ライフサイエンスコーパス: protein phosphatase 2A

1 ed for NF-kappaB activation by regulation of protein phosphatase 2A.

2 YAP, small t antigen brings it together with protein phosphatase 2A.

3 e 406 in a rapid process that is mediated by protein phosphatase 2A.

4 se 3beta, cyclin-dependent kinase 5, and tau protein phosphatase 2A.

5 olase 15 family members and the A subunit of protein phosphatase 2A.

6 d somatic mutations in PPP2R1A, a subunit of protein phosphatase 2A.

7 that then recruits the catalytic subunit of protein phosphatase 2A.

8 f phosphorylated Akt to dephosphorylation by protein phosphatase 2A.

9 ear region as well as from the inhibition of protein phosphatase 2A.

10 ) sensor calmodulin, protein kinase CK2, and protein phosphatase 2A.

11 up a CAR surface, allowing interaction with protein phosphatase 2A.

12 are mediated by protein kinase C but not by protein phosphatase 2A.

13 We identified PROTEIN PHOSPHATASE 2A-3 (PP2A-3), a catalytic subunit o

14 ase-mediated restriction of synthesis of the protein phosphatase 2A-A (PP2A-A), a key factor that fac

15 We conclude that protein phosphatase 2A accounts for enhanced SP-1 dephos

16 s inhibition was not due to H(2)S release or protein phosphatase 2A activation, which are key propert

17 s [B56alpha, B56gamma, PR72/PR130, and PTPA (protein phosphatase 2A activator)], which when suppresse

18 tion is regulated depending on the sites and protein phosphatase 2A, active in mitosis, is essential

19 P levels and attenuates protein kinase A and protein phosphatase 2A activities.

20 Rts1 constitutively directs protein phosphatase 2A activity toward the prodomain, ef

21 (ATM) activation by a mechanism dependent on protein phosphatase 2A activity.

22 ynthase (nNOS) down-regulation and decreased protein phosphatase 2A activity.

23 to protein kinase C activation and increased protein phosphatase- 2A activity, thereby suppressing HG

24 on was conferred by Pak2 inhibition of PP2A (protein phosphatase 2A) activity.

25 re administered chemical modulators of PP2A (protein phosphatase 2A) activity.

26 by DIM may be due, in part, to inhibition of protein phosphatase 2A, an upstream regulator of ATM.

27 re known to bind to the catalytic subunit of protein phosphatase 2A and inhibit its activity.

28 In vitro, FAM13A interacts with protein phosphatase 2A and recruits protein phosphatase

29 chemical analysis showed increased levels of protein phosphatase 2A and reduced levels of activated A

30 y was associated with reduced Tau binding to protein phosphatase 2A and was dependent on Cdk5 but not

31 uced the cleavage of I2(PP2A), inhibition of protein phosphatase 2A, and hyperphosphorylation of Tau,

32 at Rts1, a regulatory subunit of the general protein phosphatase 2A, and Ptr3 have opposing roles in

33 (armadillo/huntingtin, elongation factor 3, protein phosphatase 2A, and the yeast kinase TOR1) or BE

34 in to HEAT (Huntingtin, elongation factor 3, protein phosphatase 2A, and the yeast kinase TOR1) repea

35 /MST1) signaling, stimulates the activity of protein phosphatase 2A, and thereby attenuates the phosp

36 named after Huntingtin, elongation factor 3, protein phosphatase 2A, and yeast kinase TOR1) repeat.

37 comprised of the southern hemisphere against protein phosphatase 2A are described.

38 identify CIP2A (cancerous inhibitor of PP2A [protein phosphatase 2A]) as a key modulator of mTORC1 an

39 3 (p90 ribosomal S6 kinase type 3) and PP2A (protein phosphatase 2A) at signalosomes organized by the

40 vity through the androgen receptor-STK4/MST1-protein phosphatase 2A axis, which may have important im

41 yeasts to be mediated by recruitment of the protein phosphatase 2A B' (PP2A B').

42 nd related proteins that bind to and inhibit protein phosphatase 2A/B55, the principal phosphatase fo

43 r-suppressive functions of B56gamma-specific protein phosphatase 2A (B56gamma-PP2A).

44 kinase-3 (GSK-3), and a beta-arrestin-2/AKT/protein phosphatase 2A (beta-arrestin-2/AKT/PP2A) comple

45 t, Cdr2-T166 phosphorylation is regulated by protein phosphatase 2A but not by the Sds23-PP6 pathway.

