ライフサイエンスコーパス: phosphorylation-dependent

1 d hrtAB promoter regions and that binding is phosphorylation dependent.

2 This interaction is cell-cycle regulated and phosphorylation-dependent.

3 Moreover, changes in CheV localization are phosphorylation-dependent.

4 With conserved motifs for phosphorylation-dependent 14-3-3 binding, these deacetyl

5 al SGK1 target sites on Nedd4-2 that overlap phosphorylation-dependent 14-3-3 interaction motifs.

6 Phosphorylation-dependent (40E8 and p396) and C-terminal

7 lationally arrested mRNAs) and the eIF2alpha phosphorylation-dependent accumulation of hnRNP A1 in SG

8 itive 1 (BRI1), reflects the balance between phosphorylation-dependent activation and several potenti

9 n synaptic plasticity is associated with the phosphorylation-dependent activation of Akt kinase.

10 human cultured cells, the compounds inhibit phosphorylation-dependent activation of STAT3 without af

11 The phosphorylation-dependent activation of the Janus family

12 Cytokinin signaling leads to the phosphorylation-dependent activation of two classes of A

13 by connecting functional protein dynamics of phosphorylation-dependent activation to protein folding

14 nd additional scaffolding functions with the phosphorylation-dependent, allosteric control of phospho

15 hanced RAN translation requires an eIF2alpha phosphorylation-dependent alteration in start codon fide

16 This phosphorylation-dependent alteration in the PDZ domain-l

17 We show that the phosphorylation-dependent alterations in gene and protei

18 rs to be the result of increasing GluA1-S845 phosphorylation-dependent AMPAR trafficking.

19 inding to amyloid structure assay to monitor phosphorylation-dependent amyloid conversion.

20 rs involved in the control of K(+) fluxes by phosphorylation-dependent and -independent events.

21 transcripts and fibronectin expression in a phosphorylation-dependent and -independent manner, respe

22 in the presence of SGs induced by eIF2alpha phosphorylation-dependent and -independent mechanisms.

23 ed for rapid CtrA proteolysis in vivo form a phosphorylation-dependent and cyclic diguanylate (cdG)-d

24 we report that the Ska-Ndc80 interaction is phosphorylation-dependent and does not require microtubu

25 e Hippo signaling pathway, elucidating novel phosphorylation-dependent and independent mechanisms of

26 ylation of the HM domain, demonstrating both phosphorylation-dependent and independent roles of the H

27 with betaTrCP and subsequent degradation is phosphorylation-dependent and is mediated by the Polo-li

28 branched and sponge-like topologies that are phosphorylation-dependent and self-similar over three de

29 of CaMKII activation that includes both the phosphorylation-dependent and the newly identified oxida

30 f nutrient signals and identifies a Ser(727) phosphorylation-dependent and Tyr(705) phosphorylation-i

31 We conclude that Polo/Plk1 initiates the phosphorylation-dependent assembly of a Cnn scaffold aro

32 rk structure was consistent with a step-wise phosphorylation-dependent assembly of the Grb2/Gab2/Shc1

33 This correlates with the phosphorylation-dependent association of hnRNPA1 with 14

34 have found that MEKK2 is regulated through a phosphorylation-dependent association with 14-3-3, a gro

35 increases in SC levels and reduces oxidative phosphorylation-dependent ATP production.

36 We demonstrate that phosphorylation-dependent basal activity of TAK1 is depe

37 and the Top2 C-terminal regulatory domain is phosphorylation-dependent because treatment with phospha

38 This is the first example of proteasome phosphorylation dependent binding of a proteasome regula

39 exes, revealing the structural basis of both phosphorylation-dependent binding events.

40 e axonal membrane through the reversible Cdk phosphorylation-dependent binding of Kvbeta2 to EB1.

41 Phosphorylation-dependent binding of the transmembrane p

42 ed that ChREBP is retained in the cytosol by phosphorylation-dependent binding to 14-3-3 protein dime

43 residue peptide surrounding the D1 site show phosphorylation-dependent binding to thin filaments.

