Sandbox Reserved 1452

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== Structural highlights ==
== Structural highlights ==
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Uricase is mainly located in the liver where it forms an elctron dense crystalline core in peroxisomes. It is a tetramer of identical subunits each containing copper binding sites. X-ray crystallography shows that uric acid binds to the active site as a monoanion and is deprotonated as a dianion which is then stabilized by <scene name='77/778332/1vax_substrate_binding/1'>Arg 176 and Gln 228.</scene> This specific enzyme is found in Aspergillus flavus which is a type of bacteria. Uricase can be inhibited by both cyanide and chloride ions. Oxonate competitively inhibits uricase.
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Uricase is mainly located in the liver where it forms an elctron dense crystalline core in peroxisomes. It is a tetramer of identical subunits each containing copper binding sites. One of the four identical subunits of the enzyme can be viewed <scene name='77/778332/1vaxsubunit/1'>here</scene>. X-ray crystallography shows that uric acid binds to the active site as a monoanion and is deprotonated as a dianion which is then stabilized by <scene name='77/778332/1vax_substrate_binding/1'>Arg 176 and Gln 228.</scene> This specific enzyme is found in Aspergillus flavus which is a type of bacteria. Uricase can be inhibited by both cyanide and chloride ions. Oxonate competitively inhibits uricase.
This is <scene name='77/778332/1vax/1'>uricase</scene> without a ligand.
This is <scene name='77/778332/1vax/1'>uricase</scene> without a ligand.
You can view uricase with a ligand <scene name='77/778332/4mb8/1'>here.</scene>
You can view uricase with a ligand <scene name='77/778332/4mb8/1'>here.</scene>

Revision as of 17:41, 3 May 2018

This Sandbox is Reserved from Jan 22 through May 22, 2018 for use in the course Biochemistry II taught by Jason Telford at the Maryville University, St. Louis, Missouri, USA. This reservation includes Sandbox Reserved 1446 through Sandbox Reserved 1455.
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Uricase

Caption for this structure

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References

Bonifacio, and Vicente. “Uric Acid and Evolution | Rheumatology | Oxford Academic.” OUP Academic, Oxford University Press, 13 July 2010, academic.oup.com/rheumatology/article/49/11/2010/1785765.

Gabison, et al. “Near-Atomic Resolution Structures of Urate Oxidase Complexed with Its Substrate and Analogues: the Protonation State of the Ligand.” Acta Crystallogr.,Sect.D, www.rcsb.org/structure/3L8W.

Hossain, et al. “Crystal Structure of Uricase from Arthrobacter Globiformis.” Acta Crystallogr.,Sect.D, www.rcsb.org/structure/1vax.

Kratzer, James T., et al. “Evolutionary History and Metabolic Insights of Ancient Mammalian Uricases.” PNAS, National Academy of Sciences, 11 Mar. 2014, www.pnas.org/content/111/10/3763.short.

Ortlund, E.o., and M.n. Murphy. “Evolutionary History and Metabolic Insights of Ancient Mammalian Uricases.” Evolutionary History and Metabolic Insights of Ancient Mammalian Uricases, 2014, doi:10.2210/pdb4mb8/pdb.

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