ライフサイエンスコーパス: maltose-binding protein

1 rest and a monomeric periplasmic anchor (the maltose binding protein).

2 mutant) into a reference protein (wild-type maltose binding protein).

3 on, and by fusion to marker proteins (GFP or maltose binding protein).

4 ssed using the PelB signal sequence fused to maltose binding protein.

5 tability caused by the binding of maltose to maltose binding protein.

6 a fusion protein consisting of LOOP1 and the maltose binding protein.

7 isordered human protein tau and the globular maltose binding protein.

8 N432]-N-terminal region is replaced with the maltose binding protein.

9 is responsible for the unusual resistance in maltose binding protein.

10 l tumbling: the HIV-1 protease homodimer and Maltose Binding Protein.

11 f Streptococcal protein G to the 370-residue Maltose-binding protein.

12 d purified to 95% homogeneity, as fusions to maltose-binding protein.

13 scherichia coli as a fusion protein with the maltose-binding protein.

14 , Yersinia pseudotuberculosis invasin, or to maltose-binding protein.

15 lin alpha as a bacterial fusion protein with maltose-binding protein.

16 ed by codon optimization and its fusion with maltose-binding protein.

17 and that of chimeric spinach PsbO fused with maltose-binding protein.

18 (YSX), but both bind to an identical target, maltose-binding protein.

19 ce of four coexpressed proteins: cytoplasmic maltose binding protein (42 kDa), tau-40 (45 kDa), alpha

20 in-generated C-terminal thioester on E. coli maltose-binding protein (43 kDa) and an intein-generated

21 Maltose binding protein, a survivor from thermolysin dig

22 Here we use maltose-binding protein affinity chromatography to isola

23 authors report the use of a fusion protein, maltose-binding protein alphaB-crystallin (MBP-alphaB),

24 The structure of the maltodextrin or maltose-binding protein, an initial receptor for bacteri

25 amily of proteins, consists of a periplasmic maltose binding protein and a membrane-associated transl

26 nostained with antibodies raised against the maltose binding protein and A. naeslundii T14V whole bac

27 The mutant HMG domains were fused to maltose binding protein and expressed in and purified fr

28 A)-ZW and two different His-tagged proteins, maltose binding protein and fluorescent mCherry protein.

29 rements (i.e., no meaningful differences) on maltose binding protein and infliximab, a monoclonal ant

30 The stabilities of maltose binding protein and monomeric lambda repressor v

31 targeting of two Escherichia coli proteins, maltose binding protein and OmpA.

32 properties of a fusion protein consisting of maltose binding protein and the active site region of ge

33 p33 alters folding transitions within single maltose binding proteins and aggregation transitions bet

34 frame between coding regions for the E. coli maltose-binding protein and a polypeptide containing a h

35 Tfs4 VirD2 was purified as a fusion to maltose-binding protein and demonstrated to bind and nic

36 inase, were expressed in Escherichia coli as maltose-binding protein and glutathione S-transferase fu

37 , R-phycoerythrin apo-subunits were fused to maltose-binding protein and incubated with phycoerythrob

38 ecular weight, such as the globular, soluble maltose-binding protein and the membrane protein bacteri

39 protease Factor Xa to separate Cah6 from the maltose-binding protein and the purified Cah6 protein wa

40 he binding of small molecules to immobilized maltose-binding protein and tissue transglutaminase.

41 F1845 fimbriae, DraE and DaaE, as fusions to maltose-binding protein and to oligohistidine tags and e

42 ) calmodulin-GFP Ca(2+) sensor protein, (ii) maltose binding protein, and (iii) CSL transcription fac

43 chia coli, purified as a fusion protein with maltose binding protein, and cleaved with thrombin to yi

44 scherichia coli (E. coli) in fusion with the maltose binding protein, and, after cleavage of the latt

45 oes not form in the absence of MgCl(2) or of maltose-binding protein, and ADP or another nonhydrolyza

46 re of a monobody in complex with its target, maltose-binding protein, and mutation analysis revealed

