ライフサイエンスコーパス: serine residue

1 ted following phosphorylation at a conserved serine residue.

2 tly phosphorylates SRF on a highly conserved serine residue.

3 e and perturbs the position of the catalytic serine residue.

4 ch is controlled by an N-terminal regulatory serine residue.

5 s a G-to-S change at the predicted catalytic serine residue.

6 is primed by the phosphorylation of a single serine residue.

7 , Cdc8, is regulated by phosphorylation of a serine residue.

8 s partially rescued by removing the adjacent serine residue.

9 ced the highly conserved cysteine 107 with a serine residue.

10 n responded to modification of even a single serine residue.

11 oteins, and (iii) phosphorylation of various serine residues.

12 ciated with dephosphorylation of the Ntcp on serine residues.

13 of three hydrophobic amino acids flanked by serine residues.

14 mapping and mutating the key O-GlcNAcylated serine residues.

15 ons, including modification of glutamine and serine residues.

16 -acetylglucosamine (O-GlcNAc) also occurs on serine residues.

17 cted kinase that phosphorylates cyclin L2 at serine residues.

18 inase 1 (Clk1) phosphorylates SPF45 on eight serine residues.

19 ymes through nonenzymatic acetylation of key serine residues.

20 rane binding and phosphorylation at specific serine residues.

21 step formal cycloaddition between two distal serine residues.

22 elium SCAR is basally phosphorylated at four serine residues.

23 effects based on phosphorylation at specific serine residues.

24 CaMKK2 by phosphorylation of three conserved serine residues.

25 hosphorylation switch of adjacent lysine and serine residues.

26 ic peptide containing N-terminal alanine and serine residues.

27 tion has to precede phosphorylation of other serine residues.

28 that it is phosphorylated mainly on multiple serine residues.

29 directly interacting with its two canonical serine residues.

30 the change of phosphorylation state of other serine residues.

31 function of each of these two phosphorylated serine residues.

32 Here we identify serine residue 1166 (Ser1166) in the carboxy-terminal ta

33 ion of the Na-K-2Cl cotransporter (NKCC2) at serine residue 126 (pS126 NKCC2) and of the Na-Cl cotran

34 Here we report that phosphorylation of serine residues 17 and 24 flanking the Bnip3 LIR promote

35 that constitutively active IKKbeta in which serine residues 177/181 were mutated into negatively cha

36 We discovered that dual serine (traditional serine residues 177/181) and tyrosine (188/199) phosphor

37 PKC-dependent NMDAR insertion, and identify serine residue-187 as the molecular target of PKC phosph

38 ndividually contained one of six cysteine-to-serine (residues 193, 197, 209, 211, 214, and 218) subst

39 Mass spectrometry shows that serine residues 2 and 5 of the pol II C-terminal domain

40 CK2 phosphorylated 14-3-3gamma at serine residue 235 and Dok-7 at several serine residues

41 o 2.8-fold increased phosphorylation of Cx43 serine residues 255, 262, 279/282, and 368, and appeared

42 ion with MEF2s in nuclear speckles requiring serine residues 259 and 498, whose phosphorylations cont

43 RK1A can specifically phosphorylate LIN52 on serine residue 28, and that this phosphorylation is requ

44 somal neural-derived IRS-1 phosphorylated at serine residue 307 (corresponding to serine residue 312

45 ated at serine residue 307 (corresponding to serine residue 312 in humans) negatively correlated with

46 sulin receptor substrate-1 phosphorylated at serine residue 312 in neurons and oligodendrocytes in th

47 ceptor substrate 1 (IRS-1) phosphorylated at serine residue 312 was more apparent in inclusion bearin

48 MST4 phosphorylates ATG4B at serine residue 383, which stimulates ATG4B activity and

49 CDK5 phosphorylated PER2 at serine residue 394 (S394) in a diurnal fashion.

50 ABAARs is potentiated via phosphorylation of serine residues 408 and 409 (S408/9) in the beta3 subuni

51 tion, the beta3 subunit is phosphorylated on serine residues 408/409 by PKC activity, whereas the del

52 Furthermore, phosphorylation of TDP-43 at serine residues 409/410 drives mutant TDP-43 toxicity.

53 site-directed mutagenesis, which identified serine residues 421 and 423 as critical for its nuclear

54 GSK3beta was found to interact with ST2L on serine residue 446 in response to IL-33 treatment.

55 phate 5-kinase type-l gamma (PIP5Klgamma) at serine residue 448.

