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

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3MGH	Binary complex of a DNA polymerase lambda loop mutant 分子名称: DNA (5'-D(*CP*AP*GP*TP*AP*C)-3'), DNA (5'-D(*CP*GP*GP*CP*AP*GP*TP*AP*CP*TP*G)-3'), DNA (5'-D(P*GP*CP*CP*G)-3'), ... 著者 Garcia-Diaz, M, Bebenek, K, Zhou, R.Z, Povirk, L.F, Kunkel, T. 登録日 2010-04-06 公開日 2010-05-19 最終更新日 2017-11-08 実験手法 X-RAY DIFFRACTION (2.4 Å) 主引用文献 Loop 1 modulates the fidelity of DNA polymerase lambda Nucleic Acids Res., 38, 2010
6MES	Trypanosoma brucei methionyl-tRNA synthetase in complex with inhibitor (Chem 1907) 分子名称: 1-[(1H-benzimidazol-2-yl)methyl]-4-[(2,4-dichlorophenyl)methyl]-1,3-dihydro-2H-imidazol-2-one, GLYCEROL, METHIONINE, ... 著者 Barros-Alvarez, X, Hol, W.G.J. 登録日 2018-09-07 公開日 2019-09-18 最終更新日 2024-03-13 実験手法 X-RAY DIFFRACTION (2.9 Å) 主引用文献 Structure-guided discovery of selective methionyl-tRNA synthetase inhibitors with potent activity against Trypanosoma brucei Rsc Med Chem, 2020
3QZF	CDK2 in complex with inhibitor JWS-6-52 分子名称: 2-(4,6-diamino-1,3,5-triazin-2-yl)benzene-1,4-diol, Cyclin-dependent kinase 2 著者 Betzi, S, Alam, R, Han, H, Becker, A, Schonbrunn, E. 登録日 2011-03-06 公開日 2012-08-08 最終更新日 2023-09-13 実験手法 X-RAY DIFFRACTION (2 Å) 主引用文献 Structure-guided optimization of novel CDK2 inhibitors discovered by high-throughput screening To be Published
6LXX	Frog EPDR1 with an Ir atom 分子名称: CALCIUM ION, CHLORIDE ION, Ependymin-related 1, ... 著者 Park, S, Park, J. 登録日 2020-02-12 公開日 2021-02-17 最終更新日 2023-11-29 実験手法 X-RAY DIFFRACTION (2.4 Å) 主引用文献 A Single Soaked Iridium (IV) Ion Observed in the Frog Ependymin-Related Protein. Bull.Korean Chem.Soc., 41, 2020
6LYM	Crystal structure of D657A mutant of formylglycinamidine synthetase 分子名称: 1,2-ETHANEDIOL, ADENOSINE-5'-DIPHOSPHATE, GLYCEROL, ... 著者 Sharma, N, Tanwar, A.S, Anand, R. 登録日 2020-02-14 公開日 2021-02-17 最終更新日 2023-11-29 実験手法 X-RAY DIFFRACTION (2.46 Å) 主引用文献 Mechanism of Coordinated Gating and Signal Transduction in Purine Biosynthetic Enzyme Formylglycinamidine Synthetase. Acs Catalysis, 12, 2022
6LYO	Crystal Structure of H296A mutant of Formylglycinamidine Synthetase 分子名称: 1,2-ETHANEDIOL, ADENOSINE-5'-DIPHOSPHATE, GLYCEROL, ... 著者 Sharma, N, Tanwar, A.S, Anand, R. 登録日 2020-02-15 公開日 2021-02-17 最終更新日 2023-11-29 実験手法 X-RAY DIFFRACTION (1.87 Å) 主引用文献 Mechanism of Coordinated Gating and Signal Transduction in Purine Biosynthetic Enzyme Formylglycinamidine Synthetase. Acs Catalysis, 12, 2022
3RJ0	Plant steroid receptor BRI1 ectodomain in complex with brassinolide 分子名称: 2-acetamido-2-deoxy-beta-D-glucopyranose, Brassinolide, Protein BRASSINOSTEROID INSENSITIVE 1, ... 著者 Hothorn, M. 登録日 2011-04-14 公開日 2011-06-22 最終更新日 2020-07-29 実験手法 X-RAY DIFFRACTION (2.541 Å) 主引用文献 Structural basis of steroid hormone perception by the receptor kinase BRI1. Nature, 474, 2011
6LYL	Crystal structure of S1052D mutant of Formylglycinamidine synthetase 分子名称: 1,2-ETHANEDIOL, ADENOSINE-5'-DIPHOSPHATE, GLYCEROL, ... 著者 Sharma, N, Tanwar, A.S, Anand, R. 登録日 2020-02-14 公開日 2021-02-17 最終更新日 2023-11-29 実験手法 X-RAY DIFFRACTION (2.1 Å) 主引用文献 Mechanism of Coordinated Gating and Signal Transduction in Purine Biosynthetic Enzyme Formylglycinamidine Synthetase. Acs Catalysis, 12, 2022
