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Literature summary for 2.4.2.1 extracted from

  • Fateev, I.V.; Antonov, K.V.; Konstantinova, I.D.; Muravyova, T.I.; Seela, F.; Esipov, R.S.; Miroshnikov, A.I.; Mikhailopulo, I.A.
    The chemoenzymatic synthesis of clofarabine and related 2-deoxyfluoroarabinosyl nucleosides: the electronic and stereochemical factors determining substrate recognition by E. coli nucleoside phosphorylases (2014), Beilstein J. Org. Chem., 10, 1657-1669.
    View publication on PubMedView publication on EuropePMC

Organism

Organism UniProt Comment Textmining
Escherichia coli
-
-
-

Substrates and Products (Substrate)

Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
2,6-diaminopurine ribonucleoside + phosphate
-
Escherichia coli 2,6-diaminopurine + alpha-D-ribose 1-phosphate
-
?
2-chloroadenosine + phosphate
-
Escherichia coli 2-chloroadenine + alpha-D-ribose 1-phosphate
-
?
5-aza-7-deazaguanine + phosphate
-
Escherichia coli ?
-
r
inosine + phosphate
-
Escherichia coli hypoxanthine + alpha-D-ribose 1-phosphate
-
r

Synonyms

Synonyms Comment Organism
DeoD
-
Escherichia coli
PNP
-
Escherichia coli
purine nucleoside phosphorylase
-
Escherichia coli