ライフサイエンスコーパス: signal peptide

1 owing transport of a Tat substrate lacking a signal peptide.

2 s observed when it was expressed without its signal peptide.

3 signal peptidase II (LspA) that removes the signal peptide.

4 gineered ruminant expressed CD18 without the signal peptide.

5 gion, which potentially acts as GPI-addition signal peptide.

6 in intracellular because of the absence of a signal peptide.

7 ceptor expression through binding to the CD4 signal peptide.

8 associates with plasma HDL via its uncleaved signal peptide.

9 map to the C1 region of gp120 and one to the signal peptide.

10 splanted into a variant form of FGF4 without signal peptide.

11 media and the impact of either PelB or DsbA signal peptide.

12 al secretion in the absence of an N-terminal signal peptide.

13 2 to 27 that may represent an unconventional signal peptide.

14 ing a prodomain in addition to an N-terminal signal peptide.

15 ized to the cytosol and both proteins lack a signal peptide.

16 cifically bind the RR proximal region of the signal peptide.

17 be significantly enhanced by optimizing the signal peptide.

18 eavage with complete removal of the bombyxin signal peptide.

19 vector, pCI-neo, with and without a collagen signal peptide.

20 ere found in 463 of these putative secretory signal peptides.

21 ed as putative secretory proteins containing signal peptides.

22 l or the ER using ER-targeting and retention signal peptides.

23 Targeting to the translocase is mediated by signal peptides.

24 s the primary docking site for twin-arginine signal peptides.

25 binding cavity for twin-arginine-containing signal peptides.

26 cted by a limited set of naturally occurring signaling peptides.

27 ing cell wall-associated extensins and small signaling peptides.

28 reciated route for the secretion of amidated signaling peptides.

29 wnstream main ORFs, whereas sORFs may encode signaling peptides.

30 large-scale discovery of O-glycosylation on signaling peptides.

31 s, glycoproteins, as well as flavonoids, and signaling peptides.

32 mmunoglobulin (Ig) domain and a high-quality signal peptide [9], and we show evidence that it is secr

33 al consensus domain architecture comprises a signal peptide, a 60-90-residue globular prodomain with

34 glycoprotein complex consisting of a stable-signal peptide, a receptor-binding subunit, GP1, and a v

35 proteins, comprising a cleavable N-terminal signal peptide, a surface-exposed central passenger and

36 el missense mutations were discovered in the signal peptide (A13V) and the extracellular domains (E31

37 It remains unknown, however, how far these signaling peptides act.

38 which binds and sequesters the secreted agr-signaling peptide (AIP).

39 nd found that Astn2 has a cleaved N-terminal signal peptide, an N-terminal domain located in the lume

40 o HDL is mediated by its retained N-terminal signal peptide, an unusual feature for a secreted protei

41 ipt encodes a precursor protein comprising a signal peptide and 5 repeats of variegin-like sequences

42 regions: an N-terminal region codifying for signal peptide and a C-terminal (C-term) region, which p

43 g glycine (G) results in the cleavage of the signal peptide and abrogation of leukotoxin-induced cyto

44 on of effectors(4), despite possessing a Sec signal peptide and being mainly secreted via the T2SS.

45 glucanotransferase, devoid of its N-terminal signal peptide and C-terminal nonconserved regions, was

46 Pasteurella) haemolytica binds to the intact signal peptide and causes cytolysis of ruminant leukocyt

47 served hairpin-like structure comprised of a signal peptide and early mature region initiates protein

48 by a nonclassical mechanism, not involving a signal peptide and not requiring transport from the endo

49 port through interactions with the substrate signal peptide and other Tat components, notably the Tha

50 antagonist, all IL-1 family cytokines lack a signal peptide and require proteolytic processing into a

51 Conserved residues from the signal peptide and residues downstream of the canonical

52 plasmic reticulum (ER) upon emergence of the signal peptide and return to the cytosol after terminati

53 the cell envelope following cleavage of its signal peptide and that this process is required for TPP

54 Clustering strictly required an intact RR signal peptide and the presence of the TatABC subunits,

55 The location of the inserted signal peptide and the Tha4-cpTatC contact data suggest

56 n structure as a CMCMC-type, consisting of a signal peptide and three chitin-binding (C) domains with

57 as precursors containing amino-terminal Sec signal peptides and are exported through the inner-membr

58 e helices, intrinsically disordered regions, signal peptides and other motifs.

