1qxw

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{{STRUCTURE_1qxw| PDB=1qxw | SCENE= }}
{{STRUCTURE_1qxw| PDB=1qxw | SCENE= }}
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'''Crystal structure of Staphyloccocus aureus in complex with an aminoketone inhibitor 54135.'''
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===Crystal structure of Staphyloccocus aureus in complex with an aminoketone inhibitor 54135.===
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==Overview==
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High-resolution crystal structures of Staphylococcus aureus methionine aminopeptidase I in complex with various keto heterocycles and aminoketones were determined, and the intermolecular ligand interactions with the enzyme are reported. The compounds are effective inhibitors of the S. aureus enzyme because of the formation of an uncleavable tetrahedral intermediate upon binding. The electron densities unequivocally show the enzyme-catalyzed transition-state analogue mimicking that for amide bond hydrolysis of substrates.
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(as it appears on PubMed at http://www.pubmed.gov), where 14998322 is the PubMed ID number.
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{{ABSTRACT_PUBMED_14998322}}
==About this Structure==
==About this Structure==
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[[Category: Oefner, C.]]
[[Category: Oefner, C.]]
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Revision as of 23:22, 28 July 2008

Image:1qxw.png

Template:STRUCTURE 1qxw

Crystal structure of Staphyloccocus aureus in complex with an aminoketone inhibitor 54135.

Template:ABSTRACT PUBMED 14998322

About this Structure

1QXW is a Single protein structure of sequence from Staphylococcus aureus. Full crystallographic information is available from OCA.

Reference

Crystal structures of Staphylococcusaureus methionine aminopeptidase complexed with keto heterocycle and aminoketone inhibitors reveal the formation of a tetrahedral intermediate., Douangamath A, Dale GE, D'Arcy A, Almstetter M, Eckl R, Frutos-Hoener A, Henkel B, Illgen K, Nerdinger S, Schulz H, Mac Sweeney A, Thormann M, Treml A, Pierau S, Wadman S, Oefner C, J Med Chem. 2004 Mar 11;47(6):1325-8. PMID:14998322

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