ライフサイエンスコーパス: phosphatase activity

1 r factor-kappaB ligand (RANKL), and alkaline phosphatase activity.

2 ated PTEN mutations block its essential PIP3 phosphatase activity.

3 nd B subunits were stable and uncoupled from phosphatase activity.

4 iptional coactivators with intrinsic protein phosphatase activity.

5 ad deficient mineral apposition and alkaline phosphatase activity.

6 Asn394 as a critical amino acid involved in phosphatase activity.

7 e that help decipher the mechanism of glucan phosphatase activity.

8 phosphorylation of Shp2, which inhibits Shp2 phosphatase activity.

9 ed ligands and inhibits its protein-tyrosine phosphatase activity.

10 brane electrical potential to inositol lipid phosphatase activity.

11 y with Ssu72 and strongly stimulates its CTD phosphatase activity.

12 roximately 5-fold increase in Cps2B-mediated phosphatase activity.

13 nsport, PSRP1-sRNPC is stable against phloem phosphatase activity.

14 mplex and reduces but does not fully abolish phosphatase activity.

15 sociated with significant reduction in local phosphatase activity.

16 ase activity must be counteracted by protein phosphatase activity.

17 means for modulating the balance of CDK and phosphatase activity.

18 duced type 1 collagen secretion and alkaline phosphatase activity.

19 in the stimulation (6-fold) of phosphatidate phosphatase activity.

20 XNWD motif, results in maximal activation of phosphatase activity.

21 0 has been shown to bind PP5 to activate its phosphatase activity.

22 lkaline phosphatase has an enhanced alkaline phosphatase activity.

23 ts SRC basal activation independently of its phosphatase activity.

24 nserved domain is not sufficient for maximal phosphatase activity.

25 fects of Ssu72 with respect to its Ser(P)(5) phosphatase activity.

26 e its subcellular location and phosphatidate phosphatase activity.

27 ose production despite the loss of glucose-6-phosphatase activity.

28 h GADD34-PP1 holoenzymes, thereby inhibiting phosphatase activity.

29 reased protein abundance but suppressed PTEN phosphatase activity.

30 regulation of both FGFR2's kinase and Shp2's phosphatase activity.

31 which occurs in cells lacking phosphatidate phosphatase activity.

32 on of proteotoxic stress and loss of protein phosphatase activity.

33 PPP1CB protein that demonstrated diminished phosphatase activity.

34 h FliM is not required for binding CheY-P or phosphatase activity.

35 irectly binds to RapP and inhibits its Spo0F phosphatase activity.

36 EOPARD syndrome SHP2 mutants exhibit reduced phosphatase activity.

37 pathway and inhibition of myosin light chain phosphatase activity.

38 abundance of PTEN protein but increased PTEN phosphatase activity.

39 ority of them stained intensely for alkaline phosphatase activity.

40 membrane and nucleus without affecting lipid phosphatase activity.

41 calcium release on its way to activation of phosphatase activity.

42 ssed by staining for tartrate-resistant acid phosphatase activity.

43 human Treg cells and provides complementary phosphatase activity.

44 tion of purified PP2Ac with CIN85 suppressed phosphatase activity.

45 ons leads to significant or complete loss of phosphatase activity.

46 SUMOylated, yet is independent of its lipid phosphatase activity.

47 dependent platelet function by dampening the phosphatase activity.

48 f LC20 upon inhibition of myosin light chain phosphatase activity.

49 or and OC protein addition enhanced alkaline phosphatase activity.

50 e effect associated with intestinal alkaline phosphatase activity.

51 , which occurs independently of antagonizing phosphatase activity.

52 ction networks depends on protein kinase and phosphatase activities.

53 SIK2-PP2A complex preserves both kinase and phosphatase activities.

54 nonrobust phosphorylation due to diminished phosphatase activities.

55 regulation of HisKA and HisKA_3 transmitter phosphatase activities.

56 tion of the local balance between kinase and phosphatase activities.

57 Together, the RVLM phosphatase activity acts tonically to attenuate the ERK

58 des for ITM, we investigated whether protein phosphatase activity affected circadian modulation.