47 itially coated with a two-domain recombinant maltose-binding protein appended with a positively charg

48 gical ligands, galactose-binding protein and maltose-binding protein, are in rapid, dynamic equilibri

49 g glutathione S-transferase, thioredoxin, or maltose binding protein as N-terminal fusion tags did no

50 containing five native N-extein residues and maltose binding protein as the N-extein with the C-termi

51 Here we report that the maltose-binding protein becomes tightly associated with

52 thermal analysis using experimental data for maltose binding protein binding to maltose, and for two

53 system of Escherichia coli, the periplasmic maltose-binding protein binds its substrate maltose with

54 em is not only determined by the periplasmic maltose-binding protein but that a further level of subs

55 gth HbhA and the C terminus of HbhA fused to maltose-binding protein, but not recombinant HbhA lackin

56 sible to radically change the specificity of maltose binding protein by converting it into a zinc sen

57 ty, in complex with alkaline phosphatase and maltose-binding protein captured in their unfolded state

58 purified tafazzin construct, tagged with the maltose-binding protein, catalyzed both forward and reve

59 Maltose-binding protein caveolin and glutathione S-trans

60 tions by expressing them in the context of a maltose binding protein chimera containing a portion of

61 2 domains were prepared recombinantly as the maltose binding protein constructs, and their interactio

62 n confirmed earlier findings on the CCS-MBP (maltose binding protein) constructs, namely, that Cu(I)

63 Bacterial maltose-binding proteins containing the CPV or ECT CrmD

64 sport-specific interactions between MalG and maltose-binding protein, defining a novel class of MalG

65 For a mutant of maltose-binding protein (DM-MBP), the rate of folding in

66 teins that are resistant to proteases (e.g., maltose-binding protein) do not return accurate results;

67 The maltose-binding protein does not bind calmodulin, and th

68 posed of GFP and a cytoplasmically localized maltose binding protein domain moves more slowly, with D

69 natively, as a fusion to the C terminus of a maltose-binding protein domain (MalE) with the peptide s

70 When fused to maltose-binding protein, domain 3 was also sufficient fo

71 gth Trm5p, purified as a fusion protein with maltose-binding protein, exhibited robust methyltransfer

72 ORF was fused to the 3'-end of the gene for maltose binding protein, expressed in bacteria and the p

73 as well as novel fragments of Jo-1 into the maltose-binding protein expression vector pMALc2.

74 s structure to other proteins that adopt the maltose-binding protein fold but bind monosaccharides, d

75 s sensing modalities have been utilized with maltose-binding protein for both in vitro and in vivo de

76 main antibody (sdAb) with the thermal stable maltose binding protein from the thermophile Pyrococcus

77 richia coli the full-length HA(2) chain with maltose-binding protein fused at its N-terminus.

78 ated severely, studies were carried out with maltose-binding protein fused to A22 as well as to RuvC.

79 lectrophoretic mobility shift assays, a GbdR-maltose binding protein fusion bound specifically to bot

80 using a polyclonal antibody raised against a maltose binding protein fusion construct containing UL15

81 l in vitro, we first purified NasR as both a maltose binding protein fusion form (MBP-NasR) and a His

82 ce immobilization, we have constructed a CaM/maltose binding protein fusion protein, which renders Ca

83 Two maltose binding protein fusion proteins, 2B7F1 and 2B7F2

84 mic domain of MisS were purified as His6 and maltose binding protein fusion proteins, respectively.

85 Cysteine-to-serine mutants of a maltose binding protein fusion with the human copper cha

86 d starch nanoparticles via construction of a maltose binding protein fusion.

87 es, was purified as the native protein, as a maltose-binding protein fusion and with an N-terminal ta

88 ere efficiently expressed and purified using maltose-binding protein fusion constructs.

