ライフサイエンスコーパス: polypeptide

1 vasopressin) and VIP (vasoactive intestinal polypeptide).

2 igate real-time cotranslational folding of a polypeptide.

3 can also function when anchored by an apolar polypeptide.

4 onally interacts with newly synthesized Var1 polypeptide.

5 facilitate dimerization of the 90 amino acid polypeptide.

6 s oligomeric solution of human islet amyloid polypeptide.

7 ould facilitate the recruitment of a nascent polypeptide.

8 ecomposition or in their polymerization into polypeptide.

9 uiring two domains to be present on the same polypeptide.

10 ent antibody conjugated with an elastin-like polypeptide.

11 inct non-canonical amino acids into a single polypeptide.

12 atory properties are present within a single polypeptide.

13 ich include a variety of polysaccharides and polypeptides.

14 e composed of sixteen pairs of the alphabeta-polypeptides.

15 ion of faulty mRNA and partially synthesized polypeptides.

16 onic, anionic, short oligopeptides, and long polypeptides.

17 paucimannose structures to nascent secretory polypeptides.

18 ynthesis to prevent accumulation of aberrant polypeptides.

19 t for understanding associations of l- and d-polypeptides.

20 composed of bound water and unwound gelatin polypeptides.

21 processes that determine the fate of nascent polypeptides.

22 rnal out-of-frame ORFs, which generate novel polypeptides.

23 ator (CFTR) have distinct effects on nascent polypeptides.

24 n-functional and potentially toxic truncated polypeptides.

25 modifications and elimination of individual polypeptides.

26 r nuclear membrane protein lamina-associated polypeptide 1 (LAP1) caused defective VLDL secretion and

27 embrane-spanning cofactor, lamina associated polypeptide 1 (LAP1) or lumenal domain like LAP1 (LULL1)

28 lance in the levels of the lamina-associated polypeptide 1 (LAP1), an activator of ER-resident Torsin

29 r torsinA or its cofactor, lamina-associated polypeptide 1 (LAP1), resulted in fatty liver disease an

30 ol-cytochrome c reductase Rieske iron-sulfur polypeptide 1 (UQCRFS1), the Rieske FeS protein in RCIII

31 well as wild-type C57BL/6 and glucagon-like polypeptide 1 receptor deficient (Glp-1r(-/-)) mice on c

32 C19 (cytochrome P450, family 2, subfamily C, polypeptide 19) *2 and *3 alleles leads to a loss of fun

33 Apolipoprotein B editing enzyme, catalytic polypeptide 3 (APOBEC3) family members are cytidine deam

34 riphosphatase/RNA helicase X-linked DEAD-box polypeptide 3 (DDX3X) emerged as a novel therapeutic tar

35 ogy in the presence of vasoactive intestinal polypeptide, a potent stimulator of ion secretion classi

36 The human lysosomal polypeptide ABC transporter TAPL (ABC subfamily B member

37 onal repression mechanism that reduces eEF2K polypeptide abundance to preclude eEF2 phosphorylation,

38 itions exhibits increased thermal stability, polypeptide accessibility and ceruloplasmin-mediated inh

39 Amyloidoses (misfolded polypeptide accumulation) are among the most debilitatin

40 ocon" sufficient for translocation of the AC polypeptide across the plasma membrane of target cells.

41 pose secretome have predominantly focused on polypeptide adipokines.

42 n (Delta(Spont)) contained mainly C-terminal polypeptides akin to C1, the cell-surface anchored C-ter

43 This review focuses on the applications of polypeptides alongside the synthetic advances in the rin

44 the amyloid-beta peptide, the islet amyloid polypeptide, alpha-synuclein, and the hungingtin protein

45 via immunoglobulin-G1 Fc domains and 2 XTEN polypeptides (Amunix Pharmaceuticals, Inc, Mountain View

46 t PPXY motifs at the C-terminus of the Warts polypeptide and additional WW domains bind unoccupied mo

47 -stabilizing interactions at early stages of polypeptide and nucleic acid co-existence.

