ライフサイエンスコーパス: polypeptide

1 mers, cationic polysaccharides, and cationic polypeptides).

2 rchitectures have been reported for the same polypeptide.

3 enables robust ubiquitination of the nascent polypeptide.

4 tems, these proteins are fused into a single polypeptide.

5 h the surface along the entire length of the polypeptide.

6 in polysaccharide biosynthesis into a single polypeptide.

7 translationally incorporated into the parent polypeptide.

8 s when the domains are expressed as separate polypeptides.

9 tion of reaction centre and light-harvesting polypeptides.

10 unction in the presence of aggregation-prone polypeptides.

11 s in chaperone holdase activity for unfolded polypeptides.

12 form a disulfide bridge between two Siglec-E polypeptides.

13 re protein complexes formed by six different polypeptides.

14 n of cytochrome P450, family 7, subfamily b, polypeptide 1 (CYP7B1) and results in increased plasma l

15 Lamina-associated polypeptide 1 (LAP1) is an integral protein of the inner

16 r nuclear membrane protein lamina-associated polypeptide 1 (LAP1), are required for rearward nuclear

17 lipoprotein B mRNA-editing enzyme, catalytic polypeptide-1 (APOBEC1), together with its cofactor RBM4

18 that apolipoprotein B mRNA-editing catalytic polypeptide 3 expression and editing function was heat s

19 that apolipoprotein B mRNA-editing catalytic polypeptide 3A (A3A) and A3G expression levels were sign

20 l:betaGlcNAc beta-1,4-galactosyltransferase, polypeptide 5 (B4GALT5) expression in lung tissue (P = 1

21 els, higher insulin, and lower islet amyloid polypeptide accumulation were observed.

22 cluding increased enzyme activity, increased polypeptide accumulation, and possibly reduced substrate

23 de variety of cargo including nucleic acids, polypeptides, adeno-associated viruses, and nanodots.

24 d dynamics of a self-assembling elastin-like polypeptide along its entire self-assembly pathway, from

25 es that contact an 80-angstrom-long unfolded polypeptide along the axial channel.

26 genes found in C-fibers: calcitonin-related polypeptide alpha (Calca/Cgrpalpha), specific to pain-se

27 rt, and are regulated by stable tubulin-only polypeptide, an MT-associated protein.

28 ntial enzymatic activities from a single Sde polypeptide: an ADP-ribosyltransferase and a nucleotidas

29 etween two polypeptides, or between a single polypeptide and a new molecule (polymer, small molecule,

30 d-beta, alpha synuclein, human islet amyloid polypeptide and prions, the peptides and proteins associ

31 ss to multiple activity states from the same polypeptide and transmission of that information across

32 to probe the mobility and density of the FG-polypeptides and embedded macromolecules within intact N

33 re the hydration water dynamics on different polypeptides and liposome surfaces and find the DW dynam

34 to trigger the rapid degradation of aberrant polypeptides and mRNAs.

35 Polypeptides and polynucleotides are natural programmabl

36 metabolism, as they are cleaved from larger polypeptides and proteins.

37 The RQC complex polyubiquitylates aberrant polypeptides and recruits a Cdc48 hexamer to extract the

38 amides, anionic polysaccharides, and anionic polypeptides) and polybases (e.g., polyamines, pyridine

39 n, vasoactive intestinal peptide, pancreatic polypeptide, and 24-hour urinary 5-hydroxyindoleacetic a

40 , oxyntomodulin (enteroglucagon), pancreatic polypeptide, and somatostatin.

41 wers into iDR-NCs using PEG-grafted cationic polypeptides, and (4) physically loading neoantigen into

42 tified mitotic regulators, misfolded nascent polypeptides, and pathological Huntingtin variants as th

43 Apolipoprotein B mRNA-editing catalytic polypeptide (APOBEC) 3 proteins have been identified as

44 significant upregulation of fibrinogen gamma polypeptide, apolipoproteins A-Ib and A-II, galectin-1,

45 Polypeptides are generally too large and polar to passiv

46 high density of initiating groups from which polypeptides are grown, forming a brush polymer.

