ライフサイエンスコーパス: glycosylation site

1 tides with glycans attached to each specific glycosylation site.

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

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

4 envelope proteins or introduction of a novel glycosylation site.

5 extensive heterogeneity associated with each glycosylation site.

6 in the V3 region rather than losing the N332 glycosylation site.

7 g specificity and remove a critical N-linked glycosylation site.

8 s associated with the presence of a specific glycosylation site.

9 on sequence motif will lead to the loss of a glycosylation site.

10 structural determination of the alpha7 nAChR glycosylation site.

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

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

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

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

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

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

17 g glycan structures with their corresponding glycosylation sites.

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

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

20 a reesei Family 7 cellobiohydrolase at three glycosylation sites.

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

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

23 te domains incorporated at all of the native glycosylation sites.

24 of HIV diversity by tracking gp120 N-linked glycosylation sites.

25 IL-15Ralpha and characterization of multiple glycosylation sites.

26 labelling to be the hexose at several of the glycosylation sites.

27 id of glycans at the first, second or both N-glycosylation sites.

28 inatorial mutagenesis of all six potential N-glycosylation sites.

29 involved modifications of potential N-linked glycosylation sites.

30 -fold depletion in substitutions at O-linked glycosylation sites.

31 , FM/47, and FW/50 differ in the presence of glycosylation sites.

32 the disaccharide chitobiose at the natural N-glycosylation sites.

33 ndered nonfunctional by disruption of single glycosylation sites.

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

35 nto glycosylation, resulting in unoccupied N-glycosylation sites.

36 It bears 11 glycosylation sites.

37 e high evolutionary conservation of all four glycosylation sites.

38 acid substitutions and continual addition of glycosylation sites.

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

40 98 degrees C), and absence of cysteines and glycosylation sites.

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

42 Exon 16 also includes two O-glycosylation sites.

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

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

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

46 We show that KCNE1 has two distinct N-glycosylation sites: a typical co-translational site and

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

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

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

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

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

52 The HIV N-linked Glycosylation Site Analyzer web server is available at h

53 web server described here, the HIV N-linked Glycosylation Site Analyzer, was developed to facilitate

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

55 ot ROM1, is glycosylated and we examined the glycosylation site and glycan composition of ROM1 by liq

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

74 or wild type KCNE1, the overlapping N- and O-glycosylation sites are innocuous for subunit biogenesis

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

76 of FlgA1 confirm that its three predicted N-glycosylation sites are modified with covalently linked

77 ere linkers connect to structured domains, O-glycosylation sites are observed less frequently, wherea

78 Putative N-glycosylation sites are quite rare in cellulase linkers,

79 As a result, some N-glycosylation sites are unoccupied.

80 analysis revealed that all eight potential N-glycosylation sites are utilized.

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

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

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

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

85 procal experimental approach, deletion of HA glycosylation sites (Asn 142 and Asn 177, but not Asn 71

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

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

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

89 N-glycosylation of the two glycosylation sites, Asn393 and Asn366, has differential

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

91 attenuated in mice by adding two additional glycosylation sites (asparagine [Asn] 71 and Asn 286) on

92 ibiting complex-type N-glycans at a single N-glycosylation site, asparagine 42.

93 The N-glycosylation site at Asn-644 in the LOX catalytic domai

94 A mutation which introduces a potential glycosylation site at Asn123 in the NL219 hemagglutinin

95 on at position 125, resulting in loss of the glycosylation site at Asn123.

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

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

100 tudy, we have introduced individual N-linked glycosylation sites at several positions spaced at inter

101 ssociated with changes in potential N-linked glycosylation sites but not CD4 independence or CXCR4 us

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

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

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

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

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

107 es have been identified for the selection of glycosylation sites by GalNAc-Ts: confined sequence reco

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

109 In particular, enrichment of N-linked glycosylation sites can be found within Envelope variabl

110 re conditions, or introduction of artificial glycosylation sites, can alter CBM binding affinity to c

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

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

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

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

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

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

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

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

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

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

121 The modification of glycosylation sites for the 1918 and SI/06 viruses also

122 lycosylation sites to 1918 HA and removal of glycosylation sites from SI/06 HA imposed constraints on

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

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

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

126 CasBrE Env possesses 6/8 consensus MLV glycosylation sites (gs) but is missing gs3 and gs5 and

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

128 Although the loss of these glycosylation sites has seemingly occurred naturally (pr

129 Since then, variants with additional glycosylation sites have been detected, and the location

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

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

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

133 Reintroduction of the N-glycosylation site in either GP3 or GP5 allowed recovery

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

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

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

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

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

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

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

141 activity toward an Env variant that lacked a glycosylation site in V4.

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

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

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

145 ring MCTC, with viruses of shorter and fewer glycosylation sites in env present in IP transmission, o

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

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

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

149 1,4-glucanase and contains eight potential N-glycosylation sites in its extracellular domain.

