ライフサイエンスコーパス: carrier protein

1 an extended beta-ketoacyl chain (ACP = acyl carrier protein).

2 ozoite surface protein 8 (MSP8) as a vaccine carrier protein.

3 a chain linker to a diphtheria toxin mutant carrier protein.

4 array of tertiary and heteroaryl amines to a carrier protein.

5 th siderophores conjugated to an immunogenic carrier protein.

6 l length polysaccharide for conjugation to a carrier protein.

7 sence of a prior immune response against the carrier protein.

8 ratase, a decarboxylase and a dedicated acyl carrier protein.

9 gnition of peptides derived from the coupled carrier protein.

10 vaccine that used SIIL tetanus toxoid as the carrier protein.

11 shear conditions FVIII is released from its carrier protein.

12 surrogate of BDE-47 covalently attached to a carrier protein.

13 exclusive of the native substrate, acyl-acyl carrier protein.

14 harides of varying chain length to CRM197 as carrier protein.

15 ation of the identified minimal epitope on a carrier protein.

16 ith favourable dynamic properties of an acyl carrier protein.

17 ons ready for activation and coupling to the carrier protein.

18 supercomplex (termed III-IV) and the ADP/ATP carrier proteins.

19 sponses to Pfs25 when coupled to immunogenic carrier proteins.

20 nd NFU5 proteins with the ISCA class of Fe-S carrier proteins.

21 f genes encoding mitochondrial dicarboxylate carrier proteins.

22 fits to including non-conserved pneumococcal carrier proteins.

23 h CD45 expression, were examined for SC-PNAL carrier proteins.

24 along with a reduction in mitochondrial acyl carrier proteins.

25 ting functional overlap between BSH and Fe-S carrier proteins.

26 of B. pseudomallei and covalently linked to carrier proteins.

27 ately being incorporated into essential acyl carrier proteins.

28 FabZ dehydratase subunits with six AcpP acyl carrier proteins.

29 (Ppt) from coenzyme A (CoA) to diverse acyl carrier proteins.

30 nd that the evaluated proteins are potential carrier proteins.

31 chondrial presequence-containing but not for carrier proteins.

32 f novel fentanyl-based haptens conjugated to carrier proteins.

33 other mitochondrial proteins such as ADP/ATP carrier proteins.

34 Moreover, imported protein sterol carrier protein 2 (SCP2) occupies only a subregion of la

35 t function in vivo, we focused on the Sterol Carrier Protein 2 (scp2), a multifunctional protein that

36 Sterol Carrier Protein-2 (SCP-2) is an important non-specific l

37 H-Asn-Phe-Gly-Ala-Ile-Leu-Gly-NH2) and acyl carrier protein (65-74) fragment (H-Val-Gln-Ala-Ala-Ile-

38 ssion of uncoupling protein (UCP) 3, ADP/ATP carrier protein (AAC) 1 and AAC2, and pyruvate dehydroge

39 tein ISCU, accessory protein ISD11, and acyl-carrier protein ACP.

40 th PKSs are able to use dimethylmalonyl acyl carrier protein (ACP) as an extender unit.

41 ucing polyketide synthases (NR-PKS) the acyl-carrier protein (ACP) carries the growing polyketide int

42 TE1 for the acyl chain attached to the acyl carrier protein (ACP) domain of FASN is unknown.

43 an acyl-adenylate and ligation onto the acyl carrier protein (ACP) domain of MbtB to form covalently

44 Mutation of the acyl carrier protein (ACP) domain of the upstream module in o

45 a reaction chamber for the intramodule acyl carrier protein (ACP) domain that carries building block

46 Acyl carrier protein (ACP) domains act as interaction hubs wi

47 le, which forms extensive contacts with acyl carrier protein (ACP) during catalysis.

48 s DSF by dehydration of a 3-hydroxyacyl-acyl carrier protein (ACP) fatty acid synthetic intermediate

49 The acyl carrier protein (ACP) from fatty acid synthases sequeste

50 le for the C2-methylation of 3-ketoacyl-acyl carrier protein (ACP) intermediates to give the correspo

51 Acyl carrier protein (ACP) is a highly conserved cofactor pro

52 cleavage of the ester bond of pimeloyl-acyl carrier protein (ACP) methyl ester.

