ライフサイエンスコーパス: N-terminal extension

1 ontains an additional alpha-helix in a novel N-terminal extension.

2 ntiholin, S107, which differs by its Met-Lys N-terminal extension.

3 gth chains the groove is likely filled by an N-terminal extension.

4 sses a novel first exon that encodes a 51 aa N-terminal extension.

5 from restricted removal of the cTnI-specific N-terminal extension.

6 der of the pilus, with the assistance of the N-terminal extension.

7 hile RGS4-3 encodes a 302 aa protein with an N-terminal extension.

8 immunoglobulin-like fold (pilin body) and an N-terminal extension.

9 weakly stimulates motor domains without the N-terminal extension.

10 , a variant of TUC-4a that includes a unique N-terminal extension.

11 w ionic strength upon addition of this extra N-terminal extension.

12 obed the protein-protein interactions of the N-terminal extension.

13 be sensitive to the nature of the protruding N-terminal extension.

14 mally stabilized form of Mcl1 due to a 13-aa N-terminal extension.

15 odulates the actin binding properties of the N-terminal extension.

16 rel domain connected to a positively charged N-terminal extension.

17 interaction domains located at their unique N-terminal extension.

18 y unobserved HXH motif located in its unique N-terminal extension.

19 ke region and a approximately 400 amino acid N-terminal extension.

20 motif, but it also carries an arginine-rich N-terminal extension.

21 d MCM2 are unusual in having long and unique N-terminal extensions.

22 structure with structurally uncharacterised N-terminal extensions.

23 h contain the DNA binding domain and various N-terminal extensions.

24 RPs) contain a C-terminal RFamide but unique N-terminal extensions.

25 with DNA to analyse functional roles of the N-terminal extensions.

26 ic of other L23a family members and a unique N-terminal extension, absent from Saccharomyces cerevisi

27 g the HB-EGF membrane anchor, but lacking an N-terminal extension, activated EGFR during their transi

28 These observations show that the N-terminal extension affects the conformational state of

29 Deletion of the betaB2-crystallin N-terminal extension alone (rbetaB2Ntr) gave almost no c

30 Bacteria encoding L27 with this N-terminal extension also encode a sequence-specific cys

31 These and other results suggest that the N-terminal extension alters the accessibility of the sig

32 site of interaction of Mal3 with Tea2 is the N-terminal extension, although a weaker interaction is a

33 the channels include a 71 amino acid CLH-3a N-terminal extension and a 270 amino acid extension of t

34 These studies reveal that SRPK1 uses an N-terminal extension and a large, intrinsically disorder

35 I1-64 contains the phosphorylatable N-terminal extension and a region that anchors I1-64 to

36 ed in the KE-rich region at the start of the N-terminal extension and appears to mediate ATP-independ

37 -24 (also PKA sites) in the cardiac-specific N-terminal extension and at Thr-144, a unique residue in

38 ric Mdv1-Fis1 complex that contains both the N-terminal extension and coiled-coil regions of Mdv1.

39 Surprisingly, the commonly cited V2-specific N-terminal extension and cysteines were found to be disp

40 This homology region is preceded by an N-terminal extension and followed by a C-terminal extens

41 The ARF binding site is located in the N-terminal extension and is separate from the core three

42 The N-terminal extension and phosphorylation of the myosin r

43 ecular autoinhibitory mechanism involving an N-terminal extension and phosphorylation of tyrosine res

44 verall architectural topology; however, each N-terminal extension and pilin body has specific functio

45 e intrasubunit interactions between the cTnI N-terminal extension and the cTnI inhibitory peptide, wh

46 ating intramolecular interaction between the N-terminal extension and the inhibitory region of cTnI.

47 ity to the intrinsic effects of Motif 3, the N-terminal extension and their synergistic effect, and (

48 up I intron binding surface that includes an N-terminal extension and two small insertions (insertion

49 on those of bacterial TyrRSs, except for an N-terminal extension and two small insertions not found

50 eptides from ERAAP-deficient cells contained N-terminal extensions and had a different molecular comp

51 These new compstatin peptides contain polar N-terminal extensions and non-natural amino acid substit

52 ethyltransferase and beta-barrel domains, an N-terminal extension, and a dimerization arm.

