ライフサイエンスコーパス: binding of

1 nt isothermal titration calorimetry data for binding of 11 tryptophan ligands to the homo-undecameric

2 was quantified as the difference in specific binding of [(11)C]raclopride (nondisplaceable binding po

3 NMR studies confirmed the pocket of binding of 12 as predicted by the Glide docking software

4 Because of the binding of (123)I-CLINDE to blood cells and peripheral t

5 The binding of 16 to BRPF1B was rationalized through an X-ra

6 Binding of (18)F-GP1 to GPIIb/IIIa receptors was investi

7 of the new products were formed via covalent binding of 3-QCA with DOM molecules of above-average O/C

8 CD4 binding substantially increases the binding of 36D5 to gp120 in the intact Env trimer, consi

9 D-aspartate receptor activation requires the binding of a coagonist, D-serine, which is synthesized f

10 O cell fibronectins were able to mediate the binding of a diverse panel of gp120 proteins to alpha4be

11 We have explored the interdependence of the binding of a DNA triplex and a repressor protein to dist

12 ty acids was found to play a key role in the binding of a glycolipid to the carbohydrate recognition

13 y can define the subunit topology and copper binding of a manganese oxidizing complex, and describe e

14 monomeric Delta123 predominantly blocked the binding of a non-neutralizing antibody to Delta123, whil

15 This transition is controlled by binding of a novel tetrameric form of the second messeng

16 bstitution of Lys51 to Ala in LC3B abrogates binding of a phosphomimetic Nix mutant.

17 ption in vivo by analyzing motor defects and binding of a positron emission tomography (PET) radiolig

18 aper describes an assay that can profile the binding of a protein to ligands and can rank the affinit

19 We investigated whether variation in binding of a transcription factor, the vitamin D recepto

20 is approach has broad potential to probe the binding of a variety of ligands to metal nanoparticles.

21 Upon binding of a Wnt ligand to a receptor of the Fz family,

22 However, differences in the predicted binding of A-867744, compared with TBS-516 and TQS, may

23 namics simulations, elucidating preferential binding of Abeta42 with the A2V and A2T hexapeptides com

24 gus Ashbya gossypii, we demonstrate that the binding of adenine and guanine nucleotides to the canoni

25 We observe that binding of agonists to VFD2 of TAS1R2 leads to major con

26 on of the signal transduction cascade, after binding of all investigated products to the receptor pre

27 Binding of allergen-specific IgE to its high-affinity re

28 y conformational changes associated with the binding of allosteric regulatory proteins, and show that

29 layers previously oxidized, and the covalent binding of amino-oligonucleotides to pure p-MBA monolaye

30 Synaptic dysfunction due to the disrupting binding of amyloid beta (Abeta) and tau oligomers is one

31 novel mechanism of MAPK activation requiring binding of an activator and also shows that MAPKs can be

32 onclude that phosphorylation can disrupt the binding of an E3 ubiquitin ligase to an E2-conjugating e

33 differences from wild-type IL-23 except for binding of and signaling blockade by the 7B7 anti-IL-23

34 was optimized to eliminate the non-specific binding of antigen on the membrane surface.

35 nding specificities, why lipid increases the binding of apoE to its receptor, and why specific residu

36 Furthermore, binding of ArfA and RF2 induces conformational changes i

37 lysozyme demonstrate how nanomolar affinity binding of asymmetrical antigen is enabled through selec

38 s would disrupt critical interactions in the binding of ATP and thereby impair ATP-induced nucleotide

39 and its chaperone function are regulated by binding of ATP/ADP to mtHsp70's nucleotide-binding domai

40 inium-labeling of AtRALF1 indicated that the binding of AtRALF1 to intact roots is CML38-dependent.

41 We show that this is due to sustained binding of B-Raf to Rap1.

42 Noncovalent binding of biopharmaceuticals to human serum albumin pro

43 In vitro binding of biotinylated Cry proteins and competition ass

44 for both alphavbeta5 and alpha5beta1, while binding of biotinylated cyclo[RGDfK] was very weak and o

45 (ii) Selective and cooperative binding of both an acetato ligand and an amino ligand to

46 d enabled identification of allele-dependent binding of both, transcription factors and coregulators

47 This recruitment requires binding of BRD2's tandem bromodomains to H4Ac, which is

48 factors through inhibiting the acetyllysine binding of BRD4 and the kinase activity of PI3K.

