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 Moreover, changes in CheV localization are phosphorylation-dependent.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

18 inactivated by hypertrophic stimuli through phosphorylation-dependent and -independent mechanisms.

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

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

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

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

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

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

25 lex between Akt, Mdm2 and AR, which promotes phosphorylation-dependent AR ubiquitination and its degr

26 ation of other MCM proteins, suggesting that phosphorylation-dependent assembly is essential for stab

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

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

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

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

31 respectively, which oppositely regulate the phosphorylation-dependent asymmetric activity of ADF/cof

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

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

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

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

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

37 In vitro phosphorylation-dependent binding of recombinant CsrR to

38 Phosphorylation-dependent binding of the transmembrane p

39 Here, we define a phosphorylation-dependent binding site on the receptor t

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

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

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

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

44 ough post-translational mechanisms involving phosphorylation-dependent cellular localization.

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

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

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

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

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

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

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

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

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

54 Phosphorylation-dependent conversion of PrP from alpha-h

55 The phosphorylation-dependent cooperativity between Ngn2 and

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

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

58 cooperates with ER stress stimuli to mediate phosphorylation-dependent degradation of IFNAR1.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

74 ivity are predicted to contribute equally to phosphorylation-dependent enhancement of NO production d

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

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

77 The phosphorylation-dependent equilibrium between active and

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

79 RLC phosphorylation-dependent force development is regulated

80 B as a model system, we were able to observe phosphorylation-dependent FRET between fluorescent prote

81 Thus, Shc has an intrinsic phosphorylation-dependent gating mechanism where the SH2

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

83 This phosphorylation-dependent GSK3beta inhibition is mediate

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

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

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

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

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

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

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

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

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

93 Q might function as a catalytic component in phosphorylation-dependent inhibition.

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

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

96 The phosphorylation-dependent interaction between CAR and ER

97 e also extended the method to imaging of the phosphorylation-dependent interaction between Cdc25C pho

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

99 A represses collagen transcription through a phosphorylation-dependent interaction between its prolin

100 gether these data suggest that the TOC1/PRR3 phosphorylation-dependent interaction may protect TOC1 f

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

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

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

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

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

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

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

108 ible pocket to integrate ligand binding- and phosphorylation-dependent interactions and to modulate t

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

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

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

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

113 ling by the type-A ARRs most likely involves phosphorylation-dependent interactions.

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

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

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

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

118 between the molecular mechanisms regulating phosphorylation-dependent kinase activation in plant and

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

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

121 ould always be attached to a tether that has phosphorylation-dependent length regulation.

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

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

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

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

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

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

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

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

130 on 3 (STAT3) can interact with ephrinB1 in a phosphorylation-dependent manner that leads to enhanced

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

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

133 associated with CD4-beta loop chimeras in a phosphorylation-dependent manner, and that agrin increas

134 3beta to CARD9 in a stimulation-specific and phosphorylation-dependent manner, disassembling the CBM

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

164 ex (SCF(beta-TrCP)) E3 ubiquitin ligase in a phosphorylation-dependent manner.

165 ClpV1 is recruited to the T6S apparatus in a phosphorylation-dependent manner.

166 ociated with cytoplasmic dynein in a Ser-732 phosphorylation-dependent manner.

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

168 motor-cargo interactions are regulated in a phosphorylation-dependent manner.

169 which binds at the C terminus (Ser367) in a phosphorylation-dependent manner.

170 g during glaucomatous neurodegeneration in a phosphorylation-dependent manner.

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

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

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

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

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

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

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

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

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

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

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

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

183 We identified a phosphorylation-dependent mechanism that regulates selec

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

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

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

187 y sequester CRTC2 in the cytoplasm through a phosphorylation-dependent mechanism.

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

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

190 BK channel current through both Ca(2+)- and phosphorylation-dependent mechanisms in vascular smooth

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

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

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

194 synaptic membranes where they facilitate the phosphorylation dependent modulation of certain ion chan

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

196 t gating properties and lack the bulk of the phosphorylation-dependent modulation of channel gating.

197 on, voltage-dependent activation gating, and phosphorylation-dependent modulation of Kv2.1 are regula

198 action and surface expression, function, and phosphorylation-dependent modulation of Kv2.1 channels.

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

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

201 Phosphorylation-dependent modulation of the vanilloid re

202 regulation of Kv2.1 trafficking, gating, and phosphorylation-dependent modulation through cytoplasmic

203 and rescues their expression, function, and phosphorylation-dependent modulation.

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

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

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

207 D1 levels are maintained at steady state by phosphorylation-dependent nuclear export and polyubiquit

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

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

210 ctivation of protein kinase D (PKD) with the phosphorylation-dependent nuclear export of the class II

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

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

213 Mutation of R16 to A or E prevented this phosphorylation-dependent ordering.

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

215 Phosphorylation-dependent PHF8 dismissal from chromatin

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

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

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

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

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

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

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

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

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

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

226 hosphorylation sites, provided that there is phosphorylation-dependent receptor-SFK association and a

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

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

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

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

231 Ang1 halts the ability of VEGF to induce the phosphorylation-dependent redistribution of the adhesion

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

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

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

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

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

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

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

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

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

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

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

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

244 ules from invertebrate striated muscles with phosphorylation-dependent regulation showed head-head in

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

246 rther addressed that IkappaB kinase (IKK), a phosphorylation-dependent regulator of NF-kappaB, plays

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

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

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

250 s showed that axon pruning requires tyrosine phosphorylation-dependent reverse signaling and coupling

251 We demonstrate that both PDZ and phosphorylation-dependent reverse signaling by ephrin-B1

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

253 an additional tier of control over tyrosine phosphorylation-dependent signal transduction by transie

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

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

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

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

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

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

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

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

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

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

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

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

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

267 residues is a common regulatory mechanism in phosphorylation-dependent signalling cascades.

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

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

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

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

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

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

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

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

276 GTPases in podocytes, thereby preserving the phosphorylation-dependent synaptopodin-14-3-3 beta inter

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

278 lase (AC) isoforms is thought to enhance the phosphorylation dependent termination of cAMP synthesis.

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

280 seeking is associated with increases in the phosphorylation-dependent trafficking of GluR2-containin

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

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

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

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

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

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

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

288 Phosphorylation-dependent ubiquitination and degradation

289 Phosphorylation-dependent ubiquitination and ensuing dow

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

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

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

293 " element in SRC-3 that is required for this phosphorylation-dependent ubiquitination event and ident

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

295 Herein, we provide evidence that coordinated phosphorylation-dependent ubiquitination regulates SRC-3

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