89 i-AflR antibody and co-purified with an AflR-maltose-binding protein fusion demonstrating a physical

90 NN was expressed as a maltose-binding protein fusion in Escherichia coli.

91 We describe here experiments in which a maltose-binding protein fusion protein bearing the CD4 t

92 Experiments with maltose-binding protein fusion proteins containing segme

93 Using proteolytic fragments and maltose-binding protein fusion proteins that together sp

94 mutations altered the capacity of ToxR-VacA-maltose-binding protein fusion proteins to insert into a

95 1c, Delta N4, and Delta N5, was expressed as maltose-binding protein fusion proteins.

96 toring production of PE in reactions using a maltose-binding protein fusion with Plasmodium knowlesi

97 PDPr was expressed in Escherichia coli as a maltose-binding protein fusion, and the recombinant prot

98 ved by expressing the redesigned Urzyme as a maltose-binding protein fusion.

99 y crystal structure of the dimeric SarR-MBP (maltose binding protein) fusion protein.

100 s developed using bacterially expressed IE62-maltose binding protein fusions as substrates for immuno

101 region, we expressed and analyzed ToxR-VacA-maltose binding protein fusions using the TOXCAT system,

102 es against CFA/I and CS17 whole fimbriae and maltose-binding protein fusions with the amino-terminal

103 NA synthetase were constructed, expressed as maltose-binding protein fusions, and assayed for histidi

104 In vivo and in vitro characterization of maltose-binding-protein fusions between the wild-type Cp

105 By using maltose-binding protein, glutathione S-transferase, and

106 (PBP) superfamily members, in particular the maltose-binding protein, have been used extensively to p

107 in beta in bacteria as a fusion protein with maltose-binding protein (hereafter referred to as recomb

108 The strategy utilizes a dual His6-maltose binding protein (HisMBP) affinity tag that can b

109 The maltose-binding protein-human FAS (MBP-hFAS) catalyzed p

110 rated by following the induced expression of maltose binding protein in E. coli.

111 open reading frame to the coding sequence of maltose-binding protein in a pMal expression vector.

112 sion proteins at the carboxy terminus of the maltose-binding protein in Escherichia coli or independe

113 n 10 nonoverlapping segments as fusions with maltose-binding protein in pMAL-C2 (pVP1, pVP2a through

114 show that interactions with substrate-loaded maltose-binding protein in the periplasm induce a partia

115 d LamB and some periplasmic proteins such as maltose-binding protein, in Escherichia coli.

116 mbinant PDK2, expressed as a fusion with the maltose-binding protein, inactivated kinase-depleted mai

117 xpressed and affinity-purified as fusions to maltose-binding protein, incubated with purified synthet

118 nds to 12% of the total protein molecule, to maltose binding protein is sufficient to endow the prote

119 onal rabbit antiserum was prepared against a maltose binding protein-LMP2a cytoplasmic domain fusion

120 The purified maltose binding protein-LuxI fusion protein catalyzes th

121 using three soluble protein-ligand systems (maltose binding protein, lysozyme, and nitrogen regulato

122 ement in the recognition of substrate by the maltose-binding protein MalE.

123 sed of ChiA fused at the N terminus with the maltose-binding protein (MalE) of Escherichia coli and f

124 tact maltose transporter in complex with the maltose-binding protein, maltose and ATP.

125 Using epitope tags, antibodies, and maltose-binding protein markers, we find that syntaxin a

126 Using epitope tags, antibodies and maltose-binding protein markers, we find that the helica

127 expression vectors encoding polyhistidine or maltose binding protein (MBP) affinity purification tags

128 By using Escherichia coli maltose binding protein (MBP) and E. coli ribonuclease H

129 onstrated that presecretory proteins such as maltose binding protein (MBP) and outer membrane protein

130 HP), a protective amebic antigen, fused to a maltose binding protein (MBP) and to CTA2.

131 a translational fusion was made between the maltose binding protein (MBP) and UreD, with the resulti

132 er AlexaFluor 488 or Cy3 dye was attached to maltose binding protein (MBP) and used with various QD a

133 Engineered maltose binding protein (MBP) appended with an oligohist

134 S protein was expressed as a fusion with the maltose binding protein (MBP) at its amino-terminal end

135 , quencher-dye-labeled biotin-linked E. coli maltose binding protein (MBP) bound in a specific orient