3R6X	CDK2 in complex with inhibitor KVR-1-158 分子名称: 1,2-ETHANEDIOL, 4-[(3-hydroxypropyl)amino]-5-nitro-2-[(pyridin-3-ylmethyl)amino]benzamide, 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 (1.75 Å) 主引用文献 Structure-guided optimization of novel CDK2 inhibitors discovered by high-throughput screening To be Published
3R7U	CDK2 in complex with inhibitor KVR-1-75 分子名称: 1,2-ETHANEDIOL, 2-{[4-(aminomethyl)benzyl]amino}-5-nitrobenzamide, Cyclin-dependent kinase 2 著者 Betzi, S, Alam, R, Han, H, Becker, A, Schonbrunn, E. 登録日 2011-03-23 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
3R9H	CDK2 in complex with inhibitor RC-2-142 分子名称: 4-amino-N-(2,6-difluorophenyl)-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 2011-03-25 公開日 2012-10-31 最終更新日 2023-09-13 実験手法 X-RAY DIFFRACTION (2.1 Å) 主引用文献 Development of highly potent and selective diaminothiazole inhibitors of cyclin-dependent kinases. J.Med.Chem., 56, 2013
6LZB	crystal structure of Human Methionine aminopeptidase (HsMetAP1b) in complex with AN-P2-5H-06 分子名称: 1-[(3-methoxyphenyl)methyl]-~{N}-oxidanyl-pyrrolo[2,3-b]pyridine-5-carboxamide, COBALT (II) ION, GLYCEROL, ... 著者 sandeep, C.B, Addlagatta, A. 登録日 2020-02-18 公開日 2021-02-24 最終更新日 2023-11-29 実験手法 X-RAY DIFFRACTION (1.29 Å) 主引用文献 Selective inhibition of Helicobacter pylori methionine aminopeptidase by azaindole hydroxamic acid derivatives: Design, synthesis, in vitro biochemical and structural studies. Bioorg.Chem., 115, 2021
6M0U	Structure of AhSYMRK kinase domain mutant - K625E 分子名称: CACODYLATE ION, CALCIUM ION, Symbiosis receptor kinase SymRK, ... 著者 Datta, A.B, Naskar, P. 登録日 2020-02-22 公開日 2021-02-24 最終更新日 2023-11-29 実験手法 X-RAY DIFFRACTION (2.29 Å) 主引用文献 Structure of AhSYMRK kinase domain mutant - K625E To Be Published
3MQS	Crystal Structure of the USP7:Hdm2(PSTS) complex 分子名称: Hdm2 peptide, Ubiquitin carboxyl-terminal hydrolase 7 著者 Saridakis, V. 登録日 2010-04-28 公開日 2010-08-25 最終更新日 2023-09-06 実験手法 X-RAY DIFFRACTION (2.4 Å) 主引用文献 Crystal Structure of USP7 To be Published
6M2Z	Crystal structure of a formolase, BFD variant M3 from Pseudomonas putida 分子名称: Benzoylformate decarboxylase, MAGNESIUM ION, THIAMINE DIPHOSPHATE 著者 Wei, H.L, Liu, W.D, Li, T.Z, Zhu, L.L. 登録日 2020-03-02 公開日 2021-03-03 最終更新日 2023-11-29 実験手法 X-RAY DIFFRACTION (2.35 Å) 主引用文献 Totally atom-economical synthesis of lactic acid from formaldehyde: combined bio-carboligation and chemo-rearrangement without the isolation of intermediate. Green Chem, 22, 2020
6M2Y	Crystal structure of a formolase, BFD variant M6 from Pseudomonas putida 分子名称: Benzoylformate decarboxylase, MAGNESIUM ION, THIAMINE DIPHOSPHATE 著者 Wei, H.L, Liu, W.D, Li, T.Z, Zhu, L.L. 登録日 2020-03-02 公開日 2021-03-03 最終更新日 2023-11-29 実験手法 X-RAY DIFFRACTION (2.1 Å) 主引用文献 Totally atom-economical synthesis of lactic acid from formaldehyde: combined bio-carboligation and chemo-rearrangement without the isolation of intermediate. Green Chem, 22, 2020
6M4I	Structure of CENP-E motor domain at 1.9 angstrom resolution 分子名称: ADENOSINE-5'-DIPHOSPHATE, Centromere-associated protein E, MAGNESIUM ION 著者 Shibuya, A, Yokoyama, H. 登録日 2020-03-07 公開日 2021-03-10 最終更新日 2023-11-29 実験手法 X-RAY DIFFRACTION (1.9 Å) 主引用文献 Structure and comparison of the motor domain ofcentromere-associated protein E Acta Crystallogr.,Sect.D, 77, 2021
