ライフサイエンスコーパス: C-terminal region

1 t ion-permeation properties are conferred by C-terminal region.

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

3 ptor, CdiA delivers a toxin derived from its C-terminal region.

4 ion range, and are partly conferred by WRN's C-terminal region.

5 nding site to the conformationally malleable C-terminal region.

6 ontains a tryptophan-rich (TR) domain in the C-terminal region.

7 ng at the N terminus propagates to the ATP7B C-terminal region.

8 bohydrate binding module (CBM) followed by a C-terminal region.

9 E activation within the switch regions and a C-terminal region.

10 to force owing to the high stability of the C-terminal region.

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

12 of MBD1-c but HDAC3 preferably bound to the C-terminal region.

13 causes an increase of the flexibility of the C-terminal region.

14 n the N-terminal region and the other in the C-terminal region.

15 posure of a hydrophobic motif located at the C-terminal region.

16 ys similarities to gp18-like proteins in its C-terminal region.

17 ich Sec insertion is normally limited to the C-terminal region.

18 mains, a DNA-binding homeodomain (HD), and a C-terminal region.

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

20 o conserved cysteine residues located in the C-terminal region.

21 gh mediating the local unfolding of the Mad2 C-terminal region.

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

23 he reported functional regulation of the p53 C-terminal region.

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

25 regions of Abeta: the central region and the C-terminal region.

26 uggesting enhanced local cleavage of the CgA C-terminal region.

27 rming a catalytic domain and extended N- and C-terminal regions.

28 with Titin truncations in the N-terminal and C-terminal regions.

29 are involved in RAD51 interaction via their C-terminal regions.

30 BC-ATPase fold embedded between novel N- and C-terminal regions.

31 ger composite NC domain formed by the N- and C-terminal regions.

32 erwise highly divergent nature of the N- and C-terminal regions.

33 n complex with a segment of their respective C-terminal regions.

34 N-terminal domain of sigma(B) via its N- and C-terminal regions.

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

36 rent dynamic interactions involving loop and C-terminal regions.

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

38 ays a previously unrecognized element in its C-terminal region, a 'gatekeeper' helix, which extends o

39 In the Ca(2+)/NCS-1.D2R peptide complex, the C-terminal region adopts a 310 helix-turn-310 helix, whe

40 In addition, the C-terminal region alone induces vacuolization in a manne

41 Deletion of the C-terminal region also creates a hyperactive SMARCAL1 pr

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

43 sensor that detects RNA viruses through its C-terminal region and activates the production of antivi

44 Rather, EGCG immobilizes the C-terminal region and moderately reduces the degree of b

45 hen constructed two deletion mutants lacking C-terminal regions and mutants with point mutations of t

46 unique arrangement of the CBS domains in the C-terminal region, and propose how they interact with th

47 of PINK1, including the architecture of the C-terminal region, and reveals how the N lobe of PINK1 b

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

49 AF2 binds to multiple motifs within the TAF8 C-terminal region, and these interactions dictate TAF2 i

50 , palm, and thumb subdomains), a hydrophobic C-terminal region, and two magnesium ions coordinated in

51 All mutants contained the essential N- and C-terminal regions, and as expected, all maintained the

52 wo Plus-C proteins localizes in their N- and C-terminal regions, and their concerted conformational c

53 sing truncated MeCP2 lacking both the N- and C-terminal regions (approximately half of the native pro

54 ent selection pressures acting on the N- and C-terminal regions are consistent with their protein str

55 ed type-III effector AvrRps4; however, their C-terminal regions are dissimilar, indicating that they

56 ia the IgA-binding region but rather via the C-terminal region, as demonstrated by flow cytometry.

57 r report the crystal structure of the MMADHC C-terminal region at 2.2 A resolution, revealing a modif

58 ates of Cdk5, which phosphorylates it in its C-terminal region at Ser(549) (site 6) and Ser(551) (sit

59 y a globular head at the apex and a globular C-terminal region at the base.

60 ues in the vicinity of the pocket and in the C-terminal region at the dimeric interface exhibits pert

61 to attach to mitotic chromosomes, while the C-terminal region binds TR DNA and also associates with

62 1-mediated retroviral silencing requires the C-terminal region, but not the enzymatic activity, of th

63 -607 and SmgGDS-558 directly bind the GTPase C-terminal region, but the specificity of the SmgGDS spl

64 The USP7 C-terminal region (C-USP7) contains five ubiquitin-like

65 putative transmembrane domain [TM], and the C-terminal region [C]) were obtained commercially and va

66 inal half of the MHD1 with the corresponding C-terminal region can bind to syntaxin-1.