44 Although aspects of this response were HDAC5 phosphorylation dependent, blocking HDAC5 phosphorylatio

45 Designed assemblies perform efficient phosphorylation-dependent capture and release of cargo p

46 onstrating that the loop functions to couple phosphorylation-dependent CBS domain conformational chan

47 the E267-K1060 electrostatic interaction in phosphorylation-dependent CFTR gating.

48 Importantly, the rate of phosphorylation-dependent channel activation was comprom

49 lix valine residue V228 to leucine prevented phosphorylation-dependent channel regulation.

50 /p97UFD1-NPL4 segregase cooperate to promote phosphorylation-dependent, chromatin-associated Lys-SDE2

51 d functions of phosphoproteins by catalyzing phosphorylation-dependent cis/trans isomerization of pep

52 ar communication whereby ethylene stimulates phosphorylation-dependent cleavage and nuclear movement

53 al structures of the mycobacterial upstream (phosphorylation-dependent) complex PknB-GarA and the dow

54 f caveolae are associated with a Cav1 Tyr-14 phosphorylation-dependent conformational change, which s

55 second beta-propeller, ruling out models of phosphorylation-dependent conformational change.

56 at this region of THEMIS might control local phosphorylation-dependent conformational changes importa

57 rylated and phosphorylated states identified phosphorylation-dependent conformational changes in the

58 sults point to a molecular mechanism for the phosphorylation-dependent control of ICAP-1alpha functio

59 We conclude that phosphorylation-dependent control of TAA1 enzymatic acti

60 Phosphorylation-dependent conversion of PrP from alpha-h

61 periodicity during the cell cycle, including phosphorylation-dependent cyclin E ubiquitylation by the

62 at Ser268 and ATG16L1beta at Ser269, driving phosphorylation-dependent degradation of ATG16L1 protein

63 In cells exposed to VEGF, phosphorylation-dependent degradation of IFNAR1 leads to

64 t the hypoxic activation of ATR leads to the phosphorylation-dependent degradation of the cdc25a phos

65 R kinase (PERK) were shown to accelerate the phosphorylation-dependent degradation of the IFNAR1 chai

66 ng the ligand-stimulated and specific serine phosphorylation-dependent degradation of the IFNAR1 chai

67 The latter promotes an accelerated phosphorylation-dependent degradation of the interferon-

68 Taken together, our results reveal that phosphorylation-dependent derepression of HDAC5 mediates

69 lso initiates signalling cascades leading to phosphorylation-dependent desensitization of MLCK.

70 he GR transcriptome through a coordinated GR phosphorylation-dependent detection mechanism.

71 the alpha 4-beta 5-alpha 5 surface disrupts phosphorylation-dependent dimerization and DNA binding a

72 The data suggest that the activity of the phosphorylation-dependent dimers, such as RcsA-RcsB and

73 ough the neuronal P2X purinoreceptors led to phosphorylation-dependent down-regulation of GABAA recep

74 hmania CK1 in mammalian cells stimulated the phosphorylation-dependent downregulation of IFNAR1 and a

75 essing the phosphosite variant, suggesting a phosphorylation-dependent effect.

76 rylation and the coupling of this process to phosphorylation-dependent EGFR endocytosis.

77 n stress granules is associated with G3BP, a phosphorylation-dependent endoribonuclease.

78 diac isoform cMyBP-C plays a key role in the phosphorylation-dependent enhancement of cardiac functio

79 elease of basal autoinhibition is coupled to phosphorylation-dependent enzyme activation.

