ライフサイエンスコーパス: phosphoprotein

1 A expression of VASP (vasodilator-stimulated phosphoprotein).

2 1 and inactivation of vasodilator-stimulated phosphoprotein.

3 e, and phosphorylated vasodilator-stimulated phosphoprotein.

4 nds to the nucleocapsid template through the phosphoprotein.

5 acid analysis, we show that yeast MIPS is a phosphoprotein.

6 rotubule-associated protein tau is an axonal phosphoprotein.

7 d mass spectrometry analysis of the enriched phosphoproteins.

8 , respectively, both the PSII core and LHCII phosphoproteins.

9 ifically bind to the phosphate groups on any phosphoproteins.

10 tion, which requires effective enrichment of phosphoproteins.

11 e than 11,000 phosphorylation sites in 2,500 phosphoproteins.

12 by general methods to biosynthesize defined phosphoproteins.

13 olding and thereby activity and stability of phosphoproteins.

14 rotein 79 (AKAP79) delineates PP2B access to phosphoproteins.

15 orylation in both phosphopeptides and intact phosphoproteins.

16 enic markers, alkaline phosphatase, secreted phosphoprotein 1 (osteopontin), and bone gamma-carboxygl

17 ther adapter proteins, Src kinase-associated phosphoprotein 1 (SKAP1) and SKAP2.

18 s SNPs associated with Src kinase-associated phosphoprotein 1 (SKAP1), matrix metallopeptidase 12 (MM

19 Secreted phosphoprotein 1 (SPP1, also known as osteopontin) incre

20 Stress-inducible phosphoprotein 1 (STI1), an Hsp90 cochaperone secreted b

21 The target's identity, stress-induced phosphoprotein 1 (STIP1), was determined by mass spectro

22 Secreted phosphoprotein 1 and sex-specific differences in silica-

23 PGC-1alpha induces the secretion of secreted phosphoprotein 1 and the recruitment of macrophages.

24 Secreted phosphoprotein 1 stimulates macrophages to secrete monoc

25 ontrast, induction of PGC-1alpha in secreted phosphoprotein 1(-/-) mice leads to immature capillariza

26 Pb induced the expression of SPP1 (secreted phosphoprotein 1), which has known neuroprotective effec

27 terix, osteocalcin, and dentin matrix acidic phosphoprotein 1.

28 The Src kinase-associated phosphoprotein 2 (Skap2) is involved in integrin functio

29 conserved disulfide bonded loop of secreted phosphoprotein 2 (Spp-24) encoded by SPP2.

30 Recently, the Golgi phosphoprotein 3 (GOLPH3) and its yeast homolog Vps74p h

31 Recently, Golgi phosphoprotein 3 (GOLPH3), the mammalian homolog of Vps7

32 lls gain metastatic capacity through a Golgi phosphoprotein 3-dependent (GOLPH3-dependent) Golgi memb

33 cAMP], dopamine- and cAMP-regulated neuronal phosphoprotein 32 kDa [DARPP-32], and cAMP responsive el

34 ne and abnormal dopamine- and cAMP-regulated phosphoprotein 32 kDa signal integration.

35 In total, we identified 2,080 phosphoproteins (4,621 peptides), of which 385 proteins

36 that the scaffolding protein, ezrin-binding phosphoprotein 50 (EBP50), is a central regulator of mac

37 filamentous actin (F-actin) and ERM-binding phosphoprotein 50 (EBP50).

38 adaptor protein named Src kinase-associated phosphoprotein 55 homologue (SKAP-Hom) as a novel substr

39 and CD8(+) CMV-specific memory responses to phosphoprotein 65 (pp65) in a prospective cohort of 18 D

40 ination with DCs pulsed with Cytomegalovirus phosphoprotein 65 (pp65) RNA.

41 cytomegalovirus (HCMV) is the immunodominant phosphoprotein 65 (pp65), which is frequently included i

42 correlated with granzyme B loading, and CMV phosphoprotein 65 (pp65)-specific CD8(+)IFN-gamma(+) and

43 fit of adoptive T-cell therapy (ATCT) of CMV phosphoprotein 65 (pp65)-specific T cells.

