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1 C) has recently been identified as the Golgi casein kinase.
2 clear translocation of PER2 are regulated by casein kinase.
3 ity 20C (Fam20C), is the physiological Golgi casein kinase.
4 ubiquitylation were blocked by disruption of casein kinase 1 (CK1) activity, and mass spectrometry an
5 lation was reduced by specific inhibitors of casein kinase 1 (CK1) and casein kinase 2 (CK2) (10 muM
6 such as phosphorylation of clock proteins by casein kinase 1 (CK1) and glycogen synthase kinase 3 (GS
7 ligase complex upon dual phosphorylation by casein kinase 1 (CK1) and glycogen synthase kinase 3beta
8 under physiological conditions and identify Casein Kinase 1 (CK1) as an upstream effector that bidir
10 lated in vitro and in vivo by members of the casein kinase 1 (CK1) family and by glycogen synthase ki
15 at Ser680 promotes Ser683 phosphorylation by casein kinase 1 (CK1), and these phosphorylation events
17 nes; rephosphorylation by kinases, including casein kinase 1 (CK1), restores NFAT to its latent state
18 elsr1, Prickle1, FZD3, FZD7, Dvl2, Dvl3, and casein kinase 1 (CK1)-epsilon are upregulated in B lymph
26 protein stability of FOXO3A is regulated by Casein Kinase 1 alpha (CK1alpha) in an oncogenic RAS-spe
36 requires both non-canonical Wnt5a ligand and casein kinase 1 epsilon (CK1varepsilon), and that this e
38 be our isolation and characterization of the casein kinase 1 family member Hhp2 as a novel regulator
42 a multifaceted approach, we have found that casein kinase 1 gamma 1 (CK1gamma1) carries out this fun
50 ing protein (IQGAP); and three NFAT kinases, casein kinase 1, glycogen synthase kinase 3, and dual sp
51 e sensitive to pharmacological inhibition of Casein kinase 1, suggesting the possibility of shared cl
53 involves SOD1-mediated stabilization of two casein kinase 1-gamma (CK1gamma) homologs, Yck1p and Yck
54 psis (Arabidopsis thaliana) CK1 member named casein kinase 1-like 6 (CKL6) associates with cortical m
57 In this study, we determined the role of casein kinase-1 (CK1) in regulating NMDAR activity in th
63 clock, a protein complex of frequency (FRQ), casein kinase 1a (CK1a), and the FRQ-interacting RNA Hel
65 t lenalidomide induces the ubiquitination of casein kinase 1A1 (CK1alpha) by the E3 ubiquitin ligase
67 Here we report that both screens identified casein kinase 1alpha (CK1alpha) as a bifunctional regula
68 report purification and characterization of casein kinase 1alpha (CK1alpha) as a bona fide major IFN
70 iRNA kinome screen, we identify and validate casein kinase 1alpha (CK1alpha) as being responsible for
71 caused by GLIPR1-mediated redistribution of casein kinase 1alpha (CK1alpha) from the Golgi apparatus
72 demonstrate that RAS-dependent elevation of casein kinase 1alpha (CK1alpha) negatively regulates aut
73 trate that the destruction complex component casein kinase 1alpha (CK1alpha) phosphorylates Jade-1 at
75 and metastasis in vivo via downregulation of casein kinase 1alpha (CK1alpha), a suppressor of pro-met
77 nhibitor), adenomatous polyposis coli (APC), casein kinase 1alpha (CK1alpha), and glycogen synthase k
78 inc finger proteins 1 (IKZF1) and 3 (IKZF3), casein kinase 1alpha (CK1alpha), and the translation ter
79 IFN in the context of intestinal knockout of casein kinase 1alpha (CK1alpha), which controls the ubiq
81 o impacted by lenalidomide, which suppressed casein kinase 1alpha expression while augmenting glycoge
83 ion in the beta-Catenin degradation complex, Casein Kinase 1alpha mutant cells accumulate beta-Cateni
84 , we could not detect any effect of the same Casein Kinase 1alpha mutation on Hedgehog signaling.
