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Article
Nature Structural Biology  4, 947 - 952 (1997)
doi:10.1038/nsb1197-947

Crystal Structure of the protein drug urate oxidase-inhibitor complex at 2.05 Å resolution

Nathalie Colloc'h1, 6, Mohamed El Hajji2, Bernard Bachet1, Guillaume L'Hermite1, Marc Schiltz3, Thierry Prangé3, 4, Bertrand Castro5 & Jean-Paul Mornon1

  1Systèmes Moleculaires et Biologic Structurale, Laboratoire de Minéralogie-Cristallographie, CNRS URA09, Université Paris VI et Paris VII, case 115,4 place Jussieu, 75252 Paris cedex 05, France.

  2SANOFI Chimie, route d'Avignon, 30390 Aramon, France.

  3LURE, Université Paris-Sud, Bat. 209d, 91405 Orsay cedex, France

  4Chimie Structurale Biomoléculaire, CNRS URA1430, 93017 Bobigny cedex, France.

  5SANOFI Chimie, 82 avenue Raspail, 94255 Gentilly cedex, France.

  6colloch@lmcp.jussieu.fr

The gene coding for urate oxidase, an enzyme that catalyzes the oxidation of uric acid to allantoin, is inactivated in humans. Consequently, urate oxidase is used as a protein drug to overcome severe disorders induced by uric acid accumulation. The structure of the active homotetrameric enzyme reveals the existence of a small architectural domain that we call T-fold (for tunnelling-fold) domain. It assembles to form a perfect unusual dimeric alpha8beta16 barrel. Urate oxidase may be the archetype of an expanding new family of tunnel-shaped proteins that now has three members; tetrahydropterin synthase, GTP cyclohydrolase I and urate oxidase. The structure of the active site of urate oxidase around the 8-azaxanthine inhibitor reveals an original mechanism of oxidation that does not require any ions or prosthetic groups.

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