56 that O-GlcNAc transferase (OGT) modified CTD serine residues 5 and 7.

57 RP1 and PARP2 from aspartate or glutamate to serine residues(5-10).

58 y catalyzing the dephosphorylation of PDE4D3 serine residue 54.

59 tivate SP-1 through dephosphorylation at its serine residue 59.

60 Serine residues 6 and/or 533, potential kinase target si

61 ational modification occurs predominantly on serine residues(6-8) and requires HPF1, an accessory fac

62 d decreased levels of DRP1 phosphorylated at serine residue 616 (P-DRP1(S616)), a post-translational

63 on cascade that modulates phosphorylation of serine residue 863 (S863) in the GluA1 AMPAR subunit and

64 Allodynia suppression was a consequence of serine residue 896/897 phosphorylation of NMDA receptor

65 els purified from brain is phosphorylated on serine residues 9 and 31, and that cyclin-dependent kina

66 intracellular inhibitor of PP2A (I2PP2A) on serine residues 9 and 93, resulting in enhanced binding

67 We conclude that serine residue 96 of human KCC3 is a third site that has

68 er, our data suggest that phosphorylation of serine residues adjacent to the PIAS1 SUMO-interacting m

69 O-palmitoylation of a threonine or serine residue, along with a characteristic and highly c

70 ht chain last amino acid, which was either a serine residue, an alanine residue or deleted.

71 tly phosphorylated mTOR and RAPTOR on unique serine residues, an effect that was independent of insul

72 ate that Scute is phosphorylated by Sgg on a serine residue and that mutation of this residue results

73 d an ester bond formed between a thermolysin serine residue and the A2ML1 thiol ester.

74 diversity, consisting mostly of tyrosine and serine residues and a small but significant contribution

75 ion, we induced a mutation in the C-terminal serine residues and examined their effects on the intera

76 minal domain of DGLalpha, phosphorylated two serine residues and inhibited DGLalpha activity.

77 sues, is phosphorylated on more than a dozen serine residues and interacts with a variety of protein

78 horylation of NRF1 can occur at two distinct serine residues and negatively regulates NRF1 DNA bindin

79 (AICAR) resulted in STIM1 phosphorylation on serine residues and prevented protease-activated recepto

80 structural changes due to phosphorylation of serine residues and shown a correlation between the CTD

81 erichia coli was phosphorylated by CKII on a serine residue, and its phosphorylation was dependent on

82 -unsaturated fatty acyl group at a conserved serine residue, and this modification is required for Wn

83 y, induced IRS-1 phosphorylation at multiple serine residues, and inhibited physiological IRS-1pTyr i

84 Occasionally, serine residues are also incorporated into the cross-bri

85 otably, these two clusters of closely spaced serine residues are located in disordered domains flanki

86 The modified serine residues are located in the phospho-tyrosine bind

87 A serine residue at P3 was required for the stable binding

88 On the other hand, a serine residue at position 105, which is a known target

89 signature depends on phosphorylation of the serine residue at position 273 of PPARgamma, in striking

90 tudies have shown that cannabinoids target a serine residue at position 296 in the third transmembran

91 smic tail of rat ADAM17 contains a conserved serine residue at position 811, which resides in a canon

92 AOX1A carrying a serine residue at position CysI was activated by succina

93 ed that the phosphate moiety attached to the serine residue at position P5 of pMART-1 is available fo

94 f-function" mutation [a leucine mutated to a serine residue at the 9' position (Leu9'Ser)] in VTA GAB

95 or tryptophan residue in Env with a natural serine residue at this position (S375H/W) increased the

96 o Uniprot entry P50286 (WoA-S121) that has a serine residue at this position.

97 ur findings show enhanced phosphorylation of serine residues at amino acid positions 15 and 46 in the

98 quent mutagenesis analysis demonstrated that serine residues at amino acids 225 and 232 in NS5A (geno

99 ion in cells leads to phosphorylation of two serine residues at analogous sites on both SH2 domains o

100 FmhA incorporates serine residues at positions 3 and 5 of the cross-bridge

101 o restrict MLV/GaLV Env, but mutation of the serine residues at positions 52 and 56 completely allevi

102 pha-helices have an L-shape, with proline or serine residues at the kinks, which functions as a lever

103 Mutating these serine residues attenuates the ability of Smo to transdu

104 ers with a phosphorylation pocket flanked by serine residues between their N-terminal domains.

105 sphorylate TC21 and R-Ras on this C-terminal serine residue both in vitro and in vivo.

