PYCR1
PYCR1
The PYCR1 gene encodes the enzyme pyrroline-5-carboxylate reductase 1, which is involved in the proline biosynthesis pathway. This enzyme plays a crucial role in cellular metabolism and is essential for the synthesis of proline from pyrroline-5-carboxylate. Proline is an amino acid that is important for protein synthesis, cellular signaling, and stress responses.
Function
The PYCR1 enzyme catalyzes the conversion of pyrroline-5-carboxylate (P5C) to proline, using NAD(P)H as a cofactor. This reaction is a key step in the proline biosynthesis pathway, which is important for maintaining cellular redox balance and osmotic stress resistance. Proline also serves as a source of energy and carbon under certain conditions.
Clinical Significance
Mutations in the PYCR1 gene have been associated with a rare genetic disorder known as Cutis Laxa, Autosomal Recessive, Type 2B (ARCL2B). This condition is characterized by loose, wrinkled skin, growth retardation, and developmental delay. The disorder results from impaired proline biosynthesis, leading to defects in collagen and elastin, which are critical components of the extracellular matrix.
Structure
The PYCR1 protein is a member of the pyrroline-5-carboxylate reductase family and is localized in the mitochondria. It is composed of several domains that facilitate its enzymatic activity, including a binding site for NAD(P)H and a catalytic site for the reduction of P5C to proline.
Pathways
PYCR1 is involved in the proline biosynthesis pathway, which is part of the larger amino acid metabolism network. This pathway is interconnected with other metabolic pathways, such as the urea cycle and the citric acid cycle, highlighting the enzyme's role in maintaining metabolic homeostasis.
Research
Ongoing research is focused on understanding the broader implications of PYCR1 function in cellular metabolism and its potential role in various diseases, including cancer and metabolic disorders. Studies are also exploring the therapeutic potential of targeting PYCR1 in conditions where proline metabolism is dysregulated.
Also see
Template:Amino acid metabolism
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Contributors: Prab R. Tumpati, MD