44 significantly rescued, most effectively with phosphoprotein 65 Ag and combined exogenous IL-2 and IL-

45 -specific CTLs responded specifically to CMV-phosphoprotein 65 stimulation by secreting IFN-gamma and

46 e early 1 or 100 spots per 250 000 cells for phosphoprotein 65) identified patients who were protecte

47 However, the capacity for in vitro CMV phosphoprotein 65-specific proliferation and CD4(+)T-bet

48 hort that were specific for epitopes of HCMV phosphoprotein-65, tetanus toxoid precursor, EBV nuclear

49 ent of maize leaves, we analyzed protein and phosphoprotein abundance as maize leaves transition from

50 dence that lack of secretory calcium-binding phosphoproteins accounts for the evolutionary loss of sc

51 Phosphoprotein activation of several MAPK signaling comp

52 Scc2 is a phosphoprotein, although the functions of phosphorylatio

53 ids followed by quantitative phenotyping and phosphoprotein analyses uncover key changes in the signa

54 Phosphoprotein analysis showed restoration of wild-type

55 Ure2 is a phosphoprotein and central negative regulator of nitroge

56 In addition, FDH is a phosphoprotein and dephosphorylation was found to increa

57 RCM-1 is a phosphoprotein and is a substrate of PKA in vivo and in

58 nt protein (EGFP) was introduced between the phosphoprotein and matrix genes (position 5) of the geno

59 Furthermore, PPM1G is a phosphoprotein and this phosphorylation appears to be re

60 We biosynthesize several phosphoproteins and demonstrate phosphoprotein structure

61 Our study provides a unique resource of phosphoproteins and phosphorylation sites that may gener

62 ficant challenge due to the low abundance of phosphoproteins and the low stoichiometry of phosphoryla

63 tein (DSPP) into dentin sialoprotein, dentin phosphoprotein, and dentin glycoprotein.

64 NS5A is a phosphoprotein, and it has been proposed that differenti

65 Phosphoprotein antibody array analysis revealed that PL

66 ay in Dajiao, along with other cold-specific phosphoproteins, appears to be associated with the molec

67 Characteristic phosphopeptides of phosphoproteins are identified from human serum after th

68 invasion-related proteins, of them 43 (>70%) phosphoproteins are unrecognized.

69 Phosphoprotein array analysis established that AKT1S1, a

70 zation from synapses, thereby indicating the phosphoprotein as a novel target through which S1P contr

71 hemistry, we identify more than 100 secreted phosphoproteins as genuine Fam20C substrates.

72 Protein lysates were processed for phosphoprotein assays and a wound healing assay performe

73 tance aggregometry or vasodilator-stimulated phosphoprotein assays, was numerically but not significa

74 proteins, can reinvigorate studies of 14-3-3/phosphoprotein assemblies, including those with challeng

75 binding to a transmembrane adaptor known as phosphoprotein associated with glycosphingolipid-enriche

76 Of these proteins, phosphoprotein associated with glycosphingolipid-enriche

77 antigen (Sjogren's syndrome antigen B) is a phosphoprotein associated with nascent precursor tRNAs a

78 were limited to the analysis of one or a few phosphoproteins at a time.

79 remained limited by our inability to produce phosphoproteins at high yields.

80 The results for phosphoprotein beta-casein show that, under mild subcrit

81 nhibition was abolished by truncation of the phosphoprotein-binding Breast Cancer 1 C-terminal domain

82 The 14-3-3 family of phosphoprotein-binding proteins regulates many cellular

83 orylation and the levels of 14-3-3epsilon, a phosphoprotein-binding regulatory protein.

84 ic screens have revealed many Rab GTPases as phosphoproteins, but the effects of this modification ar

85 Pin1 regulates the levels and functions of phosphoproteins by catalyzing phosphorylation-dependent

86 rom a recombinant baculovirus vector and the phosphoprotein cofactor (P) in Escherichia coli and puri

87 Full processivity of L requires its phosphoprotein cofactor and the template-associated N.

88 Silaffins are a group of phosphoproteins constituting the main components of the

89 atform for direct expression of programmable phosphoproteins containing multiple phosphorylated resid

90 ecline in G-actin; reduced cofilin and HSP27 phosphoprotein content, respectively; and blocked the my

91 e and drug-induced changes in the metabolite-phosphoprotein correlation network.

