ライフサイエンスコーパス: terminal region

1 mediating the local unfolding of the Mad2 C-terminal region.

2 m the presence of an acidic residue at its N-terminal region.

3 state, with structure apparent only in the C-terminal region.

4 nding protein C (cMyBP-C), focusing on the N-terminal region.

5 reported functional regulation of the p53 C-terminal region.

6 ucture of a stable domain (CHD4-N) in this N-terminal region.

7 gion and residues 30-36 (AIIGLMV) from the C-terminal region.

8 tivity, and a functionally uncharacterized N-terminal region.

9 gions of Abeta: the central region and the C-terminal region.

10 gesting enhanced local cleavage of the CgA C-terminal region.

11 ease domain, but instead binds to the EsaD N-terminal region.

12 ion-permeation properties are conferred by C-terminal region.

13 against Plasmodium should include the CSP N-terminal region.

14 of the amino acid changes occurring in the C-terminal region.

15 nt segment (positions 61-67) in the FLIL33 N-terminal region.

16 ecifically at the chromatin via its carboxyl-terminal region.

17 or, CdiA delivers a toxin derived from its C-terminal region.

18 cb1 and Lhcb2 can be phosphorylated in the N-terminal region.

19 cting on different receptors within the same terminal region.

20 e domain at the C terminus and an extended N-terminal region.

21 n range, and are partly conferred by WRN's C-terminal region.

22 emely transient helices are present in the N-terminal region.

23 function for other amino acids within this C-terminal region.

24 -binding sequence (CBS) located within its C-terminal region.

25 conserved cysteine residues located in the C-terminal region.

26 mental evidence of O-linked glycans in the N-terminal region.

27 more prominent in the most distal axons and terminal regions.

28 was likely affected by its N-terminal and C-terminal regions.

29 nt dynamic interactions involving loop and C-terminal regions.

30 heterogeneity arises due to variation in the terminal regions.

31 ing a catalytic domain and extended N- and C-terminal regions.

32 th Titin truncations in the N-terminal and C-terminal regions.

33 domain (DUF583) that is flanked by variable terminal regions.

34 re involved in RAD51 interaction via their C-terminal regions.

35 e-binding domains were mapped within their N-terminal regions.

36 male mouse dopaminergic somatodendritic and terminal regions.

37 Among the basic amino acids in the PA-X C-terminal region, 3 residues, 195K, 198K, and 199R, were

38 ts the nucleus to the cytoskeleton via its N-terminal region [5-7].

39 ta8.1, 8.2(+) immune T cells recognize the N-terminal region (aa 41-152) of dense granule protein 6 (

40 present study, we identified a NiV-G stalk C-terminal region (amino acids 159 to 163) that is importa

41 ensor that detects RNA viruses through its C-terminal region and activates the production of antivira

42 of two monomers that each contain a folded N-terminal region and an intrinsically disordered C-termin

43 Hsc70 dynamically associated with the N-terminal region and Rac1 GEF domain of Trio.

44 form higher-order oligomers through their N-terminal region and that the same AT-rich site is recogn

45 BP3 to chromatin depends on both its C and N terminal regions and is affected by the cell cycle and p

46 n constructed two deletion mutants lacking C-terminal regions and mutants with point mutations of two

47 tive groups of hnRNP proteins, through its N-terminal region, and directly regulates pre-mRNA splicin

48 hanges that affect the solvent exposure of N-terminal region, and hence the redox sensitivity of the

49 f PINK1, including the architecture of the C-terminal region, and reveals how the N lobe of PINK1 bin

50 to ECL2 established the importance of its C-terminal region, and site-directed mutagenesis of each n

51 olecular rationale for the function of the N-terminal region, and support the idea that Cerberus coul

52 ng truncated MeCP2 lacking both the N- and C-terminal regions (approximately half of the native prote

53 abolites (most likely depending on the amino-terminal region around the highly conserved cysteine res

54 mediated cleavage mechanism, featuring the N-terminal region as an anchor for at least one of the DNA

55 activation required not only the conserved N-terminal region but also permissive communication of the

56 protein that may be cleaved in vivo at the N-terminal region by neutrophil proteases including elasta

57 inear extension of the filament, while the N-terminal region can serve as a branch-point.

