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1 g no functional group with which to bind the saccharide.
2 he lipid may not be covalently linked to the saccharide.
3 which contained Vsa protein, lipid, DNA, and saccharide.
4 shows that Trp49 does not contact the bound saccharide.
5 ril interactions from the perspective of the saccharide.
6 form, and in complex with a tetra- or hepta-saccharide.
7 ows high selectivity for glucose, over other saccharides.
8 es, which could be inhibited by N-acetylated saccharides.
9 produce near-quantitative levels of soluble saccharides.
10 ancer cells manifested by truncated O-linked saccharides.
11 quence of variable recognition of peripheral saccharides.
12 be due to the molecular architectures of the saccharides.
13 removal of side-chain Kdo from the LPS core saccharides.
14 hat contain purified, or partially purified, saccharides.
15 red to have progressively truncated LPS core saccharides.
16 n shown to be effective for the synthesis of saccharides.
17 nd cAMP was triggered by the introduction of saccharides.
18 detection of characteristic oxonium ions of saccharides.
19 rin since they shared the same compositional saccharides.
20 determined to be fructose > glucose > other saccharides.
21 stress, with carbon accumulating as complex saccharides.
22 a nontypical binding preference with sample saccharides.
23 t eliminated the mitogenic activity of these saccharides.
24 tions of J(CH) and J(CC) values in ionizable saccharides.
25 y and a different acetylation pattern of the saccharides.
26 ain enhanced selectivity for ribose and rare saccharides.
27 hing, which is diminished in the presence of saccharides.
28 importance of the multivalent binding to PG saccharides.
29 eUmChlE was also active towards feruloylated saccharides.
30 p, deprotection affords water-soluble 2-thio saccharides.
31 ed MOS indicated minimal amounts of branched saccharides.
32 ers to conjugates bearing a larger number of saccharides.
33 nation complexes, peptides, nucleobases, and saccharides.
34 f alpha-FucN3 linkages relevant to bacterial saccharides.
35 enzyme, the glycan chains consist of 8 or 4 saccharides.
36 d to be glycosylated with a similar terminal saccharide, 4-(3-hydroxybutanamido)-4,6-dideoxy-2-O-meth
37 lectronegative substituent effect on 3JCC in saccharides, a structural factor undocumented previously
38 minimal functional units and that additional saccharides adjacent to these units can alter binding ou
39 physiologically important substances such as saccharides, alpha-hydroxycarboxylates, and catecholamin
40 LMW) organic compounds, including alkaloids, saccharides, amino acids, nucleosides, nucleic bases, an
41 ns in cellular components (lipids, proteins, saccharides, amino acids...) and cellular functions (cel
42 purine moiety as well as the polyoxygenated saccharide and a labile glycosidic bond in the nucleosid
45 BaF3/FGFR2b cells, heparin with at least 10 saccharides and 6-O-, 2-O-, and N-sulfates were required
46 sidues at the reducing ends of the S. sonnei saccharides and aminooxy linkers bound to BSA or a recom
48 mall intestine accumulate mannose-containing saccharides and glycogen particles in their apical cytop
49 ropolymerized 3-aminophenylboronic acid with saccharides and hydroxy acids also confirm that the obse
51 rmed to determine the relative enrichment of saccharides and inorganic ions in nascent fine (PM2.5) a
53 329S, was found to bind the tetra- and hepta-saccharides and may represent a higher-affinity site emp
54 sity B-coefficients of transfer (DeltatB) of saccharides and other parameters such as isobaric expans
55 n regarding the hydration characteristics of saccharides and play a pivotal role in the study of tast
57 This study aimed to assess the contents of saccharides and potential fructooligosaccharides (FOS) o
58 J-couplings within the N-acetyl fragment of saccharides and related structures to be used for more c
60 emand for chemosensors which target multiple saccharides and saccharide derivatives, in aqueous media
62 ctures and physicochemical properties of the saccharides and their degradation species correlate well
63 information available in the NMR spectra of saccharides and to advance our understanding of the corr
64 apid and sensitive analysis of underivatized saccharides and was used for determination of sugars in
65 kDa), heparin-derived oligosaccharides (4-22 saccharides), and chemically modified heparins (2-O-, 6-
66 stances (EPS), and lipids using the protein, saccharide, and lipid signatures, respectively, together
67 drolyze lignocellulosic biomass into soluble saccharides, and the bacterium Escherichia coli, which m
68 cation and order of activation for potential saccharide antigens used in conjugate vaccine developmen
72 manipulations at the C1 anomeric position of saccharides are one of the central goals of preparative
73 is labeling pattern is expected for 4-carbon saccharides arising from the pentose phosphate pathway.