92 e assigned all phosphorylation sites to 3013 phosphoproteins, covering the entire dynamic range from

93 are altogether 47 923 phosphosites in 16 477 phosphoproteins curated across nine plant organisms from

94 ion of dopamine- and cAMP-regulated neuronal phosphoprotein (DARPP-32) exclusively in D2R-expressing

95 rons expressing dopamine- and cAMP-regulated phosphoprotein (DARPP-32+), known to be modulated by dop

96 We used phosphoprotein data from cancer cell lines as well as in

97 Integration of mRNA, protein, and phosphoprotein data sets greatly improved the predictive

98 Using the phosphoprotein data, we scored more than 2,000 networks

99 ublished pseudopodium-enriched (PDE) protein/phosphoprotein datasets to identify novel PDAC-specific

100 are dissociated by WNTs and regulated by the phosphoprotein Dishevelled (DVL).

101 Dentin phosphoprotein (DPP) is the most abundant noncollagenous

102 (DSP), dentin glycoprotein (DGP) and dentin phosphoprotein (DPP).

103 We used Enabled/vasodilator-stimulated phosphoprotein (Ena/VASP)-deficient MV(D7) fibroblasts,

104 We have identified a previously unidentified phosphoprotein encoded by MDV ORF012.

105 hat neuronal levels of the survival protein, phosphoprotein enriched in astrocytes at approximately 1

106 Global phosphoprotein enrichment analysis revealed involvement

107 gel electrophoresis, as well as column-based phosphoprotein enrichment followed by liquid chromatogra

108 we performed and compared phosphopeptide and phosphoprotein enrichment methodologies after activation

109 Phosphopeptides/phosphoproteins enrichment from biological samples is cu

110 he late endosome in a vasodilator-stimulated phosphoprotein envelope.

111 However, several protein/phosphoprotein events such as overexpression of AKT prot

112 Synapsin I is part of a phosphoprotein family involved in neuronal regulation of

113 ins of the Mena/VASP (vasodilator-stimulated phosphoprotein) family.

114 th the phosphoprotein-specific Pro-Q Diamond phosphoprotein fluorescent stain and chemical dephosphor

115 ssociations involving vasodilator-stimulated phosphoprotein, focal adhesion kinase, and protein-disul

116 ssociations involving vasodilator-stimulated phosphoprotein, focal adhesion kinase, the H(+)/K(+) ATP

117 rosylation, including vasodilator-stimulated phosphoprotein, focal adhesion kinase, the membrane phos

118 vers kinase consensus motifs and prioritizes phosphoproteins for kinase target validation.

119 mmunization with rBCG strains expressing the phosphoprotein from hMPV also can induce protective Th1

120 ated RABV expressing the glycoprotein or the phosphoprotein from wt RABV) demonstrate that DC activat

121 These NPs enrich phosphoproteins from complex cell and tissue lysates wit

122 tative phosphoproteomics analysis, isolating phosphoproteins from whole brain derived from E18.5 Cdk5

123 identical to those of the nucleoprotein and phosphoprotein genes except that it contains an apparent

124 tative binding partner, the Golgi-associated phosphoprotein GOLPH3.

125 RNAs), 17,862 nonmodified proteins, and 6227 phosphoproteins harboring 31,595 phosphorylation sites q

126 The existence of extracellular phosphoproteins has been acknowledged for over a century

127 Although numerous extracellular phosphoproteins have been identified, the protein kinase

128 nfection and requires an active large T (LT) phosphoprotein helicase to replicate.

129 minal EVH1 (Ena/VASP [vasodilator-stimulated phosphoprotein] homology domain 1) binding domains of Lp

130 The major phosphoprotein in dentin is the aspartic acid and serine

131 Here, we provide evidence that MKP1 is a phosphoprotein in vivo and that MKP1 accumulates in resp

132 role of a disordered secondary structure in phosphoproteins in bone-like apatite formation.

