ライフサイエンスコーパス: phosphorylated protein

1 utations resulting in lower abundance of the phosphorylated protein.

2 e previous lower-resolution structure of the phosphorylated protein.

3 as Delta Np63 alpha, and it was present as a phosphorylated protein.

4 tent with a chaperoning role for this highly phosphorylated protein.

5 er reaction and decrease in stability of the phosphorylated protein.

6 also observed in the presence of the 97-kDa phosphorylated protein.

7 RasGAP, and an unidentified 145-kDa tyrosine-phosphorylated protein.

8 ipitate with an unidentified 87 kDa tyrosine-phosphorylated protein.

9 ed an additional 2 mol of phosphate into the phosphorylated protein.

10 be easily modified to evaluate any tyrosine-phosphorylated protein.

11 serines are replaced with glutamate to mimic phosphorylated protein.

12 nd IRAK4 mRNA as well as increased total and phosphorylated protein.

13 me-mediated degradation of the mature, fully phosphorylated protein.

14 plex between c-Src and at least one tyrosine-phosphorylated protein.

15 This study revealed a plethora of newly phosphorylated proteins.

16 c kinase activity and PP2-sensitive tyrosine-phosphorylated proteins.

17 reflecting the experimental data, including phosphorylated proteins.

18 ern blotting with antibodies specific to the phosphorylated proteins.

19 Western blotting with antibodies specific to phosphorylated proteins.

20 motility, and alters the pattern of tyrosine phosphorylated proteins.

21 tacts containing enriched levels of tyrosine-phosphorylated proteins.

22 ellular location, and/or turnover of certain phosphorylated proteins.

23 trometric analysis of proteolytic digests of phosphorylated proteins.

24 rafts colocalized with the BCR and tyrosine-phosphorylated proteins.

25 when the SH2 domains of p85 bind to tyrosyl-phosphorylated proteins.

26 tion and proteasome-dependent degradation of phosphorylated proteins.

27 ate the conformation and function of certain phosphorylated proteins.

28 o catalyze the dephosphorylation of tyrosine-phosphorylated proteins.

29 greatly enhanced by enriching the sample of phosphorylated proteins.

30 -induced functional changes in other heavily phosphorylated proteins.

31 phosphate groups, such as phospholipids and phosphorylated proteins.

32 components paxillin, vinculin, and tyrosine-phosphorylated proteins.

33 as associated with 100- and 180-kDa tyrosine phosphorylated proteins.

34 ellular activity by binding and sequestering phosphorylated proteins.

35 regulation of the turnover of sumoylated and phosphorylated proteins.

36 tography (IMAC), which specifically binds to phosphorylated proteins.

37 oxal 5'-phosphate (PLP) and serine/threonine-phosphorylated proteins.

38 nes by lowering the levels of both total and phosphorylated proteins.

39 hich are known to interact with and regulate phosphorylated proteins.

40 Cool-associated tyrosine-phosphorylated protein 1 (Cat-1) is a signaling scaffold

41 cumulation of tyrosine- and serine/threonine-phosphorylated proteins, a marked increase in cellular T

42 ppressor protein with various functions) and phosphorylated proteins (Abraxas/BACH1/CtIP), implicated

43 ociation of PAK with 60- and 90-kDa tyrosine-phosphorylated proteins accompanied this.

44 Here, we report that multiple tyrosine-phosphorylated proteins accumulate transiently upon BCR

45 tified 11,552 distinct nonmodified and 2,852 phosphorylated proteins across the four root tissues.