67 epsin B cleaved chemokines especially in the C-terminal region, cathepsins K, L, and S cleaved chemok

68 nnan-binding lectin (MBL) likely through its C-terminal region (CCP22-30).

69 cteria and delivers a toxin derived from its C-terminal region (CdiA-CT).

70 and delivers a toxin domain derived from its C-terminal region (CdiA-CT).

71 ion to binding to the thick filament via its C-terminal region, cMyBP-C can also interact with actin

72 NX1a has unique functions due to its lack of C-terminal regions common to RUNX1b and c.

73 f low complexity and unknown function, and a C-terminal region composed of five SH3b peptidoglycan (P

74 ealing a pilin-like protein with an extended C-terminal region composed of two discrete domains conne

75 enhancement of fragmentation near the N- and C-terminal regions consistent with slight fraying.

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

77 This analysis also revealed that the C-terminal region contains a previously unrecognized WRD

78 The C-terminal region contains the catalytic glucosyltransfe

79 CC MBS (localized within and adjacent to the C-terminal region) contributing to the dimer-dimer inter

80 uced splice-site mutation that truncates the C-terminal region (CTR) domain of RELN protein and displ

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

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

83 Here we show that the acetylation of the C-terminal region (CTR) of S6K1 blocks mTORC1-dependent

84 exhibits shifts in cytoplasmic loops and the C-terminal region (CTR) to occlude the cytoplasmic exit

85 of commonality in the function of the N- and C-terminal regions during the mechanochemical cycle of a

86 horylation of Ngn2 occurs in both the N- and C-terminal regions, either side of the conserved basic H

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

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

89 In contrast, TIR2, located at the C-terminal region encompassing the PH domain, decreases

90 ctivity and generated fragments (lacking the C-terminal region) endowed of potent proangiogenic activ

91 odel of 13 transmembrane helices and a large C-terminal region exposed to the periplasm.

92 However, the realization that the N- and C- terminal regions flanking the repeats play essential

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

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

95 lar dichroism of the isolated CBM, and a CBM-C-terminal region fusion revealed folded domains dominat

96 tutions in the conserved helix alpha6 of the C-terminal region generated Spx substrates that were deg

97 The present article shows that the WDR62 C-terminal region harbors a novel dimerization domain co

98 This C-terminal region harbors several protein-protein intera

99 nuclear localization of PA-X mediated by its C-terminal region has a significant impact on shutoff ac

100 erase and methyltransferase (MTase), and the C-terminal region has the polymerase (POL), all of which

101 with deletion of residues 338 to 347 in the C-terminal region, has been an enigma, because the basis

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

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

104 To ensure helical C-terminal regions in the truncated peptides, we produce

105 ed on the crystal structures of the p25 (p35 C-terminal region including AD)-Cdk5 complex, we simulat

106 has some severing activity, addition of the C-terminal region increases severing potency by 40-fold,

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

108 nt forms an intricate closed ring, while the C-terminal region is a more regular, superhelical struct

109 a mouse model in which the entire Ub-binding C-terminal region is deleted (Optn(470T)).

110 We propose that the flexible nature of the C-terminal region is essential to allow it to modulate i

111 h kinase-mediated phosphorylation within the C-terminal region is inhibitory and regulates catalytic

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

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

114 bacterial orthologs because of an additional C-terminal region, known as domain B.

115 odimers linked to DNA-PKcs via flexible Ku80 C-terminal regions (Ku80CTR) in a complex stabilized thr

116 of nucleocapsid borne NP and display of the C-terminal region likely serves as a bountiful affinity

117 n against hydrogen/deuterium exchange in the C-terminal region near the N-glycan sites, suggesting th

118 The C-terminal region of a truncated LcrG (residues 52-73) s

119 Abeta and residues 30-36 (AIIGLMV) from the C-terminal region of Abeta assemble to form homotetramer

120 Deletion of the C-terminal region of ABI5 or substituting lysine 344 for

121 By interacting directly with the C-terminal region of activation-induced cytidine deamina

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

123 e increased conformational distortion at the C-terminal region of alphaF helix containing 110-114 res

124 igate the interaction between the disordered C-terminal region of Artemis and the DNA binding domain

125 motif (proteolytic signal) is located at the C-terminal region of AtWRI1(IDR) (3).

126 a sequence stretch of 250 amino acids in the C-terminal region of BAG-6 (BAG-6(686-936)).

