PDB: 45176 件ウェブページステータス検索Chemie searchBIRD

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6BTV	Solution NMR structures for CcoTx-II 分子名称: Beta-theraphotoxin-Cm1b 著者 Agwa, A.J, Schroeder, C.I. 登録日 2017-12-07 公開日 2018-05-09 最終更新日 2023-06-14 実験手法 SOLUTION NMR 主引用文献 Gating modifier toxins isolated from spider venom: Modulation of voltage-gated sodium channels and the role of lipid membranes. J. Biol. Chem., 293, 2018
3P4L	Crystal structure of a hemojuvelin-binding fragment of neogenin 分子名称: Neogenin 著者 Yang, F, West Jr, A.P, Bjorkman, P.J. 登録日 2010-10-06 公開日 2010-11-17 最終更新日 2023-09-06 実験手法 X-RAY DIFFRACTION (1.8 Å) 主引用文献 Crystal structure of a hemojuvelin-binding fragment of neogenin at 1.8A. J.Struct.Biol., 174, 2011
6BR0	Solution NMR structure for CcoTx-I 分子名称: Beta-theraphotoxin-Cm1a 著者 Agwa, A.J, Schroeder, C.I. 登録日 2017-11-29 公開日 2018-05-16 最終更新日 2023-06-14 実験手法 SOLUTION NMR 主引用文献 Gating modifier toxins isolated from spider venom: Modulation of voltage-gated sodium channels and the role of lipid membranes. J. Biol. Chem., 293, 2018
3P1Y	Crystal structure of the chimeric Archaeoglobus fulgidus RNA splicing endonuclease with the broadest substrate specificity 分子名称: tRNA-splicing endonuclease 著者 Hirata, A. 登録日 2010-10-01 公開日 2011-08-10 最終更新日 2024-03-20 実験手法 X-RAY DIFFRACTION (2.05 Å) 主引用文献 Cleavage of intron from the standard or non-standard position of the precursor tRNA by the splicing endonuclease of Aeropyrum pernix, a hyper-thermophilic Crenarchaeon, involves a novel RNA recognition site in the Crenarchaea specific loop Nucleic Acids Res., 39, 2011
3P44	Human carbonic anhydrase II in complex with p-(4-ruthenocenyl-1H-1,2,3-triazol-1-yl)benzenesulfonamide 分子名称: Carbonic anhydrase 2, GLYCEROL, ZINC ION, ... 著者 Salmon, A.J. 登録日 2010-10-06 公開日 2011-10-12 最終更新日 2023-11-01 実験手法 X-RAY DIFFRACTION (2.2 Å) 主引用文献 Protein crystal structures with ferrocene and ruthenocene-based enzyme inhibitors. Chem.Commun.(Camb.), 48, 2012
3WU0	Crystal structure of phosphorylated ETS-1 DNA binding and autoinhibitory domains (276-441) 分子名称: Protein C-ets-1 著者 Shiina, M, Hamada, K, Ogata, K. 登録日 2014-04-21 公開日 2014-08-20 最終更新日 2023-11-08 実験手法 X-RAY DIFFRACTION (2.6 Å) 主引用文献 A novel allosteric mechanism on protein-DNA interactions underlying the phosphorylation-dependent regulation of Ets1 target gene expressions. J.Mol.Biol., 427, 2015
3WCT	The structure of a deoxygenated 400 kda hemoglobin provides a more accurate description of the cooperative mechanism of giant hemoglobins: Oxygenated form 分子名称: A1 globin chain of giant V2 hemoglobin, A2 globin chain of giant V2 hemoglobin, B1 globin chain of giant V2 hemoglobin, ... 著者 Numoto, N, Nakagawa, T, Ohara, R, Hasegawa, T, Kita, A, Yoshida, T, Maruyama, T, Imai, K, Fukumori, Y, Miki, K. 登録日 2013-06-01 公開日 2014-06-04 最終更新日 2023-11-08 実験手法 X-RAY DIFFRACTION (2.4 Å) 主引用文献 The structure of a deoxygenated 400 kDa haemoglobin reveals ternary- and quaternary-structural changes of giant haemoglobins Acta Crystallogr.,Sect.D, 70, 2014
