ライフサイエンスコーパス: subdomain

1 he OHIP-G49 was limited to the physical pain subdomain.

2 helicase is regulated specifically by its 2B subdomain.

3 he rotational conformational state of its 2B subdomain.

4 nd the integrin-binding properties of its F3 subdomain.

5 a summary narrative synthesis by domain and subdomain.

6 ses indicated that it can insert into the F2 subdomain.

7 structural parts, called the alpha- and beta-subdomain.

8 IDOL and multiple conformations of its F3ab subdomain.

9 the interaction network at the 3D(pol) palm subdomain.

10 serotonergic group distributed throughout DR subdomains.

11 a QDE2 revealed that the PIWI domain has two subdomains.

12 s in the context of known structural domains/subdomains.

13 accessible to regulation and organized into subdomains.

14 mbrella term, encompassing several disparate subdomains.

15 short segment around V2547 connecting the 2 subdomains.

16 etermined the main input structures to these subdomains.

17 guing that they bud continuously from stable subdomains.

18 nd gamma-catenin reside within its F1 and F3 subdomains.

19 sphatidylinositol synthase (PIS)-enriched ER subdomains.

20 annels cluster together in specific cellular subdomains.

21 omization of Re-chains and formation of ReS2 subdomains.

22 iation with different cellular membranes and subdomains.

23 wo unc-13 (Unc13) isoforms to presynaptic AZ subdomains.

24 provokes a reorganisation of plasma membrane subdomains.

25 score improved significantly, as did 3 of 4 subdomains.

26 omain align more linearly with its F2 and F3 subdomains.

27 tion of IEGs in SPN subtypes within striatal subdomains.

28 e energy profiles for unfolding of talin rod subdomains.

29 sensitive to a specific interaction between subdomains.

30 omatin droplets, mimicking nuclear chromatin subdomains.

31 inct circuit and behavioral functions of its subdomains.

32 ich is involved in physical interaction with subdomain 1 of actin and in stimulating the ATPase activ

33 ns, we mapped the BMP-binding epitope on the subdomain 1 of the vWC domain.

34 sts of three subdomains: core, insertion and subdomain-1 (SD-1).

35 nteractions with the DNase-I binding loop in subdomain 2 of the adjacent subunit.

36 state, and the conformation of the flexible subdomain 2B.

37 In particular, conformational changes in subdomain 3 open up multiple favorable interactions with

38 We have identified an interface on IFNAR1-subdomain-3 that is differentially utilized by IFN-beta

39 ture revealed that the CCSSD consists of two subdomains: a juxta-membrane subdomain, which has a nove

40 istinct vertical segments, each with 3 major subdomains: A membrane-connected basal lobe and an apica

41 nly mediated by N- and C-terminal protruding subdomains (aa 1-27 and aa 355-372).

42 r to those of other beta-CoVs, the insertion subdomain adopts a novel fold, which is largely invisibl

43 he structures also reveal refolding of an S1 subdomain after ACE2 binding that disrupts interactions

44 hat PINK1 recruits Parkin onto mitochondrial subdomains after actinonin-induced mitochondrial proteot

45 n talin1, its F1 subdomain and additional F0 subdomain align more linearly with its F2 and F3 subdoma

46 ic structural information about the globular subdomains, along with coevolutionary information and an

47 yIIC reveals a novel fold, consisting of two subdomains alphaA-beta1-beta2 and beta3-beta4-alphaB-bet

48 gase domain of SspH1 can be divided into two subdomains: an N-terminal subdomain that harbors the act

49 , and a bundle of 3 helices: 1 from the palm subdomain and 2 from the N-terminal domain.

50 binding site in the vestigial 3' exonuclease subdomain and a non-catalytic water-bridged magnesium co

51 the PROMIS Global Satisfaction With Sex Life subdomain and a single item from the PROMIS Interest in

52 resemble a cloverleaf, but in talin1, its F1 subdomain and additional F0 subdomain align more linearl

53 firm the mechanosensory role of the talin R3 subdomain and exclude the possibility that the observed

54 acting with a glutamate residue in the 'lid' subdomain and the catalytic glutamate upon ATP binding;

55 of the membrane-binding functions of the F2 subdomain and the integrin-binding properties of its F3

56 ten transmembrane helices organized into two subdomains and bisected by a long diagonal helix.

57 equired for proper designation of chromosome subdomains and normal chromosome remodeling in late meio

58 ee enzymatic functions and over 30 conserved subdomains and topological regions.