74 or use in other real-world samples involving saccharides as well as for sensing other desired analyte
76 chromatography and identified as HA-[32P]UDP saccharides based on their degradation by snake venom ph
80 particularly useful for the sequencing of HS saccharides, because the lack of contaminating isomeric
83 pothesized that one or more of the secondary saccharide-binding sites harboring the aromatic residues
84 that the aromatic residues at the secondary saccharide-binding sites in HSAmy play a critical role i
86 that a conjugate of nucleobase, peptide, and saccharide binds to peptides from molecular nanofibrils
88 s on the concentration of negatively charged saccharides but is independent of oligosaccharide length
89 tocks that harbor easy-to-access fermentable saccharides by incorporating self-destructing lignin; an
90 ates that present patches of electropositive saccharide C-H bonds engage more often in CH-pi interact
92 nstrate how these nanomolecules grafted with saccharides can exhibit dramatically improved binding af
93 use of phenylboronic acid as a receptor for saccharide capture onto the substrate and the ability of
95 at binding of two FGF1 molecules to the same saccharide chain is a prerequisite for subsequent FGFR2c
96 antibody levels were a function of both the saccharide chain length and their loading on the protein
97 doglycan (PG), a complex polymer composed of saccharide chains cross-linked by short peptides, is a c
98 pecies were covalently attached to polyamino-saccharide chains of chitosan (CHIT) and allowed to inte
101 of three allosteric ligands: muramic acid (a saccharide component of the peptidoglycan), the cell wal
102 ) but instead 4-linked glucose as their main saccharide component, with low levels of glucosamine and
104 nd/or nitrogen sources could alter monomeric saccharide composition and concentrations of the free EP
105 omeric oligosaccharides, which have the same saccharide composition but different types of sequences,
106 mass spectrometry due to their complexity in saccharide composition, polydispersity, and sequence het
107 he most complex natural matrices in terms of saccharides composition, this innovative approach can be
114 of synthetic antifouling polymer composed of saccharide containing N-substituted polypeptide (glycope
117 acid on the terminal galactose of a neutral saccharide core (binding order GT1b = GD1a >> GM3; no bi
118 determined and discussed in terms of solute (saccharide)-cosolute (sodium gluconate) interactions.
121 e used a set of mutants that have successive saccharide deletions from the nLc4 alpha chain to charac
122 A chemosensor array for saccharides and saccharide derivatives, fully operational in aqueous med
123 ensors which target multiple saccharides and saccharide derivatives, in aqueous media at physiologica
124 ducing three membrane protein complexes from saccharide detergents and show how reducing their overal
126 nknown phase II metabolites, conjugates with saccharides, disaccharides, malonic acid, and sulfate, w
127 ed with the capability of adapting the inter-saccharide distances and orientations in the presence of
128 sition, without regard to the arrangement of saccharide domains typically found in vertebrate HS.
