ライフサイエンスコーパス: binding site for

1 ant levels of recently proposed 'off target' binding sites for [(18)F]AV-1451, such as neuronal monoa

2 To date, a receptor/binding site for 20-HETE has been implicated based on th

3 additional plant families and identified 715 binding sites for 501 genes conserved in dicots, monocot

4 y potential score, for accuracy in detecting binding sites for 75 vertebrate transcription factors.

5 tructures of the RNA molecule and provided a binding site for a biotinylated capture probe.

6 sal that residues in this motif serve as the binding site for a divalent transition metal cofactor [e

7 ted markers, rs11855145, directly alters the binding site for a nuclear factor.

8 c cleft between the domains might serve as a binding site for a potential host cell interaction partn

9 nding pocket in BGT1, which accommodates the binding site for a series of novel noncompetitive inhibi

10 determines whether it can serve as a robust binding site for a suitably optimized ligand.

11 incorporates competition between neighboring binding sites for a local pool of TF molecules explains

12 q analysis was used to determine genome-wide binding sites for a range of different TFs in multiple c

13 metry (MS) can be used to map small-molecule binding sites for a rapidly aggregating protein.

14 Promoters often contain multiple binding sites for a single factor.

15 The specific binding sites for acetylene are validated by modeling an

16 pha4, and alpha6 accessory subunits can form binding sites for ACh and NS9283 at interfaces with alph

17 specific RpL4 extension harbours overlapping binding sites for Acl4 and the nuclear transport factor

18 h is known to be phosphorylated as part of a binding site for activating 14-3-3 protein, but was crit

19 important role of beta-catenin and TCF4/LEF binding-sites for activating (alpha)-promoter, while act

20 cular modelling, we provide evidence for the binding site for adamantane derivatives and their putati

21 0-bp region in the moricin promoter contains binding sites for additional transcription factors.

22 tive site, whereas GtfB provides the primary binding site for adhesin.

23 terminus of Nup214 that acts as a direct NPC binding site for AdV.

24 senchymal stem cell PCMs possess many unused binding sites for aggrecan, showing a 2.5x increase in P

25 g of this role, we have identified chromatin binding sites for AGO2 throughout the 45S region of the

26 on, docking calculations around the observed binding site for all three states of the receptor, inclu

27 the reaction rate and reduced the number of binding sites for allicin, whereas the number of non-cov

28 Although the donor binding site for alpha-maltose 1-phosphate had been prev

29 nit is a multi-segmented nexus with distinct binding sites for Ame1, Nkp1-Nkp2 and Ctf19-Mcm21.

30 These include the three substrate-binding sites for amino acid, ATP and tRNA associated wi

31 The binding site for amlodipine and other dihydropyridines i

32 s may not be rare since such high numbers of binding sites for an anion are also found in analogous t

33 One core element, containing binding sites for AP1 family and the macrophage-specific

34 open sites at active enhancer regions and at binding sites for AP1-complex components, including c-Fo

35 mics enhanced sampling reveal three distinct binding sites for arginine vasopressin (AVP) within its

36 Here, we defined the binding site for Atg30 on the peroxisomal membrane prote

37 boxyl terminus of hClC-Kb is not part of the binding site for barttin, but functionally modifies the

38 The Kindlin-2 binding sites for beta- and gamma-catenin reside within

39 We found that the binding sites for betaEST and dFBr communicate with the

40 thesized that this ACE mutation disrupts the binding site for blood components which may stabilize AC

41 r, but also as high affinity (KD </= 0.8 nM) binding site for both high molecular weight kininogen (H

42 5-bp consensus sequence GGC(GC)|(CG) as the binding site for both TGF-beta and BMP-activated Smads a

43 RGS14 contains distinct binding sites for both active (GTP-bound) and inactive (

44 % of Dux-responsive genes contained ChIP-seq binding sites for both Dux and DUX4, and both proteins h

45 rved scaffold protein TOPBP1(Dpb11) provides binding sites for both pro- and anti-resection factors a

46 Lysine acetylation often creates binding sites for bromodomain-containing 'reader' protei

47 full-length Plasmodium enolase suggested one binding site for BV.

48 Our results demonstrate that the binding site for C1 represents a new pharmacological vul

49 (TnC) as the Ca(2+)-binding moiety, has two binding sites for calcium ions, providing a linear respo

50 that the presence of high-nanomolar affinity binding sites for CaM at its universal gating brake and

51 This analysis identifies a binding site for canonical recycling signals at the inte

52 more, phosphatidylinositol lipids occupy the binding site for capsaicin and other vanilloid ligands,

53 s hypothesized to support negatively charged binding sites for cations.