106 a at serine residue 235 and Dok-7 at several serine residues but does not phosphorylate Rapsyn or Rac

107 Finally, only the addition of 10 serine residues (but not 2 or 4) between the extracellul

108 defined, conserved N-terminal threonine and serine residues, but the kinase pathways that mediate th

109 c intermediate as well as phosphorylation of serine residues by protein kinase D (PKD).

110 vation, we mutated cysteine 203 of CypD to a serine residue (C203S) and determined its effect on mPTP

111 n article, we show that five, and only five, serine residues can be phosphorylated both in vitro and

112 sidue plays a role in activating an adjacent serine residue carrying out nucleophilic attack, opening

113 y ERK-mediated phosphorylation of ERG at one serine residue causes a conformational change that allow

114 assays showed that Cdc5 phosphorylates nine serine residues clustered within the N-terminus of Cse4.

115 osophospecific antibody, and substitution of serine residues demonstrate phosphorylation of candidate

116 dehydratases such as aconitase, which use a serine residue deprotonated by an oxyanion hole.

117 the observation that mutation of Cys475 to a serine residue eliminates the formation of the protein a

118 cytosolic S4-S5 linker of both proteins by a serine residue forces the channels into an open conforma

119 -R353A, but not FXII lacking the active site serine residue (FXII-S544A), shortened the clotting time

120 Conversely, the replacement of His 375 by a serine residue (H375S) within HIV-1 CRF01_AE decreased t

121 In contrast, this mutant at serine residues had no demonstrable impact on apelin-13-

122 Although mutating these serine residues had no effect on binding between ORF59 a

123 ough its serine-rich domain in which most of serine residues have the propensity to be phosphorylated

124 duced by phosphorylation of highly conserved serine residues (human S183/S185, mouse S180) in the DNA

125 lation analysis of Pah1, we identified eight serine residues (i.e. Ser-114, Ser-475, Ser-511, Ser-602

126 Two serine residues, i.e. serine 362 and serine 604, were id

127 The serine residues identified here provide a genetic tool f

128 n I; group B, comprising mutations affecting serine residues important for hyperphosphorylation and a

129 ime, the occurrence of O-xylosylation at the serine residue in (G4S)n>2 linkers.

130 sporter EAAT2, and we identified a conserved serine residue in Flot1 that is essential for transporte

131 The cysteine residue is followed by a serine residue in IgG1lambda.

132 In addition, a modification to an adjacent serine residue in Rab1 was discovered, which was indepen

133 nRK2.6-mediated phosphorylation of a defined serine residue in SNACS.

134 Mutation of an additional serine residue in the active site causes the enzyme to b

135 iety as the warhead to react with the active serine residue in the active site of SBLs.

136 (APC/C); while phosphorylation of a specific serine residue in the APC/C coactivator Cdc20 prevents d

137 ntered on two hydrogen bonds with a specific serine residue in the bound peptide.

138 nthesis by transfer of its acetyl group to a serine residue in the cyclooxygenase (COX) active site.

139 Here, we show that a conserved serine residue in the Golgi GDP-fucose transporter (GFR)

140 Phosphorylation at a conserved serine residue in the KXGS motif in PSD-95 regulates spi

141 d the consequences of changing the conserved serine residue in the P-loop to asparagine, within a chi

142 mline mutation (S631G) at a highly conserved serine residue in the uncharacterized gene VSIG10L that

143 he enzyme is regulated by phosphorylation of serine residues in a regulatory domain and by binding of

144 s inhibited by phosphorylation of up to four serine residues in a repeating sequence in the C-termina

145 ly at Ser12, indicating that the pore-facing serine residues in BM2 mediate proton relay to the proto

146 equires phosphorylation at three clusters of Serine residues in Drosophila Hedgehog (Hh) signaling.

147 nM, can covalently transacylate arginine and serine residues in GSTP and cross-link them to adjacent

148 ened interactions between formoterol and two serine residues in H5 at the orthosteric binding site of

149 a signature 25-residue insert of glycine and serine residues in loop L11 of its motor domain, and thi

150 Mutation of the two C-terminal serine residues in MKP-1 and MKP-2 to alanine decreased

151 oselective, and modular functionalization of serine residues in native polypeptides, which uses a rea

152 t AvrPtoB phosphorylation occurs at multiple serine residues in planta, with S258 phosphorylation sig

153 entially phosphorylated at three clusters of serine residues in response to levels of Hh activity.