46 hase kinase 3beta, protein phosphatase 1, or protein phosphatase 2A, but reduces p35 subunit of Cdk5.

47 Furthermore, we noted that protein phosphatase 2A can interact with TET2 and dephos

48 showed that Len inhibits the haplodeficient protein phosphatase 2A catalytic domain alpha (PP2Acalph

49 e for KPNA1, the mTOR-associated phosphatase protein phosphatase 2A catalytic interacted directly wit

50 dose-dependent increase in the levels of the protein phosphatase 2A catalytic subunit (PP2Ac) but not

51 -155-mediated suppression of the phosphatase protein phosphatase 2A catalytic subunit alpha (PPP2CA).

52 at low mitogen or nutrient levels, mTOR and protein phosphatase 2A catalytically control the constit

53 Cancerous inhibitor of protein phosphatase 2A (CIP2A) is overexpressed in most

54 berrant expression of cancerous inhibitor of protein phosphatase 2A (CIP2A), a recently identified en

55 d by proteins such as cancerous inhibitor of protein phosphatase 2A (CIP2A), protein phosphatase meth

56 Among these, the protein phosphatase 2A-dependent dephosphorylation of Ak

57 Protein phosphatase 2A dephosphorylates JAM-A at S285, s

58 ostulated to target the catalytic subunit of protein phosphatase 2A for degradation.

59 Here we discovered that the protein phosphatase 2A heterotrimer, PP2A(Ppp2r2d), regu

60 key regulatory subunit (B56alpha) of the PP (protein phosphatase) 2A holoenzyme displayed aberrant ac

61 s, of which three (two peptide inhibitors of protein phosphatase 2A (I1PP2A and I2PP2A) and prostagla

62 this is mediated by metabolic activation of protein phosphatase 2A in complex with the B55beta targe

63 as driven by dysfunction of serine/threonine protein phosphatase 2A in the nerve terminals.

64 PKC activation and protein phosphatase 2a inhibition increased the open pro

65 e important structural features required for protein phosphatase 2A inhibition, the mechanism of acti

66 Induction of transport was abolished by the protein phosphatase 2A inhibitor, OA.

67 ties of tau kinases and phosphatases such as protein phosphatase 2A, irrespective of fisetin treatmen

68 Protein phosphatase 2A is known to activate SP-1 through

69 more, we show that a novel host cell factor, protein phosphatase 2A, is involved in NS2 dephosphoryla

70 whereas dephosphorylation by a mitochondrial protein phosphatase 2A isoform and the calcium-calmoduli

71 tion of a beta-arrestin 2-associated pool of protein phosphatase 2A, leading to activation of Akt and

72 related with reduced Akt activity, increased protein phosphatase 2A levels, derepression of FoxO3a, a

73 ulated kinase pathways, and independently of protein phosphatase 2A, liver kinase B1/AMP-activated pr

74 Protein phosphatase 2A mediated the reduction in NF-kapp

75 itory effect was caused by BTK inhibition of protein phosphatase 2A-mediated (PP2A-mediated) dephosph

76 a (alpha isoform of the catalytic subunit of protein phosphatase 2A) negatively regulate the adhesion

77 BR1) interacted with the B'' subunit of rice protein phosphatase 2A (OsPP2A B'') and underwent revers

78 untingtin, elongation factor 3, a subunit of protein phosphatase 2A, PI3 kinase target of rapamycin 1

79 We discovered that a specific form of protein phosphatase 2A (PP2A(Cdc55)) opposes the initial

80 d sphingolipids are required to activate the protein phosphatase 2A (PP2A(Cdc55)) to attenuate Swe1 p

81 tein kinase C (Pkc1), and a specific form of protein phosphatase 2A (PP2A(Cdc55)).

82 endometrial cancers harbor mutations in the protein phosphatase 2A (PP2A) Aalpha scaffold subunit en

83 Somatic missense mutations in the Ser/Thr protein phosphatase 2A (PP2A) Aalpha scaffold subunit ge

84 Somatic mutation of the protein phosphatase 2A (PP2A) Aalpha-subunit gene PPP2R1

85 dding yeast, protein phosphatase 1 (PP1) and protein phosphatase 2A (PP2A) activities have each been

86 We found a decrease in protein phosphatase 2A (PP2A) activity associated with a

87 Here we analyzed an endogenous inhibitor of protein phosphatase 2A (PP2A) activity called SET, and i

88 Protein phosphatase 2A (PP2A) activity can be enhanced p

89 ral human malignancies via the inhibition of protein phosphatase 2A (PP2A) activity toward c-Myc.