53 d a candidate gene encoding a beta-keto acyl carrier protein (ACP) reductase (BKR) putatively associa

54 bits the essential NADH-dependent enoyl-acyl-carrier protein (ACP) reductase, InhA.

55 many complex biosynthetic pathways, the acyl carrier protein (ACP) shuttles substrates to appropriate

56 lytic (NFS1), LYRM protein (ISD11), and acyl carrier protein (ACP) subunits.

57 ia esterification by the bacterial acyl-acyl carrier protein (ACP) synthase AasC but inhibitors of th

58 due to decreased activity of 3-ketoacyl-acyl carrier protein (ACP) synthase II.

59 ich BioZ proteins catalyze a 3-ketoacyl-acyl carrier protein (ACP) synthase III-like reaction to prod

60 polyketide biosynthesis, beta-ketoacyl-acyl carrier protein (ACP) synthases (KS), catalyze this proc

61 parate domains of the bifunctional acyl-acyl carrier protein (ACP) synthetase/2-acylglycerolphosphoet

62 Acyl-CoA and acyl-acyl carrier protein (ACP) synthetases activate exogenous fat

63 specialized acyl-transferase that uses acyl carrier protein (ACP) to covalently link fatty acids, vi

64 er of an R-3-hydroxyacyl chain from its acyl carrier protein (ACP) to the 3-OH group of UDP-GlcNAc.

65 We reveal that subunit B22 anchors an acyl carrier protein (ACP) to the complex, replicating the LY

66 Acyl carrier protein (ACP) transports the growing fatty acid

67 ype I PKS module minimally contains AT, acyl carrier protein (ACP), and ketosynthase (KS) domains.

68 esulfurase (NFS1), LYR protein (ISD11), acyl-carrier protein (ACP), and the iron-sulfur cluster assem

69 he PKS and NRPS modules mediated by the acyl carrier protein (ACP), condensation (C) and ketoreductas

70 on a thioesterase specific for butyryl-acyl carrier protein (ACP), which allows native fatty acid bi

71 , we demonstrate that the mitochondrial acyl carrier protein (ACP), which has a well-known role in FA

72 enosyl-l-methionine and either cellular acyl carrier protein (ACP)-coupled fatty acids or CoA-aryl/ac

73 d extender units switches largely to an acyl carrier protein (ACP)-independent mode.

74 inges on improving our understanding of acyl-carrier protein (ACP)-protein interactions.

75 ubunit (NFS1), LYR protein (ISD11), and acyl carrier protein (ACP).

76 , a polyene was detected in the tryptic acyl carrier protein (ACP).

77 ftD is non-covalently complexed with an acyl carrier protein (ACP).

78 single enzymatic step to an orthogonal acyl carrier protein (ACP).

79 PlsX is an acyl-acyl carrier protein (ACP):phosphate transacylase that interc

80 l transcriptional regulator Fis and the acyl carrier protein AcpP, were identified in P. aeruginosa.

81 selects from the bacterial pool of acyl-acyl carrier proteins (ACPs) an acyl chain of a specific leng

82 Acyl carrier proteins (ACPs) are essential to the production

83 Acyl carrier proteins (ACPs) are the scaffolds for fatty acid

84 Acyl carrier proteins (ACPs) are universal and highly conserv

85 ratory has developed methods to prepare acyl carrier proteins (ACPs) loaded with substrate mimetics a

86 Prior work showed that expression of acyl carrier proteins (ACPs) of a diverse set of bacteria rep

87 is highly selective for two specialized acyl carrier proteins (ACPs) that deliver the donor and accep

88 se (AT), which loads monomer units onto acyl carrier proteins (ACPs), small, flexible proteins that s

89 tics are positioned on the actinorhodin acyl carrier protein (actACP) to probe the underpinnings of s

90 n is laid for defining the dynamic action of carrier-protein activity in primary and secondary metabo

91 It makes acylphosphate from acyl-acyl carrier protein (acyl-ACP) and is also involved in coord

92 Cyanobacteria possess two enzymes, acyl-acyl carrier protein (acyl-ACP) reductase (AAR) and aldehyde-

93 omprehensive evaluation of hapten structure, carrier protein, adjuvant and dosing.

