PDB: 72655 件ウェブページステータス検索Chemie searchBIRD

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3LIG	Crystal structure of fructosyltransferase (D191A) from A. japonicus 分子名称: Fructosyltransferase 著者 Chuankhayan, P, Chen, C.J, Chiang, C.M. 登録日 2010-01-24 公開日 2010-05-12 最終更新日 2024-03-20 実験手法 X-RAY DIFFRACTION (1.8 Å) 主引用文献 Crystal structure of Aspergillus japonicus fructosyltransferase complex with donor/acceptor substrates reveal complete sbusites in the active site for catalysis To be Published
3LEM	Crystal structure of fructosyltransferase (D191A) from A. japonicus in complex with Nystose 分子名称: Fructosyltransferase, beta-D-fructofuranose-(2-1)-beta-D-fructofuranose-(2-1)-beta-D-fructofuranose-(2-1)-alpha-D-glucopyranose 著者 Chuankhayan, P, Chen, C.J, Chiang, C.M. 登録日 2010-01-15 公開日 2010-05-12 最終更新日 2024-03-20 実験手法 X-RAY DIFFRACTION (2.1 Å) 主引用文献 Crystal structure of Aspergillus japonicus fructosyltransferase complex with donor/acceptor substrates reveal complete sbusites in the active site for catalysis To be Published
7QGP	STK10 (LOK) bound to Macrocycle CKJB51 分子名称: 1,2-ETHANEDIOL, 1-[(4-chloranyl-2-methyl-phenyl)methyl]-3-(7,10-dioxa-13,17,18,21-tetrazatetracyclo[12.5.2.1^{2,6}.0^{17,20}]docosa-1(20),2(22),3,5,14(21),15,18-heptaen-5-yl)urea, CHLORIDE ION, ... 著者 Berger, B.-T, Schroeder, M, Kraemer, A, Schwalm, M.P, Kurz, C.G, Amrhein, J.A, Hanke, T, Knapp, S, Structural Genomics Consortium (SGC) 登録日 2021-12-09 公開日 2022-01-26 最終更新日 2024-01-31 実験手法 X-RAY DIFFRACTION (1.9 Å) 主引用文献 STK10 bound to CKJB51 To Be Published
3LDR	Crystal structure of fructosyltransferase (D191A) from A. japonicus in complex with 1-Kestose 分子名称: Fructosyltransferase, beta-D-fructofuranose-(2-1)-beta-D-fructofuranose-(2-1)-alpha-D-glucopyranose 著者 Chuankhayan, P, Chen, C.J, Chiang, C.M. 登録日 2010-01-13 公開日 2010-05-12 最終更新日 2024-03-20 実験手法 X-RAY DIFFRACTION (2.1 Å) 主引用文献 Crystal structure of Aspergillus japonicus fructosyltransferase complex with donor/acceptor substrates reveal complete sbusites in the active site for catalysis To be Published
3LFI	Crystal structure of fructosyltransferase (wild-type) from A. japonicus in complex with glucose 分子名称: Fructosyltransferase, beta-D-glucopyranose 著者 Chuankhayan, P, Chen, C.J, Chiang, C.M. 登録日 2010-01-17 公開日 2010-05-12 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 Aspergillus japonicus fructosyltransferase complex with donor/acceptor substrates reveal complete sbusites in the active site for catalysis To be Published
5D0Y	Substrate bound S-component of folate ECF transporter 分子名称: Conserved hypothetical membrane protein, FOLIC ACID 著者 Swier, L.J.Y.M, Guskov, A, Slotboom, D.J. 登録日 2015-08-03 公開日 2016-04-06 最終更新日 2024-01-10 実験手法 X-RAY DIFFRACTION (3.014 Å) 主引用文献 Structural insight in the toppling mechanism of an energy-coupling factor transporter. Nat Commun, 7, 2016
