1dcs: Difference between revisions

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[[Image:1dcs.gif|left|200px]]
{{Seed}}
[[Image:1dcs.png|left|200px]]


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{{STRUCTURE_1dcs|  PDB=1dcs  |  SCENE=  }}  
{{STRUCTURE_1dcs|  PDB=1dcs  |  SCENE=  }}  


'''DEACETOXYCEPHALOSPORIN C SYNTHASE FROM S. CLAVULIGERUS'''
===DEACETOXYCEPHALOSPORIN C SYNTHASE FROM S. CLAVULIGERUS===




==Overview==
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Penicillins and cephalosporins are among the most widely used therapeutic agents. These antibiotics are produced from fermentation-derived materials as their chemical synthesis is not commercially viable. Unconventional steps in their biosynthesis are catalysed by Fe(II)-dependent oxidases/oxygenases; isopenicillin N synthase (IPNS) creates in one step the bicyclic nucleus of penicillins, and deacetoxycephalosporin C synthase (DAOCS) catalyses the expansion of the penicillin nucleus into the nucleus of cephalosporins. Both enzymes use dioxygen-derived ferryl intermediates in catalysis but, in contrast to IPNS, the ferryl form of DAOCS is produced by the oxidative splitting of a co-substrate, 2-oxoglutarate (alpha-ketoglutarate). This route of controlled ferryl formation and reaction is common to many mononuclear ferrous enzymes, which participate in a broader range of reactions than their well-characterized counterparts, the haem enzymes. Here we report the first crystal structure of a 2-oxoacid-dependent oxygenase. High-resolution structures for apo-DAOCS, the enzyme complexed with Fe(II), and with Fe(II) and 2-oxoglutarate, were obtained from merohedrally twinned crystals. Using a model based on these structures, we propose a mechanism for ferryl formation.
The line below this paragraph, {{ABSTRACT_PUBMED_9723623}}, adds the Publication Abstract to the page
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{{ABSTRACT_PUBMED_9723623}}


==About this Structure==
==About this Structure==
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[[Category: Merohedral twinning]]
[[Category: Merohedral twinning]]
[[Category: Oxidoreductase]]
[[Category: Oxidoreductase]]
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