53 ), a histidine-tagged analogue containing an N-terminal extension, and five different terminus-trunca

54 interactions are lost after exit of the VP1 N-terminal extension, and that the RNA also interacts wi

55 ly of bacteria that contain MetAPs with such N-terminal extensions, and we classify these as MetAP ty

56 The switch II helix has an N-terminal extension, apparently stabilized by conserved

57 pe of a truncated form of DrDps1 without the N-terminal extensions appears as a dodecameric sphere, c

58 tor domain only or the motor domain plus the N-terminal extension are monomeric, whereas a construct

59 We hypothesize that the N-terminal extensions are responsible for localizing com

60 H16 that makes specific contacts with the S4 N-terminal extension, as well as a right-angle motif bet

61 Replacement of an N-terminal extension at either the amino or carboxyl ter

62 We identify an N-terminal extension ("ATP-binding loop", ABL) that is c

63 to its operator sequence, revealing that the N-terminal extension binds in the minor groove.

64 ements of the zinc finger as well as a short N-terminal extension but is restricted to the switch and

65 Ligands lacking an N-terminal extension, but possessing the membrane-anchor

66 ates the ATPase of constructs containing the N-terminal extension by decreasing the K0.5(MT) for stim

67 in vitro motility assay, suggesting that the N-terminal extension can act in a modular manner to incr

68 presence of calcium nor deletion of the MTIP N-terminal extension changed the speed of actin movement

69 hGNE2 and hGNE7 display a 31-residue N-terminal extension compared to hGNE1.

70 residue N-terminal deletion and a 50-residue N-terminal extension compared to hGNE1.

71 lumen are synthesized in the cytosol with an N-terminal extension consisting of transient signals for

72 Mammalian Icmt has an N-terminal extension consisting of two TM segments not f

73 Other type Ib and type Ic MetAPs with N-terminal extensions contain similarly located PxxP mot

74 bacterial orthologs, plant UreGs possess an N-terminal extension containing a His- and Asp/Glu-rich

75 This longer form has an 80-residue N-terminal extension containing an additional, distal, C

76 A unique N-terminal extension contributes to the observed dual ta

77 Surprisingly, deletion of the N-terminal extension decreased steady-state levels of th

78 taT2) in a dose-dependent manner, whereas an N-terminal extension deletion mutant did not.

79 The phosphorylation and N-terminal extension-dependent boost in cross-bridge kin

80 escued null or control (Dmlc2(+)), truncated N-terminal extension (Dmlc2(Delta2-46)), disrupted myosi

81 e is not sufficient for cytotoxicity and the N-terminal extension does not affect the conformation of

82 HK97, T5 encodes the scaffold function as an N-terminal extension (-domain) to the major head protein

83 nzymes, however, TgVP1 contains a 74-residue N-terminal extension encompassing a 42-residue N-termina

84 Our results showed that MPG lacking N-terminal extension excises hypoxanthine with significa

85 Structural pilus subunits consist of an N-terminal extension followed by an incomplete immunoglo

86 ain of Bub1, revealing the requirement of an N-terminal extension for its kinase activity.

87 eal a 'budded' PH domain fold, possessing an N-terminal extension forming an integral part of the ove

88 aturally occurring 12-amino acid hydrophilic N-terminal extension found on s2 VacA blocks vacuolating

89 gondii lacks this type of translocator, the N-terminal extension from the Plasmodium falciparum sequ

90 rge spacer insert domain and a portion of an N-terminal extension function cooperatively to increase

91 cardiac stress to remove the unique cardiac N-terminal extension functions to improve cardiac contra

92 Removal of the N-terminal extension had no detectable effects on MCM1 b

93 Removal of the N-terminal extension has little effect on this activity.

94 show that the native signal peptide, or any N-terminal extension, has an inhibitory effect on SplB.

95 rion and the evolutionary conservation of an N-terminal extension have remained mysteries.

96 on of an invariant asparagine residue in the N-terminal extension, however, restored cotranslational

97 ting evidence as to the functions of the BNP N-terminal extension; however, this has never been asses

98 led oxidation of Fe(2+), and possess a short N-terminal extension implicated in stabilizing cellular

99 ers of the ABCC subfamily, Ycf1p contains an N-terminal extension in addition to its ABC "core" domai

100 rough the ASTS USP7 binding motif within its N-terminal extension in an identical manner with other k

101 The deletion of the N-terminal extension in betaB1 resulted in maximum expos

102 However, this N-terminal extension in hEFO1p is unlike Rad30p, but ins

103 we were able to probe the environment of the N-terminal extension in intact troponin.