94 generally consists of an integrated peptidyl carrier protein, an amino acid-loading adenylation domai

95 terase-mediated offloading reaction from the carrier protein and activates the biosynthetic intermedi

96 The carrier protein and enzyme interact only weakly, but we

97 only when present at the amino-terminus of a carrier protein and even conservative peptide amino acid

98 ocking crosslinking of Escherichia coli acyl carrier protein and FabA, a direct mimic of the biologic

99 g (SAXS), the positions of the flanking acyl carrier protein and ketosynthase domains have been ident

100 cular level and is performed by at least one carrier protein and two channels in Arabidopsis (Arabido

101 dent tailoring enzymes, a free-standing acyl carrier protein and two hypothetical proteins in oocydin

102 ng to transfer clusters between scaffold and carrier proteins and in the final stages of FeS protein

103 g enzyme can adenylate each of these sulphur-carrier proteins and probably also catalyses the subsequ

104 ol-linker to serve as a conjugation point to carrier proteins and surfaces for immunological experime

105 me this limitation, including conjugation to carrier proteins and/or formulation with potent adjuvant

106 protein domain of the synthase to a separate carrier protein, and a non-ribosomal peptide synthetase

107 oesterase that hydrolyzes beta-ketoacyl acyl-carrier protein, and ShMKS1 is a decarboxylase that conv

108 olysaccharides were conjugated to the CRM197 carrier protein, and the resulting glycoconjugates were

109 f protein: E1 Ubl-activating enzymes, E2 Ubl carrier proteins, and E3 Ubl ligases.

110 osphate (S1P) is present in plasma, bound to carrier proteins, and involved in many physiological pro

111 nstable mutant variants of the mitochondrial carrier protein, Ant1, also induces aggresomes despite a

112 tent immunogens by chemically coupling to a "carrier protein" antigen.

113 s identified four stable complexes: the acyl-carrier proteins ApeE and ApeF bound to the thioesterase

114 ing, and its ability to interact with acidic carrier proteins are critical steps for proper enamel de

115 Specific carrier proteins are required to distribute these cofact

116 e reaction is an acyl chain bound to an acyl carrier protein, are classified so that unusual reaction

117 (e.g., a hormone carrier or a small-molecule carrier protein) as well as enzymes.

118 carboxyltransferase (CT) and biotin carboxyl carrier protein (BCCP) components.

119 oforms interact with the two biotin carboxyl carrier protein (BCCP) isoforms of A. thaliana ACCase.

120 domain-containing (BADC) and biotin carboxyl carrier protein (BCCP) subunits from Arabidopsis indicat

121 ion reaction of the acceptor biotin carboxyl carrier protein (BCCP), through the expected biotinoyl-A

122 is linked covalently to the biotin carboxyl carrier protein (BCCP).

123 ase (CT)-alpha, CT-beta, and biotin carboxyl carrier protein (BCCP1 or BCCP2).

124 is able to provide selectivity for both the carrier protein-bound amino acid and the amine substrate

125 hydroxylates C5 of norvaline appended to its carrier protein but can either chlorinate or hydroxylate

126 f the thioester bond to the structure of the carrier protein by using solution NMR spectroscopy and m

127 In addition, we show that different vaccine carrier proteins can be glycosylated using this system.

128 of a native siderophore and the immunogenic carrier protein cholera toxin subunit B (CTB).

129 oduced, to our knowledge, a novel carotenoid carrier protein, COCP, which consists of dimerized C-dom

130 al description of transport by mitochondrial carrier proteins, consistent with an alternating-access

131 Carrier proteins consume fuel in order to pump ions or m

132 ed by a docking domain, whereas an NRPS EpoB carrier protein contributes l-cysteine.

