ライフサイエンスコーパス: attachment site

1 in the phage DNA) and attB (the chromosomal attachment site).

2 RNA biogenesis that generates the amino acid attachment site.

3 aquaporin 1 (Aqp1), a water channel, at the attachment site.

4 t that is equivalent to a single microtubule attachment site.

5 stretched entropically depending on the tip attachment site.

6 ated directly above the molecule's substrate attachment site.

7 after precise excision from its tRNA-serine attachment site.

8 osylphosphatidylinositol-dependent cell wall attachment site.

9 SGLT1-dependent glucose uptake occurs at the attachment site.

10 aquaporin 1 (AQP1), a water channel, to the attachment site.

11 but decreases the membrane protrusion at the attachment site.

12 he first sugar residue (GlcNAc) at the N1574 attachment site.

13 ng either the 2' or 3'-hydroxyl group as the attachment site.

14 to induce host cell actin remodeling at the attachment site.

15 ediction of the family of glycoforms at each attachment site.

16 o a single amino acid exchange in the SUMO-1 attachment site.

17 the building of the kinetochore-microtubule attachment site.

18 in, with the C2 domain providing a secondary attachment site.

19 eins that create the kinetochore-microtubule attachment site.

20 in protein-DNA interactions at the viral DNA attachment site.

21 res polymerization of host cell actin at the attachment site.

22 ,4,5)P3 and F-actin response at the particle attachment site.

23 in the protein specifically near the GPtdIns-attachment site.

24 n adverse event was mild itching at the tick attachment site.

25 e number of mannose units on the CBM and the attachment site.

26 number of Ndc80 molecules at the microtubule attachment site.

27 ay explain tandem insertions into the SCCmec attachment site.

28 oil adjacent to the gamma chain carbohydrate attachment site.

29 perties of the protein backbone at the probe attachment site.

30 is located in the neighborhood of the probe attachment site.

31 Lys-122 was identified as the major labeling attachment site.

32 cally vary in terms of linkages, length, and attachment sites.

33 combination does not require homology in the attachment sites.

34 with the cortex may be regulated by cortical-attachment sites.

35 nectin fibril growth at discrete cell-matrix attachment sites.

36 t not IRSp53, was recruited to the bacterial attachment sites.

37 ndroitin sulfate glycosaminoglycans serve as attachment sites.

38 uences on human cells at the recognition and attachment sites.

39 on between bacterial (attB) and phage (attP) attachment sites.

40 mplex are specifically enriched at merotelic attachment sites.

41 lymerization/depolymerization at kinetochore attachment sites.

42 but SUMO can also act by blocking ubiquitin attachment sites.

43 sequences with prokaryotic lipoprotein lipid attachment sites.

44 4), exhibit structural defects of the muscle attachment sites.

45 ted with mutant Sdc1 lacking heparan sulfate attachment sites.

46 r about the overall structure of microtubule-attachment sites.

47 g of an exon encoding several O-linked sugar attachment sites.

48 DNA identity between the bacterial and phage attachment sites.

49 athogen genomes beyond the confines of their attachment sites.

50 recombination at one of five different phage attachment sites.

51 n and for diffusion to discrete cytoskeleton attachment sites.

52 anizing centers that may function as nuclear attachment sites.

53 Robo to extend toward Slit-expressing muscle attachment sites.

54 This complex is flanked by nuclear matrix attachment sites.

55 s thetaiotaomicron (Bt), is resident at EHEC attachment sites.

56 ve along KFs as they approach their cortical attachment sites.

57 ells, with clusters of TG2 seen at bacterial attachment sites.

58 ents, localizes specifically to the muscular attachment sites.

59 ecombination occur between other pairings of attachment sites.

60 ust sister chromatid cohesion at microtubule attachment sites.

61 tions to coordinate dynamics across multiple attachment sites.

62 ion in isolated Int and when Int is bound to attachment sites.