3RPO	CDK2 in complex with inhibitor KVR-1-156 分子名称: 1,2-ETHANEDIOL, 4-({4-carbamoyl-2-nitro-5-[(pyridin-3-ylmethyl)amino]phenyl}amino)butanoic acid, 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 2012-08-08 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
3MGM	Crystal structure of human NUDT16 分子名称: U8 snoRNA-decapping enzyme 著者 Yan, J, Lu, G, Zhang, J, Qi, J, Li, Z, Gao, F. 登録日 2010-04-07 公開日 2011-04-20 最終更新日 2023-11-01 実験手法 X-RAY DIFFRACTION (1.801 Å) 主引用文献 Crystal structure and the template mRNA decapping activity of human NUDT16 To be Published
3RPV	CDK2 in complex with inhibitor RC-2-88 分子名称: 1,2-ETHANEDIOL, 4-{[4-amino-5-(3-aminobenzoyl)-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 2011-04-27 公開日 2012-10-31 最終更新日 2023-09-13 実験手法 X-RAY DIFFRACTION (1.8 Å) 主引用文献 Development of highly potent and selective diaminothiazole inhibitors of cyclin-dependent kinases. J.Med.Chem., 56, 2013
3LB9	Crystal structure of the B. circulans cpA123 circular permutant 分子名称: Endo-1,4-beta-xylanase 著者 D'Angelo, I, Reitinger, S, Ludwiczek, M, Strynadka, N, Withers, S.G, Mcintosh, L.P. 登録日 2010-01-08 公開日 2010-03-23 最終更新日 2023-09-06 実験手法 X-RAY DIFFRACTION (3 Å) 主引用文献 Circular permutation of Bacillus circulans xylanase: a kinetic and structural study. Biochemistry, 49, 2010
3RQ7	Polo-like kinase 1 Polo box domain in complex with a C6H5(CH2)8-derivatized peptide inhibitor 分子名称: C6H5(CH2)8-derivatized peptide inhibitor, Serine/threonine-protein kinase PLK1 著者 Liu, F, Park, J.-E, Qian, W.-J, Lim, D.C, Graber, M, Berg, T, Yaffe, M.B, Lee, K.S, Burke Jr, T.R. 登録日 2011-04-27 公開日 2011-07-20 最終更新日 2012-12-12 実験手法 X-RAY DIFFRACTION (1.55 Å) 主引用文献 Serendipitous alkylation of a Plk1 ligand uncovers a new binding channel. Nat.Chem.Biol., 7, 2011
6M5Y	Structure of human galectin-1 tandem-repeat mutant with lactose 分子名称: Galectin-1,Galectin-1, beta-D-galactopyranose-(1-4)-alpha-D-glucopyranose, beta-D-galactopyranose-(1-4)-beta-D-glucopyranose 著者 Nonaka, Y, Kamitori, S, Nakamura, T. 登録日 2020-03-12 公開日 2021-03-17 最終更新日 2023-11-29 実験手法 X-RAY DIFFRACTION (1.38 Å) 主引用文献 Crystal structure and conformational stability of a galectin-1 tandem-repeat mutant with a short linker. Glycobiology, 2021
3R7V	CDK2 in complex with inhibitor KVR-1-9 分子名称: 1,2-ETHANEDIOL, 5-nitro-2-[(pyridin-2-ylmethyl)amino]benzamide, Cyclin-dependent kinase 2 著者 Betzi, S, Alam, R, Han, H, Becker, A, Schonbrunn, E. 登録日 2011-03-23 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
6M73	Crystal structure of Enterococcus hirae L-lactate oxidase in complex with D-lactate form ligand 分子名称: 1,2-ETHANEDIOL, 1-DEOXY-1-(7,8-DIMETHYL-2,4-DIOXO-3,4-DIHYDRO-2H-BENZO[G]PTERIDIN-1-ID-10(5H)-YL)-5-O-PHOSPHONATO-D-RIBITOL, 2-AMINO-2-HYDROXYMETHYL-PROPANE-1,3-DIOL, ... 著者 Yoshida, H, Hiraka, K, Tsugawa, W, Sode, K. 登録日 2020-03-16 公開日 2021-03-17 最終更新日 2023-11-29 実験手法 X-RAY DIFFRACTION (1.7 Å) 主引用文献 Structure of lactate oxidase from Enterococcus hirae revealed new aspects of active site loop function: Product-inhibition mechanism and oxygen gatekeeper Protein Sci., 31, 2022

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