2BYA
| Is radiation damage dependent on the dose-rate used during macromolecular crystallography data collection | 分子名称: | BENZAMIDINE, CALCIUM ION, CATIONIC TRYPSIN, ... | 著者 | Leiros, H.-K.S, Timmins, J, Ravelli, R.B.G, McSweeney, S.M. | 登録日 | 2005-07-29 | 公開日 | 2006-02-06 | 最終更新日 | 2021-08-04 | 実験手法 | X-RAY DIFFRACTION (1.3 Å) | 主引用文献 | Is Radiation Damage Dependent on the Dose-Rate Used During Macromolecular Crystallography Data Collection? Acta Crystallogr.,Sect.D, 62, 2006
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2BY9
| Is radiation damage dependent on the dose-rate used during macromolecular crystallography data collection | 分子名称: | BENZAMIDINE, CALCIUM ION, CATIONIC TRYPSIN, ... | 著者 | Leiros, H.-K.S, Timmins, J, Ravelli, R.B.G, McSweeney, S.M. | 登録日 | 2005-07-29 | 公開日 | 2006-02-06 | 最終更新日 | 2021-08-04 | 実験手法 | X-RAY DIFFRACTION (1.3 Å) | 主引用文献 | Is Radiation Damage Dependent on the Dose-Rate Used During Macromolecular Crystallography Data Collection? Acta Crystallogr.,Sect.D, 62, 2006
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1IT3
| Hagfish CO ligand hemoglobin | 分子名称: | CARBON MONOXIDE, PROTOPORPHYRIN IX CONTAINING FE, hemoglobin | 著者 | Mito, M, Chong, K.T, Park, S.-Y, Tame, J.R. | 登録日 | 2002-01-05 | 公開日 | 2002-01-23 | 最終更新日 | 2023-10-25 | 実験手法 | X-RAY DIFFRACTION (2.1 Å) | 主引用文献 | Crystal structures of deoxy- and carbonmonoxyhemoglobin F1 from the hagfish Eptatretus burgeri J.Biol.Chem., 277, 2002
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2BY5
| Is radiation damage dependent on the dose-rate used during macromolecular crystallography data collection | 分子名称: | BENZAMIDINE, CALCIUM ION, CATIONIC TRYPSIN, ... | 著者 | Leiros, H.-K.S, Timmins, J, Ravelli, R.B.G, McSweeney, S.M. | 登録日 | 2005-07-29 | 公開日 | 2006-02-06 | 最終更新日 | 2021-08-04 | 実験手法 | X-RAY DIFFRACTION (1.3 Å) | 主引用文献 | Is Radiation Damage Dependent on the Dose-Rate Used During Macromolecular Crystallography Data Collection? Acta Crystallogr.,Sect.D, 62, 2006
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1ILQ
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2BY8
| Is radiation damage dependent on the dose-rate used during macromolecular crystallography data collection | 分子名称: | BENZAMIDINE, CALCIUM ION, CATIONIC TRYPSIN, ... | 著者 | Leiros, H.-K.S, Timmins, J, Ravelli, R.B.G, McSweeney, S.M. | 登録日 | 2005-07-29 | 公開日 | 2006-02-06 | 最終更新日 | 2021-08-04 | 実験手法 | X-RAY DIFFRACTION (1.3 Å) | 主引用文献 | Is Radiation Damage Dependent on the Dose-Rate Used During Macromolecular Crystallography Data Collection? Acta Crystallogr.,Sect.D, 62, 2006
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2BQM
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1IVE
| STRUCTURES OF AROMATIC INHIBITORS OF INFLUENZA VIRUS NEURAMINIDASE | 分子名称: | 2-acetamido-2-deoxy-alpha-D-glucopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose, 2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose, 4-(ACETYLAMINO)-3-AMINO BENZOIC ACID, ... | 著者 | Jedrzejas, M.J, Luo, M. | 登録日 | 1994-12-12 | 公開日 | 1995-03-31 | 最終更新日 | 2020-07-29 | 実験手法 | X-RAY DIFFRACTION (2.4 Å) | 主引用文献 | Structures of aromatic inhibitors of influenza virus neuraminidase. Biochemistry, 34, 1995