59 port the solution-phase structures of native signal peptides and related analogs capable of either st

60 d ProtComp v9.0 were utilized to predict the signal peptides and the signal peptide-dependent secrete

61 ly transport substrate proteins implies that signal peptides and transmembrane domains pass through t

62 involving a complex ensemble of host-derived signaling peptides and bacterial modifier enzymes capabl

63 distribution of a set of negatively charged signaling peptides and proteins - known as the HS intera

64 native receptor for growth factors and other signaling peptides and sequestering and localizing them,

65 e the likelihood of capturing these modified signaling peptides and to provide improved sequence cove

66 9 amino acids, reveals a predicted cleavable signal peptide, and suggests structural homology with th

67 molecular distinction between TM domains and signal peptides, and the propensity for hydrophobic H-se

68 activity impairs processing of preproinsulin signal peptide antigen and its recognition by specific a

69 Signal peptides appear to have evolved only in some eudi

70 Accordingly, the MDK signal peptide appeared to be rich in good binders to co

71 the significant upregulation of VGF-derived signaling peptide AQEE-30 upon high caloric feeding.

72 Upon crossing the plasma membrane, signal peptides are cleaved off and mature domains reach

73 Small posttranslationally modified signaling peptides are proteolytically derived from larg

74 ulation in Medicago truncatula in which root signaling peptides are translocated to the shoot where t

75 thermore, our results highlight the bombyxin signal peptide as a reliable secretion sequence applicab

76 form or in complex with nuclear localization signal peptides as the starting conformation.

77 After SecA2 engagement with the signal peptide, Asp1 to Asp3 promote SecA2 engagement wi

78 rminal amino acids 35-80 of DGAT1, but not a signal peptide at the N terminus of MGAT2, is required f

79 ays suggest an impaired functionality of the signalling peptides at low pH.

80 om plants, and in addition to removal of the signal peptide, at least one cleavage processing step be

81 d hypothesized that, given the presence of a signal peptide, BB0744 may be a surface-exposed protein.

82 Sec61 is the channel that translocates signal peptide-bearing nascent polypeptides into the end

83 act sites on cpTatC and assessed the role of signal peptide binding on Tha4 assembly with the cpTatC-

84 suppressed inactivating substitutions in the signal peptide binding site on TatC.

85 rt of substrate proteins cross-linked to the signal peptide binding site tentatively identified mutan

86 Preprotein or signal peptide binding to the purified and reconstituted

87 ors did not function by restoring detectable signal peptide binding to the TatBC complex.

88 d silkworm expression system with its innate signal peptide, bombyxin, secures structural homogeneity

89 A point mutation in the signal peptide breaks the alpha helix allowing co-transl

90 its sequence orthologue hFPR3 also react to signal peptides but are much more narrowly tuned in sign

91 Signal peptide cleavage and N-glycosylation of proteins

92 ysis mapped structural microheterogeneity of signal peptide cleavage at the amino terminus of FGF2, w

93 stn2, but we did not observe any evidence of signal peptide cleavage in Astn1.

94 byxin, secures structural homogeneity at the signal peptide cleavage site regardless of the native se

95 Q), at amino acid position 5 upstream of the signal peptide cleavage site, with cleavage-inducing gly

96 tail the mechanism by which co-translational signal-peptide cleavage is prevented.

97 Signal-peptide cleavage occurs only late after gp160 cha

98 phobic nature and is located adjacent to the signal peptide cleft.

99 rboring a more hydrophobic h-region in their signal peptides confirmed that unlike in TorA[KQ]-30aa-M

100 but does not affect binding indicates that a signal peptide conformational change is required during

101 , the Jek1 and Jek3 proteins share identical signal peptides, conserved cysteine positions and direct

102 Thus, bacterial signal peptides constitute a novel class of immune activ

103 s greatly enhanced by binding of an extended signal peptide containing 19 additional residues.

104 adhesins typically have a 90-amino acid-long signal peptide containing an elongated N-region and a hy

105 Proteins are targeted to TatBC by signal peptides containing an essential pair of arginine

106 Because the majority of signal peptide-containing proteins encoded by A. oris po

107 periplasm in a piggyback fashion by the Tat signal peptide-containing subunit PaoA.

