ライフサイエンスコーパス: protein phosphatase 1

1 f KIBRA on Ser(539), probably via regulating protein phosphatase 1.

2 1epsilon (CK1epsilon) and was antagonized by protein phosphatase 1.

3 hereas the carboxyl-terminal domain binds to protein phosphatase 1.

4 is effect is exacerbated by pretreating with protein phosphatase 1.

5 ssive tension, an effect that is reversed by protein phosphatase 1.

6 ty but modulated the binding and activity of protein phosphatase 1.

7 M phase with the mitotic kinase Aurora B and protein phosphatase 1.

8 other proteins such as protein kinase A and protein phosphatase 1.

9 rough the activation of specific isoforms of protein phosphatase 1.

10 okadaic acid, suggesting the involvement of protein phosphatase 1.

11 resistant to serine 133 dephosphorylation by protein phosphatase 1.

12 rmones or by dephosphorylation of lipin with protein phosphatase 1.

13 induced Ser(847)-PO(4) dephosphorylation by protein phosphatase 1.

14 acting proteins such as protein kinase A and protein phosphatase 1.

15 rora B, Mps1, and Plx1) and is suppressed by protein phosphatase 1.

16 ethod was expanded to detect the activity of protein phosphatase 1.

17 inactivation of CaMKII bound to caspase 2 by protein phosphatase 1.

18 kinase-3 and the glycogen-associated form of protein phosphatase 1.

19 n phospho-protein kinase A and a decrease in protein phosphatase-1.

20 e derivative of the protein kinase inhibitor protein phosphatase 1 (1NM-PP1), it is possible to produ

21 at could be achieved in vitro by recombinant protein phosphatase 1 (230 +/- 30%) was significantly gr

22 lular signal activated kinase 1/2), p38MAPK, protein phosphatase 1/2A (PP1/2A), and reactive oxygen s

23 (CaMKII) but was augmented by inhibition of protein phosphatase 1/2A (PP1/2A).

24 T840 dephosphorylation could be blocked by a protein phosphatase 1/2A (PP1/PP2A) inhibitor and was pa

25 brain slices of WKY rats pretreated with the protein phosphatase 1/2A, calcineurin, or casein kinase-

26 cAMP-regulated phosphoprotein-32--> increase protein phosphatase 1/2A--> decrease GABA(A).

27 in hippocampal slices induces a calcium and protein phosphatase 1/2A-dependent dephosphorylation of

28 as mediated through Src tyrosine kinases and protein phosphatase-1/2A.

29 ttributed to the intracellular inhibition of protein phosphatases 1/2A due to lack of specific transm

30 A) versus agents that act on microtubules or protein phosphatases 1/2A.

31 The protein phosphatase 1 a (PP1a)-specific phosphatase inhi

32 Inhibition of protein phosphatase 1 action on phospho-eIF2alpha by kno

33 The increased protein phosphatase 1 activity is partially due to depho

34 Protein phosphatase 1 activity negatively regulates this

35 also show that pharmacological inhibition of protein phosphatase 1 activity, which will result in pRb

36 and cardiomyocytes, related to inhibition of protein phosphatase 1 activity.

37 Finally, inhibition of protein phosphatase-1 activity by calyculin A or knockdo

38 tus of inhibitor-1, which in turn suppresses protein phosphatase-1 activity, thus modulating phosphol

39 These results demonstrate that protein phosphatase 1 acts as a major phosphatase to dep

40 d a direct association between InsP(3)R1 and protein phosphatase 1 alpha (PP1 alpha).

41 In addition, dephosphorylation of BRCA1 by protein phosphatase 1 alpha enhances the E3 ubiquitin li

42 ligase is controlled by Aurora-A kinase and protein phosphatase 1 alpha-mediated phosphoregulation t

43 ed by PC1 binding through the recruitment of protein phosphatase-1 alpha (PP1alpha).

44 erature upon incubation with okadaic acid, a protein phosphatase 1 and 2A inhibitor.

45 Neurabin and spinophilin are homologous protein phosphatase 1 and actin binding proteins that re

46 n of glycogen synthase due to codigestion by protein phosphatase 1 and beta-d-N-acetylglucosaminidase

47 Moreover, inhibition of protein phosphatase 1 and glycogen synthase kinase 3beta

48 ciated protein Doublecortin is controlled by protein phosphatase 1 and its regulator spinophilin.