129 diverse organisms utilizes the in vivo oligo saccharide donor in preference to certain larger and/or
132 ng drug molecules, amino acids and peptides, saccharides, dyes, hydrocarbons, perfluorinated hydrocar
135 stereoselective synthesis of beta-(1-->2)-C-saccharides employing 3-deoxy- and 3-C-branched glycals
136 elective fucose cleavage from the H2-antigen saccharide enables efficient removal of H2 antigen from
137 chain conformation in biologically important saccharides, especially those where this structural elem
138 gh this was improved through the addition of saccharide excipients without detriment to the biologica
139 ferent from that of phages binding cell wall saccharides, for which structural information is availab
142 rides, the structural diversity displayed in saccharides from tissue or cell sources cannot be readil
143 of multiple concentrations of each of seven saccharides (glucose, galactose, fructose, sucrose, treh
144 ing this method, bioactive molecules such as saccharides, glycoalkaloids, flavonoids, organic acids,
145 on of a group of small molecules, called non-saccharide glycosaminoglycan mimetics (NSGMs), as direct
148 ion behaviour and the basic taste quality of saccharides have been studied from measured apparent mol
149 en unmet as existing molecular receptors for saccharides have generally not shown sufficient degrees
150 re of lignin coexisting with poly- and oligo-saccharides, have very low but variable oxygen permeabil
151 and chain length of heparin, since long (>22 saccharides) heparin chains with sulfation on the 6-O an
157 ETD effectively dissociates GAGs up to eight saccharides in length, but the low resolution of the ion
159 ng showed the presence of mannose-containing saccharides in the epithelium of proximal kidney tubules
160 c owing to the frequent occurrence of acidic saccharides in the glycan, rendering traditional proteom
162 etching vibration were determined in various saccharides including FOS (1-kestose, nystose and kestop
163 ereas the stabilizing effect per mole of all saccharides increased, and that the absolute stability o
165 creen-printed electrode through boronic acid-saccharide interactions, with the boronic acid units spe
170 ural and semi-synthetic heparan sulfate (HS) saccharide libraries are a valuable resource for investi
172 r generation of structurally diverse natural saccharide libraries from HS variants that is fast (appr
174 The galectin family of lectins recognizes saccharide ligands on a variety of microbial pathogens,
175 aose, cross-ring cleavage, which can provide saccharide linkage information, is the dominant fragment
176 he complexity of heparin and heparan sulfate saccharides makes their purification, including many iso
178 e three-dimensional conformation of terminal saccharides may partly explain reduced enzymatic activit
179 erial surface, CA forms a loosely associated saccharide mesh that coats the bacteria, often within bi
180 ies involved in osmotic stress tolerance and saccharide metabolism that support phenomic studies.
182 the distinct stimuli-sensitive properties of saccharide-modified polymers to mediate drug release und
184 t heparin fragments containing two- or eight-saccharide monomers protect against amylin cytotoxicity
185 supramolecular entities displaying different saccharide motifs in a controlled manner is of critical
186 mutual influence of varying densities of the saccharide motifs in the binding properties toward diffe
187 ugar, strongly suggesting that "mismatching" saccharide motifs may modulate carbohydrate-lectin speci
188 ermined for use in conformational studies of saccharide N-acetyl side-chains in solution by NMR spect
190 lysis of vinyl ether groups from unsaturated saccharides occurs independently of the alpha or beta co
191 HIL on APC to a heparin/heparan sulfate-like saccharide of syndecan-4 on activated T cells, we posite
194 The design and synthesis of amide-linked saccharide oligomers and polymers, which are predisposed
200 ns to evaluate the effects of peptide versus saccharide pathway structure on coupling magnitude.