108 re corroborated by experiments redirecting a signal-peptide-containing FGF family member from the end

109 features of FGF2 as they are absent from all signal-peptide-containing members of the FGF protein fam

110 The OPH signal peptide contains an invariant cysteine residue at

111 SCUBE3 (signal peptide CUB-EGF-like domain-containing protein 3)

112 scube1 (signal peptide-CUB (complement protein C1r/C1s, Uegf, an

113 Signal peptide-CUB-EGF domain-containing protein 3 (SCUB

114 atocyte S1P secretion and that its uncleaved signal peptide delays apoM trafficking out of the cell,

115 However, when KISS1 is missing the secretion signal peptide (DeltaSS), invasion and metastasis are no

116 In mammalian cells, signal peptide-dependent protein transport into the endo

117 lized to predict the signal peptides and the signal peptide-dependent secreted proteins among the 35,

118 Ghrelin, a hunger signalling peptide derived from the peripheral tissues,

119 peptide of the Spike protein with an optimal signal peptide did not enhance or reduce infectious part

120 central role in Tat operation: It binds the signal peptide, directs translocase assembly, and may fa

121 SPaseII cleaves the signal peptide during bacterial lipoprotein processing.

122 ted to the endoplasmic reticulum (ER) by its signal peptide during synthesis.

123 These findings suggest that the GspB signal peptide electrostatically binds anionic lipids at

124 Furthermore, all signal peptides examined here function as potent activat

125 e of naturally O-linked glycosylation on the signaling peptides extracted from mouse and human pancre

126 VEN (GLV)/ROOT GROWTH FACTORS/CLE-Like small signaling peptide family is encoded by 11 genes in Arabi

127 protein (AhAI) encoding a 26 amino acid (aa) signal peptide followed by the 43 aa region and the prev

128 MAN2A1-FER protein retained the signal peptide for Golgi localization from MAN2A1 and tr

129 ave been described that harbor an N-terminal signal peptide for release along the classical secretory

130 extension protein (UBCEP) that consists of a signal peptide for secretion, a mono-ubiquitin domain, a

131 38 amino acids long, possessed an N-terminal signal peptide for secretion, and contained a conserved

132 788 amino acids in P. jirovecii, including a signal peptide for the former 2 but not the latter.

133 N-terminally formylated signal peptide fragments with variable sequence and leng

134 nd secretion of S100b-a protein that lacks a signal peptide-from brown adipocytes.

135 The removal of the N-terminal signal peptide further increased phytase activity.

136 Tha4-cpTatC contact data suggest a model for signal peptide-gated Tha4 entry into the chamber to form

137 ex (GPC) of arenaviruses, composed of stable signal peptide, GP1, and GP2, is the only antigen correl

138 BC complex catalyzes insertion of a pre-SufI signal peptide hairpin that penetrates about halfway acr

139 ge, a novel hairpin-hinge model in which the signal peptide hairpin unhinges during movement of the m

140 ugh diverse, contain an absolutely conserved signal peptide hydrophobic (H) domain.

141 We also found that the putative signal peptide in CwlT is required for CwlT to function

142 es clearly indicated the involvement of AhAI signal peptide in extracellular secretion.

143 We demonstrated that EmbC has a functional signal peptide in M. tuberculosis.

144 coli trimethylamine N-oxide reductase (TorA) signal peptide in TatBC receptor binding in vivo and in

145 mRNAs containing an amber-stop codon in the signal peptide in the presence of the N(epsilon)-(5-azid

146 ing in particular on the roles played by Tat signal peptides in protein targeting and translocation.

147 stable signal peptide (SSP) is unique among signal peptides in that it is an integral component of t

148 transporters export antimicrobial or quorum signaling peptides in Gram-positive bacteria.

149 CLV3/ESR (CLE) proteins are important signaling peptides in plants.

150 e required for generating amidated bioactive signaling peptides, in Chlamydomonas and mammalian cilia

151 titutive secretion of FGF1 with an exogenous signal peptide increased beta-cell number in the absence

152 that the TatB F13Y substitution resulted in signal peptide-independent assembly of the Tat transloca

153 vitro overexpression of G1 or G2 lacking the signal peptide inhibited cell viability, triggered phosp

154 We provide evidence that the substrate signal peptide inserts between cpTatC subunits arranged

155 sis, we report that the N-region of the GspB signal peptide interacts with anionic lipids through ele

156 interferes with the deep insertion of a Tat signal peptide into the TatBC receptor complex.