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2BQE
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2BQO
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2BQH
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2R3L
| Crystal Structure of Cyclin-Dependent Kinase 2 with inhibitor | 分子名称: | 3-bromo-6-phenyl-N-(pyrimidin-5-ylmethyl)imidazo[1,2-a]pyridin-8-amine, Cell division protein kinase 2 | 著者 | Fischmann, T.O, Hruza, A.W, Madison, V.M, Duca, J.S. | 登録日 | 2007-08-29 | 公開日 | 2008-01-22 | 最終更新日 | 2011-07-13 | 実験手法 | X-RAY DIFFRACTION (1.65 Å) | 主引用文献 | Structure-guided discovery of cyclin-dependent kinase inhibitors. Biopolymers, 89, 2008
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2BQK
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1IVP
| THE CRYSTALLOGRAPHIC STRUCTURE OF THE PROTEASE FROM HUMAN IMMUNODEFICIENCY VIRUS TYPE 2 WITH TWO SYNTHETIC PEPTIDIC TRANSITION STATE ANALOG INHIBITORS | 分子名称: | 4-[(2R)-3-{[(1S,2S,3R,4S)-1-(cyclohexylmethyl)-2,3-dihydroxy-5-methyl-4-({(1S,2R)-2-methyl-1-[(pyridin-2-ylmethyl)carba moyl]butyl}carbamoyl)hexyl]amino}-2-{[(naphthalen-1-yloxy)acetyl]amino}-3-oxopropyl]-1H-imidazol-3-ium, HIV-2 PROTEASE | 著者 | Mulichak, A.M, Watenpaugh, K.D. | 登録日 | 1993-03-18 | 公開日 | 1993-07-15 | 最終更新日 | 2024-02-07 | 実験手法 | X-RAY DIFFRACTION (2.5 Å) | 主引用文献 | The crystallographic structure of the protease from human immunodeficiency virus type 2 with two synthetic peptidic transition state analog inhibitors. J.Biol.Chem., 268, 1993
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2BQF
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1X4X
| Solution structure of the 6th fibronectin type III domain from human fibronectin type III domain containing protein 3 | 分子名称: | Fibronectin type-III domain containing protein 3a | 著者 | Tomizawa, T, Kigawa, T, Koshiba, S, Inoue, M, Yokoyama, S, RIKEN Structural Genomics/Proteomics Initiative (RSGI) | 登録日 | 2005-05-15 | 公開日 | 2005-11-15 | 最終更新日 | 2024-05-29 | 実験手法 | SOLUTION NMR | 主引用文献 | Solution structure of the 6th fibronectin type III domain from human fibronectin type III domain containing protein 3 To be Published
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2BQG
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2BQN
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1X5D
| The solution structure of the second thioredoxin-like domain of human Protein disulfide-isomerase A6 | 分子名称: | Protein disulfide-isomerase A6 | 著者 | Tochio, N, Koshiba, S, Inoue, M, Kigawa, T, Yokoyama, S, RIKEN Structural Genomics/Proteomics Initiative (RSGI) | 登録日 | 2005-05-15 | 公開日 | 2005-11-15 | 最終更新日 | 2024-05-29 | 実験手法 | SOLUTION NMR | 主引用文献 | The solution structure of the second thioredoxin-like domain of human Protein disulfide-isomerase A6 To be Published
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2BPR
