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 The structure reveals a ligand-binding site for 24(S),25-epoxycholesterol in the 7-tran

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

5 Here, we predict gain or loss of binding sites for 741 transcription factors (TFs) across

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

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

8 st that this may represent an as-yet-unknown binding site for a partner protein required for tumorige

9 as it took 10-20 s on average to predict the binding site for a protein complex whereas the state-of-

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

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 reds of thousands of energetically favorable binding sites for a target ligand.

15 recipitation-tiling array experiments to map binding sites for ABI3 globally.

16 scan" approach, we show that the orthosteric binding sites for acetylcholine and nicotine in the two

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

18 Modeling studies unveil the specific binding sites for acetylene capture as well as the inter

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

20 0-bp region in the moricin promoter contains binding sites for additional transcription factors.

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

22 pha6 loop might block access to the proposed binding site for alpha2-3-sialyllactose.

23 However, whether RGD is the sole binding site for alphav-class integrins is unclear.

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

25 The binding site for amlodipine and other dihydropyridines i

26 loss of hyaluronan, which harbors a specific binding site for angiopoietin and a key regulator of end

27 during infection without the need to evolve binding sites for antisilencing proteins at each foreign

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

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

30 These include binding sites for architectural proteins, such as CTCF,

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

32 A single class of binding sites for beta-C on whey fractions was recognize

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

34 es ASIC1a, identify the acidic pocket as the binding site for BigDyn, and thus highlight this cavity

35 his assay allows distinction of two separate binding sites for BODIPY-cyclopamine on the SMO transmem

36 AZ resistant isolates involved AmpC, a known binding site for both ceftolozane and ceftazidime, and D

37 ecause DapF (Ct) utilizes a shared substrate-binding site for both racemase and epimerase activities,

38 5-bp consensus sequence GGC(GC)|(CG) as the binding site for both TGF-beta and BMP-activated Smads a

39 d TRPM8 structures have uncovered unforeseen binding sites for both cooling agonists and membrane lip

40 Relevant to this, binding sites for both HIF-1alpha and ERalpha overlap in

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

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

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

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

45 5 can form oligomers that possess additional binding sites for C3b in FHR5.

46 The binding sites for Ca(2+)-free and Ca(2+)-occupied CaM co

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

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

49 harboring a weak SigA-dependent promoter and binding sites for cap repressors such as SaeR, CodY and

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

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

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

53 on strategy, we determined the preferred DNA-binding site for CDA-KLF1.

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

55 tor (GPCR) to be swept rapidly for potential binding sites for cholesterol at the bilayer interfaces

56 g WS-12 and PIP(2) Our structures reveal the binding sites for cooling agonists and PIP(2) in TRPM8.

57 dentified putative transcription factor (TF)-binding sites for cortical hem-patterning TFs.

58 TNFAIP1, and affect the transcription factor binding sites for CTCF, NFATc1 and NR3C1.

59 Furthermore, Sec63 optimally positions binding sites for cytosolic and luminal chaperones in th

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

61 site ligands identify an additional membrane binding site for diazepam and suggest an allosteric mech

62 rials with sensitive nanospace and selective binding sites for discriminating the subtle structural d

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

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

65 ibodies neutralize P. vivax by targeting the binding site for Duffy antigen receptor for chemokines (

66 ly by populating microtubules with defective binding sites for dynein.

67 However, while individual ribosomal binding sites for each functional half of everninomicin

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

69 on, and the regions that close contain known binding sites for effectors of mitogenic signaling pathw

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

71 D'D3 forms the binding site for factor VIII.

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

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

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

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

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

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

78 response and implying that the SSD is not a binding site for GGPP.

79 ke SS4, SS5 has a conserved putative surface binding site for glucans and also interacts with MYOSIN-

80 omplexes and a competitive loss of available binding sites for glyphosate-functionalized poly(ethylen

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

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

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

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

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

86 as simultaneously, suggesting two different binding sites for H2A/H2B and H3/H4.

87 as performed on NKAP to identify the minimal binding site for HDAC3.

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

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

90 lutionary paths to (i) optimize their glycan binding site for higher glycan binding function and (ii)

91 401W, places a bulky tryptophan opposite the binding site for HMG Box A at both 12- and 23-spacer rec

92 tes HSR, and heat shock elements (HSEs), the binding sites for HSF1 - between Antarctic fishes and th

93 ng of the types of glycans that may serve as binding sites for human lung pathogens.

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

95 and mutagenesis analysis identified specific binding sites for hypoxia-inducible factors (HIF) and TG

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

97 heterodimer (IL-2Rbetagamma(c)) but have no binding site for IL-2Ralpha (also called CD25) or IL-15R

98 eostat positions located near the allosteric binding sites for inhibitor alanine (Ala) and activator

99 We assess common and distinct binding sites for Insv and ELBA and their genetic interd

100 rates how mRNA junctions can create specific binding sites for interacting RNAs of prescribed sequenc

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

102 hromatin accessibility at PPARgamma and EBF2 binding sites for key thermogenic genes.