47 M) and closely related calmodulin-like (CML) polypeptides are principal sensors of Ca(2+) signals.

48 EGF Arg(1023) to citrulline with recombinant polypeptide arginine deiminase 4 (PAD4) abolished ADAMDE

49 Detoxification of aggregated reporter polypeptides as well as misfolded endogenous proteins in

50 o actin subunits connected by a single Lmod2 polypeptide, as reported in the original structure, the

51 NUCB1 inhibits aggregation of islet-amyloid polypeptide associated with type 2 diabetes mellitus, a-

52 ome-associated complex (RAC) but not nascent polypeptide-associated complex (NAC).

53 o acid becomes incorporated into the nascent polypeptide at the site of the PTC.

54 RMM36m, with improved accuracy in generating polypeptide backbone conformational ensembles for intrin

55 The polypeptide backbone forms transient, sparse hydrogen-bo

56 Here we measure intramolecular polypeptide backbone reconfiguration as a way to underst

57 The enzyme showed pI of 4.1 and a single polypeptide band of 83.1kDa after SDS-PAGE.

58 Here, we report a polypeptide-based macromolecule with spatially organized

59 mmarize the recent advances in the design of polypeptide-based supramolecular structures, including c

60 stem is developed to easily tune the size of polypeptide-based, thermoresponsive hydrogel particles,

61 e ribonucleoproteins (RNPs) with a family of polypeptides bearing different arrangements of cationic

62 ee protein subpopulations, including nascent polypeptides being translated and post-translationally m

63 ndependent growth, whereas its chaperone and polypeptide-binding functionalities are dispensable.

64 c understanding of the dynamic nature of the polypeptide-binding pocket in the Hsp70 chaperone cycle.

65 Strikingly, the polypeptide-binding pocket is completely closed, seeming

66 e RQC component, Rqc2p, modifies the nascent polypeptide by adding a carboxyl-terminal alanine and th

67 tagged CEPs and identified stably associated polypeptides by precision mass spectrometry.

68 a partly conserved 40-residue nonstructural polypeptide, called the delta peptide, that is produced

69 d a paradigm by which lncRNAs encoding small polypeptides can modulate general biological pathways an

70 Using a combination of small molecule and polypeptide CCS calibrants, we successfully determined t

71 of beta-cells lacking Abcc8 into pancreatic polypeptide cells but not to alpha- or delta-cells.

72 mical protein synthesis to prepare three ShK polypeptide chain analogues, each containing either an a

73 Interaction between the nascent polypeptide chain and the ribosomal exit tunnel can modu

74 at of an overall extended and highly dynamic polypeptide chain comprising three helical segments and

75 nd addition of the amino acid to the growing polypeptide chain during protein synthesis.

76 g, including the balance between solvent and polypeptide chain entropies.

77 observe simultaneous folding of the nascent polypeptide chain in real time.

78 donor to the asparagine residue of a nascent polypeptide chain is catalyzed by an oligosaccharyltrans

79 m a trefoil knot in the denatured state of a polypeptide chain of 120 residues is 5.8 +/- 1 kcal mol(

80 is is the first evidence that folding of the polypeptide chain precedes disulfide formation within a

81 tudied folding events at the early stages of polypeptide chain translocation into the mammalian ER us

82 le of hindered dihedral rotations within the polypeptide chain, with a proportionality coefficient b

83 known about spontaneous knot formation in a polypeptide chain-an event that can potentially impair i

84 of an IgG1 and at multiple sites in the same polypeptide chain.

85 nce, but rather to the mature portion of the polypeptide chain.

86 It is now clear which polypeptide chains become disordered and which become re

87 plings between amino acids within and across polypeptide chains have allowed for inference of native

88 and allo-Ile, both l-allo-ShK and d-allo-ShK polypeptide chains were prepared by total chemical synth

89 isms as well as the interactions of unfolded polypeptide chains with other cell components.