| NMR STRUCTURE OF THE SUBSTRATE BINDING DOMAIN OF DNAK, 25 STRUCTURES | 分子名称: | DNAK | 著者 | Wang, H, Kurochkin, A.V, Pang, Y, Hu, W, Flynn, G.C, Zuiderweg, E.R.P. | 登録日 | 1998-08-11 | 公開日 | 1999-03-02 | 最終更新日 | 2024-05-22 | 実験手法 | SOLUTION NMR | 主引用文献 | NMR solution structure of the 21 kDa chaperone protein DnaK substrate binding domain: a preview of chaperone-protein interaction. Biochemistry, 37, 1998
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1IWI
| Putidaredoxin-Binding Stablilizes an Active Conformer of Cytochrome P450cam in its Reduced State; Crystal Structure of Cytochrome P450cam | 分子名称: | CAMPHOR, CYTOCHROME P450-CAM, PROTOPORPHYRIN IX CONTAINING FE | 著者 | Nagano, S, Shimada, H, Tarumi, A, Hishiki, T, Kimata-Ariga, Y, Egawa, T, Park, S.-Y, Adachi, S, Shiro, Y, Ishimura, Y, RIKEN Structural Genomics/Proteomics Initiative (RSGI) | 登録日 | 2002-05-15 | 公開日 | 2002-06-05 | 最終更新日 | 2023-12-27 | 実験手法 | X-RAY DIFFRACTION (2 Å) | 主引用文献 | Infrared spectroscopic and mutational studies on putidaredoxin-induced conformational changes in ferrous CO-P450cam Biochemistry, 42, 2003
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1IWV
| Crystal Structure Analysis of Human lysozyme at 147K. | 分子名称: | CHLORIDE ION, LYSOZYME C | 著者 | Joti, Y, Nakasako, M, Kidera, A, Go, N. | 登録日 | 2002-06-03 | 公開日 | 2002-09-04 | 最終更新日 | 2023-12-27 | 実験手法 | X-RAY DIFFRACTION (1.4 Å) | 主引用文献 | Nonlinear temperature dependence of the crystal structure of lysozyme: correlation between coordinate shifts and thermal factors. Acta Crystallogr.,Sect.D, 58, 2002
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2C68
| Crystal structure of the human CDK2 complexed with the triazolopyrimidine inhibitor | 分子名称: | (5Z)-5-(3-BROMOCYCLOHEXA-2,5-DIEN-1-YLIDENE)-N-(PYRIDIN-4-YLMETHYL)-1,5-DIHYDROPYRAZOLO[1,5-A]PYRIMIDIN-7-AMINE, CELL DIVISION PROTEIN KINASE 2 | 著者 | Richardson, C.M, Dokurno, P, Murray, J.B, Surgenor, A.E. | 登録日 | 2005-11-08 | 公開日 | 2005-12-07 | 最終更新日 | 2023-12-13 | 実験手法 | X-RAY DIFFRACTION (1.95 Å) | 主引用文献 | Triazolo[1,5-A]Pyrimidines as Novel Cdk2 Inhibitors: Protein Structure-Guided Design and Sar. Bioorg.Med.Chem.Lett., 16, 2006
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2QHN
| Crystal Structure of Chek1 in Complex with Inhibitor 1a | 分子名称: | 5-ETHYL-3-METHYL-1,5-DIHYDRO-4H-PYRAZOLO[4,3-C]QUINOLIN-4-ONE, Serine/threonine-protein kinase Chk1 | 著者 | Yan, Y, Munshi, S. | 登録日 | 2007-07-02 | 公開日 | 2008-03-18 | 最終更新日 | 2023-08-30 | 実験手法 | X-RAY DIFFRACTION (1.7 Å) | 主引用文献 | Optimization of a pyrazoloquinolinone class of Chk1 kinase inhibitors. Bioorg.Med.Chem.Lett., 17, 2007
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1IXX
| CRYSTAL STRUCTURE OF COAGULATION FACTORS IX/X-BINDING PROTEIN (IX/X-BP) FROM VENOM OF HABU SNAKE WITH A HETERODIMER OF C-TYPE LECTIN DOMAINS | 分子名称: | CALCIUM ION, COAGULATION FACTORS IX/X-BINDING PROTEIN | 著者 | Mizuno, H, Fujimoto, Z, Koizumi, M, Kano, H. | 登録日 | 1997-05-01 | 公開日 | 1998-05-06 | 最終更新日 | 2011-07-13 | 実験手法 | X-RAY DIFFRACTION (2.5 Å) | 主引用文献 | Structure of coagulation factors IX/X-binding protein, a heterodimer of C-type lectin domains. Nat.Struct.Biol., 4, 1997
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