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1                                              CaMKI binds MARK2 within its kinase domain, but only if
2                                              CaMKI docks within the CCTalpha membrane-binding domain
3                                              CaMKI is a Ca2+/calmodulin-dependent protein kinase that
4                                              CaMKI is found throughout the cell cytosol, including th
5                                              CaMKI is required and serves as both a PINK1 and Parkin
6                                              CaMKI-mediated phosphorylation of Ser516 in betaPIX enha
7                                              CaMKI-WT was essentially inactive in the absence of CaM
8                                              CaMKI-WT, in the absence of CaM, or CaMKI-299 and CaMKI-
9 in gene expression are mediated by the CMK-1 CaMKI enzyme, which exhibits T(c)-dependent nucleocytopl
10 ntify a gain-of-function allele of the cmk-1 CaMKI gene in C. elegans and show that loss of the regul
11 tin 1 for access to a NES, and assembly of a CaMKI-14-3-3 zeta-CCTalpha complex is a key effector mec
12    The sustained cytosolic Ca(2+) triggers a CaMKI-Fray-JNK signaling relay, leading to the transcrip
13 he CaMKs and will phosphorylate and activate CaMKI, CaMKIV, and AMP-activated protein kinase.
14 r-dependent LTP induction robustly activated CaMKI, the Ca2+-stimulated Ras activator Ras-GRF1 (Ras-g
15              To understand how CaM activates CaMKI, we have characterized the activation of the enzym
16       Co-expression of constitutively active CaMKI and IV, which do not bind to alphaKAP, interfered
17          Expression of constitutively active CaMKI induced formation of multiple axons, whereas block
18 d by transfection with constitutively active CaMKI.
19 r by transfection with constitutively active CaMKI.
20                                       Again, CaMKI and CaMKIV were different, this time in kinetics a
21    Mutation of Ile294 and Phe298 to alanine (CaMKI-2A) resulted in measurable basal enzyme activity.
22 al mutation of Ile286 and Val290 to alanine (CaMKI-4A) increased this basal activity.
23 f the enzyme by calmodulin (CaM) also allows CaMKI to be phosphorylated and activated by a second enz
24 -WT, in the absence of CaM, or CaMKI-299 and CaMKI-298 were autoinhibited and could not be phosphoryl
25 iochemical homologues of CaMKKalpha/beta and CaMKI/IV.
26 lted in a rapid inhibition of both CaMKK and CaMKI activity.
27                                    CaMKK and CaMKI form a multiprotein signaling complex with the gua
28 ata indicate an essential role for CaMKK and CaMKI to link NMDA receptor-mediated Ca2+ elevation with
29 lmodulin-dependent kinase kinase (CaMKK) and CaMKI to promote formation of spines and synapses in hip
30 , we examined the potential for [Ca2+]i- and CaMKI-dependent phosphorylation of eIF4GII in vitro and
31 gulatory loop comprised of the SIK2-PP2A and CaMKI and PME-1 networks may function in fine-tuning cel
32  The functionally antagonistic SIK2-PP2A and CaMKI and PME-1 networks thus constitute a negative feed
33  indicating that activation of autoinhibited CaMKI by CaM requires a costly energetic disruption of t
34                      The interaction between CaMKI and MARK2 was confirmed in vitro and in vivo by co
35                     CaMKKbeta activates both CaMKI and CaMKIV when coexpressed in Jurkat T cells as j
36 rotein, and examined as a substrate for both CaMKI and CaMKIV.
37 as determined by the phosphorylation of both CaMKI and AMP-activated protein kinase (AMPK), two of Ca
38 tured rat hippocampal neurons is enhanced by CaMKI-mediated phosphorylation of Ser1156 in eukaryotic
39    In vitro, CaMKK is also phosphorylated by CaMKI at the same sites as PKA, suggesting that this reg
40 ted from HEK293T cells was phosphorylated by CaMKI, in vitro as was a recombinant fragment of eIF4GII
41 cking serine 246 cannot be phosphorylated by CaMKI/IV, a similar mutant is still phosphorylated by Ca
42 transfection with constitutively active (ca) CaMKI was blocked by dnRas.
43 context, the observed similarity between CaM.CaMKI enzyme and peptide complexes is striking, indicati
44  chain kinase are also compared with the CaM.CaMKI complexes.
45  members of the CaMK cascade, such as CaMKK, CaMKI, and CaMKIV.
46 ovide a new physiological role for the CaMKK-CaMKI pathway.
47 ify a new signaling complex containing CaMKK/CaMKI/betaPIX/Rac that regulates the morphogenesis of sp
48 t of synaptic strength that depends on CaMKK/CaMKI signaling, actin dynamics, and the pattern of syna
49 ss-talk with other signaling pathways: CaMKK/CaMKI can activate the mitogen-activated protein kinase
50  that in vitro and in intact cells the CaMKK/CaMKI cascade is subject to inhibition by PKA-mediated p
51  Here we report that inhibition of cytosolic CaMKI, but not CaMKII or nuclear CaMKIV, dramatically de
52           Overexpression of kinase-deficient CaMKI, but not CaMKII, prevented cdk4 activation, mimick
53 tion experiments revealed [Ca2+]i-dependent, CaMKI site-specific, eIF4GII phosphorylation in vivo.
