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 gnition of peptides derived from the coupled carrier protein.

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

4 shear conditions FVIII is released from its carrier protein.

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

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

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

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

9 alamin II receptor and the transcobalamin II carrier protein.

10 entified as proteolytic products of the acyl carrier protein.

11 via the synthesis of [(14)C]linolenoyl-acyl carrier protein.

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

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

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

15 th siderophores conjugated to an immunogenic carrier protein.

16 l length polysaccharide for conjugation to a carrier protein.

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

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

19 along with a reduction in mitochondrial acyl carrier proteins.

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

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

22 ately being incorporated into essential acyl carrier proteins.

23 antigens were coupled to immune stimulating carrier proteins.

24 protein-protein interactions with noncognate carrier proteins.

25 glycopeptide antibiotics to three different carrier proteins.

26 6-aminohexyl glycosides to be conjugated to carrier proteins.

27 to the target molecule or additional sulfur carrier proteins.

28 immunization strategies based on the use of carrier proteins.

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

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

31 sponses to Pfs25 when coupled to immunogenic carrier proteins.

32 f genes encoding mitochondrial dicarboxylate carrier proteins.

33 ible nitric oxide synthase (iNOS) and solute carrier protein 11A1 (SLC11A1).

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 results for the protein Aedes aegypti sterol carrier protein 2.

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

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

39 initial cluster assembly and transfer to FeS carrier proteins, accessory factors such as monothiol gl

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 shuttle acyl intermediates

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

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

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

50 pical primer is transformed to pimeloyl-acyl carrier protein (ACP) methyl ester by two cycles of fatt

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

52 Enoyl-acyl carrier protein (ACP) reductase catalyzes the last step

53 Enoyl-acyl carrier protein (ACP) reductase, FabI, is a key enzyme i

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

55 ze the reduction of 2-methyl-3-ketoacyl acyl carrier protein (ACP) substrates and in certain cases ep

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

57 e KASIII domain of the beta-acetoacetyl-acyl carrier protein (ACP) synthase FabH.

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

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

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

61 fatty acid synthetic intermediate, the acyl carrier protein (ACP) thioester of 3-hydroxydodecanoic a

62 d for the Umbellularia californica acyl-acyl carrier protein (ACP) thioesterase was shown to have hig

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

64 yl coenzyme A (acetyl-CoA) with malonyl-acyl carrier protein (ACP) to make the FAS primer beta-acetoa

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

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

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

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

72 both acyltransferases catalyze an acyl-acyl carrier protein (ACP)-dependent transfer of a fatty acyl

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

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

75 coupled via a phosphopantetheine to an acyl carrier protein (ACP).

76 8:1 free fatty acid, 18:1-CoA, and 18:1-acyl-carrier protein (ACP).

77 ster bond to either coenzyme A (CoA) or acyl carrier protein (ACP).

78 ubunit (NFS1), LYR protein (ISD11), and 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 Acyl carrier proteins (ACPs) are universal and highly conserv

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

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

84 Acyl carrier proteins (ACPs) play a central role in acetate b

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

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

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

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

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

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

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

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

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

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

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

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

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

98 nslocase, which is involved in the import of carrier proteins and other, hydrophobic membrane protein

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

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

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

102 ed around novel emerging cofactors (tRNA and carrier proteins) and then more complex cofactor structu

103 activities of an E1 activating enzyme, an E2 carrier protein, and an E3 ligase.

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

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

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

107 specificities and can employ acyl-CoAs, acyl carrier proteins, and galactolipids as acyl donors.

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

109 h we covalently link the target molecules to carrier proteins, and then crystallize the entire carrie

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

111 Notably, the carrier protein approach is not limited to peptide ligan

112 A few LeX carrier proteins are known, but a systematic analysis of

113 Specific carrier proteins are required to distribute these cofact

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

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

116 rboxyl of either malonyl-CoA or malonyl-acyl carrier protein based on the ability of O-methylated (bu

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

118 of the vitamin biotin to the biotin carboxyl carrier protein (BCCP) domain of five biotin-dependent c

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

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

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

122 The carrier protein can accomplish this task only because pr

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

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

125 ionalized with a cocaine multivalent antigen-carrier protein conjugate.

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

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

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

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

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

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

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

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

134 lease and analysis of intermediates bound to carrier proteins (CPs), providing access to these specie

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

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

137 omprehensive characterization of the vaccine carrier protein, CRM197.

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

139 ABC genes encoding the (3R)-hydroxyacyl-acyl carrier protein dehydratases resulted in more than a 16-

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

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

142 These carrier protein-dependent pathways require fundamental p

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

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

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

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

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

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

149 itope fragment) conjugated to an immunogenic carrier protein, diphtheria toxoid (DT), and formulated

150 is governed by interactions between the acyl carrier protein domain and the ketosynthase domain plus

151 in, transfer of the acetyl group to the acyl carrier protein domain is suppressed.

