PDB: 4080 件ウェブページステータス検索Chemie searchBIRD

---

1C2G	RECRUITING ZINC TO MEDIATE POTENT, SPECIFIC INHIBITION OF SERINE PROTEASES 分子名称: BIS(5-AMIDINO-2-BENZIMIDAZOLYL)METHANE KETONE HYDRATE, CALCIUM ION, DIMETHYL SULFOXIDE, ... 著者 Katz, B.A, Luong, C. 登録日 1999-07-21 公開日 2000-07-26 最終更新日 2023-12-27 実験手法 X-RAY DIFFRACTION (1.65 Å) 主引用文献 Design of potent selective zinc-mediated serine protease inhibitors. Nature, 391, 1998
1C2E	RECRUITING ZINC TO MEDIATE POTENT, SPECIFIC INHIBITION OF SERINE PROTEASES 分子名称: BIS(5-AMIDINO-2-BENZIMIDAZOLYL)METHANE KETONE, CALCIUM ION, MAGNESIUM ION, ... 著者 Katz, B.A, Luong, C. 登録日 1999-07-22 公開日 2000-07-26 最終更新日 2024-10-16 実験手法 X-RAY DIFFRACTION (1.65 Å) 主引用文献 Design of potent selective zinc-mediated serine protease inhibitors. Nature, 391, 1998
2XTY	Structure of QnrB1 (R167E-Trypsin Treated), a plasmid-mediated fluoroquinolone resistance protein 分子名称: QNRB1 著者 Vetting, M.W, Hegde, S.S, Park, C.H, Jacoby, G.A, Hooper, D.C, Blanchard, J.S. 登録日 2010-10-13 公開日 2010-10-27 最終更新日 2023-12-20 実験手法 X-RAY DIFFRACTION (1.8 Å) 主引用文献 Structure of Qnrb1, a Plasmid-Mediated Fluoroquinolone Resistance Factor. J.Biol.Chem., 286, 2011
1NN6	Human Pro-Chymase 分子名称: 2-acetamido-2-deoxy-beta-D-glucopyranose, 2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose, Chymase 著者 Reiling, K.K, Krucinski, J, Miercke, L.J.W, Raymond, W.W, Caughey, G.H, Stroud, R.M. 登録日 2003-01-12 公開日 2003-03-04 最終更新日 2023-08-16 実験手法 X-RAY DIFFRACTION (1.75 Å) 主引用文献 Structure of human pro-chymase: a model for the activating transition of granule-associated proteases. Biochemistry, 42, 2003
2XTX	Structure of QnrB1 (M102R-Trypsin Treated), a plasmid-mediated fluoroquinolone resistance protein 分子名称: QNRB1, SULFATE ION 著者 Vetting, M.W, Hegde, S.S, Park, C.H, Jacoby, G.A, Hooper, D.C, Blanchard, J.S. 登録日 2010-10-12 公開日 2010-10-20 最終更新日 2024-05-08 実験手法 X-RAY DIFFRACTION (2.2 Å) 主引用文献 Structure of Qnrb1, a Plasmid-Mediated Fluoroquinolone Resistance Factor. J.Biol.Chem., 286, 2011
1EFM	STRUCTURE OF THE GDP DOMAIN OF EF-TU AND LOCATION OF THE AMINO ACIDS HOMOLOGOUS TO RAS ONCOGENE PROTEINS 分子名称: ELONGATION FACTOR TU, GUANOSINE-5'-DIPHOSPHATE, MAGNESIUM ION 著者 Jurnak, F. 登録日 1987-05-29 公開日 1987-07-16 最終更新日 2024-02-07 実験手法 X-RAY DIFFRACTION (2.7 Å) 主引用文献 Structure of the GDP domain of EF-Tu and location of the amino acids homologous to ras oncogene proteins. Science, 230, 1985
1VTP	VACUOLAR TARGETING PEPTIDE FROM NA-PROPI 分子名称: VACUOLAR TARGETING PEPTIDE 著者 Nielsen, K.J, Hill, J.M, Anderson, M.A, Craik, D.J. 登録日 1995-11-14 公開日 1996-03-08 最終更新日 2024-05-22 実験手法 SOLUTION NMR 主引用文献 Synthesis and structure determination by NMR of a putative vacuolar targeting peptide and model of a proteinase inhibitor from Nicotiana alata. Biochemistry, 35, 1996