59 ive impairment at 3 years affected all ACE-R subdomains and was associated with ACE-R 1 year (beta=1.

60 ingernail, attached to the conserved fingers subdomain, and a bundle of 3 helices: 1 from the palm su

61 hagy-initiation complex, the PIS-enriched ER subdomain, and ATG9A vesicles together initiate autophag

62 Lro1 is active at this nuclear subdomain, and its compartmentalization is critical for

63 he rotational conformational state of its 2B subdomain, and its helicase activity has been correlated

64 ing microtubule (MT) arrays, plasma membrane subdomains, and nuclear compartments.

65 located in the interface between 2 distinct subdomains, and structural modeling revealed conservatio

66 ains of integrin alphaIIbbeta3, talin1 F2/F3 subdomains, and the kindlin2 FERM domain in an explicit

67 Model structures of the subdomains are combined to generate a model of t/PK.

68 95-144 of RCHY1 and 389-652 of SUD (SUD-NM) subdomains are crucial for interaction.

69 d that topologically associating domains and subdomains are fundamental building blocks of the three-

70 mapping, we demonstrate that the F2PH and F3 subdomains are important for kindlin self-association.

71 aturation CD spectroscopy, we show that both subdomains are required for binding the NTSD with microm

72 st that the intermediate states in talin rod subdomains are stabilized by force during unfolding, and

73 cture further revealed an unusually hinged 2-subdomain arrangement.

74 e identified a histone deacetylase 4 (HDAC4) subdomain as a molecular checkpoint of adaptive and mala

75 actins can be explained by treating the four subdomains as rigid bodies.

76 The TlpC dCACHE LBD has two PAS-like subdomains, as predicted.

77 ollowed by a secretin/TonB, short N-terminal subdomain at the C terminus of the CCSSD, a previously u

78 the position of the AdnA iron-sulfur cluster subdomain at the Y junction and its likely role in maint

79 esults in repositioning of the tetrathiolate subdomain away from the rest of the catalytic domain, th

80 These subdomains become enriched in DAG.

81 iately adjacent to the SecA two-helix finger subdomain before channel entry.

82 ed that the linker in H. pylori MotB forms a subdomain between the plug and the C-terminal domain, th

83 difference in global cognition or cognitive subdomains between cohorts.

84 CUP expression becomes cleared from boundary subdomains between petal primordia, most likely contribu

85 GerK(3) GR, revealing two distinct globular subdomains bisected by a cleft, a fold with strong homol

86 cer cells reveals several unique features of subdomain boundary as compared to domain boundary, inclu

87 cts with the preceding ZPC and following ZPN subdomains by beta-sheet complementation.

88 cket at the junction of the fingers and palm subdomains by displacing residue V603 in motif B.

89 associates with Domain III of the rRNA and a subdomain called "DIII(core)".

90 t a closed, right-handed fold with conserved subdomains called palm, fingers, and thumb1,2.

91 a membrane (PM) is composed of heterogeneous subdomains, characterized by differences in protein and

92 ic interactions between two semi-independent subdomains connected by an allosteric switch at Asp52(2.

93 architecture formed by an N- and C-terminal subdomain consisting of eight beta-strands and an alpha-

94 Two subdomains contain tetratricopeptide-like motifs that fo

95 rs the active-site cysteine and a C-terminal subdomain containing the Ube2D~Ub-binding site.

96 suppresses the segregation of mitochondrial subdomains containing DeltaOTC, it does not decrease the

97 of the duplex-which does not require the 2B subdomain, contrary to a previous proposal.

98 The structure consists of three subdomains: core, insertion and subdomain-1 (SD-1).

99 KH2 and KH3 bind adjacently to an IRES subdomain (d10b) that is unrelated to dIV, with KH3 in a

100 so contains an essential GNRA tetraloop in a subdomain (d10c) that is homologous to poliovirus dIVc.

101 ins, D00-D2, extending into the fifth lectin subdomain (D3) that binds to the Tir-receptor on the hos

102 stepwise destabilization of the talin rod R3 subdomain decreases cellular traction force generation,

103 ases Lro1 and Dga1 are formed at discrete ER subdomains defined by seipin (Fld1), and a regulator of

104 ystal structure, revealing that its F0-F1 di-subdomain displays another unprecedented constellation,

105 Moreover, discriminant analysis using ASD subdomains distinguished between CNV cases with 76% accu

106 he structure, we observed 5 intra- and inter-subdomain disulfide bridges, of which 1 is unique in the

107 Together with 2 nearby inter-subdomain disulfide bridges, this hinge induces slow con

108 oordinated by an independent movement of two subdomains, dsRBD1 and dsRBD2, in which the diffusion di

109 affects the formation of distinct chromosome subdomains during meiotic chromosome remodeling.