3OS5	SET7/9-Dnmt1 K142me1 complex 分子名称: 1,2-ETHANEDIOL, BETA-MERCAPTOETHANOL, Dnmt1, ... 著者 Esteve, P.-O, Chang, Y, Samaranayake, M, Upadhyay, A.K, Horton, J.R, Feehery, G.R, Cheng, X, Pradhan, S. 登録日 2010-09-08 公開日 2010-12-15 最終更新日 2023-09-06 実験手法 X-RAY DIFFRACTION (1.69 Å) 主引用文献 A methylation and phosphorylation switch between an adjacent lysine and serine determines human DNMT1 stability. Nat.Struct.Mol.Biol., 18, 2011
3X44	Crystal structure of O-ureido-L-serine-bound K43A mutant of O-ureido-L-serine synthase 分子名称: (E)-O-(carbamoylamino)-N-({3-hydroxy-2-methyl-5-[(phosphonooxy)methyl]pyridin-4-yl}methylidene)-L-serine, O-ureido-L-serine synthase 著者 Matoba, Y, Uda, N, Oda, K, Sugiyama, M. 登録日 2015-03-13 公開日 2015-07-29 最終更新日 2024-05-29 実験手法 X-RAY DIFFRACTION (1.9 Å) 主引用文献 The structural and mutational analyses of O-ureido-L-serine synthase necessary for D-cycloserine biosynthesis. Febs J., 282, 2015
3M4W	Structural basis for the negative regulation of bacterial stress response by RseB 分子名称: Sigma-E factor negative regulatory protein, Sigma-E factor regulatory protein rseB, ZINC ION 著者 Kim, D.Y, Kwon, E, Choi, J.K, Hwang, H.-Y, Kim, K.K. 登録日 2010-03-12 公開日 2010-05-05 最終更新日 2023-11-01 実験手法 X-RAY DIFFRACTION (2.3 Å) 主引用文献 Structural basis for the negative regulation of bacterial stress response by RseB Protein Sci., 19, 2010
3SPB	Unliganded E. Cloacae MurA 分子名称: UDP-N-acetylglucosamine 1-carboxyvinyltransferase 著者 Zhu, J.-Y, Yang, Y, Schonbrunn, E. 登録日 2011-07-01 公開日 2012-03-07 最終更新日 2023-09-13 実験手法 X-RAY DIFFRACTION (2.3 Å) 主引用文献 Functional Consequence of Covalent Reaction of Phosphoenolpyruvate with UDP-N-acetylglucosamine 1-Carboxyvinyltransferase (MurA). J.Biol.Chem., 287, 2012
3YAS	HYDROXYNITRILE LYASE COMPLEXED WITH ACETONE 分子名称: ACETONE, PROTEIN (HYDROXYNITRILE LYASE), SULFATE ION 著者 Zuegg, J, Wagner, U.G, Gugganig, M, Kratky, C. 登録日 1999-03-15 公開日 1999-10-13 最終更新日 2023-09-13 実験手法 X-RAY DIFFRACTION (1.85 Å) 主引用文献 Three-dimensional structures of enzyme-substrate complexes of the hydroxynitrile lyase from Hevea brasiliensis. Protein Sci., 8, 1999
3ZFF	Human enterovirus 71 in complex with capsid binding inhibitor WIN51711 分子名称: 5-(7-(4-(4,5-DIHYDRO-2-OXAZOLYL)PHENOXY)HEPTYL)-3-METHYL ISOXAZOLE, VP1, VP2, ... 著者 Plevka, P, Perera, R, Yap, M.L, Cardosa, J, Kuhn, R.J, Rossmann, M.G. 登録日 2012-12-11 公開日 2013-03-27 最終更新日 2023-12-20 実験手法 X-RAY DIFFRACTION (3.4 Å) 主引用文献 Structure of Human Enterovirus 71 in Complex with a Capsid-Binding Inhibitor. Proc.Natl.Acad.Sci.USA, 110, 2013
3DP6	Crystal structure of the binding domain of the AMPA subunit GluR2 bound to glutamate 分子名称: GLUTAMIC ACID, Glutamate receptor 2, ZINC ION 著者 Ahmed, A.H, Wang, Q, Sondermann, H, Oswald, R.E. 登録日 2008-07-07 公開日 2008-11-25 最終更新日 2023-08-30 実験手法 X-RAY DIFFRACTION (1.55 Å) 主引用文献 Structure of the S1S2 glutamate binding domain of GLuR3. Proteins, 75, 2008
3DRT	Crystal structure of the HIV-1 broadly neutralizing antibody 2F5 in complex with the gp41 scrambledFP-MPER scrHyb3K construct GIGAFGLLGFLAAGSKK-Ahx-K656NEQELLELDKWASLWN671 分子名称: 2F5 Fab' heavy chain, 2F5 Fab' light chain, GLYCEROL, ... 著者 Julien, J.-P, Bryson, S, de la Torre, B.G, Andreu, D, Nieva, J.L, Pai, E.F. 登録日 2008-07-11 公開日 2009-06-23 最終更新日 2023-11-15 実験手法 X-RAY DIFFRACTION (3.3 Å) 主引用文献 Structural constraints imposed by the conserved fusion peptide on the HIV-1 gp41 epitope recognized by the broadly neutralizing antibody 2F5. J.Phys.Chem.B, 113, 2009