157 vely impermeable macromolecule tagged with a signal peptide is chaperoned through the nanopore by nuc

158 The 18-amino acid signal peptide is necessary for binding to HDL and inter

159 motif, a minimal, functional h-region in the signal peptide is required for Tat-dependent export in E

160 SRP receptor (SR) on the membrane, where the signal peptide is transferred to the translocon.

161 sides the Tat motif, the h-region of the Tat signal peptides is another important binding determinant

162 ions results in a GhV-F that now possesses a signal peptide, is efficiently cell surface expressed, e

163 CR1 was expressed in N. benthamiana with its signal peptide, it provoked the plant immune system, whe

164 attention has been directed to glycosylated signaling peptides, largely due to lack of enabling anal

165 ptide forms present today and the protonated signalling peptides likely to be dominating in future oc

166 N-terminal signal peptide; second, internal signal peptide-mediated secretion and third, non-convent

167 leased from a reporter construct by internal signal peptide-mediated secretion it can be incorporated

168 lar space was believed to strictly depend on signal peptide-mediated translocation into the lumen of

169 Overexpression of p.Gly97Arg and another signal peptide mutation, p.Gly29Asp, caused cellular ret

170 pically synthesized as preproteins, carrying signal peptides N-terminally fused to their mature domai

171 by these results, we discover that bacterial signal peptides, normally used to translocate proteins a

172 ed to a single-point mutation, rendering the signal peptide of a seed storage protein kafirin resista

173 atidylinositol anchor signal region with the signal peptide of cell wall protein alpha-agglutinin of

174 downregulation of the fusion activity by the signal peptide of F, which has not been reported for oth

175 and secretion experiments revealed that the signal peptide of Gp3 does not act as a membrane anchor,

176 Since the signal peptide of HER2 directed mCherry to the mitochond

177 Deletion of the N-terminal signal peptide of IL-12 can effect such a change by prev

178 The signal peptide of Midkine is accessible to HLA class II

179 The signal peptide of preproinsulin is a major source for HL

180 reported that, contrary to the paradigm, the signal peptide of ruminant CD18, the beta subunit of bet

181 lysis of chimeric proteins revealed that the signal peptide of the bat MuV fusion protein is responsi

182 binds the Sec61 translocon and prevents the signal peptide of the nascent HER3 protein from initiati

183 In this work, we demonstrate that the signal peptide of the S. aureus quorum-sensing signal, A

184 Replacement of the signal peptide of the Spike protein with an optimal sign

185 Signal peptides of membrane proteins are cleaved by sign

186 This signaling pathway consists of small signaling peptides of the CLE family interacting with CL

187 s in protease cleavage, glycosylation sites, signal peptides or trans-membrane domains between Africa

188 rized plant peptides to date acting as small signaling peptides or antimicrobial peptides are derived

189 essing either wild-type DeltaspAvr2 (deleted signal-peptide) or the DeltaspAvr2(R45H) variant become

190 d protein substrates we show that the native signal peptide, or any N-terminal extension, has an inhi

191 How these signalling peptides orchestrate pattern formation at a m

192 factor activated upon binding of its cognate signaling peptide PapR on a tetratricopeptide repeat-typ

193 P and ATP-gammaS-bound states shows that the signal peptide partially inserts into the SecY channel i

194 in the bacterial periplasm with the help of signal peptide paves the way for a large scale identific

195 The signal peptide peptidase (SPP) is an intramembrane cleav

196 Here, we show that signal peptide peptidase (SPP) modulates the ER shape th

197 lex virus (HSV) glycoprotein K (gK) binds to signal peptide peptidase (SPP), also known as minor hist

198 the intramembrane-cleaving aspartyl protease signal peptide peptidase (SPP), is involved in this path

199 The signal peptide peptidase (SPP)-related intramembrane asp

200 While the combined action of signal peptide peptidase and endoplasmic reticulum (ER)

201 d by a host intramembrane-cleaving protease, signal peptide peptidase, and is required for cell fusio

202 Another intramembrane protease, signal peptide peptidase, predominantly co-purified with

203 74 is mediated by the intramembrane protease signal peptide peptidase-like (SPPL)2a, a process critic

204 Signal peptide peptidase-like 2a (SPPL2a) is an aspartyl

205 ating mutation in the intramembrane protease signal peptide peptidase-like 2A (SPPL2A) unexpectedly e

206 ion was mapped to the intramembrane protease signal peptide peptidase-like 2a (Sppl2a), a gene not pr

207 psin S (CatS) and the intramembrane protease signal peptide peptidase-like 2a (SPPL2a).