110 rts" between genomics and other data-science subdomains (e.g., astronomy).

111 elucidate a mechanism by which a peripheral subdomain enforces stable gene repression and maintains

112 prime CDTa for translocation as the adaptor subdomain enters the lumen of the preinsertion state cha

113 modules and an inward motion of the fingers subdomain-especially the O helix-to engage the primer-te

114 Overall mean miniRQLQ score and all subdomains except the "eye" domain showed significantly

115 loped for monitoring the rates of individual subdomain folding transitions in situ, in the context of

116 nearly scan upstream chromatin in the 3' Igh subdomain for convergently oriented D-12RSSs and, thereb

117 that dCACHE domain proteins can utilise both subdomains for ligand recognition.

118 We found that conserved subdomains generally are critical for channel function a

119 Force induced unfolding of talin rod subdomains has been proposed to act as a cellular mechan

120 icopeptide (HAT) repeats, organized into two subdomains, HAT-N and HAT-C.

121 an unusual sequence and structure containing subdomain homology to thrombospondin type 1 and interleu

122 (TGN) is a central hub divided into multiple subdomains hosting distinct trafficking pathways, includ

123 the SAP domain engages the cleft between NBD subdomains Ia and IIa, stabilizing the ADP-bound conform

124 bumin at drug site 3, which is also known as subdomain IB.

125 further close the interdomain cleft between subdomains IB and IIB.

126 ne substitutions for the invariant lysine in subdomain II or the aspartate in the DYG-loop of GC-A an

127 ing results revealed beta-C was bound to the subdomain IIA of BSA, the residues of aromatic cluster I

128 This 18-mer peptide, which lies in Subdomain IIIA of human serum albumin, blocks binding of

129 its pairwise arrangement with the companion subdomain in each brace of protomers of the DnaB hexamer

130 dies had implicated only the membrane-distal subdomain in ligand recognition.

131 e synthesized, to which pre- or postsynaptic subdomains in a given neuron type they localize, and whe

132 entify topologically associating domains and subdomains in Hi-C data.

133 oscopy to visualize organization of synaptic subdomains in hippocampal neurons.

134 sed model that the interface between the two subdomains in the NTD of GR A subunits serves as the ger

135 lators bind to a conserved cleft between two subdomains in the sGC heme domain.

136 veral other components and the definition of subdomains in the tip structures.

137 Identification of these functional subdomains in TP will facilitate its targeting for antiv

138 The membrane-proximal subdomain, in contrast, had a well-delineated pocket wit

139 how genomics fits as a specific application subdomain, in terms of well-known 3 V data and 4 M proce

140 tream constant region exon-containing 3' Igh subdomain, in which scanning can be impeded by targeted

141 We find that Fld1 and Nem1 localize to ER subdomains independently of each other and of LDs, but b

142 cial impairment, as well as higher scores on subdomains, indicating deficits in social cognition, soc

143 We found that the pinky finger subdomain is a major regulator of initiation and that th

144 /6J mice in which the Nr4a1 superenhancer E2 subdomain is ablated (E2 (-/-) mice).

145 In turn, the Amo1-enriched subdomain is critical for Swi6 association with FACT tha

146 The UvrD 2B subdomain is regulatory and can exist in extreme rotatio

147 This subdomain is susceptible to proteolysis, consistent with

148 Compartmentalized signaling in dendritic subdomains is critical for the function of many central

149 containing a Zn(2+)-binding G5 and a spacer subdomain, is responsible for Zn(2+)-dependent assembly

150 to show that nanocompartmentalization of IDR subdomains leads to a remarkably elaborate gating struct

151 The kernel of this algorithm is the subdomain level discontinuous Galerkin time domain (DGTD

152 ognition is mediated via a four-helix bundle subdomain located in the cytoplasm, which functions as t

153 d weaker synergistic effects at a distal GHI-subdomain locus.