90 Hsp70 that binds ribosome-associated nascent polypeptide chains, also binds to the TPR domain of Sec7

91 xpression of the corresponding complementary polypeptide chains, retain tetrameric architecture and a

92 MCM2-7 is a heterocomplex made of different polypeptide chains, the MCM complexes of many Archaea fo

93 increase of the number of GABs on individual polypeptide chains.

94 tively affected the retention of most of the polypeptides chains.

95 a large channel that contains three types of polypeptide clamp sites: an alpha clamp, a phenylalanine

96 Polypeptide clamps located throughout the PA channel cat

97 This activity is in addition to its viral polypeptide cleavage function.

98 UN, ATP hydrolysis by the D2 ring moves the polypeptide completely through the double ring, generati

99 Muscle sarcomeres contain giant polypeptides composed of multiple immunoglobulin and fib

100 nit and the smallest of its kind, the 23-kDa polypeptide comprises a metallonuclease domain only.

101 X5(1-125)-DTM interaction was inhibited by a polypeptide comprising PEX5 residues 138-639.

102 Here, the authors show that control over a polypeptide conformation can be achieved by altering the

103 racellular fate of micelles of a recombinant polypeptide conjugated with doxorubicin via an acid-labi

104 esigned and tested simple de novo 98-residue polypeptides containing 7-residue repeats (AEEEXXX, wher

105 RPM6/7 are the only known examples of single polypeptides containing both an ion channel pore and a s

106 Our results suggest that an appropriate polypeptide context or other adequate structural element

107 Interestingly, when placed in the V3 polypeptide context, a mature bi-antennary complex-type

108 in the -1 frame, and generate the 70 aa-long polypeptide CopA(Z), which helps cells survive toxic cop

109 e main fraction as well as small fraction of polypeptides could lower the denaturation of crayfish my

110 uch as with the erythropoietin protein, a V3 polypeptide derived from HIV-1 gp120, or a simple 9-fluo

111 V whole-virus (WV) particles and recombinant polypeptides derived from the four PEDV structural prote

112 evolution of inter-monomer distances within polypeptides deviates both from the predictions of those

113 The core polypeptide dimer and two small subunits coordinate 54 b

114 gration, including the efficiency with which polypeptide domains integrate into the membrane, the var

115 We report herein that Chimeric Polypeptide Doxorubicin (CP-Dox), a nanoparticle formula

116 i) to obtain a reduced dynamical model for a polypeptide dynamics in water and (ii) to identify diagn

117 N-myristoyltransferase with an elastin-like polypeptide (ELP) fused to a short recognition sequence

118 versus uncollapsed state of an elastin-like polypeptide (ELP), an uncharged thermoresponsive polymer

119 the hydrophobic collapse of an elastin-like polypeptide (ELP).

120 Elastin-like polypeptides (ELPs) derived from the tropoelastin sequen

121 ymmetric structure within the homodimeric Fc polypeptide, enable completely selective binding to the

122 entify and functionally characterize a novel polypeptide encoded by the lncRNA LINC00961.

123 We investigated the polypeptides encoded by two genes upregulated during gro

124 enylalanine, l-tyrosine, l-tryptophan) and a polypeptide (epsilon-poly-l-lysine) in prolonging the co

125 erics, partially mediated by an unusual heme-polypeptide ester bond.

126 ound to also bind ribosomes near the nascent polypeptide exit tunnel, but the function of this SecA-r

127 ribosomal proteins with rRNA surrounding the polypeptide exit tunnel.

128 heir activity, whereas vasoactive intestinal polypeptide-expressing interneurons increased their acti

129 Spasmolytic polypeptide-expressing metaplasia (SPEM) develops in pat

130 mediated anion-exchange activity and surface polypeptide expression did not change.

131 Neither the l-allo-ShK nor the d-allo-ShK polypeptides folded, whereas both l-ShK and d-ShK folded

132 Our results demonstrate that polypeptide folding can occur without complete domain tr

133 QC), which targets the partially synthesized polypeptide for proteasomal degradation through the acti

134 Synthetic polypeptides from the ring-opening polymerization of N-c

135 Here we demonstrate that the polypeptide GalNAc-transferase 2 (GalNAc-T2) specificall

136 The polypeptide GalNAc-transferases (GalNAc-Ts), that initia

137 used by mutations in the neurofilament light polypeptide gene (NEFL).