63 Int in solution and when Int is bound to the attachment sites.

64 r results suggest that elimination of glycan attachment sites 3 and 11 enhanced the exposure of conta

65 We successfully introduced a new attachment site 70 kb from the existing attP using this

66 athway to induce actin polymerization at the attachment site, a process associated with microbial sec

67 and DPAB are only loosely connected to basal attachment sites, allowing for two distinct cellular sig

68 iated by pN-level forces applied at integrin attachment sites along both appositional and distal unap

69 here mechanotransduction occurs at substrate attachment sites along the processes at force levels pre

70 he formation and maintenance of PM-sarcomere attachment sites also known as costameres.

71 n of cI and cro homologs but lacks the phage attachment site and integrase necessary to establish lys

72 ther a transmembrane domain nor a GPI-anchor attachment site and must utilize an adaptor molecule to

73 ted integration of plasmids carrying an attB attachment site and the desired mutation.

74 f a molecular linker between the kinetochore attachment site and tubulin subunits within the lattice

75 The covalent flavin attachment site and two residues that bind substrate car

76 Here we identified the polySia attachment sites and demonstrate that NRP2 is recognized

77 the TSP transcript is concentrated at muscle attachment sites and is expressed by a subset of myoblas

78 is of general significance in understanding attachment sites and may explain the diverse pathologic

79 using a dedicated MS method to determine the attachment sites and micro-heterogeneity.

80 vents led to the modulation of potential GAG attachment sites and other ECM-binding motifs.

81 rategy that used insertion of ectopic glycan attachment sites and terminal fusions of green fluoresce

82 e potentially between the cysteine-rich acyl attachment sites and the C-terminal coiled-coil domain.

83 module comprised of an integrase, associated attachment sites and, in some cases, a recombination dir

84 radation of this mutant, implying that other attachment sites and/or proteolytic pathways exist.

85 The cassette contains the device, an attachment site, and a reporter of state.

86 acid substitutions, elimination of N-glycan attachment sites, and a 100-amino-acid deletion spanning

87 f the seven REP13E12 sites present in BCG as attachment sites, and can occupy more than one site simu

88 on of kinetochore microtubules through their attachment sites, and that the polymerization state of t

89 viral constructs revealed that the N-glycan attachment sites are largely dispensable for viral repli

90 n organization revealed that all chondroitin attachment sites are located in unstructured regions.

91 eocyte cell body and processes with no local attachment sites are not.

92 levels of the Egfr ligand Vein at the muscle attachment sites are reduced in PS mutant embryos.

93 Although the muscle-tendon attachment sites are reduced in size, components of the

94 thetic genetic circuits as the attP and attB attachment sites are small (<50 bp), there are no host f

95 r system produces focal strains at localized attachment sites around the osteocyte cell process.

96 letal muscle for the maintenance of integrin attachment sites at MTJs.

97 erpart via competition for glycosaminoglycan attachment sites at the cell surface.

98 on of the kinetochore, distal to microtubule attachment sites at the outer plate.

99 the phage attachment site attP and the host attachment site attB to form the hybrid sites attL and a

100 that in the absence of the primary bacterial attachment site (attB) in trnS-leu2, ICEBs1 integrated i

101 al chromosome at a locus known as the SCCmec attachment site (attB).

102 ng recombination between bacterial and phage attachment sites (attB and attP, respectively).

103 asily adapted to different mycobacteriophage attachment sites (attB) due to its modular design.

104 nce, which presumably contains the bacterial attachment site, attB, for phiRv1.

105 me and additionally containing the bacterial attachment site, attB.

106 age attachment site, attP, and the bacterial attachment site, attB.

107 mutant proteins to cleave and ligate CTnDOT attachment site (attDOT) DNA in vitro in general paralle

108 I footprinting experiments with the excisive attachment sites attL and attR.

109 Moreover, the phage-like attachment site, attL, encoded within ssrA, serves as th

110 A binds to the bacteriophage lambda (lambda) attachment site, attL, producing SarA-DNA complexes simi

111 The attachment site (attlambda) of bacteriophage lambda was

112 directional; recombination between the phage attachment site attP and the host attachment site attB t

113 plasmid was constructed containing the phage attachment site attP from the mycobacteriophage L5 genom

114 The phage attachment site attP is located within the phage repress

115 The PhiCD119 attachment site attP lies in a noncoding region close to

116 lysis of integration revealed that the phage attachment site (attP) is contained in the int gene and

117 h binding to arm-type sites within the phage attachment site (attP).