49 We further show that the Reg1-Glc7 protein phosphatase 1 and Sit4 type 2A-like phosphatase

50 accharomyces cerevisiae SNF1/AMPK, Reg1-Glc7 protein phosphatase 1 and Sit4 type 2A-related phosphata

51 strate that Myosin phosphatase, a complex of Protein phosphatase 1 and the scaffolding protein Mypt1,

52 ted by 2 phosphoproteins, the inhibitor-1 of protein phosphatase 1 and the small heat shock protein 2

53 m that involves activation by this kinase of protein phosphatase 1 and/or 2A and resultant increased

54 Spinophilin is a protein that binds to protein phosphatase-1 and actin and modulates excitatory

55 g complex promoted Axin dephosphorylation by protein phosphatase-1 and inactivated ("closed") Axin th

56 Inhibition of protein phosphatases 1 and 2A and activation of PKC incr

57 Inhibition of protein phosphatases 1 and 2A blocked ITM when animals w

58 yrosine phosphatases or the serine/threonine protein phosphatases 1 and 2A decreased Ih at maximal ac

59 Inhibition of serine/threonine protein phosphatases 1 and 2A decreased maximal Ih and H

60 nd okadaic acid indicated that inhibition of protein phosphatases 1 and 2A dramatically enhanced ERK2

61 dent of Ca2+ and independent of calcineurin, protein phosphatase 1, and/or protein phosphatase 2A act

62 containing substrates for protein kinase A, protein phosphatase-1, and matrix metalloproteinases 2 a

63 , bath application of NMDA induced a strong, protein phosphatase 1- and/or 2A-mediated decrease in T8

64 regulators identified different kinases and protein phosphatase 1 as the molecules that control reve

65 at involves the phosphatases calcineurin and protein phosphatase-1, as well the serine/threonine kina

66 The interaction with protein phosphatase 1 beta/Mypt1 resulted in exclusion o

67 Here, we show that the neuronal actin- and protein phosphatase-1-binding protein, neurabin-I, promo

68 h forms of LTD were blocked by inhibitors of protein phosphatase 1, but only LTD of AMPAR EPSCs was a

69 MDARs was independent of protein kinase A or protein phosphatase 1, but was abolished by incubation o

70 Pi04314 interacts with three host protein phosphatase 1 catalytic (PP1c) isoforms, causing

71 eurabin II may induce the association of the protein phosphatase 1 catalytic subunit (PP1) with neura

72 oduct of which recruits the alpha-isoform of protein phosphatase 1 catalytic subunit (PP1alpha) and e

73 Through interaction with the protein phosphatase 1 catalytic subunit (PP1c), Gadd34 r

74 The serine/threonine protein phosphatase-1 catalytic subunit (PP-1c) is a maj

75 in phosphatase (MP) holoenzyme consisting of protein phosphatase-1 catalytic subunit (PP1c) and MP ta

76 Dephosphorylation studies showed that protein phosphatase 1 catalyzed near-complete in vitro d

77 Exposure of these CCM cells to protein phosphatase 1 caused a transitory increase in Ca

78 Therefore, Sgo1, Ipl1 kinase, Dam1, and protein phosphatase 1 comprise the SAC silencing network

79 Finally, we show that protein phosphatase 1 counteracts Aurora B activity to e

80 neurons, NMDA receptor stimulation induces a protein phosphatase 1-dependent dephosphorylation of CDK

81 lated by A20/glycogen synthesis kinase-3 and protein phosphatase 1-dependent mechanisms.

82 First, purified protein phosphatase-1 directly dephosphorylates Pax-6 in

83 Perturbation of both microtubule binding and protein phosphatase 1 docking at the KNL-1 N terminus ad

84 A reg1Delta mutant, lacking Reg1-Glc7 protein phosphatase 1, exhibits elevated glycogen accumu

85 The involvement of protein phosphatase 1 explains why second messengers lik

86 RK-1/2 via increased DUSP1 (dual-specificity protein phosphatase 1) expression.

87 Ser-518/Thr-514/Thr-509) is carried out by a protein phosphatase 1 family member in vitro, in neurobl

88 gamma(1)34.5 recruits both IKKalpha/beta and protein phosphatase 1, forming a complex that dephosphor

89 ated with a parallel depletion of G beta and protein phosphatase 1 from the oligomeric GIRK1 complexe

90 Dephosphorylation of channels by protein phosphatase 1 (from 75% to near 0% at serine-280

91 Repo-Man targets protein phosphatase 1 gamma (PP1gamma) to chromatin at a

92 e phosphorylation of Rpt6 were reversible by protein phosphatase 1 gamma.