49 that the intragenic DNA methylation-mediated binding of Brother of Regulator of Imprinted Sites (BORI

50 e structure of free CheR1, revealed that the binding of c-di-GMP induces dramatic structural changes

51 Binding of C. albicans to EphA2 on oral epithelial cells

52 This promotes the binding of C/EBPbeta at enhancers controlling the expres

53 Binding of Ca(2+) induced an increase in the alpha-helic

54 Accordingly, increased binding of Ca(2+)/CaM to PSD-95 induced by a chronic inc

55 eriments revealed that FGF13 potentiates the binding of calmodulin to NaV1.5 and that phosphomimetic

56 affinity than Ca(2+)-free CaM (apoCaM); the binding of CaMKII peptide to CaM in return increases the

57 Covalent binding of capturing biomolecule (anti-TNF-alpha antibod

58 mics simulations to investigate the specific binding of cardiolipins to yAAC3.

59 er landscapes and associate with coordinated binding of CEBPD, IRF1, and NFkappaB.

60 minal domain (NTD) with implications for the binding of certain adaptors, providing insight into how

61 MP persistence arose secondary to binding of CFH to CD11b, which obstructed the homeostati

62 Nanoparticle tilting after binding of chiral amino acids is proposed as a chiral gr

63 Transcription factor (TF) binding of cis-elements is often associated with accessi

64 ve mass spectra matching, the promiscuity of binding of cisplatin to ubiquitin is revealed, with 14 d

65 e increase in probe-to-probe spacing enables binding of cisplatin via the intrastrand GNG motif (N =

66 species in human-inflamed tissue and allows binding of complement factor 1q (C1q) and activation of

67 e central methylene considerably affects the binding of compound 1 analogues to PI3Kdelta enzyme.

68 Competition between binding of copper ions to a membrane-embedded synthetic

69 noprecipitation analyses reveal constitutive binding of CREB to target gene promoters in the absence

70 ylation of CRMP-2, which results in elevated binding of CRMP-2 to microtubules and a concomitant incr

71 Vinblastine inhibited the binding of crocin to tubulin while podophyllotoxin did n

72 n, and 80% of HNRNPU peaks coincide with the binding of CTCF or RAD21.

73 toplasmic relocalization of Cat L, decreased binding of CUX1 to Snail and the E-cadherin promoter, re

74 Binding of DDX1 results in enhancement of Rev oligomeriz

75 Binding of dead cells via receptors present on the macro

76 ing site provide the molecular mechanism for binding of dectin-2 to fungal mannans and also to bacter

77 biochemical influences that probably include binding of degraded hemoglobin, among other things, that

78 e explore how shape and charge contribute to binding of diverse inhibitors of these enzymes.

79 The vast majority of mutations do not affect binding of dynein to dynactin and BICD2 and are therefor

80 ys residues to Glu markedly reduced integrin binding of E128K IL-1beta, suggesting that the Lys resid

81 n thus would be favorable for the postulated binding of E7 to phosphatidylethanolamine lipid headgrou

82 ed by a concerted transition model where the binding of each GABAergic drug additively and independen

83 structural and thermodynamic consequences of binding of each ligand to its allosterically coupled sit

84 Based on these results, we propose that the binding of each stator-unit is enhanced by the force it

85 d substitutions have damaging effects on DNA binding of EBF3.

86 hat ENb-TRAIL blocks EGFR signalling via the binding of ENb to EGFR which in turn induces DR5 cluster

87 cts also promoted the cytotoxic activity and binding of enterotoxin and beta toxin more strongly than

88 onal studies have provided insights into the binding of ERCC1-XPF to various DNA substrates.

89 Binding of FACT to these genomic regions triggers a p53

90 soform containing extradomain B enhances the binding of fibronectin through the RGD sequence to beta3

91 Here, we assayed the binding of five essential TFs over multiple stages of em

92 Binding of FK506 to the FKBP domain causes the target do

93 lected between 1979 and 2010 to block glycan binding of four pandemic GII.4 noroviruses isolated in t

94 Plk1 phosphorylation sites in regulating the binding of FoxM1b to Rb and DNMT3b.

95 Preferential binding of G-quadruplex RNA is conserved, surprisingly u

96 Receptor-specific binding of gallium-labeled HZ220 was characterized in PC

97 complex architecture and to investigate the binding of GPCRs and other receptors to the BBSome.