118 een two DNA recognition sequences, the phage attachment site, attP, and the bacterial attachment site

119 t) from phage C31 acts on the phage and host-attachment sites, attP and attB, to form an integrated p

120 integrase, which acts on the phage and host attachment sites, attP and attB, to form an integrated p

121 egration reaction between the phage and host attachment sites, attP x attB to generate the hybrid sit

122 ic, inserting into its specific target site, attachment site attTn7 (attTn7) in a single orientation.

123 ts insertion into its preferred target site, attachment site attTn7, is mediated by four Tn7-encoded

124 The attachment site (base) of stems to blood vessels was ext

125 prfC, SXT integrated into several secondary attachment sites but preferentially into the 5' end of p

126 competent myoblasts and the epidermal muscle attachment site cells.

127 umber of spirochetes in the skin at the tick attachment sites compared to the number of spirochetes i

128 y linked to the core kinetochore microtubule attachment site comprised of the Knl1-Mis12-Ndc80 (KMN)

129 ated that inhibition of alphaVbeta3 integrin attachment sites compromises the response to probe stimu

130 l senses tension across multiple microtubule attachment sites, considering the stochastic dynamics of

131 rough a mechanism that is independent of the attachment site differentiation initiated by stripe.

132 Although the attachment site DNA of mycobacteriophage Pukovnik is lik

133 discriminate between attP and attB, cleaves attachment site DNA to form a 6-base overlap region, and

134 nd the linear organizations of the P22 phage attachment site DNA-binding sites have differences that

135 the component half-sites within each of the attachment site DNAs.

136 ein and bind weakly to discrete cytoskeleton attachment sites either associated with flexible actin n

137 Muscle attachment sites (entheses) on dry bones are regularly u

138 Of the 24 NBD attachment sites examined, all but three gave results qu

139 sed of a polar segment that includes the GPI-attachment site followed by a hydrophobic segment locate

140 ccharide that, in some bacteria, provides an attachment site for a long-chain O-antigenic polysacchar

141 n plays a more passive role by serving as an attachment site for astral MTs to pull centrosomes apart

142 zation of PGA at the cell poles, the initial attachment site for biofilm formation.

143 s footprint analyses predicted a unique cell attachment site for HRV-Cs.

144 The attachment site for Nup133 lies at the very end of an ex

145 . diverse xenobiotics, haemolysin) and as an attachment site for phage and colicins.

146 ology to the chromosomal region flanking the attachment site for phage lambda.

147 assembled at each centromere, serves as the attachment site for spindle microtubules and the site at

148 EBS1-TE, in which the 4'-phosphopante-theine attachment site for starter acyl groups was specifically

149 ysine residue of each C/EBP RDM served as an attachment site for SUMO-1.

150 ge, an amine group was left that provided an attachment site for the environmentally sensitive fluore

151 hloride-bicarbonate exchange and provides an attachment site for the erythrocyte membrane skeleton on

152 1 of the U1A protein, was used as a specific attachment site for the fluorophore pair IAEDANS [N'-iod

153 truncated soluble forms of CR-1 based on the attachment site for the GPI moiety (omega-site), which w

154 mediated repeated targeting" (SIRT), an attP attachment site for the phage phiC31 integrase is first

155 Utilizing an attP attachment site for the phiC31 integrase previously targ

156 ypothesis that the LCR serves as the primary attachment site for the recruitment of macromolecular co

157 phas, but also suggest an alternate membrane attachment site for this G protein.

158 pothesis predicts contiguous Hyp residues as attachment sites for arabino-oligosaccharides (arabinosi

159 These are candidate attachment sites for cargo-specific receptors.

160 was the best plane to observe the course and attachment sites for each ligament.

