ライフサイエンスコーパス: binding of

1 Regional grey matter volumes, and regional binding of 18F-AV-1451 and 11C-PK11195 were derived from

2 The binding of [(3)H]muscimol has been used to evaluate the

3 In contrast, the binding of a 12-porphyrin nanoring to two hexadentate li

4 tracellular free iron content via reversible binding of a [2Fe-2S] cluster.

5 t structural definition to support the rapid binding of a heme cofactor.

6 ion of the motor switch protein FliM and the binding of a member of the CheY protein family to the ou

7 Binding of a nucleosome to SAGA displaces the HAT and DU

8 tional changes a cell undergoes upon the DNA binding of a POI.

9 The IHZ assay involves imaging the binding of a protease-activated monoclonal antibody prod

10 The virus enters host cells through binding of a receptor-binding domain within its trimeric

11 olar range (K (diss) ~ 17 and ~ 31 muM), but binding of a second molecule of profilin is negatively c

12 dpiece underlie PLB inhibition of SERCA, and binding of a single Ca(2+) ion is sufficient to shift th

13 al changes of PLB-bound SERCA in response to binding of a single Ca(2+) ion.

14 We conclude that binding of a single Ca(2+) is a critical mediator of all

15 revealed an overlap between LRP1 binding and binding of a small-molecule inhibitor of PAI-1, CDE-096,

16 ization of reactants induced by the bivalent binding of a specific IgG antibody to two antigen-conjug

17 Binding of a target analyte can disrupt the hybridizatio

18 ning it in an "off" state until the specific binding of a true substrate.

19 on PrP(C) that underlies the stereoselective binding of Abeta (1-30).

20 either impaired RISC formation or increased binding of AGO2 to mRNA targets as mutation specific fun

21 he RIFIN disrupts the complex, blocks LILRB1 binding of all tested RIFINs and abolishes signalling in

22 nvestigate the effects of photolysis and the binding of amino acid residues in cytochrome c and neuro

23 The binding of ammonium ions by two homooxacalix[3]arene-bas

24 of RSK2 on autophagy resulted from directly binding of AMPKalpha2 in nucleus and phosphorylating it

25 The binding of amyloid-beta peptides of different concentrat

26 we demonstrate that fusion is abrogated when binding of an adaptor protein is prevented and that dire

27 s a valuable moiety that can induce covalent binding of an inhibitor to its target.

28 ace coverage assays, including heterogeneous binding of analyte molecules on bead or sensor surfaces,

29 of apoptosis, which is characterized by the binding of Annexin V, demonstrates that programmed cell

30 Binding of another compound (NITD-640) ordered the finge

31 f one ligand thermodynamically activates the binding of another, different ligand or substrate, is a

32 Recent work shows that binding of antagonists to these receptors is complex, wi

33 Receptor crosslinking requires binding of antibodies to multiple epitopes on the allerg

34 We demonstrate that IL-2 activates binding of AP-1 and STAT5 at sites that can subsequently

35 sults support the relevance of high-affinity binding of ARF transcription factors to uniquely spaced

36 Sulfur bridges provide efficient binding of As to organic carbon (C), but the formation o

37 The chromatin binding of Ascl1 and Myod1 was surprisingly similar in f

38 ssays with newly replicated DNA revealed the binding of ATAD2, a bromodomain-containing posttranslati

39 Luciferase assays revealed binding of ATOH1 and subsequent activation to the promot

40 osterically turn the enzyme on or off by the binding of ATP or dATP, respectively.

41 four activation-loop threonine residues and binding of ATP-Mg(2+).

42 lar response to external signals, such as in binding of B cell receptors (BCR) to antigen, which init

43 To contrast the binding of B2 versus DDM in tubulin, X-ray crystallograp

44 Specifically, we realized rapid binding of bacterial cells to a G-FET by electrical fiel

45 e of Apurinic/apyrimidinic (AP) site damage, binding of BER proteins, and G4 structures revealed that

46 the agonist, ATR, as well as the noncovalent binding of beta-ionone, an antagonist for G protein acti

47 nd-activated transcription factor that, upon binding of bile acids, regulates the expression of genes

48 role in the endothelial homeostasis and the binding of BMP-9 to the receptor activin-like kinase 1 (

49 itation experiments demonstrate preferential binding of both gephyrin and collybistin to WT and an S3

50 nt cells, however, can demonstrate increased binding of both MDM2 and MDM4 to p53 but in absence of c

51 show that PBRM1/Pbrm1 deficiency reduces the binding of brahma-related gene 1 (BRG1) to the IFNgamma

52 Binding of Ca(2+) at the LBD subunit interface was assoc

53 Taken together, these results show that the binding of calcium-calmodulin to the C-terminus has long

54 During small molecule screens, we observed binding of carbamazepine to the cysteine-rich domain (CR

55 We show that NVS-CECR2-1 inhibits chromatin binding of CECR2 BRD and displaces CECR2 from chromatin

56 and TOP1 interacts with cGAS to enhance the binding of cGAS to DNA.

