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1 s a diacylated substrate and does not cleave CDP-diacylglycerol.
2 the affinity of the enzyme for its substrate CDP-diacylglycerol.
3 ynthesis of CL from phosphatidylglycerol and CDP-diacylglycerol.
4                                              CDP-diacylglycerol, a phospholipid pathway intermediate
5              Cardiolipin (A0.5 = 1.9 mol %), CDP-diacylglycerol (A0.5 = 2.6 mol %), and phosphatidyli
6 , indicating that the capacity to synthesize CDP-diacylglycerol affects gene expression.
7 s the formation of phosphatidylinositol from CDP-diacylglycerol and inositol.
8 lcholine is synthesized by the complementary CDP-diacylglycerol and Kennedy pathways.
9 e synthesis of CL from two lipid substrates, CDP-diacylglycerol and phosphatidylglycerol.
10  phosphatidylserine (PS) is synthesized from CDP-diacylglycerol and serine, a route that is different
11 ynthase catalyzes the synthesis of PG-P from CDP-diacylglycerol and sn-glycerol 3-phosphate and funct
12  membrane phospholipids and was inhibited by CDP-diacylglycerol and sphingoid bases.
13 hosphatidylglycerol, phosphatidylserine, and CDP-diacylglycerol) and inhibited by zwitterionic (phosp
14                                 Cardiolipin, CDP-diacylglycerol, and phosphatidylinositol were mixed
15    The activation constants for cardiolipin, CDP-diacylglycerol, and phosphatidylinositol were within
16             While both phosphatidic acid and CDP-diacylglycerol appeared to be activators, the most s
17 transferases, transmembrane enzymes that use CDP-diacylglycerol as donor substrate for this reaction,
18       Unlike eukaryotic Cls (that use PG and CDP-diacylglycerol as substrates) or ClsA, the combined
19 ces cerevisiae starts with the conversion of CDP-diacylglycerol (CDP-DAG) and serine to phosphatidyls
20 ytidine 5'-diphospho-1,2-diacyl-sn-glycerol (CDP-diacylglycerol; CDP-DG) is an important intermediate
21 a method that localizes membrane-bound [(3)H]CDP-diacylglycerol (DAG) produced from the precursor [(3
22 id biosynthesis, including reduced levels of CDP-diacylglycerol (DAG) synthase activity.
23 sequences of a number of enzymes involved in CDP-diacylglycerol-dependent phosphatidyltransfer identi
24 hase (CDS), which catalyzes the formation of CDP-diacylglycerol from phosphatidic acid, is a key regu
25 hase (CDS), which catalyzes the formation of CDP-diacylglycerol from phosphatidic acid, is a key regu
26 e for the conversion of phosphatidic acid to CDP-diacylglycerol in phospholipid biosynthesis.
27                                 Radiolabeled CDP-diacylglycerol is unavailable commercially.
28 he CHO1-encoded phosphatidylserine synthase (CDP-diacylglycerol:l-serine O-phosphatidyltransferase, E
29    Enzyme activation by cardiolipin (n=2.8), CDP-diacylglycerol (n=2.1), and phosphatidylinositol (n=
30 e purified Cho1 has a K(m) for its substrate CDP-diacylglycerol of 72.20 muM with a V(max) of 0.079 n
31 portional increase in the cellular levels of CDP-diacylglycerol or phosphatidylinositol.
32 he CHO1-encoded phosphatidylserine synthase (CDP-diacylglycerol pathway enzyme) and loss of the zinc-
33 idylcholine is balanced by the repression of CDP-diacylglycerol pathway enzymes and the induction of
34  in a decrease in the activity levels of the CDP-diacylglycerol pathway enzymes phosphatidylserine sy
35 elated with increased activity levels of the CDP-diacylglycerol pathway enzymes phosphatidylserine sy
36 the synthesis of major phospholipids via the CDP-diacylglycerol pathway.
37 tion of phosphatidylcholine synthesis by the CDP-diacylglycerol pathway.
38 thanolamine, and phosphatidylcholine via the CDP-diacylglycerol pathway.
39                                   The enzyme CDP-diacylglycerol:sn-glycerol-3-phosphate 3-phosphatidy
40  A photoreceptor-specific form of the enzyme CDP-diacylglycerol synthase (CDS), which catalyzes the f
41  A photoreceptor-specific form of the enzyme CDP-diacylglycerol synthase (CDS), which catalyzes the f
42 aled reduced expression of the gene encoding CDP-diacylglycerol synthase 1 (Cds1), an enzyme that cat
43 s a genetic dependency in the context of low CDP-diacylglycerol synthase 1 gene (CDS1) expression.
44 ial cells in vitro, we show ECs deficient in CDP-diacylglycerol synthase 2 are uniquely sensitive to
45  gene pairs, we identified and validated the CDP-diacylglycerol synthase 2 gene (CDS2) as a genetic d
46 C59-encoded dolichol kinase and CDS1-encoded CDP-diacylglycerol synthase enzymes.
47 nsduction genes as a model system, two human CDP-diacylglycerol synthase genes (CDS1 and CDS2) were c
48 ling, rdgB (retinal degeneration B) and cds (CDP-diacylglycerol synthase).
49 y also caused increases in the activities of CDP-diacylglycerol synthase, phosphatidylserine decarbox
50  and 37% amino acid sequence identities with CDP-diacylglycerol synthases reported from Escherichia c
51                                 In contrast, CDP-diacylglycerol synthases that provide PIS with its s
52 s report, we demonstrate the central role of CDP-diacylglycerol synthetase (CDS) in the regulation of
53                                        Human CDP-diacylglycerol synthetase (cds1) and phosphatidylino
54 s, a cDNA predicted to encode a second human CDP-diacylglycerol synthetase (cds2) was also uncovered
55 e including DKs, phytol kinases, and several CDP-diacylglycerol synthetases has been identified, and
56 cterium salmoninarum, with and without bound CDP-diacylglycerol to 3.6 and 2.5 A resolution, respecti