ライフサイエンスコーパス: C-terminal extension

1 RT folding by interacting with both TRBD and C-terminal extension.

2 he rare amino acid selenocysteine (Sec) on a C-terminal extension.

3 domains, box A and box B, and a lysine-rich C-terminal extension.

4 e disparately affected by dimeric LC8 with a C-terminal extension.

5 cting together with a functionally important C-terminal extension.

6 rthologs are notable for their highly acidic C-terminal extension.

7 N-1 consists of a nuclease core domain and a C-terminal extension.

8 ely 15 A) from the flavin chromophore in the C-terminal extension.

9 de spanning the transmembrane region and its C-terminal extension.

10 ctivity included the leucine-rich repeat and C-terminal extension.

11 drophobic sterol-binding pocket and a unique C-terminal extension.

12 ite effects were observed on deletion of the C-terminal extension.

13 changes of the central beta hairpin and the C-terminal extension.

14 by an N-terminal extension and followed by a C-terminal extension.

15 3 (FSD3) apparently linked to binding of the C-terminal extension.

16 d hCenexin1 variant 1, that possess a unique C-terminal extension.

17 icted to adopt a HMG fold, and a lysine-rich C-terminal extension.

18 ains hydrophobic residues clustered near the C-terminal extension.

19 cturally unique secretory PLA(2) with a long C-terminal extension.

20 hing studies and antibody recognition of the C-terminal extension.

21 within a fragment encompassing ABS2 and the C-terminal extension.

22 inding of the second messenger c-di-GMP to a C-terminal extension.

23 top codon and production of a protein with a C-terminal extension.

24 have either a short (Map53) or long (Map73) C-terminal extension.

25 the amino terminus and residues 69-93 of the C-terminal extension.

26 packaged DyP interacts with Enc via a unique C-terminal extension.

27 tuberculosis DyP (Mt-DyP), which contains a C-terminal extension.

28 ant active site loop alterations and a large C-terminal extension.

29 ongation is affected mainly by the length of C-terminal extension.

30 15 A apart and separated by residues in the C'-terminal extension.

31 es through the LOV domain core to the N- and C-terminal extensions.

32 OB-fold present in bacterial IF1 plus N- and C-terminal extensions.

33 strin homology (PH) domain with short N- and C-terminal extensions.

34 onserved changes in loop structure and N and C-terminal extensions.

35 hesion molecules and flanked by large N- and C-terminal extensions.

36 a helical motif flanked by disordered N- and C-terminal extensions.

37 vity and is flanked on either side by N- and C-terminal extensions.

38 terdomain insertion (4-helical bundle) and a C-terminal extension (3-helical bundle) and it packs as

39 The V143A mutation is in the C-terminal extension, a region predicted to form an olig

40 Mutation of residues 247 and 248 in the C-terminal extension abolished the ability of IF3(mt) to

41 Brf1 and Brf2 both have a C-terminal extension absent in TFIIB, but their C-termin

42 The N- and C-terminal extensions add additional structural elements

43 Notably, Mss116p's C-terminal extension also bends RNA 5' of the central nu

44 ogues form heteromultimers and indicate that C-terminal extensions alter virus recognition by multime

45 rearrangement due to the removal of the pD1 C-terminal extension, altering the Psb27-CP43 binding in

46 The helicase core of each protein precedes a C-terminal extension and a basic tail, whose structural

47 rom similar and diverse origins highlights a C-terminal extension and a pi-cation interaction within

48 tants with deletions of N-terminal domain or C-terminal extension and also with deamidation plus abov

49 ses an immunoglobulin fold flanked by a long C-terminal extension and an N-terminal hairpin loop.

50 o somatic centrosomes via a variant-specific C-terminal extension and recruits Plk1 through a Cdc2-de

51 We demonstrate here that processing of the C-terminal extension and sequences at the C-terminus of

52 in became water insoluble on the deletion of C-terminal extension and subsequent deletions of the C-t

53 Both the C-terminal extension and the linker are required for thi

54 Mounting evidence suggests that both C-terminal extensions and N-terminal truncations help pr

55 vements are largest on datasets containing N/C-terminal extensions and on datasets containing long an

56 amino acid residues flanked by varied N- and C-terminal extensions and usually exist as oligomers.