127 he structural pocket proximal to S184 in the C-terminal region of Bax, directly activating its proapo

128 Replacing the C-terminal region of beta-arrestin-1 with its counterpar

129 from synthetic peptides corresponding to the C-terminal region of beta3-tubulin, whereas cytosolic ca

130 dies identified phosphorylation sites in the C-terminal region of BRM at SnRK2 target sites that are

131 hat the barrel partially opens, allowing the C-terminal region of BSSalpha that houses the glycyl rad

132 MAD-1 coiled-coil segment interacted with a C-terminal region of BUB-1 that contains its kinase doma

133 nding question concerns the structure of the C-terminal region of CA and the peptide SP1 (CA-SP1), wh

134 The C-terminal region of capsid (CA) and the p2 region of Pr

135 -binding homeodomain) we discovered that the C-terminal region of Caudal contributes to the preferent

136 vator CBP by masking its binding site in the C-terminal region of Ci.

137 fied and conserved Sufu-binding motif in the C-terminal region of Ci/Gli and provides mechanistic ins

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

139 The C-terminal region of CPEB may participate in assembly of

140 Thus, the C-terminal region of Dcx dynamically regulates formation

141 dies showed the existence of epitopes in the C-terminal region of DENV nonstructural protein 1 (NS1)

142 ne mAb designated 2E8 does not recognize the C-terminal region of DENV NS1 in which host-cross-reacti

143 potentially harmful events, we replaced the C-terminal region of DENV NS1 with the corresponding reg

144 p C, comprising a single mutation within the C-terminal region of domain II.

145 The C-terminal region of DP2 contains two conserved cysteine

146 and structural approaches, we find that the C-terminal region of DRC2 is critical for the coassembly

147 Tau and EBs form a complex via the C-terminal region of EBs and the microtubule-binding sit

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

149 The C-terminal region of Fen was necessary for interaction w

150 ance and suggests that this highly conserved C-terminal region of ferlins represents a functionally s

151 ight conserved motifs were identified in the C-terminal region of fish and frog proteins.

152 The C-terminal region of FLASH contains a highly conserved d

153 was identified around residue Ser-250 in the C-terminal region of FtsQ and a membrane-proximal intera

154 which efficiently competes with ZipA for the C-terminal region of FtsZ, a central hub for multiple in

155 2' sugar modifications and revealed that the C-terminal region of FUS is sufficient to retain ASOs in

156 In this way, the C-terminal region of gamma-tubulin regulates S-phase pro

157 art of an amphipathic alpha-helix within the C-terminal region of GobX.

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

159 We found that quercetin bound the C-terminal region of hnRNPA1, impairing the ability of h

160 These results suggest that a dynamic C-terminal region of Hsc70 provides for flexibility betw

161 In addition, residues 153-171 in the C-terminal region of HscB exhibited NMR signal perturbat

162 pendent binding site for HscA resides in the C-terminal region of HscB.

163 an E3 ubiquitin ligase, interacted with the C-terminal region of HSPA5 and mediated HSPA5 ubiquitina

164 ial nuclear localization signal (NLS) in the C-terminal region of I2 (PP2A) containing a conserved ba

165 Mutagenesis defined the C-terminal region of JP2 as the predominant calpain clea

166 We show that the C-terminal region of KDM4D mediates its rapid recruitmen

167 ap the RNA chaperone domain (RCD) within the C-terminal region of La in close proximity to a novel AK

168 cal assays and mutagenesis indicate that the C-terminal region of LcrG (residues 52-73) is important

169 f Ly49B, demonstrating unexpectedly that the C-terminal region of Ly49s can play a significant role i

170 This was dependent on a C-terminal region of M45, which is not required for inte

171 Although the C-terminal region of MBP1-64 is required for interaction

172 itulated in a strain lacking only the unique C-terminal region of MceG, suggesting an important funct

173 glutamate-rich protein fused in frame to the C-terminal region of merozoite surface protein 3 (MSP3).

174 n, and to a 25-residue-long peptide from the C-terminal region of MG491 by surface plasmon resonance

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

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

177 cture of MtTOP1 by first predicting that the C-terminal region of MtTOP1 contains four repeated domai

178 region of MUC5B (D1-D2-D'-D3 domains, NT5B), C-terminal region of MUC5B (D4-B-C-CK domains, CT5B) and

179 erved regions I and II (CRI and CRII) at the C-terminal region of murine Rif1.