1SFI	High resolution structure of a potent, cyclic protease inhibitor from sunflower seeds 分子名称: CALCIUM ION, SULFATE ION, TRYPSIN, ... 著者 Luckett, S, Garcia, R.S, Barker, J.J, Konarev, A.V, Shewry, P, Clarke, A.R, Brady, R.L. 登録日 1998-12-16 公開日 1999-07-09 最終更新日 2024-10-30 実験手法 X-RAY DIFFRACTION (1.65 Å) 主引用文献 High-resolution structure of a potent, cyclic proteinase inhibitor from sunflower seeds. J.Mol.Biol., 290, 1999
1GI2	A NOVEL SERINE PROTEASE INHIBITION MOTIF INVOLVING A MULTI-CENTERED SHORT HYDROGEN BONDING NETWORK AT THE ACTIVE SITE 分子名称: 2-(2-HYDROXY-PHENYL)-3H-BENZOIMIDAZOLE-5-CARBOXAMIDINE, BETA-TRYPSIN, CALCIUM ION, ... 著者 Katz, B.A, Elrod, K, Luong, C, Rice, M, Mackman, R.L, Sprengeler, P.A, Spencer, J, Hatayte, J, Janc, J, Link, J, Litvak, J, Rai, R, Rice, K, Sideris, S, Verner, E, Young, W. 登録日 2001-01-22 公開日 2002-01-22 最終更新日 2024-10-30 実験手法 X-RAY DIFFRACTION (1.38 Å) 主引用文献 A novel serine protease inhibition motif involving a multi-centered short hydrogen bonding network at the active site. J.Mol.Biol., 307, 2001
1GI6	A NOVEL SERINE PROTEASE INHIBITION MOTIF INVOLVING A MULTI-CENTERED SHORT HYDROGEN BONDING NETWORK AT THE ACTIVE SITE 分子名称: 2-(2-HYDROXY-PHENYL)-1H-INDOLE-5-CARBOXAMIDINE, BETA-TRYPSIN, CALCIUM ION, ... 著者 Katz, B.A, Elrod, K, Luong, C, Rice, M, Mackman, R.L, Sprengeler, P.A, Spencer, J, Hatayte, J, Janc, J, Link, J, Litvak, J, Rai, R, Rice, K, Sideris, S, Verner, E, Young, W. 登録日 2001-01-22 公開日 2002-01-22 最終更新日 2023-12-27 実験手法 X-RAY DIFFRACTION (1.49 Å) 主引用文献 A novel serine protease inhibition motif involving a multi-centered short hydrogen bonding network at the active site. J.Mol.Biol., 307, 2001
1GI1	A NOVEL SERINE PROTEASE INHIBITION MOTIF INVOLVING A MULTI-CENTERED SHORT HYDROGEN BONDING NETWORK AT THE ACTIVE SITE 分子名称: 2-(2-HYDROXY-PHENYL)-1H-BENZOIMIDAZOLE-5-CARBOXAMIDINE, BETA-TRYPSIN, CALCIUM ION, ... 著者 Katz, B.A, Elrod, K, Luong, C, Rice, M, Mackman, R.L, Sprengeler, P.A, Spencer, J, Hatayte, J, Janc, J, Link, J, Litvak, J, Rai, R, Rice, K, Sideris, S, Verner, E, Young, W. 登録日 2001-01-22 公開日 2002-01-22 最終更新日 2024-10-09 実験手法 X-RAY DIFFRACTION (1.42 Å) 主引用文献 A novel serine protease inhibition motif involving a multi-centered short hydrogen bonding network at the active site. J.Mol.Biol., 307, 2001
1GI0	A NOVEL SERINE PROTEASE INHIBITION MOTIF INVOLVING A MULTI-CENTERED SHORT HYDROGEN BONDING NETWORK AT THE ACTIVE SITE 分子名称: 2-(2-HYDROXY-PHENYL)-1H-BENZOIMIDAZOLE-5-CARBOXAMIDINE, BETA-TRYPSIN, CALCIUM ION, ... 著者 Katz, B.A, Elrod, K, Luong, C, Rice, M, Mackman, R.L, Sprengeler, P.A, Spencer, J, Hatayte, J, Janc, J, Link, J, Litvak, J, Rai, R, Rice, K, Sideris, S, Verner, E, Young, W. 登録日 2001-01-22 公開日 2002-01-22 最終更新日 2023-12-27 実験手法 X-RAY DIFFRACTION (1.42 Å) 主引用文献 A novel serine protease inhibition motif involving a multi-centered short hydrogen bonding network at the active site. J.Mol.Biol., 307, 2001