161 random coil but contain a variable number of attachment sites for heparan sulfate chains.

162 bornene)-derived support containing multiple attachment sites for high loading capacities and solubil

163 cultures and that these structures serve as attachment sites for leukocytes.

164 uence epithelial cells to differentiate into attachment sites for muscle, the expression of stripe, a

165 anodal junctions flank nodes and function as attachment sites for myelin and as paracellular and memb

166 consistent with their roles as cell surface attachment sites for perlecan.

167 Retinal basement membranes (BMs) serve as attachment sites for retinal pigment epithelial cells on

168 ons of the protein surface, and were used as attachment sites for spectroscopic probes.

169 Kinetochores provide the attachment sites for spindle microtubules and are requir

170 n, kinetochores form the primary chromosomal attachment sites for spindle microtubules.

171 the extending myotubes and resolves into the attachment sites for the dorsal abdominal muscles.

172 s Cep192 at several residues to generate the attachment sites for the gamma-tubulin ring complex and,

173 differentiate as "tendon cells," serving as attachment sites for the indirect flight muscles (IFMs)

174 mes are intercellular adhesive junctions and attachment sites for the intermediate filament (IF) cyto

175 and two lysine residues that could serve as attachment sites for ubiquitin.

176 different positions in NM to provide unique attachment sites for various probes.

177 c papillar plasma membrane, under the pollen attachment site, for pollen hydration and pollen tube en

178 ycocyanobilin, combined with a switch of the attachment site from a cysteine near the N terminus to o

179 The removal of specific N-glycan attachment sites from V1 and V2 led to increased sensiti

180 l-length sequence mutated at the chromophore attachment site had no effect on phenotype, indicating t

181 transfer measurements made using several dye attachment sites illustrates that dye labeling of comple

182 or curing endogenous prophages from the comK attachment site in 10403S-derived strains were developed

183 Mutation of the covalent flavin attachment site in MSOX produces a catalytically inactiv

184 ranscriptional fusions integrated at a phage attachment site in the chromosome but not at the normal

185 when fused to lacZ and integrated at a phage attachment site in the M. xanthus chromosome, showed a s

186 a viruses were labeled to identify the virus attachment site in the mouse cornea.

187 ite-specific recombination between attP (the attachment site in the phage DNA) and attB (the chromoso

188 pe PSI1 or PSI1 G2A with a mutated myristate attachment site in the psi1-1 background suggesting that

189 dhesome and 48 proteins known to localize to attachment sites in C. elegans muscle.

190 d are coincident at the integrin-rich muscle-attachment sites in embryonic muscle.

191 ot ubiquitinated and the major ubiquitin-His attachment sites in HIV-1 Nef were determined to be lysi

192 Msk protein is enriched at muscle attachment sites in late embryogenesis and msk mutant em

193 number and location of the glycosaminoglycan attachment sites in the core protein were determined by

194 of the integrin to recruit laminin to muscle attachment sites in the embryo and caused detachment of

195 e transverse plane for evaluation of the CLC attachment sites in the phalanges.

196 urther experiments demonstrate that two acyl attachment sites in the Wg protein are required for the

197 force levels predicted to occur at integrin attachment sites in vivo.

198 nome by site-specific recombination between 'attachment sites' in the phage (attP) and the host (attB

199 of talin, an adapter protein at cell-matrix attachment sites, in outside-in signaling.

200 erally be attributed to the loss of a muscle attachment site induced by some other aspect of the Pitx

201 suggest that a collection of 1200 lines with attachment sites inserted every 140 kb throughout the ge

202 The attachment site is controlled by cysteine mutations of s

203 tein kinase Calpha (PKCalpha) at the E. coli attachment site is critical for the invasion of HBMEC.