57 rge subunit, endoproteolytic cleavage of the C-terminal extension, and dimerization with the small su

58 oforms: the calmodulin-binding sequence, the C-terminal extension, and the autoregulatory loop in the

59 proach by tracking the effects of mutations, C-terminal extensions, and ribosomal tethering on the st

60 The C-terminal extension appears to be essential for nucleot

61 However, both the N-terminal domain and C-terminal extension are also important for the chaperon

62 ntramolecular disulfide bond in ABri and the C-terminal extension are required to elongate initially

63 , Phe(116), Val(118), and Tyr(119)) near the C-terminal extension are responsible for these activitie

64 C-terminal extensions are a common feature of kinetoplas

65 erminal extension absent in TFIIB, but their C-terminal extensions are unrelated.

66 tic functions of Rny1 are independent of the C-terminal extension, are affected by many mutations in

67 icate that these elements, together with the C-terminal extension, are involved in scaffold formation

68 This points to an important role for the C-terminal extension, Arg-163 in particular, and no sign

69 The lack of any light response in the C-terminal extension as evidenced by FTIR spectroscopy d

70 rk at 0.5 mm injected concentration with the C-terminal extension as the dimerization site.

71 cause it induces phosphorylation of the Mpk1 C-terminal extension at Ser423 and Ser428.

72 arrel core, it possesses unstructured N- and C-terminal extensions bearing several highly conserved a

73 264 amino acid fragment contains the entire C-terminal extension beginning after the EF-Tu-homologou

74 f II + connecting peptide [betaB1(149-252)], C-terminal extension [betaB1(1-234)], C-terminal extensi

75 Generation and analysis of a series of C-terminal extensions beyond residue 219 yielded a stabl

76 ng NMR spectroscopy, we now show that N- and C-terminal extensions beyond the predicted C2B domain co

77 gh gives rise to low abundance proteins with C-terminal extensions beyond the stop codon.

78 orm activase to form a disulfide bond in the C-terminal extension (C-extension) significantly increas

79 elongation factor eEF1A, eEFSec has a unique C-terminal extension called Domain IV.

80 f RNA polymerase II (RNA pol II) is its long C-terminal extension, called the carboxy-terminal domain

81 complex, in which the acidic residues of the C-terminal extension cannot interact with the heparin-bi

82 ucleotide (FAD) cofactor, and a cryptochrome C-terminal extension (CCT), which is essential for signa

83 The large subunit is synthesized with a C-terminal extension, cleaved off by a specific endopept

84 of CfaE, the CFA/I adhesin, incorporating a C-terminal extension comprising a flexible linker and 10

85 The second domain has a C-terminal extension consisting of two additional helice

86 of the thylakoid Tat machinery, a 25-residue C-terminal extension containing a 13-residue in vivo bio

87 s lack TMBS2 and half of ABS1, and present a C-terminal extension containing a proline-rich domain an

88 The Drosophila insulin receptor (dIR) C-terminal extension contains potential binding sites fo

89 ning the tetramer after its assembly but the C-terminal extension contributes to the overall stabilit

90 Moreover, we found that N- and C-terminal extensions create a highly unusual all alpha-

91 The redox regulated C-terminal extension (CTE) and the associated alternate

92 es in homodimerization and the impact of the C-terminal extension (CTE) by contrasting HP1a to its pa

93 minal GTPase domain and, except for Cdc10, a C-terminal extension (CTE) containing a predicted coiled

94 tumefaciens VirE2 and VirD2 proteins and the C-terminal extension (CTE) domain of Arabidopsis thalian

95 ified guanosine-binding "AT-hook" within the C-terminal extension (CTE) flanking the DBD, which makes

96 RNA, as in other DEAD-box proteins, while a C-terminal extension (CTE) induces a second bend, result

97 We show here that this C-terminal extension (CTE) mediates in vivo localization

98 is minor groove interaction is mediated by a C-terminal extension (CTE) of the DNA binding domain and

99 onsiveness to HMGB-1/-2 was dependent on the C-terminal extension (CTE) region of the ER DNA binding

100 ls that this selectivity is dependent on the C-terminal extension (CTE), amino acid sequences adjacen

101 nts and deamidated plus N-terminal domain or C-terminal extension deleted mutants: (i) alphaA-NT (NT,

102 (iv) alphaA-N101/123D-NT, (v) alphaA-CT (CT, C-terminal extension deleted), (vi) alphaA-N101D-CT, (vi

103 C-terminal extension (deletion) requires ss-sheet rearra

104 that the Escherichia coli enzyme contains a C-terminal extension displaying sequence similarity to t

105 nd that the 25 residues comprising the novel C-terminal extension do not participate in receptor acti

106 tch of pentatricopeptide repeats (PPR) and a C-terminal extension domain ending with the amino acids

107 the essential loop L6.1 adjacent to the TERT C-terminal extension domain.

