Literature summary extracted from

Stachelska-Wierzchowska, A.; Wierzchowski, J.; Bzowska, A.; Wielgus-Kutrowska, B.
Tricyclic nitrogen base 1,N6-ethenoadenine and its ribosides as substrates for purine-nucleoside phosphorylases spectroscopic and kinetic studies (2018), Nucleosides Nucleotides Nucleic Acids, 37, 89-101 .

Organism

EC Number	Organism	UniProt	Comment	Textmining
2.4.2.1	Escherichia coli	P0ABP8	-	-

Substrates and Products (Substrate)

EC Number	Substrates	Comment Substrates	Organism	Products	Comment (Products)	Rev.	Reac.
2.4.2.1	1,N6-ethenoadenine + alpha-D-ribose 1-phosphate	-	Escherichia coli	1,N6-ethenoadenine N7-riboside + phosphate	-	r
2.4.2.1	1,N6-ethenoadenine + alpha-D-ribose 1-phosphate	-	Escherichia coli	1,N6-ethenoadenine N9-riboside + phosphate	-	r

Synonyms

EC Number	Synonyms	Comment	Organism
2.4.2.1	PNP	-	Escherichia coli

General Information

EC Number	General Information	Comment	Organism
2.4.2.1	physiological function	PNP catalyzes a reversible phosphorolysis of the N-glycosidic bond in natural purine nucleosides, as well as inmany purine analogs, some of them displaying marked biological and pharmacological activity	Escherichia coli

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Release 2023.1 (January 2023)