ライフサイエンスコーパス: binding activity of

1 We demonstrate that the cap-binding activity of 4EHP contributes to the translationa

2 Alp7R also shows the typical nonspecific binding activity of a DNA-binding protein: Alp7R-GFP (gr

3 -TRAP, the intracellular folding and antigen-binding activity of a human single-chain antibody fragme

4 results suggest that EGF regulates the actin binding activity of ACTN4 by inducing tyrosyl-directed p

5 ied as selective materials for assessing the binding activity of agonist and antagonist of dopamine D

6 We show that Hex-hA20 retains the binding activity of all six Fabs, associates with CD20 i

7 ylation are associated with a loss of ligand-binding activity of alpha-DG and are causal for various

8 alpha-dystroglycan glycosylation and laminin binding activity of alpha-dystroglycan in the morphants.

9 utation analyses demonstrate that the ligand-binding activity of alpha-dystroglycan is conferred prim

10 rated ROS enhanced the activation and ligand-binding activity of alphaMbeta2 integrin following N-for

11 Hippo pathway negatively regulates the actin-binding activity of Amot family members through direct p

12 help elucidate this process, we examined the binding activities of an MA mutant that stabilizes MA tr

13 We utilize the binding activity of an RNA-editing enzyme to visualize t

14 we hypothesize that RNPC1 modulates the RNA-binding activity of, and cooperates with, HuR to regulat

15 demonstrate by microarray analyses distinct binding activities of antibodies and a lectin toward var

16 The DNA-binding activity of AP-1 increased after stretch stimula

17 Here we found that the promoter DNA-binding activity of AP-1 transcription factors is select

18 receptor-binding region ablated the heparin-binding activity of apoE, as determined by an in vitro h

19 ability of CRISPR-Cas12a and the competitive binding activities of aTFs for small molecules and doubl

20 s are promising leads for suppression of DNA binding activities of B-ZIP and B-HLH-ZIP transcription

21 The structures and DNA-binding activities of basal NF-kappaB proteins resemble

22 The results indicate that the binding activities of beta-catenin decreased in mouse ce

23 We determined the transthyretin (TTR)-binding activity of blood-accumulating contaminants in b

24 DHX30 interaction in vivo requires the dsRNA-binding activity of both DHX30N and the NS1 RBD.

25 S-/IgG immune complexes-induced ALI, the DNA binding activities of C/EBPgamma are obviously reduced.

26 ynamic high-capacity and low-affinity Ca(2+)-binding activity of calsequestrin.

27 for optimal DNA binding or can stimulate the binding activity of CAP variants that only transiently p

28 multidomain proteins that regulate the actin-binding activity of capping protein (CP), a major capper

29 dicate that impairment of the membrane lipid binding activity of Cb and a consequent defect in inhibi

30 10 by arsenic is associated with reduced DNA-binding activity of CCAAT/enhancer-binding protein beta

31 a point mutation (C169A) that abolishes DNA-binding activity of Cfp1 ablates the rescue activity of

32 pression of hmuO and the hrtAB genes and the binding activity of ChrA is dependent on phosphorylation

33 ity of other members of this family, the DNA-binding activity of Clp is allosterically inhibited by i

34 However, whether the collagen binding activity of cnm-positive S. mutans is related to

35 The binding activity of cockroach allergens to CD206 was det

36 Here, the ligand binding activity of CqsS is probed with structural analo

37 e at pH 7.0, for example, the phosphocholine-binding activity of CRP, which was reduced at acidic pH,

38 at the protection was independent of the PCh-binding activity of CRP.

39 at the protection was independent of the PCh-binding activity of CRP.

40 ot monomerize CRP and did not affect the PCh binding activity of CRP.

41 that the protection was dependent on the PCh-binding activity of CRP.

42 lis, a model Gram-positive organism, the DNA binding activity of CtsR is regulated by McsAB-mediated

43 for the enzymatic or the hydrophobic pocket binding activity of CypA.