58 ed rates of MT polymerization, whereas the N-terminal region cannot bind to MT plus ends but can act

59 the presence of two conserved regions: an N-terminal region codifying for signal peptide and a C-ter

60 lographic structure of the Arabidopsis TPL N-terminal region comprising the LisH and CTLH (C-terminal

61 We also show that the N-terminal region, conserved across all group 4 LEA protei

62 hancement of fragmentation near the N- and C-terminal regions consistent with slight fraying.

63 angiosperms and possess a highly conserved C-terminal region containing linear motifs (CKII-acidic, L

64 This analysis also revealed that the C-terminal region contains a previously unrecognized WRDPL

65 Here, we demonstrate that this N-terminal region contains a ubiquitin (Ub)-associated (UB

66 The C-terminal region contains the catalytic glucosyltransfera

67 MBS (localized within and adjacent to the C-terminal region) contributing to the dimer-dimer interac

68 ed splice-site mutation that truncates the C-terminal region (CTR) domain of RELN protein and display

69 A new Reln mutant with a truncation of the C-terminal region (CTR) domain shows that Reln mutation ca

70 inhibits the RNA chaperone activity of the C-terminal region (CTR) of Gag-p45.

71 hibits shifts in cytoplasmic loops and the C-terminal region (CTR) to occlude the cytoplasmic exit of

72 hermore, we found that deletion of the F1L N-terminal region does not impede F1L antiapoptotic activi

73 By contrast, a mutation in the whirlin C-terminal region eliminated all normal whirlin isoforms b

74 fting that often results in synthesis of a C-terminal region encoded by a new frame.

75 leucine-rich repeats (LRRs) and having an N-terminal region enriched in alternating lysine and gluta

76 ies are indirectly regulated by the N- and C-terminal regions flanking the FH1-FH2 domains.

77 The amino-terminal region forms a tight dimerization domain with a

78 n TRP structures, together with the carboxyl-terminal region, forms a large two-layered cytosolic rin

79 We demonstrate here that a yeast-specific C-terminal region from Pat1 interacts with several short m

80 CYP1A2, containing the N-terminal regions from CYP1A1, no longer localized in ord

81 clear localization of PA-X mediated by its C-terminal region has a significant impact on shutoff acti

82 ase and methyltransferase (MTase), and the C-terminal region has the polymerase (POL), all of which a

83 SAAS (named after four residues in the amino terminal region) has many attractive properties.

84 ith deletion of residues 338 to 347 in the C-terminal region, has been an enigma, because the basis f

85 opy assays indicated that the Rec10 N- and C-terminal regions have complex interactions with Rec25.

86 ement of RNA-binding sites, although these N-terminal regions have only limited sequence conservation

87 se R, whereas the Walker B motif is in its N-terminal region implying that the two parts of the prote

88 regulate DNA-damage responses through its N-terminal region in a poly(ADP-ribose) polymerase-depende

89 monstrate that the established role of the N-terminal region in dimerization is not conserved; instea

90 at both mutations lead to unfolding of the C-terminal region in the t-SNARE complex.

91 To ensure helical C-terminal regions in the truncated peptides, we produced

92 Both the N- and C-terminal regions inhibited viral RNA replication.

93 lded side of the main barrier in which the N-terminal region is disordered.

94 kinase-mediated phosphorylation within the C-terminal region is inhibitory and regulates catalytic ac

95 zation, it has also been reported that the C-terminal region is involved in p130Cas FA targeting.

96 The C-terminal region is required for CofB to initiate pilus a

97 onserved membrane-proximal amino-terminal (N-terminal) region, is distinct from other lipid-activated

98 cterial orthologs because of an additional C-terminal region, known as domain B.

99 imers linked to DNA-PKcs via flexible Ku80 C-terminal regions (Ku80CTR) in a complex stabilized throu

100 best-scoring receptor structures have the N-terminal region lid region bound in a helical conformati

101 hannel that otherwise binds ppGpp, and its N-terminal region, like the coiled-coil tip of DksA, engag

102 against hydrogen/deuterium exchange in the C-terminal region near the N-glycan sites, suggesting this

103 of an auto-regulatory motif, AutoN, in the N-terminal region (NTR) of ISWI, indicating that AutoN doe

104 netic techniques to show that the myosin-I N-terminal region (NTR) plays a critical role in tuning my

105 e shows the stalk region and the essential N-terminal region (NTR) previously unseen in our DNA unbou

106 vealed that PA2588 has a novel fold at the N-terminal region (NTR), and its C-terminal HTH (helix-tur

107 a central Trp-Gly-Arg (WGR) domain and an N-terminal region (NTR).