54                                 Two distinct CaMKI/IV kinases, CaMKKalpha and CaMKKbeta, were purifie
55  by transfection with dominant-negative (dn) CaMKI but not dnCaMKIV.
56 consistent with a requirement for endogenous CaMKI for in vivo eIF4GII phosphorylation.
57                        Our results establish CaMKI as a key regulator of the operating range for noci
58                                     Finally, CaMKI phosphorylates MARK2 on novel sites within its kin
59  increase in the CaM activation constant for CaMKI and suggests the involvement of methionine 124 in
60 aM increased the CaM activation constant for CaMKI by 10-190-fold and lowered the maximal enzyme acti
61  The kinetics of bacterially expressed human CaMKI show that the peptide syntide-2 is a relatively po
62  Ca2+/calmodulin-dependent protein kinase I (CaMKI) and the TAX-4 cyclic nucleotide-gated channel reg
63 ly activates CaM-dependent protein kinase I (CaMKI) by binding to a region in the C-terminal regulato
64 ly activates CaM-dependent protein kinase I (CaMKI) by binding to the enzyme and indirectly promotes
65  Calcium- and calmodulin-dependent kinase I (CaMKI) can regulate neurite outgrowth; however, the sign
66 tracellular infusion of active CaM-kinase I (CaMKI) into cultured hippocampal neurons enhances miniat
67  Ca2+/calmodulin-dependent protein kinase I (CaMKI) is maintained in an autoinhibited state by the in
68  Ca2+/calmodulin-dependent protein kinase I (CaMKI) is phosphorylated and activated by a protein kina
69 w that Ca(2+)/calmodulin-dependent kinase I (CaMKI) regulates thermal preferences according to past e
70     We identified a new calmodulin kinase I (CaMKI) substrate, cytidyltransferase (CCTalpha), a cruci
71 nd activates CaM-dependent protein kinase I (CaMKI) through interactions with a short sequence in its
72 a2(+)/calmodulin-dependent protein kinase I (CaMKI), an upstream kinase for phosphorylating PME-1/Ser
73 09), the upstream activator of CaM-kinase I (CaMKI), as well as by transfection with dominant-negativ
74 ownstream target Ca(2+)/calmodulin kinase I (CaMKI).
75 nt activation of Ca(2+)/calmodulin kinase-I (CaMKI), which triggers cAMP response element binding pro
76                       These results identify CaMKI as a positive transducer of growth cone motility a
77 KKalpha was robustly expressed and increased CaMKI (Thr(177/180)) phosphorylation, a known CaMKK subs
78  also determined for CaM bound to the intact CaMKI enzyme.
79 ep in cyclin D/cdk4 activation that involves CaMKI and follows complex assembly, nuclear entry, and p
80 rols the actions of a CaMK cascade involving CaMKI, CaMKIV or AMPK.
81 lmodulin-dependent protein kinases I and IV (CaMKI and CaMKIV) are closely related by primary sequenc
82 lmodulin-dependent protein kinases I and IV (CaMKI and CaMKIV, respectively) require phosphorylation
83 modulin-dependent protein kinases-I and -IV (CaMKI and CaMKIV) also induce hypertrophic responses in
84 Caenorhabditis elegans ortholog of mammalian CaMKI/IV, in thermosensory neurons in vivo.
85 tor of CaMKK, STO-609, and dominant-negative CaMKI (dnCaMKI), a downstream target of CaMKK, blocked n
86 osphorylation was blocked by kinase-negative CaMKI consistent with a requirement for endogenous CaMKI
87 y, inhibition of the CaMKKbeta-AMPK, but not CaMKI, signaling axis in prostate cancer cells by pharma
88  a position equivalent to that of Thr-177 of CaMKI, the activation loop site for regulation by CaM ki
89 drophobic interaction with tryptophan 303 of CaMKI.
90                               The ability of CaMKI, which regulates the actin cytoskeleton, to recrui
91 hosphorylation and synergistic activation of CaMKI by an exogenous kinase.
92  mitochondrial recruitment and activation of CaMKI that precedes the colocalization of PINK1/Parkin a
93 tion of the SIK2-PP2A complex, activation of CaMKI, and downstream effects, including phosphorylation
94 rization are mediated by CaMKK activation of CaMKI.
95 dnCaMI or dnCaMKK, the upstream activator of CaMKI, exhibit collapsed morphology with a prominent red
96 CaM kinase kinase, the upstream activator of CaMKI.
97 se kinase (CaMKK), the upstream activator of CaMKI.