54 his SNP is on chromosome 8q24, adjacent to a binding site for CCAAT/enhancer-binding protein beta, a

55 The C allele of rs35767 provides a binding site for CCAAT/enhancer-binding-protein delta (C

56 tu neutron powder diffraction studies on the binding sites for CD4 within MFM-132a and MFM-115a revea

57 (E2RE), a region that contains at least two binding sites for cellular factors; one of these sites,

58 ive drug target carrying different potential binding sites for chemical modulators, particularly agon

59 n side chains was hypothesized as a possible binding site for chlorogenic acids in coffee melanoidins

60 l domain of NPC1, which contains the initial binding site for cholesterol.

61 We describe a completely novel allosteric binding site for class B receptors, providing an opportu

62 These results identify a potential binding site for collectrin and other SLC6 ancillary pro

63 No validated microRNA-binding sites for cZNF292 were detected in Argonaute hig

64 R into its monomers, exposing the PP2A/RACK1 binding site for dephosphorylation.

65 s situated at or near the negatively charged binding site for dihydrostreptomycin within the permeati

66 of the genome can be genetically encoded by binding sites for DNA-binding proteins and can also invo

67 Because each receptor has a unique set of binding sites for downstream signaling partners and diff

68 provide a promising alternative to classical binding sites for drug development.

69 now provides a three-dimensional view of the binding sites for drugs acting on sodium and calcium cha

70 binding, and we identified novel and unique binding sites for each protein.

71 In addition, the PGC-1alpha promoter has binding sites for early growth response 3 (Egr3), which

72 ne-arginine (SR)-rich region, which contains binding sites for EB1.

73 ta(1-40) oligomers with multiple independent binding sites for EGCG with a Kd approximately 10-fold l

74 ch coincide with CCCTC-binding factor (Ctcf) binding sites, for example, the clustered protocadherin

75 y little phosphatidylserine (PS) but express binding sites for factor VIII (fVIII), casting doubt on

76 ge-CH2 region, structurally distant from the binding site for FcRn at the CH2-CH3 elbow region.

77 nesis and biochemical studies, revealed dual binding sites for fedratinib.

78 e show that the fourth helix constitutes the binding site for FlhA, a membrane protein at the export

79 By inserting binding sites for fluorescent proteins adjacent to the r

80 tibodies (sABs) against LD2 and LD4 that are binding sites for focal adhesion kinase (FAK) and other

81 thin the previously determined fVa-dependent binding site for fXa (amino acid region 473-487 of FII).

82 Fibrinogen alphaC (233-425) contains a binding site for FXIIIa and three glutamines Q237, Q328,

83 dent way, resulting in the proposal of a new binding site for GAGs.

84 GIRK2-4, and located within their C-terminal binding sites for Gbetagamma proteins that mediate membr

85 kinase homology domain harbored an exclusive binding site for GCAP1 with similar affinities as the fu

86 use models expressing SORLA variants lacking binding sites for GGA or retromer to query this concept

87 lex, which correlated with the two suggested binding sites for GMF.

88 g the CD33 IgV domain, which is the antibody-binding site for GO, as well as diagnostic immunophenoty

89 ied the N-terminal domain of FH as the major binding site for GP patient IgG.

90 ciency (Mac-1(-/-)) or mutation of the Mac-1-binding site for GPIbalpha have delayed thrombosis after

91 ble chromatin regions, as well as sex-biased binding sites for growth hormone-regulated transcription

92 ate anions and phenyl groups create multiple binding sites for guest and/or solvent molecules.

93 functional groups in the pore as the primary binding sites for guest molecules.

94 us HSF sequence-binding elements (HSEs), the binding sites for heat shock factor-1 (HSF-1), located i

95 H3 with an excess positive charge may be the binding site for heparin.

96 rotein footprinting to identify two separate binding sites for heparin interaction with Robo1: one bi

97 We identified a putative binding site for hepatic nuclear factor 4 alpha (HNF4alp

98 ethylation of Lys9 of histone H3 (H3K9me), a binding site for heterochromatin protein 1 (HP1).

99 SOX9 binding peaks precisely overlapped with binding sites for histone-fold NF-Y transcription factor

100 the LARP7 family of proteins and defines the binding site for hLARP7 on the 7SK RNA, providing insigh

101 This region of gD contains most of the binding site for HVEM, an HSV receptor important for vir

102 ately apolar pocket representing a potential binding site for hydrophobic ligands.