44 formation about the domain structure and DNA-binding activity of D5, the poxvirus helicase-primase.

45 Both helicase and nuclear pore-binding activities of Ddx19 are dispensable for MKL1 nuc

46 vivo, enzymatic (ATPase or helicase) or ATP binding activities of Dhh1 or those of any its many high

47 The binding activity of DIP2A-PXXP motifs (P, proline; X, an

48 sed the level of p53, independent of the DNA-binding activity of Dmp1.

49 srupting TGFbeta signaling decreased the DNA binding activity of DNA methyltransferase DNMT1, suggest

50 tide exchange predominantly regulate the DNA binding activity of DnaA and that those with low rates o

51 Furthermore, the DNA binding activity of DnaD is redundant for this filament

52 mpared the previously documented microtubule binding activity of dystrophin with utrophin and analyze

53 Id2 inhibits the DNA binding activity of E proteins, whereas ankyrin-repeat S

54 om a variety of sources, we measured protein-binding activities of each individual compound against e

55 findings indicate that the site-specific DNA-binding activity of EBNA1 or its derivatives when expres

56 In line with the double-stranded RNA-binding activity of EBP1 in human (Homo sapiens) cells,

57 ding region for EphA2, we compared the EphA2 binding activity of EBV gH/gL and the EBV gH/gL-N(69)L/S

58 ing protein (eIF4E-BP), lowered the cap site binding activity of eIF4E and directly inhibited activit

59 acterized the growth properties and receptor-binding activities of eight mutants.

60 phenotype requires the BAR-mediated membrane binding activity of endophilin B2.

61 Moreover, Adora1 ablation decreased binding activity of ERalpha to the promoter of its targe

62 Thus, it is likely that the lower ethylene binding activity of ETR1 with silver is due to fewer eth

63 MED25 also stimulates the in vitro DNA binding activity of ETV4 by relieving autoinhibition.

64 -induced RPA foci formation requires the DNA-binding activity of FAAP24 but not the DNA translocase a

65 attachment had no effect on the plasminogen binding activity of FBA-tb, it competed with the natural

66 his GLD-3FBF complex does not impact the RNA-binding activity of FBF.

67 The properties and ligand binding activity of FhbA suggest that it plays multiple

68 We queried whether the elevated actin binding activity of FSGS mutants can be downregulated by

69 anges to the catalytic activity and membrane binding activity of FTT258.

70 The DNA binding activity of full-length Brh2 appears to correlat

71 The DNA binding activity of full-length SaeR could be restored b

72 utational analysis suggest that the membrane-binding activity of Gag is a major requirement for the a

73 sion in CD4(+) T cells by regulating the DNA-binding activity of GATA-3 and limiting GATA-3 regulatio

74 ts cognate binding site can increase the DNA binding activity of GEF to Domain I, suggesting a novel

75 nt on the SMN mRNA with Gemin5, but the mRNA-binding activity of Gemin5 is dependent on SMN levels, p

76 ns than the wild-type GS to regulate the DNA-binding activities of GlnR and TnrA in vitro.

77 The DNA-binding activity of GlnR is activated by a transient pro

78 lective pathology of CMT2D to the neomorphic binding activity of GlyRS(CMT2D) that antagonizes the VE

79 onal signaling also required the G betagamma binding activity of GRK2 but did not involve the GRK2 N-

80 mechanism that allosterically regulates DNA-binding activity of GT2-LIKE 1 (GTL1), a transrepressor

81 Also, we found that the porphyrin binding activity of GUN4 and Mg-chelatase affect the ass

82 ticular mutants, we found that the porphyrin binding activity of GUN4 and Mg-chelatase contribute to

83 s of these micelles with the in vitro ligand-binding activity of hA(2)aR in these systems.