98 pecific amino acids in the autoinhibition of CaMKI and also in its activation by CaM and phosphorylat
99 a role for this residue in autoinhibition of CaMKI.
100                      Downstream effectors of CaMKI include the MAP-kinase pathway of Ras/MEK/ERK and
101                                Expression of CaMKI and MARK2 in Neuro-2A (N2a) cells and in primary h
102 7) generated a constitutively active form of CaMKI that was also phosphorylated by CaMKK-433.
103 t activation of the unphosphorylated form of CaMKI.
104 G(1), we expressed kinase-deficient forms of CaMKI and CaMKII.
105 combinant wild-type (WT) and mutant forms of CaMKI and CaMKK.
106       CaMKK signals via the gamma-isoform of CaMKI as shRNA to CaMKIgamma, but not the other CaMKI is
107  of the membrane-associated gamma isoform of CaMKI.
108  was identified as an interacting partner of CaMKI in three independent screens.
109 ffinity complex with a 25-residue peptide of CaMKI (residues 294-318) has been determined by X-ray cr
110 ace expression as well as phosphorylation of CaMKI, AKT(T308), and mTOR.
111 re thoroughly characterize the regulation of CaMKI by CaM and its interrelationship with phosphorylat
112  important consequences in the regulation of CaMKI, CaMKIV, protein kinase B, and ERK signaling pathw
113  thermal analgesia through the regulation of CaMKI-dependent signaling.
114 corresponding to the CaM-binding sequence of CaMKI.
115 d for searching for intracellular targets of CaMKI and may have identified a new role of Ca2+ signali
116      The similarity of this motif to that of CaMKI is consistent with the 59% level of amino acid seq
117          CaMKI-WT, in the absence of CaM, or CaMKI-299 and CaMKI-298 were autoinhibited and could not
118 of multiple axons, whereas blocking CaMKK or CaMKI activity with pharmacological, dominant-negative,
119                      Suppression of CaMKK or CaMKI by pharmacological inhibitors, dominant-negative (
120 KI as shRNA to CaMKIgamma, but not the other CaMKI isoforms, inhibited axon formation.
121                          Mutation of Phe307 (CaMKI-F307A) resulted in increased basal enzyme activity
122 is regulated by Ca2+/CaM, and phosphorylates CaMKI and CaMKIV on Thr177 and Thr200, respectively.
123 phorylation of synapsin IIa on a distant PKA/CaMKI consensus site known to be essential for vesicle r
124 n lung cDNA expression library for potential CaMKI substrates by solid phase in situ phosphorylation
125                                        Since CaMKI/IV are conserved regulators of adaptable behaviors
126 aMKK) and its primary downstream substrates, CaMKI and CaMKIV.
127 ((32)P) release sequencing, established that CaMKI and CaMKIV phosphorylate completely different site
128             These data support the idea that CaMKI links mitochondrial stress with the PINK1/Parkin a
129                    Our results indicate that CaMKI-mediated changes in sensory gene expression contri
130                                          The CaMKI site, Ser(89) ((84)LLRSGSSPNL(93)), fits the expec
131       NMR spectra of CaM bound to either the CaMKI enzyme or peptide are virtually identical, indicat
132                  Upon complex formation, the CaMKI peptide adopts an alpha-helical conformation, whil
133 ow that loss of the regulatory domain of the CaMKI enzyme produces thermal analgesia and shifts the o
134            We tested the hypothesis that the CaMKI-CREB-Wnt2 signaling pathway couples NDL PCB-enhanc
135 metic for interaction of calmodulin with the CaMKI enzyme.
136 ified a requirement for CaMKK acting through CaMKI in the stimulation of ERKs upon depolarization of
137                                         Thus CaMKI vies with CRM1/exportin 1 for access to a NES, and
138 in of CaM in regulating the access of ATP to CaMKI.
139 (2+) levels in Or47b ORNs, likely leading to CaMKI-mediated activation of the histone-acetyl transfer
140 inase, Pnck, that is most closely related to CaMKI.
141                          Mutation of Trp303 (CaMKI-W303S) resulted in a large increase in the K0.5 fo
142 t that synaptic recruitment of CP-AMPARs via CaMKI may provide a mechanistic link between NMDAR activ
143 tic architecture in response to NDL PCBs via CaMKI-CREB-Wnt2 signaling in rats.
144 ulation of cap-dependent RNA translation via CaMKI activation and selective recruitment of phosphoryl
145                            Post hoc in vitro CaMKI phosphorylation assays confirm that activity promo
146                         To determine whether CaMKI substrates identified by phosphorylation screening
147 ity with CaMKKalpha and 30-40% identity with CaMKI and CaMKIV themselves.
148                    Interaction of MARK2 with CaMKI results in a novel, calcium-dependent pathway that
149 chiometry of the phosphorylation sites, with CaMKI preferring Ser(15) ((10)LLRTPSWGPF(19)) to Ser(85)

 
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