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New page: left|200px<br /><applet load="1dj5" size="450" color="white" frame="true" align="right" spinBox="true" caption="1dj5, resolution 1.93Å" /> '''CRYSTAL STRUCTURE OF...
 
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[[Image:1dj5.gif|left|200px]]<br /><applet load="1dj5" size="450" color="white" frame="true" align="right" spinBox="true"  
[[Image:1dj5.gif|left|200px]]<br /><applet load="1dj5" size="350" color="white" frame="true" align="right" spinBox="true"  
caption="1dj5, resolution 1.93&Aring;" />
caption="1dj5, resolution 1.93&Aring;" />
'''CRYSTAL STRUCTURE OF R48A MUTANT OF CYTOCHROME C PEROXIDASE WITH N-HYDROXYGUANIDINE BOUND'''<br />
'''CRYSTAL STRUCTURE OF R48A MUTANT OF CYTOCHROME C PEROXIDASE WITH N-HYDROXYGUANIDINE BOUND'''<br />


==Overview==
==Overview==
Heme enzymes are capable of catalyzing a range of oxidative chemistry with, high specificity, depending on the surrounding protein environment. We, describe here a reaction catalyzed by a mutant of cytochrome c peroxidase, which is similar but distinct from those catalyzed by nitric-oxide, synthase. In the R48A mutant, an expanded water-filled cavity was created, above the distal heme face. N-hydroxyguanidine (NHG) but not guanidine was, shown to bind in the cavity with K(d) = 8.5 mM, and coordinate to the heme, to give a low spin state. Reaction of R48A with peroxide produced a, Fe(IV)=O/Trp(.+) center capable of oxidizing either NHG or, N(omega)-hydroxyarginine (NHA), but not arginine or guanidine, by a, multi-turnover catalytic process. Oxidation of either NHG or NHA by R48A, did not result in the accumulation of NO, NO(2)(-), NO(3)(-), urea, or, citrulline, but instead afforded a yellow product with absorption maxima, of 257 and 400 nm. Mass spectrometry of the derivatized NHA products, identified the yellow species as N-nitrosoarginine. We suggest that a, nitrosylating agent, possibly derived from HNO, is produced by the, oxidation of one molecule of substrate. This then reacts with a second, substrate molecule to form the observed N-nitroso products. This complex, chemistry illustrates how the active sites of enzymes such as nitric-oxide, synthase may serve to prevent alternative reactions from occurring, in, addition to enabling those desired.
Heme enzymes are capable of catalyzing a range of oxidative chemistry with high specificity, depending on the surrounding protein environment. We describe here a reaction catalyzed by a mutant of cytochrome c peroxidase, which is similar but distinct from those catalyzed by nitric-oxide synthase. In the R48A mutant, an expanded water-filled cavity was created above the distal heme face. N-hydroxyguanidine (NHG) but not guanidine was shown to bind in the cavity with K(d) = 8.5 mM, and coordinate to the heme to give a low spin state. Reaction of R48A with peroxide produced a Fe(IV)=O/Trp(.+) center capable of oxidizing either NHG or N(omega)-hydroxyarginine (NHA), but not arginine or guanidine, by a multi-turnover catalytic process. Oxidation of either NHG or NHA by R48A did not result in the accumulation of NO, NO(2)(-), NO(3)(-), urea, or citrulline, but instead afforded a yellow product with absorption maxima of 257 and 400 nm. Mass spectrometry of the derivatized NHA products identified the yellow species as N-nitrosoarginine. We suggest that a nitrosylating agent, possibly derived from HNO, is produced by the oxidation of one molecule of substrate. This then reacts with a second substrate molecule to form the observed N-nitroso products. This complex chemistry illustrates how the active sites of enzymes such as nitric-oxide synthase may serve to prevent alternative reactions from occurring, in addition to enabling those desired.


==About this Structure==
==About this Structure==
1DJ5 is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Saccharomyces_cerevisiae Saccharomyces cerevisiae] with HEM and HGU as [http://en.wikipedia.org/wiki/ligands ligands]. Active as [http://en.wikipedia.org/wiki/Cytochrome-c_peroxidase Cytochrome-c peroxidase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=1.11.1.5 1.11.1.5] Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1DJ5 OCA].  
1DJ5 is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Saccharomyces_cerevisiae Saccharomyces cerevisiae] with <scene name='pdbligand=HEM:'>HEM</scene> and <scene name='pdbligand=HGU:'>HGU</scene> as [http://en.wikipedia.org/wiki/ligands ligands]. Active as [http://en.wikipedia.org/wiki/Cytochrome-c_peroxidase Cytochrome-c peroxidase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=1.11.1.5 1.11.1.5] Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1DJ5 OCA].  


==Reference==
==Reference==
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[[Category: Saccharomyces cerevisiae]]
[[Category: Saccharomyces cerevisiae]]
[[Category: Single protein]]
[[Category: Single protein]]
[[Category: Goodin, D.B.]]
[[Category: Goodin, D B.]]
[[Category: Hirst, J.]]
[[Category: Hirst, J.]]
[[Category: HEM]]
[[Category: HEM]]
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[[Category: oxidoreductase]]
[[Category: oxidoreductase]]


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