57 conformational changes to GAFab induced upon binding of cGMP and the PDE6 inhibitory gamma-subunit (P

58 e Sec14-fold as scaffold for translating the binding of chemically distinct ligands to the control of

59 rial flagellar motility is controlled by the binding of CheY proteins to the cytoplasmic switch compl

60 Enantioselective binding of chiral guests, with energetic differences Del

61 Direct binding of CHL1-Fc to the first extracellular loop of DR

62 gth of the reactant and product states: weak binding of CO is desirable from a selectivity perspectiv

63 ble from a selectivity perspective, but weak binding of CO(2) leads to low activity.

64 E did not alter C1q interaction but affected binding of complement inhibitors factor H and C4b-bindin

65 Apparently, the binding of content and context features is not erased bu

66 via increased transcription, but instead via binding of CPEB4 to cytoplasmic polyadenylation elements

67 We have analyzed the interdependence of binding of CTCF and cohesin and demonstrate that while C

68 In conclusion, our results demonstrate the binding of CTRP6 to a variety of microbial and endogenou

69 ing of Cu(I) binding by SRFA and concomitant binding of Cu(I) by Cl(-) stabilizes Cu(I).

70 CNG channels open upon direct binding of cyclic nucleotides (cAMP and/or cGMP), but th

71 Finally, a Trp quenching study revealed binding of cyclic-di-GMP with FlrC(C) Excess cyclic-di-G

72 out-coupled angle resulting from successful binding of d-biotin to streptavidin immobilized on funct

73 Binding of DDX3 and PAF1 to the Nanog promoter, and the

74 W mutation formed alternative holoenzymes by binding of different PP2A regulatory subunits compared w

75 pocket considered critical for back-to-back binding of dimers.

76 ave been developed in recent years, but even binding of dinitrogen to an f-block metal cation is extr

77 nformational dynamics of protein folding and binding of disordered proteins.

78 Human research suggests that the binding of diverse stimuli into one attended percept req

79 ctivity in nuclear extracts and enhance TDP2 binding of DNA-protein crosslinks in vitro.

80 Binding of DSS1 to RAD52 changes the RAD52 oligomeric co

81 The binding of E. coli to the M13 phage on the cytosensor su

82 ain in CBP/p300 does not completely abrogate binding of E2A and E2A-PBX1.

83 don loop (nucleotides 32 and 38) to tune the binding of each tRNA to the decoding center in the ribos

84 ctivation promotes nuclear translocation and binding of Egr2 to SOCS1 promoter for its early inductio

85 efield-based refinement, we characterize the binding of eight analogues to the bacterial ribosome at

86 (2)) species, and Ni-Sc showed no detectable binding of either substrate.

87 ct" in barium block experiments, whereby the binding of external K(+) impedes the forward translocati

88 Intriguingly, initial binding of FAK to the membrane causes steric clashes tha

89 Binding of FH increases meningococcal resistance to comp

90 at PF-PC synapses, and demonstrates that the binding of filamentous actin to CaMKII can enable the be

91 imulations reveal that the limiting step for binding of flexible molecules to ice is not the alignmen

92 We capture real-time binding of fluorophore-labeled biomolecules, utilizing t

93 The binding of Fpr to various DNA motifs are mediated by its

94 We determined genome-wide binding of FXR isoforms in mouse liver organoids that ex

95 ere performed to shed light on the selective binding of G(i) to mu-OR.

96 ligands can contribute significantly to the binding of GBPs with multiple binding sites through a pr

97 Specifically, binding of gD to one of its receptors induces a conforma

98 We describe parameters known to control the binding of generic or gene-specific cofactors that regul

99 Binding of GIV's TILL motif to TIR modules inhibits proi

100 ted STAT3 or GLI1 knockdown reduced promoter binding of GLI1 and STAT3, respectively.