46 One or more phosphorylated proteins activate GFA1 transcription beca

47 First, it is not known whether highly phosphorylated proteins alone can induce matrix minerali

48 Of 38 phosphorylated proteins analyzed, 8 were significantly d

49 AT5B mutations are associated with increased phosphorylated protein and a growth advantage to transdu

50 on the simultaneous measurement of multiple phosphorylated protein and phospholipid components in th

51 t, in dark-grown seedlings, NPH3 exists as a phosphorylated protein and that BL stimulates its dephos

52 n this study, we demonstrate that Atg29 is a phosphorylated protein and that this modification is cri

53 The newly tyrosine phosphorylated proteins and activated Src-family members

54 nd vinculin, have a central core of tyrosine phosphorylated proteins and are depleted of integrins at

55 in proteomics studies to effectively detect phosphorylated proteins and avoid time-consuming and exp

56 e results in decreased affinity for tyrosine-phosphorylated proteins and decreased PI3K membrane loca

57 ieval of rich biological information for the phosphorylated proteins and facilitates database annotat

58 mass spectrometry identification of tyrosine phosphorylated proteins and growth inhibition in the pre

59 ytes, M-CSF increased the levels of tyrosine-phosphorylated proteins and induced Akt activation in a

60 Clusters recruited tyrosine-phosphorylated proteins and induced spatially restricted

61 orylation, decreased the numbers of tyrosine-phosphorylated proteins and levels of type I collagen, a

62 ation of PI3-kinase associated with tyrosine-phosphorylated proteins and of p85/PI3-kinase associated

63 ing network describing the interaction of 11 phosphorylated proteins and phospholipids in human immun

64 tes the conformation and function of certain phosphorylated proteins and plays an important role in c

65 Furthermore, tyrosine-phosphorylated proteins and PLC-gamma2 were colocalized

66 14-3-3 proteins bind to phosphorylated proteins and regulate a variety of cellul

67 to both substrates and appropriate tyrosine-phosphorylated proteins and therefore can compete with t

68 Among the information were three partially phosphorylated proteins and three proteins heterozygous

69 ome mobility shift assays with both in vitro-phosphorylated proteins and with point mutants bearing n

70 CARP-1 is a tyrosine-phosphorylated protein, and ERRP treatments cause elevat

71 ORF45 was characterized as a phosphorylated protein, and it is localized in the cytop

72 s demonstrate that both Vac8p and Apg13p are phosphorylated proteins, and Apg13p phosphorylation is r

73 plicable to serine-, threonine- and tyrosine-phosphorylated proteins, and is capable of selectively i

74 organic phosphoesters such as phospholipids, phosphorylated proteins, and nucleic acids.

75 th ligand stimulation, a broader spectrum of phosphorylated proteins appears compared with EGF-treate

76 These Tyr33-phosphorylated proteins are mostly located in the mitoch

77 Interactions between FHA domains and phosphorylated proteins are thought to have essential ro

78 the past, identifying spectral variations in phosphorylated proteins arising from either the phosphat

79 the important regulatory event of selecting phosphorylated proteins as endocytic cargo.

80 immunoprecipitates for the existence of such phosphorylated proteins as targets for barrier regulatio

81 Phosphorylated proteins, as defined by the fluorescence

82 rometric identification of a 155-kD tyrosine phosphorylated protein associated with src homologous an

83 pectrometry was used to identify three major phosphorylated proteins associated with this PSI-Cyt b(6

84 Binding of the tyrosyl-phosphorylated proteins at the fructose 1,6-bisphosphate

85 chromatin-associated proteins, with the most phosphorylated protein band being near the same molecula

86 light chain 2 were identified in the highly phosphorylated protein bands with the highest scores.

87 The phosphorylated proteins bear the same phosphoepitope fou

88 VCaB45 are modulated by phosphorylation; the phosphorylated protein binds up to 100-fold more calcium

89 The phosphorylated protein bound significantly more calcium

90 The purified phosphorylated protein bound to a phosphotyrosine specif

91 ed with the tryptic digests of the naturally phosphorylated proteins bovine alpha- and beta-casein.

92 ide G(M1), a lipid raft marker, and tyrosine-phosphorylated proteins, but not CD45 and transferrin re

93 ells showed a small set of discrete tyrosine-phosphorylated proteins, but these proteins were not rec

94 Standards of phosphorylated proteins can be used to correct for hydro

95 in a sequential gel staining procedure, the phosphorylated proteins can be visualized in the same ge

96 duced specific differences in the pattern of phosphorylated proteins, caused changes in lipid metabol

97 demonstrated here with the synthesis of the phosphorylated protein CHK2.

