PDB ID: 1B0F
Hetero Atom Contents
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Code | Name | Style | Show | Link | |
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SEI | 1-{3-methyl-2-[4-(morpholine-4-carbonyl)-benzoylamino]-butyryl}-pyrrolidine-2-carboxylic acid (3,3,4,4,4-pentafluoro-1-isopropyl-2-oxo-butyl)-amide | PoSSuM |
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FUC | Alpha-L-fucopyranose | |
NAG | 2-acetamido-2-deoxy-beta-D-glucopyranose |
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Download interaction data: 1B0F
Structure summary
Code : | 1B0F PDBj RCSB PDB PDBe | ||||||||||||
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Header : | HYDROLASE | ||||||||||||
Title : | CRYSTAL STRUCTURE OF HUMAN NEUTROPHIL ELASTASE WITH MDL 101, 146 | ||||||||||||
Release Data : | 1998-11-09 | ||||||||||||
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Authors : | Schreuder, H.A., Metz, W.A., Peet, N.P., Pelton, J.T., Tardif, C. | ||||||||||||
Keywords : | SERINE PROTEASE, FLUOROETHYL KETONES, HYDROLASE | ||||||||||||
Exp. method : | X-RAY DIFFRACTION ( 3.00 Å ) | ||||||||||||
Citation : |
Inhibition of human neutrophil elastase. 4. Design, synthesis, X-ray crystallographic analysis, and structure-activity relationships for a series of P2-modified, orally active peptidyl pentafluoroethyl ketones.
Cregge, R.J.,Durham, S.L.,Farr, R.A.
et al.
PubMed: 9651152 |
Reaction
Chain : | A | ||||||||
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UniProt : | P08246 (ELNE_HUMAN) | ||||||||
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