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Yorodumi- PDB-1eas: NONPEPTIDIC INHIBITORS OF HUMAN LEUKOCYTE ELASTASE. 3. DESIGN, SY... -
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Open data
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Basic information
| Entry | Database: PDB / ID: 1eas | ||||||
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| Title | NONPEPTIDIC INHIBITORS OF HUMAN LEUKOCYTE ELASTASE. 3. DESIGN, SYNTHESIS, X-RAY CRYSTALLOGRAPHIC ANALYSIS, AND STRUCTURE-ACTIVITY RELATIONSHIPS FOR A SERIES OF ORALLY ACTIVE 3-AMINO-6-PHENYLPYRIDIN-2-ONE TRIFLUOROMETHYL KETONES | ||||||
Components | PORCINE PANCREATIC ELASTASE | ||||||
Keywords | HYDROLASE (SERINE PROTEASE) | ||||||
| Function / homology | Function and homology informationpancreatic elastase / serine-type endopeptidase activity / proteolysis / extracellular space / metal ion binding Similarity search - Function | ||||||
| Biological species | ![]() | ||||||
| Method | X-RAY DIFFRACTION / Resolution: 1.8 Å | ||||||
Authors | Ceccarelli, C. | ||||||
Citation | Journal: J.Med.Chem. / Year: 1994Title: Nonpeptidic inhibitors of human leukocyte elastase. 3. Design, synthesis, X-ray crystallographic analysis, and structure-activity relationships for a series of orally active 3-amino-6- ...Title: Nonpeptidic inhibitors of human leukocyte elastase. 3. Design, synthesis, X-ray crystallographic analysis, and structure-activity relationships for a series of orally active 3-amino-6-phenylpyridin-2-one trifluoromethyl ketones. Authors: Bernstein, P.R. / Andisik, D. / Bradley, P.K. / Bryant, C.B. / Ceccarelli, C. / Damewood Jr., J.R. / Earley, R. / Edwards, P.D. / Feeney, S. / Gomes, B.C. / Kosmider, B.J. / Steelman, G.B. / ...Authors: Bernstein, P.R. / Andisik, D. / Bradley, P.K. / Bryant, C.B. / Ceccarelli, C. / Damewood Jr., J.R. / Earley, R. / Edwards, P.D. / Feeney, S. / Gomes, B.C. / Kosmider, B.J. / Steelman, G.B. / Thomas, R.M. / Vacek, E.P. / Veale, C.A. / Williams, J.C. / Wolanin, D.J. / Woolson, J.A. #1: Journal: To be PublishedTitle: Nonpeptidic Inhibitors of Human Leukocyte Elastase. 6. Design of a Potent, Intratracheally Active, Pyridone-Based Trifluoromethyl Ketone Authors: Bernstein, P.R. / Gomes, B.C. / Kosmider, B.J. / Vacek, E.P. / Williams, J.C. #2: Journal: To be PublishedTitle: Nonpeptidic Inhibitors of Human Leukocyte Elastase. 5. Design, Synthesis, and X-Ray Crystallography of a Series of Orally Active 5-Amino-Pyrimidin-6-One-Containing Trifluoromethylketones Authors: Veale, C.A. / Bernstein, P.R. / Bryant, C. / Ceccarelli, C. / Damewood, J.R. / Earley, R. / Feeney, S.W. / Gomes, B. / Kosmider, B.J. / Steelman, G.B. / Thomas, R.M. / Vacek, E.P. / ...Authors: Veale, C.A. / Bernstein, P.R. / Bryant, C. / Ceccarelli, C. / Damewood, J.R. / Earley, R. / Feeney, S.W. / Gomes, B. / Kosmider, B.J. / Steelman, G.B. / Thomas, R.M. / Vacek, E.P. / Williams, J.C. / Wolanin, D.J. / Woolson, S. #3: Journal: To be PublishedTitle: Nonpeptidic Inhibitors of Human Leukocyte Elastase. 4. Design, Synthesis,in Vitro, and in Vivo Activity of a Series of Beta-Carbolinone-Containing Trifluoromethyl Ketones Authors: Veale, C.A. / Damewood, J.R. / Steelman, G.B. / Bryant, C. / Gomes, B. / Williams, J. #4: Journal: J.Med.Chem. / Year: 1994Title: Nonpeptidic Inhibitors of Human Leukocyte Elastase. 2. Design, Synthesis and in Vitro Activity of a Series of 3-Amino-6-Arylpyridin-2-One Trifluoromethyl Ketones Authors: Damewood, J.R. / Edwards, P.D. / Feeney, S. / Gomes, B.C. / Steelman, G.B. / Tuthill, P.A. / Warner, P. / Williams, J.C. / Woolson, S.A. / Wolanin, D. / Veale, C. #5: Journal: J.Med.Chem. / Year: 1994Title: Nonpeptidic Inhibitors of Human Leukocyte Elastase. 1. The Design and Synthesis of Pyridone-Containing Inhibitors Authors: Warner, P. / Green, R.C. / Gomes, B.C. / Williams, J.C. #6: Journal: J.Med.Chem. / Year: 1994Title: Design of Orally Active, Nonpeptidic Inhibitors of Human Leukocyte Elastase Authors: Brown, F.J. / Andisik, D.W. / Bernstein, P.R. / Bryant, C.B. / Ceccarelli, C. / Damewood, J.R. / Edwards, P.D. / Earley, R. / Feeney, S.W. / Green, R.C. / Gomes, B. / Kosmider, B.J. / Krell, ...Authors: Brown, F.J. / Andisik, D.W. / Bernstein, P.R. / Bryant, C.B. / Ceccarelli, C. / Damewood, J.R. / Edwards, P.D. / Earley, R. / Feeney, S.W. / Green, R.C. / Gomes, B. / Kosmider, B.J. / Krell, R. / Shaw, A. / Steelman, G.B. / Thomas, R.M. / Vacek, E.P. / Veale, C.A. / Tuthill, P.A. / Warner, P. / Williams, J.C. / Wolanin, D.J. / Woolson, S.A. #7: Journal: J.Am.Chem.Soc. / Year: 1992Title: Design, Synthesis, and