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<< < Results 11 - 20 of 20
EC Number Natural Substrates Commentary (Nat. Sub.)
Show all pathways known for 2.7.4.14Display the word mapDisplay the reaction diagram Show all sequences 2.7.4.14ATP + dCMP higher activity with the D-enantiomer compared to the L-enantiomer
Show all pathways known for 2.7.4.14Display the word mapDisplay the reaction diagram Show all sequences 2.7.4.14ATP + dUMP -
Show all pathways known for 2.7.4.14Display the word mapDisplay the reaction diagram Show all sequences 2.7.4.14ATP + dUMP higher activity with the D-enantiomer compared to the L-enantiomer
Show all pathways known for 2.7.4.14Display the word mapDisplay the reaction diagram Show all sequences 2.7.4.14ATP + gemcitabine i.e. 2',2'-difluorodeoxycytidine
Show all pathways known for 2.7.4.14Display the word mapDisplay the reaction diagram Show all sequences 2.7.4.14ATP + UMP -
Show all pathways known for 2.7.4.14Display the word mapDisplay the reaction diagram Show all sequences 2.7.4.14ATP + UMP the enzyme plays a crucial role in the formation of UDP, CDP and dCDP which are required for cellular nucleic acid synthesis
Show all pathways known for 2.7.4.14Display the word mapDisplay the reaction diagram Show all sequences 2.7.4.14ATP + UMP the enzyme catalyses an important step in the phosphorylation of UTP, CTP and cCTP. It is also involved in the necessary phosphorylation by cellular kinases of nucleoside analogs used in antiviral therapies
Show all pathways known for 2.7.4.14Display the word mapDisplay the reaction diagram Show all sequences 2.7.4.14more the enzyme is involved in the phosphorylation of nucleic acid precursors, and is critical in the ribo- and deoxyribonucleoside salvage pathway, as well as the anabolic phosphorylation of nucleoside analogues used in viral and anticancer therapies, e.g. cidofovir, which is activated by the enzyme, overview
Show all pathways known for 2.7.4.14Display the word mapDisplay the reaction diagram Show all sequences 2.7.4.14more UMP-CMPK2 may have other functions in addition to the supply of substrates for mtDNA synthesis, it is highly expressed in leukemia cells, in bone marrow, and is tightly correlated with macrophage activation and inflammatory response
Show all pathways known for 2.7.4.14Display the word mapDisplay the reaction diagram Show all sequences 2.7.4.14more hyperensitivity and resistance against anti-cancer drugs in the different cervical tumour cell lines, effects of changes on UMP/CMPK1 expression on CTP and UTP synthesis , overview
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