1VI9
| Crystal structure of pyridoxamine kinase | 分子名称: | BETA-MERCAPTOETHANOL, Pyridoxamine kinase, SULFATE ION | 著者 | Structural GenomiX | 登録日 | 2003-12-01 | 公開日 | 2003-12-30 | 最終更新日 | 2023-12-27 | 実験手法 | X-RAY DIFFRACTION (1.96 Å) | 主引用文献 | Structural analysis of a set of proteins resulting from a bacterial genomics project Proteins, 60, 2005
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1VH6
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1VHK
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3NMI
| Crystal structure of the phenanthroline-modified cytochrome cb562 variant, MBP-Phen2 | 分子名称: | ACETATE ION, N-1,10-phenanthrolin-5-ylacetamide, PROTOPORPHYRIN IX CONTAINING FE, ... | 著者 | Radford, R.J, Tezcan, F.A. | 登録日 | 2010-06-22 | 公開日 | 2010-11-24 | 最終更新日 | 2023-12-27 | 実験手法 | X-RAY DIFFRACTION (2.01 Å) | 主引用文献 | Porous protein frameworks with unsaturated metal centers in sterically encumbered coordination sites. Chem.Commun.(Camb.), 47, 2011
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3NSH
| BACE-1 in complex with ELN475957 | 分子名称: | Beta-secretase 1, N-[(1S,2R)-1-(3,5-difluorobenzyl)-3-({1-[4-(2,2-dimethylpropyl)thiophen-2-yl]cyclopropyl}amino)-2-hydroxypropyl]acetamide | 著者 | Probst, G.D, Bowers, S, Sealy, J.M, Brecht, E, Yao, N. | 登録日 | 2010-07-01 | 公開日 | 2010-09-22 | 最終更新日 | 2023-12-27 | 実験手法 | X-RAY DIFFRACTION (2.2 Å) | 主引用文献 | Design and synthesis of hydroxyethylamine (HEA) BACE-1 inhibitors: structure-activity relationship of the aryl region. Bioorg.Med.Chem.Lett., 20, 2010
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1S8E
| Crystal structure of Mre11-3 | 分子名称: | MANGANESE (II) ION, exonuclease putative | 著者 | Hopfner, K.P. | 登録日 | 2004-02-02 | 公開日 | 2004-08-10 | 最終更新日 | 2024-05-29 | 実験手法 | X-RAY DIFFRACTION (2.3 Å) | 主引用文献 | Structural and functional analysis of Mre11-3 Nucleic Acids Res., 32, 2004
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3NSJ
| The X-ray crystal structure of lymphocyte perforin | 分子名称: | 2-acetamido-2-deoxy-beta-D-glucopyranose, CALCIUM ION, CHLORIDE ION, ... | 著者 | Law, R.H, Whisstock, J.C, Caradoc-Davies, T.T. | 登録日 | 2010-07-01 | 公開日 | 2010-11-03 | 最終更新日 | 2023-12-27 | 実験手法 | X-RAY DIFFRACTION (2.75 Å) | 主引用文献 | The structural basis for membrane binding and pore formation by lymphocyte perforin. Nature, 468, 2010
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3NWW
| P38 Alpha kinase complexed with a 2-aminothiazol-5-yl-pyrimidine based inhibitor | 分子名称: | 1-[2-(2-{[2-(dimethylamino)ethyl]amino}-6-{2-[(1-methylethyl)amino]-1,3-thiazol-5-yl}pyrimidin-4-yl)benzyl]-3-ethylurea, Mitogen-activated protein kinase 14 | 著者 | Sack, J.S. | 登録日 | 2010-07-12 | 公開日 | 2010-09-08 | 最終更新日 | 2024-02-21 | 実験手法 | X-RAY DIFFRACTION (2.09 Å) | 主引用文献 | Utilization of a nitrogen-sulfur nonbonding interaction in the design of new 2-aminothiazol-5-yl-pyrimidines as p38alpha MAP kinase inhibitors. Bioorg.Med.Chem.Lett., 20, 2010
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1ICA
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1I6B
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3Q4F
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1I1Y
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3Q0D
| Crystal structure of SUVH5 SRA- hemi methylated CG DNA complex | 分子名称: | CHLORIDE ION, DNA (5'-D(*CP*TP*GP*AP*CP*GP*TP*GP*GP*A)-3'), DNA (5'-D(*TP*CP*CP*AP*(5CM)P*GP*TP*CP*AP*G)-3'), ... | 著者 | Eerappa, R, Simanshu, D.K, Patel, D.J. | 登録日 | 2010-12-15 | 公開日 | 2011-02-23 | 最終更新日 | 2024-04-03 | 実験手法 | X-RAY DIFFRACTION (2.3704 Å) | 主引用文献 | A dual flip-out mechanism for 5mC recognition by the Arabidopsis SUVH5 SRA domain and its impact on DNA methylation and H3K9 dimethylation in vivo. Genes Dev., 25, 2011