133 k of genes encoding secreted calcium-binding phosphoproteins in cartilaginous fishes explains the abs

134 al phosphorylation dynamics of 1,887 cardiac phosphoproteins in early affected heart tissue in a tran

135 ck of technologies for specific detection of phosphoproteins in gels.

136 the level of 133 key signaling proteins and phosphoproteins in laser capture microdissected (LCM) pr

137 of cocaine-induced dephosphorylation of key phosphoproteins in the prefrontal cortex related to syna

138 e for phosvitin, an intrinsically disordered phosphoprotein, in chick embryo skeletal development, an

139 e was assessed by the vasodilator-stimulated phosphoprotein index.

140 at draws on biophysical data from SH2 domain-phosphoprotein interactions to predict the functional ef

141 20), is critical for coordinating 14-3-3zeta-phosphoprotein interactions.

142 BRCA1 is a phosphoprotein involved in many biological processes, in

143 study, we identify Synapsin I, a presynaptic phosphoprotein involved in the control of availability o

144 Phosducin (Pdc), a highly conserved phosphoprotein involved in the regulation of retinal pho

145 Synapsin I (SynI), a major SV phosphoprotein involved in the regulation of SV traffick

146 Numerous phosphoproteins involved in actin dynamics including Wis

147 Phosphopeptide abundances of five phosphoproteins involved in MKK2 interaction network, in

148 Phosphoprotein is the main cofactor of the viral RNA pol

149 hment of pY-containing peptides derived from phosphoproteins is commonly facilitated by use of immobi

150 esized that nucleophosmin (NPM), a nucleolar phosphoprotein, is critical for Bax-mediated cell death.

151 (GAP43), a protein kinase C (PKC)-activated phosphoprotein, is often implicated in axonal plasticity

152 S to characterize six bovine alpha-S1-casein phosphoprotein isoforms.

153 with the v-ATPase and the associated LAMTOR1 phosphoprotein, key components of the lysosomal nutrient

154 Mononegavirales phosphoproteins lack sequence conservation, but contain

155 RGS9-2 affects several protein interactions, phosphoprotein levels, and the function of the epigeneti

156 sessments measured by vasodilator-stimulated phosphoprotein, light transmittance aggregometry, and Mu

157 ding VerifyNow P2Y12, vasodilator-stimulated phosphoprotein, light transmittance aggregometry, and Mu

158 d for arousal-related and sleep need-related phosphoprotein markers from the diencephalon.

159 and cyclic adenosine monophosphate-regulated phosphoprotein, Mr 32000) in promoting tumor growth thro

160 We previously identified the centrosomal phosphoprotein NDE1 as a negative regulator of ciliary l

161 and biophysical data to model the human SH2-phosphoprotein network in normal and cancer cells.

162 Furthermore, the nucleolar phosphoprotein nucleophosmin (NPM1) acts as a scaffold f

163 In consonance, phosphoproteins obtained after co-expression of PknA wit

164 hat Bcl-2 binds dopamine- and cAMP-regulated phosphoprotein of 32 kDa (DARPP-32), a protein kinase A

165 lling, dopamine- and cAMP-regulated neuronal phosphoprotein of 32 kDa feedback, and synaptic plastici

166 ignaling protein dopamine-and-cAMP-regulated phosphoprotein of 32 kDa, DARPP32.

167 ated apical scaffolding proteins ERM-binding phosphoprotein of 50 kDa (EBP50) and NHE3 kinase A regul

168 n Src homology 2 domain-containing leukocyte phosphoprotein of 76 kDa (SLP-76) plays a crucial role i

169 The phosphoprotein of human metapneumovirus (HMPV) forms hom

170 Dopamine- and cAMP-regulated phosphoprotein of molecular weight 32 kDa (DARPP-32 or P

171 ocyte-directed overexpression of B56alpha, a phosphoprotein of the PP2A-B56 family.