203 annan trisaccharide [beta-(Man)(3)] by novel saccharide-peptide linker chemistry to create glycopepti
205 n isolated from cloudwaters, to biotransform saccharides present in the atmosphere was evaluated usin
206 acrocycle and especially the topology of the saccharide presentation in space influence the biologica
213 lead to antibody responses to the inner core saccharides provides an impetus to further explore this
216 es that do not process 6''-carboxyl-modified saccharides, recent structural studies reveal that this
220 pecific sulfatases selective for the type of saccharide residue and the attachment position of the su
221 mdiolates of structure R 2NN(O)NO-R' (R' = a saccharide residue) are potential prodrugs of the nitric
222 namics revealed a tight complex in which all saccharide residues are restrained without undergoing su
223 barrier' effect associated with the hydrated saccharide residues as well as steric hindrance from the
224 eak noncovalent interactions influence which saccharide residues bind to proteins, and how they are p
227 ealed that an oligosaccharide longer than 19 saccharide residues is necessary to display anti-IIa act
228 to saccharide-free peptoids, the interfacial saccharide residues of glycopeptoids formed a higher num
229 Heparin oligomers with chain lengths of 10 saccharide residues or higher provide strong inhibition
233 estigated why low levels of glucose or other saccharides restored growth of an apbC strain on Tcb.
234 e enabled exact mass measurements of heparin saccharides roughly up to degree-of-polymerization 20, l
235 insertion contributes to the differences in saccharide selectivity and host defense function and com
237 fficult challenge of heparin/heparan sulfate saccharide separation and will enhance structure-activit
238 and other alcohol) groups characteristic of saccharides, similar to biogenic carbohydrates found in
242 arensis requires a detailed knowledge of the saccharide structures that can be recognized by protecti
246 ronate esters with the 1,2- and 1,3-diols of saccharides, such as those that coat the surface of mamm
248 h distributions were obtained from the (poly)saccharide taylorgrams, including non-UV absorbing polym
250 egulated by the sulphation pattern of nearby saccharides that is genetically controlled by the hepara
251 n (GAG) family are highly polyanionic linear saccharides that play important roles in a variety of ph
252 immune system, metabolic pathways involving saccharides that provide cells with energy, and energy a
253 ype capsules differed in the identity of one saccharide, the pendant phosphopolyalcohol, and the O-ac
254 (NAG) and N-acetylmuramic disaccharide (NAM) saccharides, the latter of which has a peptide stem.
255 emical or in vitro enzymatic synthesis of HS saccharides, the structural diversity displayed in sacch
256 are critical for the development of related saccharide therapeutics, and the data here establish tha
258 hesis of highly yielding and alpha-selective saccharide thioglycosides containing 1,2-cis-2-amino gly
259 -cis-2-amino glycosidic linkages because the saccharide thioglycosides obtained can serve as donors f
260 hanged the inhibitory potencies of competing saccharides to more closely resemble those of CL-43.
263 visualization of glycoconjugates in alkynyl-saccharide-treated cells at extremely low concentration
264 se, etc.), the recognition of other types of saccharide under natural (aqueous) conditions is less we
266 al and biological properties imparted by the saccharide units and are unique from synthetic polymers.
267 ed to achieve stepwise removal of individual saccharide units from the nonreducing termini of the mul
277 for their bioorthogonal ligation to a model saccharide using a Huisgen alkyne-azide cycloaddition, t
279 n-specific immunogold label showed that this saccharide was distributed evenly over the fiber surface
282 ar interactions between the antibody and the saccharide, we determined the X-ray crystal structure of
284 lcohols, polyols, ethyl esters, mono- and di-saccharides were associated with the classification of s
286 rates of these receptors in the presence of saccharides were exploited in order to identify patterns
290 ses, containing mainly hemicellulose-derived saccharides, were refined by physicochemical methods to
291 in recognizing the terminal HBGA fucose, the saccharide which forms the primary conserved interaction
292 d derivative binds even at neutral pH to the saccharides which could expand the application towards b
295 s are observed for oxides in the presence of saccharides with closely related compositions and struct
296 ith mono- and oligosaccharides, deoxysugars, saccharides with free hydroxyl groups, pyranose, and fur
299 consist of tetra-, penta-, hexa-, and hepta-saccharides with molecular weights of 689, 851, 1013 and
300 ymerization efficiency of the alpha(2 --> 8) saccharides; with the treatment all oligomers produced a
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