154 Concomitant reorientation of the lid subdomain may mediate mechanochemical coupling of ATP hy

155 minus of the beta2AR with the GRK5 RH bundle subdomain, membrane-binding surface, and kinase catalyti

156 al score 3.6% versus 3.7% (p = 0.62) and for subdomains (memory, 5.8% vs. 6.0%; total executive, 3.6%

157 SspH1 mutations designed to restrict subdomain motions show rapid formation of an E3~Ub inter

158 rthermore, MD simulations support rigid body subdomain motions within the FabD structure that may pla

159 Domains and subdomains mutual to both perspectives are related to "A

160 -terminal domain bears closest homology to a subdomain of 6-phosphofructokinase, an important enzyme

161 olecule FRET approaches, we show that the 2B subdomain of a UvrD monomer bound to DNA exists in equil

162 s designed to target the central alpha-helix subdomain of Abeta (Abeta13-26).

163 mmetry and spindle pole movement towards the subdomain of cortical ER, whereas locally increasing mic

164 s that microtubules are less abundant in the subdomain of cortical ER.

165 rotubule depolymerase Kif2 localizes to this subdomain of cortical ER.

166 -like motif, directly interact with the Hel2 subdomain of Dicer-2's helicase domain.

167 ly ascidian embryos possess a large cortical subdomain of endoplasmic reticulum (ER) that causes asym

168 ision.Early ascidian embryos have a cortical subdomain of endoplasmic reticulum (ER) that controls as

169 depolymerase Kif2 is localized to a cortical subdomain of endoplasmic reticulum that is involved in a

170 e rotational conformational states of the 2B subdomain of fluorescently labeled UvrD and their rates

171 By fusing an oxygen sensitive subdomain of HIF1alpha to a CAR scaffold, we generated C

172 leotide/oligosaccharide fold (OB-fold) and A subdomain of Mcm2.

173 terminal domain of the PA subunit, the thumb subdomain of PB1 and the N1 subdomain of PB2.

174 bunit, the thumb subdomain of PB1 and the N1 subdomain of PB2.

175 , reside exclusively within the patatin-like subdomain of PNPLA1 containing the catalytic site.

176 tic acid fragment 3, which bound in the palm subdomain of RdRp.

177 The alpha/beta core subdomain of SHR forms the BIRD binding groove, which sp

178 The inner nuclear membrane (INM) is a subdomain of the endoplasmic reticulum (ER) that is gate

179 are associated with functions localized to a subdomain of the endoplasmic reticulum (ER), known as mi

180 ipid droplet (LD) assembly at the LD-forming subdomain of the endoplasmic reticulum (ER).

181 depolymerase Kif2 is localized to a cortical subdomain of the ER that is involved in asymmetric spind

182 o-TEM revealed IRX9 is present in a specific subdomain of the Golgi stack and was most abundant in th

183 elocates from the endoplasmic reticulum to a subdomain of the inner nuclear membrane.

184 ted glycan remodeling that forms a localized subdomain of the native mannose patch.

185 ntify a new population of Tbx6(+) cells in a subdomain of the NMP niche in mouse embryos.

186 Amino acid substitutions in the thumb subdomain of the RNA-dependent RNA polymerase (RdRp) and

187 ctivity of a chimeric UvrD containing the 2B subdomain of the structurally similar Rep helicase.

188 We find that the 2B subdomain of the UvrD monomer can rotate between an open

189 The influenza endonuclease is an essential subdomain of the viral RNA polymerase.

190 patients harbour a missense mutation in the subdomain of TLDc between residues 500 and 511.

191 localized in the sarcoplasmic reticulum (SR) subdomain of triads where it forms large multimers.

192 NSs bound to the carboxyl-terminal SPRY subdomain of TRIM21, enhancing p62 stability and oligome

193 recovering the conformational ensemble of a subdomain of TrpS affecting the relative stabilities of

194 The base and glycan cap subdomains of all filovirus GPs tested suffered a concer

195 The F1-F3 FERM subdomains of cytoskeletal proteins resemble a cloverlea

196 ound at the meeting point of three different subdomains of desmoplakin: two spectrin repeats and a Sr

197 The immunoglobulin-like ZPN and ZPC subdomains of each monomer are separated by a long linke

198 The data suggest that the two Ig-like subdomains of each Rel-homology region, which are connec

199 While the structure of the core and SD-1 subdomains of HKU1 are highly similar to those of other

200 -glucosamine residues in the highly sulfated subdomains of HSPGs.