80 A transient increase of phosphorylation-dependent ephrin-B (pEB) reverse signali

81 Such protection of PSI results from LHCII phosphorylation-dependent equal distribution of excitati

82 The phosphorylation-dependent equilibrium between active and

83 Further, we demonstrate that phosphorylation-dependent excess stabilization of the ac

84 RLC phosphorylation-dependent force development is regulated

85 Both tyrosine phosphorylation-dependent GRB4 SH2/SH3 adaptor-mediated

86 This phosphorylation-dependent GSK3beta inhibition is mediate

87 ylinositol 4,5-bisphosphate (PIP(2)) is also phosphorylation-dependent, implying a highly effective p

88 n involves modulation of specific HNF-4alpha phosphorylation dependent, in part, on a PKA signaling p

89 ic genes through direct interaction with and phosphorylation-dependent inactivation of ATF4 during th

90 functions antagonistically against pUL27 by phosphorylation-dependent inactivation of pUL27-mediated

91 e yellow-to-cyan emission ratio because of a phosphorylation-dependent increase in FRET between two f

92 nsport following osmotic change may be due a phosphorylation-dependent increase in the level of AQP1

93 y the RXL motif and mediates the bulk of the phosphorylation-dependent inhibition of helicase loading

94 ly, our findings support a mechanism whereby phosphorylation-dependent inhibition of IRSp53 by 14-3-3

95 Here, we show that phosphorylation-dependent inhibition of IRSp53 by 14-3-3

96 -mediated neuroprotective effects are due to phosphorylation-dependent inhibition of mutant HTT exon

97 Here we demonstrate phosphorylation-dependent inhibition of polarized bud gr

98 f pyruvate dehydrogenase kinase 4 (PDK4) and phosphorylation-dependent inhibition of pyruvate dehydro

99 addition to turning off the immune/eIF2alpha phosphorylation-dependent inhibition of translation, the

100 slation initiation factor 2alpha (eIF2alpha) phosphorylation-dependent integrated stress response (IS

101 Here we identify a novel phosphorylation-dependent interaction between 14-3-3 and

102 The phosphorylation-dependent interaction between CAR and ER

103 n together, this study demonstrates that the phosphorylation-dependent interaction between cMyBP-C an

104 Here we report a unique phosphorylation-dependent interaction between drug trans

105 We target the phosphorylation-dependent interaction between the hub pr

106 regulating S-phase entry is controlled by a phosphorylation-dependent interaction of 53BP1 and TOPBP

107 racellular signal-regulated kinase (ERK) and phosphorylation-dependent interaction of Elk-1 with co-a

108 XRCC1 and PNKP interact via a high-affinity phosphorylation-dependent interaction site in XRCC1 and

109 regulated, among other mechanisms, by Ser19-phosphorylation-dependent interaction with 14-3-3 protei

110 by multiple cellular interactions, including phosphorylation-dependent interaction with Pin1, a proli

111 -secretase to late endosomes/lysosomes via a phosphorylation-dependent interaction with the AP-1 adap

112 oA, and Cdc42, is shown to be regulated by a phosphorylation-dependent interaction with the ArfGAP PK

113 regulation of peroxisome division through a phosphorylation-dependent interaction with the fission m

114 istically, TOPBP1 recruitment is mediated by phosphorylation-dependent interactions between three of

115 Phosphorylation-dependent interactions inform a mechanis

116 In conclusion, this study demonstrates phosphorylation-dependent interactions of AQP2 with 14-3

117 Phosphorylation-dependent interactions play crucial regu

118 ti-recombinogenic functions of 53BP1 require phosphorylation-dependent interactions with PTIP and RIF

119 domain architecture, and characterized their phosphorylation-dependent interactions with Rad9 and Crb

120 ) functions in apical-basal polarity through phosphorylation-dependent interactions with several othe

121 versus Rap1B, due in part to their different phosphorylation-dependent interactions with the chaperon

122 ks with information on the directionality of phosphorylation-dependent interactions.

123 1) as an ATM (ataxia-telangiectasia mutated) phosphorylation-dependent interactor of 53BP1 and show t

124 d involved a D(1)/(5) dopamine receptor- and phosphorylation-dependent internalization of GABA(B)R an

125 n in renal epithelial cells and suggest that phosphorylation-dependent internalization of PC1 is clos

126 otein expression coordinated by specialized, phosphorylation-dependent intracellular signaling.

