ライフサイエンスコーパス: glycosylation site

1 sitive samples (i.e. experimentally verified glycosylation sites).

2 five silent sites in addition to the normal glycosylation site.

3 extensive heterogeneity associated with each glycosylation site.

4 of this viral strain lacks the new putative glycosylation site.

5 en to modify the mouse genome to remove this glycosylation site.

6 rands, with the former burying one prominent glycosylation site.

7 tides with glycans attached to each specific glycosylation site.

8 subclasses and heterogeneities at each head glycosylation site.

9 he N38S amino acid change and a loss of an N-glycosylation site.

10 main, was not affected by mutation of this N-glycosylation site.

11 envelope proteins or introduction of a novel glycosylation site.

12 cale mapping of Tn-glycosylated proteins and glycosylation sites.

13 SIGN is better correlated with the number of glycosylation sites.

14 he constant domains and disrupting predicted glycosylation sites.

15 acid substitutions and continual addition of glycosylation sites.

16 rved N-glycan or the deletion of predicted O-glycosylation sites.

17 e high evolutionary conservation of all four glycosylation sites.

18 but failed to detect those further from the glycosylation sites.

19 98 degrees C), and absence of cysteines and glycosylation sites.

20 se is glycosylated at all twelve potential N-glycosylation sites.

21 Exon 16 also includes two O-glycosylation sites.

22 h of gp120 at the Asn332, Asn392, and Asn386 glycosylation sites.

23 roxylases (P4Hs), defines their subsequent O-glycosylation sites.

24 sion protein that contains multiple N- and O-glycosylation sites.

25 beta-hCG bearing model glycans at all native glycosylation sites.

26 g glycan structures with their corresponding glycosylation sites.

27 was then used to pinpoint the 12 occupied O-glycosylation sites.

28 O-linked glycans and located the occupied O-glycosylation sites.

29 a reesei Family 7 cellobiohydrolase at three glycosylation sites.

30 hat of JR-FL or with mutations in putative N-glycosylation sites.

31 enaviruses is glycosylated at 11 conserved N-glycosylation sites.

32 n sites, with acquisition of around 10 new O-glycosylation sites.

33 within MIC2, with >95% occupancy at these O-glycosylation sites.

34 ave shorter variable loops or fewer N-linked glycosylation sites.

35 glycosylated and contains numerous O- and N-glycosylation sites.

36 ependent test for predicting human and mouse glycosylation sites.

37 s were found to have a dramatic influence on glycosylation sites.

38 hages transfected with FcgammaRIa in which N-glycosylation sites 1, 4, and 5 are mutated to alanines

39 heavily modified as it harbors 5 putative N-glycosylation sites (10 in the mature dimer).

40 Additionally, next to the two known glycosylation sites, a third novel, albeit low abundant,

41 In contrast, mutations of NKCC2 N-glycosylation sites abolished the effects of OS9, indica

42 However, mutating the two TRPC6 N-glycosylation sites abrogated the cytotoxicity of mutant

43 oward a differential selection pressure of N-glycosylation site acquisition during affinity maturatio

44 strategy to simultaneously monitor over 100 glycosylation sites across 50 serum glycoproteins.

45 mapping and comparing variable loop N-linked glycosylation sites across populations of HIV-1 sequence

46 Moreover, classical cadherins have multiple glycosylation sites along their extracellular regions.

47 antibody sensitivity, and putative N-linked glycosylation sites along with a comprehensive sequence

48 f gp120, here we report the first systematic glycosylation site analysis of gp120 derived from virion

49 tionic 6-deoxymannose sugar at the canonical glycosylation site and a second sugar, an unusual 4-O-me

50 igns of an immunogenic region to add a new N-glycosylation site and mask it from antibody binding.

51 ed for extracting DIA data is common to that glycosylation site and not dictated by a specific MS1 va

52 able the identification of peptide sequence, glycosylation site and the structure of intact glycopept

53 hod allowed for the identification of 2172 N-glycosylation sites and 1047 surface glycoproteins.