98 TB domains are important for stabilizing the binding of Grb2 and Shc to the single-Tyr EGF receptors.

99 est whether this occurs in vivo, we used the binding of growth factor receptor bound 2 (GRB2) to phos

100 Here, we find that the binding of guanosine triphosphate (GTP) to one subunit i

101 al His(64) residue to alanine promotes rapid binding of H2S and its efficient conversion to oxidized

102 absence of IRF4, chromatin accessibility and binding of Helios at PD-1 cis-regulatory elements were i

103 the effect of N-linked glycosylation on the binding of Herceptin to HER2 protein in breast cancer an

104 ilayer model, we show GTP-dependent membrane binding of hGBP1F In addition, we demonstrate nucleotide

105 Binding of Hic to hTSP-1 is inhibited by heparin and cho

106 of epigenetic writers/erasers and chromatin-binding of histone deacetylases (HDACs) and Polycomb-gro

107 single domain antibody mimics the effect of binding of HIV integrase to LEDGF which is crucial for H

108 moter and enhancer activity and differential binding of HNF4alpha, a key regulator of expression of v

109 to, performing the separation function, the binding of HP-MBs and SG could be avoided while a low ba

110 than murine (m) PD-1 interactions, stronger binding of hPD-1 to hPD-L2 than hPD-L1, and comparable b

111 cytometry, we demonstrate a strong and quick binding of HRV types 16 and 1B to monocytes, and slower

112 emagglutinin (HA) glycoprotein that abrogate binding of human antibodies.

113 The binding of human IgG1 to human Fc gamma receptors (hFcga

114 The binding of human plasminogen (hPg) to the surface of the

115 IgG antibodies, which were able to block the binding of human serum IgE.

116 Furthermore, dose-dependent binding of human VWF to purified recombinant human MGL w

117 nd in cultured cells by interfering with the binding of HuR to RNA.

118 The aim of this study was to evaluate the binding of IgE to five recombinant beta-conglutin isofor

119 maRIIB on myeloid cells and its differential binding of IgG subclasses controls the contributions of

120 ral and acidic pH, prevents the simultaneous binding of IgG, and reduces circulating IgG levels in pr

121 ha electrostatically repels the DNA, and the binding of IkappaBalpha appears to twist the NFkappaB he

122 lack Etv5 restored IL-10 production and the binding of IL-10-inducing transcription factors includin

123 n studied extensively for their roles in the binding of information and gaze function, respectively.

124 ctions, posttranslational modifications, and binding of inhibitors such as the p27 tumor suppressor p

125 We detected prominent binding of intravenously injected F-Dapa in the kidney c

126 HCFC2 promoted the binding of IRF1 and IRF2 to the Tlr3 promoter, without w

127 ements, as well as an over-representation of binding of key B-cell transcription factors.

128 understanding of the factors involved in the binding of KIR2DS1 and its inhibitory counterpart KIR2DL

129 Binding of knottin-RGD peptide was strongest for alphavb

130 ragmentation to give ethylene is promoted by binding of l-arginine in a nonoxidized conformation and

131 Binding of La ribonucleoprotein domain family, member 6

132 TAX1BP1 binding of LC3 and GABARAP via its LC3-interacting regio

133 Binding of Lin28a to TRBP in vitro is also enhanced by p

134 in its coiled-coil 1 domain that impedes the binding of linear (M1-linked) di-ubiquitin to its coiled

135 n the context of dynein alone, we found that binding of LIS1 to DDB does not strongly disrupt process

136 insic fluorescence enhancement observed upon binding of LM pectin to lysozyme was correlated with the

137 t, we show that direct, cell-cycle-regulated binding of M18BP1 to CENP-A nucleosomes recruits the Mis

138 NA structural alterations can promote direct binding of m6A-modified RNAs to low-complexity regions i

139 iquitination by MDM2, a process initiated by binding of MDM2 to the intrinsically disordered transact

140 e improvements were accompanied by increased binding of MeCP2 T158M to DNA.

141 t could trigger changes (for example, in the binding of microcystin to proteins).

142 sful remediation in coastal areas, permanent binding of mobile P in anoxic sediments may be needed to

143 ed an off-cycle pathway involving reversible binding of molecular oxygen to iridium, which contribute

144 providing the substrate for phase-dependent binding of mossy fiber spikes to repetitive theta-freque

145 hPD-1 to hPD-L2 than hPD-L1, and comparable binding of mPD-1 to both ligands.

146 C terminus deletion (Cox1DeltaC15), reduced binding of Mss51 and Cox14 to COA complexes.

147 ulated Raw 264.7 macrophages resulted in the binding of mu1A of the clathrin-coated vesicle AP-1 comp

148 infra-slow bursting enables integration and binding of multiple chemosensory stimuli over a prolonge

149 The binding of multiple fullerenes was observed to increase

150 e adhesins has been shown to be required for binding of multiple glycan receptors.