59 8(MAPK) determines signal amplitude, whereas phosphatase activity affects both signal amplitude and d

60 receptors interacted with and inhibited PP2C phosphatase activity against the SnRK2-type kinase, rele

61 genic related markers (osteopontin, alkaline phosphatase activity, Alizarin red, and Von Kossa) compa

62 ssential for parental levels of capsule, but phosphatase activity alone could be eliminated without a

63 The phosphatase activity also occurs with nonpeptidic substr

64 osphorylation of Synj at S1029 enhances Synj phosphatase activity, alters interaction between Synj an

65 tional model that combines MAPK scaffold and phosphatase activities and is sufficient to account for

66 on in ICL repair is dependent on its protein phosphatase activity and ability to be SUMOylated, yet i

67 This was confirmed by alkaline phosphatase activity and Alizarin red and Von Kossa stai

68 Root phosphatase activity and AM colonisation were higher for

69 e found an inverse relationship between root phosphatase activity and AM colonization in field-collec

70 l differentiation such as increased alkaline phosphatase activity and an elevated level of matrix met

71 We measured root phosphatase activity and arbuscular mycorrhizal (AM) col

72 esulting in significantly increased alkaline phosphatase activity and calcium deposition of encapsula

73 The osteoblastic functions of alkaline phosphatase activity and calcium mineralization were als

74 in MK migration due to the reduction in SHP1 phosphatase activity and consequent increase in the phos

75 trasting requirements for protein kinase and phosphatase activity and differential impact on CP-AMPAR

76 s from increased tissue-nonspecific alkaline phosphatase activity and diminished ATP availability cau

77 cleaved by calpain-2, which inactivates its phosphatase activity and generates stable breakdown prod

78 R306, of EYA1 are essential for its in vitro phosphatase activity and in vivo function during Drosoph

79 nstrate that PTPN1 mutations lead to reduced phosphatase activity and increased phosphorylation of JA

80 d in partial inhibition of its ATP-dependent phosphatase activity and inhibited subsequent phosphoryl

81 were decreased, as evidenced by low alkaline phosphatase activity and matrix mineralization.

82 tation of allosteric sites that can regulate phosphatase activity and may enable the discovery of nov

83 P-activated signaling pathway controls SHP-1 phosphatase activity and may regulate numerous receptor

84 r, the p85alpha homodimer enhances the lipid phosphatase activity and membrane association of PTEN.

85 function mutations in PTEN that impair lipid phosphatase activity and membrane binding are oncogenic,

86 rotein levels and induced increased alkaline phosphatase activity and mineralization in osteoblast cu

87 rt1(DeltaOsx1) mice exhibited lower alkaline phosphatase activity and mineralization, as well as decr

88 mber of committed osteoprogenitors, alkaline phosphatase activity and mineralization.

89 competition, however, AM colonization, root phosphatase activity and N2 fixation increased in the N2

90 formance remain unclear: biomass allocation, phosphatase activity and phosphorus-use efficiency did n

91 We also found increased alkaline phosphatase activity and reduced ATP and pyrophosphate l

92 show that FTY720-P enhances TNF-induced PP2A phosphatase activity and significantly represses TNF-ind

93 nt in polyP coincided with enhanced alkaline phosphatase activity and substitution of sulfolipids for

94 suggesting a functional correlation between phosphatase activity and systemic autoimmunity.

95 phate and tensin homolog through its protein phosphatase activity and that the increase in INPP4B is

96 mains of Pah1 are required for phosphatidate phosphatase activity and the in vivo function of the enz

97 tion based on the maintenance of the Ser/Thr phosphatase activity and their neuroprotection against t

98 only tyrosine phosphatase activity, has dual phosphatase activities, and both the N- and C-terminal d

99 ulation of organic acids, enhanced secretory phosphatase activity, and depletion of ATP in overexpres

100 ant effects on protein synthesis or alkaline phosphatase activity, and drove discrete changes in a pa

101 disrupted sebocyte cell membranes, alkaline phosphatase activity, and significantly reduced sebocyte

102 Myosin light chain kinase and phosphatase activities are known to be increased and dec

103 ponent analysis shows that dehydrogenase and phosphatase activities are the vital variables contribut

104 tection from proteolysis, and stimulation of phosphatase activity are linked to oligomerization of Sp

105 Moreover, the PST/TPM and the threonine phosphatase activity are not required for in vitro inter

106 we report inherited dysregulation of protein phosphatase activity as a cause of intellectual disabili

107 y interacted with PTP1B and suppressed PTP1B phosphatase activity as well as the association of PTP1B

108 9D) constructs, in vitro binding assays, and phosphatase activity assays, we demonstrate that phospho

109 Thus, a pool of phosphatase activity associated with a kinetochore-local

110 PHLPP phosphatase network allows coordinated phosphatase activities at the site of T-cell receptor ac

111 ive estimates for the intracellular alkaline phosphatase activity at five different temperatures in d

