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Results 1 - 10 of 10
EC Number Application Commentary Reference
Show all pathways known for 2.7.4.22Display the reaction diagram Show all sequences 2.7.4.22drug development as bacterial UMP kinases have no counterpart in eukaryotes, the information provided here can help the design of new antibiotics 665637
Show all pathways known for 2.7.4.22Display the reaction diagram Show all sequences 2.7.4.22drug development potential drug target for development of antimicrobial agents, diseases such as urethritis and prostatitis 692284
Show all pathways known for 2.7.4.22Display the reaction diagram Show all sequences 2.7.4.22drug development potential target for antibacterial drugs 665362
Show all pathways known for 2.7.4.22Display the reaction diagram Show all sequences 2.7.4.22drug development since bacterial UMPKs are specific for the phosphorylation of UMP only and differ from eukaryotic dual-specificity UMP/CMP kinases -, 690286
Show all pathways known for 2.7.4.22Display the reaction diagram Show all sequences 2.7.4.22drug development the enzyme is a potential antibacterial drug target 692284
Show all pathways known for 2.7.4.22Display the reaction diagram Show all sequences 2.7.4.22drug development the enzyme is a potential drug target for developing novel anti-tuberculosis drugs -, 738429
Show all pathways known for 2.7.4.22Display the reaction diagram Show all sequences 2.7.4.22drug development the enzyme is a target for antimicrobial drug development 671130
Show all pathways known for 2.7.4.22Display the reaction diagram Show all sequences 2.7.4.22drug development the enzyme is found only in bacteria and is a target for the discovery of antibacterials -, 737591
Show all pathways known for 2.7.4.22Display the reaction diagram Show all sequences 2.7.4.22drug development UMP kinase may be a potential antimicrobial target 666054
Show all pathways known for 2.7.4.22Display the reaction diagram Show all sequences 2.7.4.22medicine interest in new therapies against anthrax has arisen from its potential for bioterrorism. The allosteric pocket of the enzyme, with its atypical configuration of side chains, may provide a particularly suitable site for pharmacological intervention -, 693652
Results 1 - 10 of 10