54 Furthermore, it included two additional N-glycosylation sites and a pair of cysteines suggestive o

55 esults demonstrate a critical role for the N glycosylation sites and cysteines for the structure and

56 -III, di-sialylated glycans at multiple A1AT glycosylation sites and desialylated A2HSG, and depleted

57 have enabled the identification of specific glycosylation sites and glycan structures that modulate

58 correlates inversely with putative N-linked glycosylation sites and positively with virion infectivi

59 almost no correlation between the number of glycosylation sites and protein length, but the number o

60 Primarily, the pattern of glycosylation sites and residues in the Sa antigenic reg

61 Promyeloperoxidase hosts five occupied glycosylation sites and six intrachain cystine bridges w

62 Occlusion of the Asn355/Asn391-glycosylation sites and the Asn323-/Asn483-glycans, loca

63 shown to be heavily N-glycosylated, but the glycosylation sites and the biological role of N-linked

64 Envelope second variable region length, glycosylation sites and V3 amino acids were signatures o

65 lating H3N2 viral strain (that possesses the glycosylation site) and humans vaccinated with baculovir

66 eneity (different glycoforms attached to one glycosylation site) and macroheterogeneity (site occupan

67 fied as a 73 amino acid protein having one N-glycosylation site, and a variant 74 residue non-glycosy

68 Remarkably, the glycan patterns, glycosylation site, and their occupancy by N-glycans are

69 edicted secretion leader sequences, N-linked glycosylation sites, and a putative site of tyrosine sul

70 uence coverage, including seven of the eight glycosylation sites, and has been used to study the impa

71 he K(2P) channels possess consensus N-linked glycosylation sites, and here we demonstrate that the co

72 in the stalk region abolishing the N-linked glycosylation site; and 2 variants represented the head

73 elucidation of the glycan structure and the glycosylation site are needed to reveal the biological f

74 ested that mutations and changes in N-linked glycosylation sites are associated with the rise of anti

75 N-glycosylation sites are clustered around CDRs and the DE

76 NA head domain of H1N1 IAVs, three N-linked glycosylation sites are conserved and that a fourth site

77 of 25, 22, and 34 glycopeptides covering all glycosylation sites are enriched by the modified tips fr

78 Knowing the Tn-glycosylated proteins and glycosylation sites are essential to the prevention, dia

79 ons in both the number and distribution of N-glycosylation sites are found in the 18 alpha and 8 beta

80 Mutations on and in the proximity of glycosylation sites are highly associated with human dis

81 lastidal reporter proteins with artificial N-glycosylation sites are indeed glycosylated during trans

82 t form, three of the four potential N-linked glycosylation sites are modified by carbohydrate attachm

83 large portion of negative samples (i.e. non-glycosylation sites) are mislabelled due to the limitati

84 lidated the congruence of the potential HA N-glycosylation sites as well as the presence of the HA pe

85 y of previously unobserved putative N-linked glycosylation sites, as well as codons that evolve under

86 We recently reported that the N-glycosylation sites Asn-168, Asn-538, and Asn-745 in rec

87 andemic H1N1 [A(H1N1)pdm] expressed a single glycosylation site (Asn(104)) on the head of HA.

88 We found that a single N-glycosylation site (Asn(8)) was important for MICA018 su

89 1)NDS N-glycosylation motif, but not other N-glycosylation sites (Asn(260), Asn(371), and Asn(394)),

90 Next, we showed that the cluster of N-glycosylation sites (Asn-467, Asn-473, and Asn-494) was

91 tryptic cleavage site is located between the glycosylation sites Asn24 and Asn38.

92 ding details on the hitherto uncharacterized glycosylation site Asn392 of the CH3 domain.

93 pies Cys200/Cys209 residues, one of the SERT glycosylation sites, Asp208 located between the two Cys

94 SHM introduces DNA sequences encoding N-glycosylation sites asparagine-X-serine/threonine (N-gly

95 d an incentive to modify the unique N-linked glycosylation site at Asn(297), either through chemical

96 nsitive to the presence of a single N-linked glycosylation site at asparagine 297 of the Fc, with deg

97 epeats contain an evolutionarily conserved O-glycosylation site at position -1 of the first cysteine

98 th VLPs expressing HA antigens that lacked a glycosylation site at residue 144 and a deleted lysine a

99 X-ray crystallography showed that the glycosylation site at residue 245 is within a conserved

100 5, 247 (S245N/S247T; introducing an N-linked glycosylation site at residue 245) and 468.

101 ion of an additional fully occupied N-linked glycosylation site at the N terminus at position 1 (equi

102 milarity with beta-hLH, including a common N-glycosylation site at the N-terminus but differs mainly

103 sylated trimer that lacks potential N-linked glycosylation sites at positions 230, 241, and 289.

104 bunits of hK(2P)17.1 harbor two functional N-glycosylation sites at positions N65 and N94.