90 Furthermore, we found that a lower protein phosphatase 2A (PP2A) activity, a phosphatase re

91 , also called SET, in rat brain, decrease in protein phosphatase 2A (PP2A) activity, abnormal hyperph

92 etaphase entry or progression by suppressing protein phosphatase 2A (PP2A) activity.

93 phorylation correlated with an inhibition of protein phosphatase 2A (PP2A) activity.

94 A-depleted cells was the result of increased protein phosphatase 2A (PP2A) activity.

95 Here, we show that protein phosphatase 2A (PP2A) acts as opsin phosphatase

96 ells was associated with a lower activity of protein phosphatase 2A (PP2A) and augmented activity of

97 requires inhibition of the tumor suppressor protein phosphatase 2A (PP2A) and expression--but not ac

98 regulates the methylesterification state of protein phosphatase 2A (PP2A) and has been implicated in

99 associated with decreased phosphorylation of protein phosphatase 2A (PP2A) and increased phosphorylat

100 /ERK and its subsequent dephosphorylation by protein phosphatase 2A (PP2A) and inhibition of focal ad

101 regulates the methylesterification state of protein phosphatase 2A (PP2A) and is implicated in cance

102 Non-canonically activated ERK activates protein phosphatase 2A (PP2A) and lengthens cell cycle d

103 Alpha4 (alpha4) is a key regulator of protein phosphatase 2A (PP2A) and mTOR in steps essentia

104 It has been reported that protein phosphatase 2A (PP2A) and the Far3-7-8-9-10-11 c

105 dynamics of PIN proteins are affected by the protein phosphatase 2A (PP2A) and the PINOID kinase, whi

106 eres, the cohesin protector shugoshin (Sgo1)-protein phosphatase 2A (PP2A) antagonizes Aurora B and C

107 per in Immunity, Long et al. (2014) identify protein phosphatase 2A (PP2A) as a deactivator of phosph

108 phosphoprotein-32A (ANP32A), an inhibitor of protein phosphatase 2A (PP2A) as a direct target of sphi

109 We identified Cdc55-protein phosphatase 2A (PP2A) as a key phosphatase that

110 In this study, we identify serine/threonine protein phosphatase 2A (PP2A) as a key regulator of Bcl-

111 oupled with mass spectrometry, we identified protein phosphatase 2A (PP2A) as a perphenazine target.

112 We identified the A1 subunit of Ser/Thr protein phosphatase 2A (PP2A) as interacting with full-l

113 We now show that protein phosphatase 2A (PP2A) associated with mAKAP comp

114 l that de novo ceramide biosynthesis induced protein phosphatase 2A (PP2A) association directly with

115 We show here that PI3Kgamma inhibits protein phosphatase 2A (PP2A) at the beta-adrenergic rec

116 Here we show that cytoplasm-localized protein phosphatase 2A (PP2A) B' regulatory subunits int

117 Protein phosphatase 2A (PP2A) became more eNOS-associate

118 of the general serine-threonine phosphatase protein phosphatase 2A (PP2A) can replace ST in this par

119 Protein phosphatase 2A (PP2A) complexes counteract many

120 Protein phosphatase 2A (PP2A) complexes function as tumo

121 un with chromatin is positively regulated by protein phosphatase 2A (PP2A) complexes targeted to c-Ju

122 A particular form of protein phosphatase 2A (PP2A) containing a B55delta subu

123 Protein phosphatase 2A (PP2A) critically regulates cell

124 Protein phosphatase 2A (PP2A) dephosphorylates several t

125 kinase 1 (RACK1) as the regulatory subunit, protein phosphatase 2A (PP2A) dephosphorylates threonine

126 Protein phosphatase 2A (PP2A) enzyme consists of a heter

127 Protein phosphatase 2A (PP2A) enzymes can suppress tumor

128 endent PKA activity but specifically reduced protein phosphatase 2A (PP2A) expression and activity in