112 We assessed soil and root phosphatase activity between fixers and non-fixers in tw

113 ssion of OsHAD1 in rice resulted in enhanced phosphatase activity, biomass, and total and soluble P c

114 s no change in glycogen content or glucose 6-phosphatase activity but increased Slc2a2 glucose transp

115 of ethanol, caused no changes in BP or RVLM phosphatase activity but it produced significant increas

116 usually is attributed to myosin light chain phosphatase activity, but findings in non-VSM identified

117 r-72 phosphorylation and activation of PP-1I phosphatase activity by GSK-3.

118 Finally, inhibition of SHP phosphatase activity by NSC87877 abrogated B. pertussis

119 In addition, inhibition of protein phosphatase activity by OA increases CaBP4 phosphorylati

120 Inhibition of the RVLM ser/thr phosphatase activity by okadaic acid (OKA, 0.4 mug) or f

121 c homology 2 domain-containing phosphatase 2 phosphatase activity by scavenging reactive oxygen speci

122 burgdorferi CheD significantly enhances CheX phosphatase activity by specifically interacting with th

123 Moreover, alkaline phosphatase activity, calcium deposition and acidic poly

124 greatly promote MSC proliferation, alkaline phosphatase activity, calcium deposition and total prote

125 defects in balancing cytoplasmic kinase and phosphatase activities, changing their activation thresh

126 BL) and enhanced the respiratory burst, acid phosphatase activity, chemotactic activity, and gene exp

127 emur length, and 30% elevated serum alkaline phosphatase activity compared to wild type.

128 inhibiting kinase activity while stimulating phosphatase activity, consistent with the selective inac

129 Impaired phosphatase activity contributes to the persistent activ

130 BCR expression level and phosphatase activity could both contribute to such heter

131 sponse to TNF, and this increased GADD34-PP1 phosphatase activity, dephosphorylating eukaryotic trans

132 Alkaline phosphatase activity did not increase in response to inf

133 The change in Cps2B phosphatase activity did not result from alterations in

134 ediated inductions of PAH1 and phosphatidate phosphatase activity do not correlate with the amount of

135 ion, some dividing cells, and clear alkaline phosphatase activity (early bone marker).

136 phosphorylated RyRs because of reduced local phosphatase activity enhance triggered activity in LQT2

137 or of STAT5 through liberation of endogenous phosphatase activity following NADPH oxidase (NOX) inhib

138 transduction results from sensor transmitter phosphatase activity for phospho-receiver dephosphorylat

139 itant with a significant increase in protein phosphatase activity for two colon cancer cell lines in

140 mong all the compounds screened for alkaline phosphatase activity, four compounds 10, 14, 18, and 22

141 We enriched the phosphatase activity from a B. subtilis cell extract and

142 promoted DP markers and functional alkaline phosphatase activity from the DP cells.

143 tes, including bile acids transfer, alkaline phosphatase activity, gamma-glutamyl-transpeptidase acti

144 the N2 fixer with high N2 fixation and root phosphatase activity grew best on organic P, whereas the

145 , a GAS strain selectively deficient in CovS phosphatase activity had a distinct transcriptome relati

146 Although in vitro CTD phosphatase activity has been established for some CPLs,

147 Furthermore, Eya phosphatase activity has been shown to mediate transform

148 hich has been reported to have only tyrosine phosphatase activity, has dual phosphatase activities, a

149 we manipulated native loci to ablate hCDC14A phosphatase activity (hCDC14A(PD)) in untransformed hTER

150 Unexpectedly, we observed that inhibiting a phosphatase activity highly sensitive to OA caused an ab

151 he coronavirus macrodomain has ADP-ribose-1"-phosphatase activity; however, its function during infec

152 The values of soil dehydrogenase and phosphatase activities in the four wetlands follow the o

153 Chlamydomonas GPD2 showed both reductase and phosphatase activities in vitro and it can work as a bif

154 merize with wild-type PTEN and constrain its phosphatase activity in a dominant-negative manner.