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

153 es that are ready for transfer from its acyl carrier protein domain to its ketosynthase domain and as

154 malonyl group can be transferred to the acyl carrier protein domain, transfer of the acetyl group to

155 s from isochorismic acid, but lacks the aryl carrier protein domain, which is needed for tethering ac

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

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

158 ubiquitin-activating enzymes), E2 (ubiquitin-carrier proteins), E3 (ubiquitin-protein ligases), and E

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

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

161 ber of the LDL receptor family, as a new LeX carrier protein expressed by mouse neural stem cells.

162 iosynthesis of the unusual aminomalonyl-acyl carrier protein extender unit and the signature carbamoy

163 nce of specific members of the mitochondrial carrier protein family that have previously been associa

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

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

166 Being naturally nontoxic, CRM197 is an ideal carrier protein for conjugate vaccines against encapsula

167 ate studies identify UbcH7 as the cognate E2 carrier protein for E6AP, although related Ubc5 isoforms

168 Finally, VWF, the carrier protein for fVIII in plasma, may play a role in

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

170 roposal that A-type proteins can function as carrier proteins for clusters assembled on U-type protei

171 bolism using inhibitors to prevent acyl-acyl carrier protein formation or glycerol-phosphate acyltran

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

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

174 hen loaded onto phosphopantetheinylated acyl carrier protein (holo-MbtL) to form covalently acylated

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

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

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

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

179 Enzymes and carrier proteins in the visual cycle function sequential

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

181 we chemically synthesized and linked GH to a carrier protein, including keyhole limpet hemocyanion, d

182 Increased expression of additional solute carrier proteins, including Slc5a12 (>10-fold) were also

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

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

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

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

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

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

189 2 complex mediates the import of hydrophobic carrier proteins into the mitochondrial inner membrane.

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

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

192 cate that biotin transfer to biotin carboxyl carrier protein is impacted by seven substitutions, the

193 The carrier protein is planned to be genetically altered per

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

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

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

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

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

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

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

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

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

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

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

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

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

207 tochondrial proteins including the phosphate carrier protein, NADH dehydrogenase 1alpha subcomplexes

208 as monothiol glutaredoxin, GrxD, and the FeS carrier protein NfuA are located outside of these define

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

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

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

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

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

214 pecific deletions of ketosynthase (KS), acyl carrier protein, or ketoreductase.

215 ithout the need for any additional adjuvant, carrier protein, or special pharmaceutical preparation (

216 cs is not compromised by the presence of the carrier protein partner, and use this approach to determ

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

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

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

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

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

222 sphacan, tenascin-C, and L1-CAM as major LeX carrier proteins present in vivo.

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

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

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

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

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

228 ylococcus aureus that targets the enoyl-acyl carrier protein reductase (FabI).

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

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

235 Acyl carrier protein represents one of the most highly conser

236 a FAAL that transfers fatty acids to an acyl carrier protein (Rv0100).

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

238 Apolipoprotein (Apo) E is a lipid carrier protein secreted by astrocytes, which shows inhe

239 me polysaccharide conjugated to heterologous carrier proteins selects for and expands carbohydrate-sp

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

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

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

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

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

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

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

247 Carrier-protein specific immunity was also shown to be e

248 l-CoA, suggesting a strong preference toward carrier protein starter unit transfer.

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

250 tty acyl-coenzyme A (CoA) or fatty acyl-acyl carrier protein substrates to primary fatty alcohols.

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

252 jugate vaccines recruit CD4(+) T cells via a carrier protein, such as tetanus toxoid (TT), resulting

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

254 ehydrogenase complex and beta-keto acyl-acyl carrier protein synthase III from Bacillus subtilis to s

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

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

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

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

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

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

261 the only cytoplasmic Synechocystis acyl-acyl carrier protein synthetase (SynAas) were highly resistan

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

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

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

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

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

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

268 In sum, our results established NIS as a carrier protein that interacts with a major cell signali

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

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

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

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

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

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

275 heterologous over-expression of an acyl-acyl carrier protein thioesterase, or by suppression of fatty

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

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

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

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

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

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

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

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 om initial assembly on scaffold proteins via carrier proteins to final incorporation into FeS apoprot

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

287 expression of mitochondrial malonyl CoA-acyl carrier protein transacylase, a key enzyme in the pathwa

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

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

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

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

292 ethodology in vitro to reversibly label acyl carrier protein variants and apply these tools to NMR st

293 oligosaccharides can be covalently bound to carrier proteins via the reducing end pentyl amine linke

294 nyl-CoA as the methyl acceptor, malonyl-acyl carrier protein was a far better acceptor of methyl grou

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

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

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

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

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

300 Wnt palmitoylation, Wnt interaction with the carrier protein Wntless/WLS, Wnt secretion, and Wnt acti