Target type: biologicalprocess
The chemical reactions and pathways involving a purine nucleotide, a compound consisting of nucleoside (a purine base linked to a deoxyribose or ribose sugar) esterified with a phosphate group at either the 3' or 5'-hydroxyl group of the sugar. [GOC:go_curators, ISBN:0198506732]
Purine nucleotide metabolic process is a fundamental biological pathway that encompasses the synthesis, breakdown, and interconversion of purine nucleotides, which are essential building blocks of DNA, RNA, and various cellular coenzymes. This intricate process involves a series of enzymatic reactions, each catalyzed by specific enzymes, and is tightly regulated to maintain a delicate balance between the supply and demand for purine nucleotides.
The synthesis of purine nucleotides, often referred to as de novo purine biosynthesis, begins with the formation of inosine monophosphate (IMP) from simple precursors like amino acids, carbon dioxide, and tetrahydrofolate. The pathway proceeds through a series of steps, including the formation of 5'-phosphoribosyl-1-pyrophosphate (PRPP) from ribose-5-phosphate, followed by the sequential addition of glycine, formate, and glutamine to PRPP. This complex series of reactions ultimately leads to the formation of IMP, which serves as the precursor for the biosynthesis of both adenosine monophosphate (AMP) and guanosine monophosphate (GMP).
AMP and GMP, the two primary purine nucleotides, are derived from IMP through separate pathways. AMP synthesis involves the addition of aspartate to IMP, followed by a series of enzymatic reactions, while GMP synthesis involves the oxidation of IMP to xanthosine monophosphate (XMP) and the subsequent addition of glutamine.
In addition to de novo biosynthesis, purine nucleotides can also be salvaged from pre-existing purine bases. This salvage pathway utilizes specific enzymes to recycle purine bases, such as hypoxanthine, guanine, and adenine, back into their corresponding nucleotides. The salvage pathway is particularly important for cells that lack the capacity for de novo purine biosynthesis or require a rapid supply of purine nucleotides.
Purine nucleotide breakdown, also known as purine catabolism, is an essential process for removing excess purine nucleotides from the cell. This process involves the sequential degradation of purine nucleotides to uric acid, the primary end product of purine metabolism in humans. Uric acid is excreted in urine, and its accumulation can lead to a condition known as gout.
The regulation of purine nucleotide metabolism is crucial for maintaining cellular homeostasis. Various regulatory mechanisms, including feedback inhibition, allosteric regulation, and gene expression, are employed to ensure that the production and breakdown of purine nucleotides are tightly controlled in response to cellular needs.
The purine nucleotide metabolic process is essential for life, playing critical roles in DNA and RNA synthesis, cellular signaling, and energy metabolism. Disruptions in this pathway can lead to a range of disorders, including cancer, immune deficiency, and gout.'
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Protein | Definition | Taxonomy |
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Bis(5'-adenosyl)-triphosphatase | A bis(5-adenosyl)-triphosphatase that is encoded in the genome of human. [PRO:DNx, UniProtKB:P49789] | Homo sapiens (human) |
Compound | Definition | Classes | Roles |
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diadenosine triphosphate | diadenosyl triphosphate | mouse metabolite | |
4,9-dimethyl-3-(2H-tetrazol-5-ylmethoxy)-7,8,9,10-tetrahydrobenzo[c][1]benzopyran-6-one | coumarins |