172 ly disordered regions account for 80% of the phosphoprotein of the respiratory syncytial virus.

173 enriched within the microenvironment and the phosphoproteins of CD147.

174 We find that mutations mapping to phosphoproteins often create new interactions but that m

175 belled in fixed cells, for example levels of phosphoproteins or total cellular mass.

176 Osteopontin (OPN) is a secreted phosphoprotein, originally characterized in malignant-tr

177 The rabies virus (RABV) phosphoprotein P is a multifunctional protein: it plays

178 Levels of the phosphoprotein p-ERK in the mitogen-activated protein ki

179 ome of them are multifunctional, such as the phosphoprotein P.

180 s not correlated with vasodilator-stimulated phosphoprotein (p = 0.16).

181 ent RNA polymerase minimally consists of the phosphoprotein (P) and the large protein (L).

182 In addition, copies of the phosphoprotein (P) and the large RNA polymerase (L) deco

183 We also observed the effects of phosphoprotein (P) binding on the MuV NC structure.

184 al polymerase L in complex with its cofactor phosphoprotein (P) binds the nucleocapsid that constitut

185 otein is the main catalytic subunit, and the phosphoprotein (P) is an essential cofactor for polymera

186 The Nipah virus phosphoprotein (P) is multimeric and tethers the viral p

187 The viral phosphoprotein (P) is necessary and sufficient to inhibi

188 The phosphoprotein (P) is the main and essential cofactor of

189 The phosphoprotein (P) is virally encoded by the Rhabdovirid

190 ucture of an intermediate of the X domain of phosphoprotein (P) of measles virus.

191 The mumps virus (MuV) genome encodes a phosphoprotein (P) that is important for viral RNA synth

192 nucleocapsid protein (N) and associated by a phosphoprotein (P) with the large polymerase protein (L)

193 lysis in HEp-2 cells, the nucleoprotein (N), phosphoprotein (P), matrix protein (M), and fusion prote

194 s were discovered, including epitopes in the phosphoprotein (P), polymerase protein (L), M2-1 protein

195 polymerase protein (L) and its cofactor, the phosphoprotein (P), which associate with the viral ribon

196 t of the enzymatic large protein (L) and the phosphoprotein (P).

197 onstituent of the replication machinery, the phosphoprotein (P).

198 of the large polymerase subunit (L) and the phosphoprotein (P).

199 (MoRE) domain mediates binding of the viral phosphoprotein (P).

200 ical enrichment analysis of the differential phosphoprotein patterns revealed selective perturbation

201 The small phosphoprotein pCPI-17 inhibits myosin light-chain phosp

202 als PP5 utilization of conserved elements of phosphoprotein phosphatase (PPP) structure to bind subst

203 ough a process that requires the activity of phosphoprotein phosphatase (PPP)-family members.

204 18 and 24 months following control, BDNF or phosphoprotein phosphatase 1 derivative (1NMPP1) treatme

205 Phosphoprotein phosphatase 4 (PP4) has been recently sho

206 Instead, we identify phosphoprotein phosphatase 4 catalytic subunit (PP4) to

207 ated by the Ca(2+)- and calmodulin-dependent phosphoprotein phosphatase calcineurin/PP2B.

208 Previously, three bacterial-like phosphoprotein phosphatase classes were uncovered in euk

209 rn of evolution of eukaryotic bacterial-like phosphoprotein phosphatase sequences, which are predomin

210 Phosphoprotein phosphatase-1 derivatives such as 1NMPP1

211 Kelch-like domains (PPKL) are members of the phosphoprotein phosphatases family present only in plant

212 nchoring proteins direct protein kinases and phosphoprotein phosphatases toward selected substrates t

213 Similarly, global inhibition of phosphoprotein phosphatases with orthovanadate or fluori

214 ar Pi concentration, which directly inhibits phosphoprotein phosphatases, triggering a global increas

215 ynaptic expression of vasodilator-stimulated phosphoprotein phospho-mimetic or phospho-resistant muta

216 The cardiac phosphoprotein phospholemman (PLM) regulates the cardiac

217 ophosphate (cAMP) and vasodilator-stimulated phosphoprotein phosphorylation (VASP-P).