103 The major groove of this helix provides the binding site for L-glutamine, which is extensively hydro

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

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

106 entification and characterization of protein-binding sites for ligands are crucial for the understand

107 inus of the peptide chain, distinct from the binding site for Lipid II.

108 cost and demonstrated to possess sufficient binding sites for LPS adsorption and removal with ~100%

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

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

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

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

113 factor 1 (MACF1), a scaffolding protein with binding sites for microtubules (MT) and actin, is concen

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

115 ever, only one, possessing multiple putative binding sites for miR-145, was highly conserved between

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

117 s of CYCLIN D1 and c-MYC mRNAs revealed that binding sites for miR33b, miR96, and miR503 are critical

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

119 rtate substrate-binding domains at the known binding site for MK2.

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

121 mers, study of flexibility of side chains in binding site for molecular docking preparations, use of

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

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

124 ined the roles of RNA elements identified as binding sites for NC, a Gag-derived RNA-binding protein.

125 ion and (ii) acquire a completely new glycan binding site for new ligands.

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

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

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

129 Lack of a binding site for one of three betaI domain divalent cati

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

131 To date, a binding site for P on L had not been described.

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

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

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

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

136 o an open major groove with enough potential binding sites for peptide recognition.

137 ction of channels presenting a high-affinity binding site for PF-05089771 and suggesting that combina

138 roscopy (cryo-EM) structures reveal that the binding sites for PF 06882961 and GLP-1 substantially ov

139 iching specific lipids and forming essential binding sites for phosphoinositides and cholesterol that

140 n autoantibodies endowed with stereospecific binding sites for phospholipids.

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

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

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

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

145 tified using the polyclonal antisera overlap binding sites for previously reported monoclonal antibod

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

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

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

149 attachment of biomolecules or as reversible binding sites for proteins on cell surfaces.

150 ional analysis and molecular modeling of the binding site for prototypical NAMs to provide new molecu

151 tin activates Sirt6 via the isoform-specific binding site for pyrrolo[1,2-a]quinoxalines.

152 ysis of both RBDs suggests that the receptor-binding site for QX is located at a different location o

153 ational change of the ELMO1 subunit, exposes binding sites for RAC1 on DOCK2(DHR2), and RHOG and BAI

154 in of PLCepsilon was proposed to the primary binding site for Rap1A, we first confirmed using purifie

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

156 n transcribed into RNA, as they serve as the binding sites for RBPs that control post-transcriptional

157 omain (Delta1-147), suggesting an allosteric binding site for recifin A on the regulatory domain of T

158 mes and shape genome regulation by harboring binding sites for regulatory factors.

159 s may result in presence or absence of miRNA binding sites for regulatory miRNAs with consequences on

160 also shown to be dependent on its calmodulin-binding site for retention in the cytosol.

161 ciating domain (TAD), rich in enhancers with binding sites for retinal transcription factors.

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

163 hare common sequence motifs and overlap with binding sites for RNA-binding proteins crucial for neuro

164 nic frameworks allows design of well-defined binding sites for selective molecular adsorption, which

165 ieval method, here we comprehensively define binding sites for Semliki Forest virus (SFV) Cp on the g

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

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

168 12-amino-acid region of VP1 that is also the binding site for several previously identified monoclona

169 ition model was used to determine overlap of binding sites for several inhibitory and potentiating st

170 with the established views of the overlap of binding sites for several pairs of orthosteric (GABA, be

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

172 dered non-druggable because they do not have binding sites for small drug-like ligands.

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

174 Although binding sites for some activators have been identified,

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

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

177 reporter assay (MPRA) libraries composed of binding sites for SOX2, POU5F1 (OCT4), KLF4, and ESRRB.

178 nsupervised method that accurately annotates binding sites for specific TFs automatically with no req

179 RK channels indicates a structurally altered binding site for spermine.

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

181 wed that lincRNA exons contain less putative binding sites for SR proteins.

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

183 The AMH promoter contains two binding sites for steroidogenic factor 1 (SF1), one at -

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

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

186 We identify binding sites for substrate K(+) and Cl(-) ions, demonst

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

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

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

190 ment of single nucleotide variants in active binding sites for TEAD4 (P = 6 x 10-11) and its binding

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

192 signature encompasses and better defines the binding site for TFIID and is surprisingly invariant ove

193 uPol(A) bound to the cRNA template reveals a binding site for the 3' cRNA at the dimer interface.

194 ctural studies have identified a new surface binding site for the 3' vRNA and cRNA promoters on FluPo

195 Here, we functionally characterize a binding site for the 3' vRNA and cRNA promoters.

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

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

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

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

200 nformational changes that create a potential binding site for the CaM binding domain of a target prot

201 l from the enzyme active site, namely at the binding site for the cellular cofactor lens epithelium-d

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

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

204 ubunit of AP-2 to a beta hairpin, creating a binding site for the DIWK sequence.