155 A3 (RON3) protein as a regulator of the PP2A phosphatase activity in Arabidopsis thaliana.

156 nt hops induced estrogen responsive alkaline phosphatase activity in endometrial cancer cells, estrog

157 Increased phosphatase activity in light-dependent conditions rever

158 Upregulation of CD45 tyrosine phosphatase activity in MDSCs exposed to hypoxia in tumo

159 prelamin A-expressing VSMCs induced alkaline phosphatase activity in mesenchymal progenitor cells, an

160 We demonstrate that phosphatase activity in natural biofilm samples decrease

161 ion of OC protein partially rescued alkaline phosphatase activity in periodontal ligament (PDL) cells

162 cant increases in BP and inhibition of local phosphatase activity in rats treated with OKA or fostrie

163 ly members, serving as a platform to control phosphatase activity in response to diverse inputs.

164 Under laboratory conditions, BvgS shifts to phosphatase activity in response to modulators, notably

165 ate, showing that BvgS shifts from kinase to phosphatase activity in response to this modulator via a

166 aining protein tyrosine phosphatase 2 (Shp2) phosphatase activity in the absence of extracellular sti

167 tion uncover a novel mechanism whereby lipid phosphatase activity in the nucleus can regulate mammali

168 ed on the inhibition of immobilized alkaline phosphatase activity, in the presence of the phosphate i

169 ulate actin cytoskeleton dynamics and myosin phosphatase activity, including focal adhesion kinase, p

170 dramatic increases in hydrolase EEAs (e.g., phosphatase activity increased >28-fold) supporting the

171 Inhibiting serine phosphatase activity increased Ser(P)-IRS-2 and decrease

172 s of perturbations can influence transmitter phosphatase activity indirectly.

173 strain, indicating that both CovS kinase and phosphatase activities influence the CovR phosphorylatio

174 al RNA-binding NSP2 octamer with nucleotidyl phosphatase activity is central to viroplasm formation a

175 ining phosphatase 1 (SHP)-1, SHP-2, and SHIP phosphatase activity is dispensable for this function.

176 Here, we report that PTEN phosphatase activity is inhibited via a transnitrosylati

177 nd maintain 1 null allele, we show that PTEN phosphatase activity is required for preventing the emer

178 AtSAL1 phosphatase activity is suppressed by dimerization, intr

179 ow that PTEN requires both lipid and protein phosphatase activity, its extreme C-terminal PDZ binding

180 - 0.31 mumol min(-)(1) mg protein(-)(1)) and phosphatase activity (Km 27.38 +/- 3.1 mM and Vmax 0.077

181 h in vivo and in vitro, loss of EYA tyrosine phosphatase activity leads to defective assembly of gamm

182 We find that loss of Ppz phosphatase activity leads to defects in ubiquitin homeo

183 confounders, such as inflammation, alkaline phosphatase activity, low serum albumin, renal function,

184 hanced differentiation indicated by alkaline phosphatase activity, mineral deposition, and transcript

185 entiation as indicated by increased alkaline phosphatase activity, mineralization, and up-regulation

186 Phosphatase activity must subsequently be restored to pr

187 These results indicate that neither Cps2B phosphatase activity nor Cps2D phosphorylation levels pe

188 ies of the bifunctional 5-InsP7 kinase/InsP8 phosphatase activities of full-length diphosphoinositol

189 Moreover, we report that InsP8 phosphatase activities of PPIP5Ks are strongly inhibited

190 We hypothesize that the reductase and phosphatase activities of PSP-GPD multidomain enzymes ma

191 Recognition properties and phosphatase activities of site-directed mutants identify

192 , in vivo characterization of the kinase and phosphatase activities of TCS proteins is often limited

193 ere, we identified tumor inhibitory and RelA phosphatase activities of the protein phosphatase 2C (PP

194 , we show that the nuclease, polymerase, and phosphatase activities of yeast CPF are organized into t

195 nteraction with AtMIA40 is necessary for the phosphatase activity of AtSLP2 and is dependent on the f

196 at dimerization is important for controlling phosphatase activity of CacyBP/SIP and for regulating th

197 N-terminal domain is indispensable for full phosphatase activity of CacyBP/SIP.

198 alpha-syn enhanced the phosphatase activity of CN in both cell-free assays and

199 Calcineurin phosphatase activity of cyclophilin-trialysin-treated pa

200 This was dependent on the 2'-5' phosphatase activity of DBR1, since it did not occur whe

201 with our previous results that the tyrosine phosphatase activity of Eya is dispensable for normal Ey

202 The phosphatase activity of Eya is important for the transcr

203 ible inhibitors that selectively inhibit the phosphatase activity of Eya2, but not Eya3.

204 86Ser) transgenic mice demonstrates that the phosphatase activity of FIG4 has an essential role in vi

205 the nuclear translocation and phosphatidate phosphatase activity of lipin-1.

