2FPP
| Crystal structure of pig GTP-specific succinyl-CoA synthetase from polyethylene glycol with chloride ions | 分子名称: | CHLORIDE ION, SULFATE ION, Succinyl-CoA ligase [GDP-forming] alpha-chain, ... | 著者 | Fraser, M.E, Hayakawa, K, Hume, M.S, Ryan, D.G, Brownie, E.R. | 登録日 | 2006-01-16 | 公開日 | 2006-02-21 | 最終更新日 | 2017-10-18 | 実験手法 | X-RAY DIFFRACTION (2.35 Å) | 主引用文献 | Interactions of GTP with the ATP-grasp Domain of GTP-specific Succinyl-CoA Synthetase J.Biol.Chem., 281, 2006
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6L93
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3MGF
| Crystal Structure of Monomeric Kusabira-Orange (MKO), Orange-Emitting GFP-like Protein, at pH 7.5 | 分子名称: | Fluorescent protein | 著者 | Ebisawa, T, Yamamura, A, Ohtsuka, J, Kameda, Y, Hayakawa, K, Nagata, K, Tanokura, M. | 登録日 | 2010-04-06 | 公開日 | 2011-03-16 | 最終更新日 | 2023-11-15 | 実験手法 | X-RAY DIFFRACTION (1.8 Å) | 主引用文献 | Crystal Structure of Monomeric Kusabira-Orange (MKO), Orange-Emitting GFP-like Protein, at pH 7.5 To be Published
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1FU0
| CRYSTAL STRUCTURE ANALYSIS OF THE PHOSPHO-SERINE 46 HPR FROM ENTEROCOCCUS FAECALIS | 分子名称: | PHOSPHOCARRIER PROTEIN HPR | 著者 | Audette, G.F, Engelmann, R, Hengstenberg, W, Deutscher, J, Hayakawa, K, Quail, J.W, Delbaere, L.T.J. | 登録日 | 2000-09-13 | 公開日 | 2000-11-22 | 最終更新日 | 2022-12-21 | 実験手法 | X-RAY DIFFRACTION (1.9 Å) | 主引用文献 | The 1.9 A resolution structure of phospho-serine 46 HPr from Enterococcus faecalis. J.Mol.Biol., 303, 2000
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1KWP
| Crystal Structure of MAPKAP2 | 分子名称: | MAP Kinase Activated Protein Kinase 2, MERCURY (II) ION | 著者 | Meng, W, Swenson, L.L, Fitzgibbon, M.J, Hayakawa, K, ter Haar, E, Behrens, A.E, Fulghum, J.R, Lippke, J.A. | 登録日 | 2002-01-30 | 公開日 | 2002-09-18 | 最終更新日 | 2024-02-14 | 実験手法 | X-RAY DIFFRACTION (2.8 Å) | 主引用文献 | Structure of Mitogen-activated Protein Kinase-activated Protein (MAPKAP) Kinase 2 Suggests a Bifunctional Switch That
Couples Kinase Activation with Nuclear Export J.Biol.Chem., 277, 2002
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3ADF
| Crystal structure of a monomeric green fluorescent protein, Azami-Green (mAG) | 分子名称: | Monomeric Azami Green | 著者 | Ebisawa, T, Yamamura, A, Kameda, Y, Hayakawa, K, Nagata, K, Tanokura, M. | 登録日 | 2010-01-20 | 公開日 | 2010-05-19 | 最終更新日 | 2023-11-15 | 実験手法 | X-RAY DIFFRACTION (2.2 Å) | 主引用文献 | The structure of mAG, a monomeric mutant of the green fluorescent protein Azami-Green, reveals the structural basis of its stable green emission Acta Crystallogr.,Sect.F, 66, 2010
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1QY6
| Structue of V8 Protease from Staphylococcus aureus | 分子名称: | POTASSIUM ION, serine protease | 著者 | Prasad, L, Leduc, Y, Hayakawa, K, Delbaere, L.T.J. | 登録日 | 2003-09-09 | 公開日 | 2004-02-17 | 最終更新日 | 2024-02-14 | 実験手法 | X-RAY DIFFRACTION (1.9 Å) | 主引用文献 | The structure of a universally employed enzyme: V8 protease from Staphylococcus aureus. Acta Crystallogr.,Sect.D, 60, 2004
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2ERZ
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3D9V
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3UFX
| Thermus aquaticus succinyl-CoA synthetase in complex with GDP-Mn2+ | 分子名称: | GUANOSINE-5'-DIPHOSPHATE, MANGANESE (II) ION, Succinyl-CoA synthetase beta subunit, ... | 著者 | Fraser, M.E. | 登録日 | 2011-11-01 | 公開日 | 2012-06-27 | 最終更新日 | 2023-09-13 | 実験手法 | X-RAY DIFFRACTION (2.35 Å) | 主引用文献 | Biochemical and structural characterization of the GTP-preferring succinyl-CoA synthetase from Thermus aquaticus. Acta Crystallogr.,Sect.D, 68, 2012
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5WVU
| Crystal structure of carboxypeptidase from Thermus thermophilus | 分子名称: | GLYCEROL, Thermostable carboxypeptidase 1, ZINC ION | 著者 | Okai, M, Nagata, K, Tanokura, M, RIKEN Structural Genomics/Proteomics Initiative (RSGI) | 登録日 | 2016-12-29 | 公開日 | 2017-02-22 | 最終更新日 | 2024-03-20 | 実験手法 | X-RAY DIFFRACTION (2.6 Å) | 主引用文献 | Insight into the transition between the open and closed conformations of Thermus thermophilus carboxypeptidase. Biochem. Biophys. Res. Commun., 484, 2017
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1PPK
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1DZO
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3MWD
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3MWE
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3PFF
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3OXO
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2FPG
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2FP4
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2FPI
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2REN
| STRUCTURE OF RECOMBINANT HUMAN RENIN, A TARGET FOR CARDIOVASCULAR-ACTIVE DRUGS, AT 2.5 ANGSTROMS RESOLUTION | 分子名称: | 2-acetamido-2-deoxy-beta-D-glucopyranose, RENIN | 著者 | Sielecki, A.R, James, M.N.G. | 登録日 | 1992-02-05 | 公開日 | 1994-01-31 | 最終更新日 | 2020-07-29 | 実験手法 | X-RAY DIFFRACTION (2.5 Å) | 主引用文献 | Structure of recombinant human renin, a target for cardiovascular-active drugs, at 2.5 A resolution. Science, 243, 1989
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1ALQ
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1APV
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5BML
| ROCK 1 bound to a pyridine thiazole inhibitor | 分子名称: | N-[4-(2-fluoropyridin-4-yl)thiophen-2-yl]-2-{3-[(methylsulfonyl)amino]phenyl}acetamide, Rho-associated protein kinase 1 | 著者 | Jacobs, M.D. | 登録日 | 2015-05-22 | 公開日 | 2015-06-10 | 最終更新日 | 2024-03-06 | 実験手法 | X-RAY DIFFRACTION (2.95 Å) | 主引用文献 | Design, Synthesis, and Structure-Activity Relationships of Pyridine-Based Rho Kinase (ROCK) Inhibitors. J.Med.Chem., 58, 2015
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1APW
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