208 el substrates of the intramembrane proteases signal peptide peptidase-like 2a and b (SPPL2a/b).

209 ment of ODZ1 through proteolytic cleavage by signal peptide peptidase-like 2a.

210 Signal peptide peptidase-like 3 (SPPL3) is a poorly char

211 tub of NRG1 type III is further processed by signal peptide peptidase-like proteases SPPL2a and SPPL2

212 The presenilin homologue signal-peptide-peptidase-like 2a (SPPL2a) has been impli

213 A plasmid-encoded signalling peptide, Phr*pLS20, inactivates the anti-repr

214 We conclude that Tat signal peptides play roles in substrate targeting and in

215 Disruption of the N-terminal NMB0419 signal peptide, predicted to export the protein beyond t

216 subunit genes) with AAF/III, as well as the signal peptide present in the beginning of the agg3A gen

217 ow that a second antagonistic "self-sensing" signaling peptide, previously known to suppress self-ind

218 enome-wide association study and reveal that signal peptide processing of Cytokinin Oxidase 2 (CKX2)

219 t-dispersing factor (PDF), a neuromodulatory signaling peptide produced only by circadian clock circu

220 es acting in shoots and proposed to perceive signaling peptides produced in roots depending on soil n

221 hains while the incomplete processing of the signal peptide produces N-terminal elongated polypeptide

222 f protease cleavage sites, identification of signal peptides, protein interactions, determination of

223 her study shows that FER is a receptor for a signaling peptide (Rapid Alkalinization Factor 1 [RALF1]

224 lishing FPR1 and FPR2 as sensitive and broad signal peptide receptors.

225 55 proteins contained the lipoprotein signal peptide recognition site of signal peptidase II (

226 peptides but are much more narrowly tuned in signal peptide recognition.

227 stromal loop (S2) caused specific defects in signal peptide recognition.

228 t is caused by co-translational insertion of signal peptides recognized by the signal-recognition par

229 ctedly large proportion of ATs with extended signal peptide regions (ESPRs).

230 l patterning factor (EPF) family of secreted signaling peptides regulate the frequency of stomatal de

231 in intermediate (p22) without the N-terminal signal peptide, remains elusive.

232 Truncations, N-terminal methionine excision, signal peptide removal, and some post-translational modi

233 h post-translational modifications including signal peptide removal, N-terminal methionine excision,

234 least 175,542 predicted sequences, bacterial signal peptides represent the largest and structurally m

235 nd 14-28, located in and overlapping the MDK signal peptide, respectively.

236 ssical secretion by virtue of the N-terminal signal peptide; second, internal signal peptide-mediated

237 Lipoproteins are synthesized with a signal peptide securing them to the cytoplasmic membrane

238 amine the effect of a cleavable leucine-rich signal peptide sequence (Lucy tag) on OR surface express

239 The signal peptide sequence of MBLs dictates their adaptabil

240 e pathway combined with reengineering of the signal peptide sequence results in display levels 24-fol

241 l canine MDA-7 has a potential 28 amino acid signal peptide sequence that can target it for active se

242 rotein isoforms have a conserved N-terminus (signal peptide sequence) and are dissimilar in amino aci

243 second is an uncharacterized protein with a signal peptide sequence, and the third is an ortholog of

244 as to why so many large proteins, without a signal peptide sequence, are present in the prostatic fl

245 fficult to identify as they lack discernable signal peptide sequences and can make use of diverse sec

246 iation of this pathway normally requires two signals: peptide sequences in unassembled outer-membrane

247 eted to the yeast cell wall by replacing its signal peptide, serine-threonine-rich region, and glycop

248 entified 16 new superfamilies showing unique signal peptide signatures.

249 However, inactivation of both signal peptides simultaneously was found to completely a

250 escent protein mCherry, linked to endogenous signal peptide (SP) and glycophosphatidylinositol-anchor

251 s B GPCRs, the GLP-1R contains an N-terminal signal peptide (SP) and undergoes N-linked glycosylation

252 eting machinery that binds to the N-terminal signal peptide (SP) of nascent proteins.