98 table differences in the pattern of tyrosine phosphorylated proteins compared with that obtained in c

99 r networks indicated differences in tyrosine phosphorylated proteins compared with the poorly aggress

100 Osteopontin (OPN) is a multifunctional phosphorylated protein containing the integrin binding s

101 phorylated by Btk; however, a third tyrosine-phosphorylated protein coprecipitated with Bright.

102 We discovered 2449 phosphorylated proteins corresponding to 4079 identified

103 The tyrosine phosphorylated protein Crk-associated substrate (CAS) ha

104 Analysis of tyrosine-phosphorylated proteins demonstrated that Crk-associated

105 The availability of large pools of tyrosine-phosphorylated proteins derived from normal tissues faci

106 ed by MALDI-MS was then utilized to identify phosphorylated proteins detected by autoradiography.

107 E4 in the Nova-1 pre-mRNA itself, encoding a phosphorylated protein domain, as an additional target o

108 teome analysis identified 310 differentially phosphorylated proteins (DP) from 350 phosphopeptides wi

109 d recombinant PP(240), and the native highly phosphorylated protein (equivalent to the PP(523) isofor

110 The prominent tyrosine-phosphorylated proteins focal adhesion kinase, paxillin,

111 To enable the synthesis of phosphorylated proteins for in vitro studies, we have ex

112 ), a protein complex implicated in targeting phosphorylated proteins for ubiquitination [7-10].

113 JIP1 is a multiply phosphorylated protein; for this reason, it was hypothes

114 les (AuNPs) can then be attached to the thio-phosphorylated proteins, forming a Au-film/AuNP plasmoni

115 hat is suited for nucleocapsid assembly, and phosphorylated protein forms a liquid-like compartment f

116 ion of TGF beta1, Smad2, and Samd3 and their phosphorylated protein forms, and cell cycle inhibitors,

117 e have partially purified a 105-kDa tyrosine-phosphorylated protein from platelets stimulated with ph

118 zation Protein 1 (CMP-1), an abundant mildly phosphorylated protein from the flexible membrane sugges

119 phosphorylated peptides corresponding to 449 phosphorylated proteins from 200 mug of zebrafish embryo

120 1 interacted with a small subset of tyrosine-phosphorylated proteins from lysates of the human breast

121 we performed a global profiling of tyrosine-phosphorylated proteins from mutant Kit-driven murine le

122 included redistribution of epithelial serine-phosphorylated proteins from the cytoplasm to the nucleu

123 the levels of the early apoptosis-associated phosphorylated protein, H2A-X (ser 139), as well as decr

124 have opposing effects on degradation of the phosphorylated protein; Hsp90 is protective, whereas Hsp

125 Additionally, we examined multiple phosphorylated proteins (i.e., protein kinase B/Akt and

126 precipitating high molecular weight tyrosine-phosphorylated protein identified as desmoglein 2.

127 ped to simultaneously measure both total and phosphorylated protein in a single sample.

128 n to be the major CSF-1R-associated tyrosine-phosphorylated protein in CSF-1-treated BMM.

129 ote cell migration, as a major hyper-tyrosyl-phosphorylated protein in mouse and zebrafish models of

130 The GluN2B subunit is the major tyrosine-phosphorylated protein in synapses.

131 sumes that vitellogenin is the most abundant phosphorylated protein in the analyzed tissue.

132 Pah1p is a highly phosphorylated protein in vivo and has been previously s

133 y proteomic approaches were used to identify phosphorylated proteins in a chronic pressure-induced ra

134 he difficulty of obtaining site-specifically phosphorylated proteins in adequate amounts.

135 -Cbl is one of the most prominently tyrosine-phosphorylated proteins in Bcr-Abl-expressing cells.

136 were prepared and used to pull down tyrosine-phosphorylated proteins in bovine ROS.