101 Binding of GPIHBP1 to LPL alone or to 5D2-bound LPL coun

102 The binding of GTP or GDP constitutes a selective switch for

103 catalytic activity. We further show that the binding of GTP to the NADH-bound GDH activates a triangu

104 aromatic residues at the tip of the LBL for binding of HC/DC to lipid membranes.

105 Herein, we investigate the binding of heteromultivalent DNA-nanoparticle conjugates

106 ome buried at the complex interface, disrupt binding of hIL-23p19 to hIL-23R.

107 ommodation surfaces may assist high-affinity binding of HIV-1 MPER epitope at membrane interfaces.

108 murine ISG15 of 2 aa recently implicated in binding of human ISG15 to LFA-1 in vitro were required f

109 Interestingly, our results suggest that binding of HVEM to gD may contribute to efficient upregu

110 virus (IAV) entry process, including initial binding of IAV to sialylated glycans, fusion between the

111 i-IFN-gamma-induced increase in the specific binding of IFN-gamma to its receptor in U937 cells, enha

112 II reduces bacterial clearance by decreasing binding of IgA to commensal and pathogenic bacteria.

113 In the immunoblot assay, binding of IgE antibody was observed with CC38K (the mai

114 Simultaneous binding of IgE to FcepsilonRI and CD23 is blocked by rec

115 or (Gal4-VP16) greatly stimulated reversible binding of individual RNApII molecules to template DNA.

116 e this repression is released indicates that binding of inhibited Rubisco to the C-terminal CbbO VWA

117 hat similar levels of Ca(2+) instead promote binding of inosine without cleavage and thus enable high

118 High-affinity binding of InsP(8) to the XPR1 N-terminus (K (d) = 180 n

119 duction reaction (CO(2)RR), control over the binding of intermediates is key for tuning product selec

120 Binding of inverse agonists suppresses this population.

121 igomerization of mutant CSPalpha via ectopic binding of iron-sulfur (Fe-S) clusters.

122 o results in monomerization of the receptor, binding of IT1t to this variant promotes receptor dimeri

123 by its intrinsically disordered regions and binding of its bromodomains to DNA and acetylated chroma

124 e the ncAA serves as an anchor to direct the binding of its peptides to the target's active site.

125 The reversible binding of JMS-053 to serum albumin may serve to increas

126 ystallographic observation of stereospecific bindings of l- and d-lysine (Lys) in achiral MFI zeolite

127 Reducing actin binding of L253P is thus a potential therapeutic approac

128 oters and found that while sequence-specific binding of late gene promoters requires ORF24, it additi

129 We show that binding of Latrophilins to Teneurins and FLRTs directs t

130 erial infections are frequently based on the binding of lectin-like adhesins to specific glycan deter

131 r membrane protein complexes and noncovalent binding of ligands and lipids to membrane proteins.

132 Binding of ligands is often crucial for function yet the

133 ium-activated calcium channel engaged in the binding of ligands.

134 rmodynamics of protein functions such as the binding of ligands.

135 Binding of ligelizumab to IgE in a 2:1 stoichiometry ind

136 TA transferases provide new insight into the binding of lipid-linked WTA and enable assignment of the

137 exes are yielding valuable insights into the binding of lipids and their structural and functional ro

138 The binding of lipoprotein lipase (LPL) to GPIHBP1 focuses t

139 Enhanced RIC exploits the stronger binding of locked nucleic acid (LNA)-containing oligo(dT

140 Virion stabilization required binding of long GlcNAc polymers of greater than 20 units

141 Our results revealed that the binding of m102.4 is mediated predominantly by two resid

142 ction may occur on endothelial cells because binding of MBL to beta2-GPI was detected on the surface

143 he ORC5-depleted cells show normal chromatin binding of MCM2-7 and initiate replication from a simila

144 robustly detected DNA methylation-dependent binding of MeCP2 to mCG and mCAC, neither showed evidenc

145 o the main factors driving collaborative DNA binding of MEF2A and into its role in B cell-specific ge

146 This modification blocked the binding of members of the E26 transcription factor famil

147 downregulation of FERMT2 expression through binding of miR-4504 among others.