48 asis, including folding of newly synthesized polypeptides and clearance of degraded proteins.

49 anged symmetrically along the D1 and D2 core polypeptides and comprise four chlorophyll (P(D1), P(D2)

50 accumulate increased amounts of certain Coq polypeptides and display a stabilized CoQ synthome.

51 However, lipidated polypeptides and integral membrane proteins-an important

52 ClpB3 specifically targets unstructured polypeptides and mediates the reactivation of heat-denat

53 ycle arrested ribosomes and degrade aberrant polypeptides and mRNAs.

54 t lead to change in aggregation rates for 23 polypeptides and proteins.

55 s tuned by intrinsic features of the nascent polypeptides and timely association of factors with the

56 yloids, including Abeta, human islet amyloid polypeptide, and tau have been found to assemble as fibr

57 istry of alpha-amino acids, on occurrence of polypeptides, and more generally on organic electrochemi

58 ure has three biopolymers: oligonucleotides, polypeptides, and oligosaccharides.

59 heat-induced misfolding of newly synthesized polypeptides, and so has been thought to depend on ongoi

60 rophobic residues in the constituent keratin polypeptides, and the extent to which the electrolyte io

61 This unique polypeptide appears to be highly flexible and turned out

62 role of a cotranslational chaperone, nascent polypeptide-associated complex (NAC), in regulating subs

63 d palmitoylation, reduced the level of beta1 polypeptides at the plasma membrane, and reduced the ext

64 ein, Na(+)/taurocholate (TCA) cotransporting polypeptide, at the site of a pharmacologically relevant

65 ons between O, N, and C unified atoms of the polypeptide backbone and side chains.

66 ins in which the chemical composition of the polypeptide backbone has been partially altered; and pro

67 d homologs indicate that the knot within the polypeptide backbone plays a significant role in the bio

68 Alfalfa protein isolates exhibited complex polypeptide banding ranging from molecular weight of 11-

69 Nascent polypeptides begin to fold in the constrained space of t

70 Folding of polypeptides begins during their synthesis on ribosomes.

71 ging from 10 to 225 kDa, built from the same polypeptide blocks with no post-translational and other

72 emained an outstanding challenge for natural polypeptides, building blocks of life, which are fragile

73 In vertebrates, RTKs are mostly activated by polypeptides but are not naturally sensitive to amino ac

74 n, not only at the same or proximal sites on polypeptides, but also by regulating each other's enzyme

75 rence for association with newly synthesized polypeptides, but each responds differently to changes i

76 ly extended viral proteins or entirely novel polypeptides by genetic overprinting.

77 ngly heterogeneous because multiple distinct polypeptides can be synthesized from a single mRNA seque

78 a specialized scaffold against which nascent polypeptides can begin to form structure in a highly coo

79 Understanding how polypeptides can efficiently and reproducibly attain a s

80 Although relatively large polypeptides cannot be thoroughly characterized using tr

81 t time the SFC-MS separation of a mixture of polypeptides carried out using poly(styrene-co-divinylbe

82 resence of topological permutations within a polypeptide chain and/or subunit rearrangements.

83 also correlate with increased intermolecular polypeptide chain association and aggregation.

84 y the cotranslational folding of the nascent polypeptide chain can also enhance PRF.

85 irmed that fennel nsLTP1 is a 9433 Da single polypeptide chain consisting of 91 amino acids with eigh

86 and translocates to the periplasm where the polypeptide chain does an about turn in order to enter a

87 hoice of dye attachment positions within the polypeptide chain has a substantial impact on which unfo

88 hich the conformational state of the nascent polypeptide chain has been linked to PRF.