201 sis on the sequence conservation patterns of subdomains of KCNQ1 and the distribution of pathogenic v

202 in binding site resides within the F1 and F3 subdomains of Kindlin-2 but not the integrin binding sit

203 The thumb, palm, and fingers subdomains of POL form an extensive interface with the p

204 Problem rating of hot flushes and subdomains of quality of life did not improve.

205 classes on the basis of their reactivity to subdomains of S protein as well as their cross-reactivit

206 xposed regions and the interface between the subdomains of SERINC5 as critical for HIV-1-restriction

207 e propose that structural differences in the subdomains of the Ag43 classes account for different aut

208 of glutelin and prolamine mRNAs to distinct subdomains of the cortical endoplasmic reticulum is a mo

209 etory protein trafficking by assembling onto subdomains of the endoplasmic reticulum (ER) in two laye

210 hrough the endomembrane system from specific subdomains of the endoplasmic reticulum.

211 d, relocalizes VPS13A from lipid droplets to subdomains of the endoplasmic reticulum.

212 on and the GGA2 GAE domain bound to multiple subdomains of the loop.

213 synthetase and the leader- and core-peptide subdomains of the modular HalA2 precursor peptide substr

214 ularly, functionally, and spatially distinct subdomains of the plant TGN and suggest that functional

215 oteins in lipid rafts-the dynamic functional subdomains of the plasma membrane.

216 eurons, with each ipRGC innervating specific subdomains of the SCN.

217 rbon atoms are enriched in secretory vesicle subdomains of the TGN and are critical for de novo polar

218 dCACHE family, a structure with two PAS-like subdomains, one membrane-proximal and the other membrane

219 tion, but the specific roles of different ZI subdomains or cell types have not been well examined.

220 FERM domain structure but show that the F3c subdomain orientation obscures the target-binding site.

221 All vertebrate pseudoknots include two subdomains: P2ab (helices P2a and P2b with a 5/6-nt inte

222 ral features: an additional novel alpha+beta subdomain placed close to the putative transmembrane alp

223 ease-causing mutations indicate that the two subdomains play pivotal but distinct roles and that the

224 spots are significantly smaller than a Golgi subdomain positive for scaffolding protein AKAP450, whic

225 136 (I136N) and Thr for Ile-142 (I142T) in a subdomain previously named the helical hairpin in the NT

226 HTLV-1 CA CTD, indicating that the HTLV-1 CA subdomains provide distinct contributions to Gag-Gag oli

227 mposition to functional polar sorting at TGN subdomains remain unknown.

228 cting WGR domain (W) and the catalytic (Cat) subdomain responsible for the poly(ADP ribosyl)ating rea

229 1 with a mutation in the ligand-binding CRD2 subdomain retained the monomer-to-dimer ratio of the unl

230 S-CoV Sia-binding activity was assigned to S subdomain S1(A) When multivalently displayed on nanopart

231 Mean EPIC subdomain score changes at each serial time point were c

232 There was no significant change in EPIC subdomain scores from baseline over the 24 months.

233 s disorder (PTSD), all SF-12 physical health subdomain scores were significantly below US norms, and

234 key interactions implicated in IFNAR1 inter-subdomain (SD1-SD4) movements.

235 Notably, introducing disulfide bonds between subdomains SD2 and SD3 modulated IFN binding and activit

236 plays a bi-modular structure composed of two subdomains separated by a flexible serine-rich linker.

237 ther demonstrate in vivo that the N-terminal subdomain serves as a pedestal for the C-terminal subdom

238 and of MutL-dependent changes in the UvrD 2B subdomain show that the transition from an open to an in

239 Our data support the hypothesis that subdomain-sized fragments can provide structural versati

240 These subdomain-specific forebrain spheroids can be assembled

241 ransition from an open to an intermediate 2B subdomain state is on the pathway to helicase activation

242 rates of folding of two or more neighboring subdomain structures using a single mutant to facilitate

243 ither enrichment in or specificity to apical subdomains such as emerging flower primordia, and a larg

244 flexibility is evident throughout the first subdomain, suggesting that the HlyIIC structure may have

245 How Zeb2 subdomains support cell differentiation in various conte

246 ia a series of constant region shuffling and subdomain swapping approaches to create improved ("i") c

247 Here we use high-throughput and DR subdomain-targeted single-cell transcriptomics and inter

248 We identify five residues in the insertion subdomain that are critical for binding of neutralizing

249 ra, Chm7, is recruited to a nuclear envelope subdomain that expands upon inhibition of NPC assembly a

250 fied a flexible region within the rigid beta-subdomain that gives way under load, thus opening up the

251 e divided into two subdomains: an N-terminal subdomain that harbors the active-site cysteine and a C-

