Target type: molecularfunction
Catalysis of the reaction: purine nucleoside + phosphate = purine + alpha-D-ribose 1-phosphate. [EC:2.4.2.1]
Purine-nucleoside phosphorylase (PNP) activity is a critical enzymatic process involved in the catabolism of purine nucleosides, such as guanosine and inosine. This activity is catalyzed by the enzyme purine nucleoside phosphorylase (PNP), which plays a vital role in the salvage pathway for purine bases and the regulation of purine nucleotide levels. The molecular function of PNP involves the following steps:
1. **Substrate Binding:** PNP binds to a purine nucleoside, such as guanosine or inosine. The nucleoside is positioned in the active site of the enzyme, where it interacts with specific amino acid residues.
2. **Phosphorolysis:** PNP catalyzes the phosphorolytic cleavage of the glycosidic bond between the purine base and the sugar moiety (ribose or deoxyribose) of the nucleoside. This reaction requires the presence of inorganic phosphate (Pi). The reaction proceeds through a two-step mechanism involving the formation of a covalent intermediate between the enzyme and the purine base.
3. **Product Release:** The reaction releases the purine base (e.g., guanine or hypoxanthine) and the sugar-1-phosphate (e.g., ribose-1-phosphate or deoxyribose-1-phosphate).
4. **Phosphate Utilization:** The inorganic phosphate that was used in the phosphorolysis reaction is regenerated.
The purine base is further metabolized by other enzymes, while the sugar-1-phosphate can be recycled for nucleotide biosynthesis. The molecular function of PNP is essential for maintaining the proper levels of purine nucleotides in cells. Mutations in the PNP gene can lead to a deficiency in PNP activity, which can result in various metabolic disorders, including immunodeficiency and neurodevelopmental issues.'
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Protein | Definition | Taxonomy |
---|---|---|
Purine nucleoside phosphorylase | [no definition available] | Bos taurus (cattle) |
Purine nucleoside phosphorylase | A purine nucleoside phosphorylase that is encoded in the genome of human. [PRO:DNx, UniProtKB:P00491] | Homo sapiens (human) |
Compound | Definition | Classes | Roles |
---|---|---|---|
sk&f 29661 | 1,2,3,4-tetrahydroisoquinoline-7-sulfonamide: structure | ||
3-deazaguanine | 3-deazaguanine: structure | ||
adenosine | quinquefolan B: isolated from roots of Panax quinquefolium L.; RN not in Chemline 10/87; RN from Toxlit | adenosines; purines D-ribonucleoside | analgesic; anti-arrhythmia drug; fundamental metabolite; human metabolite; vasodilator agent |
ly 134046 | LY 134046: RN given refers to parent cpd; structure in first source | ||
7,8-dichloro-1,2,3,4-tetrahydroisoquinoline | 7,8-dichloro-1,2,3,4-tetrahydroisoquinoline : A 1,2,3,4-tetrahydroisoquinoline hacing chloro substituents at the 7- and 8-positions. 7,8-dichloro-1,2,3,4-tetrahydroisoquinoline: potent reversible inhibitor of phenylethanolamine N-methyltransferase; structure | isoquinolines; organochlorine compound | |
3-deazaguanosine | 3-deazaguanosine: structure | ||
4,9-dihydro-7-methoxy-3h-pyrido(3,4b)indole | 4,9-dihydro-7-methoxy-3H-pyrido(3,4b)indole: structure given in first source | ||
ag 99 | tyrphostin A46: epidermal growth factor-urogastrone receptor antagonist | ||
galidesivir | |||
acyclovir | acyclovir : An oxopurine that is guanine substituted by a (2-hydroxyethoxy)methyl substituent at position 9. Used in the treatment of viral infections. Acyclovir: A GUANOSINE analog that acts as an antimetabolite. Viruses are especially susceptible. Used especially against herpes. | 2-aminopurines; oxopurine | antimetabolite; antiviral drug |
guanosine monophosphate | guanosine 5'-monophosphate : A purine ribonucleoside 5'-monophosphate having guanine as the nucleobase. Guanosine Monophosphate: A guanine nucleotide containing one phosphate group esterified to the sugar moiety and found widely in nature. | guanosine 5'-phosphate; purine ribonucleoside 5'-monophosphate | biomarker; Escherichia coli metabolite; metabolite; mouse metabolite |
guanine | 2-aminopurines; oxopurine; purine nucleobase | algal metabolite; Escherichia coli metabolite; human metabolite; mouse metabolite; Saccharomyces cerevisiae metabolite | |
guanosine | ribonucleoside : Any nucleoside where the sugar component is D-ribose. | guanosines; purines D-ribonucleoside | fundamental metabolite |
hypoxanthine | nucleobase analogue; oxopurine; purine nucleobase | fundamental metabolite | |
inosine | inosines; purines D-ribonucleoside | Escherichia coli metabolite; human metabolite; mouse metabolite; Saccharomyces cerevisiae metabolite | |
8-amino-9-(2-thienylmethyl)guanine | |||
allopurinol riboside | allopurinol riboside : A nucleoside analogue that is allopurinol with a beta-D-ribofuranosyl moiety at the 1-position. | nucleoside analogue | metabolite |
8-amino-9-benzylguanine | 8-amino-9-benzylguanine: structure given in first source | ||
forodesine | forodesine: structure in first source | dihydroxypyrrolidine; pyrrolopyrimidine | |
peldesine | peldesine: potent inhibitor of human CCRF-CEM T-cell proliferation; structure given in first source | ||
ci 972 | CI 972: structure given in first source | ||
8-aminoguanine | |||
acyclovir monophosphate | |||
immucillin g | immucillin G: structure in first source | dihydroxypyrrolidine; pyrrolopyrimidine | |
ulodesine | ulodesine: a purine nucleoside phosphorylase inhibitor | ||
9-deazaguanine | |||
8-bromoguanosine | purine nucleoside | ||
9-deaza-9-(3-thienylmethyl)guanine | |||
8-aminoguanosine |