1uaq: Difference between revisions
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New page: left|200px<br /><applet load="1uaq" size="450" color="white" frame="true" align="right" spinBox="true" caption="1uaq, resolution 1.6Å" /> '''The crystal structure... |
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[[Image:1uaq.gif|left|200px]]<br /><applet load="1uaq" size=" | [[Image:1uaq.gif|left|200px]]<br /><applet load="1uaq" size="350" color="white" frame="true" align="right" spinBox="true" | ||
caption="1uaq, resolution 1.6Å" /> | caption="1uaq, resolution 1.6Å" /> | ||
'''The crystal structure of yeast cytosine deaminase'''<br /> | '''The crystal structure of yeast cytosine deaminase'''<br /> | ||
==Overview== | ==Overview== | ||
Yeast cytosine deaminase is an attractive candidate for anticancer gene | Yeast cytosine deaminase is an attractive candidate for anticancer gene therapy because it catalyzes the deamination of the prodrug 5-fluorocytosine to form 5-fluorouracil. We report here the crystal structure of the enzyme in complex with the inhibitor 2-hydroxypyrimidine at 1.6-A resolution. The protein forms a tightly packed dimer with an extensive interface of 1450 A2 per monomer. The inhibitor was converted into a hydrated adduct as a transition-state analog. The essential zinc ion is ligated by the 4-hydroxyl group of the inhibitor together with His62, Cys91, and Cys94 from the protein. The enzyme shares similar active-site architecture to cytidine deaminases and an unusually high structural homology to 5-aminoimidazole-4-carboxamide-ribonucleotide transformylase and thereby may define a new superfamily. The unique C-terminal tail is involved in substrate specificity and also functions as a gate controlling access to the active site. The complex structure reveals a closed conformation, suggesting that substrate binding seals the active-site entrance so that the catalytic groups are sequestered from solvent. A comparison of the crystal structures of the bacterial and fungal cytosine deaminases provides an elegant example of convergent evolution, where starting from unrelated ancestral proteins, the same metal-assisted deamination is achieved through opposite chiral intermediates within distinctly different active sites. | ||
==About this Structure== | ==About this Structure== | ||
1UAQ 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 ZN and DUC as [http://en.wikipedia.org/wiki/ligands ligands]. Active as [http://en.wikipedia.org/wiki/Cytosine_deaminase Cytosine deaminase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=3.5.4.1 3.5.4.1] Full crystallographic information is available from [http:// | 1UAQ 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=ZN:'>ZN</scene> and <scene name='pdbligand=DUC:'>DUC</scene> as [http://en.wikipedia.org/wiki/ligands ligands]. Active as [http://en.wikipedia.org/wiki/Cytosine_deaminase Cytosine deaminase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=3.5.4.1 3.5.4.1] Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1UAQ OCA]. | ||
==Reference== | ==Reference== | ||
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[[Category: Saccharomyces cerevisiae]] | [[Category: Saccharomyces cerevisiae]] | ||
[[Category: Single protein]] | [[Category: Single protein]] | ||
[[Category: Hsu, Y | [[Category: Hsu, Y H.]] | ||
[[Category: Hu, C | [[Category: Hu, C Y.]] | ||
[[Category: Ko, T | [[Category: Ko, T P.]] | ||
[[Category: Liaw, S | [[Category: Liaw, S H.]] | ||
[[Category: Lin, J | [[Category: Lin, J J.]] | ||
[[Category: Wang, A | [[Category: Wang, A H.J.]] | ||
[[Category: DUC]] | [[Category: DUC]] | ||
[[Category: ZN]] | [[Category: ZN]] | ||
[[Category: alpha-beta-alpha]] | [[Category: alpha-beta-alpha]] | ||
''Page seeded by [http:// | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 15:22:24 2008'' | ||