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

181 indicates that dramatic rearrangement of the C-terminal region of Nop15 in the pre-ribosome exposes t

182 n of human FLASH and YARP interacts with the C-terminal region of NPAT and that this interaction is e

183 The C-terminal region of NSm, which contains a basic amino a

184 Substitutions in the conserved C-terminal region of Oma1 impair its ability to form a l

185 Antibody binding studies revealed that the C-terminal region of one of the two b subunits is princi

186 ociation required B domain in OsRBR1 and the C-terminal region of OsPP2A B''.

187 The C-terminal region of p130Cas or Cas family homology doma

188 full-length p17 demonstrating that the final C-terminal region of p17 is irrelevant for the protein's

189 Moreover, the largely dispensable C-terminal region of pp150 is critical for pp150-pUL96 i

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

191 ever, the N-terminal region of pp150 and the C-terminal region of pUL96, which are critical for these

192 he RbpA-sigma interaction is mediated by the C-terminal region of RbpA and sigma domain 2, and S. coe

193 In addition, the C-terminal region of Redbeta corresponding to residues 1

194 the central part of M-Tha, and the specific C-terminal region of RelAp43 are required for this inter

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

196 tingly, the Walker A motif is located in the C-terminal region of RNase R, whereas the Walker B motif

197 nd identify an 18 amino acid sequence in the C-terminal region of S2 -SLF1 (SLF1 of S2 haplotype) tha

198 Replacing the diverged C-terminal region of SA1 with the corresponding region o

199 We found that the C-terminal region of Spt16 binds specifically to the his

200 Expression of the C-terminal region of SS4 alone increased granule initiat

201 ture-function analysis demonstrates that the C-terminal region of TACC2 is both necessary and suffici

202 The C-terminal region of TDP-43 was required for this functi

203 ersa, by stabilizing the L12-G2 loop and the C-terminal region of the alpha3 helix on KIX.

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

205 is proposed to be its active state, but the C-terminal region of the enzyme adopts a distinct confor

206 ibrinogen induced a structural change in the C-terminal region of the fibrinogen beta-chain (beta384-

207 lasia (mes) mice harbour a truncation in the C-terminal region of the Hh-ligand receptor, Patched-1 (

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

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

210 Additionally, the C-terminal region of the linker forms previously unrepor

211 WY domain of ATR1, partially specified by a C-terminal region of the LRR domain.

212 ring the parasite's hepatic replication, the C-terminal region of the parasitic PV membrane protein e

213 atory mechanism does not require the diverse C-terminal region of the PilA pilins but specifically in

214 The C-terminal region of the protein contains a predicted Do

215 y the presence of distinct insertions at the C-terminal region of the protein responsible for a struc

216 static interaction of the positively charged C-terminal region of the protein with a negatively charg

217 The C-terminal region of the RTA is involved in the respondi

218 These new structures reveal the C-terminal region of the small coat protein subunit, whi

219 S889 lies within a C-terminal region of the SMARCAL1 protein.

220 a small conformational change induced in the C-terminal region of the tetratricopeptide repeat (TPR)

221 ated by a conserved PP1-binding motif in the C-terminal region of the V protein.

222 IgG that targets amino acid residues in the C-terminal region of the V3 loop crown, suggesting the i

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

224 plex activity, likely through binding to the C-terminal region of Tim44.

225 eractions of the central part of Tm with the C-terminal region of TnI.

226 The C-terminal region of TOPBP1 interacts with TOP2A, and TO

227 n of a glutamic acid residue (DeltaE) in the C-terminal region of torsinA.

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

229 nserved catalytic site was identified in the C-terminal region of TRP120, and TRP120 autoubiquitinati

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

231 Mutational analyses indicated that the C-terminal region of VPg is important for the VPg-eIF4G

232 that synthetic peptides corresponding to the C-terminal region of wt-MoaA rescue the GTP 3',8-cyclase

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

234 ion/translocation region, kinase domain, and C-terminal region of YpkA.

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

236 bilized trimers derived from the central and C-terminal regions of Abeta.

237 ins the two surfaces to which the apical and C-terminal regions of AgI/II noncompetitively adhere.

238 termolecular interactions between the N- and C-terminal regions of alpha-syn play critical roles in m

239 tramolecular interactions between the N- and C-terminal regions of alpha-Syn, resulting in the protei

240 millisecond-timescale dynamics of the N- and C-terminal regions of C2alpha.

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

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

243 hat are localized within and adjacent to the C-terminal regions of each homodimer.

