De novo synthesis of purine nucleotides. provide every information involved in the synthesis, and the answer should be about 4 pages

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De novo synthesis of purine nucleotides is a complex biochemical pathway that utilizes various enzymes and metabolic intermediates to produce the building blocks required for the synthesis of purine nucleotides, such as ATP, GTP, and other important molecules involved in energy metabolism and nucleic acid synthesis. This process is important for cellular growth and proliferation, and any disruption in the pathway can lead to serious health consequences.

The de novo synthesis of purine nucleotides begins with the formation of the precursor molecule 5-phosphoribosyl-1-pyrophosphate (PRPP), which serves as the starting point for the synthesis of purine nucleotides. PRPP is formed from ribose-5-phosphate and ATP in a reaction catalyzed by the enzyme ribose-phosphate pyrophosphokinase.

The next step in the pathway involves the sequential assembly of the purine ring system, starting with the formation of inosine 5'-monophosphate (IMP). This process requires several enzymatic reactions and metabolic intermediates, with each step catalyzed by a specific enzyme.

The first committed step in the pathway is the conversion of PRPP to 5-phosphoribosylamine, which is catalyzed by the enzyme amidophosphoribosyltransferase. This reaction is regulated by feedback inhibition by purine nucleotides, ensuring the proper balance of purine nucleotide synthesis in the cell.

The next step involves the synthesis of the purine ring system, starting with the formation of 5-phospho-D-ribosylamine (PRA) from 5-phosphoribosylamine and ATP. This reaction is catalyzed by the enzyme phosphoribosylamine-glycine ligase. PRA then undergoes a series of enzymatic reactions to form IMP, including the addition of a glycine moiety and the removal of a carbon and nitrogen atom.

IMP serves as the precursor for the synthesis of various purine nucleotides, including AMP and GMP. The conversion of IMP to AMP involves the addition of an aspartate moiety to IMP, followed by the removal of a phosphate group. This process is catalyzed by the enzyme adenylosuccinate synthase and adenylosuccinate lyase, respectively.

Similarly, the conversion of IMP to GMP involves the addition of a glutamine moiety to IMP, followed by the removal of a phosphate group. This process is catalyzed by the enzyme IMP dehydrogenase and GMPS (guanosine monophosphate synthetase), respectively.

Overall, the de novo synthesis of purine nucleotides is a highly regulated and complex pathway that involves multiple enzymatic reactions and metabolic intermediates. Any disruption in this pathway can lead to imbalances in purine nucleotide levels, which can have serious consequences for cellular function and health. Therefore, understanding the mechanisms involved in purine nucleotide synthesis is crucial for developing therapies for diseases related to purine metabolism.