148 ivalent binding of TNRC6 enables cooperative binding of miRNA-AGO complexes to target RNAs, thereby e

149 radigm for a lipid storage response in which binding of MLX transcription factors to LD surfaces adju

150 SA (g-iELISA) is based on the principle that binding of monoclonal antibodies to specific epitopes of

151 Specifically, the binding of morphine, methadone, and cocaine to antimorph

152 amics simulations also suggest that membrane binding of MreB double protofilaments induces a stable m

153 w these mitoribosomal proteins assist in the binding of mt-mRNA and to what extent they are involved

154 This process was likely accomplished by the binding of Mt2 ectodomain to Hjv and Hfe.

155 However, how the binding of multiple factors at any given locus is coordi

156 439, was critical for both transport and the binding of multiple substrates and inhibitors.

157 singly charged metals differ profoundly from binding of multiply charged ions, often leading to overa

158 ived from functional studies to describe the binding of muscimol to the receptor.

159 Binding of N(2) by nitrogenase requires a reductive acti

160 This binding of NAD(+) to the ARM domain facilitated the inhi

161 tified, and the key residues involved in the binding of NADP(+) and L-AHG and the catalysis are revea

162 res show that either flavin reduction or the binding of NADP(H) is sufficient to drive the FAD to the

163 phB2-ephrinB1 boundary formation, as well as binding of Nck, RasGAP, and the chimaerins, respectively

164 ChIP assays showed enhanced binding of NF-[Formula: see text] to the Mef2c promoter.

165 tomic difference was not correlated with DNA binding of NF-Y but with splicing of NF-YA.

166 high importance of the P2/P3 pockets for the binding of nonpeptide ligands.

167 We find that binding of NSD2 and NSD3 to mononucleosomes causes DNA n

168 Binding of NucC trimers to a cyclic tri-adenylate second

169 We show that the rate of binding of O(2) is faster than that of NO and also leads

170 ations involving the strong and/or selective binding of O(2).

171 hat oxidized base-derived AP site damage and binding of OGG1 and APE1 are predominant in G4 sequences

172 ion, while the other only requires substrate binding of OGG1--both resulting in conformational adjust

173 of in vitro selection, revealed that strong binding of OLE RNA by OapB requires a stem containing a

174 horetic mobility shift assays to examine the binding of OLE RNA fragments by OapB and found that OapB

175 These data show that binding of one agonist leads to conformational flexibili

176 NMR experiments revealed that binding of one divalent metal ion per C2 domain results

177 imetric studies (ITC) show that the stronger binding of one enantiomer is accompanied by an increased

178 ric activation of protein function, in which binding of one ligand thermodynamically activates the bi

179 ace of the phagophore serve as scaffolds for binding of other core autophagy proteins and various eff

180 lagen molecules has been shown to affect the binding of other ECM components to collagen.

181 tein [RBP] yeast) two-hybrid assay to assess binding of our CEH mutant RNAs to TERT, we find that the

182 erization, thus enhancing insulin-stimulated binding of p110-p85alpha heterodimers to IRS1 and activa

183 Binding of p27 to LAMTOR1 prevents Ragulator assembly an

184 Importantly, DFO induced binding of p53 as well as HIF-1alpha to Zp in chromatin

185 t reaction selectivity arises from preferred binding of pairs through intermolecular interactions of

186 adaptive immune response triggered upon the binding of pathogenic superantigens to T cell receptors

187 currently available tools for predicting the binding of peptides to a selection of HLA-I allomorphs.

188 Furthermore, binding of PFN2 to NAA80 via the proline-rich loop promo

189 F8 is phosphorylated by CK2, which regulates binding of PHF8 to TopBP1.

190 Finally, SOB3 reduces binding of PIF4 to shared target loci.

191 iochemical, and biologic work has shown that binding of PIP(3) to the pleckstrin homology (PH) domain

192 tor gamma (ESRRG), which results in stronger binding of pituitary-specific positive transcription fac

193 Binding of platelet alpha(IIb)beta(3) to SLC44A2 on neut

194 n sharp contrast, kinetic studies showed the binding of POT1 to an initially folded 24 nt G-quadruple

195 Binding of PP2A-B56 to ADAM17 protease decreases growth

196 uch allosteric coupling leads to cooperative binding of proteasomal ATPases to 20S and promotes forma

197 ke only protein sequence as input to predict binding of protein to DNA, RNA, and other proteins.

198 article characterization can directly detect binding of proteins to functionalized colloidal probe pa

199 ally acquired antibodies highly blocking the binding of PvDBP to the Duffy receptor.

200 r, we generated a knock-in mouse model where binding of Pygo2 to H3K4me(2/3) was rendered ineffective

201 ivating protein (GAP) activity, and effector binding of RAC2(E62K) Our findings indicate the E62K mut

202 To detect any NR2B-specific binding of radioligand in brain, various preblocking or

203 chains that are critical for the inhibitory binding of RD3 to RetGC.