7SD2	Murine Fab that recognizes Hev b 8 (profilin for Hevea brasiliensis) 分子名称: Heavy Chain Antibody IgE/Fab anti-profilin Hev b 8, Light Chain Antibody IgE/Fab anti-profilin Hev b 8 著者 Rodriguez-Romero, A, Garcia-Ramirez, B. 登録日 2021-09-29 公開日 2022-08-10 最終更新日 2023-10-18 実験手法 X-RAY DIFFRACTION (3.75 Å) 主引用文献 A native IgE in complex with profilin provides insights into allergen recognition and cross-reactivity. Commun Biol, 5, 2022
3CHE	Crystal structure of Aspergillus fumigatus chitinase B1 in complex with tripeptide 分子名称: Chitinase, Peptide inhibitor, SULFATE ION 著者 Andersen, O.A, van Aalten, D.M.F. 登録日 2008-03-09 公開日 2008-03-25 最終更新日 2023-08-30 実験手法 X-RAY DIFFRACTION (2.05 Å) 主引用文献 Structure-based dissection of the natural product cyclopentapeptide chitinase inhibitor argifin. Chem.Biol., 15, 2008
3CH9	Crystal structure of Aspergillus fumigatus chitinase B1 in complex with dimethylguanylurea 分子名称: 1-methyl-3-(N-methylcarbamimidoyl)urea, Chitinase, SULFATE ION 著者 Andersen, O.A, van Aalten, D.M.F. 登録日 2008-03-09 公開日 2008-03-25 最終更新日 2023-08-30 実験手法 X-RAY DIFFRACTION (2.2 Å) 主引用文献 Structure-based dissection of the natural product cyclopentapeptide chitinase inhibitor argifin. Chem.Biol., 15, 2008
3CHC	Crystal structure of Aspergillus fumigatus chitinase B1 in complex with monopeptide 分子名称: (2S)-2-acetamido-N-methyl-5-[[N-(methylcarbamoyl)carbamimidoyl]amino]pentanamide, Chitinase, SULFATE ION 著者 Andersen, O.A, van Aalten, D.M.F. 登録日 2008-03-09 公開日 2008-03-25 最終更新日 2023-08-30 実験手法 X-RAY DIFFRACTION (1.9 Å) 主引用文献 Structure-based dissection of the natural product cyclopentapeptide chitinase inhibitor argifin. Chem.Biol., 15, 2008
5P9J	BTK1 COCRYSTALLIZED WITH IBRUTINIB 分子名称: 1-[(3~{R})-3-[4-azanyl-3-(4-phenoxyphenyl)pyrazolo[3,4-d]pyrimidin-1-yl]piperidin-1-yl]propan-1-one, Tyrosine-protein kinase BTK 著者 Gardberg, A.S. 登録日 2016-09-20 公開日 2017-05-24 最終更新日 2021-11-17 実験手法 X-RAY DIFFRACTION (1.08 Å) 主引用文献 Ability of Bruton's Tyrosine Kinase Inhibitors to Sequester Y551 and Prevent Phosphorylation Determines Potency for Inhibition of Fc Receptor but not B-Cell Receptor Signaling. Mol. Pharmacol., 91, 2017
5P9L	BTK1 IN COMPLEX WITH CC 292 分子名称: Tyrosine-protein kinase BTK, ~{N}-[3-[[5-fluoranyl-2-[[4-(2-methoxyethoxy)phenyl]amino]pyrimidin-4-yl]amino]phenyl]propanamide 著者 Gardberg, A.S. 登録日 2016-09-20 公開日 2017-05-24 最終更新日 2021-11-17 実験手法 X-RAY DIFFRACTION (1.25 Å) 主引用文献 Ability of Bruton's Tyrosine Kinase Inhibitors to Sequester Y551 and Prevent Phosphorylation Determines Potency for Inhibition of Fc Receptor but not B-Cell Receptor Signaling. Mol. Pharmacol., 91, 2017
5P9H	BTK1 COCRYSTALLIZED WITH RN983 分子名称: 6-~{tert}-butyl-8-fluoranyl-2-[3-(hydroxymethyl)-4-[1-methyl-5-[[5-(1-methylpiperidin-4-yl)pyridin-2-yl]amino]-6-oxidanylidene-pyridazin-3-yl]pyridin-2-yl]phthalazin-1-one, Tyrosine-protein kinase BTK 著者 Gardberg, A.S. 登録日 2016-09-20 公開日 2017-05-24 最終更新日 2024-05-22 実験手法 X-RAY DIFFRACTION (1.95 Å) 主引用文献 Ability of Bruton's Tyrosine Kinase Inhibitors to Sequester Y551 and Prevent Phosphorylation Determines Potency for Inhibition of Fc Receptor but not B-Cell Receptor Signaling. Mol. Pharmacol., 91, 2017