108 spliced isoforms, differing only in their N-terminal regions (NTRs).

109 (NoLS) localization signals near the carboxy-terminal region of AAP2 (amino acid positions 144 to 184

110 serine 8 causes structural changes in the N-terminal region of Abeta aggregates in favor of less com

111 d other biological events that involve the N-terminal region of Abeta aggregates.

112 beta and residues 30-36 (AIIGLMV) from the C-terminal region of Abeta assemble to form homotetramers

113 deling revealed that two residues near the N-terminal region of alpha-helix 1 in GPPrP might mediate

114 Moreover, we showed that the N-terminal region of alpha-syn is important for PLK2-media

115 Glycation affected primarily the N-terminal region of alpha-synuclein, reducing membrane bi

116 In yeast and humans, the unstructured C-terminal region of alpha7 contains an acidic patch with

117 ns to refine structure and topology of the N-terminal region of alphaS bound to the surface of synapt

118 Thus, an NH2-terminal region of approximately 30 amino acids of Swi1

119 ate the interaction between the disordered C-terminal region of Artemis and the DNA binding domain of

120 We used a peptide of the carboxyl-terminal region of AtABP1 as a tool.

121 ATXN7L3B shares 74% identity with the N-terminal region of ATXN7L3, but the functions of ATXN7L3

122 structural pocket proximal to S184 in the C-terminal region of Bax, directly activating its proapopt

123 238, which specifically interacts with the N-terminal region of BB0323.

124 Replacing the C-terminal region of beta-arrestin-1 with its counterpart

125 es identified phosphorylation sites in the C-terminal region of BRM at SnRK2 target sites that are ev

126 The N-terminal region of BubR1 binds to both Cdc20 and Mad2, t

127 ing question concerns the structure of the C-terminal region of CA and the peptide SP1 (CA-SP1), whic

128 y binding of the Hsp90 middle domain to an N-terminal region of Caenorhabditis elegans Cdc37 (CeCdc37

129 The C-terminal region of capsid (CA) and the p2 region of Pr55

130 We further identified a conserved N-terminal region of CDH23-C that binds to the CKK domain.

131 We also show that the N-terminal region of CHD4, although not CHD4-N alone, is e

132 tor CBP by masking its binding site in the C-terminal region of Ci.

133 ed and conserved Sufu-binding motif in the C-terminal region of Ci/Gli and provides mechanistic insig

134 CDI(+) bacteria deliver the toxic C-terminal region of contact-dependent inhibition A protei

135 a structural description of the Fn binding N-terminal region of CshA, derived from a combination of X

136 ional analysis predicted that the extended N-terminal region of CYP144A1-FLV is largely unstructured.

137 es showed the existence of epitopes in the C-terminal region of DENV nonstructural protein 1 (NS1) wh

138 mAb designated 2E8 does not recognize the C-terminal region of DENV NS1 in which host-cross-reactive

139 otentially harmful events, we replaced the C-terminal region of DENV NS1 with the corresponding regio

140 The N-terminal region of DNA-binding domain of STAT3 is respon

141 The C-terminal region of DP2 contains two conserved cysteine c

142 nd structural approaches, we find that the C-terminal region of DRC2 is critical for the coassembly o

143 n at Y102 disrupts the helical fold of the N-terminal region of E2 and its interaction with key cellu

144 Tau and EBs form a complex via the C-terminal region of EBs and the microtubule-binding sites

145 In this study, we discovered that the N-terminal region of Efb (Efb-N) promotes platelet binding

146 non-synonymous substitution (A120G) in the N-terminal region of eIF2Bbeta was responsible for the TuM

147 In contrast, the C-terminal region of Ets-1, including its Pointed (PNT) do

148 played by a stretch of 17 residues in the N-terminal region of EZH2, we call the activation loop, in

149 Lsm11, in addition to interacting with the N-terminal region of FLASH, also contacts the C-terminal S

150 Thus, the N-terminal region of FMDV 3D that acts as a nuclear locali

151 ich efficiently competes with ZipA for the C-terminal region of FtsZ, a central hub for multiple inte

152 sugar modifications and revealed that the C-terminal region of FUS is sufficient to retain ASOs in c

153 t of an amphipathic alpha-helix within the C-terminal region of GobX.