151 n the mutant CALR C terminus influences both binding of mutant CALR to MPL and activation of MPL sign

152 s, we propose that this initial prerequisite binding of MVAPP enhances ATP binding.

153 This analysis highlights that the strong binding of myosin Ic to actin is dominated by the ADP st

154 NA motif that mediates the homo-trimeric DNA binding of Myrf N-terminal fragments.

155 ectivity filter in which to test competitive binding of Na(+) These experiments disclosed a marked de

156 luciferase reporter assays revealed a direct binding of NANOG to a transcriptionally active site in a

157 g domains efficaciously blocked reticulocyte binding of native PvRBPs, suggesting that the human immu

158 ecovery phase from a hypoxic injury and that binding of neuronal uPA to astrocytic uPAR induces astro

159 This import involves binding of newly synthesized proteins by cytosolic perox

160 ls, which exhibited an aging-related loss in binding of NF-kappaB and STAT factors.

161 Binding of nitric oxide in the reduced Miner2 [2Fe-2S] c

162 h acts as a specificity filter that prevents binding of non-NES peptides.

163 The binding of NR3C1 but not HES1 to CLDN1 promoter signific

164 analysis revealed that OA-NO2 increased the binding of Nrf2 to an antioxidant response element in th

165 obably because these mutations decreased the binding of NS1 to the cleavage and polyadenylation speci

166 hether this modification is required for the binding of NS5A to other cellular proteins.

167 ysis confirmed that clofibrate abrogates the binding of nuclear factor-kappaB to the PTPRZ1 and Wnt8a

168 scribe a detailed protocol based on covalent binding of nucleophilic groups on Wnt proteins to activa

169 Olfaction is mediated by the binding of odorant molecules to olfactory receptors (ORs

170 nding domain (GluA2-LBD) are consistent with binding of one molecule of 11m per dimer interface, cont

171 This indicates that OA may inhibit the binding of other RRM-containing protein/s necessary for

172 ChIp analyses indicated the binding of p53 to the promoter region of miR-199a-3p.

173 comparable in oxLDL-loaded Mvarphis, yet the binding of p65/RelA (the prototypic NF-kappaB family mem

174 The binding of pairs of fullerene guests was observed to eff

175 Upon DNA damage, binding of PARylated PARP1 by the macro domain induces a

176 fused to the C-terminus of Bet v 1 inhibited binding of patients' IgE antibodies to Bet v 1.

177 A general method for sequence-specific binding of peptides remains elusive despite decades of r

178 The binding of PF4 to perlecan was found to inhibit both FGF

179 step in merozoite invasion is the essential binding of PfRh5/CyRPA/PfRipr complex to basigin, a step

180 ol 3-kinase VPS34 activity by increasing the binding of phosphatidylinositol to VPS34.

181 Moreover, binding of phospho-SRC1 to RORgammat displaced bound Fox

182 nd is inhibited by mutations that compromise binding of phosphorylated Thr-348 to an allosteric bindi

183 Binding of PHR1 and PHL1 factors to P1BS was confirmed b

184 Particular attention has focused on the binding of plasminogen (Plg) to bacterial surfaces, as i

185 We further show that binding of Plexin-B1 to Sema4A promotes the interaction

186 We found extensive binding of PPARalpha near genes involved in glycolysis/g

187 ion is directed in part by sequence-specific binding of PRDM9, a polymorphic histone H3 (H3K4Me3) met

188 not allow discrimination between the initial binding of properdin and binding secondary to C3b deposi

189 Similarly, binding of properdin to the surface of human umbilical v

190 jacent residues that facilitate the specific binding of proteins and modulate the global folding and

191 N)6](3-)/[Fe(CN)6](4-)) that is altered upon binding of PSMA with PSMA-Ab immobilized on N-AuNPs/ITO.

192 and enzyme activity are regulated in part by binding of purine nucleotides to an allosteric regulator

193 The binding of pVIIn2-and, by extension, that of genome-cond

194 in, or phosphorylation site causes excessive binding of RAD51 to CFS loci and impairs CFS expression.