137 blot analysis, enables detection of specific phosphorylated proteins in complex mixtures such as cell

138 ever, current methods for analyzing tyrosine-phosphorylated proteins in crude protein extracts provid

139 kinase) substrates indicated the presence of phosphorylated proteins in cytosolic, membrane, and nucl

140 mutant (YF-Brk) and associates with tyrosine-phosphorylated proteins in deregulated signaling complex

141 d by immunoaffinity purification of tyrosine-phosphorylated proteins in GIST cells before and after t

142 Phosphoprotein profiling identified diverse phosphorylated proteins in glutamate-treated SCs in addi

143 SHP-1 is associated with two major tyrosine-phosphorylated proteins in hematopoietic cells treated w

144 These data provide a detailed annotation of phosphorylated proteins in human lymphoid cancer.

145 n cell culture (SILAC), to identify tyrosine phosphorylated proteins in isogenic human bronchial epit

146 sed for restoring the function of aberrantly phosphorylated proteins in lung cancer.

147 we found there were complex interactions of phosphorylated proteins in modulating cancer stemness in

148 low abundance tissue-annotated proteins and phosphorylated proteins in plasma, as well as quantitate

149 se) markedly increase the number of tyrosine-phosphorylated proteins in platelets.

150 Recruitment of GRB2 by tyrosine-phosphorylated proteins in response to TPO and convulxin

151 ing set of serine-, threonine-, and tyrosine-phosphorylated proteins in the Archaea that may offer ne

152 nity profiling strategy to identify tyrosine-phosphorylated proteins in the KG-1 cell line.

153 s in the rapid accumulation of many tyrosine-phosphorylated proteins in the liver and kidney of treat

154 Measurements of phosphorylated proteins in the RLC signalling and actin

155 es in the profiles of 75- and 80-kD tyrosine-phosphorylated proteins in the zyxin-null cells.

156 sphoisoform-specific regulation of histidine-phosphorylated proteins in vivo, and we link these modif

157 , we analyzed the levels of nuclear tyrosine phosphorylated proteins in WT and Itgalpha1-null kidney

158 urther phosphorylation to produce the doubly phosphorylated protein inactivates ER.

159 GP Ib, and associates with several tyrosine-phosphorylated proteins including the Fc receptor gamma-

160 hich, when activated, initiates a cascade of phosphorylated proteins including the SRC family of kina

161 ry that identifies large numbers of tyrosine-phosphorylated proteins, including active kinases.

162 involve up-regulated expression of tyrosine-phosphorylated proteins, including beta-catenin.

163 ormed stable complexes with several tyrosine-phosphorylated proteins, including PLCgamma2, only in Bt

164 lls, SLAP-2 associated with several tyrosine phosphorylated proteins, including the ubiquitin ligase

165 were incubated with ATP, the peak levels of phosphorylated proteins increased in the presence of the

166 domains serve an essential role as histidine-phosphorylated protein intermediates during phosphoryl t

167 CD2-binding protein 1 (CD2BP1)], a tyrosine-phosphorylated protein involved in cytoskeletal organiza

168 croscopy studies revealed that this tyrosine-phosphorylated protein is localized to the cytoplasmic f

169 The 18-kDa phosphorylated protein is subunit ESSS from complex I an

170 RAP-HAP interaction in the N-terminus of the phosphorylated protein is very stable to changing soluti

171 One of these tyrosine phosphorylated proteins is identified as p130Cas (Crk-as

172 actin cup and local recruitment of tyrosine phosphorylated proteins is markedly attenuated.

173 nformation and function of a subset of these phosphorylated proteins is regulated by the prolyl isome

174 nine or cysteine) and phosphorus (present in phosphorylated proteins) is presented.

