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Results 1 - 10 of 45

EC Number	Substrates	Commentary Substrates	Organism	Products	Commentary (Products)	Reversibility
2.6.1.28	L-tryptophan + 2-oxobutanoate	weak activity	Pseudomonas sp.	3-indole-2-oxopropanoate + 2-aminobutanoate	-	r
2.6.1.28	L-tryptophan + 4-hydroxyphenylpyruvate	15% of the activity with phenylpyruvate	Aspergillus nidulans	3-indole-2-oxopropanoate + ?	-	?
2.6.1.28	L-tryptophan + pyruvate	2% of the activity with alpha-ketoisocaproate	Pseudomonas sp.	3-indole-2-oxopropanoate + L-alanine	-	r
2.6.1.28	L-tryptophan + 2-oxoglutarate	-	Agrobacterium tumefaciens	3-indole-2-oxopropanoate + L-glutamate	-	r
2.6.1.28	L-tryptophan + 2-oxoglutarate	no activity	Pseudomonas sp.	3-indole-2-oxopropanoate + L-glutamate	-	?
2.6.1.28	L-tryptophan + 2-oxoisohexanoate	-	Pseudomonas sp.	3-indole-2-oxopropanoate + L-leucine	-	r
2.6.1.28	L-tryptophan + 2-oxohexanoate	-	Pseudomonas sp.	3-indole-2-oxopropanoate + L-norleucine	-	r
2.6.1.28	L-tryptophan + phenylpyruvate	-	Aspergillus nidulans	3-indole-2-oxopropanoate + L-phenylalanine	-	?
2.6.1.28	L-tryptophan + phenylpyruvate	-	Pseudomonas sp.	3-indole-2-oxopropanoate + L-phenylalanine	i.e. indolepyruvate + L-Phe	r
2.6.1.28	L-tryptophan + phenylpyruvate	phenylpyruvate is the most effective amino acceptor, in the reverse reaction phenylalanine is the most effective amino donor	Agrobacterium tumefaciens	3-indole-2-oxopropanoate + L-phenylalanine	i.e. indolepyruvate + L-Phe	r

Results 1 - 10 of 45

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Release 2023.1 (January 2023)