5P9F	BTK IN COMPLEX WITH GDC-0834 分子名称: 1,2-ETHANEDIOL, GLYCEROL, N-{3-[6-({4-[(2R)-1,4-dimethyl-3-oxopiperazin-2-yl]phenyl}amino)-4-methyl-5-oxo-4,5-dihydropyrazin-2-yl]-2-methylphenyl }-4,5,6,7-tetrahydro-1-benzothiophene-2-carboxamide, ... 著者 Gardberg, A.S. 登録日 2016-09-20 公開日 2017-05-24 最終更新日 2024-05-22 実験手法 X-RAY DIFFRACTION (1.71 Å) 主引用文献 Ability of Bruton's Tyrosine Kinase Inhibitors to Sequester Y551 and Prevent Phosphorylation Determines Potency for Inhibition of Fc Receptor but not B-Cell Receptor Signaling. Mol. Pharmacol., 91, 2017
5P9G	Structure of BTK with RN486 分子名称: 6-cyclopropyl-8-fluoranyl-2-[2-(hydroxymethyl)-3-[1-methyl-5-[[5-(4-methylpiperazin-1-yl)pyridin-2-yl]amino]-6-oxidanylidene-pyridin-3-yl]phenyl]isoquinolin-1-one, Tyrosine-protein kinase BTK 著者 Gardberg, A.S. 登録日 2016-09-20 公開日 2017-05-24 最終更新日 2024-05-22 実験手法 X-RAY DIFFRACTION (1.75 Å) 主引用文献 Ability of Bruton's Tyrosine Kinase Inhibitors to Sequester Y551 and Prevent Phosphorylation Determines Potency for Inhibition of Fc Receptor but not B-Cell Receptor Signaling. Mol. Pharmacol., 91, 2017
5P9M	BTK1 BINDS COVALENTLY TO HY-15771 ONO-4059 分子名称: 6-azanyl-9-[(3~{R})-1-[(~{E})-but-2-enoyl]pyrrolidin-3-yl]-7-(4-phenoxyphenyl)purin-8-one, DIMETHYL SULFOXIDE, Tyrosine-protein kinase BTK 著者 Gardberg, A.S. 登録日 2016-09-20 公開日 2017-05-24 最終更新日 2021-11-17 実験手法 X-RAY DIFFRACTION (1.41 Å) 主引用文献 Ability of Bruton's Tyrosine Kinase Inhibitors to Sequester Y551 and Prevent Phosphorylation Determines Potency for Inhibition of Fc Receptor but not B-Cell Receptor Signaling. Mol. Pharmacol., 91, 2017
5P9I	BTK1 SOAKED WITH IBRUTINIB-Rev 分子名称: 1-{(3R)-3-[4-amino-3-(4-phenoxyphenyl)-1H-pyrazolo[3,4-d]pyrimidin-1-yl]piperidin-1-yl}prop-2-en-1-one, DIMETHYL SULFOXIDE, Tyrosine-protein kinase BTK 著者 Gardberg, A.S. 登録日 2016-09-20 公開日 2017-05-24 最終更新日 2024-05-22 実験手法 X-RAY DIFFRACTION (1.11 Å) 主引用文献 Ability of Bruton's Tyrosine Kinase Inhibitors to Sequester Y551 and Prevent Phosphorylation Determines Potency for Inhibition of Fc Receptor but not B-Cell Receptor Signaling. Mol. Pharmacol., 91, 2017
3G0H	Human dead-box RNA helicase DDX19, in complex with an ATP-analogue and RNA 分子名称: 5'-R(P*UP*UP*UP*UP*UP*UP*U)-3', ATP-dependent RNA helicase DDX19B, GLYCEROL, ... 著者 Karlberg, T, Lehtio, L, Collins, R, Arrowsmith, C.H, Berglund, H, Bountra, C, Dahlgren, L.G, Edwards, A.M, Flodin, S, Flores, A, Graslund, S, Hammarstrom, M, Johansson, A, Johansson, I, Kotenyova, T, Moche, M, Nilsson, M.E, Nordlund, P, Nyman, T, Persson, C, Sagemark, J, Schutz, P, Siponen, M.I, Thorsell, A.G, Tresaugues, L, Van Den Berg, S, Weigelt, J, Welin, M, Wisniewska, M, Schuler, H, Structural Genomics Consortium (SGC) 登録日 2009-01-28 公開日 2009-02-17 最終更新日 2023-09-06 実験手法 X-RAY DIFFRACTION (2.7 Å) 主引用文献 The DEXD/H-box RNA Helicase DDX19 Is Regulated by an {alpha}-Helical Switch. J.Biol.Chem., 284, 2009