93 effect of activating the inhibitor (I-1c) of protein phosphatase 1 (I-1) through gene transfer on car

94 insulin intolerance and inactivated adipose protein phosphatase 1 in association with the up-regulat

95 o-Ser(65) inhibitor-1 is dephosphorylated by protein phosphatase 1 in the striatum.

96 er(65) inhibitor-1 from dephosphorylation by protein phosphatase 1 in vivo.

97 electively inhibited a regulatory subunit of protein phosphatase 1 in vivo.

98 Increased protein phosphatase-1 in heart failure (HF) induces mole

99 Third, overexpression of protein phosphatase-1 in human lens epithelial cells lea

100 Phosphorylation of the protein phosphatase 1 inhibitor 1 (I-1), a direct calcin

101 athway using PKC-alpha and the PKC-regulated protein phosphatase 1 inhibitor 14D that is required for

102 MBS85), paxillin and CPI-17 (PKC-potentiated protein phosphatase 1 inhibitor protein of 17 kDa) phosp

103 Calyculin A, a protein phosphatase 1 inhibitor, blocked the hypertonici

104 This approach identified protein phosphatase 1 inhibitor-1 (I-1) as a DCT-enriche

105 r Ser(67) did not convert inhibitor-1 into a protein phosphatase 1 inhibitor.

106 PHLPP1 (PH domain leucine-rich repeat protein phosphatase 1) is a protein-serine/threonine pho

107 clude that PDE4D3, like protein kinase A and protein phosphatase 1, is recruited to the I(Ks) channel

108 ein lipase (Lpl), lactamase beta (Lactb) and protein phosphatase 1-like (Ppm1l), are validated as pre

109 ade of RCAN1-CaN interaction reduced CaN and protein phosphatase-1 localization to nuclear-enriched p

110 Protein phosphatase 1 mediated the dephosphorylation eve

111 increase in GIRK surface expression requires protein phosphatase-1-mediated dephosphorylation of a se

112 A (PP2A) is responsible for DHEA action, and protein phosphatase 1 might be involved in nafenopin ind

113 by protein kinase A and dephosphorylation by protein phosphatase 1 modulate the inhibitory activity o

114 n is an actin binding protein that positions protein phosphatase 1 next to its substrates in dendriti

115 s alpha or beta of the catalytic subunits of protein phosphatase 1 not only increased phosphorylation

116 In this study, we identified the protein phosphatase-1 nuclear targeting subunit PNUTS (P

117 Protein phosphatase 1 occurs in all tissues and regulate

118 Here we show that either protein phosphatase 1 or 2A is sufficient to suppress ac

119 se 5 (Cdk5), glycogen synthase kinase 3beta, protein phosphatase 1, or protein phosphatase 2A, but re

120 RPP-32), a potent and selective inhibitor of protein phosphatase-1, or the protein tyrosine kinase Fy

121 trin homology domain and leucine-rich repeat protein phosphatase 1 (PHLPP1) as a regulatory phosphata

122 eckstrin homology domain leucine-rich repeat protein phosphatase 1 (PHLPP1) differentially attenuates

123 trin homology domain and leucine rich repeat protein phosphatase 1 (PHLPP1) is a member of the serine

124 ariants of PH domain and Leucine-rich repeat Protein Phosphatase 1 (PHLPP1), PHLPP1alpha and PHLPP1be

125 ion of the PH domain and leucine-rich repeat protein phosphatases 1 (PHLPP1), a phosphatase of Akt.

126 eckstrin-homology domain leucine-rich repeat protein phosphatases 1 (PHLPP1).

127 ications implicated an indirect role of PP1 (protein phosphatase 1), potentially via its interphase r

128 ase 1I (PP-1I) is a major endogenous form of protein phosphatase 1 (PP-1) that consists of the core c

129 the first identified endogenous inhibitor of protein phosphatase 1 (PP-1), was previously reported to

130 ously demonstrated that the serine/threonine protein phosphatase-1 (PP-1) plays an important role in

131 inhibitor-1 (I-1), altering the activity of protein phosphatase-1 (PP-1), which may account for the

132 require the kinetochore-localized isoform of protein phosphatase 1 (PP1(Dis2)).