206 we show is critical for the specific glucan phosphatase activity of LSF2 toward native Arabidopsis s

207 Our data collectively show that the phosphatase activity of OsPP2A against OsRBR1 is regulat

208 The mechanisms that regulate the phosphatase activity of PGAM5 are poorly understood.

209 ular allosteric regulation mechanism for the phosphatase activity of PGAM5, in which the assembly of

210 hat function as allosteric regulators of the phosphatase activity of PGAM5.

211 of multimeric complexes and markedly reduce phosphatase activity of PGAM5.

212 For example, the phosphatase activity of PP2A is suppressed in chronic my

213 a negative feedback loop that modulates the phosphatase activity of PP2A.

214 Furthermore, increased phosphatase activity of PP5 correlated with impaired pho

215 ever, Hsp70 binding to PP5 stimulates higher phosphatase activity of PP5 than the binding of Hsp90.

216 PTEN mutant constructs, we show that protein phosphatase activity of PTEN targets PTK6, with efficien

217 tumors, functionally caused the loss of the phosphatase activity of PTPRD, and were associated with

218 vels increased mRNA, protein expression, and phosphatase activity of SHP-1, which remained elevated d

219 steine residue, which inhibited the tyrosine-phosphatase activity of SHP-1.

220 Tim50 was overexpressed, suggesting that the phosphatase activity of TbTim50 plays a role in regulati

221 Phytohormone binding inactivates the phosphatase activity of the coreceptor, permitting phosp

222 oadly conserved mechanism that regulates the phosphatase activity of the largest family of bifunction

223 lacking the WDXNWD motif markedly increases phosphatase activity of the mutant protein.

224 RCAR7 regulated the phosphatase activity of the PP2Cs ABI1, ABI2, and PP2CA

225 In contrast, phosphatase activity of the TbTim50 is required neither

226 The lipid phosphatase activity of the tumor suppressor phosphatase

227 d, in this active conformation, exerts lipid phosphatase activity on PtdIns(3,4,5)P3.

228 PHO13-overexpressing strain showed a higher phosphatase activity on xylulose-5-phosphate (X-5-P), su

229 in tumors, most often by loss of PTEN lipid phosphatase activity or the amplification or mutation of

230 enopus early embryonic extract revealed that phosphatase activity other than PP1 continuously suppres

231 15 (P = 0.0001), and calcification (alkaline phosphatase activity, P < 0.01; osteocalcin, P < 0.05).

232 ere, we use fission yeast to investigate how phosphatase activity participates in this interplay duri

233 GAS mutants lacking SP-PTP revealed that the phosphatase activity per se positively regulates growth,

234 hese data reinforce the hypothesis that CpxA phosphatase activity plays a critical role in controllin

235 We also find that the threonine phosphatase activity plays only a minor role during Dros

236 hese requirements, namely segregation of the phosphatase activity predominantly onto the free form of

237 acdc55 mutation affecting Cdc55-PP2A protein phosphatase activity prevented Orm dephosphorylation and

238 sion of a mutated form of PTEN with enhanced phosphatase activity prevented the TGF-beta-induced coll

239 1 directly binds to STRIPAK and inhibits its phosphatase activity, protecting MST2 activation-loop ph

240 fferences we observed in voltage-sensing and phosphatase activity provide a starting point for future

241 with helix disruption decreasing the kinase/phosphatase activity ratio, as required to modulate the

242 ho85-Pho80 kinase complex, maximum Nem1-Spo7 phosphatase activity required Mg(2+) ions (8 mm) and Tri

243 Fig4 mutations predicted to inactivate FIG4 phosphatase activity rescue lysosome expansion phenotype

244 tracellular stores and increased calcineurin phosphatase activity, resulting in NFATc1 nuclear transl

245 Within target tissues, phosphatase activity results in disassembly of PSRP1-sRN

246 Moreover, PTPRO phosphatase activity shortened the half-life of ERBB2 by

247 c, and it possesses carbohydrate binding and phosphatase activity similar to human laforin.

