Recombinant Human QDPR/DHPR protein is a Human Full Length protein, in the 1 to 244 aa range, expressed in Escherichia coli, with >90% purity and suitable for SDS-PAGE, MS.
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Catalyzes the conversion of quinonoid dihydrobiopterin into tetrahydrobiopterin.
DHPR, SDR33C1, QDPR, Dihydropteridine reductase, HDHPR, Quinoid dihydropteridine reductase, Short chain dehydrogenase/reductase family 33C member 1
Recombinant Human QDPR/DHPR protein is a Human Full Length protein, in the 1 to 244 aa range, expressed in Escherichia coli, with >90% purity and suitable for SDS-PAGE, MS.
pH: 8.5
Constituents: 10% Glycerol (glycerin, glycerine), 0.32% Tris HCl, 0.04% (R*,R*)-1,4-Dimercaptobutan-2,3-diol
ab113148 was purified using conventional chromatography techniques.
Catalyzes the conversion of quinonoid dihydrobiopterin into tetrahydrobiopterin.
Belongs to the short-chain dehydrogenases/reductases (SDR) family.
Previously labelled as QDPR.
QDPR also known as Quinoid Dihydropteridine Reductase or DHPR is an enzyme that plays an important role in tetrahydrobiopterin (BH4) regeneration. It has a molecular mass of approximately 25 kDa and is found in various tissues such as the liver and brain where it contributes to neurotransmitter synthesis and other physiological processes. The DHPR protein is encoded by the QDPR gene in humans and is highly conserved across species indicating its essential function.
QDPR catalyzes the reduction of quinonoid dihydrobiopterin (qBH2) to tetrahydrobiopterin maintaining BH4 homeostasis. This process supports neurotransmitter synthesis by replenishing BH4 a cofactor for aromatic amino acid hydroxylases. QDPR does not operate as part of a large multi-protein complex but has a significant role as a standalone enzyme that assists hydroxylating enzymes important for dopamine serotonin and nitric oxide production.
QDPR contributes to the biosynthesis of catecholamines and serotonin both essential neurotransmitter pathways. It supports phenylalanine hydroxylase tyrosine hydroxylase and tryptophan hydroxylase activities by sustaining BH4 levels. These pathways are integral to proper neurological function and are tightly regulated due to their dependence on QDPR's enzymatic activity. The function of QDPR aligns with the regulation of neurotransmitter metabolism working alongside other critical proteins in these pathways.
QDPR deficiency can result in hyperphenylalaninemia a condition characterized by elevated phenylalanine levels leading to cognitive impairments. This deficiency affects neurotransmitter synthesis linking it to neurological diseases such as depressive disorders. Additionally QDPR-related disruptions can implicate other proteins like phenylalanine hydroxylase showing how these metabolic pathways and their components are interwoven into broader physiological contexts.
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15% SDS-PAGE showing ab113148 (3 μg) at approximately 28.2 kDa.
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