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
3YGS	APAF-1 CARD IN COMPLEX WITH PRODOMAIN OF PROCASPASE-9 分子名称: APOPTOTIC PROTEASE ACTIVATING FACTOR 1, PROCASPASE 9 著者 Qin, H, Srinivasula, S, Wu, G, Fernandes-Alnemri, T, Alnemri, E, Shi, Y. 登録日 1999-05-08 公開日 2000-04-19 最終更新日 2023-12-27 実験手法 X-RAY DIFFRACTION (2.5 Å) 主引用文献 Structural basis of procaspase-9 recruitment by the apoptotic protease-activating factor 1. Nature, 399, 1999
3NB7	Crystal structure of Aquifex Aeolicus Peptidoglycan Glycosyltransferase in complex with Decarboxylated Neryl Moenomycin 分子名称: Penicillin-binding protein 1A 著者 Sliz, P, Yuan, Y, Walker, S. 登録日 2010-06-02 公開日 2011-05-18 最終更新日 2023-09-06 実験手法 X-RAY DIFFRACTION (2.65 Å) 主引用文献 Functional and structural analysis of a key region of the cell wall inhibitor moenomycin. Acs Chem.Biol., 5, 2010
3DJA	Crystal Structure of cpaf solved with MAD 分子名称: Protein CT_858 著者 Chai, J, Huang, Z. 登録日 2008-06-22 公開日 2009-01-13 最終更新日 2011-07-13 実験手法 X-RAY DIFFRACTION (2.9 Å) 主引用文献 Structural basis for activation and inhibition of the secreted chlamydia protease CPAF Cell Host Microbe, 4, 2008
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
3NER	Structure of Human Type B Cytochrome b5 分子名称: Cytochrome b5 type B, MAGNESIUM ION, PROTOPORPHYRIN IX CONTAINING FE, ... 著者 Terzyan, S, Zhang, C, Rivera, M, Benson, D.B. 登録日 2010-06-09 公開日 2011-05-25 最終更新日 2023-09-06 実験手法 X-RAY DIFFRACTION (1.45 Å) 主引用文献 Accommodating a Non-Conservative Internal Mutation by Water-Mediated Hydrogen-Bonding Between beta-Sheet Strands: A Comparison of Human and Rat Type B (Mitochondrial) Cytochrome b5 Biochemistry, 50, 2011
3ZBF	Structure of Human ROS1 Kinase Domain in Complex with Crizotinib 分子名称: 3-[(1R)-1-(2,6-dichloro-3-fluorophenyl)ethoxy]-5-(1-piperidin-4-yl-1H-pyrazol-4-yl)pyridin-2-amine, PROTO-ONCOGENE TYROSINE-PROTEIN KINASE ROS 著者 McTigue, M, Deng, Y, Liu, W, Brooun, A, Stewart, A. 登録日 2012-11-08 公開日 2013-06-12 最終更新日 2023-12-20 実験手法 X-RAY DIFFRACTION (2.2 Å) 主引用文献 Acquired Resistance to Crizotinib from a Mutation in Cd74-Ros1 N.Engl.J.Med., 368, 2013
3NJT	Crystal structure of the R450A mutant of the membrane protein FhaC 分子名称: Filamentous hemagglutinin transporter protein fhaC 著者 Clantin, B, Delattre, A.S, Jacob-Dubuisson, F, Villeret, V. 登録日 2010-06-18 公開日 2010-11-03 最終更新日 2023-09-06 実験手法 X-RAY DIFFRACTION (3.5 Å) 主引用文献 Functional importance of a conserved sequence motif in FhaC, a prototypic member of the TpsB/Omp85 superfamily. Febs J., 277, 2010
3R8Z	CDK2 in complex with inhibitor RC-1-136 分子名称: Cyclin-dependent kinase 2, [4-amino-2-(prop-2-en-1-ylamino)-1,3-thiazol-5-yl](pyridin-4-yl)methanone 著者 Betzi, S, Alam, R, Han, H, Becker, A, Schonbrunn, E. 登録日 2011-03-24 公開日 2012-10-31 最終更新日 2023-09-13 実験手法 X-RAY DIFFRACTION (1.85 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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