103 a indicate that polymeric C4BP with multiple binding sites for IAPP neutralizes lytic activity of IAP

104 -terminal UBL1-2 domains and mapped the USP7-binding site for ICP0.

105 ineered high-specificity M6P/IGF2R domain 11 binding site for IGF2 may improve therapeutic targeting

106 eceptor (M6P/IGF2R), domain 11 has evolved a binding site for IGF2 to negatively regulate ligand bioa

107 ompound 6 and cereblon away from the modeled binding site for Ikaros/Aiolos.

108 r length counting and also indicate that the binding site for initiating NTP is located on p58C.

109 an residue, and consequent opening up of the binding site for interaction.

110 eukaryotic inner centromere and provides the binding site for Ipl1/Aurora B.

111 extremely hydrophobic, but in complex I the binding site for its redox-active quinone headgroup is a

112 g PopZ independently of the previously known binding sites for its client proteins.

113 sion of GAB2 but not by GAB2 mutants lacking binding sites for its effectors phosphatidylinositol 3-k

114 domains of plectin and other plakins harbor binding sites for junctional proteins.

115 They find a progressive degeneration of binding sites for key transcription factors, mirroring t

116 s within cCpG-II and tCpG, which contain two binding sites for Kruppel-like transcription factors, in

117 The structure also reveals an exo binding site for L-Trp, located ~42 A from the active si

118 The sigma-holes are binding sites for Lewis bases, and binding energies corr

119 The identification of the binding sites for low affinity molecular encounters is e

120 hat contains the following two high affinity binding sites for LRP1: one is located within domains 1

121 BP-1c promoter in a region that contains two binding sites for LXRalpha and is known to be required f

122 allographic loop contacts, we determined the binding site for magnesium protoporphyrin IX.

123 y against the kinase C-lobe, adjacent to the binding site for Mam1.

124 annose termini, which create potential novel binding sites for mannose-specific lectins.

125 In Drosophila, PREs consist of binding sites for many different DNA-binding proteins, s

126 Causal variants tend to occur near binding sites for master regulators of immune differenti

127 Moreover, the binding site for Mcm10 on MCM includes the Mcm2 and Mcm6

128 view the regulatory roles of the 3'UTRome as binding sites for microRNAs or RNA binding proteins, or

129 renalase 3'-UTR (C/T; rs10749571) creates a binding site for miR-146a; consistently, miR-146a down-r

130 he 3'UTR of Kr-h1 mRNA contains a functional binding site for miR-2 family miRNAs (for miR-2, miR-13a

131 Interestingly, GDF15 mRNA contains a binding site for miR-21.

132 nt at the 3'-UTR of CDKN1A, which contains a binding site for miR-95-3p.

133 CUG-BP1 mRNA were found to contain potential binding sites for miR-214-3p.

134 nce that repression of egl-1 is dependent on binding sites for miR-35 and miR-58 family miRNAs within

135 n InsP3R3 mRNA revealed two highly conserved binding sites for miR-506.

136 KEY MESSAGE: The binding site for miR398 in an isoform of Cu/Zn superoxid

137 The unexpected position of the binding site for MK-0893, which is structurally similar

138 ed a preference in the enzyme's second metal binding site for Mn(II) over Mg(II), suggesting that T7

139 The mutation lies near the binding site for most PCNA-interacting proteins.

140 and CtrA and overlap with nearly all of the binding sites for MucR1, a regulator that controls the e

141 The promoter region contained putative binding sites for multiple transcription factors includi

142 normal pigmentation and identify a critical binding site for Munc13-4 on Rab27a, revealing the molec

143 Doc2B is a cytosolic protein with binding sites for Munc13 and Tctex-1 (dynein light chain

144 he acidic pocket form an allosteric effector binding site for Na(+).

145 The extrinsic arm contains binding sites for NADH, the primary electron acceptor FM

146 KD1 expression is increased and identify the binding sites for NF-kappaB in the PRKD1 promoter.

147 cessible regions were enriched for consensus binding sites for NFAT and Nr4a family members, indicati

148 n B7-H6 that is completely distinct from the binding site for NKp30, such that 17B1.3 does not block

149 Our in silico analysis revealed tandem binding sites for nuclear respiratory factor 2 (NRF-2) o

150 es, which contain phenylalanine-glycine (FG) binding sites for nuclear transport receptors.