136 energy transfer (BRET) biosensor, comprising maltose binding protein (MBP) flanked by a green fluores

137 altose biosensor was constructed, comprising maltose binding protein (MBP) flanked by a green fluores

138 form of the complex, which requires liganded maltose binding protein (MBP) for ATPase activity, the p

139 chemical shift data is illustrated using the maltose binding protein (MBP) from Escherichia coli as a

140 When expressed as a maltose binding protein (MBP) fusion protein by bacteria

141 ed in baculovirus and in Escherichia coli as maltose binding protein (MBP) fusions and immunocytochem

142 sphorylation of soluble sensors in which the maltose binding protein (MBP) has replaced the amino-ter

143 ational shifts, we have instead utilized the maltose binding protein (MBP) in lieu of an antibody in

144 sor based on the surface immobilization of a maltose binding protein (MBP) nitroreductase (NR) fusion

145 equences (DeltaTF and DeltaPol) fused to the maltose binding protein (MBP) of Escherichia coli, was r

146 (WZA2), through a linker L1 and possesses a Maltose Binding Protein (MBP) tag at the N terminal end.

147 gG1 at the C terminus (GCSF-Fc) and with the maltose binding protein (MBP) tag at the N-terminus and

148 eta-lactamase (BLA) and the Escherichia coli maltose binding protein (MBP) to create a family of MBP-

149 For these measurements, maltose binding protein (MBP) was isotopically labeled w

150 In one approach, a maltose binding protein (MBP) was systematically fused t

151 ing known binders of three proteins, pepsin, maltose binding protein (MBP), and carbonic anhydrase (C

152 d to protein treatment with HIV-1 integrase, maltose binding protein (MBP), and MBP-Vpr in the undiff

153 subunits of MccB17 synthetase as fusions to maltose binding protein (MBP), and the in vitro reconsti

154 odulin (CaM), by fusion to a larger protein, maltose binding protein (MBP), for single-molecule fluor

155 Conjugation of DHLA-capped QDs to maltose binding protein (MBP), the immunoglobulin-G-bind

156 on of the CrpE epoxidase using an engineered maltose binding protein (MBP)-CrpE fusion.

157 By solving crystal structures of maltose binding protein (MBP)-fused AID alone and in com

158 e analyze the interaction between R2TP and a Maltose Binding Protein (MBP)-fused Nop58p by biophysica

159 A crystal structure of a maltose binding protein (MBP)-L30 fusion protein with tw

160 pressed, purified, and characterized several maltose binding protein (MBP)-NDM-1 fusion proteins with

161 To identify Rns-regulated genes, a maltose binding protein (MBP)-Rns fusion protein was use

162 synthetic degenerate' DNA motif and fused to Maltose Binding Protein (MBP).

163 l sequence of alkaline phosphatase (PhoA) or maltose binding protein (MBP).

164 coli malE gene, which encodes the bacterial maltose binding protein (MBP).

165 sed in Escherichia coli as a fusion with the maltose binding protein (MBP).

166 in Escherichia coli as fusion proteins with maltose binding protein (MBP).

167 oli and purified as fusion proteins with the maltose binding protein (MBP).

168 pressed in bacteria as a fusion protein with maltose binding protein (MBP).

169 neered the sequences of one subdomain within maltose binding protein (MBP, alpha/beta/alpha-sandwich)

170 was purified as a chimeric protein fused to maltose binding protein (MBP-Orf20).