108 6SS effectors consists of VgrG proteins with C-terminal extension domains carrying various enzymatic

109 site of post-transfer editing, or the N- or C-terminal extension domains of eukaryotic and archaeal

110 This C-terminal extension encodes an ERK5 docking site requir

111 The HP1 C-terminal extension enhances the affinity, as does the

112 ably the lack of TMBS2 and the presence of a C-terminal extension featuring a proline-rich domain and

113 Lmods additionally contain a C-terminal extension featuring an actin-binding WH2 doma

114 We also found that the C-terminal extension flanking the catalytic core of Dbp4

115 st two zinc fingers, whereas residues in the C-terminal extension following the third zinc finger bin

116 hemical studies proved the importance of the C-terminal extension for MgCh stimulation and inactivati

117 dopts an extended conformation, exposing the C-terminal extension for prenylation or enabling OsCaM61

118 CL3 can be relieved by exchanging its acidic C-terminal extension for that of PLP2.

119 tic of C2 domains and that the unique N- and C-terminal extensions form a small subdomain that packs

120 ously reported analogs and relies on the HPF C-terminal extension forming the binding platform for th

121 In particular, the C-terminal extension found in all apicomplexan PBGS enzy

122 s it affected by removal of the unique 20-aa C-terminal extension found in Ly49B.

123 Removal of either the N- or C-terminal extension has almost no effect on this value.

124 The exact role of the C-terminal extension has remained elusive; however, clea

125 r eukaryotes, PNGase has an N-terminal and a C-terminal extension in addition to its central catalyti

126 ed form of Rv2466c revealed the binding of a C-terminal extension in alpha-helical conformation to a

127 and/or deletion of the N-terminal domain or C-terminal extension in alphaA-crystallin.

128 demonstrate the intrinsic flexibility of the C-terminal extension in CDK12 and highlight its importan

129 these two stealth family proteins revealed a C-terminal extension in CsxA, which conferred processivi

130 Aquifex aeolicus (Aacpn10) has a 25-residue C-terminal extension in each monomer not found in any ot

131 phaB-crystallin increased on deletion of the C-terminal extension in the deamidated alphaA mutants, b

132 This in turn suggests that the C-terminal extensions in Brf1 and Brf2 are crucial to sp

133 ons among NADP (+), FAD, and residues in the C'-terminal extension indicate that the gross conformati

134 pha-crystallin domain with disordered N- and C-terminal extensions, indicating that the extensions ar

135 A mutant lacking this C-terminal extension interacts more tightly with both hC

136 In yeast Brf1, the C-terminal extension interacts with the TBP/TATA box com

137 ide A-183 (EEWEVLCWTWETCER) suggested that a C-terminal extension into the FVIIa active site could yi

138 d them to open the F pocket and expose their C-terminal extension into the solvent.

139 al of the 1291-1302-amino acid region of the C-terminal extension is critical for relieving the auto-

140 imeras we demonstrated that the ER alpha DBD C-terminal extension is required for directed DNA bendin

141 n1 is a critical centrosomal component whose C-terminal extension is required for proper recruitment

142 ation of serines 261 and 289, located in the C-terminal extension, is required for Gem-mediated cytos

143 However, removal of the C-terminal extension leads to a complex dissociation pat

144 ates strongly decreased with increase of the C-terminal extension length.

145 first binding all phage containing A-183 and C-terminal extension libraries to immobilized and inacti

146 re domain harbors the nuclease activity, the C-terminal extension may be important for protein-protei

147 Our major finding is that the C-terminal extension (motif 3) is critical to 4E-BP1-med

148 extension plus motif IV [betaB1(1-190)], or C-terminal extension + motif III + motif IV [betaB1(1-14

149 the cellular level we have characterized the C-terminal extension mutants and other mutants, addressi

150 C-terminal extension mutants generally showed dramatical

151 Co-localization of the N terminus and the C-terminal extension near the hinge of the kinase domain

152 Here, we provide evidence that the unusual C-terminal extension negatively regulates phospholipid t

153 lic cpn10 sequences, except for a 25-residue C-terminal extension not found in any other cpn10.

154 e precursor of gallinacin-3 contained a long C-terminal extension not present in the prepropeptide.