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

151 Several glycosylation sites in proteins that participate in the

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

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

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

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

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

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

158 ations (Asn to Gln) at the seven potential N-glycosylation sites in the NiV G ectodomain (G1 to G7) i

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

160 were shorter and had fewer putative N-linked glycosylation sites in the V1-V5 region than matched mat

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

162 Mass spectrometric analysis identified five glycosylation sites in type I collagen (i.e. alpha1,2-87

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

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

165 2 is insensitive to disruption of multiple N-glycosylation sites, in contrast with the related recept

166 haracterize C. jejuni JHH1 and identified 93 glycosylation sites, including 34 not previously reporte

167 SSG for multiple N- and O-glycosylation sites, including extensive glycan heteroge

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

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

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

171 We thus evaluated topology by N-linked glycosylation site insertion and protein lipidation mapp

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

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

174 Different from N-linked glycans, the O-glycosylation site is not within a known consensus seque

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

176 data indicate that utilization of several N-glycosylation sites is important for KOR1 activity, wher

177 The stochastic distribution of glycoforms at glycosylation sites is revealed.

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

179 Furthermore, a potential N-linked glycosylation site located close to the HIR and postulat

180 we found that the elimination of a conserved glycosylation site located in Loop D and two glycosylati

181 glycosylation site located in Loop D and two glycosylation sites located in variable region 5 of Env

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

183 the most N-terminal of three beta3 subunit N-glycosylation sites, might reduce GABAergic inhibition b

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

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

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

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

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

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

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

191 A glycosylation site, N116, in this region did not affect

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

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

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

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

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

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

198 nce analysis shows that PRRSV-01 lacks two N-glycosylation sites, normally present in wild-type (wt)

199 r Envs displayed marked differences in their glycosylation site occupancies and in their amounts of c

200 Glycosylation site occupancy alteration has been implica

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

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

203 nsmitted/founder Envs had similar degrees of glycosylation site occupancy as well as similar glycan p

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

205 marker is a highly sensitive tool to study N-glycosylation site occupancy.

206 to screen for compounds that reverse poor N-glycosylation site occupancy.

207 rescent protein (GFP) construct to measure N-glycosylation site occupancy.

208 marker is a highly sensitive indicator of N-glycosylation site occupancy.

209 8% of the variations that lead to changes in glycosylation sites occur at the loop and bend regions o

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

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

212 mycin treatment and mutation of the specific glycosylation site of the PiT1 receptor.

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

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

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

216 o elucidate the functional significance of N-glycosylation sites of STIM1, we created different mutat

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

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

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

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

221 Mutations in the glycosylation site on ephrin-A1 result in protein aggreg

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

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

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

225 ered A(H1N1)pdm IAV with differing potential glycosylation sites on HA for sensitivity to collectins

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

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

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

229 Mutation of predicted N-glycosylation sites on SIRPalpha indicates that Sp-D bin

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

231 In this study, we analyzed all glycosylation sites on synaptotagmin 1, synaptophysin, a

232 o determine the influence of these missing N-glycosylation sites on the distinct neutralization pheno

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

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

235 her attenuated by introducing two additional glycosylation sites on the top of the HA head at Asn 142

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

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

238 creases directly with the number of N-linked glycosylation sites, our results indicate that additiona

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

240 VWF variant that predicts disruption of an O-glycosylation site (p.Ser1486Leu) and a rare variant enc

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

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

243 smission E1E2s had lost a potential N-linked glycosylation site (PNGS) in E2.

244 contained fewer potential asparagine-linked glycosylation sites (PNGSs) in variable region 5 (V5) th

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

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

247 Combined mutagenesis of all N-glycosylation sites resulted in the accumulation of the

248 by generating an additional (third) N-linked glycosylation site, resulting in protein misfolding and

249 Processing of N-glycosylation site(s) is dispensable for the overall TcS

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

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

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

253 on or by mutation of all of the 10 predicted glycosylation sites, ST binding and surface localization

254 han nonsynonymous mutations, and conserved N-glycosylation sites, suggesting that some of the HERV-K

255 rfusogenic NiV-F protein lacking an N-linked glycosylation site (T5FDeltaN3).

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

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

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

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

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

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

262 of FI carrying additional surface-exposed N-glycosylation sites that were expected to sterically hin

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

264 tures), PRRSV-01 virus quickly regains these glycosylation sites through replication in vivo, suggest

265 The addition of glycosylation sites to 1918 HA and removal of glycosylat

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

267 Of these, the predominant glycosylation site was alpha1-87, one of the major helic

268 Each glycosylation site was characterized individually, with

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

270 Each N-glycosylation site was eliminated individually by replac

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

272 terization of complex proteins with multiple glycosylation sites we utilized 2D LC, where RP separati

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

274 on and sequential mutagenesis of potential N-glycosylation sites, we identified TMEM106B as a type 2

275 Because this site has two potential O-glycosylation sites, we tested whether recombinant GalNA

276 Vpp and HCVcc that contained this new HVR495 glycosylation site were less sensitive to antibody neutr

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

278 Glycosylation sites were clearly localized from the ETD

279 Several known glycosylation sites were confirmed.

280 del for this antibody indicated that several glycosylation sites were critical for neutralization.

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

282 Six of the seven N-glycosylation sites were found to be glycosylated.

283 glycoproteins showed that extreme C-terminal glycosylation sites were modified by an STT3B-dependent

284 Eleven of 13 possible SUATM129 N-linked glycosylation sites were modified with carbohydrate.

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

286 Indeed, changes in glycosylation sites were observed with the appearance of

287 N-glycosylation sites were reintroduced into GP3 and GP5 o

288 Glycopeptides from two different N-linked glycosylation sites were separated from all other trypti

289 tries in mouse Notch1 and identified a novel glycosylation site with alanine in place of proline, sug

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

291 EDEM1 has five N-linked glycosylation sites with the most C-terminal site recogn

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

293 the latter introducing a potential N-linked glycosylation site within a predicted CD4-binding pocket

294 s were observed with the appearance of a new glycosylation site within HVR495.

295 1Delta phenotype, while mutation of a single glycosylation site within Msb2 was sufficient to confer

296 An artificially introduced glycosylation site within the HIR was also not utilized

297 We identified a new glycosylation site within the HVR495 region of HCV subty

298 ty assays on CDKAL1 constructs carrying an N-glycosylation site within the luminal domain, we further

299 bution, and mutation of a predicted N-linked glycosylation site within the N-terminus disrupts GAR-3-

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