218 12 reaction units and vasodilator-stimulated phosphoprotein phosphorylation and platelet reactivity i

219 Inhibition of vasodilator-stimulated phosphoprotein phosphorylation and prostaglandin E1-indu

220 let reactivity index (vasodilator-stimulated phosphoprotein phosphorylation assay) at baseline (befor

221 correlations with the vasodilator-stimulated phosphoprotein phosphorylation assay.

222 g VerifyNow P2Y12 and vasodilator-stimulated phosphoprotein phosphorylation assays.

223 rachidonic acid), and vasodilator-stimulated phosphoprotein phosphorylation assays.

224 onfirmed by increased vasodilator-stimulated phosphoprotein phosphorylation in MRP4-deficient platele

225 by Rap1 activity and vasodilator-stimulated phosphoprotein phosphorylation, respectively.

226 sion aggregometry and vasodilator-stimulated phosphoprotein phosphorylation.

227 ation, p = 0.005) and vasodilator-stimulated phosphoprotein platelet reactivity index (20.7% relative

228 as well as changes in vasodilator-stimulated phosphoprotein platelet reactivity index and P-selectin

229 APTITUDE-CABG) study, vasodilator-stimulated phosphoprotein-platelet reactivity index, a specific mar

230 eal-time polymerase chain reaction (qPCR) or phosphoprotein (pp65) antigenemia (pp65emia) for startin

231 BD retained inflammation-associated tyrosine phosphoprotein profiles ex vivo.

232 gnaling that is expressed as different brain phosphoprotein profiles.

233 Phosphoprotein profiling identified diverse phosphorylat

234 s a member of the Ena/vasodilator-stimulated phosphoprotein protein family, which facilitates the ass

235 demonstrates that proteins and particularly phosphoproteins provide information for predicting drug

236 in live cells and has future applications in phosphoprotein purification and analysis.

237 rotein (NT) and the C-terminal domain of the phosphoprotein (PX).

238 pd and the host VASP (vasodilator-stimulated phosphoprotein) recruited to the bacterial cell surface

239 MN), a cytoplasmic microtubule-destabilizing phosphoprotein, regulates interphase microtubules during

240 he role of Synapsin, a conserved presynaptic phosphoprotein regulating the balance between the reserv

241 re epilepsy susceptibility genes that encode phosphoproteins reversibly associated with synaptic vesi

242 Using a phosphoprotein-screening array, we found that Benzyl Iso

243 We also identify new interactions between phosphoprotein signaling and cellular energy processes t

244 I TGF-beta receptor (TbetaRI) with TGF-beta phosphoprotein signaling assays.

245 energy potential even as glucose uptake and phosphoprotein signaling is repressed.

246 al performance via the PDE4D/PRKAR1alpha/PKA phosphoprotein signaling pathway.

247 onal electrophoresis in combination with the phosphoprotein-specific Pro-Q Diamond phosphoprotein flu

248 ity as confirmed by SDS-PAGE analysis with a phosphoprotein-specific stain and mass spectrometry anal

249 Phosphoprotein staining after two-dimensional polyacryla

250 ys, galectin phosphorylation was detected by phosphoprotein staining and autoradiography.

251 Phosphoprotein staining confirmed the association betwee

252 size several phosphoproteins and demonstrate phosphoprotein structure determination and synthetic pro

253 How phosphatases target specific phosphoprotein substrates and reverse the action of kina

254 The trypsin-digested products of phosphoproteins, such as casein, nonfat milk, egg yolk,

255 The phosphoprotein synapsin I (Syn I) plays a crucial role d

256 a functional complex with the SV-associated phosphoprotein synapsin, previously implicated in SV clu

257 The microtubule-associated phosphoprotein tau regulates microtubule dynamics and is

258 ribution of Synapsin I (SynI), a presynaptic phosphoprotein that controls the availability of synapti

259 d by phospholamban (PLB), a small inhibitory phosphoprotein that decreases the Ca(2+) affinity of SER