133 icates that the protein regulators governing protein phosphatase 1 (PP1) activity have crucial functi

134 receptors through a dominant coupling to the protein phosphatase 1 (PP1) activity in postsynaptic neu

135 h similarity to Sds22p, a regulator of yeast protein phosphatase 1 (PP1) activity in the nucleus.

136 have studied Sds22, a conserved regulator of protein phosphatase 1 (PP1) activity, and determined its

137 t long-lasting tolerance, was facilitated by protein phosphatase 1 (PP1) activity.

138 rora B inhibition, is rescued by restraining protein phosphatase 1 (PP1) activity.

139 sphorylation in IL-2 signaling, the roles of protein phosphatase 1 (PP1) and 2A (PP2A) were examined.

140 utation disrupts Phactr4, an uncharacterized protein phosphatase 1 (PP1) and actin regulator family m

141 spindle MTs in vivo, Mars binds directly to protein phosphatase 1 (PP1) and coimmunoprecipitates fro

142 axonal transport (FAT) by activating axonal protein phosphatase 1 (PP1) and glycogen synthase kinase

143 ivities of cyclin-dependent kinase 5 (CDK5), protein phosphatase 1 (PP1) and glycogen synthase kinase

144 disrupt protein-protein interactions between protein phosphatase 1 (PP1) and its regulator CPI-17, re

145 nhibits many protein phosphatases, including protein phosphatase 1 (PP1) and PP2A, that can reverse P

146 atase drives this reversal in budding yeast, protein phosphatase 1 (PP1) and protein phosphatase 2A (

147 e (MP), which includes the catalytic subunit protein phosphatase 1 (PP1) and the regulatory targeting

148 Additionally, we show that protein phosphatase 1 (PP1) antagonizes rpS6 C terminus

149 t wild-type, but not catalytically inactive, protein phosphatase 1 (PP1) associates with KIBRA.

150 d amino acid within the domain important for protein phosphatase 1 (PP1) binding.

151 SAMe and MTA increased protein phosphatase 1 (PP1) catalytic subunit mRNA and p

152 Protein phosphatase 1 (PP1) catalytic subunits dephospho

153 rmed, and it was observed that knock-down of protein phosphatase 1 (PP1) catalytic subunits significa

154 C-3 prostate cancer cells by disrupting HDAC-protein phosphatase 1 (PP1) complexes.

155 We also show that host cell protein phosphatase 1 (PP1) controls VP30 dephosphorylat

156 The serine-threonine protein phosphatase 1 (PP1) deactivates this pathway whe

157 The serine/threonine protein phosphatase 1 (PP1) dephosphorylates hundreds of

158 Cut12 harbors a bipartite protein phosphatase 1 (PP1) docking domain.

159 Opposing roles of Aurora kinases and protein phosphatase 1 (PP1) during mitosis have long bee

160 In one approach, a recombinant protein phosphatase 1 (PP1) has been conjugated to MPs v

161 Recently, protein phosphatase 1 (PP1) has been shown to interact w

162 t the catalytic subunit of the budding yeast protein phosphatase 1 (PP1) homolog, Glc7, regulates exi

163 acid, implicating PDGF-induced activation of protein phosphatase 1 (PP1) in CRMP2 regulation.

164 Dephosphorylation of CDK9 on Thr(186) by protein phosphatase 1 (PP1) in stress-induced cells or b

165 Here we demonstrate a role for protein phosphatase 1 (PP1) in the regulation of the maj

166 Here we show in vitro and in Drosophila that Protein Phosphatase 1 (PP1) inactivates Mps1 by dephosph

167 However, pretreatment of GCs with the protein phosphatase 1 (PP1) inhibitor tautomycin increas

168 regulatory subunit 1A (PPP1R1A) is a potent protein phosphatase 1 (PP1) inhibitor; however, its role

169 strated that NKCC1 activity is stimulated by protein phosphatase 1 (PP1) inhibitors.