105 dentification and orthogonal validation of N-glycosylation sites based on alternating sequential samp

106 ed as rmAb, 35 out of 38 (92%) nongermline N-glycosylation sites became occupied.

107 quantification of glycosylated peptides and glycosylation sites but not glycosylation occupancy or g

108 eted protein was due not to the loss of an N-glycosylation site, but rather an SNP-specific targeting

109 red for histamine catabolism, has multiple N-glycosylation sites, but their roles, for example in DAO

110 ein abundance but also the occupancy of each glycosylation site by different glycoforms during biolog

111 ssess the relative occupancies of numerous N-glycosylation sites by endoglycosidase H-resistant N-gly

112 enetically introducing aspartates at these N-glycosylation sites bypasses the requirement for PNG-1/N

113 an side chain remains intact in ETD, and the glycosylation site can be localized on the basis of the

114 e that in addition to antigenicity, N-linked glycosylation sites can alter NA enzymatic stability and

115 ddition to antigenicity, changes in N-linked glycosylation sites can alter other properties of viral

116 location and heterogeneity of surrounding N-glycosylation sites can be altered, resulting in exposur

117 carrying key hemagglutinin (HA) head region glycosylation sites can be removed from the lung by pulm

118 in PNS myelin and mutations in which at the glycosylation site cause Charcot-Marie-Tooth neuropathy,

119 Differences in hemagglutinin glycosylation site composition and heterogeneity seen in

120 CL2 has a predicted N-linked glycosylation site confirmed by using mass spectrometry.

121 (i) We determined which glycosylation sites contain conserved glycan profiles ac

122 oplasmic reticulum or mutation of the Asn-24 glycosylation site decreased GC activity, but neither in

123 uences into NCAM Ig5, including an "extra" N-glycosylation site, decreases or completely blocks NCAM

124 ng approaches have been proposed to identify glycosylation sites, demonstrating a promising predictiv

125 al elimination of evolutionarily conserved N-glycosylation sites did not abolish proper KOR1 folding,

126 of FL-BCRs is the acquisition of potential N-glycosylation sites during somatic hypermutation.

127 We suggest that the occasional absence of glycosylation sites encoded in the conserved regions of

128 verall selection bias against acquiring an N-glycosylation site, except for the CDR3 of the H chain.

129 t at least seven C-linked and three O-linked glycosylation sites exist within MIC2, with >95% occupan

130 IgM exhibits different accessibility of the glycosylation sites, explaining site-specific glycosylat

131 Vs of human origin, where the number of head glycosylation sites first increased over time and then d

132 Six glycosylation sites fitting the sequon N-X-S/T were succ

133 expose the CD4bs by selective elimination of glycosylation sites flanking the CD4bs, and 2) minimize

134 rked by analyzing Jurkat cells, where 947 Tn-glycosylation sites from 480 glycoproteins were mapped.

135 s focus mainly on either the de-glycosylated glycosylation site (glycosite)-containing peptides or th

136 s accommodating 19 N-linked and one O-linked glycosylation sites (glycosites).

137 we confirmed that such mutations at multiple glycosylation sites greatly diminish viral infectivity a

138 However, the presence or absence of glycosylation sites had differential effects on neutrali

139 n and swine origin, where the number of head glycosylation sites has mainly increased over time.

140 LC/MS(E) glycomics analysis revealed that glycosylation sites have specific proportions of N-glyca

141 All of the three N-linked glycosylation sites (i.e. sequons NCSV at HA 54, NHTV at

142 accharides and an aromatic ring close to the glycosylation site in an N-glycoprotein host.

143 C.2a H3N2 viruses possessing a new predicted glycosylation site in antigenic site B of HA emerged, an

144 e ~10 amino acids that surround the Asn(154) glycosylation site in each of the 180 envelope glycoprot

145 ession and that a mutation that eliminates a glycosylation site in HA(1) allows the Israel810 HA to g

146 ion CLRN1(N48K), which affects a conserved N-glycosylation site in hCLRN1, is a common causative USH3

147 we demonstrate that the conserved putative N-glycosylation site in K(2P)3.1 and K(2P)9.1 is a glycan

148 , providing additional information about the glycosylation site in the E protein.