154 characterization of the previously unknown N-terminal region of HAI-1, we provide new insight into th

155 The C-terminal region of HELLP, HELLP(215-278), encompassing t

156 n E3 ubiquitin ligase, interacted with the C-terminal region of HSPA5 and mediated HSPA5 ubiquitinati

157 Here, we present the structure of the N-terminal region of human BCAP and show that it possesses

158 gical missense variants cluster in the amino-terminal region of human BCL11A, and we demonstrate that

159 in the endoplasmic reticulum (ER) via the N-terminal region of human invariant chain p33, with or wi

160 be important for biological activity: the N-terminal region of human neuropeptide Y (NPY1-9, Tyr(1)-

161 An amino-terminal region of LifA shares homology with the catalyt

162 noprecipitated the recombinantly expressed N-terminal region of LRP2.

163 ulated in a strain lacking only the unique C-terminal region of MceG, suggesting an important functio

164 ctors (eIF) 2, 3, 1 and 1A, attach to the 5'-terminal region of messenger RNA and scan along it to th

165 ds via its substrate-binding domain to the C-terminal region of MRTF-A and that CCTepsilon is able to

166 We have identified a C-terminal region of MTBP (the CTM domain) that binds effi

167 TFAM tethers the N-terminal region of mtRNAP to recruit the polymerase to t

168 ure of MtTOP1 by first predicting that the C-terminal region of MtTOP1 contains four repeated domains

169 harp contrast, recombinant proteins of the N-terminal region of MUC5B (D1-D2-D'-D3 domains, NT5B), C-

170 gion of MUC5B (D1-D2-D'-D3 domains, NT5B), C-terminal region of MUC5B (D4-B-C-CK domains, CT5B) and t

171 The N-terminal region of Ndfip1 binds to UbcH7, whereas the PY

172 oteolytic product p22-FLIP all require the C-terminal region of NEMO/IKKgamma (amino acids 272-419) a

173 allow pocket adjacent to the groove in the N-terminal region of NHR trimer as a new drug target, and

174 dicates that dramatic rearrangement of the C-terminal region of Nop15 in the pre-ribosome exposes the

175 n is mediated by the J domain of Hsp40 and N-terminal region of NP.

176 nded alpha-helix from the disordered carboxy-terminal region of nucleoprotein-core links nucleoprotei

177 The C-terminal region of p130Cas or Cas family homology domain

178 ll-length p17 demonstrating that the final C-terminal region of p17 is irrelevant for the protein's b

179 its binding to specific regions within the C-terminal region of PRG-2.

180 cleaved eight amino acid residues from the N-terminal region of Prx1 inside the matrix, without inter

181 binding to polar residues in the conserved N-terminal region of PulG, we propose that PulM acts as ch

182 In addition, the C-terminal region of Redbeta corresponding to residues 182

183 he central part of M-Tha, and the specific C-terminal region of RelAp43 are required for this interac

184 The interaction occurred through the C-terminal region of RING1B (C-RING1B), with an affinity i

185 ngly, the Walker A motif is located in the C-terminal region of RNase R, whereas the Walker B motif i

186 The long N-terminal region of RTN3 contains several newly identifie

187 Scc2 binds to Scc1 through an N-terminal region of Scc1 that overlaps with its Pds5-bind

188 We determined that the amino-terminal region of SidE was essential for SidJ-mediated

189 hat links the activity of SidJ and the amino-terminal region of SidE, which is required to modulate t

190 We demonstrated that the glycine-rich N-terminal region of SPS is crucial for the SelA-tRNA(Sec)

191 We found that the C-terminal region of Spt16 binds specifically to the histo

192 Expression of the N-terminal region of SS4 alone did not alter the ss4 mutan

193 Expression of the C-terminal region of SS4 alone increased granule initiatio

194 Interestingly, the N-terminal region of SS4 alone or when fused to GS conferr

195 d versions of SS4 and a fusion between the N-terminal region of SS4 and GS in the Arabidopsis ss4 mut

196 The N-terminal region of SS4 is unique among SS isoforms and c

197 Remarkably, fusion of the N-terminal region of SS4 to A. tumefaciens GS restored the

198 re-function analysis demonstrates that the C-terminal region of TACC2 is both necessary and sufficien

199 n mutants, we further demonstrate that the N-terminal region of TALEs is required for the initial non

200 The C-terminal region of TDP-43 was required for this function

201 Here we mapped this interaction to the NH2-terminal region of the APP intracellular domain.

202 ptide-binding domain located at the carboxyl-terminal region of the avian HSPA2.