260 NS5A is a phosphoprotein that exists in hyperphosphorylated and ba

261 t PC1 interacts with Pacsin 2, a cytoplasmic phosphoprotein that has been implicated in cytoskeletal

262 Encoded on chromosome IX, GRA25 is a phosphoprotein that is secreted outside the parasites an

263 Synapsin III (SynIII) is a neuron-specific phosphoprotein that plays a unique role in neuronal deve

264 s (HCV) nonstructural protein 5A (NS5A) is a phosphoprotein that plays key, yet poorly defined, roles

265 NPM1 (nucleophosmin 1) is a nucleolar phosphoprotein that regulates many cellular processes, i

266 re associated with deficiency of synapsin, a phosphoprotein that reversibly associates with synaptic

267 s in alpha-casein, an approximately 23.5 kDa phosphoprotein that showed eight of nine known phosphory

268 , we show that alpha-arrestin Aly1/Art6 is a phosphoprotein that specifically interacts with and is d

269 Phosducin (Pdc) is a conserved phosphoprotein that, when unphosphorylated, binds with h

270 RPLP1/2 are phosphoproteins that bind the ribosome through interacti

271 napsin family of synaptic vesicle-associated phosphoproteins that is precociously expressed in neuron

272 tabolites, associated metabolic enzymes, and phosphoproteins, the resultant data provided input for a

273 As synapsin is a synaptic vesicle-clustering phosphoprotein, these observations identify a presynapti

274 capture, enrichment, and detection of intact phosphoproteins toward a comprehensive analysis of the p

275 Specifically, we measured 14 phosphoproteins under 43 different perturbed conditions

276 MVC NP1 is a 22-kDa nuclear phosphoprotein unique to the genus Bocaparvovirus of the

277 th the average number of predictor genes per phosphoprotein used by the teams ranging from 3 to 124.

278 Vasodilator-stimulated phosphoprotein (VASP) and Ena-VASP-like (EVL) are cytosk

279 Vasodilator-stimulated phosphoprotein (VASP) can catalyze actin polymerization

280 sophila enabled (Ena)/vasodilator-stimulated phosphoprotein (VASP) homology 1 (EVH1) domains.

281 Vasodilator-stimulated phosphoprotein (VASP) is active in many filopodium-based

282 to determine whether vasodilator-stimulated phosphoprotein (VASP) signaling improves lipid metabolis

283 age overexpression of vasodilator-stimulated phosphoprotein (VASP), a key downstream mediator of intr

284 2Y12), and vasodilator-associated stimulated phosphoprotein (VASP).

285 The HSV type 1 tegument virion phosphoprotein (VP) 11/12 (VP11/12) is a major Ag target

286 y member A (RhoA) and vasodilator-stimulated phosphoprotein was increased in response to 8-CPT-cGMP t

287 147 microenvironment and the CD147-dependent phosphoproteins was generated and led to the identificat

288 nd phosphorylation of vasodilator-stimulated phosphoprotein were determined.

289 total of 1,953 mRNAs, 187 proteins, and 131 phosphoproteins were differentially expressed (DE) betwe

290 phosphopeptides belonging to 3163 different phosphoproteins were efficiently identified with high-th

291 The isolated phosphoproteins were eluted and isotopically labeled for

292 f transcripts and their encoded proteins and phosphoproteins were highly congruent.

293 ly increased, whereas 113 phosphosites in 74 phosphoproteins were significantly decreased.

294 In contrast, 545 phosphosites in 266 phosphoproteins were significantly increased, whereas 11

295 a conducive environment for introduction of phosphoproteins while simultaneously modulating the spre

296 Bone sialoprotein (BSP) is an acidic phosphoprotein with collagen-binding, cell attachment, a

297 f nucleophosmin (NPM/B23), a major nucleolar phosphoprotein with diverse cellular activities linked t

298 ofiling identified a set of PfCRK4-regulated phosphoproteins with greatest functional similarity to C

299 Ping) through coupling specific detection of phosphoproteins with protein identification and phosphor

300 is a bi-phasic system containing lipids and phosphoproteins, working synergistically to maximize adh