138 IkappaBalpha (nuclear factor of kappa light polypeptide gene enhancer in B-cell inhibitor, alpha), l

139 f exogenous glucose-dependent insulinotropic polypeptide (GIP) in the splanchnic region in 10 obese p

140 er fasting and stimulated gastric inhibitory polypeptide (GIP) levels.

141 f clinical investigation, gastric inhibitory polypeptide (GIP), as proof-of-principle peptides to dem

142 rm of human glucose-dependent insulinotropic polypeptide (GIP), GIP(3-30)NH2, was recently identified

143 ghrelin, cholecystokinin, gastric inhibitory polypeptide (GIP), glucagon-like peptide 1 (GLP-1), and

144 stability in de novo and naturally-occurring polypeptides, giving new insight into how single alpha-h

145 Herein, we use a synthetic polypeptide-grafted comb macromolecule to demonstrate ho

146 atelet preparation that concentrates various polypeptide growth factors and, therefore, has the poten

147 These systems consist of a single polypeptide harboring the domains of sensor kinases and

148 ations in multi-domain nuclear receptor (NR) polypeptides has remained challenging, with few crystal

149 Synthetic polypeptides have received increasing attention due to t

150 est change in hepatitis B virus core antigen polypeptide (HBcAg/p21) synthesis, it mediates a dramati

151 Amyloid-beta (Abeta) and human islet amyloid polypeptide (hIAPP) aggregate to form amyloid fibrils th

152 eptide, derived from the human islet amyloid polypeptide (hIAPP).

153 or, human sodium-taurocholate cotransporting polypeptide (hNTCP), on macaque primary hepatocytes faci

154 tor human sodium taurocholate cotransporting polypeptide (hNTCP).

155 GPCRs; these receptors are activated by long polypeptide hormones and constitute targets of drug deve

156 ryotic PTM to recombinantly synthesize lipid-polypeptide hybrid materials.

157 ression has come far since the 'one-gene one-polypeptide' hypothesis proposed by Beadle and Tatum.

158 au in the brain during AD, and islet amyloid polypeptide (IAPP) in pancreatic islets in T2D.

159 Islet amyloid polypeptide (IAPP) is responsible for cell depletion in

160 Human islet amyloid polypeptide (IAPP) is the major component of amyloid dep

161 Aggregation of the islet amyloid polypeptide (IAPP) to form fibrils and oligomers is impo

162 (SHLP2), on the misfolding of islet amyloid polypeptide (IAPP), a critical pathogenic step in type 2

163 Aggregation of islet amyloid polypeptide (IAPP), a peptide hormone co-synthesized and

164 y effect on the aggregation of islet amyloid polypeptide (IAPP), a peptide which shares sequence simi

165 ded aggregates composed of the islet amyloid polypeptide (IAPP), its role in the disease is unknown.

166 sically disordered polypeptide islet amyloid polypeptide (IAPP), which is associated with type 2 diab

167 lpha-synuclein (alpha-Syn) and islet amyloid polypeptide (IAPP).

168 nt synthesis of a smaller number of cellular polypeptides illustrating a unique mode of action of the

169 diseases is that the level of amyloidogenic polypeptide in vivo is below the critical concentration

170 ue phase transition behavior of elastin-like polypeptides in bulk and within microfluidic-generated d

171 s) of myosin light-chain phosphatase partner polypeptides in regulation of vascular smooth-muscle cel

172 The conformational change of triazole polypeptides in response to the donor-acceptor pattern w

173 re of how Gnd(+) influences the stability of polypeptides in three distinct physical regimes by varyi

174 Contrary to the full-length polypeptide, in fact, the DFNKF sequence is not stable i

175 ranscript encoding a protein named AtC30Y, a polypeptide including most part of AtCPSF30 and a YT521B

176 The single Arf mRNA encodes two distinct polypeptides, including full-length p19(Arf) and N-termi

177 The unique features of these synthetic polypeptides, including their chemical diversity of side

178 umulation is regulated and whether the ISG15 polypeptide influences HCMV replication remain unknown.