127 These data identify a previously unknown phosphorylation-dependent KCC2 regulatory mechanism duri

128 in the cationic pocket of an activation loop phosphorylation-dependent kinase result in constitutive

129 that CDK1 and PKC act in concert to mediate phosphorylation-dependent lamin B1 disassembly during mi

130 onreceptor protein tyrosine kinase, displays phosphorylation-dependent localization in the seminifero

131 rearrangement of microvilli on cells due to phosphorylation-dependent loss of EBP50 function.

132 hat canine peri-op AF is associated with the phosphorylation-dependent loss of TASK-1 current.

133 rve as coreceptors for the TCR in a tyrosine phosphorylation dependent manner, and some are required

134 with negatively charged lipid bilayers in a phosphorylation-dependent manner and that the lipid inte

135 ulation of centrosome functions in a Ser-732 phosphorylation-dependent manner during mitosis.

136 an activate Rad53 kinase activity in an Ies4-phosphorylation-dependent manner in the absence of known

137 associates with tomato 14-3-3 proteins in a phosphorylation-dependent manner that influences HopQ1's

138 anethiosulfonate bromide (MTSET) alters in a phosphorylation-dependent manner the activity of channel

139 amatically inhibited cell proliferation in a phosphorylation-dependent manner through inhibition of E

140 racted with type-A ARR proteins, likely in a phosphorylation-dependent manner, and recruited them to

141 mes via a newly identified LxxIxE motif in a phosphorylation-dependent manner, and this recruitment i

142 3beta to CARD9 in a stimulation-specific and phosphorylation-dependent manner, disassembling the CBM

143 lation of blood pressure, is controlled in a phosphorylation-dependent manner, including the binding

144 cible domain peptides bind terbium(III) in a phosphorylation-dependent manner, showing strong terbium

145 ely erased in early pronuclei in a protamine phosphorylation-dependent manner, suggesting that SRPK1-

146 reduce the growth of NKTL cells, in an EZH2 phosphorylation-dependent manner, whereas various compou

147 act with many of their cellular targets in a phosphorylation-dependent manner.

148 feration and epithelial cell maturation in a phosphorylation-dependent manner.

149 in a Src family kinase Fyn-mediated tyrosine phosphorylation-dependent manner.

150 -infected chicken embryonic fibroblasts in a phosphorylation-dependent manner.

151 CREB-H directly interacts with Fbw1a in a phosphorylation-dependent manner.

152 interactions with FUS and BRG1 in a p38 MAPK phosphorylation-dependent manner.

153 t also binds to and activates kinesin-1 in a phosphorylation-dependent manner.

154 NKCC2 and AnxA2 interact in a phosphorylation-dependent manner.

155 which is known to regulate YAP turnover in a phosphorylation-dependent manner.

156 tructure of the C-terminal domain of H1 in a phosphorylation-dependent manner.

157 and inhibits cap-dependent translation in a phosphorylation-dependent manner.

158 x at both its N- and C-terminal regions in a phosphorylation-dependent manner.

159 endent kinase inhibitor Sic1, in a multisite phosphorylation-dependent manner.

160 h multiple endocytic accessory proteins in a phosphorylation-dependent manner.

161 ach other and to the actin cytoskeleton in a phosphorylation-dependent manner.

162 T domains of MCPH1 (C-BRCTs) bind Cdc27 in a phosphorylation-dependent manner.

163 transcription and translation processes in a phosphorylation-dependent manner.

164 itment of different functional partners in a phosphorylation-dependent manner.

165 eurofibromatosis type 2/Merlin in a Ser(539) phosphorylation-dependent manner.

166 and enhanced its deacetylation activity in a phosphorylation-dependent manner.

167 , binds and targets PML for degradation in a phosphorylation-dependent manner.

168 s directly with an SRC-3 phospho-degron in a phosphorylation-dependent manner.

169 ated degradation in a GSK3beta-mediated KLF5 phosphorylation-dependent manner.

170 naptic AMPA receptor activity in a stargazin phosphorylation-dependent manner.

171 ma membrane to perinuclear regions in a S198 phosphorylation-dependent manner.

172 ell-type-specific AS in a concentration- and phosphorylation-dependent manner.

