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EC Number General Information Commentary Reference
Display the reaction diagram Show all sequences 2.7.8.46physiological function deletion mutants of primase tarK and polymerase tarL, respectively, are viable, each gene is individually dispensable. Mutants of tarK and tarL are not compromised in growth or cell wall teichoic acid levels. A tarK and tarL double deletion cannot be created in a wild-type background -, 740613
Display the reaction diagram Show all sequences 2.7.8.46physiological function in Staphylococcus aureus, a the tarK ortholog is missing from the analyzed strains. It may be functionally replaced by one of the two tarL genes or be compensated for by the extra copy of tarL 740233
Display the reaction diagram Show all sequences 2.7.8.46physiological function TarK is a bifunctional enzyme that catalyzes both ribitol phosphate priming and polymerization, reactions of EC 2.7.18.46 and 2.7.8.47. TarK can replace polymerase TarL provided that it is sufficiently expressed. TarK directs the synthesis of a polyribitol-containing teichoic acid K-WTA. The biosynthesis of K-WTA is repressed by the accessory gene regulator (agr) system -, 740612
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