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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="450" color="white" frame="true" align="right" spinBox="true"
caption="1uaq, resolution 1.6&Aring;" />
'''The crystal structure of yeast cytosine deaminase'''<br />


==Overview==
==The crystal structure of yeast cytosine deaminase==
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.
<StructureSection load='1uaq' size='340' side='right'caption='[[1uaq]], [[Resolution|resolution]] 1.60&Aring;' scene=''>
== Structural highlights ==
<table><tr><td colspan='2'>[[1uaq]] is a 2 chain structure with sequence from [https://en.wikipedia.org/wiki/Saccharomyces_cerevisiae Saccharomyces cerevisiae]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1UAQ OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=1UAQ FirstGlance]. <br>
</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 1.6&#8491;</td></tr>
<tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=DUC:DIHYDROPYRIMIDINE-2,4(1H,3H)-DIONE'>DUC</scene>, <scene name='pdbligand=ZN:ZINC+ION'>ZN</scene></td></tr>
<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=1uaq FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1uaq OCA], [https://pdbe.org/1uaq PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=1uaq RCSB], [https://www.ebi.ac.uk/pdbsum/1uaq PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=1uaq ProSAT]</span></td></tr>
</table>
== Function ==
[https://www.uniprot.org/uniprot/FCY1_YEAST FCY1_YEAST] Converts cytosine to uracil or 5-methylcytosine to thymine by deaminating carbon number 4.
== Evolutionary Conservation ==
[[Image:Consurf_key_small.gif|200px|right]]
Check<jmol>
  <jmolCheckbox>
    <scriptWhenChecked>; select protein; define ~consurf_to_do selected; consurf_initial_scene = true; script "/wiki/ConSurf/ua/1uaq_consurf.spt"</scriptWhenChecked>
    <scriptWhenUnchecked>script /wiki/extensions/Proteopedia/spt/initialview01.spt</scriptWhenUnchecked>
    <text>to colour the structure by Evolutionary Conservation</text>
  </jmolCheckbox>
</jmol>, as determined by [http://consurfdb.tau.ac.il/ ConSurfDB]. You may read the [[Conservation%2C_Evolutionary|explanation]] of the method and the full data available from [http://bental.tau.ac.il/new_ConSurfDB/main_output.php?pdb_ID=1uaq ConSurf].
<div style="clear:both"></div>
<div style="background-color:#fffaf0;">
== Publication Abstract from PubMed ==
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==
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<ref>PMID:12637534</ref>
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://ispc.weizmann.ac.il/oca-bin/ocashort?id=1UAQ OCA].


==Reference==
From MEDLINE&reg;/PubMed&reg;, a database of the U.S. National Library of Medicine.<br>
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:[http://ispc.weizmann.ac.il//pmbin/getpm?pmid=12637534 12637534]
</div>
[[Category: Cytosine deaminase]]
<div class="pdbe-citations 1uaq" style="background-color:#fffaf0;"></div>
 
==See Also==
*[[Deaminase 3D structures|Deaminase 3D structures]]
== References ==
<references/>
__TOC__
</StructureSection>
[[Category: Large Structures]]
[[Category: Saccharomyces cerevisiae]]
[[Category: Saccharomyces cerevisiae]]
[[Category: Single protein]]
[[Category: Hsu Y-H]]
[[Category: Hsu, Y.H.]]
[[Category: Hu C-Y]]
[[Category: Hu, C.Y.]]
[[Category: Ko T-P]]
[[Category: Ko, T.P.]]
[[Category: Liaw S-H]]
[[Category: Liaw, S.H.]]
[[Category: Lin J-J]]
[[Category: Lin, J.J.]]
[[Category: Wang AH-J]]
[[Category: Wang, A.H.J.]]
[[Category: DUC]]
[[Category: ZN]]
[[Category: alpha-beta-alpha]]
 
''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Wed Nov 21 03:58:04 2007''

Latest revision as of 23:50, 27 December 2023

The crystal structure of yeast cytosine deaminase

1uaq, resolution 1.60Å

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