173 ng its nuclear-cytoplasmic localization in a phosphorylation-dependent manner.

174 luding protein tyrosine kinases (PTKs), in a phosphorylation-dependent manner.

175 a-A induces AR transactivation activity in a phosphorylation-dependent manner.

176 ificantly enhance the activity of PDE3A in a phosphorylation-dependent manner.

177 ion proteins occludin and ZO-1 in a tyrosine phosphorylation-dependent manner.

178 d SSIIa coimmunoprecipitated with SSIII in a phosphorylation-dependent manner.

179 ctile properties in a protein kinase A (PKA) phosphorylation-dependent manner.

180 rol expression of archaellum components in a phosphorylation-dependent manner.

181 ligase ubiquitinated and degraded SGT1 in a phosphorylation-dependent manner.

182 oresis to show that the AQP2 binds LIP5 in a phosphorylation-dependent manner.

183 F-box (SCF) family of ubiquitin ligases in a phosphorylation-dependent manner.

184 oligomerizes via its N-terminal domain in a phosphorylation-dependent manner.

185 othelial proliferation and angiogenesis in a phosphorylation-dependent manner.

186 del in which these enzymes modulate B12 in a phosphorylation-dependent manner.IMPORTANCE Constraints

187 hosphorylation of MAP4, thereby interrupting phosphorylation-dependent MAP4 degradation.

188 ATP hydrolysis cycle, and this is due to the phosphorylation-dependent marked decrease in the affinit

189 B1 inhibits vaccinia virus B12 protein via a phosphorylation-dependent mechanism and that this functi

190 rall, our data reveal a new Ca(2+) sensitive phosphorylation-dependent mechanism regulating Ca(v)3 ch

191 Here we report a phosphorylation-dependent mechanism that ensures timely

192 onses to DNA damage, revealing an additional phosphorylation-dependent mechanism that modulates survi

193 We identified a phosphorylation-dependent mechanism that regulates selec

194 s cell-cell fusion via an ITIM-mediated Y881 phosphorylation-dependent mechanism, supporting a unique

195 signaling, activates IRF3 through a similar phosphorylation-dependent mechanism.

196 ration can occur through an ERM-independent, phosphorylation-dependent mechanism.

197 lators of calcineurin (RCANs), through a Sra phosphorylation-dependent mechanism.

198 u directly antagonizes EB function through a phosphorylation-dependent mechanism.

199 d enzymes that are activated through similar phosphorylation-dependent mechanisms involving protein k

200 a reverse signal by either PDZ-dependent or phosphorylation-dependent mechanisms.

201 ilization of the actin cytoskeleton is a key phosphorylation-dependent mediator of the toxicity of wi

202 However as neurons become oxidative phosphorylation dependent, mitophagy is severely impaire

203 These results suggest that phosphorylation-dependent modulation of c-Myb SUMOylatio

204 sponsive cell expansion are mediated through phosphorylation-dependent modulation of ROP activity.

205 asopressin to regulate water excretion via a phosphorylation-dependent modulation of the PDZ domain-l

206 Our results establish a phosphorylation-dependent molecular mechanism that regul

207 Our data provide evidence for dynamic, phosphorylation-dependent, multisite interactions of var

208 Inhibition of phosphorylation-dependent negative-feedback pathways is

209 ls over residues (S22 and S392) that promote phosphorylation-dependent nuclear disassembly and that b

210 f transcription factor FoxO1 is regulated by phosphorylation-dependent nuclear exclusion and deacetyl

211 D1 levels are maintained at steady state by phosphorylation-dependent nuclear export and subsequent

212 , whereas PSS (12 +/- 4 dynes/cm(2)) induced phosphorylation-dependent nuclear export of class II HDA

213 Our results highlight the contribution of phosphorylation-dependent nuclear export of PER-TIM hete

214 as well as persistent focal adhesion kinase phosphorylation dependent on alphaIIbbeta3 activation.