84 red to as Hand2(EDE)) that abolished the DNA-binding activity of Hand2, leaving the remainder of the

85 HPOB does not block the ubiquitin-binding activity of HDAC6.

86 Enhanced DNA-binding activity of heat shock transcription factor 1 (H

87 gest that Aurora-A modulates the microtubule binding activity of Hice1 in a spatiotemporal manner for

88 However, whether microtubule binding activity of Hice1 is modulated by mitotic regula

89 deprivation significantly suppressed the DNA-binding activities of HNF-4alpha and PPAR-alpha, and red

90 Here, we reveal how distinct DNA-binding activities of Hop2-Mnd1 mediate the stabilizatio

91 NleE inactivates the ubiquitin chain binding activity of host proteins TAK1-binding proteins

92 The PPARgamma binding activity of house dust extracts at levels compar

93 Here, we characterize the DNA binding activity of Hox transcription factor complexes o

94 BP has been implicated in inhibiting the DNA-binding activity of HSF.

95 In aging cells, the DNA binding activity of HSF1 deteriorates correlating with t

96 We could show that binding activity of Hsp70-SPIONs to the substrate-bindin

97 The ligand-binding activity of human FcmuR was further examined.

98 ands of rare alleles likely to alter the DNA binding activity of human sequence-specific TFs.

99 To better understand the DNA-binding activity of human XPA in NER, we used NMR to inv

100 -239) is a suitable model to examine the DNA binding activity of human XPA.

101 Finally, we showed that the RNA-binding activity of HuR to p21 transcript was enhanced b

102 effects appear to depend on the G-quadruplex binding activity of HXDV as its non-G-quadruplex binding

103 In functional assays, DNA-binding activity of I184M was reduced, resulting in impa

104 e PAR polymer binding site abolishes the PAR binding activity of Iduna and attenuates its protective

105 evidence that the cell cycle arrest and DNA binding activities of IE2 appear to be responsible for t

106 d and substantially enhanced by the receptor binding activity of incorporated HA.

107 Ligand binding activity of indoor dust and its bioactivated ext

108 ty, and invasion are regulated by the ligand-binding activity of integrin receptors, transmembrane pr

109 horter p87 PIP5KIgamma, regulates the ligand-binding activity of integrins via talin.

110 Vpx expression results in decreased promoter binding activity of IRF5.

111 uppression activated iron-responsive element-binding activity of iron regulatory protein 1, increased

112 ed, the iron-responsive element-binding (IRE-binding) activity of iron regulatory protein 1 (IRP1) wa

113 latory protein 2 (IRP2) and/or increased IRE-binding activity of IRP1.

114 cellular glucose deprivation reduces the RNA-binding activity of IRP2 but not IRP2-C512S or IRP2-C516

115 that Y4/31E significantly reduced the actin binding activity of K255E, T259I and S262P, dramatically

116 mbinant form of Leish4E-IP2 inhibits the cap-binding activity of LeishIF4E-1 and LeishIF4E-3.

117 es, suggesting that it could inhibit the cap-binding activity of LeishIF4Es.

118 n (DNAm) profiles, we infer the landscape of binding activity of lung-specific transcription factors

119 In this work, we found that the zinc binding activity of M2-1 is essential for virus replicat

120 ctivated HSCs have higher nuclear levels and binding activity of MafG to the antioxidant response ele

121 The RNA binding activity of MBNL3 requires the CX(7)CX(4-6)CX(3)

122 d the low-resolution molecular structure and binding activity of Merlin and a Merlin(S518D) mutant th

123 roversy about the molecular conformation and binding activity of Merlin.

