1uaq

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[[Image:1uaq.gif|left|200px]]
[[Image:1uaq.gif|left|200px]]
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{{Structure
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<!--
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|PDB= 1uaq |SIZE=350|CAPTION= <scene name='initialview01'>1uaq</scene>, resolution 1.6&Aring;
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The line below this paragraph, containing "STRUCTURE_1uaq", creates the "Structure Box" on the page.
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|SITE=
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You may change the PDB parameter (which sets the PDB file loaded into the applet)
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|LIGAND= <scene name='pdbligand=DUC:DIHYDROPYRIMIDINE-2,4(1H,3H)-DIONE'>DUC</scene>, <scene name='pdbligand=ZN:ZINC+ION'>ZN</scene>
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or the SCENE parameter (which sets the initial scene displayed when the page is loaded),
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|ACTIVITY= <span class='plainlinks'>[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] </span>
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or leave the SCENE parameter empty for the default display.
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|GENE= fcy1 ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=4932 Saccharomyces cerevisiae])
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-->
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|DOMAIN=
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{{STRUCTURE_1uaq| PDB=1uaq | SCENE= }}
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|RELATEDENTRY=[[1k70|1k70]]
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|RESOURCES=<span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=1uaq FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1uaq OCA], [http://www.ebi.ac.uk/pdbsum/1uaq PDBsum], [http://www.rcsb.org/pdb/explore.do?structureId=1uaq RCSB]</span>
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}}
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'''The crystal structure of yeast cytosine deaminase'''
'''The crystal structure of yeast cytosine deaminase'''
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[[Category: Lin, J J.]]
[[Category: Lin, J J.]]
[[Category: Wang, A H.J.]]
[[Category: Wang, A H.J.]]
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[[Category: alpha-beta-alpha]]
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[[Category: Alpha-beta-alpha]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sat May 3 10:58:30 2008''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Mon Mar 31 00:07:45 2008''
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Revision as of 07:58, 3 May 2008

Template:STRUCTURE 1uaq

The crystal structure of yeast cytosine deaminase


Overview

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

1UAQ is a Single protein structure of sequence from Saccharomyces cerevisiae. Full crystallographic information is available from OCA.

Reference

Crystal structure of yeast cytosine deaminase. Insights into enzyme mechanism and evolution., Ko TP, Lin JJ, Hu CY, Hsu YH, Wang AH, Liaw SH, J Biol Chem. 2003 May 23;278(21):19111-7. Epub 2003 Mar 13. PMID:12637534 Page seeded by OCA on Sat May 3 10:58:30 2008

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