204 regulate cell fate selection; a recombinase attachment site is embedded within a repressor coding se

205 le image reconstruction revealed that the FX attachment site is localized to the central depression a

206 ese complexes at one kinetochore-microtubule attachment site is necessary to understand the molecular

207 The specification of proteoglycan attachment sites is defined by the Golgi enzyme polypept

208 In addition, since it retains attachment sites, it can be excised out to cure the cell

209 The PfRh4 attachment site lies within the three N-terminal complem

210 olution, reaffirms Cys 24 as the chromophore attachment site, locates key amino acids that form a sol

211 e are able to define a single AzBCQ covalent attachment site lying within the digestive vacuolar-disp

212 nslational fusion, are localized to integrin attachment sites (M-lines and dense bodies) in the body-

213 l forms, and multiple, readily derivatizable attachment sites make them valuable nanometer-size molec

214 minant ubiquitylated species, with ubiquitin attachment sites mapped to six lysines.

215 actin-rich structures in Drosophila: muscle attachment sites (MASs), which connect somatic muscles t

216 e (boron-dipyrrin, perylene, terrylene), and attachment sites (meso-position, beta-pyrrole position).

217 ernal RGD motif and four Metal Ion-Dependent Attachment Sites (MIDAS) motifs required for coordinatio

218 ficient to promote pairing and that telomere attachment sites must be coupled to cytoplasmic dynein a

219 The attachment site mutants were generated by replacing the

220 t molecular explanation of the wall-membrane attachment sites observed in vivo.

221 tes the putative translocation pore from the attachment site of an additional membrane component.

222 te 3 aa upstream of the predicted GPI anchor attachment site of ARTC2.2.

223 Here, the principal attachment site of Brf1 for the Bdp1 subunit of TFIIIB h

224 ted set of conserved sequences occurs at the attachment site of each enterobacterial element, apparen

225 ) modules found in proximity of the membrane-attachment site of N-CAM.

226 The attachment site of the 4-AzHBA probe was localized to th

227 Our data show that the MT attachment site of the budding yeast kinetochore is well

228 n extension is tolerant to variations in the attachment site of the proximal ubiquitin moiety.

229 exchanger, SLCA1, AE1) constitutes the major attachment site of the spectrin-based cytoskeleton to th

230 cryo-EM electron density, may function as an attachment site of the virus to host cells.

231 The attachment sites of all ligaments were best analyzed eit

232 lt muscle, both proteins are concentrated at attachment sites of myofibrils to the membrane.

233 the sugar composition, linkage pattern, and attachment sites of N-linked glycans.

234 lorectal epithelial cells, especially at the attachment sites of primers for MSP, although there was

235 mutants, the DA3 muscle randomly adopts the attachment sites of the DA3 or DO5 muscles that derive f

236 the PS integrins are required at the muscle attachment sites of the Drosophila embryo to regulate te

237 found that alteration of the putative lipid attachment site on CwlT had no effect on its role in con

238 on late day 4 and then in the stroma at the attachment site on days 5-6 of pregnancy, with a similar

239 Additionally, the PSA phage attachment site on the L. monocytogenes chromosome was c

240 e developed to obtain conjugates with single attachment site on the protein, based on chemical modifi

241 This result is attributed to exhaustion of attachment sites on biochar by the dissolved organic car

242 mbly of kinetochores-the primary microtubule attachment sites on chromosomes.

243 s the number of kinetochore-microtubule (MT) attachment sites on each chromosome and that CENP-A is n

244 tegrase (Int) mediates recombination between attachment sites on lambda phage and E. coli DNAs.

245 tegrase (Int) mediates recombination between attachment sites on phage and Escherichia coli DNA.

246 nt on a distinct subset of glycosaminoglycan attachment sites on syndecan-2.

247 conservation, the four N-linked carbohydrate attachment sites on the external domain of gp41 are surp

248 ith recombination occurring between specific attachment sites on the phage and mycobacterial chromoso

249 f cells and link cortical actin filaments to attachment sites on the plasma membrane.

250 hnique to design an insulating membrane with attachment sites on top of single-walled carbon nanotube

251 At each OH attachment site, only one isomeric pathway via the bicyc

252 th pyridyldithio groups for amplification of attachment sites [PEI(PDT)], and (3) a bifunctional (ami

253 e in having only one kinetochore microtubule attachment site per centromere.