89 Comparisons are usually performed at the polypeptide chain level, however the functional form of

90 ed denatured state we find that knotting the polypeptide chain of MJ0366 increase the folding energy

91 Single-chain FLARE (scFLARE) is a single polypeptide chain that incorporates a transcription fact

92 l slip site generates a force on the nascent polypeptide chain that scales with observed frameshiftin

93 ifferent icosahedral symmetries, causing the polypeptide chain to exist in seven quasi-equivalent env

94 d state presents ample opportunities for the polypeptide chain to transiently sample nonnative struct

95 RT is expressed as a single polypeptide chain within the Gag-Pol polyprotein, and ei

96 the product of both the overall fold of the polypeptide chain, and, typically, structural motifs mad

97 it players can now-starting from an extended polypeptide chain-generate a diversity of protein struct

98 nd thermodynamic consequences of threading a polypeptide chain.

99 ore with an unexpected crosslink to the main polypeptide chain.

100 chanical transduction through titin's intact polypeptide chain.

101 insic dynamic properties of emerging nascent polypeptide chains and guides them toward their biologic

102 Collagen I is a major tendon protein whose polypeptide chains are linked by covalent crosslinks.

103 genetic modifications are limited to natural polypeptide chains at the Cas9 termini, which excludes a

104 g that bound water is crucial to connect the polypeptide chains for the electron-conductivity.

105 e novo protein folding by protecting nascent polypeptide chains from misfolding and maintain translat

106 slation by labeling and releasing elongating polypeptide chains from translating ribosomes.

107 a unified picture of the nature of unfolded polypeptide chains in the absence of denaturant.

108 nfounded by release of puromycylated nascent polypeptide chains prior to fixation.

109 Our results suggest that polypeptide chains which form amyloid fibrils with narro

110 gies to label endogenously occurring nascent polypeptide chains within cells using O-propargyl-puromy

111 ycin is covalently incorporated into nascent polypeptide chains, anti-puromycin immunofluorescence en

112 hat water can be a good solvent for unfolded polypeptide chains, even those with a hydrophobic and ch

113 odel system for the study of folding of long polypeptide chains, including related phenomena such as

114 events premature degradation of such nascent polypeptide chains.

115 is to generate two non-covalently associated polypeptide chains.

116 e of ribosomes and incorporates into nascent polypeptide chains.

117 otein folding limits the lengths of cellular polypeptide chains.

118 rid biomaterials called cholesterol-modified polypeptides (CHaMPs) that exhibit programmable self-ass

119 Such HDAC4 polypeptide cleavage resulted in a ~30 kDa fragment that

120 liquid phase separation (LLPS) occurs when a polypeptide coalesces into a dense phase to form a liqui

121 All were distinguished by their polypeptide composition and partly by pigmentation.

122 However, can polypeptides confer functions of evolutionary relevance,

123 uch techniques facilitate the development of polypeptide conjugates to advance therapeutics, diagnost

124 ing several structural units within a single polypeptide, constitute a large fraction of all proteome

125 nst toxoplasmosis by (i) this novel chimeric polypeptide, containing epitopes that elicit CD8(+) T ce

126 er, we propose that individual intestinal IF polypeptides contribute in different ways to endotube mo

127 equent accumulation of partially synthesized polypeptides could explain the neurodevelopmental and ne

128 x that lacks 5 key PSII core reaction center polypeptides: D1, D2, PsbE, PsbF, and PsbI.

129 6 binds the N-terminal domain of ERFE, and a polypeptide derived from the N terminus of ERFE was suff

130 he changing information in a growing nascent polypeptide dictates the recruitment of functionally dis

131 la DEVELOPMENTALLY REGULATED PLASMA MEMBRANE POLYPEPTIDE (DREPP), a member of the MT binding DREPP/PC

132 like behavior that originates from intrinsic polypeptide dynamics.

133 old co-translationally during unidirectional polypeptide elongation by the ribosome.

134 njugated and recombinant A99 to elastin-like polypeptides (ELPs) as the scaffold and characterize the

135 tionary model whereby adaptive transmembrane polypeptides emerge de novo from thymine-rich non-genic

136 al in all cells and initiates when a nascent polypeptide emerges from the ribosome exit tunnel, where

137 drial ribosomes (mitoribosomes) with over 70 polypeptides encoded in nuclear DNA, translated on cytop

138 ight roles for glycans in sterically masking polypeptide epitopes and directly modulating Spike-ACE2

139 f evolutionary relevance, and how might such polypeptides evolve into modern proteins?

