戻る
「早戻しボタン」を押すと検索画面に戻ります。 [閉じる]

コーパス検索結果 (１語後でソート)

通し番号をクリックするとPubMedの該当ページを表示します
1 ts on the activity of coenzyme A-independent transacylase.
2 of the other KAS isozymes to malonyl-CoA:ACP transacylase.
3  an effective medium chain length fatty acyl transacylase.
4 tive malonyl coenzyme A-acyl carrier protein transacylase.
5 resent in other studied acyltransferases and transacylases.
6 tochondrial malonyl CoA-acyl carrier protein transacylase, a key enzyme in the pathway encoded by the
7  activity and acyl coenzyme A (acyl-CoA):ACP transacylase (ACAT) activity in a 1:0.12 ratio.
8 The pfKASIII also catalyzes the acyl-CoA:ACP transacylase (ACAT) reaction typically exhibited by KASI
9        Acetyl-CoA:acyl carrier protein (ACP) transacylase (ACT) activity has been demonstrated for th
10 ial isoenzymes of tafazzin that have similar transacylase activities but different membrane topologie
11  the total phospholipase B/lysophospholipase/transacylase activities of the cell.
12                           Both deacylase and transacylase activities were inhibited 50-60% by 20 micr
13 ssesses triglyceride lipase and acylglycerol transacylase activities.
14 hospholipase hydrolase and lysophospholipase transacylase activities.
15 h calcium-independent phospholipase A(2) and transacylase activities.
16 inhibited 5-lipoxygenase and CoA-independent transacylase activities.
17 hospholipase hydrolase and lysophospholipase transacylase activities.
18 ates phospholipase B, lysophospholipase, and transacylase activities.
19                      Coincidence between the transacylase activity and a stained protein of a molecul
20                      A phospholipase A and a transacylase activity are partially separated by gel per
21  phospholipase DDHD1 and a calcium-dependent transacylase activity implicated in endocannabinoid bios
22                                          The transacylase activity in the homogenate was present in t
23      Although all Drosophila isoforms showed transacylase activity in vitro, only the A-form supporte
24 ish a paradigm shift demonstrating that ATGL transacylase activity is biologically important.
25                                          The transacylase activity is independent of free fatty acid
26                            ATGL biosynthetic transacylase activity is present in human adipose tissue
27                                      Malonyl transacylase activity of the Arg-606 --> Ala and Arg-606
28  account for the decrease in CoA-independent transacylase activity or the induction of apoptosis.
29 zeta, and iPLA2eta also possess acylglycerol transacylase activity utilizing mono-olein as an acyl do
30                                              Transacylase activity was decreased in lymphoblasts from
31                          In contrast, acetyl transacylase activity was increased 6.6-fold in the Arg-
32 FL) and tafazzin lacking exon 5 (Delta5) had transacylase activity, and only these two isoforms were
33 cause the same mutations did not affect PlsX transacylase activity, we conclude that membrane associa
34                          DDHD2 also exhibits transacylase activity, which enables transfer of acyl ch
35 icant decrease in microsomal CoA-independent transacylase activity.
36 ptor and H(6)-FabD exhibited malonyl-CoA:ACP transacylase activity.
37 is gene product does not contain significant transacylase activity.
38 Mg2+ enhanced but were not essential for the transacylase activity.
39 n remodeling by sequential phospholipase and transacylase/acyltransferase activities in conjunction w
40 OCF3 is also an inhibitor of CoA-independent transacylase and 5-lipoxygenase.
41 est that 1-O-acylceramide synthase is both a transacylase and a novel phospholipase A2.
42 ubstrates, malonyl Co-A acyl carrier protein transacylase and ketopantoate hydroxymethyltransferase,
43 monstrated that transfected cells had higher transacylase and phospholipase A(2) activities than did
44  on the boundaries of the acetyl and malonyl transacylases and the beta-hydroxyacyl dehydratase, we a
45 hibited the activities of the acetyl/malonyl transacylases and the beta-hydroxyacyl dehydratase.