104 especially the role of the cardiac specific N-terminal extension in modulating actomyosin interactio

105 cal amino acid sequences except for a unique N-terminal extension in PDE3A1.

106 gers the closure of the groove and seals the N-terminal extension in place.

107 consensus sequence, and participation of the N-terminal extension in the formation of the substrate-b

108 A model of a highly mobile N-terminal extension in the monomeric enzyme is proposed

109 orrelated with the presence or absence of an N-terminal extension in the PapE pilin structure.

110 Analysis of Trx h9 revealed a 17-amino acid N-terminal extension in which the second Gly (Gly(2)) an

111 ewly identified role of the ferritin subunit N-terminal extensions in gating Fe(2+) exit from the cyt

112 Our data also suggest that various N-terminal extensions in mammalian TRs are often express

113 presentation of peptide precursors with long N-terminal extensions in TPPII gene-trapped embryonic fi

114 Bioinformatic analyses revealed N-terminal extensions in two additional Pdu proteins and

115 New studies on the 'N-terminal' extension in yeast suggest that it works wit

116 We hypothesize that the ELC N-terminal extension interaction with actin inhibits the

117 . smegmatis but included an eight amino acid N-terminal extension involving a different start codon.

118 Previous structural studies showed that the N-terminal extension is disordered in the absence of DNA

119 In this study, we show that this N-terminal extension is essential for virus viability, a

120 revented virus recovery, suggesting that the N-terminal extension is essential for virus viability.

121 Hydrodynamic analysis indicates that the N-terminal extension is in a highly extended conformatio

122 ding that the coding sequence for the entire N-terminal extension is omitted from the plasmid, transf

123 The N-terminal extension is required for quadruplex recognit

124 he molecules of the crystal, part of the RLC N-terminal extension is seen in atomic detail and forms

125 Here, we show that the N-terminal extension is sensitive to protease cleavage,

126 of available databases shows that the unique N-terminal extension is shared by multiple insect lineag

127 ed protein alpha-synuclein with a 10-residue N-terminal extension is shown to form a stable tetramer

128 2 ubiquitin conjugation enzyme with a unique N-terminal extension, is a novel USP7-interacting protei

129 ar-encoded as their precursors containing an N-terminal extension known as the transit peptide (TP).

130 activity of the protease precursor), and the N-terminal extension makes transient intra- and intersub

131 Based on data, we propose that the N-terminal extension mediates an interaction with an uni

132 The N-terminal extension mediates dimerization and tetrameri

133 The active site at the interface of the N-terminal extension, methyltransferase, and beta-barrel

134 st other Ras family members, ARHI has a long N-terminal extension, modest GTPase activity, and consti

135 Additionally, the effect of one of the L3 N-terminal extension mutants on the interaction between

136 Analysis of N-terminal extensions (N-acetylation, Gly, AlaSer) showe

137 eting an array of enzymes presenting special N-terminal extensions, namely PduC, D, E, L and P.

138 dgd1-1 mutant of Arabidopsis in fusion with N-terminal extensions (NDGD1 and NDGD2) targeting to the

139 Most strikingly, deletion of ARHI's unique N-terminal extension nearly abolished its inhibitory eff

140 that phosphorylation of Ser-251 in the Ycf1p N-terminal extension negatively regulates activity.

141 Both ALDOART1 and ALDOA_V2 have unusual N-terminal extensions not found in other aldolases.

142 ted using specific primers with deletions of N-terminal extension (NT) (named betaA3-NT), N-terminal

143 nts of betaA3-crystallin were generated: (i) N-terminal extension (NTE) 21 amino acids (betaA3[21] mu

144 erminal localization module, organized in an N-terminal extension (NTE) and a tetratricopeptide repea

145 Separate elements in the Mps1 N-terminal extension (NTE) and tetratricopeptide repeat

146 Fourth, a partial deletion of the Ssl1 N-terminal extension (NTE) domain inhibits TFIIH functio

147 replaced with a beta-strand formed from the N-terminal extension (Nte) of an incoming pilus subunit

148 Here we demonstrate that the unstructured N-terminal extension (NTE) of ClpS enters the ClpA proce

149 aracterized by a approximately 32 amino acid N-terminal extension (NTE), the function of which remain

150 ransporters is the presence of a hydrophobic N-terminal extension (NTE), whose function is not clearl

151 substrate alpha-amino group and the flexible N-terminal extension (NTE).