179 report that a systemic administration of the polypeptide insulin-like growth factor II (IGF-II) rever

180 type-2 diabetes related human islet amyloid polypeptide intermediate stabilized in nanodiscs.

181 hat brings N- and C-terminal segments of the polypeptide into proximity, high ionic strength that pro

182 translocates signal peptide-bearing nascent polypeptides into the endoplasmic reticulum (ER), and it

183 erse family of membrane-permeabilizing small polypeptides involved in replication and pathogenesis of

184 l translation of mRNA into the corresponding polypeptide is a complex multistep process, requiring ac

185 This polypeptide is conserved between human and mouse, is loc

186 ationally when the N-terminus of the nascent polypeptide is still attached to the ribosome.

187 the biological significance of these hidden polypeptides is still unclear.

188 atures a massive amount of nascent secretory polypeptides, is particularly sensitive to stress.

189 interaction of the intrinsically disordered polypeptide islet amyloid polypeptide (IAPP), which is a

190 tes I. scapularis organic anion transporting polypeptide, isoatp4056 and kynurenine amino transferase

191 ing ISG15 accumulation and whether the ISG15 polypeptide itself influences HCMV infection biology rem

192 tional and biorelated films like polymer and polypeptide layers, which is of topical interest for int

193 y associated with the trimeric LHCII protein polypeptides, Lhcb1, Lhcb2 and Lhcb3.

194 olipoprotein B mRNA editing enzyme catalytic polypeptide-like (APOBEC) genes as an important source o

195 lipoprotein B mRNA editing enzyme, catalytic polypeptide-like (APOBEC) proteins are a family of cytid

196 olipoprotein B mRNA editing enzyme catalytic polypeptide-like APOBEC3A and APOBEC3B have emerged as k

197 chored to an electrode via a short, flexible polypeptide linker.

198 S, followed by conformational changes of two polypeptide loops on the major capsid F proteins.

199 y structures and cost-effective synthesis of polypeptide materials.

200 etent states, as compared with a random-coil polypeptide, may contribute to the slow in vitro folding

201 Key features of the polypeptide-micelle interaction include the anchoring of

202 ring amyloid fibril formation, amyloidogenic polypeptides misfold and self assemble into soluble pre-

203 found that the molecular structure of these polypeptides modulates the degree of PABP-mediated enhan

204 protein-conducting conduits that facilitate polypeptide movement in the opposite direction-from the

205 rions were generated in cells overexpressing polypeptide N-acetylgalactosaminyltransferase 1 (GalNAcT

206 catalytic subunit gamma gene PPP3CC and the polypeptide N-acetylgalactosaminyltransferase 4 gene GAL

207 is initiated by a large family of UDP-GalNAc:polypeptide N-acetylgalactosaminyltransferases (GalNAc-T

208 covery of sodium taurocholate cotransporting polypeptide (NTCP) as the hepatitis B virus (HBV) recept

209 Sodium taurocholate cotransporting polypeptide (Ntcp) from the respective species was clone

210 s for the sodium-taurocholate cotransporting polypeptide (NTCP), which is a hepatocellular transporte

211 The Na(+) -taurocholate cotransporting polypeptide (NTCP/SLC10A1) is believed to be pivotal for

212 n wild-type (WT), organic anion transporting polypeptide (OATP) knockout mice (lacking Slco1a/1b isof

213 gated the role of organic anion transporting polypeptide (OATP) transporters to the disposition of do

214 uding 909 bp of coding region that encoded a polypeptide of 302 amino acids possessing all the charac

215 we termed this polypeptide 'small regulatory polypeptide of amino acid response' (SPAR).