85 mor suppressor adenomatous polyposis coli or casein kinase 1alpha uncovered new regulatory features a
88 lycogen synthase kinase-3beta (GSK3beta) and casein kinase-1alpha (CK1alpha) are multifunctional kina
89 as carried out by the combined activities of casein kinase 1delta (CK1 delta) and casein kinase 1epsi
93 Given the role of mammalian Hhp2 homologs, casein kinase 1delta and 1epsilon, in regulation of the
95 ermined whether pharmacological targeting of casein kinase 1delta and epsilon (CK1delta/epsilon), key
96 n correlated with neurite outgrowth and that casein kinase 1delta, one of the enzymes that mediate Wn
97 ithin Rec8 as well as two different kinases, casein kinase 1delta/epsilon (CK1delta/epsilon) and Dbf4
102 liver nuclei all three PERs, both CRYs, and Casein Kinase-1delta (CK1delta) are present together in
103 ties of casein kinase 1delta (CK1 delta) and casein kinase 1epsilon (CK1epsilon) and was antagonized
106 pigment aggregation signaling also involved casein kinase 1epsilon (CK1epsilon), that both enzymes w
108 earing a short-period mutation in the enzyme casein kinase 1epsilon (tau mutation), which accelerates
109 Fat-Hippo signaling requires the Drosophila Casein kinase 1epsilon encoded by discs overgrown (Dco),
110 Here, we show that fission yeast Cki3 (a casein kinase 1gamma homolog) is a critical regulator to
111 es with thapsigargin (10 mum), inhibition of casein kinase 2 (4,5,6,7-tetrabromobenzotriazole; 10 mum
112 ific inhibitors of casein kinase 1 (CK1) and casein kinase 2 (CK2) (10 muM D4476, 100 muM CK2-inhibit
118 ave identified polo-like kinase 1 (Plk1) and casein kinase 2 (CK2) as two kinases of CLIP-170 and map
120 Our previous results highlighted a role for casein kinase 2 (CK2) in the modulation of dopamine D1 r
121 iated stimulation, PTEN is phosphorylated by casein kinase 2 (CK2) in the Ser380-Thr382-Thr383 cluste
123 7 -: tetrabromobenzotriazole (TBB), a potent casein kinase 2 (CK2) inhibitor, as a strong suppressor
128 Previous in vitro studies indicated that casein kinase 2 (CK2) mediated the phosphorylation of NS
130 We demonstrated that increased activity of casein kinase 2 (CK2) observed in HPC and in MDSC could
131 w that murine caspase-9 is phosphorylated by casein kinase 2 (CK2) on a serine near the site of caspa
134 The MRE11-PIH1D1 interaction is dependent on casein kinase 2 (CK2) phosphorylation of two acidic sequ
135 The Foxc2 amino terminus has a consensus casein kinase 2 (CK2) phosphorylation site at serine 124
139 and overexpression experiments, we show that casein kinase 2 (CK2) promotes stress granule dynamics.
140 that phosphorylation of recombinant TFIIF by casein kinase 2 (CK2) reduces or eliminates some of the
141 serine residues 16 and 18, which are within casein kinase 2 (CK2) sites, and serine residue 114, whi
142 ctivated through pharmacologic inhibition of casein kinase 2 (CK2) to eradicate disease in high-risk
143 sh1 is phosphorylated by the Cka2 subunit of casein kinase 2 (CK2) to promote its E3 activity for Cse
145 ere, we report that Brg1 is also a target of casein kinase 2 (CK2), a serine/threonine kinase, in pro
146 wn previously to require the Cka2 subunit of casein kinase 2 (CK2), a ubiquitous enzyme with multiple
148 nsists of Daz interacting protein 1 (Dzip1), casein kinase 2 (CK2), and B56 containing protein phosph
149 on was dependent on XRCC1 phosphorylation by casein kinase 2 (CK2), enhancing XRCC1's interaction wit
150 on events catalyzed first by MEK and then by casein kinase 2 (CK2), followed by interaction with impo
151 e, and this phosphorylation was catalyzed by casein kinase 2 (CK2), the levels of which were dramatic
152 a striking resemblance to that of eukaryotic casein kinase 2 (CK2), which also exhibits dual nucleoti
153 d51 phosphorylation at threonine 13 (T13) by casein kinase 2 (CK2), which in turn triggers direct bin
162 minal kinase; (ii) inhibition of calpain and casein kinase 2 activity; and (iii) induction of fibrobl
165 molecular events of this modulation involved casein kinase 2 and the synaptic vesicle rapid endocytos
166 posttranslationally regulated by TNF-induced casein kinase 2 catalytic subunit (CK2alpha') phosphoryl
171 a physical interaction between S6KII and the casein kinase 2 regulatory subunit (CK2beta), suggesting
172 We now show that TFIIF phosphorylated by casein kinase 2 remains competent to support PIC assembl
178 ylation of calmodulin by protein kinase CK2 (casein kinase 2) rapidly and reversibly modulated KCNQ2
179 overed that murine Arl13b is a substrate for casein kinase 2, a contaminant in our preparation from h
181 ation of ErbB2 or loss of the betasubunit of casein kinase 2, shifted the whole population toward a f
182 uired Rab11-dependent trafficking and FAM20C/casein kinase 2-dependent C-terminal phosphorylation of
183 required for insulin induction of Sort1 in a casein kinase 2-dependent manner and that inhibition of
189 nts indicate that phosphorylation of TLE1 by casein kinase-2 (CK2) at Ser-239 and Ser-253 is necessar
192 s NMDA receptor activity by interacting with casein kinase-2 and protein phosphatases in the hypothal
193 r localization of Atx3 was not affected by a casein kinase-2 inhibitor or by mutating a predicted nuc
198 ated protein 1 (MRP1), is regulated by yeast casein kinase 2alpha (Cka1p) via phosphorylation at Ser2
199 se kinase-3beta and an increase in levels of casein kinase 2alpha, and led to increased cyclin-D1, an
200 orylation status of the downstream molecules casein kinase-2alpha and histone deacetylase 2 were sign
201 x1 regulates normal cardiac function via p27/casein kinase-2alpha/histone deacetylase 2 and indicate
202 e U.S. Food and Drug Administration-approved casein kinase activator, pyrvinium) in C57Bl/6J mice res
204 kDa enamelin that is phosphorylated by Golgi casein kinase and is thought to mediate calcium binding.