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1VES
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1VH2
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1VH9
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1HSI
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1HSG
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1HUN
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3OX2
| X-ray Structural study of quinone reductase II inhibition by compounds with micromolar to nanomolar range IC50 values | 分子名称: | 2-hydroxy-8,9-dimethoxy-6H-isoindolo[2,1-a]indol-6-one, FLAVIN-ADENINE DINUCLEOTIDE, Ribosyldihydronicotinamide dehydrogenase [quinone], ... | 著者 | Pegan, S.D, Sturdy, M, Mesecar, A.D. | 登録日 | 2010-09-21 | 公開日 | 2011-05-25 | 最終更新日 | 2024-02-21 | 実験手法 | X-RAY DIFFRACTION (2.41 Å) | 主引用文献 | X-ray structural studies of quinone reductase 2 nanomolar range inhibitors. Protein Sci., 20, 2011
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1T93
| Evidence for Multiple Substrate Recognition and Molecular Mechanism of C-C reaction by Cytochrome P450 CYP158A2 from Streptomyces Coelicolor A3(2) | 分子名称: | FLAVIOLIN, PROTOPORPHYRIN IX CONTAINING FE, putative cytochrome P450 | 著者 | Zhao, B, Sundaramoorthy, M, Waterman, M.R. | 登録日 | 2004-05-14 | 公開日 | 2005-01-25 | 最終更新日 | 2023-08-23 | 実験手法 | X-RAY DIFFRACTION (1.62 Å) | 主引用文献 | Binding of Two Flaviolin Substrate Molecules, Oxidative Coupling, and Crystal Structure of Streptomyces coelicolor A3(2) Cytochrome P450 158A2. J.Biol.Chem., 280, 2005
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1GG2
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1WBI
| AVR2 | 分子名称: | AVIDIN-RELATED PROTEIN 2, BIOTIN, GLYCEROL, ... | 著者 | Airenne, T.T, Hytonen, V.P, Maatta, J.H, Kidron, H, Halling, K.K, Horha, J, Kulomaa, T, Nyholm, T.K.M, Johnson, M.S, Salminen, T.A, Kulomaa, M.S. | 登録日 | 2004-11-01 | 公開日 | 2005-10-12 | 最終更新日 | 2023-12-13 | 実験手法 | X-RAY DIFFRACTION (1.4 Å) | 主引用文献 | Avidin Related Protein 2 Shows Unique Structural and Functional Features Among the Avidin Protein Family. Bmc Biotechnol., 5, 2005
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3PJZ
| Crystal Structure of the Potassium Transporter TrkH from Vibrio parahaemolyticus | 分子名称: | POTASSIUM ION, Potassium uptake protein TrkH | 著者 | Cao, Y, Jin, X, Huang, H, Levin, E.J, Zhou, M, New York Consortium on Membrane Protein Structure (NYCOMPS) | 登録日 | 2010-11-10 | 公開日 | 2011-01-19 | 最終更新日 | 2017-11-08 | 実験手法 | X-RAY DIFFRACTION (3.506 Å) | 主引用文献 | Crystal structure of a potassium ion transporter, TrkH. Nature, 471, 2011
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3MVM
| P38 Alpha Map Kinase complexed with pyrrolotriazine inhibitor 7V | 分子名称: | 4-{[5-(isoxazol-3-ylcarbamoyl)-2-methylphenyl]amino}-5-methyl-N-propylpyrrolo[2,1-f][1,2,4]triazine-6-carboxamide, Mitogen-activated protein kinase 14 | 著者 | Sack, J.S. | 登録日 | 2010-05-04 | 公開日 | 2010-10-13 | 最終更新日 | 2024-02-21 | 実験手法 | X-RAY DIFFRACTION (2 Å) | 主引用文献 | Discovery of 4-(5-(Cyclopropylcarbamoyl)-2-Methylphenylamino)-5-Methyl-Npropylpyrrolo[1,2-F][1,2,4] Triazine-6-Carboxamide (Bms-582949), a Clinical P38? Map Kinase Inhibitor for the Treatment of Inflammatory Diseases J.Med.Chem., 53, 2010
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