216 Islet amyloid polypeptide oligomeric assemblies were shown to contribu

217 erized alpha-helical cytotoxic islet amyloid polypeptide oligomers which interact with cell membranes

218 formation of new covalent bonds between two polypeptides, or between a single polypeptide and a new

219 y we have shown that CRM1 binds NESs in both polypeptide orientations.

220 BNST pituitary adenylate cyclase activating polypeptide (PACAP) and its cognate PAC1 receptor transc

221 n of NUPR1, mapped by NMR, was a hydrophobic polypeptide patch at the 30s region of its sequence, as

222 ellular matrices as populations of assembled polypeptide phases ranging from particles to amyloid fib

223 ugh locomotion-induced vasoactive intestinal polypeptide positive (VIP) interneuron depolarization ca

224 the less abundant delta and gamma/pancreatic polypeptide (PP) cells.

225 tor (Y4R) and its cognate ligand, pancreatic polypeptide (PP), are involved in the regulation of ener

226 her-order functions in living systems (e.g., polypeptides, proteins, and nucleic acids) cannot occur

227 factor 7-like 2 (TCF7L2), gastric inhibitory polypeptide receptor (GIPR), caveolin 2 (CAV2), and pept

228 tive GLP-1, glucose-dependent insulinotropic polypeptide receptor (Gipr)-deficient mice receiving bac

229 upled pituitary adenylate cyclase-activating polypeptide receptor (PAC1R) is a potential therapeutic

230 ability to act as H-bond acceptors, and the polypeptides regain their alpha-helical structure.

231 The organic anion-transporting polypeptides represent an important family of drug uptak

232 n elaborate multidomain architectures, these polypeptides represent challenging targets for detailed

233 logical functions supported by these diverse polypeptides require them to have an amphipathic nature,

234 1) and GIP (glucose-dependent insulinotropic polypeptide), respectively.

235 owed by degradation of the aberrant mRNA and polypeptide, ribosome disassembly and recycling.

236 te was transcribed with 12 pure proteins (80 polypeptides): RNA polymerase II, six general transcript

237 Standard methods that rely on perturbing a polypeptide's sequence and evaluating impact on folding

238 A pH titration method enhanced this polypeptide's solubility and, with the aid of </=5D NMR,

239 The polypeptide's vectorial emergence from the ribosomal tun

240 Here we identified the polypeptide segment essential for BB0238-BB0323 interact

241 us of the data analysis was on an 11-residue polypeptide segment in mouse [Formula: see text](121-231

242 he RodZ transmembrane domain dictate nascent polypeptide selection by SecA instead of the SRP machine

243 natural d-proline ((D)P) stereoisomer into a polypeptide sequence is a typical strategy to encourage

244 In addition to recognizing polypeptide sequence, the GalNAc-Ts exhibit unique long-

245 the co-translational insertion of arbitrary polypeptide sequences into the Sec translocon.

246 ,2,3-triazole groups, when incorporated onto polypeptide side-chains, serve as both H-bond donors and

247 Hence, we termed this polypeptide 'small regulatory polypeptide of amino acid

248 se CRISPR/Cas9 engineering to develop a SPAR-polypeptide-specific knockout mouse while maintaining ex

249 We characterized the LLO and polypeptide specificity of all three TbOST isoforms and

250 ir venom such as conotoxins, which are short polypeptides stabilized by disulfide bonds, and conopept

251 and facilitate the in-register alignment of polypeptide strands that is characteristic of amyloid fi

252 y is an ATP-induced allosteric regulation of polypeptide substrate binding and release.

253 ity toward the LLO and region 1 to influence polypeptide substrate specificity.

254 ding evidence for an active release of bound polypeptide substrates following ATP binding.

255 in a cooperative manner from their unfolded polypeptide subunits, without biological chaperones.

256 Swc5 is a conserved subunit of the 14-polypeptide SWR complex that is required for the histone

257 loading to HIV unspliced RNA and rate of Gag polypeptide synthesis was quantified in cellulo.