155 ion of cofactor insertion was removal of the C-terminal extension observed.

156 onical N-terminal binding core yet exhibit a C-terminal extension of 1-30 amino acids.

157 ptide consisting of native ANP((1-28)) and a C-terminal extension of 12 AA.

158 Leiomodin also contained a C-terminal extension of 150 residues.

159 hClpP has an extra C-terminal extension of 28 amino acids.

160 closely packed helical modules followed by a C-terminal extension of 32 aa.

161 a striking example of how a splice-generated C-terminal extension of a sperm tail-associating protein

162 An A. aeolicus variant lacking the unique C-terminal extension of Aacpn10 displays the same kineti

163 co-crystal structure of LeuRS showed that a C-terminal extension of about 60 amino acids forms a dis

164 ses indicate that the disulfide bond and the C-terminal extension of ABri are required for the format

165 ty than the deletion of N-terminal domain or C-terminal extension of alphaA-crystallin.

166 ding regions of alphaA and alphaB and in the C-terminal extension of alphaB.

167 he conserved phosphorylation site found in a C-terminal extension of angiosperm GUN4.

168 e for substrate conduction and a cytoplasmic C-terminal extension of approximately 25 residues.

169 A single dileucine signal in the C-terminal extension of BMPRII-LF accounted for its fast

170 The C-terminal extension of capsid protein VP3 folds into a

171 Both the C-terminal end of Bni5 and the C-terminal extension of Cdc11 make important contributio

172 s, an M-domain loop, and the cpSRP43 binding C-terminal extension of cpSRP54 are predominantly disord

173 erotetramer shows that FliW interacts with a C-terminal extension of CsrA.

174 Here, we show that the C-terminal extension of DotL interacts with DotN, IcmS,

175 A C-terminal extension of Dsn1 recruits Ndc80C to the oppo

176 thermore, we show that residues 66-72 in the C-terminal extension of Escherichia coli Hfq are essenti

177 elocalized Plk1 from the centrosomes and the C-terminal extension of hCenexin1 was crucial to recruit

178 This result shows that the C-terminal extension of Hfq may be required for some for

179 matin stabilization requires the lysine-rich C-terminal extension of HMO1 as truncation of the HMO1 C

180 by mutational and kinetic analysis that the C-terminal extension of human CysRS is used to selective

181 In addition, we show that the C-terminal extension of human FEN-1 likely interacts wit

182 Finally, we find that deleting the C-terminal extension of Lmod1 and Lmod2 results in an ap

183 Notably, we observe a role for the C-terminal extension of N in directly preventing prematu

184 Furthermore, the C-terminal extension of NAP5 surprisingly interacts with

185 constrained through two disulfide bonds to a C-terminal extension of noncanonical secondary structure

186 drG subdomains followed by the movement of a C-terminal extension of one subdomain to cover the ligan

187 avior of the calmodulin (CaM) domain and the C-terminal extension of OsCaM61 in the absence and prese

188 partic protease regions, but each also has a C-terminal extension of over 80 residues, which includes

189 ion also decreases HX in a 3-10 helix at the C-terminal extension of p38alpha.

190 A peptide corresponding to the C-terminal extension of ProP forms a homodimeric alpha-h

191 Upon binding to SBT4.13, the C-terminal extension of SPI-1 was proteolytically cleave

192 onmental persistence, the interaction of the C-terminal extension of SpoIIID with DNA is a potential

193 ween the conserved and functionally critical C-terminal extension of TetM and the decoding center of

194 ween the conserved and functionally critical C-terminal extension of TetM with a unique splayed confo

195 tein, termed transframe (TF), comprised of a C-terminal extension of the 6K protein in the -1 open re

196 by recruiting additional His ligands from a C-terminal extension of the alpha5 helix.

197 stream and is predicted to give a 21-residue C-terminal extension of the apoAII protein identical to

198 icates that the two cysteine residues in the C-terminal extension of the B subunit of the light-activ

199 icity of CM15 expressed intracellularly as a C-terminal extension of the carrier protein ketosteroid

200 Here we show that the C-terminal extension of the enzyme is not required for t

201 (KIND) of Spire directly interacts with the C-terminal extension of the formin homology domain 2 (FH

202 otein product (MCM9M) that eliminates a long C-terminal extension of the fully spliced product (MCM9L

203 An acidic C-terminal extension of the gp2.5 protein, which is requ

204 The first is the C-terminal extension of the kinase domain, which was obs

205 nd spectroscopic analysis indicated that the C-terminal extension of the large subunit is essential f

206 KK2 and MEK5 PB1 domains and a 34-amino-acid C-terminal extension of the MEK5 PB1 domain.

207 Elements within the C-terminal extension of the NC domain are highly conserv

208 rities between the PEAK1 SHED region and the C-terminal extension of the Parkinson's disease-associat

209 ain binding sites for MEKK2 and ERK5, with a C-terminal extension of the PB1 domain contributing to E

210 and Psb27 is triggered by the removal of the C-terminal extension of the pD1 protein.

