Structural and Kinetic Characterization of Quinolinate Phosphoribosyltransferase (hQPRTase) from Homo sapiens

Human quinolinate phosphoribosyltransferase (EC 2.4.2.19) (hQPRTase) is a member of the type II phosphoribosyltransferase family involved in the catabolism of quinolinic acid (QA). It catalyses the formation of nicotinic acid mononucleotide from quinolinic acid, which involves a phosphoribosyl trans...

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Published inJournal of molecular biology Vol. 373; no. 3; pp. 755 - 763
Main Authors Liu, Huanting, Woznica, Kerry, Catton, Gemma, Crawford, Amanda, Botting, Nigel, Naismith, James H.
Format Journal Article
LanguageEnglish
Published Netherlands Elsevier Ltd 26.10.2007
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Summary:Human quinolinate phosphoribosyltransferase (EC 2.4.2.19) (hQPRTase) is a member of the type II phosphoribosyltransferase family involved in the catabolism of quinolinic acid (QA). It catalyses the formation of nicotinic acid mononucleotide from quinolinic acid, which involves a phosphoribosyl transfer reaction followed by decarboxylation. hQPRTase has been implicated in a number of neurological conditions and in order to study it further, we have carried out structural and kinetic studies on recombinant hQPRTase. The structure of the fully active enzyme overexpressed in Escherichia coli was solved using multiwavelength methods to a resolution of 2.0 Å. hQPRTase has a α/β barrel fold sharing a similar overall structure with the bacterial QPRTases. The active site of hQPRTase is located at an α/β open sandwich structure that serves as a cup for the α/β barrel of the adjacent subunit with a QA binding site consisting of three arginine residues (R102, R138 and R161) and two lysine residues (K139 and K171). Mutation of these residues affected substrate binding or abolished the enzymatic activity. The kinetics of the human enzyme are different to the bacterial enzymes studied, hQPRTase is inhibited competitively and non-competitively by one of its substrates, 5-phosphoribosylpyrophosphate (PRPP). The human enzyme adopts a hexameric arrangement, which places the active sites in close proximity to each other.
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ISSN:0022-2836
1089-8638
DOI:10.1016/j.jmb.2007.08.043