195 We study the folding and binding of random sequences of hydrophobic ([Formula: se

196 Binding of receptor activator of NF-kappaB ligand (RANKL

197 number of constraints, possibly through the binding of regulatory proteins in the trans-Golgi networ

198 pidly after folic acid injection, as did DNA binding of RelB and NFkappaB2, detected in nuclei isolat

199 sitive competition ELISA to measure integrin-binding of RGD-peptides in high-throughput without using

200 ility shift assay revealed sequence-specific binding of rSaWRKY1 with MYB20 promoter.

201 Binding of S-peptide to S-protein results in the formati

202 x to poly-Fe(vbpy)2(CN)2 followed by surface binding of salts of the cations and electrochemical redu

203 erologous SNARE proteins orchestrated by the binding of Sec1/Munc18 (SM) proteins to specific syntaxi

204 ar how the immune system reconciles receptor binding of self-proteins with self/non-self-discriminati

205 hancers regulate gene expression through the binding of sequence-specific transcription factors (TFs)

206 Increased binding of serum epitope-specific IgA to CM in mothers o

207 Previous in vitro studies suggested that binding of SH2 and PTB domains can enhance protein phosp

208 Binding of sialylated glycans or other ligands triggers

209 Binding of siRNA to PEI-polymer was characterized and co

210 sis in embryonic stem cells showed extensive binding of Smad2/3/4 to GC-rich cis-regulatory elements.

211 erlies enzymatic activity and influences the binding of small-molecule inhibitors.

212 nto the structural basis for state-dependent binding of sodium channel-blocking drugs.

213 ciated with Abeta localizing to synapses and binding of soluble Abeta aggregates to synapses requires

214 Binding of specific monoclonal anti-DARC antibodies and

215 CARM1 recruitment lags behind the binding of SRC-3 and p300 to ER.

216 t-nCu exposure experiments indicate that the binding of SRE with nCu and dissolved Cu ions can signif

217 ESAT-6 induced phosphorylation and DNA binding of STAT3 and this was blocked by STAT3 inhibitor

218 Binding of STIM1 to SUR1 was enhanced by poly-lysine.

219 Notch signalling activity by inhibiting DNA-binding of Su(H), potentially affecting both activation

220 loop has an important role in the selective binding of succinyl-CoA over acetyl-CoA.

221 In particular, the selective binding of sulfate with artificial receptors is importan

222 Simultaneous binding of SWR to both H2A nucleosome and free H2A.Z ind

223 We find that binding of TDP-43 to the translational machinery is medi

224 he promoter region of MLH1 as perturbing the binding of TFAP4 and consequently increasing DCLK3 expre

225 Thus, we demonstrated peptide-dependent binding of the activating NK cell receptor KIR2DS1, prov

226 These actions result from the specific binding of the antibody to the beta-subunit of Fsh to bl

227 Moreover, binding of the antiviral drug, amantadine, at the N-term

228 ross EC-EC junctions in trans Except for the binding of the C-terminal angiopoietin domains to the Ti

229 roup and a dedicated cavity that facilitates binding of the C2 methyl branch.

230 Binding of the capsid to the nuclear pore complex (NPC)

231 These positively modulate the binding of the CB1 orthosteric agonist CP55,940 while ex

232 The consequences of the binding of the CD4-mimetic compound to the HIV-1 envelop

233 which rearrangement of a flexible loop upon binding of the correct peptide substrate is required for

234 Glycan array analysis confirmed selective binding of the CRD to glycans that contain Manalpha1-2Ma

235 -mediated phosphorylation and 14-3-3 protein binding of the cytoplasmic amino-terminus of iRhom2 alte

236 All studied iRFPs exhibited efficient binding of the endogenous biliverdin chromophore in cult

237 Binding of the gamma-tubulin receptor Spc110 to the cent

238 The phosphate and diphosphate binding of the generated channels was studied in planar

239 se observations, enhancers show TF-dependent binding of the H3K27 demethylase KDM6A.

240 The binding of the HIV-1 gp120 glycoprotein to CD4 triggers

241 Competitive binding of the human monoclonal antibody (mAb) LE2E9 rev

242 Binding of the intrinsically disordered C-terminal arm o

243 We also studied the binding of the isolated SH2 domain of Grb2 (growth facto

244 Additionally, binding of the ligand-activated AHR to the putative diox

245 fected cell lines that were unrelated to the binding of the MAb to the target cells.

246 main exerts negative allosteric control over binding of the N-terminal lectin domain to mannosylated

247 The measured enthalpy of binding of the Naph(+*)(Pyr) heterodimer (20.9 kcal/mol)

248 MCM loading is orchestrated by binding of the origin recognition complex (ORC) to DNA,

249 eral C3b-binding compounds to interfere with binding of the original C3b ligand that guided their dis

250 The compound has no effect on the binding of the orthosteric ligands, implying its alloste

251 one cationic species as product requires the binding of the other (ternary-complex mechanism).

