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1 ospho-N-acetylneuraminic acid (CMP-Neu5Ac or CMP-sialic acid).
2 ugate substrates and nucleotide sugar donor, CMP-sialic acid.
3 . cerevisiae vesicles were able to transport CMP-sialic acid.
4 ex with its physiological substrates CMP and CMP-sialic acid.
7 g pocket SLC35A1 might accommodate the bulky CMP-sialic acid and the smaller CDP-ribitol, whereas SLC
8 for polymerizing sialyl residues from donor CMP-sialic acid are not homologous glycosyltransferases.
9 rmined structure of pig ST3GAL1, including a CMP-sialic acid-binding site assembled from conserved si
10 back inhibition of GNE-epimerase activity by CMP-sialic acid causes excessive production of free sial
14 ar treatment of TNFR-IgG with alpha2,3ST and CMP-sialic acid (CMP-Sia), in the presence of MnCl(2), p
17 s were performed to predict and evaluate the CMP-sialic acid donor and glycan acceptor interactions,
18 onclusion, Ng exploits type I IFNs to obtain CMP-sialic acid for LOS sialylation, resulting in innate
19 lation of expression of the transporters for CMP-sialic acid, GDP-fucose, or both unexpectedly result
21 s are an exception, because of a mutation in CMP-sialic acid hydroxylase, which occurred after our co
23 n efficiently and effectively substitute for CMP-sialic acid in extracellular ST6Gal-1-mediated sialy
25 ans including kidney, a critical shortage of CMP-sialic acid prevented sialylation of nephrin and pod
26 n protecting the host, IFN-epsilon increases CMP-sialic acid production in epithelial cells, potentia
27 back inhibition of GNE-epimerase activity by CMP-sialic acid recovered after silencing demonstrating
28 enetic ablation of the Sia-activating enzyme CMP-sialic acid synthase (CMAS) resulted in embryonic le
29 study, we characterize the first functional CMP-sialic acid synthase (DmCSAS) from any protostome li
30 evolutionarily conserved enzymes, including CMP-sialic acid synthetase (CSAS) and sialyltransferase
32 sialic acid 9-phosphate synthase (SAS), and CMP-sialic acid synthetase (CSAS) were coexpressed in in
35 se compounds are subsequently activated by a CMP-sialic acid synthetase and transferred to a wide ran
37 e reaction could be trapped by coupling with CMP-sialic acid synthetase to yield CMP-3F(ax)Neu5Ac.
38 ed in media lacking sialic acid, and a siaB (CMP-sialic acid synthetase) mutant was deficient in biof
40 ed by serum-localized nucleotide sugar donor CMP-sialic acid that is at least partially derived from
41 er Golgi membranes were incubated with [(3)H]CMP sialic acid to radiolabel endogenous soluble and mem
42 2 catalyzes the transfer of sialic acid from CMP-sialic acid to a growing chain of polysialic acid at
43 e reactions that transfer a sialic acid from CMP-sialic acid to an acceptor (a structure terminated w
44 s helix may swing down upon binding to donor CMP-sialic acid to form the binding pocket for an accept
45 the transporter supplied limited amounts of CMP-sialic acid to Golgi sialyltransferases but was unab
46 ere very similar to the previously described CMP-sialic acid transport characteristics observed with
48 tal structures of a mammalian NST, the mouse CMP-sialic acid transporter (mCST), in complex with its
49 viously described cDNA encoding the putative CMP-sialic acid transporter encodes the transporter prot
50 ned the interactions of nucleotides with the CMP-sialic acid transporter in order to better understan
51 tionally expressed the murine Golgi putative CMP-sialic acid transporter in Saccharomyces cerevisiae.
52 red that CDP-ribitol transport relies on the CMP-sialic acid transporter SLC35A1 and the transporter
54 o the lumen of the Golgi complex through the CMP-sialic acid transporter, an antiporter that also fun
57 ctivated sugar donor cytidine monophosphate (CMP) sialic acid, which is required for all sialylation.
58 termost structures of animal cells, requires CMP-sialic acid, which is a product of the nuclear enzym
59 itutions at C-5 or C-9 of the sialic acid in CMP-sialic acid, while its acceptor substrate specificit