258 , which is reversibly conjugated to numerous polypeptide targets, impacts the proteome and physiology

259 Lysozyme is an antimicrobial polypeptide that can be used for food preservation.

260 of insulin-like growth factor II (IGF-II), a polypeptide that crosses the blood-brain barrier and act

261 n insulin mRNA encoding a highly immunogenic polypeptide that is targeted by T cells in T1D patients.

262 tudy reveals a new source of nonconventional polypeptides that act as self-epitopes in clinical autoi

263 CKS proteins are small (9-kDa) polypeptides that bind to a subset of the cyclin-depende

264 family of thermally responsive elastin-like polypeptides that exhibit temperature-triggered micelliz

265 ic phosphorylated tyrosine into the cationic polypeptide, the helical structure of AMPs was distorted

266 o drive the ligation of separately expressed polypeptides through a process termed protein trans-spli

267 cation channel for the movement of misfolded polypeptides through the endoplasmic reticulum membrane.

268 nd the global reconfiguration timescale of a polypeptide to be the sum of solvent friction and intern

269 one Ssb interacts with ribosomes and nascent polypeptides to assist protein folding.

270 ality control mechanisms eliminate defective polypeptides to ensure proteostasis and to avoid the tox

271 capture of increasingly complex motifs from polypeptides to single cell organisms and mammalian cell

272 gand binding domain to tightly clamp the two polypeptides together.

273 Using a human islet amyloid polypeptide transgenic mouse model of islet amyloidosis,

274 s a subtle increase in cytoplasmic HBcAg/p21 polypeptide translation, which shifts the equilibrium fr

275 Hsp100 polypeptide translocases are conserved members of the AA

276 nt, indicating that both the beta-barrel and polypeptide transport-associated (POTRA) domains are req

277 Arabidopsis thaliana, revealing three tandem polypeptide transport-associated (POTRA) domains, with P

278 tion of segment 7 mRNA with NXF1, mutant NS1 polypeptides unable to promote mRNA export did neither.

279 ons of a collection of labeled and unlabeled polypeptides using smFRET and SAXS, we directly assessed

280 t a strategy to modulate the conformation of polypeptides utilizing donor-acceptor interactions emana

281 PAC1/2 receptor ligand vasoactive intestinal polypeptide (VIP) had no effect on plasma corticosterone

282 f mast cells (MCs) and vasoactive intestinal polypeptide (VIP) in barrier regulation in IBS and healt

283 ice, lower activity of vasoactive intestinal polypeptide (VIP) interneurons resulted in an increased

284 Strikingly, vasoactive intestinal polypeptide (VIP), a neuropeptide critical for synchrony

285 zation of the peptides vasoactive intestinal polypeptide (VIP), calcitonin-gene related peptide (CGRP

286 tex that originates in vasoactive intestinal polypeptide (VIP)-expressing interneurons.

287 ional interactions between nucleic acids and polypeptides was a key transition in the origin of life

288 ntibody response, mainly directed against S1 polypeptides, was observed at days 7 to 10 postinfection

289 ymes, they appear as tandem repeats in large polypeptides we refer to as CSRPs (copper-only SOD-repea

290 ucagon-like peptide 1 and gastric inhibitory polypeptide were lower compared with PS-CF, and after 18

291 he three allo-Thr or allo-Ile-containing ShK polypeptides were able to fold into defined protein prod

292 ransport is an assembly of natively unfolded polypeptides, which contain phenylalanine-glycine (FG) b

293 DeActs, genetically encoded actin-modifying polypeptides, which effectively induce actin disassembly

294 rogress in the chemical design of functional polypeptides, which plays a crucial role to manipulate t

295 tu maturation of UQCRFS1 produces N-terminal polypeptides, which remain bound to holocomplex III.

296 osin alpha 1 (Talpha1)-a naturally occurring polypeptide with an excellent safety profile in the clin

297 a highly extended, intrinsically disordered polypeptide with unusually high polyproline type II heli

298 ort pore wide enough to allow the passage of polypeptides with a secondary structure.

299 ns a large diversity of essentially isomeric polypeptides with the cationic and amphiphilic character

300 orter and Na(+) -taurocholate cotransporting polypeptide, within the enterohepatic circulation.