124 H melting profiles showed 24-35% of enhanced binding activity of methylxanthines during helix-coil tr

125 Here, we describe the PG9 binding activity of monomeric gp120s from multiple strai

126 Mutagenesis experiments show that the RNA binding activity of Mov10 is required for HCV inhibition

127 scuss the possible implications of the lipid-binding activity of MpPR-1 family members with regard to

128 y, we discover a significant increase in RNA binding activity of MSI2 in leukemic stem cells compared

129 Since the enzymatic and binding activities of NAs are not routinely assessed, th

130 This interaction requires the ubiquitin-binding activity of NEMO.

131 -type specific up/down-modulation of the DNA-binding activities of NF-kappaB, AP-1, and multiple othe

132 ylation, of p38 MAPK phosphorylation, of DNA binding activity of NF-kappaB and ATP content of Kupffer

133 hermore, IL-1alpha depletion reduced the DNA binding activity of NF-kappaB and C/EBPbeta, which stimu

134 Correspondingly, P4 diminished the DNA-binding activity of NF-kappaB and the transcription of i

135 f p65 with corresponding increase in the DNA-binding activity of NF-kappaB as detected by electrophor

136 f nuclear factor-kappaB (NF-kappaB), and DNA-binding activity of NF-kappaB compared with WT.

137 apoptotic cell death and suppressed the DNA binding activity of NF-kappaB in a concentration depende

138 y silencing SOD and catalase reduced the DNA binding activity of NF-kappaB in the transformed cells.

139 The DNA binding activity of NF-kappaB is critical for VCAM-1 exp

140 DNA-binding activity of NF-kappaB was higher in HSF-1(-/-) m

141 p-Akt, VEGF, Ang-1, Bcl-2, survivin and DNA binding activity of NF-kappaB were observed in the Grx-1

142 Trx is also known to activate the DNA binding activity of NF-kappaB, an important transcriptio

143 overexpression led to an increase in the DNA-binding activity of NF-kappaB, which, in turn, led to in

144 shift assay revealed that PMA stimulated DNA binding activity of NF-kappaB.

145 on, NF-kappaB nuclear translocation, and DNA binding activity of NF-kappaB.

146 ephrine stimulated the Ca(2+) -dependent DNA-binding activities of NFAT2, NFAT4, and Sp1 (but not Sp3

147 The amounts and DNA binding activities of NFI proteins were similar in immat

148 Disruption of the cholesterol-binding activity of NHERF1 largely abrogates its dynamic

149 The binding activity of NNVs with functionalized AMPs onto a

150 In addition, we characterize RNA-binding activities of novel RBPs that have been recurren

151 The binding activities of Nrf2 on the antioxidant response e

152 nd its binding with Keap1, but decreased DNA-binding activity of Nrf2 and also its binding at the pro

153 Nrf2 protein stability, compromised the DNA-binding activity of Nrf2 in a promoter-specific manner.

154 the function of both the VEGF and Semaphorin binding activities of NRP-1 has important roles in the d

155 Despite its lack of enzymatic activity, DNA-binding activity of NrtR is antagonized by the effector

156 the NS1 protein, and establish why the dsRNA-binding activity of NS1 is required for its binding to D

157 DNA binding activity of nuclear factor kappa B (NF-kappaB) t

158 rostate cancer cells, and suppressed the DNA-binding activity of nuclear factor-kappaB (NF-kappaB) tr

159 combination gene therapy stimulated the DNA binding activity of nuclear factor-kappaB in the diabeti

160 The PI-4P and sterol binding activities of OSBP were both required for 25OH a

161 changes of the MT surface may effect the MT binding activity of other MAPs present in neurons.

162 We show that unlike the DNA-binding activity of other members of this family, the DN

163 zation) as well as scaffolding (through FACT binding) activities of OTUD5 are involved in the FACT-de

164 s accelerated in mice lacking the cyclin-cdk binding activities of p27(kip1).

165 domain in p53, which likely weakens the DNA-binding activity of p53 to the MIC-1 promoter.

166 partition complexes requires ATPase and DNA-binding activities of ParA.