151 Those methods, however, do not reveal binding sites for oligonucleotides.

152 w that most Ribi gene promoters also contain binding sites for one or more General Regulatory Factors

153 y a subset of sites; some of these sites are binding sites for other Polycomb repressive complex 1 (P

154 The MBM in MKK3 is distinct from the known binding sites for p38 or upstream kinases.

155 Transcription factor binding sites for p53, MEF2A and E2F1 were significantly

156 -type-specific and are strongly enriched for binding sites for p63, a master epidermal transcription

157 Binding sites for PAI-1 within LRP1 have been localized

158 This C-terminal tail displays the binding site for partner proteins and we report how it m

159 hromatin in hSSCs was strikingly enriched in binding sites for pioneer factors (NFYA/B, DMRT1, and ho

160 rug resistance Regulator (LmrR) as a generic binding site for planar coordination complexes that do n

161 This C terminus contains the binding site for plasmin(ogen), the key component necess

162 blood clots by providing direct and indirect binding sites for plasminogen.

163 Von Willebrand factor (VWF) contains binding sites for platelets and for vascular collagens t

164 revealed that in this setting, intravascular binding sites for platelets were exposed by neutrophils,

165 elements (CREs) comprised of combinations of binding sites for pluripotency TFs and measured their ex

166 rticularly weak splice sites and by upstream binding sites for Polypyrimidine Tract Binding protein (

167 Previous studies have shown that the binding site for potentiating betaEST is in the C-termin

168 sis and electrophysiology, we identified the binding site for potentiating dFBr on the top half of a

169 hed at mouse strain-selective adipose tissue binding sites for PPARgamma, a nuclear receptor for anti

170 with other amino acid residues in the GERAMT-binding site for proper chaperone-dependent regulation o

171 o gain insight into the number of functional binding sites for propofol and the energetic contributio

172 ne or two additional functionally equivalent binding sites for propofol, other than those modified by

173 Optimization of the models' binding sites for protein-ligand complementarity reveals

174 Furthermore, we found independent binding sites for Pto at either end of the N-terminal do

175 t of beta-sheets and loops that serve as the binding site for PU.1, and also show that unlike other I

176 RNA, an extension of MotifMap which predicts binding sites for RBP motifs across human and mouse geno

177 s NMR and calorimetric techniques to map the binding site for Rem2 on human Cavbeta4a and measure its

178 ial membrane-embedded carboxyls, generates a binding site for reserpine.

179 Iterated DNA binding sites for retinoic acid receptor, CREB, and NF-k

180 expression, we identified transcriptome-wide binding sites for RNA polymerase II and the exosome cofa

181 ChIP-Seq quantification of binding sites for RNA polymerase II was combined with RN

182 rotocol, derives a transcriptome wide set of binding sites for RNA-binding proteins.

183 cription factor overlaps with the respective binding site for RNAP.

184 The putative binding site for RPR, previously mapped to a hydrophobic

185 ducing glucans locally that provide enhanced binding sites for S. mutans.

186 epigenetic inheritance of silencing requires binding sites for sequence-dependent activating transcri

187 revealed that the exon 11 sequences contain binding sites for serine/arginine-rich splicing factor 2

188 AngII-induced enhancers/SEs are enriched in binding sites for signal-dependent transcription factors

189 st that the loops and tails may offer unique binding sites for small micropollutants which are overse

190 Although binding sites for some activators have been identified,

191 izing antibodies (bNAbs) but can also expose binding sites for some types of nonneutralizing antibodi

192 tivity and identifies transcriptome-wide RNA binding sites for SONAR-predicted RBPs, revealing unexpe

193 (3) The binding sites for SOX2 and POU5F1 in mouse embryonic ste

194 line resistant mutants suggested a different binding site for SQAs on ATP synthase.

195 ferentially expressed genes have a known DNA binding site for SR1, suggesting that they are likely di

196 The combined data globally identify binding sites for ssDNA during SsoMCM unwinding as well

197 n cyclotron resonance MS, we have probed the binding sites for ssDNA, using multiple substrates targe

198 form of Strep-Tactin that harbours a unique binding site for Strep-tag II and a single cysteine that

199 with succinate and citrate, elucidating the binding sites for substrate and two Na(+) ions.

200 an autoinhibited structure wherein both the binding sites for substrates and FlhA are occluded.

