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1 ro, consistent with it acting primarily as a diacylglycerol kinase.
2 r and generation of a functional oligomer of diacylglycerol kinase.
3 s of the polytopic integral membrane protein diacylglycerol kinase.
4  sequence similarity to the Escherichia coli diacylglycerol kinase.
5 homotrimer of the integral membrane protein, diacylglycerol kinase.
6 aining the integral membrane protein E. coli diacylglycerol kinase.
7 lical membrane protein from Escherichia coli diacylglycerol kinase.
8              We report here that Arabidopsis diacylglycerol kinase 5 (DGK5) regulates plant pattern-t
9  flg22-induced alternative splicing variant, diacylglycerol kinase 5alpha (DGK5alpha), which differs
10 so applied to the integral membrane protein, diacylglycerol kinase A where the structures determined
11 rol, suggesting that FBGC formation involves diacylglycerol kinase activation.
12                                Cells lacking diacylglycerol kinase activity (e.g. dgk1Delta mutation)
13  work, we provide evidence that DGK1-encoded diacylglycerol kinase activity is required to convert tr
14                                Inhibition of diacylglycerol kinase activity results in the detachment
15                                              Diacylglycerol kinase activity was stimulated by major m
16 dicated by analyses of DGK1 mRNA, Dgk1p, and diacylglycerol kinase activity.
17 ctions of Dgk1p were specifically due to its diacylglycerol kinase activity.
18  the CTP transferase domain caused a loss of diacylglycerol kinase activity.
19 he CTP transferase domain was sufficient for diacylglycerol kinase activity.
20                  In this paper, we show that diacylglycerol kinase alpha (DGK-alpha), which phosphory
21                  Ritanserin, an inhibitor of diacylglycerol kinase alpha (DGKA), was identified as a
22 y probe, which displayed enhanced binding to diacylglycerol kinase alpha (DGKalpha) in the presence o
23               Here we show that depletion of diacylglycerol kinase alpha (DGKalpha), a kinase devoid
24                  The data presented point to diacylglycerol kinase alpha as a novel but selective tar
25                                              Diacylglycerol kinase alpha is an 82-kDa DGK isoform tha
26 r Aggr1 and Aggr2, respectively, include the diacylglycerol kinase alpha subunit gene (Dagk1) and the
27                                              Diacylglycerol kinases alpha and zeta (DGKalpha/zeta) ar
28  on Ras-Erk1/2 signaling and is inhibited by diacylglycerol kinases alpha and zeta.
29                                              Diacylglycerol kinase-alpha (DGK-alpha) was more highly
30 iacylglycerol kinase-epsilon (DGKepsilon) or diacylglycerol kinase-alpha (DGKalpha) knockout mice wer
31 he growth of wild type cells, indicated that diacylglycerol kinase also functions to alleviate diacyl
32  recently described radioactive method using diacylglycerol kinase and 50 times more sensitive than a
33 ogenous ceramide measured by 32P labeling by diacylglycerol kinase and a 4-fold increase in ceramide
34 ide elevations were detected concurrently by diacylglycerol kinase and electrospray tandem mass spect
35 yl caged diC(8) is biologically inert toward diacylglycerol kinase and protein kinase C in vitro and
36 ition is primarily because of the failure of diacylglycerol kinase, and are consistent with the propo
37      In contrast, GOA-1 (Goalpha) and DGK-1 (diacylglycerol kinase) appear to negatively regulate syn
38                                              Diacylglycerol kinases are important mediators of lipid
39 2019;4:420-428) identify a parasite-secreted diacylglycerol kinase as a key upstream activator of sig
40                        We identify the DGK-3 diacylglycerol kinase as a thermal memory molecule that
41 ramide were detected using the enzymatic 1,2-diacylglycerol kinase assay or the non-enzymatic o-phtha
42       Ceramide levels were quantified by the diacylglycerol kinase assay using thin-layer chromatogra
43 ceramide generation (as measured by in vitro diacylglycerol kinase assay) in LLC-PK1 cells.
44                                        Using diacylglycerol kinase assays to quantify ceramide, we fo
45          In particular, forced expression of diacylglycerol kinase beta abrogated DAG accumulation at
46  of DAG kinases or expression of an inactive diacylglycerol kinase beta mutant increased the proporti
47   Consistent with the reported activation of diacylglycerol kinase by alpha-tocopherol, the diacylgly
48                                              Diacylglycerol kinase catalyses the ATP-dependent conver
49 ids were identical in DgkB and the mammalian diacylglycerol kinase catalytic cores.
