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Literature summary for 4.1.1.74 extracted from

  • Harris, D.; Berrue, F.; Kerr, R.; Patten, C.
    Metabolomic analysis of indolepyruvate decarboxylase pathway derivatives in the rhizobacterium Enterobacter cloacae (2018), Rhizosphere, 6, 98-111 .
No PubMed abstract available

Organism

Organism UniProt Comment Textmining
Enterobacter cloacae Q9FDC2
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Enterobacter cloacae UW5 Q9FDC2
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General Information

General Information Comment Organism
physiological function in a mutant lacking IpdC activity, the level of substrate indole-3-pyruvate is 2.3fold higher and the level of indole-3-lactic acid is 2.1fold higher. Phenylalanine metabolism is impacted by the loss of IpdC in the mutant strain as well as glucosinolate biosynthesis pathway Enterobacter cloacae