46 ned the activities of the acetyl and malonyl transacylases and the beta-hydroxyacyl dehydratase.
47 gments encoding the domains that contain the transacylases and the dehydratase in pET vectors and exp
48 ly, the activities of the acetyl and malonyl transacylases and the dehydratase.
49 etoacyl synthase, acetyl-CoA and malonyl-CoA transacylases, and beta-hydroxyacyl dehydratase) was clo
50 rt our hypothesis that the phospholipase and transacylase are separate enzymes essential to the synth
51     According to this line of reasoning, the transacylase assay that we have used measures the net ef
52 : beta-ketoacyl synthase, acetyl and malonyl transacylases, beta-hydroxyacyl dehydratase, enoyl reduc
53                                 The purified transacylase can use phosphatidic acid, phosphatidylinos
54            The enzyme coenzyme A-independent transacylase (CoA-IT) has been demonstrated to be the ke
55 bitors of the enzyme, coenzyme A-independent transacylase (CoA-IT), attenuates the proliferation of t
56 when cofactor thiamine pyrophosphate and the transacylase component of the BCKD complex are present.
57 and the Escherichia coli fatty acid synthase transacylase crystal structure were used to select motif
58 (BCKDHB), or dihydrolipoamide branched-chain transacylase (DBT) subunits, which interact to form the
59 Lit is a unique example of an intramolecular transacylase differentiated from that catalyzed by Lnt,
60 )-independent binding of BDP to the 24-meric transacylase (dihydrolipoyl transacylase; E2b) core of B
61                High occupancy of the malonyl transacylase domain and fast relative rate of malonyl tr
62 le in the binding of malonyl moieties to the transacylase domain but is not required for binding of a
63 ine or lysine in the context of the isolated transacylase domain, and the mutant proteins were expres
64  606, which is positionally conserved in the transacylase domains of all multifunctional fatty acid a
65              Dihydrolipoamide branched chain transacylase E2 (DBT) was found to be a robust suppresso
66 nsisting of 24 lipoate-bearing dihydrolipoyl transacylase (E2) subunits, associated with the branched
67  acid-bearing domain (LBD) from the 24-meric transacylase (E2b) core.
68  to the 24-meric transacylase (dihydrolipoyl transacylase; E2b) core of BCKDC results in a 3-fold inc
69 r monolysocardiolipin due to the loss of the transacylase enzyme tafazzin.
70  The malonyl-coenzyme A:acyl carrier protein transacylase (FabD) of P. syringae was overproduced and
71 ins, malonyl coenzyme A-acyl carrier protein transacylase (fabD), 3-ketoacyl-acyl carrier protein red
72 -coenzyme A [CoA]:acyl carrier protein [ACP] transacylase), fabG (encoding beta-ketoacyl-ACP reductas
73    BCKD kinase depends on a fully lipoylated transacylase for maximal activity, but the interaction b
74 rane protein Lit (lipoprotein intramolecular transacylase) from the opportunistic nosocomial pathogen
75 ination, a nonpolar mutation within the lktC transacylase gene of the leukotoxin operon was created.
76 n intronic nucleotide substitution in the E2 transacylase gene of type II MSUD, in which the E2 subun
77                         Application of these transacylase genes in suitable host cells can improve th
78 anched chain alpha-ketoacid dihydrolipoamide transacylase in these parasite stages was confirmed by W
79 ow that knockdown of Tafazzin (TAZ kd), a CL transacylase, in mice results in protection against the
80 nct inhibitors of the enzyme CoA-independent transacylase, including the antiproliferative alkyllysop
81 gene encodes a phospholipid-lysophospholipid transacylase involved in cardiolipin metabolism, but it
82 dular polyketide synthase by malonyl-CoA:ACP transacylase is an effective strategy for the engineered
83 t the interaction between the kinase and the transacylase is impeded in the presence of high salt con
84 dition, the level of tafazzin, a cardiolipin transacylase, is drastically reduced and the composition
85 cently discovered lipoprotein intramolecular transacylase, Lit.