1GI3	A NOVEL SERINE PROTEASE INHIBITION MOTIF INVOLVING A MULTI-CENTERED SHORT HYDROGEN BONDING NETWORK AT THE ACTIVE SITE 分子名称: 2-(2-HYDROXY-PHENYL)-1H-BENZOIMIDAZOLE-5-CARBOXAMIDINE, BETA-TRYPSIN, CALCIUM ION 著者 Katz, B.A, Elrod, K, Luong, C, Rice, M, Mackman, R.L, Sprengeler, P.A, Spencer, J, Hatayte, J, Janc, J, Link, J, Litvak, J, Rai, R, Rice, K, Sideris, S, Verner, E, Young, W. 登録日 2001-01-22 公開日 2002-01-22 最終更新日 2024-10-30 実験手法 X-RAY DIFFRACTION (1.44 Å) 主引用文献 A novel serine protease inhibition motif involving a multi-centered short hydrogen bonding network at the active site. J.Mol.Biol., 307, 2001
1GHZ	A NOVEL SERINE PROTEASE INHIBITION MOTIF INVOLVING A MULTI-CENTERED SHORT HYDROGEN BONDING NETWORK AT THE ACTIVE SITE 分子名称: 2-(2-OXO-1,2-DIHYDRO-PYRIDIN-3-YL)-1H-BENZOIMIDAZOLE-5-CARBOXAMIDINE, BETA-TRYPSIN, CALCIUM ION, ... 著者 Katz, B.A, Elrod, K, Luong, C, Rice, M, Mackman, R.L, Sprengeler, P.A, Spencer, J, Hatayte, J, Janc, J, Link, J, Litvak, J, Rai, R, Rice, K, Sideris, S, Verner, E, Young, W. 登録日 2001-01-22 公開日 2002-01-22 最終更新日 2024-11-06 実験手法 X-RAY DIFFRACTION (1.39 Å) 主引用文献 A novel serine protease inhibition motif involving a multi-centered short hydrogen bonding network at the active site. J.Mol.Biol., 307, 2001
1GI5	A NOVEL SERINE PROTEASE INHIBITION MOTIF INVOLVING A MULTI-CENTERED SHORT HYDROGEN BONDING NETWORK AT THE ACTIVE SITE 分子名称: 2-(2-HYDROXY-5-METHOXY-PHENYL)-1H-BENZOIMIDAZOLE-5-CARBOXAMIDINE, BETA-TRYPSIN, CALCIUM ION, ... 著者 Katz, B.A, Elrod, K, Luong, C, Rice, M, Mackman, R.L, Sprengeler, P.A, Spencer, J, Hatayte, J, Janc, J, Link, J, Litvak, J, Rai, R, Rice, K, Sideris, S, Verner, E, Young, W. 登録日 2001-01-22 公開日 2002-01-22 最終更新日 2023-12-27 実験手法 X-RAY DIFFRACTION (1.6 Å) 主引用文献 A novel serine protease inhibition motif involving a multi-centered short hydrogen bonding network at the active site. J.Mol.Biol., 307, 2001
1GI4	A NOVEL SERINE PROTEASE INHIBITION MOTIF INVOLVING A MULTI-CENTERED SHORT HYDROGEN BONDING NETWORK AT THE ACTIVE SITE 分子名称: 2-(2-HYDROXY-PHENYL)-3H-BENZOIMIDAZOLE-5-CARBOXAMIDINE, BETA-TRYPSIN, CALCIUM ION, ... 著者 Katz, B.A, Elrod, K, Luong, C, Rice, M, Mackman, R.L, Sprengeler, P.A, Spencer, J, Hatayte, J, Janc, J, Link, J, Litvak, J, Rai, R, Rice, K, Sideris, S, Verner, E, Young, W. 登録日 2001-01-22 公開日 2002-01-22 最終更新日 2024-10-30 実験手法 X-RAY DIFFRACTION (1.37 Å) 主引用文献 A novel serine protease inhibition motif involving a multi-centered short hydrogen bonding network at the active site. J.Mol.Biol., 307, 2001
1BT7	THE SOLUTION NMR STRUCTURE OF THE N-TERMINAL PROTEASE DOMAIN OF THE HEPATITIS C VIRUS (HCV) NS3-PROTEIN, FROM BK STRAIN, 20 STRUCTURES 分子名称: NS3 SERINE PROTEASE, ZINC ION 著者 Barbato, G, Cicero, D.O, Nardi, M.C, Steinkuhler, C, Cortese, R, De Francesco, R, Bazzo, R. 登録日 1998-09-01 公開日 1999-06-22 最終更新日 2024-05-22 実験手法 SOLUTION NMR 主引用文献 The solution structure of the N-terminal proteinase domain of the hepatitis C virus (HCV) NS3 protein provides new insights into its activation and catalytic mechanism. J.Mol.Biol., 289, 1999