248 weight, long bone length, and serum alkaline phosphatase activity, suggesting that tooth dysfunction

249 es a family of enzymes with 5'-kinase and 3'-phosphatase activities that function in nucleic acid rep

250 dystrophies to defective phosphoinositide 5-phosphatase activity that is becoming increasingly recog

251 rtantly, NFI phosphorylation is dependent on phosphatase activity that is enriched in GFAP/B-FABP+ve

252 Thus, these results identify a 5'-tri-phosphatase activity that is involved in the biogenesis

253 a novel positive regulator of lipin 1beta PA phosphatase activity that is not achieved via altering i

254 We report that Pnkp also has RNA 2'-phosphatase activity that requires Asp165 and Asp167.

255 use a significant reduction in phosphatidate phosphatase activity, the phosphorylation of Pah1p by pr

256 rovascular integrity by enabling VEC-related phosphatase activity, thereby preventing vascular leak d

257 e receptor kinase activity or enhancing CheC phosphatase activity, thereby regulating the levels of t

258 antly, S-nitrosylation of PTEN decreases its phosphatase activity, thus promoting cell survival.

259 pair factor possessing both 5'-kinase and 3'-phosphatase activities to modify ends of a DNA break pri

260 o the nucleus, where Eya1 uses its threonine phosphatase activity to control Myc phosphorylation/deph

261 horylation requires regulation of kinase and phosphatase activity to prevent aberrant signal transduc

262 To evaluate the contribution of the phosphatase activity to the in vivo function of Fig4, we

263 sequesters sigma(S) and possesses kinase and phosphatase activities toward CrsA.

264 nal HisKA family, displaying both kinase and phosphatase activities toward their substrates.

265 horylation-defective RPA2 subunit or lacking phosphatase activity toward RPA2.

266 addition, we find key differences in glucan phosphatase activity toward soluble and insoluble polygl

267 Mutations impaired phosphatase activity toward the phosphoinositide phospha

268 the C-terminus of SCP1 was essential for its phosphatase activity towards c-Myc.

269 Phosphatase activity towards phosphorylated smooth muscl

270 high basal autophagy, possess stronger basal phosphatase activity towards ULK1 and require ULK1 for s

271 ation, starvation also causes an increase in phosphatase activity towards ULK1, an mTORC1 substrate w

272 rmational switch of HK853 that shuts off its phosphatase activity under acidic conditions.

273 cherichia coli similarly exhibited increased phosphatase activity under conditions of high-oxygen gro

274 m substrate trapping complexes with impaired phosphatase activity via increased recruitment of TIPRL1

275 A significant increase in alkaline phosphatase activity was also seen on FA-coated scaffold

276 Nem1-Spo7 phosphatase activity was dependent on the concentrations

277 CD45 phosphatase activity was determined by using a novel flo

278 CD45 phosphatase activity was increased by T-cell help both i

279 Moreover, the NarX transmitter phosphatase activity was independent of nucleotides, in

280 elate with phosphorus associations; however, phosphatase activity was most strongly down-regulated in

281 creased under these conditions, but alkaline phosphatase activity was not significantly altered.

282 Glucose-6-phosphatase activity was reduced, whereas basal cytoplas

283 vitro and in vivo data demonstrated that the phosphatase activity was required for the inactivation o

284 fic functions, but how these domains control phosphatase activity was unknown.

285 uced Smad 1/5/8 phosphorylation and alkaline phosphatase activity were both enhanced by the addition

286 A on cell proliferation, migration, and PP2A phosphatase activity were investigated using ovarian and

287 genes, among which genes involved in protein phosphatase activity were overrepresented, suggesting a

288 te that Hsp70 recruits PP5 and activates its phosphatase activity which suggests dual roles for PP5 t

289 is governed by dynamic changes in kinase and phosphatase activities, which are difficult to assess wi

290 OCRL1 5-phosphatase activity, which is membrane curvature sensit

291 ressor activity depends largely on its lipid phosphatase activity, which opposes PI3K/AKT activation.

292 tion with CD45 on the T cell, inhibiting its phosphatase activity, which resulted in up-regulation of

293 tial of UBASH3B is dependent on its tyrosine phosphatase activity, which targets CBL ubiquitin ligase

294 atus of actin, as was its eIF2alpha-directed phosphatase activity, while localised G-actin depletion

295 d osteoblast differentiation marker alkaline phosphatase activity, while miR-138 inhibitor and OC pro

296 mbinant TbTim50 possesses a dual specificity phosphatase activity with a greater affinity for protein

297 tations in these allosteric clusters altered phosphatase activity with changes in kcat/KM ranging fro

298 oint mutations in cps2B demonstrated reduced phosphatase activity with corresponding increases in lev

299 enable the discovery of novel modulators of phosphatase activity with much improved pharmacological

300 n and septum formation and FgCdc14 possesses phosphatase activity with specificity for a subset of Cd