ライフサイエンスコーパス: carboxy-terminal domain

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

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

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

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

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

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

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

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

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

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

11 homology RNA-binding domains and an unusual carboxy-terminal domain.

12 e transmembrane domains and an intracellular carboxy-terminal domain.

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

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

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

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

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

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

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

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

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

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

23 A highly charged carboxy terminal domain and consensus phosphorylation si

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

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

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

27 at the domain interface, with Cys217 of the carboxy terminal domain, and we suggest that these two c

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

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

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

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

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

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

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

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

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

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

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

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

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

41 anticipated, the enzyme contains amino- and carboxy-terminal domains corresponding to the DNA-recogn

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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 s Pol II around the Rpb4-Rpb7 stalk near 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 is its long C-terminal extension, called 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 catalytic core domain flanked by amino- and carboxy-terminal domains essential for the concerted int

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

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

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

113 The carboxy-terminal domain forms a hydrophobic pocket which

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

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

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

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

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

119 The carboxy-terminal domain has DNA-binding activity coincid

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

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

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

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

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

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

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

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

128 via one transmembrane domain with amino- and carboxy-terminal domains in the cytoplasm and periplasm,

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

154 The carboxy-terminal domain of Dp140 is identical to that of

155 The approximately 25 kDa carboxy-terminal domain of Drosophila Hedgehog protein (

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

179 -transferase with the catalytically inactive carboxy-terminal domain of LPL did not activate CT despi

180 -transferase with the catalytically inactive carboxy-terminal domain of LPL that partially blocked LP

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

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

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

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

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

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

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

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

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

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

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

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

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

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

197 endent upon the phosphorylation state of 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 of the interdomain connector loop and of the carboxy-terminal domain of Saccharomyces cerevisiae prol

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

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

205 The cytoplasmic carboxy-terminal domain of SpoIIE contains a serine phos

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

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

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

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

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

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

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

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

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

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

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 e for HPV-11 capsid formation, much like the carboxy-terminal domain of the polyomavirus VP1 protein.

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

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

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

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

230 binding motifs and instead is similar to the carboxy-terminal domain of the yeast spliceosome 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 vity assays demonstrate that both amino- and carboxy-terminal domains of BSP contribute to restoratio

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

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

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

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

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

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

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

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

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

252 The conserved carboxy-terminal domains of SMADs are sufficient for ind

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

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

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

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

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

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

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

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

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

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

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

264 The carboxy-terminal domain resembles the ubiquitous cellula

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

281 and p20C/EBPbeta bind to SRF in vitro via a carboxy-terminal domain that probably does not include t

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

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

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

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

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

291 The carboxy-terminal domain was required only for homodimeri

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

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

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

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

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

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

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

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

300 The carboxy-terminal domain, whose function is unknown, is a