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  2. Phosphoribosyl pyrophosphate - Wikipedia

    en.wikipedia.org/wiki/Phosphoribosyl_pyrophosphate

    In de novo generation of purines, the enzyme amidophosphoribosyltransferase acts upon PRPP to create phosphoribosylamine. [2] The histidine biosynthesis pathway involves the reaction between PRPP and ATP, which activates the latter to ring cleavage. Carbon atoms from ribose in PRPP form the linear chain and part of the imidazole ring in histidine.

  3. Purine metabolism - Wikipedia

    en.wikipedia.org/wiki/Purine_metabolism

    Purines are biologically synthesized as nucleotides and in particular as ribotides, i.e. bases attached to ribose 5-phosphate.Both adenine and guanine are derived from the nucleotide inosine monophosphate (IMP), which is the first compound in the pathway to have a completely formed purine ring system.

  4. Purine nucleotide cycle - Wikipedia

    en.wikipedia.org/wiki/Purine_nucleotide_cycle

    Phosphagen system (ATP-PCr) and purine nucleotide cycle (PNC) [1] The Purine Nucleotide Cycle is a metabolic pathway in protein metabolism requiring the amino acids aspartate and glutamate. The cycle is used to regulate the levels of adenine nucleotides, in which ammonia and fumarate are generated. [2] AMP converts into IMP and the byproduct ...

  5. Purinosome - Wikipedia

    en.wikipedia.org/wiki/Purinosome

    The human purinosome was thought to have been identified in 2008 by the observation that transiently expressed GFP fusion constructs of purine biosynthesis proteins form macrobodies. [ 14 ] [ 15 ] A folate enzyme not directly involved in the purine biosynthesis pathway, 5,10-methenyltetrahydrofolate synthase (MTHFS), was later found to be part ...

  6. Gua Operon - Wikipedia

    en.wikipedia.org/wiki/Gua_Operon

    The first committed step of purine biosynthesis starts from 5-phosphoribosyl 1 pyrophosphate. This undergoes a series of reactions to form IMP, an important branch point in the pathway. The pathway then branches to form adenylosuccinate and then adenylate (AMP) in one branch and xanthylate (XMP) and then guanylate (GMP) in the other branch.

  7. Phosphoribosyl-N-formylglycineamide - Wikipedia

    en.wikipedia.org/wiki/Phosphoribosyl-N-formylgly...

    Phosphoribosyl-N-formylglycineamide (or FormylGlycinAmideRibotide, FGAR) is a biochemical intermediate in the formation of purine nucleotides via inosine-5-monophosphate, and hence is a building block for DNA and RNA. [1] [2] The vitamins thiamine [3] and cobalamin [4] also contain fragments derived from FGAR. [5]

  8. Hypoxanthine-guanine phosphoribosyltransferase - Wikipedia

    en.wikipedia.org/wiki/Hypoxanthine-guanine...

    n/a Ensembl n/a n/a UniProt n a n/a RefSeq (mRNA) n/a n/a RefSeq (protein) n/a n/a Location (UCSC) n/a n/a PubMed search n/a n/a Wikidata View/Edit Human Hypoxanthine-guanine phosphoribosyltransferase (HGPRT) is an enzyme encoded in humans by the HPRT1 gene. HGPRT is a transferase that catalyzes conversion of hypoxanthine to inosine monophosphate and guanine to guanosine monophosphate. This ...

  9. Phosphoribosylglycinamide formyltransferase - Wikipedia

    en.wikipedia.org/wiki/Phosphoribosylglycinamide...

    GARTfase's role in de novo purine biosynthesis makes it a target for anti-cancer drugs [6] and its overexpression during postnatal development has been connected to Down syndrome. [7] There are two known types of genes encoding GAR transformylase in Escherichia coli : purN and purT, while only purN is found in humans. [ 8 ]

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