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Literature summary for 3.2.2.9 extracted from

  • Lee, J.E.; Cornell, K.A.; Riscoe, M.K.; Howell, P.L.
    Structure of Escherichia coli 5'-methylthioadenosine/S-adenosylhomocysteine nucleosidase inhibitor complexes provide insight into the conformational changes required for substrate binding and catalysis (2003), J. Biol. Chem., 278, 8761-8770.
    View publication on PubMed

Crystallization (Commentary)

Crystallization (Comment) Organism
in complex with transition state analog formycin A and with substrate analog 5’-methylthiotubercidin Escherichia coli

Inhibitors

Inhibitors Comment Organism Structure
5'-methylthiotubercidin
-
Escherichia coli
Formycin A
-
Escherichia coli

Organism

Organism UniProt Comment Textmining
Escherichia coli P0AF12
-
-

Reaction

Reaction Comment Organism Reaction ID
S-adenosyl-L-homocysteine + H2O = S-(5-deoxy-D-ribos-5-yl)-L-homocysteine + adenine mechanism Escherichia coli