154 We identified the serine residues in Smo that can be phosphorylated by CK2

155 and E2 enzymes, SidE effectors ubiquitylate serine residues in substrates via an ADP-ribosylated ubi

156 vered a new form of ADPr that is attached to serine residues in target proteins (Ser-ADPr) and showed

157 sphorylation of PKD1 at two highly conserved serine residues in the activation loop; this modificatio

158 trometry, we first identified phosphorylated serine residues in the C terminus of APJ.

159 dy revealed extensive phosphorylation of two serine residues in the C terminus of both MKP-1 and MKP-

160 s spectrometry analysis, we identified three serine residues in the CCE domain of CRY2 (S588, S599, a

161 ificantly enhanced by phosphorylation of key serine residues in the IRF6 C-terminus.

162 ed a mutational analysis of highly conserved serine residues in the linker region between domains I a

163 Many prior papers have pinpointed several serine residues in the low complexity sequence I region

164 fy HDAC1 and the phosphorylation of specific serine residues in the molecule as potential targets for

165 sence of ROS and phosphorylation of critical serine residues in the N17 region.

166 -kinase-C-dependent phosphorylation of three serine residues in the receptor carboxy terminus.

167 thway responsible for the phosphorylation of serine residues in the Ser-x-Glu/pSer motifs in several

168 However, the role of these serine residues in tolerance and dependence for cannabin

169 PKA preferentially targeted two serine residues in TOMM34: Ser(93) and Ser(160), located

170 s can form hydrogen bonds with two conserved serine residues in transmembrane helix 5 (Ser(5.42) and

171 function mutations at either of two adjacent serine residues in TSC2 (S1365 and S1366 in mice; S1364

172 Serine residues in UbL are phosphorylated and influence

173 Two serine residues in Yorkie, S74 and S97, are Atg1/ULK1 co

174 hway, which phosphorylates Runx2 on multiple serine residues including S301 and S319 (equivalent to S

175 vates PDC by phosphorylating PDH at specific serine residues, including Ser-293, whereas dephosphoryl

176 t study of phosphorylated and phosphomimetic serine residues indicating lowered single motor stalling

177 and also SrtB from Staphylococcus aureus The serine residue indispensable for SrtB activity may be in

178 f Dazl by MK2 on an evolutionarily conserved serine residue inhibits its interaction with poly(A)-bin

179 LGST motif from bacteria to humans, only the serine residue is absolutely required for Psd1p autocata

180 reased enzymatic activity, suggesting that a serine residue is critical at that location.

181 osphorylation of kinesin motor domain at the serine residue is implicated in Huntington's disease, wi

182 the nitrogen atom of an internal cysteine or serine residue is usually cleaved by the side chain -SH

183 thermore, the presence of the phosphorylated serine residues is demonstrated to have a shielding effe

184 ation of cMyBP-C's N terminus on 3 conserved serine residues is hierarchical and antagonizes phosphor

185 n of the viral nonstructural protein NS5A at serine residues is important for the efficient assembly

186 occurs when Cdr1 phosphorylates a cluster of serine residues linking alpha-helices G and H of the Wee

187 ing PKCbeta phosphorylation of TFEB on three serine residues located in its last 15 amino acids.

188 d ERK4 are activated by phosphorylation of a serine residue lying within the activation loop signatur

189 initiation factor eIF2 alpha at a conserved serine residue mediates translational control at the ISR

190 e report the first evidence that a conserved serine residue near the active site participates in the

191 Cleavage at a serine residue near the C terminus was a major reaction

192 osphorylation at an evolutionarily conserved serine residue near the carboxyl terminus (Ser-883 in Xe

193 ndergoing inhibition by phosphorylation of a serine residue near the N terminus.

194 kt, the enzyme multi-phosphorylated a single serine residue of a diserine DCF substrate in a time-dep

195 established that transesterification of the serine residue of desmethylsalinamide E with acylated gl

196 A, that catalyzes the conjugation of Ub to a serine residue of target proteins via a phosphoribosyl l

197 We show that replacing catalytic cysteine or serine residues of enzymes with DAP permits their first-

198 l activation requires phosphorylation of two serine residues of INCENP that are conserved through evo

199 Several serine residues of IRBIT are thought to be important for

200 We recently specified three serine residues of NIPA and demonstrated a sequential ph

201 subsequent en bloc transfer of the glycan to serine residues of select periplasmic proteins.