140 The nascent polypeptide exit site of the ribosome is a crowded envir

141 The nascent polypeptide exit tunnel (NPET) is a major functional cen

142 dyl transferase center (PTC) and the nascent polypeptide exit tunnel (NPET), and export of assembling

143 n eL24, the protein-folding machinery at the polypeptide exit tunnel (PET), and the ribosomal stalk,

144 rmational changes in MRP mL45 at the nascent polypeptide-exit site within the large mitoribosomal sub

145 mouse gastric corpus metaplasia (spasmolytic polypeptide expressing metaplasia, SPEM).

146 -healing; these cells are called spasmolytic polypeptide-expressing metaplasia (SPEM) cells.

147 and, ultimately, intestinalized spasmolytic polypeptide-expressing metaplasia (SPEM) was detected in

148 flammation, oxyntic atrophy, and spasmolytic polypeptide-expressing metaplasia (SPEM), a putative pre

149 stric corpus, a process known as spasmolytic polypeptide-expressing metaplasia (SPEM), increases the

150 indispensable role for vasoactive intestinal polypeptide-expressing SCN (SCN(VIP)) neurons, including

151 of SNORC on SDS-PAGE was due to its primary polypeptide features, suggesting no additional post-tran

152 ction-to-structure relationships of the NPC1 polypeptide fold required for membrane trafficking and g

153 The catalytic domain displayed a polypeptide fold similar overall to those of other membe

154 ular chaperones have evolved to help nascent polypeptides fold correctly and multimeric protein compl

155 lled on a truncated mRNA and tag the nascent polypeptide for degradation.

156 The method can uncover numerous inhibitory polypeptides for a protein and thereby define small inhi

157 For years, polypeptide formation has fascinated the scientific worl

158 ple of AMP is Epsilon-Poly-L-lysine (EPL), a polypeptide formed by ~ 25 lysine residues with known an

159 er 9, ABCB9) transports 6-59-amino-acid-long polypeptides from the cytosol into lysosomes.

160 tro testing of nuclear factor of kappa light polypeptide gene enhancer in B cells (NF-kappaB) signali

161 Expression of nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor (IkappaB)

162 Polypeptides generated from proteolytic processing of pr

163 sistance to glucose-dependent insulinotropic polypeptide (GIP) action may occur through desensitizati

164 in hormones glucose-dependent insulinotropic polypeptide (GIP) and glucagon-like peptide 1 (GLP-1) ar

165 (GLP-1) and glucose-dependent insulinotropic polypeptide (GIP) are two incretins secreted from gastro

166 nism of the glucose-dependent insulinotropic polypeptide (GIP) receptor (GIPR) prevents weight gain a

167 -1 (GLP-1), glucose-dependent insulinotropic polypeptide (GIP), cholecystokinin (CCK), peptide YY (PY

168 incretins, glucose-dependent insulinotropic polypeptide (GIP), has garnered much attention as a pote

169 st relevant targets, including islet amyloid polypeptide, glucosidases, and cholinesterases.

170 trimeric HA consists of two disulfide-linked polypeptides, HA1 and HA2.

171 to fold during translation before the entire polypeptide has been produced, which may be particularly

172 Polypeptides have attracted considerable attention in re

173 the wide range of applications towards which polypeptides have been applied.

174 each the functional state, newly synthesized polypeptides have to become enzymatically processed, fol

175 Human pancreatic islet amyloid polypeptide (hIAPP) and beta amyloid (Abeta) can accumul

176 Human islet amyloid polypeptide (hIAPP) functions as a glucose-regulating ho

177 an Amylin, also known as human islet amyloid polypeptide (hIAPP), is the major factor for categorizin

178 n (PrP(106-126)) and the human islet amyloid polypeptide (hIAPP), with giant lipid vesicles.