167 ParB/parS partition complex requires the DNA-binding activity of ParA, which transiently tethers the

168 Z2 nor PDZ3 nor the canonical target peptide binding activity of PDZ4 were necessary for hepatic SR-B

169 The HA-binding activity of PEDF may contribute to deposition in

170 replication by disrupting viral RNA promoter binding activity of polymerase.

171 that ultimately result in the altered ssDNA-binding activity of Pot1-DBD.

172 This dual binding activity of PPM1G blocks P-TEFb reassembly onto

173 The in vitro DNA binding activity of PqrR was decreased by exposure to ai

174 e conclude that promiscuous and specific RNA-binding activities of PRC2 in vitro are not mutually exc

175 ttern controlled by the rapidly evolving DNA binding activity of PRDM9.

176 The DNA binding activity of PrgX has additional indirect regulat

177 ecognition of apoptotic T cells, whereas the binding activity of properdin in the serum appeared to b

178 ed formation is tightly regulated by the DNA binding activity of protagonist basic leucine zipper 53

179 that IL-12 stimulation alters catalytic and binding activities of proteins in CTL exosomes.

180 binding assay was performed to determine the binding activity of purified allergens and allergen extr

181 The erythrocyte-specific binding activities of PvGAMA were significantly reduced

182 estigate the functional relevance of histone-binding activity of Pygo2 in malignant progression of br

183 ancy, using compounds that stimulate the DNA-binding activity of RAD51 to promote cancer cell death.

184 However, whereas the DNA-binding activity of RAD51AP1 has been shown to be import

185 The DNA binding activity of RbkR was stimulated by CTP and suppr

186 The reduced RNA-binding activity of REF in its methylated state is essen

187 nstead, arginine methylation reduces the RNA-binding activity of REF in vitro and in vivo.

188 ore, arginine methylation fine-tunes the RNA-binding activity of REF such that the RNA-protein intera

189 egulate the phosphorylation level or the DNA-binding activity of response regulators such as Spo0F, i

190 dependent upon the RxRE element and the RNA-binding activity of Rex.

191 Analysis of the in vitro binding activity of RNAs in which internal loops and bul

192 Finally, we showed that the RNA-binding activity of RNPC1 is required for binding to MDM

193 xpressed had the general single-stranded DNA binding activity of RPA complexes, unlike the telomere-s

194 hat inhibits the in vitro and cellular ssDNA-binding activity of RPA, prevents cell cycle progression

195 inhibition of NF-kappaB signaling or the DNA-binding activity of RPA1 abrogates the pro-survival feat

196 We conclude that DNA-binding activity of RPA2 is dispensable in yeast and tha

197 on of RPT6 with XopJ is dependent on the ATP-binding activity of RPT6, but proteolytic cleavage addit

198 ner and that GTP-bound XLG2 promotes the DNA binding activity of RTV1.

199 In all cases, the RNA-binding activity of S1 is a central feature of its funct

200 readouts allowed us to characterize the DNA-binding activity of SaCas9 and to optimize its sgRNA sca

201 uted across the adjacent introns and the RNA binding activity of Sam68 are necessary to repress the S

202 We used this novel array to explore binding activity of serum IgM in healthy persons and NSC

203 r factor 1, which is able to enhance the DNA binding activity of several transcription factors throug

204 APE1's redox activity stimulates the DNA-binding activity of several transcription factors, inclu

205 we have developed assays to measure the DNA binding activity of Shelterin complexes in human cell ex

206 However, NaBu did not alter the DNA binding activities of Sp proteins or their expression.

207 TSA treatment did not alter the DNA-binding activity of Sp1 toward the P-Rex1 promoter; howe

208 However, DLX4 also bound and inhibited DNA-binding activity of Sp1.

209 neutralize the Fcgamma and the V(H)3(+) Fab binding activities of SpA and provide protection from st

210 ains (IgBDs), neutralize the Fcgamma and Fab binding activities of SpA.

211 ltrastructural regions defined by the actual binding activity of specific proteins.