170 Protein phosphatase 1 (PP1) is a ubiquitous serine/threo

171 We recently showed that protein phosphatase 1 (PP1) is activated by ATM.

172 Protein phosphatase 1 (PP1) is an essential and ubiquito

173 The serine/threonine protein phosphatase protein phosphatase 1 (PP1) is known to play an importan

174 In particular, protein phosphatase 1 (PP1) is recruited to a DSB-mimick

175 6983 prevents the dephosphorylation by pure protein phosphatase 1 (PP1) or the hydrophobic motif pho

176 hosphorylation was blocked by treatment with protein phosphatase 1 (PP1) pharmacological inhibitors a

177 ly, pharmacological or genetic inhibition of protein phosphatase 1 (PP1) prevented HTTex1 aggregation

178 biquitously expressed and highly promiscuous protein phosphatase 1 (PP1) regulates many cellular proc

179 We show that PKA directly phosphorylates the protein phosphatase 1 (PP1) regulatory subunit myosin ph

180 IF2alpha phosphatases comprising a catalytic protein phosphatase 1 (PP1) subunit in complex with a PP

181 Overexpression of the protein phosphatase 1 (PP1) subunit protein targeting to

182 Repo-Man is a protein phosphatase 1 (PP1) targeting subunit that regul

183 e targeting subunit Repo-Man from recruiting protein phosphatase 1 (PP1) to chromatin at anaphase ons

184 he mitotic chromosome periphery and recruits protein phosphatase 1 (PP1) to chromatin at anaphase ons

185 transmission through their ability to target protein phosphatase 1 (PP1) to dendritic spines where PP

186 tes with the broadly acting serine/threonine protein phosphatase 1 (PP1) to dephosphorylate eIF2alpha

187 The Ska1 C-terminal domain (CTD) recruits protein phosphatase 1 (PP1) to kinetochores to promote t

188 Here, we show that Ska complex recruits protein phosphatase 1 (PP1) to kinetochores.

189 kinase activity of the IGF-1R by activating protein phosphatase 1 (PP1) to promote dephosphorylation

190 ein KNL1 directly interacts with and targets protein phosphatase 1 (PP1) to the outer kinetochore.

191 her, Sp3 was shown to promote the binding of protein phosphatase 1 (PP1) to the p21(CIP1) promoter, l

192 We report that Ikaros interacts with protein phosphatase 1 (PP1) via a conserved PP1 binding

193 We also demonstrated that functional CK2 and protein phosphatase 1 (PP1) were selectively tethered to

194 through the RHO/ROCK pathway and coordinates protein phosphatase 1 (PP1) with cofilin activity to reg

195 ew study, we investigated the interaction of protein phosphatase 1 (PP1) with the SR protein splicing

196 Protein phosphatase 1 (PP1), a major protein phosphatase

197 Using a directed RNAi screen we find that protein phosphatase 1 (PP1), a ubiquitous serine/threoni

198 of p38 MAPK, phosphatidylinositol 3-kinase, protein phosphatase 1 (PP1), and dynamin GTPase.

199 by protein kinase A results in inhibition of protein phosphatase 1 (PP1), and phosphorylation at Thr-

200 s, we have found novel links among ERK, JNK, protein phosphatase 1 (PP1), and the eukaryotic initiati

201 /2 as a positive regulator, whereas purified protein phosphatase 1 (PP1), dephosphorylated Thr-450 in

202 es involved in glycogen synthesis, including protein phosphatase 1 (PP1), glycogen synthase, phosphor

203 amily serine/threonine phosphatases PP2A and protein phosphatase 1 (PP1), had cell type-dependent eff

204 Sds22, a regulatory subunit of protein phosphatase 1 (PP1), has recently been linked to

205 Protein phosphatase 1 (PP1), in particular, is ubiquitou

206 this study we show that Gwl associates with protein phosphatase 1 (PP1), particularly PP1gamma, whic

207 R cytoplasmic domain (cd) and the associated protein phosphatase 1 (PP1), requiring NMDARcd movement,

208 eins that are glycogen-targeting subunits of protein phosphatase 1 (PP1), the muscle-specific regulat

209 the largely uncharacterized Phactr family of protein phosphatase 1 (PP1)-and actin-binding proteins.

210 stone H3-Lys(4) methyltransferase complexes, protein phosphatase 1 (PP1)-associated proteins, a chape

211 e how Rif1 opposes DDK function by directing Protein Phosphatase 1 (PP1)-mediated dephosphorylation o

212 phosphorylated glycogen synthase at a GSK-3/protein phosphatase 1 (PP1)-regulated site in rictor kno

213 ed predominantly by an Src kinase inhibitor, protein phosphatase 1 (PP1)-sensitive but Src/Yes/Fyn-in

214 by the balance between CK1delta/epsilon and protein phosphatase 1 (PP1).