205 In contrast, resistance mutations in the HR1-binding site for the fusion inhibitors did not cause cro

206 fic modulators acting via the C1 domain, the binding site for the lipid second messenger diacylglycer

207 that the class M epitope overlapped with the binding site for the major histocompatibility complex.

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

209 rminal uncharacterized domain that harbors a binding site for the N protein.

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

211 dure in which DNA containing one copy of the binding site for the neural-inducing factor Ascl1 is inj

212 a representative ligand of the high-affinity binding site for the neuroactive substance gamma-hydroxy

213 omes, removing the glycan cap and exposing a binding site for the Niemann-Pick C1 (NPC1) receptor.

214 Together, our data identify a likely binding site for the NMDAR-positive allosteric modulator

215 PB assembly, consistent with it harboring a binding site for the PB assembly protein Edc3.

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

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

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

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

220 tion between slower dynamics of water at the binding site for the protein in solution and stronger fr

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

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

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

224 er side of the active site pocket suggests a binding site for the single-strand DNA substrate.

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

226 Notably, SNP rs17651213 created a putative binding site for the splicing factor RBFOX2 and was asso

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

228 chemical experiments have indicated that the binding site for the substrate eEF-2 is located in the C

229 nstead, these promoters are enriched for the binding site for the TALE-class homeodomain transcriptio

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

231 2149092 was predicted to disrupt a consensus binding site for the transcription factor ETS within an

232 ion in the BALB promoter creates a consensus binding site for the transcription factor MZF1 (myeloid

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

234 the ribosomal protein uL23 form a composite binding site for the transmembrane domain (TMD) on the n

235 change in the mutant exocyst that exposes a binding site for the v-SNARE.

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

237 poptotic proteins, Bim contains two distinct binding sites for the anti-apoptotic proteins Bcl-XL and

238 acement strategy, we found that multimerized binding sites for the architectural proteins Pita, Su(Hw

239 mputational analysis of single-cell data and binding sites for the CD4(+)-lineage transcription facto

240 s and identify accurate transcription factor binding sites for the core regulatory complexes in the t

241 the docking factors that specify the unique binding sites for the different dynein isoforms on the s

242 entromeric alpha-satellite repeats harboring binding sites for the DNA sequence-specific binding prot

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

244 oved from a specific tissue and the numerous binding sites for the factor in the genome.

245 The human ANO1 promoter contains binding sites for the glioma-associated oncogene (Gli) p

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

247 boxyl dopants of graphene were the efficient binding sites for the immobilization of NapCo through ax

248 ty in the particles and a total of 13 unique binding sites for the LHCIs around the PSI core.

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

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

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

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

253 led to the acquisition of hundreds of novel binding sites for the MSL complex in different species.

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

255 and de-methylesterified pectin presents more binding sites for the protein-pectin interaction than to

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

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

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

259 Binding sites for the transcription factor PITX1 were en

260 DNA binding sites for the transcription factors are closely

261 The enhancer consists of binding sites for the transcription factors jun-B, SMAD3

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

263 or transport and are candidates for possible binding sites for the two H(+) that are exchanged for on

264 molecular docking studies revealed that the binding site for these compounds overlaps with the site

265 We found that the binding site for these enzymes in the 30S subunit direct

266 Crystal structures revealed a common binding site for these monoclonal antibodies (mAbs) on F

267 sed docking simulations identified potential binding sites for these ligands.

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

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

270 al fragment C1 does not contain the reported binding sites for these oligomers.

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

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

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

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

275 bitor and its parent compound revealed novel binding sites for this channel.

276 esidues involved in the formation of the NAM binding site for three prototypical AMPAR NAMs.

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

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

279 ontains several high-affinity non-functional binding sites for transcription factors (TFs) creating a

280 tRNA genes (tDNAs) are binding sites for transcription factors and architectura

281 ls and determine the energetic properties of binding sites for transcription factors and RNA polymera

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

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

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

285 ation, mediated by DNA sequences that harbor binding sites for transcription factors, which can up- o

286 oxidation) and lack methylation at specific binding sites for transcription factors; 83% of samples

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

288 TEs frequently harbor binding sites for transcriptional regulators, thus enabl

289 ude that MHR1/2 acts as a orthostatic ligand-binding site for TRPM2.

290 The other cluster is adjacent to the binding site for two COPII components, SEC31 homolog A C

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

292 ronment-specific eQTLs reveals enrichment of binding sites for two transcription factors.

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

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

295 5, contributes to formation of a bowl-shaped binding site for ubiquitin.

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

297 near the N-terminal Arg and the carbohydrate-binding site, for which the potential function is curren

298 nt-response elements, and we also discovered binding sites for XBP1, a transcription factor of endopl

299 partners, whereas others represent putative binding sites for yet unidentified proteins.

300 Putative binding sites for Zn(++) and Cu(++) were then analyzed i