50  random equilibrium mechanism, implying that diacylglycerol kinase catalyzes direct phosphoryl transf
51 t Saccharomyces cerevisiae, the DGK1-encoded diacylglycerol kinase catalyzes the CTP-dependent phosph
52 d enzyme stalling provided evidence that the diacylglycerol kinase could desorb from these vesicles,
53                                  Prokaryotic diacylglycerol kinase (DAGK) and undecaprenol kinase (UD
54             We found here that inhibition of diacylglycerol kinase (DAGK) enzymes reduces desensitiza
55                                  Prokaryotic diacylglycerol kinase (DAGK) functions as a homotrimer o
56                 The integral membrane enzyme diacylglycerol kinase (DAGK) has long been thought to re
57                             Escherichia coli diacylglycerol kinase (DAGK) is a 13.2 kDa enzyme which
58                             Escherichia coli diacylglycerol kinase (DAGK) is a homotrimeric helical i
59 f the homotrimeric integral membrane protein diacylglycerol kinase (DAGK) is addressed.
60 ng of the trimeric integral membrane protein diacylglycerol kinase (DAGK) is documented and a method
61 due, Tyr16, of the integral membrane protein diacylglycerol kinase (DAGK) plays a critical role in th
62                             Escherichia coli diacylglycerol kinase (DAGK) represents a family of inte
63 this contribution, the catalytic activity of diacylglycerol kinase (DAGK) was measured following reco
64 lubilized membrane protein, Escherichia coli diacylglycerol kinase (DAGK), and to sustain its native
65 terface of the homotrimeric membrane protein diacylglycerol kinase (DAGK).
66 nt of cellular lipid extracts with bacterial diacylglycerol kinase (DAGK).
67                                              Diacylglycerol kinases (DagKs) are key enzymes in lipid
68 known genes are disrupted at Xp11.2, whereas diacylglycerol kinase delta (DGKD) is disrupted at 2q37.
69 t de-ubiquitination of EGFR was regulated by diacylglycerol kinase delta (DGKdelta), a lipid kinase t
70                 This pathway is regulated by diacylglycerol kinase delta (DGKdelta).
71  transcriptional activity of HIF-1alpha in a diacylglycerol kinase-dependent manner.
72 ansduction cascade rapidly increases nuclear diacylglycerol kinase (DGK) activity and PA production.
73                                              Diacylglycerol kinase (DGK) activity was important for t
74             Using the key anergy target gene diacylglycerol kinase (DGK) alpha as a focal point, we i
75 for expressing either full-length Sus scrofa diacylglycerol kinase (DGK) alpha or the catalytic domai
76                                              Diacylglycerol kinase (DGK) catalyzes the conversion of
77 mplex lipids and in intracellular signaling; diacylglycerol kinase (DGK) catalyzes the phosphorylatio
78                                              Diacylglycerol kinase (DGK) converts DG into phosphatidi
79  gating via sequential activation of PKC and diacylglycerol kinase (DGK) coupled with upregulation of
80  T cells that lacked one or both isoforms of diacylglycerol kinase (dgk) expressed highly in T cells,
81                                          The diacylglycerol kinase (DGK) family of enzymes plays crit
82                                              Diacylglycerol kinase (DGK) from Escherichia coli contai
83                The integral membrane protein diacylglycerol kinase (DGK) from Escherichia coli has be
84 active site of the trimeric membrane protein diacylglycerol kinase (DGK) from Escherichia coli.
85 nsposon was inserted into the 3' region of a diacylglycerol kinase (dgk) gene.
86                                We found that diacylglycerol kinase (DGK) inhibitor II (R59949) decrea
87              For retinal blood flow studies, diacylglycerol kinase (DGK) inhibitor R59949, at various
88                                              Diacylglycerol kinase (DGK) phosphorylates diacylglycero
89                                              Diacylglycerol kinase (DGK) plays a key role in cellular
90                                              Diacylglycerol kinase (DGK) produces PA by phosphorylati
91                                              Diacylglycerol kinase (DGK) terminates diacylglycerol (D
92       Here we report the identification of a diacylglycerol kinase (DGK) which also associates with b
93                                Inhibition of diacylglycerol kinase (DGK), an enzyme of the phosphoino
94 e we describe a solution to this problem for diacylglycerol kinase (DGK), an integral membrane protei
95 pathways generate PA: phospholipase D (PLD), diacylglycerol kinase (DGK), and lysophosphatidic acid a
96 of either phospholipase D (PLD1 and PLD2) or diacylglycerol kinase (DGK), two enzyme classes involved
97  In this study, we characterized the role of diacylglycerol kinase (DGK), which phosphorylates DAG to
98 orylation to phosphatidic acid, catalyzed by diacylglycerol kinase (DGK).
