ライフサイエンスコーパス: subdomain

1 he rotational conformational state of its 2B subdomain.

2 nduce its degradation dependent on the NS5A1 subdomain.

3 n a reliable tagger not tied to any specific subdomain.

4 onserved segment adjacent to the helical HID subdomain.

5 eEF1A interacts with Rho1p via a C-terminal subdomain.

6 ry genes operating across the border of each subdomain.

7 nges involving a large rotation of an entire subdomain.

8 ream protein partner bound to the EIN(alpha) subdomain.

9 on led to disruption of Hh signaling in this subdomain.

10 ycan and have mapped the binding to its beta subdomain.

11 s that have interrupted the closure of the N-subdomain.

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

13 a summary narrative synthesis by domain and subdomain.

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

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

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

17 individual arrangement of the characteristic subdomains.

18 guing that they bud continuously from stable subdomains.

19 (229-280), P2 (281-447), and P1-2 (448-567) subdomains.

20 terminal, alpha-helical, and alpha/beta-core subdomains.

21 omain is divided into the P1-1, P2, and P1-2 subdomains.

22 hically by sequential stabilization of their subdomains.

23 ted "puncta" positioned upon raised membrane subdomains.

24 F(0) for energy transduction between the two subdomains.

25 hain particles contain distinct cross-linked subdomains.

26 distinct functional properties of conserved subdomains.

27 ut exploring the modulatory effects of these subdomains.

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

29 etermined the main input structures to these subdomains.

30 sphatidylinositol synthase (PIS)-enriched ER subdomains.

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

32 iation with different cellular membranes and subdomains.

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 HipA forms dimers in these assemblies via N-subdomain-1 interactions that occlude their active sites

36 ingly, high-persister mutations map to the N-subdomain-1 of HipA far from its active site.

37 291, 324, and 328 were located at protruding subdomain 2 (P2) of VP1, which may influence virus bindi

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

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

40 ver, overexpression of the Rho1p-interacting subdomain affects vacuolar morphology.

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

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

43 his pocket is located in the polymerase palm subdomain and conserved across the four serotypes of den

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

45 The RH bundle subdomain and kinase C-terminal lobe form a strikingly a

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

47 , which reveals two structurally independent subdomains and an unprecedented dimer centred at the sig

48 ndapin colocalize with Past1 in distinct SSR subdomains and collapse into Amphiphysin-dependent membr

49 The roles of the subdomains and ILV clusters in frustration were tested b

50 sphorylation sites across cytoplasmic kinase subdomains and to derive a statistically significant seq

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

52 rivation and several deprivation domains and subdomains) and the 2011 England and Wales census demogr

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

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

55 the secondary structure of the various mucin subdomains, and glycosylation patterns along individual

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

57 folds the locus into several 250- to 400-kb subdomains, and Pax5 further compacts the 2-Mb region th

58 condary structural element in the peripheral subdomain appears to be the key determinant in observed

59 in the PHR is located within the alpha/beta subdomain, approximately 25 A away from the flavin.

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

61 95-144 of RCHY1 and 389-652 of SUD (SUD-NM) subdomains are crucial for interaction.

62 Here, we show how the boundaries of the CB subdomains are established, and thus ascertain the desig

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

64 PIV5-N protomer subdomains are very similar in structure to the previous

65 e at position 374 (HA0 numbering) of the HA2 subdomain as critical for HA trimer stability.

66 recise localization of SNX27 at an endosomal subdomain as well as for recycling of SNX27-retromer car

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

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

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

70 ocesses, we analysed the function of a thumb subdomain beta-hairpin using initiation, elongation and

71 ocesses, we analysed the function of a thumb subdomain beta-hairpin using initiation, elongation, and

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

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

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

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

76 ing of SV40 from BAP31 traps the virus in ER subdomains called foci, which likely serve as depots fro

77 t a closed, right-handed fold with conserved subdomains called palm, fingers and thumb(1,2).

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

79 rent types of neighbouring cells, then these subdomains can become polarised in opposite directions.

80 domain consists of two functionally distinct subdomains, CC1 (amino acids (aa) 414-530) and CC2 (aa 5

81 nsity in three distinct ways: delaying alpha-subdomain compaction, facilitating beta-strand intercala

82 more stable against unfolding than a smaller subdomain comprised of a short alpha-helix and three-str

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

84 2 subdomain is likely an insertion in the P1 subdomain; consequently, the P domain is divided into th

85 erived from the hyperstable villin headpiece subdomain consisting of helices 2 and 3 (HP24).

86 Two subdomains contain tetratricopeptide-like motifs that fo

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

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

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

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

91 red the Snail-family member Escargot and, in subdomains, Decapentaplegic signaling.

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

93 letion, mutation, or replacement by the same subdomain derived from other alphaviruses has strong neg

94 complex architectures composed of different subdomains displaying targeted characteristics.