86 hich encodes a phospholipid-lysophospholipid transacylase located in the mitochondria inner membrane.
87 protein (ACP) and possibly a malonyl CoA:ACP transacylase (MAT) forms a "minimal" PKS.
88             Malonyl-CoA:acyl carrier protein transacylase (MAT) provides acyl-ACP thioesters for the
89 cyl carrier protein (ACP), a malonyl-CoA:ACP transacylase (MAT), an acyl-ACP thioesterase, a ketoredu
90 e fatty acid synthase (fabD) malonyl CoA:ACP transacylase (MAT), recruited from primary metabolism.
91 carrier protein (ACP), and a malonyl-CoA:ACP transacylase (MAT).
92 ar to malonyl-CoA:acyl-carrier protein (ACP) transacylases (MATs).
93             Malonyl-CoA-acyl carrier protein transacylase (MCAT) is an enzyme involved in mitochondri
94 d pR212W in malonyl CoA-acyl carrier protein transacylase (MCAT), a mitochondrial protein involved in
95 he presence of S. coelicolor malonyl CoA:ACP transacylase (MCAT), the rate of loading increases and t
96 e of a malonyl-CoA:holo-acyl carrier protein transacylase (MCAT).
97 uire a third protein: malonyl-coenzyme A:ACP transacylase (MCAT).
98  transferase of Taxol biosynthesis, a set of transacylases obtained from an enriched cDNA library (co
99 sing consensus sequences from an assembly of transacylases of plant origin and from many deduced prot
100 plain these results is to postulate that the transacylase reaction occurs in two successive steps: a
101 EC and may occur through the CoA-independent transacylase remodeling pathway rather than as a direct
102                  Tafazzin is a mitochondrial transacylase required for cardiolipin remodeling.
103  tafazzin (TAZ) gene encoding a phospholipid transacylase required for cardiolipin remodeling.
104  the N-terminal domain is a starter unit:ACP transacylase (SAT domain) that selects a C(6) fatty acid
105            We show that the starter-unit:ACP transacylase (SAT) of Hpm3 is critical for crosstalk bet
106   In yeast, this process is completed by the transacylase tafazzin, which associates with intermembra
107   The maturation of cardiolipin requires the transacylase tafazzin, which is mutated in the human dis
108 ied out by the phospholipid-lysophospholipid transacylase tafazzin.
109 ations in the mitochondrial cardiolipin (CL) transacylase, tafazzin (Taz1p), result in the X-linked c
110 tis membranes contain a coenzyme A-dependent transacylase that can catalyze the preferential transfer
111                                     A unique transacylase that catalyzes esterification of a short ch
112 an acyl-acyl carrier protein (ACP):phosphate transacylase that interconverts the two acyl donors in G
113            Tafazzin (TAZ) is a mitochondrial transacylase that remodels the mitochondrial cardiolipin
114 at removes a fatty acid from CL, and Taz1, a transacylase that transfers a fatty acid from another ph
115                                Tafazzin is a transacylase that transfers acyl chains with unsaturated
116 dentify three novel TAG lipases/acylglycerol transacylases that likely participate in TAG hydrolysis
117  two other enzymes, DGAT2 and diacylglycerol transacylase, that catalyze triacylglycerol synthesis an
118            Overproduction of malonyl-CoA:ACP transacylase, the enzyme catalyzing the conversion of ma
119 itro system of Fak-PlsX (phosphate: acyl-ACP transacylase) was developed to track acyl-phosphate inte
120       The causative gene encodes tafazzin, a transacylase, which is the major determinant of the fina
121 nce that DDHD2 is a neutral lipid lipase and transacylase whose broad specificity enables TAG acyl-ch
122  CoA-independent, acyl-specific phospholipid transacylase with substrate preference for cardiolipin a

 
Page Top