99  to phosphatidic acid, which is catalyzed by diacylglycerol kinase (DGK).
100  (PA) generated by phospholipase D (PLD) and diacylglycerol kinase (DGK).
101                                              Diacylglycerol kinase (DGK)zeta is a negative regulator
102 udy, we demonstrate that genetic deletion of diacylglycerol kinase (DGK)zeta, a negative regulator of
103 (beta2AR), the peptide transporter (PepTSt), diacylglycerol kinase (DgkA), the alginate transporter (
104                        This gene encodes the diacylglycerol kinase DGKepsilon, which is an intracellu
105                                              Diacylglycerol kinases (DGKs) attenuate diacylglycerol (
106                                              Diacylglycerol kinases (DGKs) catalyze the ATP-dependent
107                                 We show that diacylglycerol kinases (DGKs) DGK1 and DGK2 form a modul
108                                              Diacylglycerol kinases (DGKs) inhibit diacylglycerol (DA
109                                              Diacylglycerol kinases (DGKs) phosphorylate diacylglycer
110                                              Diacylglycerol kinases (DGKs) phosphorylate diacylglycer
111                                              Diacylglycerol kinases (DGKs) terminate signalling from
112      beta-Arrestins physically interact with diacylglycerol kinases (DGKs), enzymes that degrade DAG.
113 G), levels of which are tightly regulated by diacylglycerol kinases (DGKs), is a lipid mediator linke
114  metabolism in T cell anergy, we manipulated diacylglycerol kinases (DGKs), which are enzymes that te
115                                              Diacylglycerol kinases (DGKs), which negatively regulate
116 ion is regulated by enzymatic degradation by diacylglycerol kinases (DGKs).
117 activity and substrate affinity of a soluble diacylglycerol kinase, DGKtheta.
118 h include loss of the GOA-1 G(o)alpha, DGK-1 diacylglycerol kinase, EAT-16 G protein gamma subunit-li
119 Saccharomyces cerevisiae DGK1 gene encodes a diacylglycerol kinase enzyme that catalyzes the formatio
120 complement defect, some have either impaired diacylglycerol kinase epsilon (DGKepsilon) activity, cob
121                                              Diacylglycerol kinase epsilon (DGKepsilon) is a membrane
122                                        Human diacylglycerol kinase epsilon (hDGK epsilon) displays hi
123 s-of-function mutations in the gene encoding diacylglycerol kinase epsilon result in atypical hemolyt
124 ansformed fibroblasts from wild-type or from diacylglycerol kinase-epsilon (DGKepsilon) or diacylglyc
125  cases; however, mutations in the non-C gene diacylglycerol kinase-epsilon have been described recent
126                               DGKE, encoding diacylglycerol kinase-epsilon, has not been implicated i
127  genome-wide association studies have linked diacylglycerol kinase eta (DGKeta) to bipolar disorder (
128  Several lines of evidence indicate that the diacylglycerol kinase eta (DGKH) gene is implicated in t
129 The mechanism of folding of Escherichia coli diacylglycerol kinase from a partially denatured state i
130  temperature-sensitive Sec14p, expression of diacylglycerol kinase from Escherichia coli further impa
131                                   Unlike the diacylglycerol kinases from bacteria, plants, and animal
132 iation rate of the trimeric membrane enzyme, diacylglycerol kinase, from Escherichia coli as a proxy
133 this clone maps to 12q13, centromeric to the diacylglycerol kinase gene (DAGK) at 12q13.3.
134 es the expression of AtDGK7, which encodes a diacylglycerol kinase in Arabidopsis.
135         This study suggests a novel role for diacylglycerol kinase in the mechanism of macrophage fus
136 tic activity of an integral membrane enzyme, diacylglycerol kinase, in the complete absence of additi
137 ells with induced expression of DGK1-encoded diacylglycerol kinase indicated that alteration in phosp
138  peroxide was suppressed by the loss of Dgk1 diacylglycerol kinase, indicating that the underpinning
139 acylglycerol kinase by alpha-tocopherol, the diacylglycerol kinase inhibitor R59022 completely abroga
140         This conversion was sensitive to the diacylglycerol kinase inhibitor R59949 and explains the
141                   Consistent with this view, diacylglycerol kinase is identified as a key enzyme requ
142 s work, we showed that a functional level of diacylglycerol kinase is regulated by the Reb1p transcri
143                        This study shows that diacylglycerol kinase is selectively activated by ANCA a
144                            While a number of diacylglycerol kinase isoforms have been implicated in c
145 P is mostly associated with one unique mRNA: diacylglycerol kinase kappa (Dgkkappa), a master regulat
146                        Our data suggest that diacylglycerol kinases limit the extent of NADPH oxidase
147                           We thus identified diacylglycerol kinase-mediated phosphatidic acid biosynt
148                              To identify the diacylglycerol kinase mediating this effect, we knocked
149 ssay is more specific than the commonly used diacylglycerol kinase method because the ubiquitous lipi
150  to that of the widely used Escherichia coli diacylglycerol kinase method.
