ライフサイエンスコーパス: signal peptide

1 eavage with complete removal of the bombyxin signal peptide.

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

3 ceptor expression through binding to the CD4 signal peptide.

4 associates with plasma HDL via its uncleaved signal peptide.

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

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

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

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

9 2 to 27 that may represent an unconventional signal peptide.

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

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

12 hibits processing of a potentially cleavable signal peptide.

13 e relies on T cell epitopes contained in its signal peptide.

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

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

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

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

18 gineered ruminant expressed CD18 without the signal peptide.

19 Targeting to the translocase is mediated by signal peptides.

20 captures substrate proteins by binding their signal peptides.

21 arginine-containing sequence motif in their signal peptides.

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

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

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

25 ed as putative secretory proteins containing signal peptides.

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

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

28 a few QS circuits known to utilize multiple signaling peptides.

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

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

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

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

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

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

35 re key enzymes involved in the regulation of signaling peptide activity.

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

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

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

39 precursor containing a 15-residue secretory signal peptide and a 90-residue peptidase inhibitor I9 d

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

41 rs (i.e., they contain a putative N-terminal signal peptide and a C-terminal conserved 13-amino-acid

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

43 requires both a unique 90-residue N-terminal signal peptide and an adjacent 24-residue segment (the A

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

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

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

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

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

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

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

51 peptide sequences have similar properties to signal peptide and signal anchor sequences.

52 peptide overlapping the junction between the signal peptide and the mature protein is not.

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

54 ctional significance, interposed between the signal peptide and the start of the conserved catalytic

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

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

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

58 Forty-four possess identifiable Sec-type signal peptides and thus are likely canonically secreted

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

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

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

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

63 equiring an intact translocase, a functional signal peptide, and a correctly folded substrate protein

64 ino-acid precursor consists of an N-terminal signal peptide, and mature Crz followed by Crz-associate

65 9 amino acids, reveals a predicted cleavable signal peptide, and suggests structural homology with th

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

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

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

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

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

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

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

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

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

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

76 d proteins, which are targeted by N-terminal signal peptides bearing conserved SRRxFLK 'twin-arginine

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

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

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

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

81 Preprotein or signal peptide binding to the purified and reconstituted

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

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

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

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

86 e that CD4(+) T cell epitopes present in the signal peptide can be accessible to recognition by CD4(+

87 Signal peptide cleavage and N-glycosylation of proteins

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

89 d via the general secretory pathway and that signal peptide cleavage is a required step in the produc

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

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

92 ing sequon and blocking glycosylation allows signal peptide cleavage, indicating that carbohydrate at

93 oxidation, acetylation, phosphorylation, and signal peptide cleavage.

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

95 Signal-peptide cleavage occurs only late after gp160 cha

96 Signal peptides cleaved from those alleles bind to HLA-E

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

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

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

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

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

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

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

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

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

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

107 The OPH signal peptide contains an invariant cysteine residue at

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

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

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

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

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

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

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

115 mber of environmental stimuli, including two signalling peptides designated as CSP and XIP.

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

117 ein insertion into the translocon, including signal-peptide docking at the translocon lateral gate (L

118 1 is secreted, confirming that the predicted signal peptide domain in MAC1 leads to secretion.

119 SPaseII cleaves the signal peptide during bacterial lipoprotein processing.

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

121 e HLA-A24 presents a naturally processed PPI signal peptide epitope.

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

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

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

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

126 known members of the CDC family, Ply lacks a signal peptide for export outside the cell.

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

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

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

130 38 amino acids long, possessed an N-terminal signal peptide for secretion, and contained a conserved

131 788 amino acids in P. jirovecii, including a signal peptide for the former 2 but not the latter.

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

133 vides an increased level of understanding of signal peptide function on the bacterial Tat pathway.

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

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

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

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

138 rk, the inter-relationship between these two signal peptides has been explored.

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

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

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

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

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

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

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

146 nsive framework to study the role of the GLV signaling peptides in plant development.

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

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

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

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

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

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

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

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

155 s reveal that the processing of the TtrB Tat signal peptide is dependent on the successful assembly o

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

157 al consequence of the presence of the pseudo signal peptide is not understood.

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

159 igotes indicate that although the N-terminal signal peptide is responsible for targeting TcSMUG produ

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 peptides mediate the interaction of native protei

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

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

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

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

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

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

173 amino acid sequence of 135 amino acids and a signal peptide of 20 amino acids.

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

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

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

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

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

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

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

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

182 We demonstrate that the N-terminal signal peptide of Sil3 mediates import into a specific s

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

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

185 that sequence these events, for example the signal peptide of the periplasmic nitrate reductase (Nap

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

187 38 or residue 17 excluding the 21-amino acid signal peptide of THPO receptor binding domain (RBD).

188 Signal peptides of HLA-A and HLA-C proteins carry methio

189 Signal peptides of membrane proteins are cleaved by sign

190 multisubunit complex with TatB and binds the signal peptides of Tat substrates.

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

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

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

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

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

196 How these signalling peptides orchestrate pattern formation at a m

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

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

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

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

201 ctive center of the gamma-secretase complex, signal peptide peptidase (SPP), and its homologues, the

202 arget a putative protease component of ERAD, signal peptide peptidase (SPP), have high selectivity an

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

204 Signal peptide peptidase (SPP), its homologs, the SPP-li

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

206 (SP) and the intramembrane-cleaving protease signal peptide peptidase (SPP).

207 butes to nisin resistance by regulation of a signal peptide peptidase (SppA), phage shock proteins (P

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

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

210 74 is mediated by the intramembrane protease signal peptide peptidase-like (SPPL)2a, a process critic

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

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

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

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

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

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

217 equences delayed processing of SP(UL40) by a signal peptide peptidase-type intramembrane protease.

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

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

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

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

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

223 fied crucial residues required for efficient signal peptide processing by SPP, which in turn has an e

224 tified crucial residues required for core-E1 signal peptide processing, including a GT3a sequence-spe

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

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

227 nalysis of a synthetic HCV JFH1 GT2a core-E1 signal peptide provides an essential structural template

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

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

230 55 proteins contained the lipoprotein signal peptide recognition site of signal peptidase II (

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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 ry receptor-1 (CD85j, ILT2, or LILRB1) and a signal peptide (SP(UL40)) that acts by upregulating cell

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

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

253 ssense mutations upstream of preproinsulin's signal peptide (SP) cleavage site were reported to cause

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

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

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

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

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

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

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

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

262 in that the mature complex retains a stable signal peptide (SSP) in addition to the conventional rec

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

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

265 strate that the resulting hydrophobic-region signal-peptide substitution (p.Thr17Arg) decreases MT1-M

266 Plants may produce signal peptides such as AtRALFL8 to induce cell wall rem

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

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

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

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

271 an overlapping sequon, NNTT, adjacent to the signal peptide that we show to be glycosylated at both a

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

273 t INS-IGF2, which contains the preproinsulin signal peptide, the B-chain, and eight amino acids of th

274 INS-IGF2 consists of the preproinsulin signal peptide, the insulin B-chain, and eight amino aci

275 As expected for a signal peptide, the Lucy tag was cleaved from the mature

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

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

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

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

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

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

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

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

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

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

286 o map the recognition site for twin arginine signal peptides to the cytosolic N-terminal region and f

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

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

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

290 The N-terminal signal peptides were cleaved, and NFR1 protein retained

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

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

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

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

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

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

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

298 Several glycosylated signaling peptides with multiple glycoforms are identifi

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