ライフサイエンスコーパス: carboxy-terminal domain

1 its catalytic domain, but rather within the carboxy-terminal domain.

2 and Pol II phosphorylated at serine 5 of the carboxy-terminal domain.

3 obic membrane domain, and a long hydrophilic carboxy-terminal domain.

4 nce in protein regulation also reside in the carboxy-terminal domain.

5 ry effects identified two residues in Sis1's carboxy-terminal domain.

6 by distinguishing amino acid changes in the carboxy-terminal domain.

7 specific signal peptide present in the Reln carboxy-terminal domain.

8 with the Arp2/3 complex through a conserved carboxy-terminal domain.

9 criptional repression mediated by the XTcf-3 carboxy-terminal domain.

10 Crk, Fyn, and others; and a highly conserved carboxy-terminal domain.

11 novel interaction between tRNA and the Elp1 carboxy-terminal domain.

12 -sensing and pore domains, and a cytoplasmic carboxy-terminal domain.

13 is activated and phosphorylates Cdc10 at its carboxy-terminal domain.

14 and increased ubiqutination within the Rbp1 carboxy-terminal domain.

15 n between FtsZ and ZipA occurs through their carboxy-terminal domains.

16 ngage the core structure via their integrase carboxy-terminal domains.

17 nteracting transactivator, with Glu/Asp-rich carboxy-terminal domain 2 (CITED2), a gene that mediates

18 clustered charged-to-alanine mutants in the carboxy-terminal domain 3 of N protein.

19 terminant of the N-M interaction maps to the carboxy-terminal domain 3 of the N protein.

20 n response to CCL5, indicating that the US28 carboxy-terminal domain also regulates agonist-dependent

21 A highly charged carboxy terminal domain and consensus phosphorylation si

22 e conserved heptapeptide repeats in the Rpb1 carboxy-terminal domain and is mediated principally by t

23 t and Val149 --> Met) are located within the carboxy-terminal domain and maintain or improve packing

24 using a recombinant OcXII harboring only the carboxy-terminal domain and this part did not exhibit an

25 lus subtilis ortholog YxiN have similar 75aa carboxy-terminal domains, and both proteins are specific

26 roteins, we find that sequences in the human carboxy-terminal domain are critical for telomere mainte

27 cretion of numerous other proteins that have carboxy-terminal domains associated with targeting to th

28 These data support a model in which the carboxy-terminal domain binds hairpin 92 to target the p

29 ge lambda nascent mRNA transcripts while the carboxy-terminal domain binds RNA polymerase and arrests

30 leosomal DNA and tethers H2A-H2B through its carboxy-terminal domain by acting as a placeholder for D

31 ST-amino-terminal domain (N-term or NTD)/GST-carboxy-terminal domain (C-term or CTD) intramolecular a

32 sense mutation occurs outside this conserved carboxy-terminal domain, closely upstream of an SIP1 (SM

33 n to target to the Golgi apparatus through a carboxy-terminal domain containing a conserved tyrosine

34 re, the cell line lex1/lex2, which lacks the carboxy-terminal domain containing the phosphorylated re

35 otein that has a unique amino-terminus and a carboxy-terminal domain containing two ankyrin-repeat mo

36 /alpha sandwich that binds OOHL, whereas the carboxy-terminal domain contains a helix turn helix DNA-

37 The Elp1 carboxy-terminal domain contains a highly conserved argi

38 a "kelch" type beta-propeller fold, and the carboxy-terminal domain contains a repeat of a fibronect

39 ces encoding the signal peptide (SS) and the carboxy-terminal domain (CT) of beta-lactamase, and clon

40 proteins are kinases which phosphorylate the carboxy terminal domain (CTD) of RNA polymerase II (Pol

41 Cyclin T1/CDK9 complexes phosphorylate the carboxy terminal domain (CTD) of RNA polymerase II (RNAP

42 purified CDK8 in vitro for RNA polymerase II carboxy-terminal domain (CTD) and histone H3 substrates.