1TNH	PREDICTION OF NOVEL SERINE PROTEASE INHIBITORS 分子名称: 4-FLUOROBENZYLAMINE, CALCIUM ION, TRYPSIN 著者 Kurinov, I, Harrison, R.W. 登録日 1994-07-21 公開日 1994-11-30 最終更新日 2024-10-23 実験手法 X-RAY DIFFRACTION (1.8 Å) 主引用文献 Prediction of new serine proteinase inhibitors. Nat.Struct.Biol., 1, 1994
1TNJ	PREDICTION OF NOVEL SERINE PROTEASE INHIBITORS 分子名称: 2-PHENYLETHYLAMINE, CALCIUM ION, TRYPSIN 著者 Kurinov, I, Harrison, R.W. 登録日 1994-07-21 公開日 1994-11-30 最終更新日 2024-06-05 実験手法 X-RAY DIFFRACTION (1.8 Å) 主引用文献 Prediction of new serine proteinase inhibitors. Nat.Struct.Biol., 1, 1994
1TNG	PREDICTION OF NOVEL SERINE PROTEASE INHIBITORS 分子名称: AMINOMETHYLCYCLOHEXANE, CALCIUM ION, TRYPSIN 著者 Kurinov, I, Harrison, R.W. 登録日 1994-07-21 公開日 1994-11-30 最終更新日 2024-10-30 実験手法 X-RAY DIFFRACTION (1.8 Å) 主引用文献 Prediction of new serine proteinase inhibitors. Nat.Struct.Biol., 1, 1994
5XX3	A BPTI-[5,55] variant with C14GA38G mutations 分子名称: Pancreatic trypsin inhibitor, SULFATE ION 著者 Islam, M.M. 登録日 2017-07-01 公開日 2018-07-04 最終更新日 2023-11-22 実験手法 X-RAY DIFFRACTION (1.12 Å) 主引用文献 Hydrophobic surface residues can stabilize a protein through improved water-protein interactions. Febs J., 2019
5XX8	Hetero-micro-seeding: Crystal structure of BPTI-[555]C14GA38I variant using micro-seeds from -C14GA38L variant 分子名称: Pancreatic trypsin inhibitor, SULFATE ION 著者 Islam, M.M. 登録日 2017-07-01 公開日 2018-07-04 最終更新日 2024-10-23 実験手法 X-RAY DIFFRACTION (1.3 Å) 主引用文献 A hetero-micro-seeding strategy for readily crystallizing closely related protein variants Biochem. Biophys. Res. Commun., 493, 2017
5XX7	Hetero-micro-seeding: Crystal structure of BPTI-[5,55]C14GA38I variant using micro-seeds from -C14GA38I variant 分子名称: Pancreatic trypsin inhibitor, SULFATE ION 著者 Islam, M.M. 登録日 2017-07-01 公開日 2018-07-04 最終更新日 2023-11-22 実験手法 X-RAY DIFFRACTION (1.38 Å) 主引用文献 A hetero-micro-seeding strategy for readily crystallizing closely related protein variants Biochem. Biophys. Res. Commun., 493, 2017
5XX6	Hetero-micro-seeding: Crystal structure of BPTI-[5,55]C14GA38I variant using micro-seeds from -C14GA38G variant 分子名称: Pancreatic trypsin inhibitor, SULFATE ION 著者 Islam, M.M. 登録日 2017-07-01 公開日 2018-07-04 最終更新日 2024-10-16 実験手法 X-RAY DIFFRACTION (1.31 Å) 主引用文献 A hetero-micro-seeding strategy for readily crystallizing closely related protein variants Biochem. Biophys. Res. Commun., 493, 2017
1ADZ	THE SOLUTION STRUCTURE OF THE SECOND KUNITZ DOMAIN OF TISSUE FACTOR PATHWAY INHIBITOR, NMR, 30 STRUCTURES 分子名称: TISSUE FACTOR PATHWAY INHIBITOR 著者 Burgering, M.J.M, Orbons, L.P.M. 登録日 1997-02-19 公開日 1998-02-25 最終更新日 2024-10-30 実験手法 SOLUTION NMR 主引用文献 The second Kunitz domain of human tissue factor pathway inhibitor: cloning, structure determination and interaction with factor Xa. J.Mol.Biol., 269, 1997

<40414243444546474849505152535455>