203 tween the PTEN C-tail and a segment in the N-terminal region of the catalytic domain.

204 ed in eukaryotic cells, the TMH-containing N-terminal region of the CbuD1884 protein trafficked to th

205 observed that HCV1, a bNAb recognizing the N-terminal region of the CD81bs, bound a soluble E2 core c

206 MORF-MORF protein connections require the C-terminal region of the central conserved MORF box.

207 s proposed to be its active state, but the C-terminal region of the enzyme adopts a distinct conforma

208 rinogen induced a structural change in the C-terminal region of the fibrinogen beta-chain (beta384-39

209 The N-terminal region of the foot-and-mouth disease virus (FMD

210 f six SN-HPCs for mutations within the amino-terminal region of the gene CTNNB1 (cadherin-associated

211 we identified a distinct domain within the N-terminal region of the HSP-16.48 protein that specified

212 Here we show that the C-terminal region of the HSV-1 pUL25 protein is required f

213 ggered by a polyglutamine expansion in the N-terminal region of the huntingtin (HTT) protein.

214 caused by a polyglutamine expansion in the N-terminal region of the huntingtin protein (N17).

215 The IP6 binding site is located within the C-terminal region of the Ino80 subunit.

216 Additionally, the C-terminal region of the linker forms previously unreporte

217 Y domain of ATR1, partially specified by a C-terminal region of the LRR domain.

218 ng the parasite's hepatic replication, the C-terminal region of the parasitic PV membrane protein exp

219 The C-terminal region of the protein contains a predicted Dot/

220 y a polyglutamine (polyQ) expansion in the N-terminal region of the protein huntingtin (HTT).

221 the presence of distinct insertions at the C-terminal region of the protein responsible for a structu

222 atic interaction of the positively charged C-terminal region of the protein with a negatively charged

223 O homooligomerization, mediated by the amino-terminal region of the protein, and carboxyl-terminal ta

224 on affecting structural aspects of the amino-terminal region of the protein, and support the concept

225 mediated by the coiled-coil domain at the N-terminal region of the protein.

226 s this activity even in the absence of the N-terminal region of the protein.

227 ed to occur via the product binding to the N-terminal region of the protein.

228 cultured cells, primarily mediated by the N-terminal region of the protein.

229 the RNA-binding motif 2 interact with the N-terminal region of the RS domain (RS1).

230 dy, we found that a 197-aa deletion in the N-terminal region of the S protein did not alter virus (TC

231 s enhanced by the presence of the unfolded N-terminal region of the sequence and by destabilization o

232 .0015, and 0.0023, respectively), in the Ch5 terminal region of the thalamus (P = 0.0003), and in the

233 gG that targets amino acid residues in the C-terminal region of the V3 loop crown, suggesting the imp

234 the potentially protective response in the C-terminal region of the V3 loop crown.

235 in the juxtaposition of the less ordered, N-terminal region of their capsid proteins, VP1/2/3.

236 An unstructured N-terminal region of Tim10 is necessary and sufficient to

237 ex activity, likely through binding to the C-terminal region of Tim44.

238 actions of the central part of Tm with the C-terminal region of TnI.

239 Our results show that the C-terminal region of TPX2 regulates Kif15 in vitro, contri

240 erved catalytic site was identified in the C-terminal region of TRP120, and TRP120 autoubiquitination

241 dies, we identified a critical role of the N-terminal region of UBXD1 (UBXD1-N).

242 cyclin F-specific amino acid motif in the C-terminal region of Vif indicated rescue of the protein f

243 The N-terminal region of vIRF-1 interacts directly with membra

244 In addition, we show that the N-terminal region of WNK1 binds to the UV radiation resist

245 ine-rich motifs (HLMs), spread in the long C-terminal region of yeast Dcp2 decapping enzyme.

246 These studies show that the central and C-terminal regions of Abeta can preferentially segregate w

247 lized trimers derived from the central and C-terminal regions of Abeta.

248 rmolecular interactions between the N- and C-terminal regions of alpha-syn play critical roles in med

249 amolecular interactions between the N- and C-terminal regions of alpha-Syn, resulting in the protein

250 (2+) binding allosterically destabilizes the terminal regions of C2alpha and thereby facilitates the

251 llisecond-timescale dynamics of the N- and C-terminal regions of C2alpha.

252 Cleavage of the N- and C-terminal regions of circulating chromogranin A (CgA, CHG

253 he FG/GLFG region of Nup98 binds to N- and C-terminal regions of DHX9 in an RNA facilitated manner.

