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 report 7mG excision and DNA binding activities of AlkD mutants, along with a compari

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

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

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

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

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

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

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

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

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

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

17 mRNA was associated with an increase in the binding activity of AP-1 but the activities of NF-kappaB

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

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

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

21 The substantial receptor-binding activity of Arg(B5)-insulin (40% relative to wil

22 reporter assay for rapidly screening the DNA-binding activities of assembled multi-finger arrays.

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

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

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

26 targeted to endosomal membranes by the lipid-binding activities of both the Vps36 GLUE domain and the

27 sites Ser-63 and Ser-73, and to increase DNA binding activity of c-Jun, detected by EMSA.

28 oth liver hepcidin transcription and the DNA-binding activity of C/EBP alpha.

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

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

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

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

33 10 by arsenic is associated with reduced DNA-binding activity of CCAAT/enhancer-binding protein beta

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

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

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

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

38 The binding activity of cockroach allergens to CD206 was det

39 Although the dsRNA-binding activity of CPL2 DRM has not been shown to date,

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

57 8ad faeG gene chimeras and characterized the binding activity of each K88 chimeric fimbria.

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

59 eracting motif ((354)LKALL(358)) and the RNA-binding activity of Ebp1.

60 essed the ability of LPS to increase the DNA binding activity of Egr-1 and p65.

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

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

63 ntegrity was not required for the HAT or RNA binding activities of Elongator.

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

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

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

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

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

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

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

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

72 genesis reveals that reducing the barbed-end binding activity of FRL1 and mDia2 greatly enhances the

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

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

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

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

77 ession and stimulated the expression and DNA-binding activity of GATA3, a key regulator of IL-4.

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

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

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

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

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

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

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

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

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

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

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

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

90 tivity and mRNA expression by inhibiting DNA-binding activity of hepatocyte nuclear factor 4alpha (HN

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

111 To evaluate the DNA binding activity of individual subunits within NS3 oligo

112 Ligand binding activity of indoor dust and its bioactivated ext

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

114 While the ligand-binding activity of integrins is known to be modulated b

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

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

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

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

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

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

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

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

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

124 NA species at least partly by disrupting the binding activities of many transcription factors which g

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

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

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

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

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

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

131 indicate that the ATP- and MuA-regulated DNA-binding activity of MuB is not essential for target deli

132 Nuclear binding activity of Myc to the E-box element of p53 and

133 eover, downregulation of TCEAL7 promotes DNA-binding activity of Myc-Max, and upregulates the promote

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

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

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

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

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

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

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

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

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

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

144 Ref-1 decrease correlated with decreased DNA-binding activity of NF-kappaB mediated by soy isoflavone

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

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

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

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

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

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

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

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

153 et merlin does not affect the GTPase nor GTP-binding activity of NGB.

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

155 The binding activity of NNVs with functionalized AMPs onto a

156 plication system to demonstrate that the RNA-binding activity of NP is not required for the unprimed

157 s out two models that postulate that the RNA-binding activity of NP mediates the switch from capped R

158 The binding activities of Nrf2 on the antioxidant response e

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

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

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

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

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

164 lso found that B-DIM treatment inhibited DNA binding activity of nuclear factor-kappaB (NF-kappaB), w

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

180 The DNA binding activity of PrgX has additional indirect regulat

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

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

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

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

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

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

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

188 e phosphorylation sites that control the DNA binding activity of RcaC.

189 ctedly found that ATP inhibited the oriCIIvc binding activity of RctB, suggesting that the ATP-bound

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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 This leads to increased binding activity of Sp1 to the mVGLUT2 promoter and resu

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

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

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

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

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

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 onsistently inhibited the expression and DNA-binding activity of T-bet, a key regulator of interferon

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

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

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

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

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 L9 might exist and serve to modulate the DNA binding activities of the C terminus.

227 The DNA binding activities of the E-proteins are regulated by a

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

229 The binding activities of the immobilized CB1/CB2 receptors

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

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

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

233 e nuclear retention, nuclear export, and RNA-binding activities of the multifunctional La protein and

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

259 u E10 splicing is mainly mediated by the RNA-binding activity of the second RRM and involves an intro

260 Binding activity of the serotonin reuptake transporter (

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

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

263 The increased DNA binding activity of the ternary complex is translated in

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

265 The iron-induced increase in DNA-binding activity of the transcription factor CCAAT/enhan

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

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

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

271 se activities having a role in vivo, the DNA binding activity of the Xilf3-containing CBTF complex an

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 Interestingly, the microtubule binding activity of this N-terminal domain is regulated

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

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

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

283 sDNA on its own, but it stimulates the ssDNA binding activity of Top3 5-fold.

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

285 ator of transcription 3 (Stat3); (b) the DNA-binding activity of transcription factors activator prot

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

287 iated with an increase in expression and RNA binding activity of tristetraprolin, an mRNA-binding pro

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

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

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

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

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

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

294 1 construct phenocopies the antiviral and NP binding activity of wild type MX1.

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

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

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

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

299 DNA binding activity of YodB is directly inhibited by thiol-

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

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