129 The adenovirus E4orf4 protein must bind protein phosphatase 2A (PP2A) for its functions.

130 Observed deficits in protein phosphatase 2A (PP2A) function in a variety of h

131 ly conserved serine (Ser)/threonine-specific protein phosphatase 2A (PP2A) functions as a heterotrime

132 The serine/threonine Protein Phosphatase 2A (PP2A) functions as a tumor suppr

133 eport show that serine (Ser)/threonine (Thr) protein phosphatase 2A (PP2A) has an important role in G

134 a direct interaction between formoterol and protein phosphatase 2A (PP2A) has been described in vitr

135 lation of AM colonization via ABA requires a PROTEIN PHOSPHATASE 2A (PP2A) holoenzyme subunit, PP2AB'

136 reviously reported that PP2A/Balpha, a major protein phosphatase 2A (PP2A) holoenzyme, binds to and d

137 Proper formation of protein phosphatase 2A (PP2A) holoenzymes is essential f

138 ivation chaperones control the biogenesis of protein phosphatase 2A (PP2A) holoenzymes that contain a

139 otential role and functional significance of protein phosphatase 2A (PP2A) in CaBP4 dephosphorylation

140 Here we report a role for protein phosphatase 2A (PP2A) in centriole duplication.

141 23 but not IL-12 was negatively regulated by protein phosphatase 2A (PP2A) in dendritic cells (DC).

142 the role of the receptor and its associated protein phosphatase 2A (PP2A) in macrophage activation.

143 s, and that serine 59 is dephosphorylated by protein phosphatase 2A (PP2A) in mitosis.

144 rectly assessed the contribution of CD25 and protein phosphatase 2A (PP2A) in promoting IL-2R signali

145 t of increased expression of the phosphatase protein phosphatase 2A (PP2A) in T cells, as recorded in

146 lst8Delta bypass mutants reveals a role for protein phosphatase 2A (PP2A) in the regulation of TORC2

147 We show that Pin1 can act along with protein phosphatase 2A (PP2A) in vitro to dephosphorylat

148 t of rapamycin (mTOR), whereas inhibition of protein phosphatase 2A (PP2A) induced phosphorylation of

149 Protein phosphatase 2A (PP2A) inhibition rescued S6K act

150 These effects did not involve protein phosphatase 2A (PP2A) inhibition.

151 enyl-4H-1-benzopyran-4-one (Ly294002) or the protein phosphatase 2A (PP2A) inhibitor okadaic acid rev

152 Here, we show that overexpression of the protein phosphatase 2A (PP2A) inhibitor protein PME-1 dr

153 Protein phosphatase 2A (PP2A) is a critical negative reg

154 Protein phosphatase 2A (PP2A) is a family of heterotrime

155 Protein phosphatase 2A (PP2A) is a family of multifuncti

156 Protein Phosphatase 2A (PP2A) is a heterotrimer composed

157 Protein phosphatase 2A (PP2A) is a heterotrimeric serine

158 Protein phosphatase 2A (PP2A) is a highly conserved and

159 Protein phosphatase 2A (PP2A) is a key signaling compone

160 Protein phosphatase 2A (PP2A) is a large enzyme family r

161 Protein phosphatase 2A (PP2A) is a member of the intrace

162 We provide evidence that protein phosphatase 2A (PP2A) is a negative regulator of

163 The tumor suppressor protein phosphatase 2A (PP2A) is a serine/threonine phos

164 Protein phosphatase 2A (PP2A) is a serine/threonine phos

165 Strong evidence has indicated that protein phosphatase 2A (PP2A) is a tumor suppressor, but

166 Herein, cellular serine/threonine protein phosphatase 2A (PP2A) is identified as a functio

167 Protein phosphatase 2A (PP2A) is one of the most abundan

168 The recruitment of substrates by the ser/thr protein phosphatase 2A (PP2A) is poorly understood, limi

169 Protein phosphatase 2A (PP2A) is regulated through a var

170 Protein phosphatase 2A (PP2A) is the major MAP phosphata

171 erine 3 by interfering with serine/threonine protein phosphatase 2A (PP2A) leads to decreased class s

172 Down-regulation of protein phosphatase 2A (PP2A) methylation occurs in Alzh

173 Protein phosphatase 2A (PP2A) negatively regulates tumor

174 cer of zeste, trithorax (SET)/inhibitor 2 of protein phosphatase 2A (PP2A) oncoprotein binds and inhi

175 termed "targeted chemotherapy" by depleting protein phosphatase 2A (PP2A) or its inhibition using a

176 We found that deletion of protein phosphatase 2A (PP2A) or of protein phosphatase

177 Protein phosphatase 2A (PP2A) participates in multiple m

178 Protein phosphatase 2A (PP2A) plays important roles in c

179 Protein phosphatase 2A (PP2A) presents unique opportunit

180 Here we show that protein phosphatase 2A (PP2A) promotes SREBP-2 LDLR prom

181 Protein phosphatase 2A (PP2A) regulates almost all cell

182 blished, far less is known regarding cardiac protein phosphatase 2A (PP2A) regulation.

