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1 ior to transfer to CMP to form the activated sugar nucleotide.
2 ucosamine (UDP-GlcNAc), forming a 3-hexulose sugar nucleotide.
3 phosphoribose diphosphate rather than from a sugar nucleotide.
4 sion strategy for the efficient synthesis of sugar nucleotides.
5 sferase 3 (PmST3) with in situ generation of sugar nucleotides.
6 ase in the synthesis rate of nucleotides and sugar nucleotides.
7 studied several model systems based on amino-sugar nucleotides.
8 d the practical synthesis of a unique set of sugar nucleotides.
9 their corresponding uridine diphosphate(UDP)-sugar nucleotides.
10 ensively for the chemoenzymatic synthesis of sugar nucleotides.
11 ]lipid IV(A) in the presence of any of these sugar nucleotides.
12 of it is synthesized from readily available sugar nucleotides.
13 up by cancer cells and then converted into a sugar nucleotide analog, GDP-5T-Fuc, that blocks FUT act
14 t the transcriptome level, genes involved in sugar nucleotide and pectin metabolism are altered in th
15 el or improved methods for regenerating ATP, sugar nucleotides and 3-phosphoadenosine-5'-phosphosulph
16 e steady state concentrations of the uridine sugar nucleotides and imply that galactose metabolism mo
17 thod for determination of cellular levels of sugar nucleotides and related nucleotides in cultured ce
18 erase catalysts for the synthesis of complex sugar nucleotides and the practical synthesis of a uniqu
19 ntral to energy transduction and amino acid, sugar, nucleotide and lipid biosyntheses can be reconsti
20 talyze nucleotidyltransfer reactions to form sugar-nucleotides and pyrophosphate in the presence of t
21 sis of most amino acids, fatty acids, simple sugars, nucleotides and core metabolites of extant livin
22 enzyme is highly specific for this acetamido sugar nucleotide, and the procedure had a detection limi
23 uded ADP-ribose, diadenosine polyphosphates, sugar nucleotides, and deoxynucleoside triphosphates.
25 e analysis identified deficiencies in simple sugars, nucleotides, and lipids in the livers of MPSI mi
33 of >700 genes, including enzymes involved in sugar-nucleotide biosynthesis, transporters, glycan exte
34 e we report a therapeutic vulnerability in a sugar nucleotide biosynthetic pathway that can be exploi
38 hesis of uridine diphosphate (UDP)-GlcNAc, a sugar nucleotide critical to multiple glycosylation path
39 phosphorylases (MTPs) that catalyze both the sugar nucleotide-dependent biosynthesis and phosphorolyt
40 utative blueprint for base specificity among sugar nucleotide-dependent dehydrogenases and, in conjun
42 It is not understood how OGT recognises its sugar nucleotide donor and performs O-GlcNAc transfer on
43 ptor and the carbohydrate moiety of either a sugar nucleotide donor or lipid-linked saccharide donor.