244 Furthermore, they act via the C-terminal regions of Gap1 not involved in ubiquitylatio

245 e N-terminal THAP DNA binding domain and the C-terminal regions of human THAP9 can also mobilize Dros

246 ion assays suggested that the N-terminal and C-terminal regions of ICP4 cooperate to mediate gene exp

247 Both the N- and C-terminal regions of LANA are essential for episome per

248 The N- and C-terminal regions of MlcC make critical contacts that c

249 this autoinhibition and that both the N- and C-terminal regions of Rhp26 are needed for its proper fu

250 nvestigated the specific roles of the N- and C-terminal regions of SS4 by expressing truncated versio

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

252 study the insertion capacity of hydrophobic C-terminal regions of the BH3-only proteins Bik, Bim, No

253 Because the C-terminal regions of the FATC domains of all known PIKK

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

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

256 lping it contact the N-terminal, middle, and C-terminal regions of the peptide.

257 332 to 543, respectively, within the N- and C-terminal regions of the protein.

258 ho and ERK pathways, with the N-terminal and C-terminal regions of the receptor playing key roles in

259 fluences interactions between N-terminal and C-terminal regions of the subdomain that are important i

260 Through manipulation of the C-terminal regions of these proteins we show the SPKTG m

261 ted peptides with sequences derived from the C-terminal regions of two LsbB-related bacteriocins inhi

262 ion inhibitory element when expressed at the C-terminal regions of ubiquitin-dependent and -independe

263 The crystal structure of the 341-residue C-terminal region outlines a unique architecture; in vit

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

265 Three basic residues at the C-terminal region play a critical role in nuclear locali

266 hat the first 15 residues of the PA-X unique C-terminal region play a critical role in shutoff activi

267 at formed a dimer, indicating that the NCS-1 C-terminal region prevents NCS-1 oligomerization.

268 c) and lower levels of fragments lacking the C-terminal region (proangiogenic) are present in circula

269 onent of PIPn regulation that depends on the C-terminal region rather than the nearby N-terminal regi

270 nature of its critical interaction with the C-terminal region remained unknown, however.

271 Deletion of the conserved C-terminal region required for 14-3-3 interaction destab

272 omprises the capsid assembly domain, and the C-terminal region (residues 150-183) is responsible for

273 Deletion mapping studies showed that the C-terminal region (residues 54-64) is required for the a

274 The adenovirus E1A C-terminal region restrains oncogenic transformation thr

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

276 but not isoform3 (i3) which shares a common C-terminal region, suppresses these malignant properties

277 ement of an N-terminal region and a proximal C-terminal region that comprises multiple cholesterol re

278 erminus, a hydrophobic core and a more polar C-terminal region that contains the cleavage site for th

279 ely dynamic region and a structured, helical C-terminal region that encompasses a membrane associated

280 s a stretch of hydrophobic residues from the C-terminal region that form a hydrophobic cleft, an adja

281 in the RNase III domain, and two were in the C-terminal region that has no homology to known motifs.

282 HCMV fusion factor has a Cys residue in the C-terminal region that is palmitoylated and mediates met

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

284 g a role of membrane anchor, an unstructured C-terminal region that is weakly associated with the mem

285 s experiments we identified a portion of the C-terminal region that mediates toxin binding to mammali

286 n into fragments containing the endorepellin C-terminal region that regulate angiogenesis and matrix

287 at SCR contains an amino acid segment at the C-terminal region that shows a remarkable affinity for c

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

289 pke in vivo and in vitro, whereas a separate C-terminal region was required for Sstn localization to

290 Hok1 binds to EEs via its C-terminal region, where it forms a complex with homolog

291 crassus TR restricted Sec insertion into the C-terminal region, whereas the 3'-UTR of TR3 conferred u

292 ponsible for periodontitis, cleaved the MUC2 C-terminal region, whereas the N-terminal region was una

293 pe G nsLTPs (LTPGs) have a GPI-anchor in the C-terminal region which attaches the protein to the exte

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

295 ficant conformational variations of the KaiB C-terminal region, which is functionally important in ma

296 ths detected using mAbs against the head and C-terminal regions, which are widely separated in the te

297 e find that deleting residues 623-641 of the C-terminal region, while retaining the IEEVD motif, caus

298 The coiled-coil comprises N- and C-terminal regions with distinct registers accommodated

299 amide shifts are localized mostly to N- and C-terminal regions within the rigid beta structure in th

300 eta42, only differ by two amino acids in the C-terminal region, yet they display markedly different a