43 ng seven alpha-helices and a beta-hairpin, a carboxy-terminal domain (CTD) comprising four alpha-heli

44 The RNA polymerase II carboxy-terminal domain (CTD) consists of tandem Y(1)S(2

45 sons revealed that multiple genes related to carboxy-terminal domain (CTD) family proteins, including

46 isomerizing peptide bonds within the pol II carboxy-terminal domain (CTD) heptapeptide repeat (YSPTS

47 ame phosphorylated at serines 2 and 5 in its carboxy-terminal domain (CTD) heptapeptide repeats (YSPT

48 n and processing, and the role of the Pol II carboxy-terminal domain (CTD) in regulating these proces

49 man immunodeficiency virus type 1 (HIV-1) CA carboxy-terminal domain (CTD) is essential for CA-CA int

50 Although Bur1 can phosphorylate the Rpb1 carboxy-terminal domain (CTD) kinase in vitro, it has no

51 We focused on acetylations of the carboxy-terminal domain (CTD) of alpha because of its re

52 dentified SEM-5 as able to interact with the carboxy-terminal domain (CTD) of EGL-15, a domain that i

53 Ess1 binds the carboxy-terminal domain (CTD) of pol II and is thought t

54 This inhibition requires the carboxy-terminal domain (CTD) of Pol II.

55 Truncation of the regulatory carboxy-terminal domain (CTD) of RNA pol II disrupts tra

56 vents that are all stimulated in vivo by the carboxy-terminal domain (CTD) of RNA Pol II.

57 In mammals, the carboxy-terminal domain (CTD) of RNA polymerase (Pol) II

58 hnRNPG directly binds to the phosphorylated carboxy-terminal domain (CTD) of RNA polymerase II (RNAP

59 i-subunit complex stably associated with the carboxy-terminal domain (CTD) of RNA polymerase II (RNAP

60 The carboxy-terminal domain (CTD) of RNA polymerase II (RNAP

61 sential for P-TEFb to hyperphosphorylate the carboxy-terminal domain (CTD) of RNA polymerase II and m

62 air which has been found associated with the carboxy-terminal domain (CTD) of RNA polymerase II holoe

63 nd P-TEFb are both able to phosphorylate the carboxy-terminal domain (CTD) of RNA polymerase II, but

64 s/trans isomerase (PPIase) that binds to the carboxy-terminal domain (CTD) of RNA polymerase II.

65 litates transcription by phosphorylating the carboxy-terminal domain (CTD) of RNA polymerase II.

66 ment of capping enzyme to the phosphorylated carboxy-terminal domain (CTD) of RNA polymerase II.

67 on of capping enzyme with the phosphorylated carboxy-terminal domain (CTD) of RNA polymerase II.

68 phosphorylation of the heptad repeat of the carboxy-terminal domain (CTD) of RNAPII.

69 ly with inhibition of phosphorylation in the carboxy-terminal domain (CTD) of RNApolII, as well as wi

70 biochemical approach, we have identified the carboxy-terminal domain (CTD) of Rpb1, the largest subun

71 The carboxy-terminal domain (CTD) of the core protein of hep

72 The carboxy-terminal domain (CTD) of the large subunit of RN

73 the failure to phosphorylate serine 2 in the carboxy-terminal domain (CTD) of the large subunit of RN

74 2)-Pro(3)-Thr(4)-Ser(5)-Pro(6)-Ser(7) in the carboxy-terminal domain (CTD) of the largest RNA polymer

75 ating Ser2 of the heptapeptide repeat of the carboxy-terminal domain (CTD) of the largest subunit of

76 mably mediated by its phosphorylation of the carboxy-terminal domain (CTD) of the largest subunit of

77 as a protein kinase that phosphorylates the carboxy-terminal domain (CTD) of the largest subunit of

78 or b (P-TEFb) through phosphorylation of the carboxy-terminal domain (CTD) of the largest subunit of

79 The carboxy-terminal domain (CTD) of the largest subunit of

80 Posttranslational modifications of the carboxy-terminal domain (CTD) of the largest subunit of

81 ach complex are known to bind pol II via the carboxy-terminal domain (CTD) of the largest subunit, Rp

82 The carboxy-terminal domain (CTD) of the RNA polymerase II (

83 The carboxy-terminal domain (CTD) of the RNA polymerase II (

84 g reactions through interactions between the carboxy-terminal domain (CTD) of the RNAP II largest sub