215 ased with IP(3) (IRBIT) and by inhibition of protein phosphatase 1 (PP1).

216 inhibition of the serine-threonine-specific protein phosphatase 1 (PP1).

217 itor-1, which, when phosphorylated, inhibits protein phosphatase 1 (PP1).

218 omitantly with dephosphorylation of PDE3A by protein phosphatase 1 (PP1).

219 d from Cdc25 and S287 is dephosphorylated by protein phosphatase 1 (PP1).

220 ctions in the checkpoint through controlling protein phosphatase 1 (PP1).

221 this phosphorylation is rapidly reversed by protein phosphatase 1 (PP1).

222 gulation, pSer-68-PLM is dephosphorylated by protein phosphatase 1 (PP1).

223 ed levels of GADD34, a regulatory subunit of protein phosphatase 1 (PP1).

224 d calcineurin (CaN)-deactivated inhibitor of protein phosphatase 1 (PP1).

225 lated by the broadly acting serine/threonine protein phosphatase 1 (PP1).

226 a master regulator of mitosis by modulating protein phosphatase 1 (PP1).

227 yeast [6], we show here that the binding of protein phosphatase 1 (PP1/Glc7) to the evolutionarily c

228 (TTN) is highly selective for a single PPP, protein phosphatase 1 (PP1/PPP1C).

229 Protein phosphatase-1 (PP1) activity is important for ma

230 sphorylation-dependent mechanism mediated by protein phosphatase-1 (PP1) and dual specificity phospha

231 nhibitor-1 (I-1) is a selective inhibitor of protein phosphatase-1 (PP1) and regulates several PP1-de

232 uires activity of NMDA receptors (NMDAR) and protein phosphatase-1 (PP1) and takes place within 15 mi

233 Protein phosphatase-1 (PP1) catalytic subunit isoforms i

234 Protein phosphatase-1 (PP1) controls many processes in e

235 PTG and G(L) are hepatic protein phosphatase-1 (PP1) glycogen-targeting subunits,

236 The reaction catalyzed by the protein phosphatase-1 (PP1) has been examined by linear

237 ively inhibit myosin phosphatase among other protein phosphatase-1 (PP1) holoenzymes.

238 ation as a targeting subunit for the Ser/Thr protein phosphatase-1 (PP1) in yeast.

239 Protein phosphatase-1 (PP1) is a major Ser/Thr phosphata

240 Protein phosphatase-1 (PP1) is a Ser/Thr protein phospha

241 Protein phosphatase-1 (PP1) is an essential protein Ser/

242 in kinase A by 8-bromo-cAMP or inhibition of protein phosphatase-1 (PP1) or calcineurin (PP2B) result

243 Our data further show that PKA targets protein phosphatase-1 (PP1) through the phosphorylation

244 in binding protein neurabin I (NrbI) targets protein phosphatase-1 (PP1) to specific postsynaptic mic

245 minal coiled-coil domains and association of protein phosphatase-1 (PP1) with neurabin-I through a ca

246 Cellular functions of protein phosphatase-1 (PP1), a major eukaryotic serine/t

247 The regulatory circuit controlling cellular protein phosphatase-1 (PP1), an abundant group of Ser/Th

248 defects did not involve changes in levels of protein phosphatase-1 (PP1), and the multinuclear phenot

249 that S135 dephosphorylation is catalyzed by protein phosphatase-1 (PP1), which directly binds C2.

250 ase SR-protein phosphorylation by activating protein phosphatase-1 (PP1).

251 -induced HIV-1 transcription is regulated by protein phosphatase-1 (PP1).

252 We find that Spinophilin, a Protein-phosphatase 1 (PP1) targeting protein, is respon

253 chemical compound that specifically inhibits protein phosphatase 1(PP1)-GADD34 phosphatase activity,

254 glycogen synthase kinase 3beta (GSK3beta) by protein phosphatase 1(PP1)-mediated dephosphorylation of

255 of Shoc2/Sur-8 and the catalytic subunit of protein phosphatase 1 (PP1c) as a highly specific M-Ras

256 We report that the catalytic subunit of protein phosphatase 1 (PP1c) constitutively associates w

257 rate specificity of the catalytic subunit of protein phosphatase 1 (PP1c) is dictated by PP1c-interac

258 n MEL-28/ELYS docks the catalytic subunit of protein phosphatase 1 (PP1c) to direct kinetochore disas

259 P)/PPP1r15B targets the catalytic subunit of protein phosphatase 1 (PP1c) to phosphorylated eIF2alpha

260 1 (MYPT1) binds to the catalytic subunit of protein phosphatase 1 (PP1C).