7NTO	The structure of RRM domain of human TRMT2A at 1.23 A resolution 分子名称: 1,2-ETHANEDIOL, CHLORIDE ION, SODIUM ION, ... 著者 Witzenberger, M, Janowski, R, Davydova, E, Niessing, D. 登録日 2021-03-10 公開日 2022-01-19 最終更新日 2024-01-31 実験手法 X-RAY DIFFRACTION (1.23 Å) 主引用文献 Small-molecule modulators of TRMT2A decrease PolyQ aggregation and PolyQ-induced cell death. Comput Struct Biotechnol J, 20, 2022
7P3R	Helical structure of the toxin MakA from Vibrio cholera 分子名称: MakA tetramer 著者 Berg, A, Nadeem, A, Uhlin, B.E, Wai, S.N, Barandun, J. 登録日 2021-07-08 公開日 2022-02-23 最終更新日 2024-07-17 実験手法 ELECTRON MICROSCOPY (3.65 Å) 主引用文献 Protein-lipid interaction at low pH induces oligomerization of the MakA cytotoxin from Vibrio cholerae . Elife, 11, 2022
7QDA	Crystal structure of CalpL 分子名称: CalpL, SULFATE ION, TETRAETHYLENE GLYCOL, ... 著者 Schneberger, N, Hagelueken, G. 登録日 2021-11-26 公開日 2022-11-16 最終更新日 2023-02-08 実験手法 X-RAY DIFFRACTION (2.1 Å) 主引用文献 Antiviral signalling by a cyclic nucleotide activated CRISPR protease. Nature, 614, 2023
3CHD	Crystal structure of Aspergillus fumigatus chitinase B1 in complex with dipeptide 分子名称: (2S)-2-[[(2S)-2-acetamido-5-[[N-(methylcarbamoyl)carbamimidoyl]amino]pentanoyl]-methyl-amino]-3-phenyl-propanoic acid, Chitinase, SULFATE ION 著者 Andersen, O.A, van Aalten, D.M.F. 登録日 2008-03-09 公開日 2008-03-25 最終更新日 2023-08-30 実験手法 X-RAY DIFFRACTION (2 Å) 主引用文献 Structure-based dissection of the natural product cyclopentapeptide chitinase inhibitor argifin. Chem.Biol., 15, 2008
3CKU	Urate oxidase from aspergillus flavus complexed with its inhibitor 8-azaxanthin and chloride 分子名称: 8-AZAXANTHINE, CHLORIDE ION, SODIUM ION, ... 著者 Colloc'h, N, Prange, T. 登録日 2008-03-17 公開日 2008-10-07 最終更新日 2023-11-01 実験手法 X-RAY DIFFRACTION (1.7 Å) 主引用文献 Oxygen pressurized X-ray crystallography: probing the dioxygen binding site in cofactorless urate oxidase and implications for its catalytic mechanism. Biophys.J., 95, 2008
3CHF	Crystal structure of Aspergillus fumigatus chitinase B1 in complex with tetrapeptide 分子名称: Argifin, Chitinase, SULFATE ION 著者 Andersen, O.A, van Aalten, D.M.F. 登録日 2008-03-09 公開日 2008-03-25 最終更新日 2023-08-30 実験手法 X-RAY DIFFRACTION (1.95 Å) 主引用文献 Structure-based dissection of the natural product cyclopentapeptide chitinase inhibitor argifin. Chem.Biol., 15, 2008
4YNT	Crystal structure of Aspergillus flavus FAD glucose dehydrogenase 分子名称: DIHYDROFLAVINE-ADENINE DINUCLEOTIDE, Glucose oxidase, putative 著者 Yoshida, H, Sakai, G, Kojima, K, Kamitori, S, Sode, K. 登録日 2015-03-11 公開日 2015-09-02 最終更新日 2023-11-08 実験手法 X-RAY DIFFRACTION (1.78 Å) 主引用文献 Structural analysis of fungus-derived FAD glucose dehydrogenase Sci Rep, 5, 2015

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