85 anylyltransferase Cgt1 cocrystallized with a carboxy-terminal domain (CTD) peptide composed of four S

86 gated the role of RNA polymerase II (pol II) carboxy-terminal domain (CTD) phosphorylation in pre-mRN

87 , polymerase II (Pol II), and phospho-Ser(2) carboxy-terminal domain (CTD) Pol II to the IFN-stimulat

88 lation of a heptapeptide repeat known as the carboxy-terminal domain (CTD) present in the largest sub

89 NAPII) foci, predominantly phosphorylated at carboxy-terminal domain (CTD) residue Tyr1, at DSBs.

90 inase 9 (CDK9) recruitment and phospho-Ser 2 carboxy-terminal domain (CTD) RNA polymerase (Pol) II fo

91 mplekin in a ternary complex with the Pol II carboxy-terminal domain (CTD) Ser 5 phosphatase Ssu72 an

92 gest subunit of Pol II contains a repetitive carboxy-terminal domain (CTD) that becomes highly phosph

93 its, a core that binds UPF1 and a protruding carboxy-terminal domain (CTD) that binds the SMG1 kinase

94 n of the amino-terminal domain (NTD) and the carboxy-terminal domain (CTD) was found to be essential

95 y consist of an approximately 100-amino acid carboxy-terminal domain (CTD) with two helix-turn-helix

96 hosphorylates the RNA polymerase II (RNApII) carboxy-terminal domain (CTD) within the transcription i

97 five SRB genes, identified as suppressors of carboxy-terminal domain (CTD)-truncation mutants; produc

98 is its long C-terminal extension, called the carboxy-terminal domain (CTD).

99 the RNA polymerase II large subunit (Pol II) carboxy-terminal domain (CTD).

100 he phosphorylated form of the RNA polymerase carboxy-terminal domain (CTD).

101 s Pol II around the Rpb4-Rpb7 stalk near the carboxy-terminal domain (CTD).

102 s secreted by T9SSs typically have conserved carboxy-terminal domains (CTDs) belonging to the TIGRFAM

103 e differences between HDAC1 and HDAC2, their carboxy-terminal domains (CTDs) were deleted, which led

104 We recently showed that the carboxy-terminal domain (Cterm) of human mt-leucyl tRNA

105 Phosphorylation within a carboxy-terminal domain, designated the hydrophobic moti

106 In contrast, transfection of the ErbB-2 carboxy-terminal domain did not induce apoptosis.

107 ishes NPK1 activity, and the presence of the carboxy-terminal domain diminishes the kinase activity.

108 eletions in the highly conserved hydrophobic carboxy-terminal domain disrupted both protein function

109 fy unique contributions for the spectrin and carboxy-terminal domains during different phases of spin

110 catalytic core domain flanked by amino- and carboxy-terminal domains essential for the concerted int

111 t of two residues in the L3 loop of the Smad carboxy-terminal domain establish the specificity of rec

112 avin dinucleotide, which binds to a distinct carboxy-terminal domain, fails to alter FAC-RED complexe

113 n that functions in flagellar assembly and a carboxy-terminal domain (FliG-C) that functions specific

114 The carboxy-terminal domain forms a hydrophobic pocket which

115 A carboxy-terminal domain from HDHB confers cell cycle-dep

116 o yield a protein that retained a 57-residue carboxy terminal domain fused to the catalytic core.

117 stabilize the protein and are located in the carboxy-terminal domain generally slow the rate of foldi

118 of the beta-promoter revealed that a smaller carboxy-terminal domain generated an open promoter confi

119 the intrinsically disordered linker histone carboxy-terminal domain (H1 CTD) influences chromatin st

120 emical and functional studies, that the Srs2 carboxy-terminal domain harbours tandem receptor motifs

121 lial monocyte-activating polypeptide II-like carboxy-terminal domain has potent leukocyte and monocyt

122 americ ring formed by the amino-terminal and carboxy-terminal domains, have been deleted; an asymmetr

123 cription, whereas phosphorylation within the carboxy-terminal domain II is necessary for replication.