149 ontemporary ZIKV isolates encode an N-linked glycosylation site in the envelope (E) protein (N154), b

150 sequence motif, VNDT, containing an N-linked glycosylation site in the envelope (E) protein, is polym

151 um channels have a highly conserved N-linked glycosylation site in the first extracellular loop, with

152 of glycosylation at both or the first PrP(C) glycosylation site in the host results in almost complet

153 Loss of the N173 glycosylation site in the non-macrophage-tropic SIVmac23

154 t and N-glycosylation analysis identified 73 glycosylation sites in 65 aleurone layer proteins, with

155 l-amino acid cassettes into closely spaced O-glycosylation sites in a single, high-yielding solid-sup

156 current study is to establish patterns of N-glycosylation sites in Ab V regions of naive and memory

157 in the greatest number of glycoproteins and glycosylation sites in biological duplicate experiments.

158 are associated with the presence of multiple glycosylation sites in close proximity and large structu

159 Previous attempts to alter glycosylation sites in Env typically involved mutating t

160 The determination of N- and O-glycans and O-glycosylation sites in etanercept provides a basis for f

161 We disrupted eight predicted N-glycosylation sites in HeV G by conservative mutations (

162 1,4-glucanase and contains eight potential N-glycosylation sites in its extracellular domain.

163 ortance of the conserved cysteines and the N-glycosylation sites in NBCe1-A EL-3, we analyzed the pot

164 Several glycosylation sites in proteins that participate in the

165 y machinery, including the identification of glycosylation sites in secreted proteins, an important g

166 upon complex oligosaccharide processing of N-glycosylation sites in the amino-terminal domain and dow

167 e investigate the contribution of individual glycosylation sites in the formation of this so-called i

168 We introduced seven N-linked glycosylation sites in the hemagglutinin head domain to

169 homa (FL), but not normal B cells, acquire N-glycosylation sites in the immunoglobulin variable regio

170 Recently we identified O-glycosylation sites in the linker regions between the ch

171 likely to predominate at all the putative N-glycosylation sites in the parasite proteome.

172 Glycosylation sites in the spike protein are highly cons

173 The presence of these extra glycosylation sites in the variable region of the molecu

174 ly shown that ablation of the three N-linked glycosylation sites in the West Nile virus NS1 protein c

175 f HIV-1 sequence alignment by using N-linked glycosylation sites in variable loops as alignment ancho

176 In 7/80 RA-rmAb, SHM resulted in ex novo N-glycosylation sites in VH and/or VL regions.

177 ides with N-linked glycans attached to their glycosylation sites, in complex proteome samples.

178 s suggest that the loss of the N173 N-linked glycosylation site increases SIVmac239 replication in ma

179 we have mutated each of the nine consensus N-glycosylation sites independently.

180 ion of a single N-linked GlcNAc at potential glycosylation sites inhibits dimer formation.

181 merization could be abolished by engineering glycosylation sites into the dimer interface; other inte

182 in the envelope (E) protein (N154), but this glycosylation site is absent in many historical ZIKV iso

183 DT motif is deleted or in which the N-linked glycosylation site is mutated by single-amino-acid subst

184 roheterogeneity of glycopeptides identifying glycosylation sites is a challenging task, and there is

185 oteotype and identification of extracellular glycosylation sites is challenging when samples are limi

186 an species from both the Fab and Fc N-Linked glycosylation sites is consistent with quantification us

187 e-rich protein that contains STT3A-dependent glycosylation sites, is poorly glycosylated in yeast cel

188 the IgG sequence, in addition to unambiguous glycosylation site localization and extensive coverage o

189 To determine whether this glycosylation site may be the binding region for EphA2,

190 to routinely assess the glycan type at each glycosylation site may facilitate design of improved vac

191 nity for EphA2, indicating that the EBV gL N-glycosylation site might be responsible for inhibiting t

192 The viral GP is characterized by a glycosylation site modification and mutations in the muc

193 This indicates that surgical glycosylation site modification may be an effective way

194 single N-acetylglucosamine at each of the N-glycosylation sites [monoglycosylated HA (HA(mg))] can e

195 irus-expressed H3 antigens (that possess the glycosylation site motif) were able to efficiently recog

196 he cellular and supernatant fractions, while glycosylation site mutants did not adversely affect viri

197 However, mutation of glycosylation site N-497 abrogates transport of ARSG to

198 atory sequences established that all eight N-glycosylation sites (N1 to N8) are used in the wild type

199 contains three highly conserved potential N-glycosylation sites (N1, N2 and N3).

