Title : Glutathione synthetase deficiency, an inborn error of metabolism involving the gamma-glutamyl cycle in patients with 5-oxoprolinuria (pyroglutamic aciduria).

Pub. Date : 1974 Jun

PMID : 4152248






1 Functional Relationships(s)
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1 Thus, 5-oxoproline is produced in amounts that exceed the normal capacity of 5-oxoprolinase to convert it to glutamate. Pyrrolidonecarboxylic Acid 5-oxoprolinase, ATP-hydrolysing Homo sapiens