254 t are localized within and adjacent to the C-terminal regions of each homodimer.

255 the presence of RNA structures within the N-terminal regions of its coding sequences.

256 ays showed that the 5' and YSS-containing 3' terminal regions of LCV RNA1 supported translation activ

257 The N- and C-terminal regions of MlcC make critical contacts that con

258 Amino-terminal regions of secretin-family peptides contain key

259 estigated the specific roles of the N- and C-terminal regions of SS4 by expressing truncated versions

260 patients were significantly lower in the Ch4 terminal regions of the anterior cingulate cortex and th

261 y of peptides derived from the central and C-terminal regions of the beta-amyloid peptide (Abeta).

262 tudy the insertion capacity of hydrophobic C-terminal regions of the BH3-only proteins Bik, Bim, Noxa

263 ntified a Y-shaped structure (YSS) in the 3' terminal regions of the bipartite genome of Lettuce chlo

264 electrophoretic mobility originate in the C-terminal regions of the gamma-tubulins.

265 The 5'- and 3'-terminal regions of the genome were determined by rapid

266 e of the JCI, Xu et al. show that specific C-terminal regions of the MOR can modulate side effects wi

267 ing it contact the N-terminal, middle, and C-terminal regions of the peptide.

268 Through manipulation of the C-terminal regions of these proteins we show the SPKTG mot

269 The N-terminal region ofSdGluc5_26A protrudes into the active

270 Although the extended transmembrane Orai N-terminal region (Orai1 amino acids 73-91; Orai3 amino ac

271 NuMA localization to minus-ends involves a C-terminal region outside NuMA's canonical microtubule-bin

272 Three basic residues at the C-terminal region play a critical role in nuclear localiza

273 t the first 15 residues of the PA-X unique C-terminal region play a critical role in shutoff activity

274 e results confirm the influential roles of N-terminal region (positions 7 and 8) and the loop 40-60 (

275 The NH2-terminal region (residues 1-543) of the cardiac ryanodin

276 g CyRPA and RIPR, and contains a conserved N-terminal region (RH5Nt) of unknown function that is clea

277 because it did not seem to contain a RecQ C-terminal region (RQC) found in the other RecQ paralogues

278 has a highly disordered conformation, its N-terminal region shows resonance broadening consistent wi

279 ine A3 receptor (A3AR) having an identical N-terminal region shows similar biological profiles to TMI

280 studies showed the alpha-actinin-4 carboxyl-terminal region specifically interacted with the NHERF1

281 formation of an AcAS-Cu(I) complex at the N-terminal region stabilizes local conformations with alph

282 midbrain DA cells and promotes DA release in terminal regions such as the nucleus accumbens (NAc).

283 ut not isoform3 (i3) which shares a common C-terminal region, suppresses these malignant properties.

284 CH1 to bind actin aided by an unstructured N-terminal region that becomes alpha-helical upon binding.

285 a stretch of hydrophobic residues from the C-terminal region that form a hydrophobic cleft, an adjace

286 CMV fusion factor has a Cys residue in the C-terminal region that is palmitoylated and mediates methy

287 In particular, it includes an extra C-terminal region that is part of the acceptor binding sit

288 ds on the presence of a basic unstructured N-terminal region that tethers SpaI to the membrane.

289 nhibitors that act by cleaving the Wnt amino-terminal region to inactivate specific Wnt ligands.

290 , yet two-state folding and binding of the N-terminal region to the p53 receptor site.

291 GAP domain, induces strong binding of that N-terminal region to the RhoGAP domain, converting DLC1 fr

292 Here, we first show that the RIG-I C-terminal region undergoes deacetylation to regulate its

293 Solution analysis of the F1L N-terminal regions using small angle x-ray scattering indi

294 e in vivo and in vitro, whereas a separate C-terminal region was required for Sstn localization to fu

295 In contrast, the C-terminal region, which contains a putative DNA-binding d

296 as RNA methyltransferase activities at its N-terminal region, which is responsible for capping the vi

297 s detected using mAbs against the head and C-terminal regions, which are widely separated in the tert

298 ons, an extended 38-amino acid-long unique N-terminal region with still unknown functions.

299 showed that replacement of the pre-TM1 amino-terminal region with the corresponding P2X2 receptor sec

300 mide shifts are localized mostly to N- and C-terminal regions within the rigid beta structure in the