133 However, no gene encoding a sulphur-carrier protein could be located in the BE-7585A cluster

134 njugate vaccines, consisting of an antigenic carrier protein coupled to the capsular polysaccharide o

135 Carrier proteins covalently tether their cargo via a thi

136 on the chemical equilibrium of Fa binding to carrier proteins Cp, like albumin in plasma and intersti

137 ction of these compounds via functionalizing carrier proteins (CPs) of biosynthetic megaenzymes.

138 Carrier proteins (CPs) play a central role in biosynthes

139 ing them to phosphopantetheinyl arms of holo carrier proteins (CPs) via a thioester bond.

140 The nuclear export carrier protein CRM1 recognizes this NES-like sequence a

141 es consisting of hexasaccharide 2 coupled to carrier protein CRM197 stimulates a T-cell-dependent B-c

142 is of either FabZ (3-R-hydroxymyristoyl acyl carrier protein dehydratase), slrA (novel RpoE-regulated

143 TY ACID DESATURASE3 (FAD3) and STEAROYL-ACYL CARRIER PROTEIN Delta9-DESATURASE6 (SAD6).

144 acids into its phospholipids by an acyl-acyl carrier protein-dependent pathway.

145 These carrier protein-dependent pathways require fundamental p

146 Stearoyl-acyl carrier protein desaturase (SACPD) activity is essential

147 ormed on plants mutated in the stearoyl-acyl carrier protein desaturase (sacpd-c) gene, which were pr

148 Stearoyl-acyl carrier protein desaturase (SACPD-C) has been reported t

149 the castor (Ricinus communis) stearoyl-Acyl Carrier Protein desaturase (T117R/G188L/D280K) that, in

150 ation of the soluble castor Delta9-18:0-acyl carrier protein desaturase, specifically, the hypothesis

151 etermined by the action of the stearoyl-acyl-carrier-protein desaturase (SAD) homolog SAD5.

152 trait loci to a region containing ACYL-ACYL CARRIER PROTEIN DESATURASE1 (AAD1) and AAD3 We found tha

153 obo H antigens were then conjugated with the carrier protein diphtheria toxoid cross-reactive materia

154 ers the polyketide chain from the final acyl carrier protein domain of the synthase to a separate car

155 -shaped structure capable of caging the acyl carrier protein domain proximal to each active site.

156 he condensation domain to recognize the acyl carrier protein domain.

157 ide assembly are covalently tethered to acyl carrier protein domains of the synthase.

158 n, suggesting that chemical modifications to carrier proteins during NRPS synthesis may impart direct

159 asis of RF in those tissues that express the carrier protein (e.g. placenta and intestine).

160 ures of three forms of Escherichia coli acyl carrier protein engaging LpxD, which represent stalled s

161 e centers of malonyl-CoA and malonyl- S-acyl carrier protein, essential to fatty acid, polyketide and

162 action and that encoding the cognate sulphur-carrier protein exist in the same gene cluster.

163 t the interface that optimally position acyl carrier protein for acyl delivery and that directly invo

164 o damaged endothelium and also serves as the carrier protein for coagulation factor VIII (FVIII), pro

165 t the use of highly immunogenic rPfMSP8 as a carrier protein for leading vaccine candidates rPfMSP1(1

166 ampsia, the serum levels of transthyretin, a carrier protein for thyroxine, are elevated.

167 preferred acyl donors, while acyl-ACP (acyl carrier protein), free fatty acids, or galactolipid-boun

168 acterization of two late-acting Fe-S cluster-carrier proteins from Arabidopsis thaliana, NFU4 and NFU

169 f structural information on substrate-loaded carrier proteins has hindered our understanding of NRPS

170 U1, a late-acting iron-sulfur (Fe-S) cluster carrier protein, has a key role in the pathogenesis of t

171 the inherent conformational mobility of acyl carrier protein have stymied previous attempts to visual

172 ctivation of apo-ACPP to generate holo-(acyl carrier protein) (holo-ACPP) in an early step of fatty a

173 ies of an adenylation domain and its partner carrier protein in apo-, holo-, and substrate-loaded for

174 TT as a carrier protein in other conjugate vaccines is known to

175 chamber shows an unprecedented role of acyl carrier protein in product release.