179 The polypeptide hormone islet amyloid polypeptide (IAPP) for

180 se cells produce, in a regulated manner, two polypeptide hormones - the natriuretic peptides - referr

181 that the antimicrobial and immunomodulatory polypeptide human cathelicidin LL-37 binds IAPP with nan

182 The polypeptide hormone islet amyloid polypeptide (IAPP) forms islet amyloid in type 2 diabete

183 Amyloid self-assembly of islet amyloid polypeptide (IAPP) is linked to pancreatic inflammation,

184 ic type II diabetes-associated islet amyloid polypeptide (IAPP), a hydrophobic-hydrophilic interface-

185 amyloid deposits derived from islet amyloid polypeptide (IAPP), a protein co-expressed with insulin

186 We trapped Rix7 with a polypeptide in the central channel, revealing Rix7's rol

187 trol (RQC) purges aberrant mRNAs and nascent polypeptides in a multi-step molecular process initiated

188 ngement of multiple forms of alpha- and beta-polypeptides in an individual LH1 ring.

189 -puromycin staining of puromycylated nascent polypeptides in fixed cells accurately reports on their

190 ical assays and live cell imaging of nascent polypeptides in mammalian cells, that puromycylated nasc

191 stress-induced misfolding and aggregation of polypeptides in most organisms and are responsible for p

192 nslational modification of newly synthesized polypeptides in the oxidizing environment of the endopla

193 step towards producing completely unnatural polypeptides in vivo.

194 t, unusually, possesses a large alpha-domain polypeptide insertion relative to other MINPPs.

195 d the SecY channel, pushing a segment of the polypeptide into the channel.

196 facilitates the lateral partitioning of the polypeptide into the membrane.

197 ergence demands a transition from disordered polypeptides into structured proteins with well-defined

198 uestration of misfolded proteins and nascent polypeptides into two distinct compartments, stress gran

199 How a polypeptide is moved through the SecA-SecY complex is po

200 erization of backbone-extended monomers into polypeptides is challenging due to their poor compatibil

201 However, how the substrate CtA, a 90-residue polypeptide, is recognized by PCAT1 remained elusive.

202 ng reductively stabilized, site-specific 5fC-polypeptide lesions and employed a quantitative MS-based

203 gous genes to understand the co-evolution of polypeptide ligands and receptors.

204 is review documents the discovery of several polypeptide ligands and their cognate receptors mainly e

205 h efficient for in vitro applications, these polypeptide ligases have not been utilized for the semis

206 lipoprotein B mRNA editing enzyme, catalytic polypeptide-like (APOBEC) cytidine deaminases, raising q

207 in B messenger RNA editing enzyme, catalytic polypeptide-like (APOBEC) family of single-stranded DNA

208 and apolipoprotein B mRNA editing catalytic polypeptide-like (APOBEC) mutagenesis over time, includi

209 olipoprotein B mRNA-editing enzyme catalytic polypeptide-like 3 (APOBEC3 or A3) family of cytidine de

210 lipoprotein B mRNA editing enzyme, catalytic polypeptide-like 3 (APOBEC3, A3) family member proteins

211 Inserting a flexible polypeptide linker into the central stalk of full-length

212 r dynamics simulation results, suggest how a polypeptide loop of an ERAD-L substrate moves through th

213 Our results suggest that phase-separating polypeptides may have been an evolutionary resource for

214 Although sHSPs are 12-25 kDa polypeptides, most assemble into oligomers with >= 12 su

215 e Small nuclear ribonucleoprotein-associated polypeptide N (Snrpn), contributing to transcriptional r

216 GALNT2 encodes the Golgi-localized polypeptide N-acetyl-d-galactosamine-transferase 2 isoen

217 levant human glycosyltransferase family, the polypeptide N-acetylgalactosaminyl transferases.

