1jrp: Difference between revisions

New page: left|200px<br /><applet load="1jrp" size="450" color="white" frame="true" align="right" spinBox="true" caption="1jrp, resolution 3.00Å" /> '''Crystal Structure of...
 
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[[Image:1jrp.gif|left|200px]]<br /><applet load="1jrp" size="450" color="white" frame="true" align="right" spinBox="true"  
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caption="1jrp, resolution 3.00&Aring;" />
caption="1jrp, resolution 3.00&Aring;" />
'''Crystal Structure of Xanthine Dehydrogenase inhibited by alloxanthine from Rhodobacter capsulatus'''<br />
'''Crystal Structure of Xanthine Dehydrogenase inhibited by alloxanthine from Rhodobacter capsulatus'''<br />


==Overview==
==Overview==
Xanthine dehydrogenase (XDH), a complex molybdo/iron-sulfur/flavoprotein, catalyzes the oxidation of hypoxanthine to xanthine followed by oxidation, of xanthine to uric acid with concomitant reduction of NAD+. The 2.7 A, resolution structure of Rhodobacter capsulatus XDH reveals that the, bacterial and bovine XDH have highly similar folds despite differences in, subunit composition. The NAD+ binding pocket of the bacterial XDH, resembles that of the dehydrogenase form of the bovine enzyme rather than, that of the oxidase form, which reduces O(2) instead of NAD+. The drug, allopurinol is used to treat XDH-catalyzed uric acid build-up occurring in, gout or during cancer chemotherapy. As a hypoxanthine analog, it is, oxidized to alloxanthine, which cannot be further oxidized but acts as a, tight binding inhibitor of XDH. The 3.0 A resolution structure of the, XDH-alloxanthine complex shows direct coordination of alloxanthine to the, molybdenum via a nitrogen atom. These results provide a starting point for, the rational design of new XDH inhibitors.
Xanthine dehydrogenase (XDH), a complex molybdo/iron-sulfur/flavoprotein, catalyzes the oxidation of hypoxanthine to xanthine followed by oxidation of xanthine to uric acid with concomitant reduction of NAD+. The 2.7 A resolution structure of Rhodobacter capsulatus XDH reveals that the bacterial and bovine XDH have highly similar folds despite differences in subunit composition. The NAD+ binding pocket of the bacterial XDH resembles that of the dehydrogenase form of the bovine enzyme rather than that of the oxidase form, which reduces O(2) instead of NAD+. The drug allopurinol is used to treat XDH-catalyzed uric acid build-up occurring in gout or during cancer chemotherapy. As a hypoxanthine analog, it is oxidized to alloxanthine, which cannot be further oxidized but acts as a tight binding inhibitor of XDH. The 3.0 A resolution structure of the XDH-alloxanthine complex shows direct coordination of alloxanthine to the molybdenum via a nitrogen atom. These results provide a starting point for the rational design of new XDH inhibitors.


==About this Structure==
==About this Structure==
1JRP is a [http://en.wikipedia.org/wiki/Protein_complex Protein complex] structure of sequences from [http://en.wikipedia.org/wiki/Rhodobacter_capsulatus Rhodobacter capsulatus] with CA, FES, MPN, MOS, FAD and 141 as [http://en.wikipedia.org/wiki/ligands ligands]. Active as [http://en.wikipedia.org/wiki/Xanthine_dehydrogenase Xanthine dehydrogenase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=1.17.1.4 1.17.1.4] Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1JRP OCA].  
1JRP is a [http://en.wikipedia.org/wiki/Protein_complex Protein complex] structure of sequences from [http://en.wikipedia.org/wiki/Rhodobacter_capsulatus Rhodobacter capsulatus] with <scene name='pdbligand=CA:'>CA</scene>, <scene name='pdbligand=FES:'>FES</scene>, <scene name='pdbligand=MPN:'>MPN</scene>, <scene name='pdbligand=MOS:'>MOS</scene>, <scene name='pdbligand=FAD:'>FAD</scene> and <scene name='pdbligand=141:'>141</scene> as [http://en.wikipedia.org/wiki/ligands ligands]. Active as [http://en.wikipedia.org/wiki/Xanthine_dehydrogenase Xanthine dehydrogenase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=1.17.1.4 1.17.1.4] Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1JRP OCA].  


==Reference==
==Reference==
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[[Category: Kisker, C.]]
[[Category: Kisker, C.]]
[[Category: Leimkuhler, S.]]
[[Category: Leimkuhler, S.]]
[[Category: Rajagopalan, K.V.]]
[[Category: Rajagopalan, K V.]]
[[Category: Rappa, R.]]
[[Category: Rappa, R.]]
[[Category: Theis, K.]]
[[Category: Theis, K.]]
[[Category: Truglio, J.J.]]
[[Category: Truglio, J J.]]
[[Category: 141]]
[[Category: 141]]
[[Category: CA]]
[[Category: CA]]
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[[Category: partial beta-barrel; xdh; xo]]
[[Category: partial beta-barrel; xdh; xo]]


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