152 TCL has an N-terminal extension of 18 amino acids in comparison to

153 binding and autophosphorylation, but has an N-terminal extension of 370 aa, lacking homology with an

154 catalytically active construct, including an N-terminal extension of 60 residues prior to the kinase

155 rocessed wild-type protein, which carries an N-terminal extension of 84 amino acids in the form of it

156 se that new gene overlaps generally arise by N-terminal extension of a downstream gene, creating a no

157 FRET from actin to a probe on the N-terminal extension of A1 showed close proximity to act

158 We conclude that the N-terminal extension of A1-ELC modulates the W-to-S stru

159 maltase with known structure and exhibits an N-terminal extension of about 140 residues, in contrast

160 The N-terminal extension of ALDOA_V2 is highly conserved in

161 change, occurring at the usher, in which the N-terminal extension of an incoming subunit completes th

162 nslated regions were noncanonical and led to N-terminal extension of annotated proteins or translatio

163 an thymidylate synthase (TS) enzymes have an N-terminal extension of approximately 27 amino acids tha

164 ion (ECF) sigma factor PvdS but possesses an N-terminal extension of approximately 29 amino acids tha

165 llins were modified by removal of either the N-terminal extension of betaA3 (rbetaA3Ntr) or betaB2 (r

166 Removal of the N-terminal extension of betaA3 had no effect on dimeriza

167 Fusion of the N-terminal extension of BimC onto the motor domain of co

168 Overall, our results demonstrate that the N-terminal extension of BNP is essential to virus viabil

169 An N-terminal extension of calmodulin, (N+3)calmodulin, tha

170 covered phosphorylation sites located in the N-terminal extension of cardiac troponin I (S4, S5, Y25)

171 Phosphorylation of the unique N-terminal extension of cardiac troponin I (TnI) by PKA

172 The N-terminal extension of cardiac troponin I (TnI) is bisp

173 These findings indicate that removal of the N-terminal extension of cTnI via restricted proteolysis

174 An N-terminal extension of Dsn1 from one head regulates int

175 We found that N-terminal extension of E-RAS is important for E-RAS sig

176 We found that ligands having the N-terminal extension of EGF could not bind to the EGFR,

177 nthesized as an inactive pre-protein with an N-terminal extension of eight amino acids.

178 nd proline-rich ligands, we suggest that the N-terminal extension of ELC interacts with actin and mod

179 Thus, in the pilus fiber, the N-terminal extension of every subunit completes the Ig f

180 The unique six amino acid N-terminal extension of Gq(alpha) when added to the N-te

181 our data support that the mRNA encoding the N-terminal extension of hcArgRS has the capacity of inde

182 the DNA-binding domain of GAL4 fused to the N-terminal extension of HDAC5 and the VP16 transcription

183 -like fold of each pilin is completed by the N-terminal extension of its neighbor.

184 taining filaments, the DFRXXL motifs and the N-terminal extension of long MLCK confer high affinity b

185 Two contain an N-terminal extension of Motif 1 and two contain Motif 3.

186 In this study we show that N-terminal extension of nominal peptide by as few as thr

187 The N-terminal extension of one isozyme, ACC1, was shown to

188 donor strand exchange mechanism in which the N-terminal extension of one subunit replaces the chapero

189 Removal of the N-terminal extension of PapE was sufficient to abolish C

190 We found that the N-terminal extension of PapF is required to adapt the Pa

191 Thus, the unphosphorylated N-terminal extension of Rlc1p can uncouple the ATPase an

192 The N-terminal extension of rusticyanin is a unique structur

193 The N-terminal extension of SK2-L is cysteine-rich and media

194 the myristoylated capsid protein VP4 and the N-terminal extension of the capsid protein VP1, both of

195 orthologues of Zta suggest that a conserved N-terminal extension of the consensus B-ZIP domain is re

196 he SH3 domain facilitates the binding of the N-terminal extension of the essential light chain isofor

197 N-terminal extension of the isolated FNIII EDA with its

198 nsect cells is multiply phosphorylated on an N-terminal extension of the protein that contains a high

199 g Gla residues are located in a four residue N-terminal extension of this contryphan.

200 domains of TnC, providing evidence that the N-terminal extension of TnI interacts with the N-termina

201 additional E2-E3 interaction mediated by the N-terminal extension of UbcH10 regulates APC activity.

202 degradation by polypeptides that include the N-terminal extension of VP1 and capsid protein VP4.