218 se, histone H3 methyltransferase SET7/9, and polypeptide N-acetylgalactosaminyltransferase with unpre

219 shed carrier-an immune-tolerant elastin-like polypeptide nanoparticle (iTEP NP)-with the peptides tha

220 xpressing sodium taurocholate cotransporting polypeptide (NTCP).

221 arget the sodium-taurocholate cotransporting polypeptide (NTCP; SLC10A1) on the sinusoidal membrane o

222 C inhibitors with organic anion transporting polypeptide (OATP) substrate properties, which facilitat

223 that a Drosophila organic anion-transporting polypeptide (OATP), which we named Ecdysone Importer (Ec

224 ced expression of organic anion transporting polypeptide (OATP)1A1, a transporter expressed in hepato

225 es overexpressing organic anion transporting polypeptides (OATP1B1, OATP1B3, and OATP2B1).

226 was co-assembled with a photo-cross-linkable polypeptide of 2-hydroxyethyl methacrylate modified poly

227 D that binds a single segment of an extended polypeptide of 3-4 residues.

228 protein MPT64, which is a highly immunogenic polypeptide of Mycobacterium tuberculosis, a causative a

229 ed when bound to a 69-residue two-PPXY motif polypeptide of the synaptic and podocyte protein synapto

230 If Ltn1 fails to ubiquitylate those stalled polypeptides or becomes limiting, CAT tails act as degro

231 r (Y(4)R) is unique as it prefers pancreatic polypeptide over NPY and peptide YY.

232 stem, pituitary adenylate cyclase-activating polypeptide (PACAP), and its cognate receptor, PAC1R, in

233 Pituitary adenylate cyclase activating polypeptide (PACAP, gene Adcyap1) is a neuropeptide and

234 tage, but favor somatostatin- and pancreatic polypeptide-positive cells at the expense of insulin- an

235 c studies of CshA_RD1-17, indicate that this polypeptide possesses a highly unusual dynamic transitor

236 Pancreatic polypeptide (PP) increased by 62%, 5 min after meal onse

237 eta-cells, namely alpha-cells and pancreatic polypeptide (PPY)-producing gamma-cells, obtained from d

238 ShK is a 35-residue disulfide-linked polypeptide produced by the sea anemone Stichodactyla he

239 ediating proteolytic targeting of incomplete polypeptides produced by ribosome stalling, and Ltn1 mut

240 n codon and primed to synthesize the encoded polypeptide product.

241 mammalian cells, that puromycylated nascent polypeptides rapidly dissociate from ribosomes even in t

242 Vasoactive intestinal polypeptide receptor (VIP1R) is a widely expressed class

243 the C-terminal tail (CTT) of SecA in nascent polypeptide recognition.

244 osphotyrosine (pY) motifs embedded in folded polypeptides remains highly challenging because of the s

245 precursor S glycoprotein into two associated polypeptides: S1 and S2.

246 cause the carbohydrases differently affected polypeptide secondary structures.

247 ptide 1 and glucose-dependent insulinotropic polypeptide secretion were lower after lunch but unalter

248 olecular interactions between the disordered polypeptide segments of protofilaments in directing the

249 These results allow preparation of polypeptide segments with different chain conformations

250 gous genes, designated NnOMT1-5 and encoding polypeptides sharing >40% amino acid sequence identity,

251 nteractions between the ribosome and nascent polypeptide skew folding pathways.

252 accommodated in the Na(+)/TCA cotransporting polypeptide structure model.

253 several rounds of binding to and release of polypeptide substrates at the substrate-binding domain (

254 tive interpretations of the translocation of polypeptide substrates longer than 100 aa.

255 (RCI, RCIII, RCIV, and RCV) by combining 13 polypeptides synthesized within mitochondria on mitochon

256 surfaces of many bacteria carry filamentous polypeptides termed adhesins that enable binding to both

257 Glatiramer acetate (GA) is a synthetic polypeptide that is used in the treatment of inflammator

258 These plaques are formed by aggregation of polypeptides that are derived from the Amyloid Precursor

259 (RQC) pathway for the degradation of nascent polypeptides that are encoded by defective messenger RNA

260 e coordinated by residues from the alphabeta-polypeptides that are hydrogen-bonded to BChl a.