95 The C-terminal subdomain displays a patch of conserved amino acids and

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

97 A small periplasmic subdomain ((E) FtsN) is required and sufficient for func

98 P dimers might expose immunoreactive S/P1-1 subdomain epitopes.

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

100 f these events was critical; premature alpha-subdomain folding prevented subsequent core formation.

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

102 hymena group I ribozyme, the separated P5abc subdomain folds to local native secondary and tertiary s

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

104 e ER-mitochondria interface, and it contains subdomains for mitochondrial as well as ER localization.

105 lity is the motion of the polymerase fingers subdomain from an open to a closed conformation upon bin

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

107 A small D'-D''-alpha1-alpha2 subdomain grafted on the immunoglobulin-like core of Fae

108 nterface, whereas a large gap between the P1 subdomains had fewer interactions.

109 This subdomain has been previously attributed a role as a put

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

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

112 find that a specific portion of the helical subdomain (HD) of the catalytic domain rapidly unfolds w

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

114 esentation of the animal kingdom ontological subdomain: how the brain represents the perceived threat

115 similarity to the human topoisomerase I core subdomains I and II (30-IXAla, 30-620A, and 30-622A).

116 Additionally, homologous substitutions in subdomains IB and IIB of Ssa1 caused defects in collabor

117 that several variants with substitutions in subdomains IB and IIB of the DnaK NBD were defective in

118 bserved that GrpE, which also interacts with subdomains IB and IIB, inhibited the interaction between

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

120 Subdomain IIA, on the other hand, is distinguished by st

121 Emphasis will be given to the IRES subdomain IIa, which currently is the most advanced targ

122 The DnaK subdomain IIB mutants were also defective in the ability

123 ding site involving four residues located on subdomain III.

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

125 iring interaction between the apical loop of subdomain IIId in the IRES and helix 26 in 18S rRNA.

126 The helical subdomain in dimeric bacteria ASADH is replaced by the c

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

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

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

130 experiments, allowed confident assignment of subdomains in a MACPF pore assembly.

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

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

133 a recognition state-facilitated by different subdomains in monomeric TALE proteins.

134 f the full-length TR pseudoknot and isolated subdomains in Oryzias latipes (Japanese medaka fish), wh

135 nsically much less stable than the other two subdomains in the M region (MII and MIII).

136 lipid rafts have been proposed to be unique subdomains in the plasma membrane that are critical for

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

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

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

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

141 kindlin 3 (K3) chimeras revealed that the F2 subdomain, in particular its C-terminal part, is crucial

142 nd the physicochemical properties of peptide subdomains, including the number and spatial location of

143 h neighboring substructures, indicating that subdomain interactions can stabilize alternative folds o

144 fer intermediate, brings the EIN(alpha/beta) subdomain into close proximity to the C-terminal dimeriz

145 The P2 subdomain is likely an insertion in the P1 subdomain; co

146 A key ciliary subdomain is the transition zone, which lies between bas

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

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

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

150 dures, we provide a structural model for the subdomain-mediated tetramer/tetramer interaction via "cr

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

152 so suggest that the vinculin-binding domain (subdomain MI) is intrinsically much less stable than the

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

154 atalytic prim fold domain, but with a unique subdomain not found in the archaeal and bacterial primas

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

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

157 Mutagenesis studies showed that an extra subdomain of about 12 amino acids contribute to C4 oxida

158 In the fusion subdomain of canine and recent equine virus HAs a unique

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

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

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

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

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

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

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

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

167 The N3 subdomain of FnBPB contains the full plasminogen-binding

168 ction and comprehension) and whether it is a subdomain of general cognitive control.

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

170 ce analysis of the C-terminal part of the F2 subdomain of K3 suggests that insertion of a variable gl

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

172 a potential targeting function of the GAPex subdomain of neurofibromin that is present in all known

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

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

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

176 ntermediate in tertiary folding of the P5abc subdomain of the 'Tetrahymena' group I intron ribozyme.

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

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

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

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

181 is caused by specific interactions between a subdomain of the non-alpha-helical N terminus (residues

182 acts with a novel binding pocket in the palm subdomain of the RdRp and exerts a promising activity ag

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

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

185 ues 403 and 404 (both Asp --> Ala) in the 2B subdomain of UvrD (uvrD303) confers an antimutator and U

186 ata demonstrate that the very amino-terminal subdomain of Venezuelan equine encephalitis virus capsid

187 al development, cells rearrange and when two subdomains of a single cell have different types of neig

188 Subdomains of cognitive function were assessed using the

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

190 b-meta-analyses were conducted in functional subdomains of emotion processing; in cool and hot execut

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

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

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

194 he larval epidermis of Drosophila, different subdomains of one cell can have opposite polarities.