176 arrier conjugates: protease digestion of the carrier protein in the endosome and presentation of a re

177 staining or to the expression levels of iron-carrier proteins in cells or bronchoalveolar lavage flui

178 Enzymes and carrier proteins in the visual cycle function sequential

179 hondrial NAD is imported from the cytosol by carrier proteins, in mammals, the mechanism of how this

180 We found that both adjuvants and carrier proteins influence the magnitude and capacity of

181 of insulin-like growth factor type 1 and its carrier protein insulin-like growth factor binding prote

182 nthetic intermediates tethered to their acyl carrier proteins interact with multiple active sites dur

183 We infer that similar principles underlie carrier protein interactions with other enzymes of the S

184 , are required to convert beta-ketoacyl acyl-carrier protein intermediates of the fatty acid biosynth

185 pimerized (2S)-2-methyl-3-ketoacyl-ACP (acyl carrier protein) intermediates.

186 rmylating oxygenase (ADO) converts acyl-Acyl Carrier Proteins into corresponding n-1 alkanes via alde

187 2 complex mediates the import of hydrophobic carrier proteins into the mitochondrial inner membrane.

188 For example, acyl carrier protein is central to the biosynthesis of the li

189 a proline-derived pyrrolyl group bound to a carrier protein is first halogenated and then elaborated

190 The carrier protein is planned to be genetically altered per

191 attachment of polysaccharide antigens to the carrier protein is thought to be imperative to the immun

192 y of BexX to selectively distinguish sulphur-carrier proteins is given a structural basis using X-ray

193 ort of presequence-containing precursors and carrier proteins is impaired in PC-deficient mitochondri

194 but detailed molecular understanding of the carrier proteins is incomplete.

195 provide evidence that covalent attachment to carrier proteins is not required for conversion of T-ind

196 nocytogenes encode two functional enoyl-acyl carrier protein isoforms based on their ability to compl

197 on, these oligosaccharides were coupled with carrier protein keyhole limpet hemocyanin.

198 usion peptide (FP8) - when conjugated to the carrier protein, keyhole limpet hemocyanin (KLH) - to be

199 Cryptosporidium ACS (and related acyl-[acyl-carrier-protein]-ligases) as pharmacological targets but

200 on partners of Spin and focused on the lipid carrier protein, Lipophorin (Lpp).

201 present the first structure of an NRPS aryl carrier protein loaded with its substrate via a native t

202 nzyme contains four subunits, having an acyl-carrier protein (MdcC subunit) with a distinct prostheti

203 ays and rewiring acyl-CoA and acyl-ACP (acyl carrier protein) metabolism in Yarrowia lipolytica hold

204 s indicated that covalent modifications to a carrier protein modulate domain communication, suggestin

205 on and thus activation of mitochondrial acyl carrier protein (mtACP) of mitochondrial fatty acid synt

206 Escherichia coli iron-sulfur (Fe-S) cluster carrier protein NfuA efficiently reconstitutes the auxil

207 Recently, it was shown that the Fe-S cluster carrier protein NfuA from Escherichia coli can regenerat

208 We have used the physiological carrier protein, NifX, which has been proposed to bind N

209 The PKS carrier protein of EpoA contributes the acetyl moiety, g

210 ne and then the nitroso, while linked to the carrier protein of PvfC.

211 Cells rely on mitochondrial carrier proteins of the SLC25 family to shuttle ions, co

212 which a molecular antigen is conjugated to a carrier protein, offer the opportunity to circumvent the

213 e vaccines by fusing the peptide epitopes to carrier proteins optimizes vaccine immunogenicity in mic

214 have been used as mimics of the natural acyl carrier protein pathway intermediates to assay FASII enz

215 delivered between enzyme centers by peptidyl carrier protein (PCP) domains, which makes PCP interacti

216 le tethered to a conserved, type II peptidyl carrier protein (PCP), as exemplified by PltL in the bio

217 re sorted according to their affinity to the carrier protein PDE6delta and the ability of Arl3 but no

218 Human serum albumin (HSA) is a natural carrier protein possessing multiple ligand binding sites

219 ding protein 4 (FABP4) is a leaderless lipid carrier protein primarily expressed by adipocytes and ma

220 Apolipoprotein E is a 299-residue lipid carrier protein produced in both the liver and the brain

221 rmational differences among the stalled acyl carrier proteins provide the molecular basis for the ass

222 f the bacterial capsular polysaccharide to a carrier protein provides CD4(+) T cells with epitopes th

223 ccine, PsA-TT, uses tetanus toxoid (TT) as a carrier protein (PsA-TT).

