, Han, H, Becker, A, Schonbrunn, E. 登録日 2011-02-23 公開日 2012-10-31 最終更新日 2023-09-13 実験手法 X-RAY DIFFRACTION (1.82 Å) 主引用文献 Development of highly potent and selective diaminothiazole inhibitors of cyclin-dependent kinases. J.Med.Chem., 56, 2013
3QTZ	CDK2 in complex with inhibitor RC-2-36 分子名称: 1,2-ETHANEDIOL, 4-{[4-amino-5-(3-fluorobenzoyl)-1,3-thiazol-2-yl]amino}benzenesulfonamide, Cyclin-dependent kinase 2 著者 Betzi, S, Alam, R, Han, H, Becker, A, Schonbrunn, E. 登録日 2011-02-23 公開日 2012-10-31 最終更新日 2023-09-13 実験手法 X-RAY DIFFRACTION (2 Å) 主引用文献 Development of highly potent and selective diaminothiazole inhibitors of cyclin-dependent kinases. J.Med.Chem., 56, 2013

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