124 results indicate that phosphorylation of the carboxy-terminal domain II residues of P protein are req

125 o examine the role of phosphorylation of the carboxy-terminal domain II residues of the P protein in

126 trate for the first time that the 57-residue carboxy-terminal domain in CCTalpha participates in lipi

127 se-resistant domain and a protease-sensitive carboxy-terminal domain in N-218 MLN64 is similar to the

128 The role of specific residues in the carboxy-terminal domain in transcription termination wer

129 The nucleotide-binding loop and the carboxy-terminal domain, including the suspected catalyt

130 B protein (CSB) or overexpression of the p53 carboxy-terminal domain induces fragility of the same lo

131 of assembly not driven by the strong capsid carboxy-terminal domain interactions that characterise c

132 We find that the carboxy-terminal domain interacts with the plus-end trac

133 and involving a region of the middle domain/carboxy-terminal domain interface previously suggested t

134 f serine residues 151 and 153 within a novel carboxy-terminal domain is critical for function in vivo

135 lyses of stable cell lines revealed that the carboxy-terminal domain is necessary to prevent the shut

136 er GCN5-related N-acetyltransferases but the carboxy-terminal domain is not.

137 ndrogen receptor (AR), ligand binding to the carboxy-terminal domain (LBD) regulates transcriptional

138 Carboxy-terminal domains line the central ion pore, and

139 utionarily restrictive catalytic core domain-carboxy-terminal domain linker regions.

140 f the carboxy terminus of Rad9 and that this carboxy-terminal domain may be a specific requirement fo

141 The carboxy terminal domain of NuMA binds MTs, allowing a Nu

142 ranscription activation domain of Gal4p, the carboxy terminal domain of Tcn1p directed strong calcine

143 nal epitope that requires both the amino and carboxy terminal domains of GPC3.

144 We have studied the contribution of the carboxy terminal domains of lipid-free apoE isolated fro

145 proteins-and each RP chaperone binds to the carboxy-terminal domain of a specific Rpt.

146 The carboxy-terminal domain of A20, composed of seven C2/C2

147 present data suggesting that the cytoplasmic carboxy-terminal domain of amphiregulin plays an importa

148 s in TNNI2 that are predicted to disrupt the carboxy-terminal domain of an isoform of troponin I (TnI

149 The carboxy-terminal domain of apo(a) containing 6 type-4 kr

150 Furthermore, the carboxy-terminal domain of Bee1p greatly stimulated the

151 Interestingly, deletion of the carboxy-terminal domain of Bee1p neither abolished the l

152 e present the X-ray crystal structure of the carboxy-terminal domain of Brd4 in complex with HPV-16 E

153 In contrast, the carboxy-terminal domain of Cbl, when attached to Grb2 SH

154 The carboxy-terminal domain of DNTTIP1 has a structure relat

155 specifically interact with the intracellular carboxy-terminal domain of EAAT4 and modulate its glutam

156 Both the carboxy-terminal domain of EEA1 (residues 1098-1411) and

157 Here we show that the carboxy-terminal domain of EED specifically binds to his

158 ding of activated CheY to FliM displaces the carboxy-terminal domain of FliG (FliGC) from FliM, modul

159 between FMRP and Ca(V)2.2 occurs between the carboxy-terminal domain of FMRP and domains of Ca(V)2.2

160 ugh a virus-specific interaction with the p6 carboxy-terminal domain of Gag.

161 The carboxy-terminal domain of gp5 is a triple-stranded beta

162 n of Rad51 by Chk1 or phosphorylation of the carboxy-terminal domain of hBRCA2 by Chk1 or Chk2 plays

163 oint kinases Chk1 and Chk2 phosphorylate the carboxy-terminal domain of hBRCA2, a protein involved in

164 histone variant that is 62% identical to the carboxy-terminal domain of histone H3 [4,5] and that res

165 w, with the use of crystallography, that the carboxy-terminal domain of human Dnmt3L interacts with t

166 owed selective competitive inhibition of the carboxy-terminal domain of human somatic ACE providing e

167 We determined the crystal structure of the carboxy-terminal domain of human SRAP and found that it

168 the amino-terminal domain is more similar to carboxy-terminal domain of I-DmoI and to I-CreI, with in

