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1 GPAT activity is known to depend upon channeling of NH(3
2 GPAT and AIRC encode enzymes for steps one and six plus
3 sition, and (3) argue against a role of sn-2-GPATs (Enzyme Commission 2.3.1.198) in membrane/storage
7 yl-CoA:glycerol-3-phosphate acyltransferase (GPAT) catalyzes the first step during de novo synthesis
11 th the glycerol-3-phosphate acyltransferase (GPAT) family, including a putative catalytic dyad locate
12 eight glycerol-3-phosphate acyltransferase (GPAT) genes that are members of a plant-specific family
13 osomal glycerol-3-phosphate acyltransferase (GPAT) increased 4-fold, liver mass of phospholipid and t
14 Four glycerol-3-phosphate acyltransferase (GPAT) isoforms, each encoded by a separate gene, catalyz
15 ndrial glycerol-3-phosphate acyltransferase (GPAT) was determined using rat liver mitochondria and mu
16 els of glycerol-3-phosphate acyltransferase (GPAT), a mitochondrial enzyme catalyzing the initial ste
17 of sn-glycerol-3-phosphate acyltransferase (GPAT), diacylglycerol acyltransferase (DGAT), and hormon
18 es [sn-glycerol-3-phosphate acyltransferase (GPAT), lysophosphatidic acid acyltransferase (LPAAT), ac
19 of sn-glycerol-3-phosphate acyltransferase (GPAT), which like MCD and ACC can be regulated by AMP-ac
20 ndrial glycerol-3-phosphate acyltransferase (GPAT)-involved in fatty acid and triacylglycerol synthes
23 rms of glycerol-3-phosphate acyltransferase (GPAT; E.C. 2.3.1.15) catalyze the committed step in glyc
24 rane-bound, eukaryotic G3P acyltransferases (GPATs) acylate the sn-1 position to produce lysophosphat
27 lysis revealed that PfGatp is a low affinity GPAT enzyme with a high specificity for C16:0 and C16:1
28 hosphoribosylpyrophosphate amidotransferase (GPAT) and glycinamide ribonucleotide synthetase (GARS) f
29 malonyl-CoA levels were reduced, and ACC and GPAT activities were diminished by 50% in muscle and liv
32 r microsomal acyltransferase enzymes such as GPAT, lysophosphatidic acid acyltransferase (LAT), or ac
33 of the endoplasmic reticulum (ER)-associated GPAT, which accounts for the majority of total GPAT acti
40 truncated nor loop-tagged enzymes conferred GPAT activity when overexpressed, suggesting that the lo
48 r oxidation of the acyl group, (2) implicate GPAT specificities as one major determinant of cutin and
51 served amino acid residues in blocks I-IV in GPAT activity through chemical modification and site-dir
53 for an endoplasmic reticulum (ER)-localized GPAT for both of these critical metabolic pathways was r
54 sults suggest that GPAT9 is the ER-localized GPAT enzyme responsible for plant membrane lipid and oil
56 milar changes in the activities of ACC, MCD, GPAT, and AMPK and the concentration of malonyl-CoA in a
59 e endoplasmic reticulum membrane (microsomal GPAT) and an NEM-resistant form in the outer mitochondri
63 s transcription of the FAS and mitochondrial GPAT genes, and glucagon antagonizes the insulin effect
64 iptional regulation of FAS and mitochondrial GPAT genes, with emphasis on elucidation of the mechanis
65 een cloned, the microsomal and mitochondrial GPAT isoforms can be distinguished, because they differ
66 lanine and histidine decreased mitochondrial GPAT activity by 90%, replacement with lysine reduced ac
67 d seven amino acid stretch for mitochondrial GPAT activity and the significance of Arg-318 for cataly
68 at Arg-318 may be critical for mitochondrial GPAT activity, whereas Arg-278 can be replaced by a basi
69 of the seven amino acids from mitochondrial GPAT, (312)IFLEGTR(318), which is highly conserved among
70 roximal promoter of the murine mitochondrial GPAT gene bound SREBP-1a and NF-Y in electromobility shi
74 nalysis of the R318K and R318A mitochondrial GPAT showed an 89 and 95%, respectively, decrease in cat
80 mido)benzoic acid (15g), possessing moderate GPAT inhibitory activity in an intact mitochondrial assa
82 MPK activator; 3) changes in the activity of GPAT and ACC paralleled that of MCD; and 4) the increase
85 ioral analysis showed that RNAi knockdown of GPAT significantly impaired the ability of females to at
92 s study, which describes the first protozoan GPAT gene, reveals an important role for the endoplasmic
95 t6-deficient mice exhibited markedly reduced GPAT activity compared with membranes from wild-type mic
97 icant increase in N-ethylmaleimide-sensitive GPAT activity, whereas acyltransferase activity toward a
98 ; however, we detected a novel NEM-sensitive GPAT activity in mitochondrial fractions and an anti-mtG
101 ment of rat liver mitochondria revealed that GPAT has a membrane-protected segment of 14 kDa that cou
104 3-phosphate and fatty acyl-CoA increased the GPAT activity, and the activity was sensitive to N-ethyl
105 ry acyl chains of lipid A are members of the GPAT family and set the stage for structural studies.
106 as co-transfected into the cells or when the GPAT promoter contained mutations in the putative bindin
112 AT, which accounts for the majority of total GPAT activity in most tissues, has remained elusive.
113 Because GPAT4 comprises 65% of the total GPAT activity in brown adipose tissue (BAT), we characte
114 des a glycerol-3-phosphate acyl transferase (GPAT) and is involved in the production of cutin monomer
120 n this work we studied the role of the yeast GPATs in the formation of LPs induced by a surplus of ol
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