Kinetic Evaluation of a Unique Class of Elastase Inhibitors, the Peptidyl Alpha-Ketobenzoxazoles,and the X-Ray Crystal Structure of the Covalent Complex between Porcine ...Title: Design, Synthesis, and Kinetic Evaluation of a Unique Class of Elastase Inhibitors, the Peptidyl Alpha-Ketobenzoxazoles,and the X-Ray Crystal Structure of the Covalent Complex between Porcine Pancreatic Elastase and Ac-Ala-Pro-Val-2-Benzoxazole Authors: Edwards, P.D. / Meyer, E.F. / Vijayalakshmi, J. / Tuthill, P.A. / Andisik, D.A. / Gomes, B. / Strimpler, A. #8: Journal: J.Am.Chem.Soc. / Year: 1989Title: Crystal Structure of the Covalent Complex Formed by a Peptidyl Alpha,Alpha-Difluoro-Beta-Keto Amide with Porcine Pancreatic Elastase at 1.78-Angstrom Resolution Authors: Takahashi, L.H. / Radhakrishnan, R. / Rosenfield, R.E. / Meyer, E.F. / Trainor, D.A. #9: Journal: J.Mol.Biol. / Year: 1988Title: X-Ray Diffraction Analysis of the Inhibition of Porcine Pancreatic Elastase by a Peptidyl Trifluoromethylketone Authors: Takahashi, L.H. / Radhakrishnan, R. / Rosenfield, R.E. / Meyer, E.F. / Trainor, D.A. / Stein, M. | ||||||
| History |
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Structure visualization
| Structure viewer | Molecule: Molmil Jmol/JSmol |
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Downloads & links
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Download
| PDBx/mmCIF format | 1eas.cif.gz | 65.2 KB | Display | PDBx/mmCIF format |
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| PDB format | pdb1eas.ent.gz | 46.2 KB | Display | PDB format |
| PDBx/mmJSON format | 1eas.json.gz | Tree view | PDBx/mmJSON format | |
| Others | Other downloads |
-Validation report
| Summary document | 1eas_validation.pdf.gz | 769 KB | Display | wwPDB validaton report |
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| Full document | 1eas_full_validation.pdf.gz | 771.1 KB | Display | |
| Data in XML | 1eas_validation.xml.gz | 12.6 KB | Display | |
| Data in CIF | 1eas_validation.cif.gz | 17.4 KB | Display | |
| Arichive directory | https://data.pdbj.org/pub/pdb/validation_reports/ea/1eas ftp://data.pdbj.org/pub/pdb/validation_reports/ea/1eas | HTTPS FTP |
-Related structure data
| Similar structure data |
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Links
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Assembly
| Deposited unit | ![]()
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| Unit cell |
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Components
| #1: Protein | Mass: 25928.031 Da / Num. of mol.: 1 Source method: isolated from a genetically manipulated source Source: (gene. exp.) ![]() | ||||||||
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| #2: Chemical | ChemComp-NA / | ||||||||
| #3: Chemical | | #4: Chemical | ChemComp-TFK / | #5: Water | ChemComp-HOH / | Has protein modification | Y | Nonpolymer details | C2 OF HET GROUP TFK IS COVALENTLY | |
-Experimental details
-Experiment
| Experiment | Method: X-RAY DIFFRACTION |
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Sample preparation
| Crystal | Density Matthews: 2.18 Å3/Da / Density % sol: 43.69 % |
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| Crystal grow | *PLUS Method: unknown |
-Data collection
| Radiation | Scattering type: x-ray |
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| Radiation wavelength | Relative weight: 1 |
| Reflection | Num. obs: 19195 / % possible obs: 88 % / Observed criterion σ(F): 2 |
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Processing
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| Refinement | Resolution: 1.8→10 Å / σ(F): 2
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| Displacement parameters | Biso mean: 19.7 Å2 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Refine analyze | Luzzati coordinate error obs: 0.2 Å | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Refinement step | Cycle: LAST / Resolution: 1.8→10 Å
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| Refine LS restraints |
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| Software | *PLUS Name: X-PLOR / Classification: refinement | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Refinement | *PLUS Rfactor obs: 0.183 / Rfactor Rwork: 0.183 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Solvent computation | *PLUS | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Displacement parameters | *PLUS | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Refine LS restraints | *PLUS
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