200 xtracellular domain of KOR1 contains eight N-glycosylation sites, N1 to N8, of which only N3 to N7 ar

201 229) is needed for TC-Cbl binding, but the N-glycosylation sites (N126, N195, and N213) are of no imp

202 A2m(1), the engineered molecule lacked two N-glycosylation sites (N166 and N337), two free cysteines

203 ere, we identify a highly conserved N-linked glycosylation site (N173 in SIV, corresponding to N160 i

204 a knockin mouse expressing RDS without the N-glycosylation site (N229S).

205 68T), with P68T generating a second N-linked glycosylation site (N66) in addition to an invariant N32

206 We found that the glycosylation site N69/S71 of gL is involved in restrict

207 To understand how individual N-glycosylation sites (NGS) coordinate to form a dynamic s

208 ses contains 2 completely conserved N-linked glycosylation sites (NGSs) at N563 and N618, suggesting

209 Glycosylation site occupancy alteration has been implica

210 The N-glycosylation site occupancy and disulfide pattern, the

211 To address N-glycosylation site occupancy and N-glycan composition of

212 ensive mass spectrometry-based analysis of N-glycosylation site occupancy in pmtDelta mutants.

213 of-function mutation (S562L) in a putative S-glycosylation site of GmCLV1A causes stem nodal identity

214 e how hemophilia mutations near the unused N-glycosylation site of the A2 domain (N582) of FVIII affe

215 The N-glycosylation sites of both inhibitors were determined t

216 r indicated that, among the four potential N-glycosylation sites of E-cadherin, Asn-554 is the key si

217 vation of any of the four predicted N-linked glycosylation sites of Ly49B, nor was it affected by rem

218 ronic acid units specifically binding to the glycosylation sites of the antibody molecules.

219 nsus amino acid sequence was evident for the glycosylation sites of the glycoproteins.

220 Asn-to-Ala substitutions at the predicted N-glycosylation sites of the M41-RBD were evaluated along

221 is heavily glycosylated at approximately 25 glycosylation sites, of which approximately 7-8 are loca

222 sites, a third novel, albeit low abundant, N-glycosylation site on C9 is identified, which surprising

223 IgG antibodies contain a conserved N-glycosylation site on the Fc domain to which a complex,

224 lation sites on the mu (heavy) chain and one glycosylation site on the J chain.

225 n chimpanzee CD4 (68T) that creates a second glycosylation site on the same virus-binding interface.

226 e-specific substitution (34T) that creates a glycosylation site on the virus binding surface of the C

227 Over half of the gp120 glycosylation sites on 11 different trimeric Envs have a

228 lly triplicate experiments, on average 953 N-glycosylation sites on 393 surface glycoproteins per exp

229 s spectrometry-based technique for mapping O-glycosylation sites on herpes simplex virus type 1.

230 O cells, the number of N-linked and O-GalNAc glycosylation sites on individual host cell proteins (HC

231 rein, we have systematically characterized O-glycosylation sites on recombinant LDLR shed from HEK293

232 dentification, delineating multiple N- and O-glycosylation sites on single glycopeptides, and derivin

233 uantification results demonstrated that many glycosylation sites on surface proteins were down-regula

234 ated from those species present at the other glycosylation sites on the molecule.

235 d of heavily glycosylated polymers with five glycosylation sites on the mu (heavy) chain and one glyc

236 N) showed that the conservation of N-linked glycosylation sites on the NA enzymatic head domain diff

237 nd N2 mutants demonstrated that the N-linked glycosylation sites on the NA head domain are required f

238 rimental analyses verified that the N-linked glycosylation sites on the NA head domain contribute to

239 Flaviviruses encode one, two, or no N-linked glycosylation sites on their envelope proteins.

240 presence of 72 additional potential O-linked glycosylation sites on this mucinous protein.

241 Ab molecule containing two distinct N-linked glycosylation sites: one present on the heavy chain (HC)

242 ainly focus on qualitative identification of glycosylation sites or intact glycopeptides.

243 are distinguished by compact Envs with fewer glycosylation sites, our study points to fusion and poss

244 Additionally, human-adapted HAs gain glycosylation sites over time, although their biological

245 PAM-1 lacking both glycosylation sites (PAM-1/OSX; where OSX is O-glycan-de

246 Residues in nsp4 distinct from glycosylation sites, particularly in the endoplasmic ret

247 concentrations, and the presence of multiple glycosylation sites per Ig.

248 glycosylated, encoding around 66-87 N-linked glycosylation sites per trimeric spike.

249 positions and numbers of potential N-linked glycosylation sites (PNGSs).

250 based on the AlphaMax algorithm for protein glycosylation site prediction.