171 This protein was expressed as a chimera with maltose binding protein (MBP::VP6) and was administered

172 Kinetic folding of the large two-domain maltose binding protein (MBP; 370 residues) was studied

173 Here we report the optimization of a maltose-binding protein (MBP) affinity-purification meth

174 Two model constructs harboring maltose-binding protein (MBP) and a His-tag as exteins w

175 ized model system, consists of a periplasmic maltose-binding protein (MBP) and a multisubunit membran

176 D) part of VP6 that was genetically fused to maltose-binding protein (MBP) and expressed in Escherich

177 in fusion protein, constructs containing the maltose-binding protein (MBP) and fragments of the C-ter

178 were overexpressed as C-terminal fusions to maltose-binding protein (MBP) and purified on amylose re

179 emblies, multiple copies of Escherichia coli maltose-binding protein (MBP) coordinate to each QD by a

180 eled engineered variants of Escherichia coli maltose-binding protein (MBP) coordinated to the surface

181 A periplasmic maltose-binding protein (MBP) delivers maltose to MalFGK

182 A periplasmic maltose-binding protein (MBP) delivers maltose to the tr

183 ly, we have shown that 5-HT(3A)-ICD fused to maltose-binding protein (MBP) directly interacts with RI

184 nd purified soluble fusion proteins with the maltose-binding protein (MBP) from Escherichia coli that

185 protein HGE-44, expressed and purified as a maltose-binding protein (MBP) fusion peptide, as an anti

186 a T7 RNA polymerase promoter system or as a maltose-binding protein (MBP) fusion protein.

187 actone synthases, we have purified AinS as a maltose-binding protein (MBP) fusion protein.

188 terminus of Kir1.1, we produced and purified maltose-binding protein (MBP) fusion proteins containing

189 By using the maltose-binding protein (MBP) fusion system, the Nqo10 s

190 erexpressed in Escherichia coli by using the maltose-binding protein (MBP) fusion system.

191 domain (ECD) of human PTH1R engineered as a maltose-binding protein (MBP) fusion that readily crysta

192 ro pull-down assays verified binding between maltose-binding protein (MBP) fusions, MBP::NaPCCP or MB

193 randomly inserted into the Escherichia coli maltose-binding protein (MBP) gene to create a domain in

194 for the latter has been recently reported on maltose-binding protein (MBP) in aqueous solution via pa

195 press both SalA and SyrF proteins fused to a maltose-binding protein (MBP) in Escherichia coli and P.

196 ing domain (HMBD, GMxCxxC) of CpATPase2 as a maltose-binding protein (MBP) in Escherichia coli reveal

197 this system are LamB in the outer membrane, maltose-binding protein (MBP) in the periplasm, and the

198 Even though the maltose-binding protein (MBP) is one of the most commonl

199 The Escherichia coli maltose-binding protein (MBP) is used to increase the st

200 A recombinant protein comprising the maltose-binding protein (MBP) of Escherichia coli fused

201 Binding of ligands to the maltose-binding protein (MBP) of Escherichia coli often

202 -kDa fusion polypeptide, in which the mature maltose-binding protein (MBP) sequence was linked to the

203 This importer requires a periplasmic maltose-binding protein (MBP) that activates ATP hydroly

204 the maltose-binding site in Escherichia coli maltose-binding protein (MBP) with an oxygen-binding sit

205 at ligands that bind to the Escherichia coli maltose-binding protein (MBP) without producing the clos

206 The maltose-binding protein (MBP), a member of the bacterial

207 A typical example is maltose-binding protein (MBP), a member of the family of

208 Maltose-binding protein (MBP), a soluble periplasmic pro

209 eins (short-lived green fluorescent protein, maltose-binding protein (MBP), and alkaline phosphatase)

210 abeled at lysine residues: calmodulin (CaM), maltose-binding protein (MBP), and dihydrofolate reducta

211 bB subunit was purified as a fusion with the maltose-binding protein (MBP), and metal analysis reveal

212 ier (Sumo), glutathione S-transferase (GST), maltose-binding protein (MBP), N-utilisation substance p

213 system, the selectivity of sugar binding to maltose-binding protein (MBP), the periplasmic binding p

214 re of the cleavable form of Escherichia coli maltose-binding protein (MBP), which does not accumulate

215 in contrast, first binds to the periplasmic maltose-binding protein (MBP), which in its ligand-stabi

216 nor-acceptor pair in the unrelated bacterial maltose-binding protein (MBP), which yielded hormone pro

217 Gel mobility shift assays with maltose-binding protein (MBP)-ExpR(71) and MBP-ExpR(153)

218 Using a 60 kDa maltose-binding protein (MBP)-GroEL(193-335) fusion prot

219 ift and DNase I footprint assays that used a maltose-binding protein (MBP)-MtrR fusion protein demons

220 ties associated with a bacterially expressed maltose-binding protein (MBP)-Rep52 fusion protein.