252 intramolecular binding motif that mimics the binding of the p53 tumor suppressor.

253 at this blocking activity may originate from binding of the peptide to a sequence of SdrC involved in

254 STD-NMR demonstrated binding of the potential substrate carveol, the potentia

255 riments revealed that Spt6 could compete for binding of the PRC2 methyltransferase Ezh2 to Suz12 and

256 Together the results shed light onto binding of the precursor peptide and the associated conf

257 as in the generally accepted P450 mechanism, binding of the primary substrate in the active-site trig

258 echanism could be inferred from the covalent binding of the proteasome-specific inhibitor epoxomicin

259 tion of hGBP1F, which competes with membrane binding of the protein.

260 misfolding of chromatin fibre and block the binding of the regulator of chromatin condensation 1 (RC

261 n reduced expression of the gene through the binding of the repressive MYB transcription factor and,

262 noprecipitation experiments reveal increased binding of the repressor factor RE1-silencing transcript

263 e and sensitivity readily exposes unexpected binding of the ribosome-associated protein SRA.

264 and mass spectrometry, we further uncovered binding of the RNA-binding protein HuR to the -44 region

265 The kinetic association rate constant of the binding of the S339D/S340D mutant to the FERM domain of

266 H3K9ac serves as a substrate for direct binding of the SEC, as does acetylation of histone H4 ly

267 ed that this association is disrupted by the binding of the second messenger Ap4A to HINT1.

268 al at the RI, hypoxia-induced expression and binding of the splicing factor SRSF3, and increased bind

269 Binding of the target triggered a release of the DNA str

270 hree-state model imply asymmetric sequential binding of the terminal domains.

271 MSC interrupted binding of the TF GATA-3 to the locus encoding TH2-cell-

272 rsensitivity site to rs7692387 and predicted binding of the transcription factor ZEB1 rather to the n

273 ctivity in patient kidney cells and impaired binding of the transcription factor ZNF143.

274 ion to exploit therapeutically.Significance: Binding of the transcription factors NFIB and YBX1 to th

275 It allows binding of the tRNAs to the ribosomal A and P sites, but

276 te with restoration of wild-type two-pronged binding of the UBXD1 adaptor protein that is impaired in

277 se a multidisciplinary approach to study the binding of the viral attachment protein G to its host re

278 idue of the N-terminal linker for inhibiting binding of the VWF A1 domain to GpIbalpha on platelets i

279 Significantly, Cripto-1 and Cryptic blocked binding of their cognate ligands to type I and type II T

280 )-Cas9 system and measured the quantities of binding of these viruses to cell surfaces.

281 ents showed that A-ZIP53 can inhibit the DNA binding of three proteins.

282 of the splicing factor SRSF3, and increased binding of total and phospho-Ser2 RNA polymerase II spec

283 tment in Arabidopsis relies in large part on binding of trans-acting factors to cis-localized DNA seq

284 ant deactivating enhancers by disrupting the binding of transcription factors (TFs) in a given cellul

285 ise that stereospecific but necessarily weak binding of tropomyosin to F-actin is required for effect

286 His96 is responsible for the binding of two haem groups within the main central cavit

287 dependent transcription is suppressed by the binding of two nucleoid associated proteins, IHF and Fis

288 Binding of TZAP to long telomeres represents the switch

289 Binding of UBA5 to UFM1 is mediated via an amino acid se

290 In conclusion, we have shown that binding of UL20 to GODZ in the Golgi apparatus regulates

291 ectrons to oxygen, and completely blocks the binding of UQ and the inhibitor HQNO.

292 s 1-101) pull downs showed sixfold-increased binding of vinculin and, to a lesser extent, alpha-actin

293 Membrane binding of viral and cellular N-myristoylated proteins c

294 Stability can be improved by binding of vitamin A to milk protein.

295 modifications significantly reduce antibody binding of waitlisted patients.

296 We evaluated antibody binding of waitlisted renal transplant patients to 3 gly

297 Binding of Wnt ligands promotes the interaction of LRP5/

298 s (T1024G and T1086G) abrogated preferential binding of WRN to G4 DNA.

299 differences in copper co-ordination upon the binding of xylan and glucans.

300 Interestingly, the binding of YscP to the slowly self-cleaving YscU variant