151                                              Diacylglycerol kinase modulates the levels of diacylglyc
152 els were reduced approximately 5-fold in the diacylglycerol kinase mutant (rdgA), but basal PLC activ
153         PhgC has a domain with similarity to diacylglycerol kinases of eukaryotes and is the first de
154 , the liver can synthesize PAs by activating diacylglycerol kinase or phospholipase D, both of which
155           Increasing or decreasing levels of diacylglycerol kinase or phospholipase D-enzymes that pr
156 atidylinositol 3-kinase, but not p38 kinase, diacylglycerol kinase, or hypoxia-inducible factor-1alph
157 dicate that the Reb1p-mediated regulation of diacylglycerol kinase plays a major role in its in vivo
158 dioctanoylphosphatidic acid by an endogenous diacylglycerol kinase present in the cell-free reaction
159 es arachidonic acid via phospholipase D2 and diacylglycerol kinase rather than phospholipase A2.
160 vity only indirectly, not by influencing the diacylglycerol kinase reaction itself.
161 lication of phorbol esters or loss of DGK-1 (diacylglycerol kinase) rescues ric-8 mutant phenotypes.
162              In this pathway, RHO-1 inhibits diacylglycerol kinase, resulting in an increase in diacy
163           However, when PI 4-kinase IIIbeta, diacylglycerol kinase, Rho, or Rho-kinase was blocked, a
164  focuses upon misfolding of a mutant form of diacylglycerol kinase (s-DAGK), a 40 kDa homotrimeric pr
165                                        While diacylglycerol kinase's kcat/Km is modest compared with
166  lipid bilayer normally plays in maintaining diacylglycerol kinase's structure and in facilitating ca
167               We show that Dgk1p is a unique diacylglycerol kinase that uses CTP, instead of ATP, to
168 lipid vesicles to partially purify a soluble diacylglycerol kinase, then studied the relation between
169                            Overexpression of diacylglycerol kinase-theta inhibited insulin signaling
170  by overexpression of phospholipase D1/D2 or diacylglycerol kinase-theta was always accompanied by di
171 , MgCl2, and ATP on the ability of a soluble diacylglycerol kinase to bind to 100-nm lipid vesicles.
172 es of the activity of the partially purified diacylglycerol kinase toward vesicle-associated diacylgl
173 tified recessive mutations in DGKE (encoding diacylglycerol kinase varepsilon) that co-segregated wit
174             Analysis of the membrane protein diacylglycerol kinase was accomplished using the combina
175 latory effects of phosphatidylserine on many diacylglycerol kinases, we examined the effects of vario
176 nd substrate specificity of Escherichia coli diacylglycerol kinase were examined.
177 ed variants of the integral membrane protein diacylglycerol kinase were measured.
178                     Loss of the DGK1-encoded diacylglycerol kinase, which converts diacylglycerol to
179                 Deletion of the DGK1-encoded diacylglycerol kinase, which counteracts PA phosphatase
180 ation product of vlmJ exhibits similarity to diacylglycerol kinases, while the translation product of
181                                              Diacylglycerol kinase z (DGKz), which phosphorylates dia
182 wild-type isocitrate dehydrogenase 1 (IDH1), diacylglycerol kinase zeta (DGKz), and p300 histone acet
183                     We demonstrate here that diacylglycerol kinase zeta (DGKzeta) interacts, via its
184 -reactive T cells deficient in the regulator diacylglycerol kinase zeta (DGKzeta) with or without PD-
185             Previous studies have shown that diacylglycerol kinase zeta (DGKzeta), which converts dia
186                                              Diacylglycerol kinase zeta (DGKzeta), which phosphorylat
187  genetic ablation of a negative regulator of diacylglycerol kinase zeta increased the suppressive abi
188 erol (DAG), and its levels are influenced by diacylglycerol kinase-zeta (DGKzeta), which metabolizes

 
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