215 GarA acts as a phosphorylation-dependent ON/OFF molecular switch.

216 Bs transduce reverse signaling in a tyrosine phosphorylation-dependent or -independent, as well as PD

217 (28) from the PA3347-FlgM complex, forming a phosphorylation-dependent partner-switching system.

218 Phosphorylation-dependent PHF8 dismissal from chromatin

219 Phosphorylation-dependent potentiation of wildtype CFTR

220 stimulus (hormone or agonist)-dependent and phosphorylation-dependent PPIs.

221 type A (vWA) domains are involved in several phosphorylation-dependent processes of multiprotein comp

222 novel form of histone H1 regulation through phosphorylation-dependent proline isomerization, which h

223 We demonstrate that the phosphorylation-dependent prolyl-isomerase Pin1 interact

224 (GSK3beta) interacts with PD-L1 and induces phosphorylation-dependent proteasome degradation of PD-L

225 hile B-Myb binding is lost when it undergoes phosphorylation-dependent, proteasome-mediated degradati

226 s on high-intensity ERK signals that trigger phosphorylation-dependent protein degradation of multipl

227 A phosphorylation-dependent protein partner switching mech

228 rm, metabolic adaptation mechanisms, such as phosphorylation-dependent protein regulation.

229 a role for Gravin as a temporal organizer of phosphorylation-dependent protein-protein interactions d

230 ol that controls contractility by modulating phosphorylation-dependent protein-protein interactions,

231 egulation of diverse biological processes by phosphorylation-dependent protein-protein interactions.

232 n codes that serve as a common mechanism for phosphorylation-dependent recruitment of arrestins by GP

233 nsable for AJ formation in vivo Nonetheless, phosphorylation-dependent recruitment of beta-Catenin is

234 Our findings uncover a signal-induced phosphorylation-dependent recruitment of OTUB1 to its ta

235 witch was identified, the basis of which was phosphorylation-dependent recruitment of the SUMO hydrol

236 We demonstrate here that phosphorylation-dependent reductions in channel activity

237 -II linker, the region of Nav1.2 crucial for phosphorylation-dependent regulation of activity.

238 y 200-residue disordered segment involved in phosphorylation-dependent regulation of channel traffick

239 We propose that phosphorylation-dependent regulation of DNA binding acti

240 ss of EZH2 K222 ubiquitination, suggesting a phosphorylation-dependent regulation of EZH2 ubiquitinat

241 We propose that phosphorylation-dependent regulation of Hts/Adducin cont

242 m for coupling intracellular Ca2+ release to phosphorylation-dependent regulation of Kv2.1 to dynamic

243 d with kinase profiling, we investigated the phosphorylation-dependent regulation of PPP holoenzymes

244 s findings represent a paradigm for tyrosine phosphorylation-dependent regulation of serine-threonine

245 xpression were accompanied by changes in the phosphorylation-dependent regulation of the key metaboli

246 We propose a model for these effects via a phosphorylation-dependent regulation of the kinetics and

247 his model has important implications for the phosphorylation-dependent regulation of the occludin:ZO-

248 ded in this motif to aspartate, suggesting a phosphorylation-dependent regulation of THIK2 traffickin

249 In addition to phosphorylation-dependent regulation of YAP, the integra

250 PP2A, and Mek-inhibitor U0126, indicative of phosphorylation-dependent regulation.

251 The eIF4E-binding protein (4E-BP) is a phosphorylation-dependent regulator of protein synthesis

252 vel function for the TFIID subunit TAF7 as a phosphorylation-dependent regulator of TAF1-catalyzed hi

253 Our results indicate a phosphorylation-dependent regulatory mechanism targeting

254 rminal transactivation domain functions as a phosphorylation-dependent regulatory switch that modulat

255 DCM-causing mutation ACTC E361G blunts this phosphorylation-dependent response without affecting oth

256 In flies, Centrosomin (Cnn) forms a phosphorylation-dependent scaffold that recruits protein

257 ntact with S. gordonii propagates a tyrosine phosphorylation-dependent signal within P. gingivalis th

258 ntial for both interrogating and redesigning phosphorylation dependent signaling pathways.

