ライフサイエンスコーパス: protein phosphatase 1

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

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

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

4 h differential activity of eIF2B mediated by protein phosphatase 1.

5 1epsilon (CK1epsilon) and was antagonized by protein phosphatase 1.

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

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

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

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

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

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

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

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

14 resistant to serine 133 dephosphorylation by protein phosphatase 1.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

29 Protein phosphatase 1 activity negatively regulates this

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

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

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

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

34 )-disrupting peptide (PDP-Nal) that triggers protein phosphatase-1 activity.

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

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

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

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

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

40 by inhibition of the catecholamine-sensitive protein phosphatase 1 and decreased by beta-blocker pret

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

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

43 h reductions in G-protein receptor kinase 2, protein phosphatase 1 and protein phosphatase 2 A abunda

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

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

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

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

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

49 coded by the PPP1R1B gene is an inhibitor of protein phosphatase-1 and protein kinase A.

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

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

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

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

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

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

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

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

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

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

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

61 -ASPP2 was dependent on its interaction with protein phosphatase 1, but not on t-ASPP2-induced YAP ac

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

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

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

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

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

67 lls to isolate NACA complexes and identified protein phosphatase 1 catalytic subunit alpha (PP1A) as

68 Furthermore, we identified protein phosphatase 1 catalytic subunit gamma (PPP1CC) a

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

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

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

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

73 ch is a stress-induced regulatory subunit of protein phosphatase 1 complex that dephosphorylates eIF2

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

101 est whether a DCT-enriched inhibitor of PP1, protein phosphatase 1 inhibitor-1 (I1), mediates cAMP's

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

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

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

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

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

107 Protein phosphatase 1 mediated the dephosphorylation eve

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

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

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

111 Nuclear inhibitor of protein phosphatase 1 (NIPP1) is a ubiquitously expresse

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

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

114 Protein phosphatase 1 occurs in all tissues and regulate

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

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

117 ysis of the Plasmodium falciparum homolog of Protein Phosphatase 1 (PfPP1), a universally conserved c

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

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

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

121 gene encoding PH domain Leucine-rich repeat Protein Phosphatase 1 (PHLPP1) protects mice from lethal

122 homology (PH) domain and leucine-rich repeat protein phosphatase 1 (Phlpp1) regulates protein kinase

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

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

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

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

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

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

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

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

131 la border cell migration model, we find that Protein phosphatase 1 (Pp1) activity controls collective

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

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

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

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

136 these events that we show are underpinned by protein phosphatase 1 (PP1) activity, the inhibition of

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

144 Evidence suggests that protein phosphatase 1 (PP1) and other protein phosphatas

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 cAMP-dependent protein kinase (PKA) and the protein phosphatase 1 (PP1) and/or PP2A.

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

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

151 We found that RIF1 mutants that block Protein Phosphatase 1 (PP1) binding activated telomeric

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

153 Protein phosphatase 1 (PP1) catalytic subunits dephospho

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

176 Protein phosphatase 1 (PP1) limits steady-state phosphor

177 6983 prevents the dephosphorylation by pure protein phosphatase 1 (PP1) or the hydrophobic motif pho

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

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

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

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

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

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

184 ctr1, an actin-binding protein that recruits protein phosphatase 1 (PP1) to certain phosphoprotein su

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

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

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

188 Biochemically, Dok3 recruited protein phosphatase 1 (PP1) to dephosphorylate Card9, an

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

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

191 etaphase II due to premature localization of protein phosphatase 1 (PP1) to kinetochores, which antag

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

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

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

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

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

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

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

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

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

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

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

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

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

205 /2 as a positive regulator, whereas purified protein phosphatase 1 (PP1), dephosphorylated Thr-450 in

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

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

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

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

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

211 The metalloenzyme protein phosphatase 1 (PP1), which is responsible for >=

212 C and error correction are both regulated by protein phosphatase 1 (PP1), which silences the SAC and

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

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

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

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

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

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

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

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

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

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

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

224 osphatase 2 phosphatase activator (PP2A) and protein phosphatase 1 (PP1).

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

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

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

228 ylation-mediated decrease in the activity of protein phosphatase 1 (PP1).

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

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

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

232 found that this motif is sufficient to bind protein phosphatase 1 (PP1)alpha, a ubiquitously express

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

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

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

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

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

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

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

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

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

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

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

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

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

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 evelopment of a photoreleasable version of a protein phosphatase-1 (PP1)-disrupting peptide (PDP-Nal)

251 ase SR-protein phosphorylation by activating 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 rate specificity of the catalytic subunit of protein phosphatase 1 (PP1c) is dictated by PP1c-interac

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

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

259 1 (MYPT1) binds to the catalytic subunit of protein phosphatase 1 (PP1C).

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

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

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

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

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

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

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

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

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

269 tic cancer cells had increased expression of protein phosphatase 1 regulatory inhibitor subunit 1B (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 Expression patterns were confirmed for protein phosphatase 1 regulatory subunit 36 (PPP1R36) an

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

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

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

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

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

279 131, which affects the expression of ORMDL3, protein phosphatase 1, regulatory inhibitor subunit 1B (

280 h de novo loss-of-function (LoF) variants in protein phosphatase 1, regulatory subunit 12a (PPP1R12A)

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

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

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

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

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

286 The MYPTs preferentially bind the catalytic protein phosphatase 1 subunit PP1cbeta, forming myosin p

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

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

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

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

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

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

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

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

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

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

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

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

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

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