183 de novo mutations revealed four mutations in protein phosphatase 2A (PP2A) regulatory subunit B famil

184 We identify Drosophila protein phosphatase 2A (PP2A) regulatory subunit B' [Wrd

185 We identify Bbeta2, a mitochondria-localized protein phosphatase 2A (PP2A) regulatory subunit, as a n

186 orylation and activation of serine/threonine protein phosphatase 2A (PP2A) regulatory subunit, B56bet

187 Protein phosphatase 2A (PP2A) represses many oncogenic s

188 beta-arrestin2/protein kinase B (PKB or Akt)/protein phosphatase 2A (PP2A) signaling complex regulate

189 The protein phosphatase 2A (PP2A) subfamily of phosphatases,

190 lternative splice mutation in the regulatory protein phosphatase 2A (PP2A) subunit PPP2R2A.

191 terase-4D3 (PDE4D3), ryanodine receptor, and protein phosphatase 2A (PP2A) to the sarcoplasmic reticu

192 e SET oncoprotein, a potent inhibitor of the protein phosphatase 2A (PP2A) tumor suppressor, is overe

193 in 2 subunits of serine/threonine (Ser/Thr) protein phosphatase 2A (PP2A) were identified in 16 indi

194 Like A1AT, protein phosphatase 2A (PP2A), a major serine-threonine

195 sferase that specifically methylates Ser/Thr protein phosphatase 2A (PP2A), a major Tau phosphatase.

196 Since MID1 ubiquitinates protein phosphatase 2A (PP2A), a negative regulator of m

197 ated that activation of the tumor suppressor protein phosphatase 2A (PP2A), a negative regulator of m

198 iquitination and blocking the recruitment of protein phosphatase 2A (PP2A), a phosphatase that inhibi

199 tors that could synergize with activation of protein phosphatase 2A (PP2A), a tumor suppressor phosph

200 Protein phosphatase 2A (PP2A), a ubiquitous and pleiotro

201 oblastoma protein (Rb) family member p107 by protein phosphatase 2A (PP2A), a ubiquitously expressed

202 udies, we identified two holoenzyme forms of protein phosphatase 2A (PP2A), ABalphaC and ABdeltaC, as

203 f key regulators of hepatic gluconeogenesis, protein phosphatase 2A (PP2A), AMP-activated protein kin

204 small t (SV40ST) oncoprotein interacts with protein phosphatase 2A (PP2A), an abundantly expressed f

205 e exchange factor (RasGEF) Aimless, RasGEFH, protein phosphatase 2A (PP2A), and a scaffold designated

206 r processes, inhibiting the tumor suppressor protein phosphatase 2A (PP2A), and inhibiting the metast

207 these pathways, including sprouty2 (SPRY2), protein phosphatase 2A (PP2A), and phosphatase and tensi

208 The MWPyV small T antigen (ST) binds protein phosphatase 2A (PP2A), and the large T antigen (

209 fied a protein serine/threonine phosphatase, protein phosphatase 2A (PP2A), as a MEKK3 phosphatase.

210 blished that Wee1 and Cdc25 are regulated by protein phosphatase 2A (PP2A), but a full understanding

211 xes that appear to act through regulation of protein phosphatase 2A (PP2A), but their functions in ma

212 Mechanistically, PI3Kgamma sequesters protein phosphatase 2A (PP2A), disrupting ERK-PP2A inter

213 we show that a regulatory pathway involving protein phosphatase 2A (PP2A), glycogen synthase kinase

214 Phosphatases, such as protein phosphatase 2A (PP2A), interestingly, also are c

215 The activity of the HDAC4 phosphatase, protein phosphatase 2A (PP2A), is downregulated by ATM-m

216 PyST enhanced YAP association with protein phosphatase 2A (PP2A), leading to decreased YAP

217 a protein complex containing Aldob, Akt, and protein phosphatase 2A (PP2A), leading to inhibition of