169 Finally, the carboxy-terminal domain of I-DmoI is smaller and has a m

170 IME2-DeltaC241, which removes the carboxy-terminal domain of Ime2, exacerbated the smk1-2

171 The carboxy-terminal domain of IN alone retained its interac

172 The carboxy-terminal domain of Int (75-356) is responsible f

173 This interaction takes place through the carboxy-terminal domain of Lig4p and is required for Lig

174 ost proteins, and nonrepeat sequences in the carboxy-terminal domain of LigB show only weak interacti

175 onse (UPR) and autophagy in B cells, and the carboxy-terminal domain of LMP1 activates cellular signa

176 lls, the apoptosis required the UPR, and the carboxy-terminal domain of LMP1 blocked this apoptosis.

177 These findings illustrate how the carboxy-terminal domain of LMP1 supports survival of B c

178 ruited to origins by an essential, conserved carboxy-terminal domain of Mcm3 that interacts with and

179 This analysis indicates that the carboxy-terminal domain of Mei3 is sufficient for functi

180 ne residues 983 and 985 contained within the carboxy-terminal domain of Mga2p120 are Rsp5p-directed U

181 Our results show that the carboxy-terminal domain of N protein, N3, is necessary a

182 n1, which directly and selectively binds the carboxy-terminal domain of NR3A through its NPF motifs a

183 s located in the surface-exposed loop of the carboxy-terminal domain of nsP2 and exhibits high variab

184 nus of Nischarin preferentially binds to the carboxy-terminal domain of PAK1 when the kinase is in it

185 interdomain connector loop (IDCL) and of the carboxy-terminal domain of PCNA in Apn2 binding and foun

186 tion via phosphorylation of cyclin H and the carboxy-terminal domain of Pol II.

187 thereby facilitating phosphorylation of the carboxy-terminal domain of Pol II.

188 domain (IR1-M) and SUMO-1 conjugated to the carboxy-terminal domain of RanGAP1.

189 is model suggested that POA binds within the carboxy-terminal domain of ribosomal protein S1 (RpsA) a

190 The carboxy-terminal domain of RIP3, like that of RIP, could

191 FCP1, a phosphatase specific for the carboxy-terminal domain of RNA polymerase II (RNAP II),

192 CDK11 phosphorylates serine 2 (Ser2) of the carboxy-terminal domain of RNA polymerase II (RNAPII), w

193 nscription elongation by phosphorylating the carboxy-terminal domain of RNA polymerase II and selecti

194 The transcriptional cdks phosphorylate the carboxy-terminal domain of RNA polymerase II, facilitati

195 on factor b (P-TEFb) hyperphosphorylates the carboxy-terminal domain of RNA polymerase II, permitting

196 endent upon the phosphorylation state of the carboxy-terminal domain of RNA polymerase II.

197 gulates transcription by phosphorylating the carboxy-terminal domain of RNA polymerase II.

198 Sub1 influences Spt5 phosphorylation of the carboxy-terminal domain of RNAPII largest subunit by the

199 study described herein demonstrates that the carboxy-terminal domain of RNase E has little structure

200 The carboxy-terminal domain of RNase E may thus act as a fle

201 y may be involved in an interaction with the carboxy-terminal domain of Rns.

202 Interaction occurred between the carboxy-terminal domain of schwannomin isoform 2 and the

203 The carboxy-terminal domain of Sec10p does not interact with

204 ce the conformational states of the proximal carboxy-terminal domain of TcdB and could contribute to

205 vitro transcription assays indicate that the carboxy-terminal domain of the alpha subunit (alpha-CTD)

206 Subsequent analysis of the carboxy-terminal domain of the alpha subunit (alphaCTD)

207 the interacting surfaces of MarA and of the carboxy-terminal domain of the alpha subunit of RNAP (al

208 t the Na(+)-K(+)-ATPase, upon binding to the carboxy-terminal domain of the alpha subunit of the chan

209 n between calmodulin and a novel site in the carboxy-terminal domain of the alpha1A subunit of P/Q-ty

210 Inclusion of the carboxy-terminal domain of the core protein modifies the

211 Slob is a novel protein that binds to the carboxy-terminal domain of the Drosophila Slowpoke (dSlo

212 Slob, a novel protein that binds to the carboxy-terminal domain of the Drosophila Slowpoke (dSlo

213 a2 that lacks the long alternatively spliced carboxy-terminal domain of the isozyme.