221 We demonstrate that a maltose-binding protein (MBP)-Rep78 fusion protein can c

222 cherichia coli as soluble proteins linked to maltose-binding protein (MBP).

223 hese proteins were soluble when fused to the maltose-binding protein (MBP).

224 ed VP7 (TrVP7) protein fused to the 42.7-kDa maltose-binding protein (MBP).

225 were isolated as chimeric proteins with the maltose-binding protein (MBP).

226 Maltose first binds to maltose-binding protein (MBP).

227 rate ligands, aspartate and substrate-loaded maltose-binding protein (MBP).

228 chia coli must first bind to the periplasmic maltose-binding protein (MBP).

229 essed as a soluble fusion protein coupled to maltose-binding protein (MBP).

230 taining the tetramer-forming domain fused to maltose-binding protein (MBP).

231 ecombinant deletion mutant enzyme fused with maltose-binding protein (MBP-G9aDelta634) was used for s

232 ified fusion of Mga to the C-terminal end of maltose-binding protein (MBP-Mga), encoded by malE-mga,

233 treptavidin (SA-CAP-1 or 2) or nonallergenic maltose-binding protein (MBP; MBP-CAP-1 to 4) and bindin

234 creating gene fusions between malE (encoding maltose-binding protein [MBP]) and a variant of gfp opti

235 immobilize a dicysteine-terminated protein (Maltose Binding Protein, MBP-cys-cys for short) at well-

236 nterface between DARPin off7 and its ligand (maltose binding protein; MBP) is characterized by a hot-

237 he PBP sequence is homologous to periplasmic maltose binding proteins (MBPs).

238 ility shift assays using purified M50 and M4 maltose binding protein-Mga found that both exhibited DN

239 o pMAL-c2 fusion vector and overexpressed as maltose-binding protein-MurD fusion proteins.

240 omplexes and gel mobility shift assays of an maltose-binding protein-MutS fusion protein bound to a s

241 d and expressed as a fusion partner with the maltose binding protein of Escherichia coli and liberate

242 ndent and dependent on the concentrations of maltose-binding protein-Opi1p (Km = 25 microg/ml) and AT

243 Using purified maltose-binding protein-Opi1p as a substrate, casein kin

244 Using a maltose-binding protein-Opi1p fusion protein as a substr

245 Using a purified maltose-binding protein-Opi1p fusion protein as a substr

246 Phosphorylation of a purified S26A mutant maltose-binding protein-Opi1p fusion protein by the kina

247 Phosphorylation of S31A and S251A mutant maltose-binding protein-Opi1p fusion proteins by protein

248 proteins, such as glutathione S-transferase, maltose-binding protein, or thioredoxin, or released in

249 tivity using a phage-based protein reporter, maltose-binding protein, over the detection of replicate

250 n binds specifically to PI(3)P when fused to maltose-binding protein, PHD2, or as an isolated peptide

251 combinatorial library of approximately 6000 maltose binding protein-PLC(Bc) fusion protein mutants c

252 o fusion failed to phosphorylate an inactive maltose-binding protein-Pto(K69Q) fusion excluding an in

253 ble form in Escherichia coli as fusions with maltose-binding protein, purified, and their metal-bindi

254 rotein as a fusion with the Escherichia coli maltose-binding protein (R), and (iii) a purified inacti

255 ous phage secretin, pIV, or to the unrelated maltose-binding protein rendered both proteins dependent

256 e resulting PCR fragments were cloned into a maltose binding protein-Rep68 fusion (MBP-Rep68delta) ex

257 Pase, and endonuclease activities by using a maltose binding protein-Rep68 fusion (MBP-Rep68Delta) pr

258 ed residues throughout the Rep68 moiety of a maltose binding protein-Rep68 fusion protein (MBP-Rep68D