218 SH-BC-893 activated protein phosphatase 2A (PP2A), leading to mislocalizatio

219 Binding of YAP to MT brings it together with protein phosphatase 2A (PP2A), leading to the dephosphor

220 Exposure of BL41-3 cells to an inhibitor of protein phosphatase 2A (PP2A), okadaic acid, resulted in

221 Protein phosphatase 2A (PP2A), one of the main serine-th

222 his study, we show that the tumor suppressor protein phosphatase 2A (PP2A), one of the major Ser/Thr

223 d that, along with the previously identified protein phosphatase 2A (PP2A), pigment aggregation signa

224 mportant myocardial proteins is regulated by protein phosphatase 2A (PP2A), representing a heterotrim

225 The proto-oncogene and inhibitor of protein phosphatase 2A (PP2A), SET, interacts with the t

226 suppression of protein phosphatases, such as protein phosphatase 2A (PP2A), that normally counteract

227 Protein phosphatase 2A (PP2A), the major serine/threonin

228 discovery of a protein network comprised of protein phosphatase 2A (PP2A), Transducer of Erb-B2 (Tob

229 r suppressor activity of protein phosphatase protein phosphatase 2A (PP2A), which by dephosphorylatin

230 The phosphorylation of Tau is regulated by protein phosphatase 2A (PP2A), which in turn is modulate

231 te require an interaction between E4orf4 and protein phosphatase 2A (PP2A), which is mediated through

232 Protein phosphatase 2A (PP2A), YAP, Src family tyrosine

233 FTY720 is also a potent protein phosphatase 2A (PP2A)-activating drug (PAD).

234 Here, we report that the protein phosphatase 2A (PP2A)-associated protein, alpha4

235 in mammalian tissue culture cells it induces protein phosphatase 2A (PP2A)-B55- and Src-dependent cel

236 signaling mechanism that involves transient, protein phosphatase 2A (PP2A)-dependent dephosphorylatio

237 amycin-induced Akt phosphorylation involving protein phosphatase 2A (PP2A)-dependent DNA protein kina

238 ll death in a number of mammalian cells in a protein phosphatase 2A (PP2A)-dependent manner.

239 n be rapidly stimulated by mGluR-induced and protein phosphatase 2a (PP2A)-mediated dephosphorylation

240 Here we report that MEF2 induces a Protein phosphatase 2A (PP2A)-mediated dephosphorylation

241 d Bub1 kinase and the Sgo1-bound phosphatase protein phosphatase 2A (PP2A)-Rts1 underlie a tension-de

242 activities of a group of phosphatases called protein phosphatase 2A (PP2A).

243 reduced Janus kinase-mediated inhibition of protein phosphatase 2a (PP2A).

244 ephosphorylated by specific heterotrimers of protein phosphatase 2A (PP2A).

245 ependent kinases (CDKs) and serine/threonine protein phosphatase 2A (PP2A).

246 o depended on Cdc55, a regulatory subunit of protein phosphatase 2A (PP2A).

247 repression and required for association with protein phosphatase 2A (PP2A).

248 ressed XPO1, followed by the reactivation of protein phosphatase 2A (PP2A).

249 s dependent on receptor dephosphorylation by protein phosphatase 2A (PP2A).

250 t also binds to the Aalpha subunit (PR65) of protein phosphatase 2A (PP2A).

251 which is a potent physiological inhibitor of protein phosphatase 2A (PP2A).

252 n dephosphorylation of myosin II mediated by protein phosphatase 2A (PP2A).

253 een SVST and POLST may lie in utilization of protein phosphatase 2A (PP2A).

254 es with tau, other molecular chaperones, and protein phosphatase 2A (PP2A).

255 its activity, an effect that is reversed by protein phosphatase 2A (PP2A).

256 raction with Cdc55p, a regulatory subunit of protein phosphatase 2A (PP2A).

257 uated eNOS S1179 phosphorylation mediated by protein phosphatase 2A (PP2A).

258 ifications, make it a nanomolar inhibitor of protein phosphatase 2A (PP2A).

259 t translational modification and activity of protein phosphatase 2A (PP2A).

