1fzz

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Revision as of 16:26, 20 November 2007 by OCA (talk | contribs) (New page: left|200px<br /><applet load="1fzz" size="450" color="white" frame="true" align="right" spinBox="true" caption="1fzz, resolution 1.86Å" /> '''THE CRYSTAL STRUCTUR...)
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File:1fzz.gif


1fzz, resolution 1.86Å

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THE CRYSTAL STRUCTURE OF THE COMPLEX OF NON-PEPTIDIC INHIBITOR ONO-6818 AND PORCINE PANCREATIC ELASTASE.

OverviewOverview

The crystal structure of a new inhibitor of human neutrophil elastase, (HNE), N-[2-[5-(tert-butyl)-1,3,4-oxadiazol-2-yl]-(IRS)-1-(methylethyl)-2-oxoethy, l]-2-(5-amino-6-oxo-2-phenyl-6H-pyrimidin-1-ly)acetamide (ONO-6818, 1), complexed to porcine pancreatic elastase (PPE) has been determined at 1.86, A resolution. Analytical results provided evidence of a 1:1 complex in, which the electrophilic ketone of 1 covalently bound to O gamma of Ser195, at the active site of PPE. The role of the unique electron-withdrawing, ketone of 1 has been elucidated.

About this StructureAbout this Structure

1FZZ is a Single protein structure of sequence from Sus scrofa with 681 as ligand. Active as Pancreatic elastase, with EC number 3.4.21.36 Full crystallographic information is available from OCA.

ReferenceReference

The crystal structure of the complex of non-peptidic inhibitor of human neutrophil elastase ONO-6818 and porcine pancreatic elastase., Odagaki Y, Ohmoto K, Matsuoka S, Hamanaka N, Nakai H, Toda M, Katsuya Y, Bioorg Med Chem. 2001 Mar;9(3):647-51. PMID:11310599

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