261 ich domains emerged from shorter and simpler polypeptides that bound phospho-ligands via N-helix site

262 o collect information about the structure of polypeptides that interact with a supported lipid bilaye

263 on is mediated by ribosome-bound nascent ATI polypeptides that interact with ATI protein in inclusion

264 ation produces incomplete, ribosome-tethered polypeptides that the ribosome-associated quality contro

265 gating mitoribosomes bound to tRNAs, nascent polypeptides, the guanosine triphosphatase elongation fa

266 ecificity factor that recognizes the nascent polypeptides they encode.

267 cooperate during the ATPase cycle to move a polypeptide through the channel.

268 adual evolutionary trajectory leading from a polypeptide to a ubiquitous nucleic acid-binding protein

269 nesis factors (RPBs) compete for the nascent polypeptide to influence their localization, folding, or

270 The failure of polypeptides to achieve conformational maturation follow

271 et the general thermodynamic tendency of all polypeptides to form beta-sheets.

272 ripts, which exposes a reservoir of variable polypeptides to natural selection.

273 otease (M(pro) ) cleaves along the two viral polypeptides to release non-structural proteins required

274 The doses are lower than reported for other polypeptide tracers such as somatostatin analogs (2.1-2.

275 ore conserved in the upper part close to the polypeptide transferase center, while in the lower part,

276 ence stopped-flow methods to the analysis of polypeptide translocation catalyzed by these ATPase moto

277 nded transmembrane beta-barrel with a single polypeptide-transport-associated (POTRA) domain extendin

278 s glycosylation, oxidation, chlorination and polypeptide truncation variants and a previously unrepor

279 t stabilize Hsp70 interaction with substrate polypeptides upon hydrolysis of its bound ATP.

280 The approach enables the rapid synthesis of polypeptides using low concentrations of reactants witho

281 llate (EGCG), found in green tea, with Abeta polypeptides, using a combination of in vitro immuno-inf

282 Incubating its polypeptides, VemG and VemH, with 3,5-dihydroxybenzoic a

283 t SCN cells expressing vasoactive intestinal polypeptide (VIP) or its cognate receptor, VPAC2, are ne

284 In particular, while vasoactive intestinal polypeptide (VIP) signalling is essential for SCN functi

285 ining five new nonionic sulfoxide containing polypeptides was described.

286 (Translational Relocalization with Aberrant Polypeptides), was generalizable beyond the ES7L mutatio

287 Synthetic genes encoding Nanoluciferase polypeptides were inserted between the variable heavy an

288 r incretin, glucose-dependent insulinotropic polypeptide, were not as profoundly affected.

289 e similarity between specific regions of the polypeptide, whereas the global structural similarity is

290 It is a heterodimer of KIF3A and KIF3C motor polypeptides which have distinct biochemical and motile

291 nctionalization of serine residues in native polypeptides, which uses a reagent platform based on the

292 They are derived from precursor polypeptides whose modification by various dedicated enz

293 several fungi, Coq10 is encoded as a fusion polypeptide with Coq11, a recently identified protein of

294 th, N-terminal Pro/Ala/Ser (PAS) random-coil polypeptide with IL-1Ra.

295 the large ribosomal subunit elongate stalled polypeptides with carboxy-terminal alanine and threonine

296 Here, using ribonucleoprotein-inspired polypeptides with low-complexity RNA-binding sequences a

297 70 client association and aggregation toward polypeptides with predicted disorder, indicating that th

298 n of mammalian cells that express the target polypeptide within a natural membrane environment on the

299 tor was seen with somatostatin, glucagon, or polypeptide Y.

300 meters, and glucagon-like peptide-1 (GLP-1), polypeptide YY (PYY), and cholecystokinin peptides were