251 sylation, and particularly the enrichment in glycosylation sites proximal to the disulfide linkages a

252 r machine classifiers to predict N-/O-linked glycosylation sites, respectively.

253 Disruption of both N-glycosylation sites results in loss of hK(2P)17.1 curren

254 re were no differences in protease cleavage, glycosylation sites, signal peptides or trans-membrane d

255 ce of protease cleavage sites, Pfam domains, glycosylation sites, signal peptides, trans-membrane pro

256 rds understanding the role of these putative glycosylation sites, site-directed mutagenesis and lecti

257 intact glycopeptides corresponding to eight glycosylation sites (six N-linked and two O-linked sites

258 s at sites 34 and 68, destroying both of the glycosylation sites, suggesting that the effects of the

259 ionally, we report a newly observed O-linked glycosylation site, T606, and we show that the full O-li

260 Specifically, mDPP4 has a nonconserved glycosylation site that acts as a barrier to MERS-CoV in

261 ence of multiple phosphorylation sites and a glycosylation site that we find to be occupied by at lea

262 riable regions (V1-V5), and also at N-linked glycosylation sites that contribute roughly half the mas

263 Because 06HA contains two potential glycosylation sites that could mask the epitope, our res

264 ligand receptor site that is ringed by four glycosylation sites that dramatically impact ligand bind

265 mplex-type biantennary N-glycans linked to N-glycosylation sites that emerge during somatic hypermuta

266 Therefore, for proteins containing multiple glycosylation sites, the individual glycan species prese

267 f cysteines in Env, and 4 potential N-linked glycosylation sites; the top features will be advanced t

268 By sequentially introducing O-glycosylation sites to ST6GAL1, we demonstrated that O-g

269 ucted the largest dataset of human and mouse glycosylation sites to train deep learning neural networ

270 this study, we tried to identify atypical N-glycosylation sites using our recently developed solid-p

271 Interestingly, beta2 with a single intact glycosylation site was as effective as the WT in promoti

272 Each glycosylation site was characterized individually, with

273 harides and the type of substitution at each glycosylation site was determined by chemical, spectrosc

274 A native N-linked glycosylation site was identified at Asn184.

275 contrast, a protein with extreme C-terminal glycosylation sites was efficiently glycosylated in yeas

276 otein-derived epitope to contain an N-linked glycosylation site, we determined that optimal CD8(+) T

277 to decipher the function of its potential N-glycosylation site, we produced pro-KLK2 in Leishmania t

278 AXL) as a model glycoprotein with multiple N-glycosylation sites, we show that those LCMS features th

279 TcdA and TcdB in which any putative N-linked glycosylation sites were altered.

280 Almost all potential N-linked glycosylation sites were at least partially occupied in

281 Glycosylation sites were clearly localized from the ETD

282 Several known glycosylation sites were confirmed.

283 In addition, putative and novel glycosylation sites were detected.

284 )17.1 channels and channels lacking specific glycosylation sites were expressed in Xenopus laevis ooc

285 ides derived from 56 glycoproteins with 83 N-glycosylation sites were identified from human serum and

286 es derived from 129 glycoproteins with 157 N-glycosylation sites were identified from mouse liver tis

287 dic N-linked oligosaccharides, the six other glycosylation sites were modified with complex N-glycans

288 series of ORF2 mutants in which the three N-glycosylation sites were mutated individually or in comb

289 The distribution and occurrence of N-glycosylation sites were systematically investigated, an

290 rometry demonstrated that all 11 predicted N-glycosylation sites were utilized in both HEK293- and Sf

291 spectrometry demonstrated that the predicted glycosylation sites were utilized in both mammalian and

292 L is at least in part proximal to the EBV gL glycosylation site, which in part accounts for differenc

293 in the native hosts, but contains potential glycosylation sites, which are aberrantly glycosylated d

294 HDX changes focused around the N221 and N255 glycosylation sites, which contain mannose-6-phosphate m

295 From this study, two atypical N-linked glycosylation sites with N-X-C and N-X-V motifs were ide

296 Several amino acid changes altered predicted glycosylation sites, with acquisition of around 10 new O

297 re was considerable variation in potential N-glycosylation sites, with GA2 and ON1 viruses showing up

298 rom the recent outbreaks contain an N-linked glycosylation site within the viral envelope (E) protein

299 alyzed the distribution and acquisition of N-glycosylation sites within Ab V regions of peripheral bl

300 ous system function - contain two putative N-glycosylation sites within the large N-terminal domain a