Undecaprenyl pyrophosphate synthase: Difference between revisions
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Michal Harel (talk | contribs) No edit summary |
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**[[1jp3]] – EcUPP (mutant) <br /> | **[[1jp3]] – EcUPP (mutant) <br /> | ||
**[[2d2r]] – HpUPP (mutant) – ''Helicobacter pylori''<br /> | **[[2d2r]] – HpUPP (mutant) – ''Helicobacter pylori''<br /> | ||
**[[2vg4]] – MtUPP – ''Mycobacterium tuberculosis''<br /> | |||
*Undecaprenyl pyrophosphate synthase complexes | *Undecaprenyl pyrophosphate synthase complexes | ||
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**[[2dtn]] – HpUPP + pyrophosphate<br /> | **[[2dtn]] – HpUPP + pyrophosphate<br /> | ||
**[[3ugs]] - UPP + FPP analog – ''Campylobacter jejuni''<br /> | **[[3ugs]] - UPP + FPP analog – ''Campylobacter jejuni''<br /> | ||
**[[2vg2]] – MtUPP + Pi + PPi + methyl butenyl diphosphate <br /> | |||
**[[2vg3]] – MtUPP + Pi + Mg + geranyl diphosphate <br /> | |||
}} | }} | ||
Revision as of 12:54, 24 June 2015
FunctionUndecaprenyl pyrophosphate synthase (UPP) catalyzes the consecutive condensation of farnesyl pyrophosphate (FPP) with 8 molecules of isopentenyl pyrophosphate (IPP) to produce undecaprenyl pyrophosphate. Undecaprenyl pyrophosphate serves as a lipid carrier for peptidoglycan synthesis of bacterial cell wall. Bisphosphonate drugs are UPP inhibitors. DiseaseRelevanceStructural highlights |
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3D structures of undecaprenyl pyrophosphate synthase3D structures of undecaprenyl pyrophosphate synthase
Updated on 24-June-2015