224 (MT) is fused with an N-terminal pseudo-acyl carrier protein (psiACP), in which the apo state of the

225 Enoyl-acyl carrier protein reductase (FabI) catalyzes a rate-contro

226 tool to specifically inhibit the enoyl-acyl carrier protein reductase (FabI) of C. trachomatis to de

227 acterial target of 6-OH-BDE-47 as enoyl-acyl carrier protein reductase (FabI), an essential and widel

228 ridone compound that inhibits the enoyl-acyl carrier protein reductase (FabI), has recently been show

229 Mycobacterial enoyl acyl carrier protein reductase (InhA) is a clinically validat

230 terial tuberculosis (Mtb) trans-2-enoyl-acyl carrier protein reductase (InhA).

231 anobacterial pathway consisting of acyl-Acyl Carrier Protein reductase and an aldehyde-deformylating

232 Enoyl-acyl carrier protein reductase catalyzes the last step in eac

233 The enoyl-acyl carrier protein reductase enzyme FabI is essential for f

234 , namely potent inhibition of the enoyl-acyl carrier protein reductase FabI, as validated by in vitro

235 lts show that FabI is the primary enoyl-acyl carrier protein reductase of type II bacterial fatty aci

236 Human enoyl-acyl carrier protein-reductase (hER) is one of the FAS cataly

237 Acyl carrier protein represents one of the most highly conser

238 Acquired haem is distributed by haemolymph carrier protein(s) and sequestered by vitellins in the d

239 in which the target region is presented on a carrier protein scaffold with preserved structural prope

240 ss requires DRAM-1, which binds the membrane carrier protein SCAMP3 and the amino acid transporters S

241 Notably, type II acyl carrier proteins serve as a crucial interaction hub in p

242 ring lipid A synthesis (Raetz pathway), acyl carrier protein shuttles acyl intermediates linked to it

243 We have investigated how the carrier protein shuttles intermediates between the enzym

244 We identify regulation of the L-glutamine carrier proteins SLC1A5 and SLC38A2 (SLC1A5/38A2) by the

245 d molecular motors, identified as the solute carrier protein SLC26a5, that drive somatic motility at

246 ember of a very interesting family of solute carrier proteins (SLCs), some of which have been suggest

247 are covalently attached to the heterodimeric carrier protein SoxYZ through conjugation to a cysteine

248 ent a low-resource method to directly reveal carrier protein-substrate interactions.

249 ALT proteins used endogenous fatty acyl-acyl carrier protein substrates to generate fatty acids that

250 d concomitant loss of the mitochondrial acyl carrier protein subunit ACPM1 from the enzyme complex an

251 lia through the coordinated actions of cargo carrier proteins such as Unc119 or PDE6delta, as well as

252 Extensive sequence conservation among carrier proteins suggests that the mechanistic insights

253 of the kasIII gene encoding 3-ketoacyl acyl carrier protein synthase III into tobacco plastids.

254 ndrial fatty acid synthesis by ketoacyl-acyl carrier protein synthase is not vital for protein lipoyl

255 ains provided by mitochondrial ketoacyl-acyl carrier protein synthase to meet the high lipoate requir

256 The Escherichia coli holo-(acyl carrier protein) synthase (ACPS) catalyzes the coenzyme

257 iosynthetic pathway, the beta-ketoacyl-(acyl carrier protein) synthase III (FabH)-like enzyme PqsBC c

258 nes (putatively encoding beta-ketoacyl-(acyl-carrier-protein) synthases, peroxisomal acyl-activating

259 ar fatty acids are activated by an acyl-acyl carrier protein synthetase (AasN) and validate type II f

260 eria harbor an enzyme known as the acyl-acyl carrier protein synthetase (AasS), which allows them to

261 in inhibitors directly inhibit the acyl-acyl carrier protein synthetase activity of FadD32.