205 " with Axin, glycogen synthase kinase 3, and casein kinase, APC targets sscatenin (sscat) for phospho
206 e interacting proteins were found to contain casein kinase (CK) 2, phosphokinase (PK)C phosphorylatio
207 acidic amino acids, is regulated in vivo by casein kinase (CK) Idelta and/or CKIepsilon, but not by
209 g peptide, we established a pivotal role for casein kinase (CK)-2-mediated circadian BMAL1-Ser90 phos
210 HDAC inhibitors transcriptionally activated casein kinase (CK)2alpha expression through increased as
219 to growth signals, and in collaboration with casein kinase I (CKI), generates a phosphodegron that bi
222 dation requires phosphorylation of PHLPP1 by casein kinase I and glycogen synthase kinase 3beta (GSK-
223 r a critical requirement for the centrosomal casein kinase I delta (CKIdelta) in centrosome transloca
225 es, we show that Hrr25p, an isoform of yeast casein kinase I, phosphorylates Tif6p both in vitro and
226 ucleation pathway were identified as well as casein kinase I, which had a similar morphological RNAi
228 When HOPS is phosphorylated by the vacuolar casein kinase I, Yck3p, tethering only takes place when
230 Set8 for ubiquitination and degradation in a casein kinase I-dependent manner, which is activated by
234 (PER) proteins, which is highly dependent on casein kinase Idelta/epsilon (CKIdelta/epsilon; termed D
236 ks, including three compounds that inhibited casein kinase Iepsilon in vitro and a unique benzodiazep
237 f Drosophila Doubletime (DBT) and vertebrate casein kinase Iepsilon/delta (CKIepsilon/delta) produce
238 f the gilgamesh (gish) gene, which encodes a casein kinase Igamma homolog that is preferentially expr
239 t sites by at minimum two different kinases, casein kinase II (CK II) and tousled-like kinase (tlk).
241 ar substrates of human protein kinases (e.g. casein kinase II (CK2) and Akt), that implicated several
242 s presented here identify the protein kinase casein kinase II (CK2) as a BMP receptor type Ia (BRIa)
247 that the conserved serine/threonine kinase, casein kinase II (CK2), promotes miRISC function in Caen
248 y, Brd4 association with p53 is modulated by casein kinase II (CK2)-mediated phosphorylation of a con
249 The N-terminal phosphorylation by cellular casein kinase II (CKII) at S21, T32, and S43, and other
250 roaches, we have identified a novel role for casein kinase II (CKII) in the modification of the polym
254 s work, we show that Pah1 is a substrate for casein kinase II (CKII); its phosphorylation was time- a
256 damage in a manner dependent on TCOF1 and on casein kinase II and ATM, which are known to modify TCOF
258 this repression by directly interacting with Casein Kinase II and preventing it from activating HDAC3
260 Thr1704-sites of phosphorylation by PKA and casein kinase II at the interface between the proximal a
261 RNA designed to knock down expression of the casein kinase II beta-subunit gene family lengthens peri
265 dition, our data indicate that inhibition of casein kinase II or GSK3beta significantly reduced hnRNP
266 uniquely possess lysine residues following a casein kinase II phosphorylation motif which is critical
267 he nuclei of infected cells, indicating that casein kinase II phosphorylation of S186 occurs in the n
270 serine 72 and pharmacological inhibition of casein kinase II reduced GTPCH-1 phosphorylation and blu
271 ll three members of the protein kinase C and casein kinase II substrate in neurons (PACSIN) family an
272 ously reported that the protein kinase C and casein kinase II substrate in neurons (PACSIN) forms a c
273 his report we identify CK2 (formerly termed "casein kinase II") as the kinase responsible for phospho
274 ned the role of protein kinase CK2 (formerly casein kinase II) in increased N-methyl-d-aspartate rece
275 ng 1 (YY1) in vitro and in vivo by CK2alpha (casein kinase II), a multifunctional serine/threonine pr
276 se A/calcium calmodulin-dependent kinase II, casein kinase II, and proline-directed kinase, indicatin
277 Ser184 of Geminin could be phosphorylated by Casein kinase II, resulting in the enhanced binding to H
278 trated that Ser(10) can be phosphorylated by casein kinase II, Ser(21) can be phosphorylated by prote
286 and signaling pathways, including CaMK, PKA, Casein kinase-II, and the Raf-MEK-ERK and PI-3K-Akt path
287 RNA synthesis through the phosphorylation of casein kinase IIalpha (CK2alpha) on a threonine residue
292 or by coexpression with protein kinase C and casein kinase substrate in neurons 3 (PACSIN3), a regula
293 eletions of YCK3, encoding a vacuolar type I casein kinase; SVP26, encoding an endoplasmic reticulum
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