195 ode sequences, which target them to specific subdomains of the cortical endoplasmic reticulum in deve

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

197 e FYVE-containing protein 1 (DFCP1)-positive subdomains of the endoplasmic reticulum (ER), distinct f

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

199 form three-way junctions found in reticular subdomains of the endoplasmic reticulum.

200 domain of FtsA in the cytoplasm and to small subdomains of the FtsB and FtsL proteins in the periplas

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

202 Subdomains of the multicopy ribosomal DNA locus containi

203 energetic and mechanical changes within the subdomains of the nucleotide binding domain (NBD) of the

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

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

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

207 mbinant proteins corresponding to particular subdomains of TspB were found to have human IgG Fcgamma-

208 cytic marker FM4-64 revealed the presence of subdomains on the apical membrane characterized by exten

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

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

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

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

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

214 136 (I136N) and Thr for Ile-142 (I142T) in a subdomain previously named the helical hairpin in the NT

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

216 city of antibodies specific to different NC1 subdomains, rabbit antibodies were generated.

217 sly suggested, and propose that a network of subdomains regulates diverse heterochromatin functions.

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

219 Moreover, deletion of the TPR2 subdomain, required for processivity, impaired primer ex

220 In particular, the subdomain rotation and loop movements, which are believe

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

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

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

224 the very amino-terminal VEEV capsid-specific subdomain SD1 is a critical player in the particle assem

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

226 particle assembly proceeds only when the two subdomains, SD1 and SD2, are derived from the same alpha

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

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

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

230 entify TZ components and localize them to TZ subdomains, showing that the Bardet-Biedl syndrome compl

231 to have arisen through the amplification of subdomain-sized peptides.

232 These subdomain-specific forebrain spheroids can be assembled

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

234 es exist within the RGS homology (RH) bundle subdomain, substrate-binding site, and kinase C-tail.

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

236 iary structural changes in the alpha-helical subdomain suffice to account for the observed conformati

237 catalytic site and a proline-rich C-terminal subdomain suggest that this protein may have a distinct

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

239 s the kinase N-terminal lobe and RH terminal subdomain surfaces are much more basic.

240 The P domain is further subdivided into two subdomains, termed P1 and P2.

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

242 een N-terminal and C-terminal regions of the subdomain that are important in the structural changes r

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

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

245 glycerol from PA, targets a nuclear membrane subdomain that is in contact with growing lipid droplets

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

247 Da CagA protein revealed a stable N-terminal subdomain that was used in a yeast two-hybrid screen tha

248 terobacteriaceae and folds into two distinct subdomains that associate with different parts of the ca

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

250 Cos proteins create discrete endosomal subdomains that concentrate Ub cargo prior to their enve

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

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

253 We report crystal structures of Arc subdomains that form a bi-lobar architecture remarkably

254 as anatomical value for revealing functional subdomains that have not been classified by conventional

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

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

257 scription factor co-associations and genomic subdomains that suggest shared patterns of regulation, a

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

259 Here, we show that the distal-most of these subdomains, the distal cap, is marked by expression of t

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

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

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

263 terminal domain alpha/beta (EIN(alpha/beta)) subdomain to the downstream protein partner bound to the

264 h precise laser microdissections of meristem subdomains to define the molecular signatures of anatomi

265 ngs define the contribution of the three CTD subdomains to the DNA replication activity of E1 in vivo

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

267 These two subdomains together appear to form the central core of V

268 mulations, the reorientation of the MII/MIII subdomains under force may constitute an initial step al

269 r is highly atypical, having a discontinuous subdomain unrelated to a WD40 motif in place of one of i

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

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

272 volved stabilizing the modified MBP and OspA subdomains via external interactions with neighboring su

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

274 We showed that the P2 subdomain was mainly involved in the homodimeric interfa

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

276 Antibodies against two of these subdomains were injected into mice carrying null mutatio

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

278 tes ankyrin-G accumulation in distinct spine subdomains, where it differentially regulates NMDA recep

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

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

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

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

283 s twofold pseudo-symmetric with two globular subdomains, which are structurally similar but functiona

284 RT induces opening of the fingers and thumb subdomains, which increases the dynamic sliding motion o

285 A mushroom body subdomain whose development or function require the tran

286 a sharing is non-uniform across neuroscience subdomains, widespread adoption of data sharing practice

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

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 approach, we engineered the sequences of one subdomain within maltose binding protein (MBP, alpha/bet

292 s/Fat system; we show that the polarity of a subdomain within one cell is its response to levels of D

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

294 ensive molecular signatures for the distinct subdomains within AC-type SAMs, an anatomical anomaly wh

295 eld contact network model reveals functional subdomains within RyR2 clusters with distinct sensitivit

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

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 ozyme's primary amino acid sequence revealed subdomains within the protein that operate either as an

300 These data define the cap and shoulder as subdomains within the repair complex accumulating distin