211 ition by interacting with a highly conserved C-terminal extension of the PH domain.

212 Importantly, aberrant C-terminal extension of the SAM domain in bpk mutant Bic

213 protein are responsible for re-directing the C-terminal extension of the second subdomain required fo

214 The unusual C-terminal extension of the U. maydis Hac1 homolog, Cib1

215 he complement proteins is a 150-residue-long C-terminal extension of their alpha-subunits that harbor

216 This activity of IF3(mt) requires the C-terminal extension of this factor.

217 C-terminal extension of this peptide has little effect,

218 In contrast, a C-terminal extension of three residues increased SspC's

219 recently provided structural evidence that a C-terminal extension of TnI is anchored on actin at low

220 Specifically, we demonstrate that the C-terminal extension of VgrG-3 acts to degrade peptidogl

221 domain-swapping analysis identified that the C-terminal extension of VgrG1 specifically confers Tde1

222 sts of an 80 amino acid J-domain, and N- and C-terminal extensions of 24 and 21 amino acid residues,

223 Src homology 3 (SH3)-like domain with N- and C-terminal extensions of about 20 aa. each.

224 ) or betaB2 (rbetaB2Ntr), or both the N- and C-terminal extensions of betaB2 (rbetaB2NCtr).

225 rotetrameric coiled coils between the paired C-terminal extensions of Cdc3 and Cdc12 projecting ortho

226 but not DP strictly requires flanking N and C-terminal extensions of minimal length.

227 Removal of both N- and C-terminal extensions of rbetaB2 also increases these pa

228 Furthermore, the plant-specific C-terminal extensions of the ClpP/R subunits were not pr

229 s predict proteins that carry N-terminal and C-terminal extensions of the guanylate kinase-like domai

230 The acidic C-terminal extensions of tubulin subunits are not essent

231 GH loops of VP3 and VP1, and disordering of C-terminal extensions of VP1 and VP2.

232 pared in which the N-terminal extension, the C-terminal extension or both extensions were deleted.

233 RGS7 for Galpha(o) does not depend on N- or C-terminal extensions or a Gbeta(5) subunit but resides

234 resent the structure of the human telomerase C-terminal extension (or thumb domain) determined by the

235 from an ancestral KH motif protein by N- and C-terminal extensions, or one of the existing topologies

236 that both the catalytic site of CtBP and the C-terminal extension play important, if nonessential rol

237 252)], C-terminal extension [betaB1(1-234)], C-terminal extension plus motif IV [betaB1(1-190)], or C

238 bsequent deletions of the C-terminal domain (C-terminal extension plus motifs III and IV) while it re

239 a sheet to the last two alpha helices in the C-terminal extension, potentially providing a mechanism

240 ression of a mutant of TbECK1 that lacks the C-terminal extension produces a slow growth phenotype, a

241 in synthesized as an 80-amino acid ubiquitin C-terminal extension protein (CEP80), functions as a nov

242 d, for example, by phosphorylation of Ser or C-terminal extensions, providing binding-incompetent PDZ

243 l phosphatidylinositol binding domain, and a C-terminal extension related to the Gbetagamma binding d

244 Moreover, TbECK1 possesses a long C-terminal extension reminiscent of those found in mamma

245 the Spn4 proteins (Spn4.1) features a unique C-terminal extension, reminiscent of an endoplasmic reti

246 of the N-terminal domain (residues 1-63) or C-terminal extension (residues 140-173) affected the str

247 N-terminal domain (residues 1-63) deleted or C-terminal extension (residues 140-173) deleted alphaA m

248 ion (residues 45-74) and a partially ordered C-terminal extension (residues 285-362) that bridges the

249 iption elongation factor SPT5 and contains a C-terminal extension rich in GW/WG repeats.

250 erse transcriptases (RTs), flanked by N- and C-terminal extensions specific to TERTs.