262 for reacylation by acyltransferase/acyl-acyl carrier protein synthetase on the inner leaflet of the m

263 ted cardiolipin by acyltransferase/acyl-acyl carrier protein synthetase, demonstrating the first evid

264 ative substrate, l-threonine appended to the carrier protein, SyrB1, but hydroxylates C5 of l-norvali

265 the biosynthetic operon for NOS, as an acyl carrier protein that delivers 3-methylindolic acid (MIA)

266 rate that SLC25A46, like Ugo1, is a modified carrier protein that has been recruited to the outer mit

267 helix-coiled-coil-helix domain 4 (CHCHD4), a carrier protein that mediates p53 import into the mitoch

268 s by coupling bacterial polysaccharides to a carrier protein that recruits heterologous CD4 T cells t

269 al absorption is thought to be mediated by a carrier protein that still remains to be identified.

270 SCL25A46 is a mitochondrial carrier protein that surprisingly localizes to the outer

271 ncing uncovered a few genes encoding sulphur-carrier proteins that are probably involved in the biosy

272 ng the 4 most prevalent FP8 sequences with 4 carrier proteins: the aforementioned KLH and rTTHC; the

273 -butoxy groups on a p-aminobenzoate peptidyl carrier protein thioester intermediate.

274 tic up-regulation of a specialized acyl-acyl carrier protein thioesterase paralog and the concerted r

275 with cDNAs for various Cuphea FatB acyl-acyl carrier protein thioesterases (FatB) that produce a vari

276 iI by donating sulfur to the thiamine sulfur carrier protein ThiS.

277 tween the substrate and product forms of the carrier protein through differences in their interaction

278 e a comprehensive molecular description of a carrier protein throughout its life cycle and demonstrat

279 ious attempts to visualize structurally acyl carrier protein tied to an overall catalytic cycle.

280 the utility of PfMSP8 as a parasite-specific carrier protein to enhance the production of complex mal

281 studied calmodulin (CaM) as a more universal carrier protein to express many types of AMPs in E. coli

282 ear ribonucleoprotein (hnRNP) A1 serves as a carrier protein to modulate nucleocytoplasmic shuttling

283 accharide and used its tetanus toxoid as the carrier protein to produce the now-licensed, highly effe

284 site at the core of the enzyme, allowing two carrier proteins to dock with Cy and deliver their subst

285 ved by the covalent conjugation of CPSs with carrier proteins to produce glycoconjugate vaccines.

286 tation p.L81R and pR212W in malonyl CoA-acyl carrier protein transacylase (MCAT), a mitochondrial pro

287 s well as decarboxylase (MdcD-MdcE) and acyl-carrier protein transferase (MdcA) catalytic activities.

288 Two serum factors, the iron-carrier protein transferrin and amino acid glutamine, we

289 rticular, we show in immunized mice that the carrier protein transthyretin simultaneously optimizes t

290 Only a single homolog to the cargo carrier protein Unc119 has been identified in T. brucei

291 The affinity between myristoylated cargo and carrier protein, Unc119, varies between subnanomolar and

292 the transport of myristoylated cargo by the carrier proteins Unc119a and Unc119b.

293 Factor VIII (FVIII) and its carrier protein von Willebrand factor (VWF) are associat

294 OTC coupled with carrier protein was placed on test line; species specifi

295 atter case, only peptides generated from the carrier protein were critical for helper T cell recognit

296 ody response against the human albumin-based carrier protein, which was prevented by using a mouse al

297 ovalently attach purified polysaccharides to carrier proteins, which is widely considered to be techn

298 e also explore the use of a mutant flagellin carrier protein with adjuvanting properties.

299 of the structure and dynamics of an apo-aryl carrier protein with those of its modified forms reveale

300 bound to transcobalamin and haptocorrin: two carrier proteins with very different biological properti