214 Using the carboxy-terminal domain of the large subunit of RNA poly

215 ates Serine 5 of heptapeptide repeats on the carboxy-terminal domain of the largest Pol II subunit Rp

216 We found that the carboxy-terminal domain of the largest Pol II subunit wa

217 juxtaposes transcription factor IIH and the carboxy-terminal domain of the largest subunit of Pol II

218 n basal transcription by phosphorylating the carboxy-terminal domain of the largest subunit of RNA po

219 An interaction between the carboxy-terminal domain of the largest subunit of RNA po

220 For example, the CTD carboxy-terminal domain of the largest subunit of RNA po

221 ix additional mutations all clustered in the carboxy-terminal domain of the MID1 protein.

222 The RVA PDE forms the carboxy-terminal domain of the minor core protein VP3 (V

223 The carboxy-terminal domain of the paused polymerase large s

224 eraction between Ceg1 and the phosphorylated carboxy-terminal domain of the Pol II largest subunit.

225 major homology region (MHR), lies within the carboxy-terminal domain of the protein.

226 The carboxy-terminal domain of the receptor shows an extensi

227 in dbp5 mutant strains are dependent on the carboxy-terminal domain of the RNA pol II largest subuni

228 Some activators contact the carboxy-terminal domain of the RNA polymerase alpha subu

229 binding motifs and instead is similar to the carboxy-terminal domain of the yeast spliceosome protein

230 via a tetraleucine motif situated within the carboxy-terminal domain of this accessory protein.

231 Models for the binding of the 200-residue carboxy-terminal domain of two mutants of apolipoprotein

232 This analysis indicated that the carboxy-terminal domain of UBF, which is necessary for t

233 (RRMs) and a SPOC domain, a highly conserved carboxy-terminal domain of unknown function [5-7].

234 The intracellular carboxy-terminal domain of US28 contains residues critic

235 tion results in premature termination of the carboxy-terminal domain of VIR, resembling McClintock's

236 s one molecule of the Vps protein Vps22, the carboxy-terminal domain of Vps36 and two molecules of Vp

237 The carboxy-terminal domain of YTHDF2 selectively binds to m

238 Here we demonstrate that the carboxy-terminal domain of YxiN is sufficient to confer

239 stent with a chaperone activity in which the carboxy-terminal domain of YxiN tethers the protein to t

240 ric and heterooligomeric ENaCs, although the carboxy-terminal domains of beta- and gamma-ENaC subunit

241 Dkk domains and chimeric Dkks shows that the carboxy-terminal domains of both Dkks associate with LRP

242 rface on FACT appears to be protected by the carboxy-terminal domains of both of its subunits, and th

243 rface on FACT appears to be protected by the carboxy-terminal domains of both of its subunits, and th

244 vity assays demonstrate that both amino- and carboxy-terminal domains of BSP contribute to restoratio

245 rowth factors depends on distinct amino- and carboxy-terminal domains of CBP, respectively.

246 The amino- and carboxy-terminal domains of E2 each form immunoglobulin-

247 ion of cells in culture, both the amino- and carboxy-terminal domains of E3L were required for full p

248 arged regions conserved in the J-domains and carboxy-terminal domains of each J-protein class, and ar

249 The amino- and carboxy-terminal domains of IDE (IDE-N and IDE-C, respec

250 The amino- and carboxy-terminal domains of mitochondrially encoded cyto

251 ilaments possess side arms that comprise the carboxy-terminal domains of neurofilament middle and hea

252 and ADA2b, respectively, with AD1, AD2, and carboxy-terminal domains of p53.

253 transfer measurements between the amino- and carboxy-terminal domains of RuBisCO.

254 The amino- and carboxy-terminal domains of the 21.5-kD sieve element-sp

255 ht about by alterations in the cysteine-rich carboxy-terminal domains of the ligands.

256 s to functionally substitute in vivo for the carboxy-terminal domains of the NS1 protein.