260 Gcn4 is dephosphorylated by the protein phosphatase 2A (PP2A); our data show that when m

261 on group A (XPA), pygopus homolog 2 (PYGO2), protein phosphatase 2A (PP2A)B subunit, Tat-interactive

262 otic entry biochemical regulators, including protein phosphatase 2A (PP2A-B55/SUR-6), biophysical reg

263 E3 ligase targeting the catalytic subunit of protein phosphatase 2A (PP2A-C) for ubiquitin-mediated d

264 thylation status of the catalytic subunit of protein phosphatase 2A (PP2A-C), but was not associated

265 Protein phosphatase-2A (PP2A) is an abundant serine/thre

266 in protein kinase A dependent activation of protein phosphatase-2A (PP2A).

267 of a feed forward mechanistic loop involving protein phosphatase 2A [PP2A] and its downstream substra

268 in and zinedin (the regulatory B subunits of protein phosphatase 2A [PP2A]), which interact with CTTN

269 The catalytic subunit of protein phosphatase 2A (PP2Ac) is stabilized in a latent

270 nvestigated whether the catalytic subunit of protein phosphatase 2A (PP2Ac), which is overexpressed i

271 that interact with the catalytic subunit of protein phosphatase 2A (PP2Ac).

272 The catalytic subunit alpha isoform of protein phosphatase 2A (PP2Acalpha) activity, protein, a

273 ), casein kinase 2 (CK2), and B56 containing protein phosphatase 2As (PP2As).

274 tors of IRF3 and STAT1 activities, including protein phosphatase 2A (PPP2CA) and tripartite motif-con

275 on did not require sTAg interaction with the protein phosphatase 2A protein complex, a tumor suppress

276 ic control of the many CaMKII-controlled and protein phosphatase 2A-regulated physiological processes

277 lex containing the ubiquitin ligase MID1 and protein phosphatase 2A regulates the nuclear localizatio

278 have previously shown that the Dictyostelium protein phosphatase 2A regulatory subunit B56, encoded b

279 s paper, we show, in budding yeast, that the protein phosphatase 2A regulatory subunit Cdc55 couples

280 ulation of Hmg1 phosphorylation requires the protein phosphatase 2A-related phosphatase Ppe1 and its

281 strate that B55beta, a regulatory subunit of protein phosphatase 2A, represents a molecular link betw

282 which results from the activity of AMPK and protein phosphatase 2A, respectively.

283 The complex between shugoshin and protein phosphatase 2A (Sgo1-PP2A) localizes to centrome

284 ial protease LON1, ribosomal protein RPL24A, protein phosphatase 2A subunit A3, a MADS box protein, a

285 deletion of the catalytic subunits of yeast protein phosphatase 2A, suggesting that lower PKA activi

286 f six (A-F) Huntingtin, elongation factor 3, protein phosphatase 2A, target of rapamycin (HEAT) repea

287 ease, and asparaginyl endopeptidase-I2(PP2A)-protein phosphatase 2A-Tau hyperphosphorylation pathway

288 Furthermore, MIG-7 protein inhibited protein phosphatase 2A to sustain Akt/GSK-3beta phosphor

289 cogene SET, thereby inducing reactivation of protein phosphatase 2A tumor suppressor and inhibition o

290 In this paper, we show that PP2A (Protein Phosphatase 2A(Twins)) counteracts Plk4 autophos

291 encodes a regulatory B subunit of the PP2A (protein phosphatase 2A), which plays important roles in

292 Inhibition of protein phosphatase 2A, which also contributes to sustai

293 The phosphorylation of Tau is regulated by protein phosphatase 2A, which in turn is regulated by in

294 stead, both agents increased the activity of protein phosphatase 2A, which inactivates protein kinase

295 d by the Arabidopsis thaliana B'' subunit of protein phosphatase 2A, which is encoded by the TONNEAU2

296 unit, as well as with protein kinase CK2 and protein phosphatase 2A, which modulate Ca(2+) sensitivit

297 ctivity of the serine/threonine phosphatase, protein phosphatase 2A, which operates at the intersecti

298 ice lacking the Bbeta2 regulatory subunit of protein phosphatase 2A, which we have shown previously a

299 tion and inactivation of a CDK-counteracting protein phosphatase 2A with a B55delta subunit (PP2A:B55

300 cts with protein phosphatase 2A and recruits protein phosphatase 2A with glycogen synthase kinase 3be