203 ggregation kinetics of Abeta42 variants with N-terminal extensions of 5-40 residues, and transmission

204 and indicated that truncation occurs within N-terminal extensions of beta-crystallins during lens ma

205 The long N-terminal extensions of beta-crystallins may influence

206 of a set of conserved serine residues in the N-terminal extensions of class II HDACs creates binding

207 interaction were the residue Met-140 and the N-terminal extensions of each subunit.

208 Relative to Phl p 7, they exhibit N-terminal extensions of one, five, and seven residues,

209 nal SUMO molecules to lysine residues in the N-terminal extensions of SUMO.

210 ion channels, cytoplasmic pores, and/or the N-terminal extensions of the helix bundles.

211 EF loop of VP2, the GH loop of VP3, and the N-terminal extensions of VP1 and VP2, which, in retrospe

212 In this study we tested the role of N-terminal extension on MPG hypoxanthine (Hx) cleavage a

213 ucleotide exchange activity requires a novel N-terminal extension on the DH domain that is predicted

214 Here, we show that a novel N-terminal extension on yeast eIF2gamma contains a PP1-b

215 ha is soluble, either phosphorylation of its N-terminal extension or DNA binding promotes the formati

216 trate that L27 variants with an un-cleavable N-terminal extension, or lacking the extension (pre-clea

217 N-terminal extension (NT) (named betaA3-NT), N-terminal extension plus motif I (named betaA3-NT + I),

218 xtension plus motif I (named betaA3-NT + I), N-terminal extension plus motifs I and II (named betaA3-

219 ning dimers, tetramers and octamers, but the N-terminal extension present in IncC1 favours nucleotide

220 efining a subtilisin-like fold with a unique N-terminal extension previously proposed to function as

221 of human PDE3A1 at a PKA site in its unique N-terminal extension promotes its incorporation into SER

222 -ray scattering (SAXS) results show that the N-terminal extensions protrude from the spherical shell

223 e new subunits were dictated by the specific N-terminal extension provided and were consistent with t

224 d with that of betaA3-crystallin missing the N-terminal extension (rbetaA3tr).

225 Loss of the unique N-terminal extension reduced lytic activity and led to a

226 ended TRPC3 having a highly homologous 73-aa N-terminal extension, referred to as hTRPC3a.

227 We hypothesized that the alpha-subunit N-terminal extension region interacts with the activin t

228 antibody directed against the alpha-subunit N-terminal extension region or by deletion of the N-term

229 G alpha13 with its N-terminal extension replaced by that of G alpha12 acqui

230 nuclear localization of BNP, with the entire N-terminal extension required for this to function effic

231 cal PTP domain (residues 44-339) and a short N-terminal extension (residues 1-43) that functions to d

232 l (betaalpha)6-barrel fold with a disordered N-terminal extension (residues 45-74) and a partially or

233 nsion of this peptide has little effect, but N-terminal extension results in higher maximal velocity

234 Bioinformatic analysis shows that an N-terminal extension rich in positively charged residues

235 including a short C-terminal tail and a long N-terminal extension rich in prolines, alanines, and lys

236 E. coli or spinach counterparts, containing N-terminal extensions (S2 and S5) or insertion sequence

237 at Cul3 interaction is dependent on a unique N-terminal extension sequence that packs against the 3-b

238 the structure uncovers a unique role for the N-terminal extension sequence, which stabilizes helix al

239 lls, with a lysine in the non-ubiquitin-like N-terminal extension serving as the major SUMO-SUMO bran

240 The structure reveals that this N-terminal extension shows no structural similarity to p

241 nscriptional regulators and also contains an N-terminal extension similar to the Ni(2+)-binding C-ter

242 duced after radiation damage and contains an N-terminal extension similar to those of proteins involv

243 Members of the first set bear N-terminal extensions similar to those that target prote

244 st likely due to cellular recognition by the N-terminal extension, since the intrinsic activity of th

245 during autoactivation at higher pH contained N-terminal extensions (starting at 6 and 14 amino acid r

246 ra crassa MMM1, which naturally lacks a long N-terminal extension, substituted for loss of Mmm1p in b

247 ophobic cleft while two other helices and an N-terminal extension target a discrete surface formed la

248 v1 has a modular structure, consisting of an N-terminal extension that binds Fis1, a central coiled c

249 approximately 150 amino acids as well as an N-terminal extension that consists of two carbohydrate b

250 I isoforms, cardiac troponin I (cTnI) has an N-terminal extension that contains phosphorylation sites

251 troponin I (cTnI) isoform contains a unique N-terminal extension that functions to modulate activati