212 s in kratom, we compared the opioid receptor binding activity of speciofoline, mitragynine, and 7-hyd

213 The ssDNA-binding activity of SpPot1 is conferred by its ssDNA-bin

214 , low oxygen increases the stability and DNA binding activity of Sre1N.

215 concentrations of SsoRal3 increase the ssDNA binding activity of SsoRadA approximately 9-fold and als

216 nds directly to the DBD and inhibits the DNA-binding activity of STAT3 both in vitro and in situ but

217 We show that IgG IC-induced DNA binding activity of Stat3 in the lung was significantly

218 cells indicated that the promiscuous antigen-binding activity of subset #8 mAbs could lead to signifi

219 tyrosine residues inhibits the promoter DNA-binding activity of T-bet.

220 These data demonstrate that the DNA-binding activity of Tal1 is not required to cooperate wi

221 nd neurofilaments, and decreased microtubule-binding activity of tau in the brains of streptozotocin-

222 ting that the L1 loop contributes to the DNA-binding activity of TEAD.

223 sion of Leish4E-IP2 also display reduced cap-binding activities of tested LeishIF4Es, and decreased g

224 chanism by which the 5mC hydroxylase and DNA binding activities of Tet3 cooperate to control target g

225 g pERK expression also declined the promoter binding activity of TFII-I to the GRP78 promoter and in

226 d by inactivation of the translocase and DNA binding activities of the FANCM/MHF complex.

227 The binding activities of the immobilized CB1/CB2 receptors

228 in regulating both the head- and microtubule-binding activities of the kinesin-1 tail.

229 tes, F-1-P and F-6-P, could modulate the DNA-binding activities of the lactose repressor.

230 We show that the C5 and LTB4 binding activities of the molecule are independent of ea

231 eting of the complex relies on the chromatin binding activities of the MRG15 (MRG stands for mortalit

232 ers in modulating nucleosome- and/or histone-binding activities of the readers.

233 ted form of B. subtilis GS regulates the DNA-binding activities of the TnrA and GlnR nitrogen transcr

234 ues within the OB fold of AAF-44 reduced DNA binding activity of the AAF-44.AAF-132 complex.

235 njugation methods retained most of the EphB4 binding activity of the antibodies (83.85% +/- 3.82%, 76

236 In addition, the surface-binding activity of the antibody-coated nanoparticles wa

237 The membrane-binding activity of the C2 domain is functionally equiva

238 Two block the DNA-binding activity of the CRISPR-Cas complex, yet do this

239 ctivity are directly attributable to the RNA binding activity of the extra dsRBD.

240 This is likely mediated by a novel lipid binding activity of the first BRCA1 C terminus domain of

241 ng the telomeric single-stranded DNA (ssDNA)-binding activity of the human telomeric protein POT1 ind

242 The PtdSer-binding activity of the immunoglobulin-like variable (Ig

243 cyclic core determined to a large extent the binding activity of the inhibitor.

244 However, it remains unknown how ligand-binding activity of the integrin is regulated.

245 omain, to allosterically modulate collagen I-binding activity of the integrin.

246 hysically interact with and modulate the DNA-binding activity of the major mitochondrial nucleoid, DN

247 We then characterized the ssDNA-binding activity of the Metnase transposase domain and f

248 initiation, it can be expected that the DNA binding activity of the mitochondrial transcription fact

249 at the binding of NSm affects the nucleotide binding activity of the NB-ARC-LRR in vitro, while Sw-5b

250 It is generally accepted that global DNA binding activity of the NF-kappaB avian reticuloendothel

251 y complementary roles in determining the DNA-binding activity of the NF-kappaB proteins encoded by th

252 fied that at least some component of the LPS binding activity of the PACs is via the lipid A moiety.

253 The fusion proteins retain the antigen binding activity of the parent antibody but have an addi

254 also result in significantly decreased metal-binding activity of the phenazine cycloadducts.