44 ytic activity due to a weak affinity for its sugar nucleotide donor, CMP-NeuAc, and that this catalyt
49 ansferases can transfer azido-functionalized sugar nucleotide donors to selected synthetic plant cell
51 ll wall polysaccharides are synthesized from sugar-nucleotides, e.g. uridine 5'-diphosphoglucose (UDP
52 eta-N-acetylglucosamine (GlcNAc), is a donor sugar nucleotide for complex glycosylation in the secret
53 pyrophosphorylase that generates the reduced sugar nucleotide for the insertion of ribitol in a phosp
54 that platelets contain sufficient levels of sugar nucleotides for detection of glycosylation of exog
55 ynthesis of a range of natural and unnatural sugar nucleotides for in vitro glycosylation studies and
57 y allows the large-scale preparation of rare sugar nucleotides from common sugars in high yields and
58 id method for efficiently removing salts and sugar nucleotides from cytosol (polyethylene glycol prec
59 with in situ generation of the corresponding sugar nucleotides from simple monosaccharides or derivat
63 nzymes involved in the biosynthesis of these sugar nucleotides have been studied in some detail in ba
64 roblem, several nucleic acids based on amino-sugar nucleotides have been studied, and as expected, th
68 erest concerns the enzymatic modification of sugar nucleotides, in relation to both secondary metabol
69 ) at comparable rates using a diverse set of sugar nucleotides, including GDP-mannose, ADP-mannose, U
70 rases coupled with effective regeneration of sugar nucleotides, including UDP-Gal, UDP-GalNAc, GDP-Fu
71 tylglucosamine from exogenously supplied UDP-sugar nucleotides into a high molecular mass (10(6) to 1
72 further demonstrate that only the formylated sugar nucleotide is converted in vitro to an undecapreny
73 or UDP-glucose mass and to test whether this sugar nucleotide is released as an extracellular signali
77 HPAEC method to determine the intracellular sugar nucleotide levels of cultured Spodoptera frugiperd
78 o enzymes that oxidize the C-4'' position of sugar nucleotides, like UDP-galactose epimerase, dTDP-gl
79 shows that small biomolecules (SBMs) such as sugars, nucleotides, metabolites such as S-adenosylmethi
81 n is catalyzed by glycosyltransferases using sugar nucleotides or occasionally lipid-linked phosphosu
82 cular weight biochemicals, including lipids, sugars, nucleotides, organic acids, and amino acids, tha
83 It is proposed that ASQD arises from the sugar nucleotide pathway of sulfolipid biosynthesis by a
84 apparently not due to better binding of the sugar nucleotide precursors complexed to Mn ion because
88 phenylboronic acids as probes to interrogate sugar nucleotide processing enzymes that recognize thymi
91 cose pyrophosphorylases, as well as of other sugar-nucleotide pyrophosphorylases, was used for compar
93 owever, the molecular mechanisms involved in sugar nucleotide recognition and transfer to protein are
95 P-GlcNAc to a novel, less negatively charged sugar nucleotide shown to be [alpha-(32)P]UDP-GlcNAc3N.
96 study confirms that oxidation occurs at the sugar nucleotide stage prior to glycosyltransfer, and su
97 sing a fluorescently labeled analogue of the sugar-nucleotide substrate, we demonstrate that E acts a
98 erase reactions in extracts with radioactive sugar nucleotide substrates and appropriate Skp1 glycofo
99 ient spectroscopy (WaterLOGSY) NMR for known sugar nucleotide substrates and selected phosphonate ana
100 O-antigen expression but, as their putative sugar nucleotide substrates are not currently available,
101 ten tolerate chemical modifications in their sugar nucleotide substrates, thus allowing the installat
102 ce of proteins were mainly involved in amino sugar, nucleotide sugar and fatty acid metabolism, one c
104 e of a bifunctional plant enzyme involved in sugar nucleotide synthesis where a single polypeptide ex
106 The conformational changes of the enzyme and sugar nucleotide that accompany metal binding may provid
107 n be obtained readily, while the majority of sugar nucleotides that exist in bacteria, plants, archae
109 amine for de novo synthesis of UDP-GlcNAc, a sugar-nucleotide that inhibits receptor endocytosis and
111 glE) have recently been shown to modify this sugar nucleotide to form UDP-2-acetamido-4-amino-2,4,6-t
115 that UXS1, a Golgi enzyme that converts one sugar nucleotide (UDP-glucuronic acid, UDPGA) to another
116 ost commonly biosynthesized as the activated sugar nucleotide uridine 5'-diphospho-beta-l-rhamnose (U
117 '-amine of UDP-L-Ara4N, generating the novel sugar nucleotide, uridine 5'-diphospho-beta-(4-deoxy-4-f
119 on and versatile precursors to various deoxy sugar nucleotides, which are substrates for the correspo
120 producible separation of all nucleotides and sugar nucleotides with high sensitivity and reproducibil