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Results 1 - 10 of 12 > >>
EC Number Protein Variants Commentary Reference
Show all pathways known for 2.7.6.2Display the word mapDisplay the reaction diagram Show all sequences 2.7.6.2more construction of a double knockout mutant lacking isozymes TPK1 and TPK2, the mutant shows severely depressed levels of TPP and elevated levels of free thiamine compared to the wild-type enzyme 676560
Show all pathways known for 2.7.6.2Display the word mapDisplay the reaction diagram Show all sequences 2.7.6.2S74A mutation causes a 1.4fold increase in turnover number, the Km-value for ATP is 2fold that of the wild-type enzyme 642743
Show all pathways known for 2.7.6.2Display the word mapDisplay the reaction diagram Show all sequences 2.7.6.2D133N mutation causes a selective decrease in the ratio of turnover-number to Km-value for thiamine 642743
Show all pathways known for 2.7.6.2Display the word mapDisplay the reaction diagram Show all sequences 2.7.6.2Q96E mutation causes an 2.5fold increase in the ratio of turnover-number to Km-value for thiamine compared to the wild-type 642743
Show all pathways known for 2.7.6.2Display the word mapDisplay the reaction diagram Show all sequences 2.7.6.2R131G mutation decreases the ratio of turnover-number to Km-value for ATP 642743
Show all pathways known for 2.7.6.2Display the word mapDisplay the reaction diagram Show all sequences 2.7.6.2T99A mutation decreases the ratio of turnover-number to Km-value for ATP 642743
Show all pathways known for 2.7.6.2Display the word mapDisplay the reaction diagram Show all sequences 2.7.6.2D100N mutation reduces turnover-number markedly 642743
Show all pathways known for 2.7.6.2Display the word mapDisplay the reaction diagram Show all sequences 2.7.6.2D71N mutation reduces turnover-number markedly 642743
Show all pathways known for 2.7.6.2Display the word mapDisplay the reaction diagram Show all sequences 2.7.6.2D73N mutation reduces turnover-number markedly 642743
Show all pathways known for 2.7.6.2Display the word mapDisplay the reaction diagram Show all sequences 2.7.6.2D222H naturally occurring homozygous TPK1 mutation in a patient with enzyme deficiency suffering neurological disorder 739080
Results 1 - 10 of 12 > >>