252 We found, in dimer, that the subdomain that makes protein-protein interactions is par

253 CR extracellular domains contain a conserved subdomain that mediates self-cleavage proximal to the st

254 2) at the 3' end of Igh contains an internal subdomain that spans the 5' CBE anchor (IGCR1)(3), the D

255 teins consist of three sequential beta-sheet subdomains that bind to specific carbohydrates to perfor

256 partition into the proximo-distally oriented subdomains that convey positional information to these d

257 in loading, leading to generation of dynamic subdomains that directionally align a downstream S regio

258 ochromatin domain, most localize to discrete subdomains that display dynamic localization patterns du

259 f the 3D fold into independent, foldspanning subdomains that govern long-range communication.

260 NSC) activation, which does not occur in the subdomains that lack progenitors.

261 zed intramolecular interactions between ZAR1 subdomains that participate in keeping ZAR1 immune compl

262 that it can be divided into three functional subdomains that roughly correspond to the three conserve

263 ising basic residues from both the N1 and N2 subdomains, that directly contributes to 30S-binding aff

264 Moreover, apPOL has an additional N-terminal subdomain, the absence of which severely diminishes its

265 at least partially mapped onto different SC subdomains, the lateral (SCl) and medial (SCm), respecti

266 ure of a cilium can be classified into three subdomains: the intracellular basal body (BB) that templ

267 Binding of guide RNA fastens the subdomains, thereby rearranging the active-site residues

268 directly convert into neuroblasts, in an IPC subdomain they generate migratory progenitors by epithel

269 ertoire by establishing protective motifs in subdomain three outside the receptor-binding and dimeriz

270 er and of LDs, but both are required for the subdomains to recruit the TAG-synthases and additional L

271 f the motions of the converter and lever arm subdomains to the rest of the protein and b) a rewiring

272 ficit maps of a broad range of psychological subdomains underlying affect and cognition.

273 terns found by microarray analysis of embryo subdomains using in situ hybridization.

274 the small and well-studied villin headpiece subdomain (VHP).

275 able region between protein kinase catalytic subdomains VII and VIII, is a common mechanism for stimu

276 To further characterize the ER subdomain, we screened phospholipid biosynthetic enzymes

277 from the PROMIS Interest in Sexual Activity subdomain were administered.

278 The beta1-alpha1-beta2 and alpha2-alpha3 subdomains were separated, and the helix alpha1 was unfo

279 s fluctuations at the interface between rRNA subdomains where bS16 binds.

280 are both necessary to recruit proteins to ER subdomains where LD biogenesis occurs.

281 a rigid and closed arrangement of the Galpha subdomain, whereas the apo and GDP-bound forms are consi

282 n, ELC1 appears to engage the MyoA converter subdomain, which couples the motor domain to the neck.

283 main serves as a pedestal for the C-terminal subdomain, which determines the ability of MapZ to mark

284 consists of two subdomains: a juxta-membrane subdomain, which has a novel all-beta-fold, followed by

285 sites of HA are located in the globular head subdomain, which is highly tolerant of amino acid substi

286 ch GRAS domain comprises one alpha/beta core subdomain with an alpha-helical cap that mediates hetero

287 , we provide evidence of a COL4A1 functional subdomain with disproportionate significance for tissue-

288 "mitochondrial RNA granules," mitochondrial subdomains with an emerging role in the regulation of ge

289 -chain length links lipid composition of TGN subdomains with polar secretory trafficking of PIN2 to a

290 to alter the surfaces and the orientation of subdomains with respect to each other, likely resulting

291 changes and positional alternations of both subdomains with respect to each other.

292 nique fold composed of three pseudosymmetric subdomains with shared sequence similarity, a feature no

293 Thus, we identified a subdomain within the CED-4 CARD that regulates the dynam

294 ngle-cell analysis, we identified a cellular subdomain within the midhypocotyl, whose expansion drive

295 ting insight into the spatial arrangement of subdomains within the adult neural subventricular zone (

296 lasses arose from shuffling of two different subdomains within the Ag43 passengers.

297 d that exhibits a major rearrangement of the subdomains within the C-terminal two-thirds of PB2 (PB2-

298 e insights into the structural properties of subdomains within the full-length vimentin, in particula

299 reconstruction microscopy (STORM) to define subdomains within the light-sensing rod sensory cilium o

300 ructure and a ZP domain that consists of two subdomains, ZP-N and ZP-C, with ZP-N of ZP2 and ZP3 requ