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Human germline mutations in glutarate metabolism highlight its fundamental biological role, with loss of function mutations in glutaryl-CoA dehydrogenase (GCDH) resulting in glutarate accumulation and glutaric aciduria type 1 (GA1)a rare autosomal disorder characterized by dystonia, developmental delay and often death in early childhood 10

however, in conditions where there is a high demand for nucleotide production (such as in the case for highly proliferative cells), the nonoxidative part of the pathway can function independently of the oxidative phase to produce ribose 5-phosphate from the glycolytic intermediates fructose 6-phosphate and glyceraldehyde 3-phosphate (figure 7.2)

Hercynine is then processed by EgtB, a sulfoxide synthase, which catalyses iron(II)-dependant oxidative sulfurisation to conjugate -glutamylcysteine to the imidazole side chain of hercynine

Glutathione (600mg) $150.00 In stock Description A single-component research material supplied for controlled research environments