254 In budding yeast, there is one microtubule attachment site per chromosome.

255 ence of the glycophosphatidylinositol anchor attachment site present in the gp15 coding sequence.

256 ubule-binding Ska complex, which enriches at attachment sites prior to anaphase onset to dampen chrom

257 10 and m242 antibodies surround the receptor-attachment site, probably inhibiting infection by blocki

258 varphi copy present between dif and its left attachment site, providing a plausible mechanism for how

259 n of the kDNA disk relative to the antipodal attachment sites results in distribution of progeny mini

260 Analysis of the 285 putative attachment sites revealed tRNAs are targets for integrat

261 SUMO attachment site(s) were identified in a subset of target

262 Ub attachment site(s) were resolved for a subset of these p

263 to identify the glycosaminoglycan side-chain attachment site(s), we further characterized HMW-DSP.

264 ts that each island encode an integrase, and attachment site sequence identity is carefully noted; th

265 and other donors containing gain-of-function attachment site sequences are specifically protected by

266 ted mutagenesis identified the N-terminal CS attachment sites Ser(507) and Ser(525) as essential for

267 A donor containing mutations in the attachment site simultaneously eliminated full-site inte

268 architecture, drug loading through multiple attachment sites, solubility through PEGylation, and dru

269 anizations on attP vs. attB half-sites allow attachment-site specific interactions to form between in

270 uppresses kMT catastrophe near the poles and attachment site tension that promotes kMT rescue at high

271 in trnS-leu2, ICEBs1 integrated in secondary attachment sites that are similar to a 17 bp sequence in

272 We show here that the SUMO attachment site (the regulatory domain motif) is necessa

273 of cortactin and actin polymerization at the attachment sites, thereby inhibiting C. parvum invasion

274 ns in the spatial and temporal regulation of attachment sites through MyoII assembly via regulation o

275 M, and can convert VF to VT by serving as an attachment site to reentrant excitation.

276 The antagonist covalent attachment site to the receptor served as a guide in the

277 importance of bioengineering optimal protein attachment sites to achieve direct protein-nanotube comm

278 mutagenesis study, we localized the polySia attachment sites to an O-glycan cluster located in the l

279 ors Sti1 and Aha1, may utilize two different attachment sites to restrict the conformational freedom

280 ts, we localized the glycosaminoglycan (GAG) attachment sites to two locations within the agrin molec

281 available lysine residues on Ub itself as Ub attachment sites, together with evidence for a branched

282 x US, two of the leaks were characterized as attachment-site (type I) leaks; these two diagnoses were

283 nt peptides we have localized the synapsin I attachment site upon the beta-spectrin isoform betaSpIIS

284 part by the integrity of putative palmitate attachment sites upstream of its GRK phosphoacceptor sit

285 tle effect on peptide binding as long as the attachment site was in the relatively hydrophobic C-term

286 se domain in the L protein, the covalent RNA attachment site was mapped.

287 om inhibition by EDTA when DNA containing an attachment site was present suggesting that the zinc fin

288 these two GAG chains, but not downstream GAG attachment sites, was cleaved efficiently.

289 1-Rng8/9 was bound to actin-tropomyosin, two attachment sites were observed: the typical ATP-dependen

290 Ub-attachment sites were resolved for a number of targets,

291 variant of g123 emerged with a new N-glycan attachment site which compensated for the loss of sites

292 grase appears to promote damage routinely at attachment sites, which may be adaptive.

293 in mutant devoid of N-linked oligosaccharide attachment sites will not be secreted by Chinese hamster

294 he WO genome sequences and identification of attachment sites will potentially advance genetic manipu

295 By substituting the attachment site with a tumor delivery agent, this potent

296 and Phe-77, are located upstream of the AMP attachment site within a conserved domain unique to the

297 e tolerance does not depend on the ubiquitin attachment site within PCNA.

298 Escherichia coli chromosome at an identical attachment site within the 5' end of prfC.

299 tilizes the listeriophage U153 integrase and attachment site within the comK gene for chromosomal ins

300 Attachment sites within the kinetochore outer plate gene