ライフサイエンスコーパス: N-terminal extension

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

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

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

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

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

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

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

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

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

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

11 enylation domain, but only one containing an N-terminal extension.

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

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

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

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

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

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

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

19 te nuclear localization signal in its unique N-terminal extension.

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

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

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

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

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

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

26 structure with structurally uncharacterised N-terminal extensions.

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

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

29 upport a model in which the isoform-specific N-terminal extensions affect chemomechanical coupling by

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

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

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

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

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

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

36 regions unique to HO2: a 20-amino acid-long N-terminal extension and a C-terminal domain containing

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

38 s of Myo18Aalpha but includes an alternative N-terminal extension and a long serine-rich C terminus.

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

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

41 -24 (also PKA sites) in the cardiac-specific N-terminal extension and at Thr-144, a unique residue in

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

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

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

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

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

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

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

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

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

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

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

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

54 escribed nonintuitive design rules governing N-terminal extensions and identified successful extensio

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

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

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

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

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

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

61 dimerization, neither the HRM region nor the N-terminal extension appeared to affect HO2 dynamics.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

80 to all viral polymerases as well as a large N-terminal extension containing a kinase-like fold and i

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

110 Currently, the role of the N-terminal extension in UFM1 activation is not clear.

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

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

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

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

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

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

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

118 Finally, the eIF4E4 N-terminal extension is an intrinsically disordered regi

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

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

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

122 sis revealed that this glycine-arginine rich N-terminal extension is present outside the animal kingd

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 The atypical propeptide, or N-terminal extension, is required only for MycP stabilit

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

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

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

133 The N-terminal extension mediates dimerization and tetrameri

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

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 eplication system, we find that the flexible N-terminal extension (NTE) of Mcm2 promotes the stable r

150 Importantly, the N-terminal extension (NTE) of MOB1A not only regulated c

151 of each FimA subunit is complemented by the N-terminal extension (Nte) of the next subunit.

152 AtPRF3 has a 37-amino acid-long N-terminal extension (NTE), and its suppressive effect o

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

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

155 RNA(Lys) Higher eukaryotic LysRSs possess an N-terminal extension (Nterm) previously shown to facilit

156 tion of the vast majority of ORFs as well as N-terminal extensions (NTEs) and truncations.

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

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

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

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

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

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

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

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

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

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

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

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

169 gated whether PIP(2) controls binding of the N-terminal extension of ARF1 to ASAP1's PH domain and th

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

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

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

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

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

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

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

177 t engagement of the intrinsically disordered N-terminal extension of ClpS by ClpA is both necessary a

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

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

180 hese phenotypes depend on the plant-specific N-terminal extension of DXO1.

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

182 inal domains of each nsp13 interact with the N-terminal extension of each copy of nsp8.

183 d donor-strand complementation, in which the N-terminal extension of each subunit, the donor strand,

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

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

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

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

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

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

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

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

192 The N-terminal extension of one regulatory light chain inter

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

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

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

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

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

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

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

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

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

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

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

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

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

206 d identity) revealed a glycine-arginine rich N-terminal extension of ~100 amino acids that, given pre

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

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

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

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

211 myosin-1C(16), and myosin-1C(35), that carry N-terminal extensions of different lengths.

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

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

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

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

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

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

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

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

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

221 y, all plant HMGLs also contained a specific N-terminal extension (P100) that is located between the

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

242 While the SEC14 domain and its CRAL-TRIO-N-terminal extension serve general membrane attachment o

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

258 Rps2 harbors a eukaryote-specific N-terminal extension that is critical for its interactio

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

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

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

262 se that mitochondrial Cbp3 homologs carry an N-terminal extension that positions the conserved C-term

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

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

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

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

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

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

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

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

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

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

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

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

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

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

277 vide structural and biochemical data on UBA5 N-terminal extension to understand its contribution to U

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

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

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

281 The N-terminal extension truncation and phosphorylation site

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

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

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

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

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

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

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

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

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 the C terminus but additionally features an N-terminal extension with low-complexity regions.

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

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

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

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

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

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