259 lpha (S413A and V415P) and conclude that PKA-phosphorylation-dependent signaling by RIM1alpha serine

260 a direct crosstalk between acetylation- and phosphorylation-dependent signaling cascades.

261 Pcdhs and Ret are functional components of a phosphorylation-dependent signaling complex.

262 Studies in cell culture suggest nephrin phosphorylation-dependent signaling events are primarily

263 ass cytometry, we measured the intracellular phosphorylation-dependent signaling events at a single-c

264 y to activate atNHE1, indicating convergent, phosphorylation-dependent signaling in atNHE1 activation

265 es of Gq/11-dependent signaling and receptor phosphorylation-dependent signaling in bronchial airway

266 host responses to infection at the level of phosphorylation-dependent signaling networks.

267 erial protein GarA is a central element of a phosphorylation-dependent signaling pathway that redirec

268 results in rapid and transient activation of phosphorylation-dependent signaling pathways that lead t

269 responses in parallel or in association with phosphorylation-dependent signaling pathways.

270 Caveolin-1 phosphorylation-dependent signaling plays a crucial role

271 The analysis of mFFA4 phosphorylation-dependent signaling was extended further

272 Our understanding of the key phosphorylation-dependent signalling pathways in the hum

273 ose a novel interplay between ubiquitin- and phosphorylation-dependent signalling, and represent the

274 Translocation to the nucleus is phosphorylation dependent since substitution of Ser-144

275 idence that Caulobacter crescentus PhyR is a phosphorylation-dependent stress regulator that function

276 This work will facilitate study of phosphorylation-dependent structure-function relationshi

277 y post-translational mechanisms that include phosphorylation-dependent subcellular localization.

278 e that promotes renal injury in part through phosphorylation-dependent suppression of pro-survival tr

279 egulation of ADAM12L induces the Akt Ser-473 phosphorylation-dependent survival pathway via stimulati

280 on, and the SH3-GK domains exhibit a Ser-561 phosphorylation-dependent switch to a closed conformatio

281 enerate, screen, align, and select potential phosphorylation-dependent Tb(3+)-sensitizing substrates

282 ed to modulate contractility via an "on-off" phosphorylation-dependent tether to myosin DeltaS2.

283 ncluded I-kappa-B kinase-alpha (CHUK), and a phosphorylation dependent transcription factor (CREB1),

284 odegron-mediated degradation and the Ser 127 phosphorylation-dependent translocation coordinately sup

285 and in LNCaP cells there is also a tyrosine phosphorylation-dependent translocation of beta-dystrogl

286 s this ubiquitination in cytosol by S13/T330 phosphorylation-dependent translocation of TRAF6 from cy

287 ting Ex to the apical membrane, Crb promotes phosphorylation-dependent ubiquitin-mediated degradation

288 activator RasGRF1 and Rap inhibitor SPAR via phosphorylation-dependent ubiquitin-proteasome degradati

289 her, this study reveals that the Akt Ser-473 phosphorylation-dependent ubiquitination and degradation

290 Phosphorylation-dependent ubiquitination and degradation

291 Phosphorylation-dependent ubiquitination and ensuing dow

292 his meiotic transition, CPEB is subjected to phosphorylation-dependent ubiquitination and partial des

293 ibitor of NF-kappaB kinase alpha), to induce phosphorylation-dependent ubiquitination and processing

294 y of proteins, some of which are involved in phosphorylation-dependent ubiquitination and/or G protei

295 Here we show that in Drosophila, a phosphorylation-dependent ubiquitination mechanism restr

296 ion and recruitment to IFNAR1 to promote the phosphorylation-dependent ubiquitination, down-regulatio

297 nthase kinase 3beta (GSK3beta) and undergoes phosphorylation-dependent ubiquitination.

298 ntial to promote granule formation through a phosphorylation-dependent unmasking of this region.

299 DAC5 nuclear export, albeit through distinct phosphorylation-dependent versus phosphorylation-indepen

300 yBP-C modulates actomyosin interactions in a phosphorylation-dependent way, but it is unclear whether