201 alphaCA possesses an additional, alternative binding site for sulfonamides that is not present in HCA

202 p in telomeric repeats, the longest reported binding site for synthetic, non-nucleic-acid-based, sequ

203 Vinculin has binding sites for talin and F-actin, but effective bindi

204 These data reveal a previously unappreciated binding site for targeted inhibition of BAX and suggest

205 s containing replication origins proximal to binding sites for Taz1, a component of the Shelterin tel

206 Remarkably, with only binding sites for telomerase reverse transcriptase (TERT

207 CdSe core and surface Cd adatoms serving as binding sites for terminal S atoms of the thiostannates

208 ructure-based mutational analyses mapped the binding site for the [GS]LFXG[ML]X[LV] motif to a conser

209 CXCR4 C-terminal domain (C-tail) also has a binding site for the actin-binding protein filamin A (FL

210 hic data show that the inhibitors occupy the binding site for the adenine ring of the ATP molecule an

211 SNP rs2227473 is located within a putative binding site for the aryl hydrocarbon receptor, a master

212 gene island and having a predicted promoter binding site for the As(III) oxidation regulator AioR.

213 KNL1 on conserved MELT motifs to generate a binding site for the Bub3-Bub1 complex [4-7].

214 olysin pore for the C4R1 dimer, but only one binding site for the C8R1 dimer.

215 D sequences, which shares homology with the binding site for the cellular NF-kappaB-repressing facto

216 croglobulin domain 4 of C3, which contains a binding site for the complement inhibitor compstatin and

217 hing data revealed the existence of the same binding site for the compounds on the enzyme molecule.

218 CATAC consensus sequence resembles the E-box binding site for the core circadian transcription factor

219 o-acid region of the nucleoporin Nup214 is a binding site for the major AdV capsid protein, hexon, an

220 It affects a binding site for the miR-16 family and miR-103/miR-107 w

221 t site, which was previously identified as a binding site for the NAM/ATAF1/CUC2 78 (NAC78) transcrip

222 the presence of low levels of H3K9me3 at the binding site for the PF3D7_1466400 AP2 transcription fac

223 se they bind to the sAC-specific, allosteric binding site for the physiological activator bicarbonate

224 g to a conformational shift that exposes the binding site for the PKR substrate eIF2alpha.

225 eletion of exon 22, due to the creation of a binding site for the pre-mRNA processing protein hnRNP A

226 model in which the POTRA domains serve as a binding site for the preprotein as it emerges from the T

227 ilar sites that overlap extensively with the binding site for the receptor (CD155).

228 otein by a conserved kinase, DDK, provides a binding site for the Scc2/4 cohesin loading complex, the

229 I and III in two different CaV isoforms as a binding site for the SH3 domains and report a crystal st

230 ssion adjacent to each finger forms a likely binding site for the sialic acid on its receptor.

231 the best-characterized pause sequences is a binding site for the sigma(70) initiation factor that in

232 r function, however, required evolution of a binding site for the spatially restricted potent repress

233 rs1076560(T) disrupted a binding site for the splicing factor ZRANB2, diminished

234 poor inhibitors of the canonical galactoside-binding site for the tested galectins, with IC50 values

235 f the ternary complex reveals a noncanonical binding site for the toxin that adopts a novel conformat

236 23457 located in an evolutionarily conserved binding site for the transcription factor Cartilage pair

237 2149092 was predicted to disrupt a consensus binding site for the transcription factor ETS within an

238 This region of the promoter contained a binding site for the transcription factor hypoxia-induci

239 through rs7278468, which lies in a consensus binding site for the transcription repressor KLF10.

240 Methylation of SAP145 on Arg 508 generates a binding site for the Tudor domain of the Survival of Mot

241 This 'E-dimer-dependent epitope' is also the binding site for the viral glycoprotein prM during virus

242 that these phosphorylations create potential binding sites for the adaptor protein 14-3-3 that links

243 BV genome, overlapping previously identified binding sites for the B cell transcription factor PAX5.

244 Binding sites for the channel activators Ca(2+), ATP, an

245 pecific serine or threonine residues creates binding sites for the COP1 tumor suppressor protein, whi

246 g alpha-satellite DNA repeats, which contain binding sites for the DNA sequence-specific binding prot

247 ement dispersed 77 functional but suboptimal binding sites for the dosage compensation complex to a n

248 A Flower mutant lacking binding sites for the endocytic adaptor AP-2 proteins fa

249 elated with rs73635312[A] occur in conserved binding sites for the GATA3 transcription factor.