175 respectively, compared with the gel from non-phosphorylated protein isolate at the same ZnSO4 level,

176 at the same ZnSO4 level, suggesting that the phosphorylated protein isolate was more crosslinked by Z

177 lts, we observed >50% reduction in levels of phosphorylated protein kinase B (Akt) and H3K36me3 in bo

178 The contents of GLUT1, GLUT4, total and phosphorylated protein kinase B (Akt), phosphorylated AM

179 n analysed for cell growth and expression of phosphorylated protein kinase B (Akt/PKB) and MMAC1/PTEN

180 tenuated senescence in part by up-regulating phosphorylated protein kinase B (p-AKT) and decreasing p

181 uch as phosphatidylinositol 3-kinase (PI3K), phosphorylated protein kinase B (PKB; also known as Akt)

182 n by more than 50% (of phosphorylated IGF1R, phosphorylated protein kinase B, and phosphorylated MAPK

183 lated extracellular signal-regulated kinase, phosphorylated protein kinase B, phosphorylated mammalia

184 n chromosome 10 protein, whereas the mass of phosphorylated protein kinase B/Akt was increased by C3a

185 ociation with an increase in CaR protein and phosphorylated protein kinase C alpha and beta in caveol

186 on chelator), a possible mechanism involving phosphorylated protein kinase C alpha and iron in Nrf2-H

187 Because we observed notably high levels of phosphorylated protein kinase C alpha and its suppressio

188 ACSL1 kd adipocytes displayed an increase in phosphorylated protein kinase C and phosphorylated JNK,

189 ng with the finding that PDK-1 does not bind phosphorylated protein kinase C effectively.

190 The interaction of caveolin-1 with phosphorylated protein kinase Calpha (PKCalpha) at the E

191 such as PEP005, reduced alpha-synuclein and phosphorylated protein kinase Calpha levels while increa

192 ation of soluble alpha-synuclein protein and phosphorylated protein kinase Calpha, as well as reduced

193 nfolded protein response (UPR), specifically phosphorylated protein kinase R-like endoplasmic reticul

194 tein were accompanied by increased levels of phosphorylated protein kinase R-like ER kinase (pPERK),

195 s: (a) the survival/rescue molecules such as phosphorylated protein kinase-like ER-resident kinase (p

196 e formats for several phosphorylated and non-phosphorylated protein kinases.

197 Western blot analysis showed that the phosphorylated protein levels of p38 and c-Jun amino-ter

198 K and its association with specific tyrosine-phosphorylated proteins may be important in insulin and

199 Macrophage actin-associated tyrosine phosphorylated protein (MAYP) belongs to the Pombe Cdc15

200 small interfering RNA to deplete a subset of phosphorylated proteins not previously linked to thrombi

201 was no difference in the pattern of tyrosine-phosphorylated proteins observed following stimulation o

202 lioside G(M1) and cholesterol where tyrosine phosphorylated proteins occur at late anaphase at the co

203 main of CMS bound specifically to a tyrosine-phosphorylated protein of 120 kDa, which we identified a

204 -immunoprecipitation of MUC1 with a tyrosine-phosphorylated protein of approximately 180 kDa.

205 imulated by casein kinase 2 (CK2) and that a phosphorylated protein of approximately 85 kDa is presen

206 ore the functions of these abundant tyrosine-phosphorylated proteins of synaptic vesicles.

207 Tyrosine-phosphorylated proteins on silver-stained gels of injure

208 of phosphorylation based on the isolation of phosphorylated proteins or peptides.

209 Following fear conditioning, the tyrosine phosphorylated protein p190 RhoGAP becomes associated wi

210 KPI-2 kinase domain phosphorylated protein phosphatase-1 (PP1C) at Thr(320),

211 al immunosensor has been developed to detect phosphorylated proteins, phospho-p53(15) and phospho-p53

212 presents extracted phosphorylation objects (phosphorylated proteins, phosphorylation sites and prote

213 Phosphorylated proteins play important roles in the regu

214 Instead, a 100-kDa tyrosine-phosphorylated protein (pp100) co-immunoprecipitated wit

215 SHPS-1 also associates with two tyrosine-phosphorylated proteins (pp55 and pp130) and a protein t

216 Dentin matrix protein 1 (DMP1), a phosphorylated protein present in the mineral phase of b

217 crease is the appearance of several tyrosine phosphorylated proteins present only in differentiated c