253 y is initiated when a hydrophobic N-terminal signal peptide (SP) on the nascent protein emerges from

254 Expressed CPPs, coupled to a secretory signal peptide (SP), can support intercellular transport

255 The latent signal peptide (SP)-coding exons were fortuitous noncodi

256 rm) region and an N-terminal codifying for a signal peptide (SP).

257 proteins were cleaved at their own internal signal peptides (SPs), in which NSm domain I functions a

258 ly understood interaction between the stable signal peptide (SSP) and the transmembrane fusion subuni

259 iral fusion proteins, GPC retains its stable signal peptide (SSP) as an essential third subunit in th

260 roteins, GPC contains a myristoylated stable signal peptide (SSP) as an essential third subunit.

261 The arenaviral glycoprotein stable signal peptide (SSP) is unique among signal peptides in

262 serine mutation at position 33 in the stable signal peptide (SSP) subunit of GPC, and we demonstrate

263 n (GP) complex, which consists of the stable signal peptide (SSP), the receptor-binding subunit GP1,

264 rus GP complex, which consists of the stable signal peptide (SSP), the receptor-binding subunit GP1,

265 Identification of splice variants lacking a signal peptide suggests the existence of novel intracell

266 An internal cross-link in the signal peptide that blocks transport but does not affect

267 ocalization did not depend on the N-terminal signal peptide that mediates APOL1 secretion into the ci

268 tions as well as the effect of inverting the signal peptide that reflects the "positive-inside" rule.

269 conserved twin-arginine (RR) motif in their signal peptides that is involved in their binding to the

270 1 (ERAP1) is required for processing of the signal peptide, the mechanisms controlling signal peptid

271 e produced as preproproteins consisting of a signal peptide, the thionin domain, and an acidic domain

272 ging TaFAR enzyme with peroxisomal targeting signal peptides, the TaFAR could be compartmentalized in

273 thesis and the glycosylation of proteins and signaling peptides, the identification of these transpor

274 TRIP-1 lacks a signal peptide, therefore, in this study, we provide evi

275 We show that signaling peptides thought to act redundantly in Arabido

276 of NKG2A(+) NK cells mediated by MHC class I signal peptides through the engagement of CD94 without a

277 teins expressed without a membrane-targeting signal peptide, thus avoiding conserved pathways that mo

278 ty against extracellular Abeta42, we added a signal peptide to Hsp70.

279 rescent protein (mRFP) fusion protein with a signal peptide to secrete it from plant cells, did not p

280 It is a new function for signal peptides to contribute to tumor-specific CD4 T ce

281 The binding of two signal peptides to SecA was also examined to determine t

282 ge sites, Pfam domains, glycosylation sites, signal peptides, trans-membrane protein domains, and pho

283 Modified oleosin with an added vacuole signal peptide transports the ER-luminal LDs to vacuoles

284 e signal peptide, the mechanisms controlling signal peptide trimming and the contribution of the T1D

285 Following cleavage of the signal peptide upon entry into the endoplasmic reticulum

286 Analysis of 512 bacterial Tat signal peptides using secondary structure prediction and

287 epitope located at the C-terminal end of the signal peptide was found to be the most prevalent in pat

288 d from 51 to 300 amino acids (aa), while the signal peptides were from 18 to 20 aa long.

289 d imply a code of conduct exists between the signal peptides where one can compensate for inactivity

290 tural genetic mutation (T to C) within FBN30 signal peptide, which changes the position 10 amino acid

291 Glycoprotein 3 (Gp3) contains an N-terminal signal peptide, which is not removed, although bioinform

292 This process is controlled by secreted RALF signaling peptides, which have previously been shown to

293 Tat substrates have hydrophobic signal peptides with an essential twin arginine (RR) rec

294 TatB that restored transport activity to Tat signal peptides with inactivating twin arginine substitu

295 ecessary recognition, the interaction of Tat signal peptides with the receptor complex plays a critic

296 lating hormone (alpha-MSH) is a melanocortin signaling peptide with anti-inflammatory properties.

297 Several glycosylated signaling peptides with multiple glycoforms are identifi

298 s constitutes the first case of a ctenophore signalling peptide with homology to a neuropeptide.

299 imultaneous generation and purification of a signal peptide within a multifunctional resin can very l

300 an acute peripheral injection of the satiety-signaling peptide YY 3-36 increased 5-HT turnover in the