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Results 1 - 7 of 7
EC Number Application Commentary Reference
Show all pathways known for 3.7.1.2Display the word mapDisplay the reaction diagram Show all sequences 3.7.1.2biotechnology participation in the synthesis of vitamin E and other tocopherols 670622
Show all pathways known for 3.7.1.2Display the word mapDisplay the reaction diagram Show all sequences 3.7.1.2degradation the enzyme is part of the key catabolic trait for biodegradation of a small number of aromatic compounds -, 669086
Show all pathways known for 3.7.1.2Display the word mapDisplay the reaction diagram Show all sequences 3.7.1.2medicine hereditary tyrosinaemia type 1 results from deficiency of fumarylacetoacetase 684964
Show all pathways known for 3.7.1.2Display the word mapDisplay the reaction diagram Show all sequences 3.7.1.2medicine in humans, deficiency of this activity is associated with the metabolic disease hereditary tyrosinaemia type 1, which is also known as hepatorenal tyrosinaemia 684183
Show all pathways known for 3.7.1.2Display the word mapDisplay the reaction diagram Show all sequences 3.7.1.2medicine plays a role in degradation pathway of phenylalanine and tyrosine 289245, 289246, 289247, 289250, 289251, 289252, 289253, 289254, 289255, 289256, 289257
Show all pathways known for 3.7.1.2Display the word mapDisplay the reaction diagram Show all sequences 3.7.1.2medicine plays a role in hereditary tyrosinemia 289244, 289246, 289247, 289248, 289249, 289251, 289252, 289253, 289255, 289256, 289257
Show all pathways known for 3.7.1.2Display the word mapDisplay the reaction diagram Show all sequences 3.7.1.2medicine type I tyrosinemia is caused by mutations in the fumarylacetoacetate hydrolase gene, the results establish worms as a model for the study of type I tyrosinemia 687809
Results 1 - 7 of 7