218 One of the phosphorylated proteins proved to be the 30-kd IL-7R fra

219 ,4,5)P3] and Src homology 2 domain [tyrosine-phosphorylated proteins, PtdIns(3,4,5)P3] of PLC-gamma;

220 It has been reported that tyrosine-phosphorylated proteins (PY) of host cells are dephospho

221 e and the interaction of AuNPs with the thio-phosphorylated proteins quantified by quartz crystal mic

222 However, after purification, the highly phosphorylated protein readily formed oligomers, whereas

223 on the contrary, detected similar amounts of phosphorylated proteins regardless of sex or gonad devel

224 14-3-3 proteins via binding serine/threonine-phosphorylated proteins regulate diverse intracellular p

225 fied protein required for NMD; (ii) SMG-2, a phosphorylated protein required for NMD in worms, yeasts

226 NFAT transcription factors are highly phosphorylated proteins residing in the cytoplasm of res

227 Analysis of tyrosine-phosphorylated proteins revealed that when 3T3 cells wer

228 his is indirect evidence suggesting that the phosphorylated protein(s) is of chlamydial origin.

229 A tyrosine-phosphorylated protein(s) of approximately 42 kDa was sp

230 The tyrosine-phosphorylated protein(s) regulates the conversion of py

231 sh condition applied in the treatment of the phosphorylated protein sample.

232 The phosphorylated protein showed competitive fragmentation

233 Diatom biomineralization involves highly phosphorylated proteins (silaffins and silacidins), anal

234 or for the selective detection of proximally phosphorylated protein sites, suitable for application i

235 ng in a less active form of PGI, whereas non-phosphorylated protein species retain cytokine activity.

236 phosphoproteins, and include several highly phosphorylated proteins such as MAP1B (33 sites) and Bas

237 es directed against known 60-70-kDa tyrosine-phosphorylated proteins suggest that pp68 may be a novel

238 he transcriptional activity of the wild-type phosphorylated protein, suggesting that the negative cha

239 facilitate the binding of BRCA1 to different phosphorylated protein targets.

240 Tau is a multiply phosphorylated protein that is essential for the develop

241 trate, was originally identified as a highly phosphorylated protein that is localized to focal adhesi

242 ve identified a high-molecular-mass tyrosine-phosphorylated protein that is rapidly phosphorylated on

243 Human cytomegalovirus pUL84 is a phosphorylated protein that is required for lytic DNA re

244 CKAP4 is a reversibly palmitoylated and phosphorylated protein that links the ER to the cytoskel

245 le minute-2 protein (Mdm2) is a multifaceted phosphorylated protein that plays a role in regulating n

246 Integrin-linked kinase (ILK) is a phosphorylated protein that regulates physiological proc

247 Phosphopeptides derived from aberrantly phosphorylated proteins that are presented on tumors and

248 NFAT transcription factors are highly phosphorylated proteins that are regulated by the calciu

249 In this study tyrosine-phosphorylated proteins that associate with PLC-gamma2 a

250 The majority of the tyrosine-phosphorylated proteins that associate with PLC-gamma2 b

251 ensing pathways, resulting in alterations of phosphorylated proteins that play a key role in the regu

252 aded filament proteins filensin and CP49 are phosphorylated proteins that undergo proteolytic degrada

253 and forms a multimeric complex with tyrosine-phosphorylated proteins, that is, Shc.

254 XA1 (ANXA1-S27-PO4) and translocation of the phosphorylated protein to the cell membrane.

255 n signal transduction pathways by binding to phosphorylated proteins to activate, inactivate, or sequ

256 subsequent, specific recruitment of tyrosine phosphorylated proteins to APP, including Lyn and Syk.