250 6me3 levels through changes in the number of binding sites for the histone methyltransferase Set2, th

251 ence motifs enriched in the PREs are cognate binding sites for the identified transcription factors a

252 Although the majority of genomic binding sites for the insulator protein CCCTC-binding fa

253 NA binding by PPR repeats to infer candidate-binding sites for the maize protein PPR103 and its ortho

254 ctra for each isomer, clearly indicating the binding sites for the major conformers in the presence o

255 f microRNA promoters revealed enrichment for binding sites for the MAPK-driven ETS1 transcription fac

256 This CpG-island contains binding sites for the methylation-sensitive transcriptio

257 arrying Clk transgenes with deletions in the binding sites for the miRNA bantam have stochastic numbe

258 ion of the 128 genes was overrepresented for binding sites for the nuclear transcription factor kappa

259 advances to rapidly mutate 10 high-affinity binding sites for the nucleoid occlusion protein SlmA an

260 anding observation of high- and low-affinity binding sites for the prototypic inhibitor rolipram.

261 complex as a tethering complex with just two binding sites for the Rab7-like Ypt7 protein to determin

262 ional repressor compete for occupancy at DNA-binding sites for the regulation of common target genes.

263 al enhancers results mainly from clusters of binding sites for the same transcription factor, and it

264 Enhancers frequently contain multiple binding sites for the same transcription factor.

265 yeast HO gene contains nine highly conserved binding sites for the SCB (Swi4/6-dependent cell cycle b

266 A, adjacent to the guide region, function as binding sites for the snoRNP proteins including the enzy

267 For example, the binding sites for the TFs Put3, Ste12, and Gcn4 are nece

268 -specific enhancers marked by H3K4me1 and at binding sites for the transcription factor p300.

269 GapR target loci are especially enriched in binding sites for the transcription factors GcrA and Ctr

270 We found that robustness is encoded by many binding sites for the transcriptional activator Arrowhea

271 cond plasmid carrying a transgene flanked by binding sites for the transposase, into the cytoplasm of

272 e then conducted a ChIP sequence analysis of binding sites for the vitamin D receptor (VDR) across th

273 ors; in addition, we have mapped the precise binding site for these factors in the BAFF promoter.

274 o regulate PTEN and identify high-confidence binding sites for these miRNAs on the 3' UTR of protein

275 ), we have identified pathways that link the binding sites for these modulators to the Cys loop, a re

276 during active disease, in order to assemble binding sites for these TFs into synthetic promoters, wh

277 Pathway analysis of binding sites for these three microRNAs revealed enrichm

278 h was recently identified as a mitochondrial binding site for thiazolidinediones, including MSDC-0602

279 of use in clinical practice, the prototypic binding site for this class of drugs within pLGICs is ye

280 The binding site for THP provides a framework for understand

281 region of human Timeless harbours a partial binding site for Tipin.

282 , leaving a cavity suggestive of a potential binding site for transcription-promoting small molecules

283 Because of the presence in area IV of binding sites for transcription factors associated with

284 Among them there are multiple binding sites for transcription factors controlling the

285 lacement with a sequence containing putative binding sites for transcription factors in, single-stran

286 red common cis-acting elements may represent binding sites for transcription factors responsible for

287 terminal (AF-1) domain of AR, which contains binding sites for transcription regulators, is not requi

288 of peptides that are long enough to present binding sites for two antibodies.

289 allography lead to the identification of new binding sites for two derivatives and of a new crystal f

290 different timing classes each associate with binding sites for two transcription factors, GAGA-factor

291 to Tx7335 as wild-type, indicating that the binding site for Tx7335 is distinct from that of canonic

292 The data suggest that there is only one binding site for ubiquinol in cyt bo3 and that site corr

293 5, contributes to formation of a bowl-shaped binding site for ubiquitin.

294 essential for NMD and independent of Upf2's binding sites for Upf1 and Upf3.

295 A removal depends on the availability of DNA binding sites for UvrD and/or the accessibility of the R

296 ined with Nanogold labeling reveals that the binding sites for vacuolar SNAREs and the Habc domain ar

297 ineering and traditional mutagenesis defined binding sites for VDR and RUNX2.

298 the nanoparticle surface to provide tailored binding sites for virtually any class of substrate.

299 n box that are transport-defective alter the binding site for vitamin B12 in BtuB.

300 e dopamine transporter carries an endogenous binding site for Zn(2+), but the nature of the Zn(2+)-de