261 of the catalytic subunit (gamma isoform) of protein phosphatase-1 (PP1c gamma) in vitro.

262 s mediated at least in part by inhibition of protein phosphatase-1 (PP1c) via persulfidation at Cys-1

263 abenz, that bound to a regulatory subunit of protein phosphatase 1, PPP1R15A/GADD34, selectively disr

264 identified a membrane-associated subunit of protein phosphatase 1 (PPP1R16A, or abbreviated as R16A)

265 Together with protein phosphatase 1, protein phosphatase 2A (PP2A) con

266 Furthermore, both the protein phosphatase 1/protein phosphatase 2A inhibitor o

267 nhibitors, but not okadaic acid (a selective protein phosphatase 1/protein phosphatase 2A inhibitor),

268 itogen-activated protein kinase pathway, and protein phosphatase 1, regulate activation of Msn2 in di

269 etermined the expression and localization of protein phosphatase 1 regulatory inhibitor subunit 11 (P

270 MPK in vivo in several substrates, including protein phosphatase 1 regulatory subunit 12C (PPP1R12C)

271 Protein phosphatase 1 regulatory subunit 1A (PPP1R1A) is

272 Protein phosphatase 1 regulatory subunit 1B(+) BLA pyram

273 , glucokinase regulatory protein (GCKR), and protein phosphatase 1 regulatory subunit 3b (PPP1R3B) th

274 ction closest to the mapped region, PPP1R3B (protein phosphatase 1 regulatory subunit 3B), encodes a

275 nophilin (abbreviated spn; gene name Ppp1r9b protein phosphatase 1 regulatory subunit 9b) and the cla

276 In this study, we propose protein phosphatase 1, regulatory (inhibitor) subunit 1A

277 line resulted in the isolation of a mutated protein phosphatase 1, regulatory (inhibitor) subunit 3B

278 131, which affects the expression of ORMDL3, protein phosphatase 1, regulatory inhibitor subunit 1B (

279 between TIBC and a variant near the gene for protein phosphatase 1, regulatory subunit 3B (PPP1R3B; r

280 in-dependent protein kinase II, calcineurin, protein phosphatase 1, Rho GTPase, mitogen-activated pro

281 Therefore the role of the protein phosphatase 1 should be considered as an additio

282 The Src homology-2 protein phosphatase-1 (SHP-1) coprecipitated with integr

283 monstrate that dephosphorylation of Pax-6 by protein phosphatase-1 significantly modulates its functi

284 Inh3 (inhibitor-3) is a potent inhibitor of protein phosphatase-1 that selectively associates with P

285 nt triggers the dephosphorylation of Dam1 by protein phosphatase 1, this dephosphorylation likely coo

286 Inhibiting protein phosphatase-1 through the overexpression of a co

287 homeostasis regulator GADD34, which recruits protein phosphatase 1 to dephosphorylate eIF2alpha durin

288 factor of herpes simplex viruses, redirects protein phosphatase 1 to dephosphorylate the alpha subun

289 ss, the gamma(1)34.5 protein associates with protein phosphatase 1 to form a large complex that depho

290 protein kinase (protein kinase A (PKA)) and protein phosphatase 1 to the carboxyl terminus of the I(

291 KAP-9), which recruits protein kinase A) and protein phosphatase 1 to the channel.

292 o-mediated targeting of protein kinase A and protein phosphatase-1 to the I(Ks) channel.

293 Expression of the catalytic subunit of protein phosphatase 1 was increased in all mutant hearts

294 NA encoding PP1cgamma1 (catalytic subunit of protein phosphatase 1) was present in several independen

295 Inhibitor-1 becomes a potent inhibitor of protein phosphatase 1 when phosphorylated by cAMP-depend

296 s dephosphorylation by kinetochore-localized protein phosphatase 1, which allows Cdc20 to activate th

297 del systems parallel the observation that in protein phosphatase-1, which has an active site that res

298 ons in PPM1D, encoding wild-type p53-induced protein phosphatase 1D (WIP1), in 37.5% of the BSGs that

299 tact has a direct parallel in the contact of protein phosphatase 1 with its regulatory proteins, sugg

300 c were determined to be potent inhibitors of protein phosphatase-1 with similar activity.