257 ly applicable tool to generate conditionally phosphorylated proteins to identify those whose dephosph

258 The tool further allows mapping of phosphorylated proteins to protein entries in the UniPro

259 dial extension, and localization of tyrosine phosphorylated proteins to the cell periphery.

260 complexes, acting as E3 ligases that target phosphorylated proteins to ubiquitylation and degradatio

261 non-phagocytic cells and elevation of their phosphorylated protein tyrosine level.

262 Wild type NHE-RF was a phosphorylated protein under basal conditions, but treat

263 ly small; only 7% of glycosylated and 13% of phosphorylated proteins undergo global changes >2 A.

264 ecifically interacted with a 75-kDa tyrosine-phosphorylated protein upon TCR stimulation.

265 able of predicting the global structure of a phosphorylated protein using only knowledge of the struc

266 st Dma1, relay checkpoint signals by binding phosphorylated proteins via their FHA domains and promot

267 d, nine-plex immunoassay measuring total and phosphorylated protein was constructed to measure tempor

268 n of the fusion protein at Ser(523), and the phosphorylated protein was found chiefly in the cytoplas

269 The 42-kDa tyrosine-phosphorylated protein was identified as Mck1, which is

270 One major tyrosine phosphorylated protein was identified as the TPR-MET onc

271 rse of this purification, a 105-kDa tyrosine-phosphorylated protein was only detected in fractions th

272 ns of a direct interaction with tubulin, the phosphorylated protein was released from microtubules.

273 scernible 2.1-fold increase in the number of phosphorylated proteins was detected when the panA gene

274 pecific phosphate binding tag for separating phosphorylated proteins, we found that Gpa2 undergoes ph

275 hotyrosine antibodies to enrich for tyrosine phosphorylated proteins, we have identified a novel sign

276 Results show that many of these phosphorylated proteins were activated specifically in t

277 Forty-five phosphorylated proteins were detected by gel electrophor

278 Tyrosyl phosphorylated proteins were detected by Western blots a

279 omes and detergent-resistant membranes, 1622 phosphorylated proteins were detected, including more th

280 A total of 34 differentially phosphorylated proteins were detected, of which 16 were

281 A total of 232 differentially expressed phosphorylated proteins were identified in this study.

282 Phosphorylated proteins were identified using 2D-DIGE an

283 hosphopeptides, corresponding to 1701 unique phosphorylated proteins, were identified and quantified.

284 Wild-type PKR is obtained as a highly phosphorylated protein when overexpressed in Escherichia

285 e of the selected sequences encoded tyrosine phosphorylated proteins when expressed on phage.

286 Scleritin is a secreted basic phosphorylated protein which exhibits a short amino acid

287 A mutant trapped primarily a 97-kDa tyrosine-phosphorylated protein, which was determined to be VCP (

288 ciated with an approximately 72-kDa tyrosine-phosphorylated protein, which we identify here as G3BP,

289 B also showed increased binding of tyrosine-phosphorylated proteins, which included the negative reg

290 e EGFR was confirmed by analysis of tyrosine phosphorylated proteins, which revealed a rapid, damage-

291 ing affinity for gefitinib is weaker for the phosphorylated protein while for the oncogenic mutant, L

292 domain of the Nck adaptor can bind tyrosine-phosphorylated proteins, while its SH3 domains can modul

293 It exists as a highly phosphorylated protein with a pI of 3 in the dentin matr

294 p65 is a multiply phosphorylated protein with phosphorylation sites in the

295 or molecule CBL, and association of tyrosine-phosphorylated proteins with phosphatidylinositol 3-kina

296 s demonstrated by immunoprecipitation of the phosphorylated proteins with specific antisera.

297 ed by an increase in association of tyrosine-phosphorylated proteins with the adapter protein Grb2.

298 Synaptogyrins comprise a family of tyrosine-phosphorylated proteins with two neuronal (synaptogyrins

299 ed with an increase in the number of Ser/Thr-phosphorylated proteins within the newly dispersed cells

300 egulated by phosphorylation, a means to cage phosphorylated proteins would be generally applicable.