204 Another early mechanism enhances the binding of Rec114 and Mer2 specifically on the shortest

205 The relative levels of membrane-binding of recombinant alphaA(N101D)- and WTalphaA prote

206 over, depletion of ATG7 markedly reduced the binding of RelA/p65 to DNA in the nucleus.

207 Binding of RePRP reduces the abundance of actin filament

208 Furthermore, our results showed increased binding of RNA-binding protein CUGBP1 with occludin and

209 Meiotic recombination proceeds via binding of RPA, RAD51, and DMC1 to single-stranded DNA (

210 resistance, probably owing to high-affinity binding of SAP2 to pyrethroid insecticides.

211 This inactive conformation is stabilized by binding of SARM1's own substrate NAD+ in an allosteric l

212 ACE2 enzymatic function was mediated by the binding of SARS-CoV-2 spike RBD domain.

213 Azide also disrupted binding of SecA to membranes.

214 y of the SM22alpha promoter by hindering the binding of serum response factor (SRF) to the proximal C

215 This modification sterically blocks binding of several classes of antibiotics to 23S rRNA, r

216 the terminator to uridines strengthened the binding of several ProQ-specific RNAs to the Hfq protein

217 lementation technology, we characterized the binding of several SHP2 allosteric inhibitors in intact

218 ne is presented, exploiting the preferential binding of silver nanoparticles (AgNPs) with sulfur-cont

219 ly with age and was accompanied by increased binding of SMAD3 to these promoters.

220 cyanine chromophores controlled by selective binding of small-molecule "anchor" groups to a specific

221 vealed that the active-site structure and Cu binding of SOD5 strongly deviate from those of Cu/Zn-SOD

222 Methods based on detecting direct binding of soluble recombinant receptor ectodomains have

223 ntifies the ability of plasma to inhibit the binding of spike protein to angiotensin-converting enzym

224 pre-mRNA splicing by sterically blocking the binding of splicing factors to the pre-mRNA, are a promi

225 cooperation of heteroduplex pairing with the binding of ssDNA to the secondary site, to extend dsDNA

226 a fluorescence-quenching assay to study the binding of ssrA-tagged substrates to ClpXP.

227 These results correlated with decreased binding of strain T3SA(+), which is capable of engaging

228 ich were previously shown to be critical for binding of Stx2A1 to the ribosome.

229 osteric systems is defined as a ratio of the binding of substrate in the absence of effector to the b

230 y competing with active phosphatases for the binding of substrates.

231 Arg/Lys residues play critical roles in the binding of suramin to the "AT-hook" DNA-binding motifs.

232 bacteriophages, and provide a substrate for binding of surface proteins such as InlB.

233 Ca(2+) induces tight binding of synaptotagmin-1 to PIP(2)-containing nanodisc

234 n of either gene did not alter the low-level binding of T3SA(-), which does not engage sialic acid.

235 t transactivation in microglia by disrupting binding of Tat to CDK9, a process key to HIV transcripti

236 it in a range of assays that measured direct binding of Tau to glycosaminoglycans and inhibition of T

237 immunoprecipitation assays confirmed direct binding of TCF/LEF factors to the promoter and putative

238 n of the WNT pathway, through preventing the binding of TCF4 to chromatin.

239 Activating beta-catenin signaling increased binding of Tcf4/beta-catenin complex and upregulated its

240 tion of the T cell receptor (TCR) results in binding of the adapter protein Nck (noncatalytic region

241 iosensors can be used to monitor equilibrium binding of the agonist, ATR, as well as the noncovalent

242 llular region allosterically elicited by the binding of the agonist.

243 ll contact, ExsA is inhibited through direct binding of the anti-activator protein ExsD.

244 tions account for the specific high-affinity binding of the c-di-AMP ligand.

245 The binding of the C2 domains to phospholipid (PSF) has been

246 Weak binding of the catalytic Mg(2+) contributes to fidelity

247 We used subtomogram averaging to image binding of the CheY family protein CleD to the cytoplasm

248 ctures in complex with HIV-1 RT/dsDNA showed binding of the conjugates at the polymerase active site,

249 th a model in which eS25 facilitates initial binding of the CrPV IGR IRES to the 40S while ensuring t

250 tion of the DH/PH-DEP1 fragment, it inhibits binding of the DEP1 domain to liposomes containing phosp

251 faces due to the difficulties with selective binding of the developing agents to the fingermark ridge

252 ation regulated EZH2 expression by enhancing binding of the E2F1 transcriptional activator to the EZH

253 Mutants engineered to disrupt binding of the embedded lipid display reduced transport

254 We found that activation was initiated by binding of the gamma9delta2TCR to BTN2A1 through the reg

255 be found within LADs, demonstrating a linear binding of the genome along the nuclear envelope.