259 The ability of a maltose binding protein-Rep68 fusion protein to bind to

260 The mutant proteins were synthesized as maltose binding protein-Rep68 fusions in Escherichia col

261 rst 200 amino acids of the Rep68 moiety of a maltose binding protein-Rep68/78 fusion protein to pheny

262 ion experiments with a bacterially expressed maltose-binding protein-Rep78 fusion protein in combinat

263 rminal amino acids from PduP to GFP, GST, or maltose-binding protein resulted in their encapsulation

264 fied preparation of MBP-ExpR(71) binds (MBP, maltose binding protein) rsmA DNA.

265 rating the leader peptidase cleavage site of maltose binding protein signal peptide, Y(NO2)-F-S-A-S-A

266 g as well as striking molecular mimicry of a maltose-binding protein substrate, beta-cyclodextrin, by

267 proteins and aggregation transitions between maltose binding protein substrates.

268 ucture crystallized in fusion with the large maltose-binding protein tag, the H2-H3 region of the AIM

269 ified from Escherichia coli as an N-terminal maltose binding protein-tagged fusion protein.

270 Those data demonstrate that the maltose-binding protein-tagged HAMP1-5 protein exist as

271 ions, both the glutathione S-transferase and maltose-binding protein tags were successful in 81% of s

272 misfolded aggregates of MalE31, a variant of maltose binding protein that forms inclusion bodies in t

273 have identified regions in Escherichia coli maltose-binding protein that are predicted to be alloste

274 Fusion Xa contains MalE (the maltose-binding protein), the four-amino acid sequence r

275 By fusion with maltose binding protein, the family IIIa recombinant wil

276 Upon stimulation by maltose-binding protein, the intact MalFGK(2) transport

277 When expressed as a C-terminal fusion with maltose-binding protein, the presence of the light chain

278 on the transposon, and the encoded trehalose/maltose-binding protein (TMBP) are induced in the presen

279 Antiserum raised to a fusion of maltose binding protein to an N-terminal 60-kDa fragment

280 protein MalK, interacts with the periplasmic maltose-binding protein to efficiently translocate malto

281 equired for integrin recognition, fusions of maltose-binding protein to fragments of p66 were tested

282 he cytoplasmic segment of DEP-1 fused to the maltose-binding protein to identify potential substrates

283 y used this method to monitor the binding of maltose-binding protein to maltose, as well as to rapidl

284 The binding of spinach PsbO fused with maltose-binding protein to PSII depleted of extrinsic su

285 used a foreign protein (the Escherichia coli maltose-binding protein) to the C-terminal region of the

286 nal DNA binding domain of Tn916 Int fused to maltose binding protein, to specific oligonucleotide sub

287 A slightly larger maltose-binding protein-transposase fusion that includes

288 Three maltose binding protein-UGT2B7 fusion proteins, 2B7F3 an

289 UL42 was mixed with a maltose-binding protein-UL42 fusion protein before being

290 re able to detect a complex between SecB and maltose-binding protein under conditions in which rapid

291 tions of a structural variant (modeled using maltose binding protein W169G mutant) into a reference p

292 Y production, a FimY fusion with the E. coli maltose-binding protein was constructed and expressed in

293 that a recombinant protein, MBP-2C, in which maltose-binding protein was fused to 2C, formed soluble

294 ivity of purified SUR1-NBD2-G1410R (bound to maltose-binding protein) was slightly inhibited when com

295 essed as a single-chain Fv (scFv) fused with maltose-binding protein were assayed for binding to NA b

296 nvestigated using three species of precursor maltose-binding protein, which differ in their stability

297 toethanesulfonic acid and released the 43kDa maltose binding protein with an active C-terminal thioes

298 cherichia coli, interaction of a periplasmic maltose-binding protein with a membrane-associated ATP-b

299 ecombinant glutathione-S-transferase:WVD2 or maltose binding protein:WVD2 protein bind to and bundle

300 se results suggest that soluble oligomers of maltose binding protein-YqgP complexes form micellelike