251 It shows that the MAPK insert and C-terminal extension, structural motifs that are unique

252 he N terminus and a particular region of the C-terminal extension suppresses the intrinsic autophosph

253 elix followed by an acidic region (AR) and a C-terminal extension termed the C-tail.

254 NADP (+), and the characteristic AFVEK (258) C'-terminal extension that is typical of bacterial FPRs

255 obic inter-domain interactions and by the N2 C-terminal extension that complements a beta-sheet on N1

256 ably expresses mouse 5-HT(3A)Rs containing a C-terminal extension that confers high-affinity binding

257 to methionine aminopeptidases, coupled to a C-terminal extension that contains important motifs for

258 Instead, they contain a C-terminal extension that directs gamma-carboxylation bu

259 Cdk12 contains a C-terminal extension that folds onto the N- and C-termin

260 complex, yet contains a eukaryotic-specific C-terminal extension that follows the tRNA anticodon-bin

261 ical RNA recognition motif with a disordered C-terminal extension that forms an alpha helix in the co

262 DbpA contain an approximately 80 amino acid C-terminal extension that has been proposed to specifica

263 ermit to drive conformational changes in the C-terminal extension that have been associated with sign

264 WH2 lacks a C-terminal extension that in Tbeta4 becomes involved in

265 known GT-B structures, however, there is no C-terminal extension that interacts with the N-terminal

266 NSUN4 lacks an N- or C-terminal extension that is commonly used for RNA recog

267 fide-rich core and a structurally disordered C-terminal extension that is essential for channel block

268 ProP contains a cytoplasmic, C-terminal extension that is essential for its activity.

269 omposed of only a core domain, followed by a C-terminal extension that may serve as a ligand for bind

270 lysine residue and a tyrosine residue of the C-terminal extension that penetrates a partner subunit t

271 eption of EsxB, B. anthracis proteins harbor C-terminal extensions that are appended to canonical WXG

272 of this protein family often contain N- and C-terminal extensions that are responsible for additiona

273 ipain-B, and we show that it contains N- and C-terminal extensions that render a low amount of latenc

274 hate isomerase (TIM) barrel fold with N- and C-terminal extensions that tailor the structure of the e

275 protein and is affected by a fungal-specific C-terminal extension, the conserved catalytic core, and

276 rystallin compared to deletion of either the C-terminal extension, the N-terminal domain, or the C-te

277 The importance of the C-terminal extension to AmtB activity remains unclear.

278 pens the HLA class I F' pocket, allowing the C-terminal extension to protrude through one end of the

279 ng a disulphide bridge that tethers the long C-terminal extension to the body of the structure.

280 s delta virus (HDV) differ only in the 19-aa C-terminal extension unique to deltaAg-L. deltaAg-S is n

281 ch differ by an approximately 500 amino acid C-terminal extension, unique among TGF-beta superfamily

282 A short helix at the C-terminal extension uniquely found in mycobacterial Glm

283 To unravel the functional role of the C-terminal extension, we used an enzymatic in vitro matu

284 a protein-peptide complex by designing N or C-terminal extensions which interact with the protein ou

285 COOH-terminal to the DNA-binding domain (the C-terminal extension), which is required for interaction

286 nal HerA-ATP synthase domain and a conserved C-terminal extension, which acts as a physical brace bet

287 nthetic organisms reveals the evolution of a C-terminal extension, which harbors the phosphorylation

288 Interestingly, the C-terminal extension, which includes two helices connect

289 This binding was not affected by cry1's C-terminal extension, which is important for signal tran

290 The precursor form of D1 (pD1) contains a C-terminal extension, which is removed by the protease C

291 A functional role for the C-terminal extension, which is unique to lymphotactin, r

292 The protein also contains a C-terminal extension, which is very uncommon among mamma

293 potexvirus CP and phlebovirus NP is in their C-terminal extensions, which appear to determine the cha

294 pneumophila, contains an ATPase domain and a C-terminal extension whose function is unknown.

295 the C-terminal lobe, and (iii) a 240 residue C-terminal extension with a modified cystine knot motif

296 OsCaM61 bears a unique C-terminal extension with a prenylation site.

297 contraction enzyme, CbiH(60), that harbors a C-terminal extension with sequence similarity to the nit

298 C-terminal extension with the KRY sequence from PACAP38

299 hanced its activity in agonizing TLR4, while C-terminal extension with the native FNIII 12-13-14 hepa

300 sequence is unchanged upon addition of a P10 C-terminal extension, yielding a critical nucleus of one