255 e enriched at hotspots determined by the DNA binding activity of the rapidly evolving zinc finger arr

256 We also show that the RNA binding activity of the Rbfox family protein is crucial

257 high levels in mammalian cells, retained the binding activity of the respective parental Fv domains a

258 t replication by being essential for the cap-binding activity of the RNA polymerase.

259 We show that the DNA-binding activity of the S. globisporus orthologue of Atr

260 urthermore, the data establish that the zinc-binding activity of the S100A12 protein represses the ac

261 Binding activity of the serotonin reuptake transporter (

262 imparted by Tbf1 can be overcome by the DNA-binding activity of the single-stranded DNA-binding prot

263 We show that the DNA binding activity of the Soj dimer is required both for a

264 esponsible for at least some of the integrin binding activity of the spirochete.

265 A) for characterization of the integrity and binding activity of the three mAbs in the drug product.

266 3) disulfide bond appears to disrupt the DNA binding activity of the transcription factor.

267 We examined the expression, structure, and binding activity of the two major S. aureus fibronectin-

268 Surprisingly, we find that the DNA binding activity of the UAF1-associated protein RAD51AP1

269 approaches to characterize the carbohydrate-binding activity of the VCC toxin.

270 individual viral particles and to study the binding activity of the viral particles.

271 recognition by Itk highlights a nonclassical binding activity of the well-studied SH2 domain providin

272 l and NMR results establish the nucleic acid-binding activity of the Zf-GRF domain.

273 fic B-cell populations and the sequences and binding activities of their antibodies before and during

274 ral basis of the alterations in the receptor binding activities of these mutants is also discussed.

275 m by which ligand binding attenuates the DNA-binding activities of these proteins.

276 The EphB4 binding activity of these probes was evaluated through t

277 el to further examine the porin and integrin-binding activities of this OMP as they relate to B. burg

278 B fold of STN1, but does not require the DNA-binding activity of this domain.

279 osphorylation of PRH by CK2 inhibits the DNA binding activity of this protein and dephosphorylation r

280 n protein (PRH/Hhex) by CK2 inhibits the DNA-binding activity of this transcription factor.

281 y disrupting the double-stranded RNA (dsRNA)-binding activity of TLR3 ablated the chemokine/cytokine

282 on, telomeres deploy the single-stranded DNA binding activity of TPP1/POT1a.

283 Taken together, inhibition of the DNA binding activity of transcriptional repressor OCT-1 is a

284 pes of structures, we evaluated the in vitro binding activities of two well-characterized DNA repair

285 s biochemical analysis revealed that the DNA-binding activity of UAF1 is indispensable for enhanced R

286 In support of the observed host membrane binding activity of VapA, we also found that rVapA(32-18

287 We first probed the monosaccharide-binding activity of VCC and demonstrated that the toxin

288 The actin-binding activity of vinculin is inhibited by an intramol

289 his study, we sought to characterize the RNA binding activity of VP6 and its functional relevance.

290 The FVIII-binding activity of VWF positively correlated with FVIII

291 ere we describe the conformations and ligand binding activities of water-soluble and membrane-bound B

292 We have examined the binding activities of wild-type (WT) MA and 62QR MA vari

293 1 construct phenocopies the antiviral and NP binding activity of wild type MX1.

294 C-terminal WRKY domain and stimulate the DNA binding activity of WRKY33.

295 performed to examine the transactivation and binding activities of WT, mutant, and chimeric AIREs on

296 nding, had only a moderate effect on the DNA-binding activity of XPA.

297 These data suggest that the intrinsic DNA-binding activities of XRCC4 and XLF may be subject to re

298 Here, we tracked the microtubule end-binding activity of yeast kinesin-8, Kip3, under varying

299 on of two of these sites can abolish the DNA-binding activity of YY1.

300 The binding activity of ZNF9 toward these TOP-containing 5'