202 rthermore, we show that SRPK1 phosphorylates serine residues of SR/RS dipeptides in the hinge region

203 ets RNA polymerase II but also the conserved serine residues of the polylinker region in Smad3, sugge

204 the N-terminal structure suggested that the serine residue (of CSQCH) would be anchored where the fi

205 The effect of the serine residue on disulfide bond susceptibility was comp

206 A serine residue on the DIV S2 helix was found to be suffi

207 Threonine and serine residues on Notch1 are functionalized with O-fuco

208 sphorylation by protein kinase A of specific serine residues on Rad decreases its affinity for beta s

209 s studies have shown that phosphorylation of serine residues on synaptic proteins is a major regulato

210 by GCK-3 kinase-mediated phosphorylation of serine residues on the cytoplasmic C-terminus linker con

211 l six cysteines were individually altered to serine residues, only C145S and C195S derivatives lost t

212 th this prediction, phosphorylation at these serine residues or mutation to aspartate inhibits bindin

213 )KVTF(901), and can dephosphorylate multiple serine residues phosphorylated by checkpoint kinases.

214 Mutations of cyclin L2 at serine residues preceding proline significantly stabiliz

215 pathway in human cells; additionally, as the serine residue promoting thermal lability is conserved a

216 erential phosphorylation of SPL tyrosine and serine residues provides a key to understanding both.

217 ations of cysteine, tyrosine, histidine, and serine residues react with octafluorocyclopentene (OFCP)

218 ing with the dockerin's critically conserved serine residues reduced the observed rupture forces.

219 Replacement of the Asp f3 cysteines with serine residues retained its dimeric structure, but dimi

220 We show that Noxa is phosphorylated on a serine residue (S(13)) in the presence of glucose.

221 in activation, we demonstrated a key role of serine residue S1163 of the alphaE chain intracellular d

222 his study, we show that phosphorylation of a serine residue (S165) within the groove of influenza A v

223 ere we show that phosphorylation of a single serine residue (S2844) in the sarcoplasmic reticulum (SR

224 es phosphorylated on at least one regulatory serine residue (S320).

225 f the STEVOR C-terminal domain at a specific serine residue (S324).

226 hypophosphorylation of Cx43 at a triplet of serine residues (S325/S328/S330) in the regulatory C-ter

227 Two neighboring serine residues, S349 and S351, are required for the ace

228 s desensitized by GRK phosphorylation at two serine residues (S426 and S430).

229 wever, RelA phosphorylation, particularly at serine residues S536 and S276, is critical for RelA func

230 lysine substrate, also involving two nearby serine residues - S566 and S527- that possess a proton r

231 ing that phosphorylation of GluA1 C-terminal serine residues S831 and S845 is not required for CaN in

232 n addition, APE2 associates with Chk1, and a serine residue (S86) in the Chk1-binding motif of APE2 i

233 tor domain by the kinase JNK3 at a conserved serine residue (Ser-175 in the B isoform and Ser-176 in

234 ntaining an aspartic acid substitution for a serine residue (Ser-189) that in GRASP65 is phosphorylat

235 NAD(+) (the oxidized form of NADH), on three serine residues (Ser(44), Ser(46), and Ser(48)) within a

236 ction, MAPK phosphorylation of the preceding serine residues (Ser(P)(279)and Ser(P)(282)) increases t

237 rylation, the phosphorylation of a conserved serine residue, Ser(779), can quantitatively control Ras

238 is regulated by phosphorylation at a single serine residue, Ser-177.

239 terized several mutants of the corresponding serine residue, Ser-364, of human glutamate transporter

240 that allows ERK phosphorylation at a second serine residue, Ser-96.

241 hat PKD1 directly phosphorylates VASP at two serine residues, Ser-157 and Ser-322.

242 ed out in Pcyt2beta and on two PKC consensus serine residues, Ser-215 and Ser-223.

243 at CK2 directly phosphorylates Dzip1 at four serine residues, Ser-664/665/706/714.

244 imuli promote Hsp27 phosphorylation on three serine residues--Ser(15), Ser(78), and Ser(82)-by a numb

245 f the MIA group from NosJ-MIA to a conserved serine residue (Ser102) on NosK.

246 s containing HSP27 mutated at three critical serine residues (Ser15, Ser78, and Ser82) to either alan

247 we investigated the roles of three conserved serine residues [Ser198(5.42), Ser199(5.43), and Ser202(

248 s from the hearts of mice in which the three serine residues (Ser273, Ser282, and Ser302) that are ph

249 The amino terminus of H3.3 contains a unique serine residue (Ser31) that is absent in 'canonical' H3.

250 implicate the phosphorylation of a specific serine residue (Ser322) on the synaptic protein UNC-18 a

251 bits increased phosphorylation of a critical serine residue (Ser354) and higher protein expression as

252 CD4 (programmed cell death protein 4) on two serine residues (Ser76 and Ser457) that regulate its sub

253 ependent phosphorylation of Hof1 at a single serine residue (serine 313) in this region diminishes th

254 Here we show that PKC phosphorylates a serine residue situated within a phospholipid binding mo

255 as determined to predominantly phosphorylate serine residues, specifically serine-18 in OLE3.