256 protein targets of herbicides, affecting the binding of the herbicide either at or near catalytic dom

257 low cytometry analysis demonstrated specific binding of the IgG1 format to cells expressing membrane-

258 RK5 transcriptional activity requires direct binding of the inhibitor to the kinase domain.

259 Binding of the inhibitor to this pocket collapsed the MK

260 ignment in the active site for high-affinity binding of the initiating nucleotides.

261 However, binding of the l- and d-enantiomers induced different co

262 MMTV share common features such as membrane binding of the MA via hydrophobic interactions and exhib

263 network of flexible interactions, including binding of the N domain of betaarr1 to phosphorylated re

264 a ligand-gated ion channel that converts the binding of the neurotransmitter serotonin (5-HT) into a

265 Additionally, binding of the PA28 regulators to the 20S proteasomes mo

266 Structural studies demonstrate specific binding of the peptide to the pore of pentameric VP1.

267 olecule of protein is extremely slow and the binding of the primary substrate, CO(2), is competitivel

268 ted in capsule alterations that affected the binding of the probe, as reducing ends were exposed and

269 Upon binding of the RNA, NMR chemical shift deviations are ob

270 by their typically low affinity and variable binding of the SIMs in parallel and antiparallel orienta

271 s in solution, it also demonstrates that the binding of the std20S or i20S subtype to any of its PA28

272 substrate in the absence of effector to the binding of the substrate in the presence of a saturating

273 e cyclic compound within this series blocked binding of the Tat-ARM peptide to TAR in solution assays

274 In particular, we found that the co-binding of the tumor suppressor BRCA1 and RNA polymerase

275 system of cell entry, which is triggered by binding of the viral spike protein to angiotensin-conver

276 The first step in SARS-CoV-2 infection is binding of the virus to ACE2 (angiotensin-converting enz

277 During HIV-1 entry into target cells, binding of the virus to host receptors, CD4 and CCR5/CXC

278 We confirm direct TPR-binding of these ligands by mapping (1)H-(15)N HSQC chem

279 Our investigation uncovered differential binding of these NPC subunits, where Nup107 preferential

280 e is still debate over what triggers the (un)binding of this transient third ion during catalysis and

281 Thus, the multivalent binding of TNRC6 enables cooperative binding of miRNA-AG

282 icult to reconcile with the high, 20 nM K(d) binding of TnT onto tropomyosin.

283 e TraJ-TraB complex formation and stimulates binding of TraI with TraB.

284 l calculations were consistent with a strong binding of trans-resveratrol to the CpLIP2 catalytic sit

285 tures of active enhancers that accompany the binding of transcription factors and local opening of ch

286 Specifically, we observed enriched binding of transcription factors associated with chromat

287 Several models of how combinatorial binding of transcription factors, i.e. the regulatory gr

288 truncated Drosophila TnT (TpnT-CD70) retains binding of tropomyosin, troponin I, and troponin C, indi

289 s that have been discussed as central to the binding of trypsin and BPTI and protein complex formatio

290 ssembled retromer coats through simultaneous binding of two VPS29s.

291 Binding of Ubiquitin to the H(abc) domain may regulate t

292 domain are responsible for the preferential binding of UDP-GlcUA.

293 We hypothesize that during nuclear budding, binding of UL25 situated at the pentagonal capsid vertic

294 measured in patient sera to characterize the binding of unconjugated bilirubin (B(T) ) to albumin (A)

295 mposition and miscibility, while competitive binding of unconnected proteins disengages networks and

296 Here we show that binding of uPA to uPAR induces not only the mobilization

297 igh affinity of the EhActn2 CaMD for Ca(2+), binding of which can only be regulated in the presence o

298 ERV into an A-repeat deficient Xist rescues binding of Xist RNA to Spen and results in strictly loca

299 Surprisingly, the binding of XPO5 to pri-miRNAs such as mir-17~92 and mir-

300 scanning fluorimetry analyses confirmed the binding of YjhC to the substrates 2,7-anhydro-Neu5Ac and