257 leavage at additional sites in the amino and carboxy-terminal domains of the protein.

258 d amino-terminal and the leucine-rich repeat carboxy-terminal domains of Tmod.

259 t on preinitiation complex assembly and Ser5 carboxy-terminal domain phosphorylation for optimal asso

260 lling polymerase II (Pol II) recruitment and carboxy-terminal domain phosphorylation on the IL-8 and

261 han does wild-type US28, indicating that the carboxy-terminal domain plays an important role in regul

262 n with an amino-terminal GTPase domain and a carboxy-terminal domain predicted to be embedded in the

263 PKBR-1 has a kinase and a carboxy-terminal domain related to those of Akt/PKB, but

264 These include rotation of the amino- and carboxy-terminal domains relative to each other, and a m

265 The carboxy-terminal domain resembles the ubiquitous cellula

266 NMR assignments were obtained for the entire carboxy-terminal domain (residues K100-I190).

267 lation of Raf-1 at serine 338 and within the carboxy-terminal domain, resulting in an electrophoretic

268 erevisiae Arp2/3 complexes bound to the WASp carboxy-terminal domain reveal asymmetric, oblate ellips

269 S11 contains an extended carboxy-terminal domain rich in basic amino acids, which

270 amino-terminal RNA recognition motif and two carboxy-terminal domains rich in serine-arginine (SR) di

271 the RNA polymerase holoenzyme alpha subunit carboxy-terminal domain (RNAP alphaCTD) and stimulate tr

272 ad2/Smad4/FAST-1 complex to DNA; through its carboxy-terminal domain, Smad4 provides an activation fu

273 the highly exposed alpha-helix 2 of the Smad carboxy-terminal domain specify the interaction with the

274 Substitutions within the carboxy-terminal domain supported identification of RscS

275 have been identified within the cytoplasmic carboxy terminal domain that activates NF-kappaB.

276 tions of Int are apportioned between a large carboxy-terminal domain that cleaves and ligates DNA at

277 eceiver domain linked by a small region to a carboxy-terminal domain that contains an amino acid sequ

278 mediated by the human protein TAP requires a carboxy-terminal domain that directly interacts with com

279 bunits, a highly charged inter-region, and a carboxy-terminal domain that encodes a functional PP2C.

280 F-box proteins contain a carboxy-terminal domain that interacts with substrates a

281 hogen Pseudomonas syringae pv. tomato, has a carboxy-terminal domain that is an E3 ubiquitin ligase.

282 of phosphorylation in the amino-terminal and carboxy-terminal domains that are positioned to alloster

283 IcsA is anchored in the outer membrane by a carboxy-terminal domain (the beta domain), such that the

284 at Thr75 is the first residue of the minimal carboxy-terminal domain, thereby identifying a specific

285 of traR, and the resulting protein lacks the carboxy-terminal domain thought to constitute the DNA-bi

286 HV terminal-repeat (TR) sequence through its carboxy-terminal domain to mediate DNA replication.

287 l as alpharetroviruses by providing critical carboxy-terminal domains to the intasome core that canno

288 and STING interacted directly, through their carboxy-terminal domains, to promote STING dimerization,

289 tructed an HCMV recombinant virus encoding a carboxy-terminal domain truncation mutant of US28, FLAG-

290 mily of traffic ATPases revealed a conserved carboxy-terminal domain unique to family members which a

291 The carboxy-terminal domain unique to SJ170 was previously s

292 The carboxy-terminal domain was required only for homodimeri

293 This carboxy-terminal domain was sufficient to repress a hete

294 in many chromatin-associated proteins, and a carboxy-terminal domain which identifies it as a member

295 in phosphorylation of the RNA polymerase II carboxy-terminal domain, which in turn affects recruitme

296 A conserved carboxy-terminal domain, which is required for the IFN r

297 n containing the Taxol-binding site, and the carboxy-terminal domain, which probably constitutes the

298 the two Moody proteins differ in their long carboxy-terminal domains, which are generated by use of

299 o-terminal DNA-binding domains but different carboxy-terminal domains, which enable them to bind spec

300 anscripts that encode proteins with modified carboxy-terminal domains, while the mitochondrial isozym