256 as been measured biochemically at C-terminal serine residues, suggesting that these residues are crit

257 tamine followed by a stretch of threonine or serine residues, suggesting the presence of structural r

258 that a stretch of consecutive threonine and serine residues, T(21) T(22) S(23) S(24,) is necessary f

259 t inhibition of p65 phosphorylation on these serine residues targets NF-kappaB activity to distinctiv

260 contains the C-terminal ITIM tyrosine and a serine residue that undergo activation-dependent phospho

261 This region contains eight serine residues that are highly conserved among HCV isol

262 egion on which lie two functionally critical serine residues that are phosphorylated during infection

263 gion of alpha7 contains an acidic patch with serine residues that are phosphorylated.

264 issociation is prevented by mutation of four serine residues that are potential sites of phosphorylat

265 on of the B55alpha subunit itself on several serine residues that drastically increases the affinity

266 Mass spectrometry identified two unique serine residues that were phosphorylated by Plk3.

267 ter mutation of the putative phosphoacceptor serine residues, the localization of the E2 protein was

268 nes through phosphorylation of different p65 serine residues, thus shedding light on novel mechanisms

269 of RdmB and show that insertion of a single serine residue to DnrK is sufficient for introduction of

270 sphorylates PYL ABA receptors at a conserved serine residue to prevent activation of the stress respo

271 he transcription factor Gata6 on a conserved serine residue to promote neural crest migration and pro

272 ally phosphorylated on specific tyrosine and serine residues to acquire full transcriptional activity

273 rom homology modeling, mutation of three TM5 serine residues to alanine (S5.42A, S5.43A, S5.46A) had

274 Mutation of these serine residues to alanine (S617A and S1179A) inhibited

275 ggest new strategies to target distinct AQP2 serine residues to induce membrane expression of this wa

276 ctivation, acting through N-terminal phospho-serine residues to regulate GR recruitment to its target

277 in HP1alpha molecules and show that specific serine residues uniquely contribute to gel formation.

278 rylation patterns across the four implicated serine residues was observed.

279 sphate precipitate core of LCP, two phosphor-serine residues were added to the N-terminal of the pept

280 enotype 1b Con1 NS5A, we found that specific serine residues were important for efficient hyperphosph

281 interact with CaWRKY40 when the relevant two serine residues were replaced by alanine.

282 re, E4orf4 reduces PARP-1 phosphorylation on serine residues, which likely contributes to PARP-1 inhi

283 s known to phosphorylate PDX-1 on C-terminal serine residues, which triggers PDX-1 proteasomal degrad

284 C-terminal domain of p53 through two unique serine residues, which were acquired during recent verte

285 e specifically phosphorylates the C-terminal serine residue while ignoring those located elsewhere.

286 Replacement of these serine residues with acidic residues, to mimic phosphory

287 sitides but undergoes phosphorylation on the serine residue within a CaMKII target motif.

288 a PXXYHXXHXP motif, and a uniquely conserved serine residue within a GS(S/T) motif, suggesting that P

289 , by phosphorylating a specific threonine or serine residue within the activation loop which is criti

290 We identified a conserved serine residue within the C terminus of CBLs as being ph

291 region (S4-S6) of TRPC4 predicts a conserved serine residue within the C-terminal sequence of the pre

292 nase A-dependent phosphorylation of a single serine residue within the core of the polybasic domain,

293 We showed that mutations in the serine residues within and outside the serine cluster di

294 MA promotes PKC-dependent phosphorylation of serine residues within CXCR4 C-tail that are required fo

295 Autophosphorylation of serine residues within TbetaRII is considered the princi

296 In both cases, in vitro phosphorylation of serine residues within the acidic tail stabilizes the as

297 Unexpectedly, mutation of serine residues within the activation segment of PINK1 u

298 forming a complex that dephosphorylates two serine residues within the catalytic domains of IkappaB

299 cultured cells, phosphorylation of specific serine residues within the cluster is also required for

300 stem enables us to map the O-linkages to the serine residues within the first SRR of PsrP.