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Literature summary for 2.4.3.4 extracted from

  • Chandrasekaran, E.V.; Xue, J.; Xia, J.; Locke, R.D.; Matta, K.L.; Neelamegham, S.
    Reversible sialylation synthesis of cytidine 5-monophospho-N-acetylneuraminic acid from cytidine 5-monophosphate with alpha2,3-sialyl O-glycan-, glycolipid-, and macromolecule-based donors yields diverse sialylated products (2008), Biochemistry, 47, 320-330 .
    View publication on PubMedView publication on EuropePMC

Application

Application Comment Organism
synthesis the enzyme can be exploited for the enzymatic synthesis of diverse sialyl products Rattus norvegicus

Inhibitors

Inhibitors Comment Organism Structure
Sodium citrate direct sialylation using CMP-N-acetyl-beta-neuraminate Rattus norvegicus

Organism

Organism UniProt Comment Textmining
Rattus norvegicus Q11205
-
-

Substrates and Products (Substrate)

Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
CMP + 3-O-[alpha-Neu5Ac-(2->3)-beta-D-Gal-(1->3)-alpha-D-GalNAc]-L-tyrosyl-[protein] the enzyme synthesizes CMP-NeuAc by transferring NeuAc from the alpha-Neu5Ac-(2->3)-beta-D-Gal-(1->3)-alpha-D-GalNAc-unit of O-glycans Rattus norvegicus CMP-N-acetyl-beta-neuraminate + 3-O-[beta-D-Gal-(1->3)-alpha-D-GalNAc]-L-tyrosyl-[protein]
-
r

Synonyms

Synonyms Comment Organism
ST3Gal-II
-
Rattus norvegicus

pH Optimum

pH Optimum Minimum pH Optimum Maximum Comment Organism
4.8 6.4 formation of CMP-N-acetyl-beta-neuraminate from CMP Rattus norvegicus
5.2 7.2 direct sialylation using CMP-N-acetyl-beta-neuraminate Rattus norvegicus