252 transcription, the Ton box is preceded by an N-terminal extension that interacts with the inner-membr

253 ns an evolutionarily conserved 50-amino-acid N-terminal extension that is absent from the NP of influ

254 C-terminal domain found in RecA, but have an N-terminal extension that is absent in the RecA protein.

255 e only identified mutation within its unique N-terminal extension that is associated with hypertrophi

256 resembles a classical signal peptide plus an N-terminal extension that is conserved in other autotran

257 reus and other Firmicutes is encoded with an N-terminal extension that is not present in most Gram-ne

258 unit protein L27 is encoded with a conserved N-terminal extension that is removed to expose residues

259 inactive mini-precursor with a four-residue N-terminal extension that mimics the transframe region p

260 family members, the neuronal protein has an N-terminal extension that shares characteristics of yeas

261 D contains an approximately 170-residue-long N-terminal extension that structurally mimics a dimer-di

262 find that TatA in Prov. stuartii has a short N-terminal extension that was atypical of TatA proteins

263 Several v-SNAREs have a Longin N-terminal extension that, by promoting a closed conform

264 Eukaryotic sirtuins have N-terminal extensions that have been linked to protein m

265 c structural elements (a beta hairpin and an N-terminal extension) that contribute to its substrate s

266 e nuclear localization signal (NLS) in their N-terminal extension, the 18-kDa FGF-2 does not contain

267 ith the exception of a unique 129-amino acid N-terminal extension, the ACH2 protein is 17-36% identic

268 letion constructs were prepared in which the N-terminal extension, the C-terminal extension or both e

269 include a zinc-binding site and a hook-like N-terminal extension, the latter representing a hallmark

270 pFurH134Y), which represent mutations in the N-terminal extension, the regulatory metal binding site

271 As the NP of influenza A virus lacks this N-terminal extension, these viruses may have evolved sep

272 o process viral peptides with C-terminal and N-terminal extensions through their proteasomal and cyto

273 cific E2-E3 interface and regulation via its N-terminal extension to limit APC activity for substrate

274 Surprisingly, we find that a basic N-terminal extension to the SET domain plays an even mor

275 Also distinctive to E1o are N-terminal extensions to the core fold, and which may me

276 ted data reveal the relative position of the N-terminal extensions to the dodecameric sphere in solut

277 s to the trimming of peptides with very long N-terminal extensions, TPPII is not essential for genera

278 The N-terminal extension truncation and phosphorylation site

279 diminished power output parameters with the N-terminal extension truncation and phosphorylation site

280 Epitope precursors with N-terminal extensions undergo a similar process.

281 f both N- and C-terminal tails, but only the N-terminal extension undergoes mechanical removal, there

282 nation was probed through the creation of an N-terminal extension variant (SliLPMO10E-Ext).

283 The N-terminal extension was also implicated in beta-lactam

284 In this study, pilus subunits in which the N-terminal extension was either deleted or swapped with

285 The function of the ELC N-terminal extension was investigated with the Tg-Delta4

286 ted by proteolytic processing and lacked the N-terminal extension was unable to bind fibrinogen.

287 C) and the physiological significance of its N-terminal extension, we generated transgenic (Tg) mice

288 nuclein construct that contains a 10-residue N-terminal extension, which forms multimers when isolate

289 DFRXXL motifs and six Ig-like modules in an N-terminal extension, which may confer unique binding pr

290 conserved among bacteria containing the L27 N-terminal extension, which performs post-translational

291 Dps-1 has an N-terminal extension with a unique metal-binding site, a

292 f actomyosin, through the interaction of its N-terminal extension with actin and its C-terminal lobe

293 lfALR has an 80-residue N-terminal extension with an additional CxxC motif requi

294 fide transporter, CcdA, which all display an N-terminal extension with respect to their bacterial cou

295 locating within the protein, or swapping its N-terminal extension with that of other subunits altered

296 In addition to an N-terminal extension with unknown function, SRPKs contai

297 Saccharomyces cerevisiae ProRS possesses an N-terminal extension with weak homology to a bacterial-s

298 s, which we named AtRibF1 and AtRibF2, carry N-terminal extensions with characteristics of organellar

299 to 5-FCLs of other organisms but containing N-terminal extensions with the features of mitochondrial

300 ble tolerance for accommodating the fly L23a N-terminal extension within the structure of the yeast r