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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
8 The pfKASIII also catalyzes the acyl-CoA:ACP transacylase (ACAT) reaction typically exhibited by KASI
10 ial isoenzymes of tafazzin that have similar transacylase activities but different membrane topologie
21 phospholipase DDHD1 and a calcium-dependent transacylase activity implicated in endocannabinoid bios
27 zeta, and iPLA2eta also possess acylglycerol transacylase activity utilizing mono-olein as an acyl do
30 FL) and tafazzin lacking exon 5 (Delta5) had transacylase activity, and only these two isoforms were
35 n remodeling by sequential phospholipase and transacylase/acyltransferase activities in conjunction w
38 ubstrates, malonyl Co-A acyl carrier protein transacylase and ketopantoate hydroxymethyltransferase,
39 monstrated that transfected cells had higher transacylase and phospholipase A(2) activities than did
40 on the boundaries of the acetyl and malonyl transacylases and the beta-hydroxyacyl dehydratase, we a
43 gments encoding the domains that contain the transacylases and the dehydratase in pET vectors and exp
45 etoacyl synthase, acetyl-CoA and malonyl-CoA transacylases, and beta-hydroxyacyl dehydratase) was clo
46 rt our hypothesis that the phospholipase and transacylase are separate enzymes essential to the synth
47 According to this line of reasoning, the transacylase assay that we have used measures the net ef
48 : beta-ketoacyl synthase, acetyl and malonyl transacylases, beta-hydroxyacyl dehydratase, enoyl reduc
51 bitors of the enzyme, coenzyme A-independent transacylase (CoA-IT), attenuates the proliferation of t
52 when cofactor thiamine pyrophosphate and the transacylase component of the BCKD complex are present.
53 and the Escherichia coli fatty acid synthase transacylase crystal structure were used to select motif
54 )-independent binding of BDP to the 24-meric transacylase (dihydrolipoyl transacylase; E2b) core of B
56 le in the binding of malonyl moieties to the transacylase domain but is not required for binding of a
57 ine or lysine in the context of the isolated transacylase domain, and the mutant proteins were expres
58 606, which is positionally conserved in the transacylase domains of all multifunctional fatty acid a
59 nsisting of 24 lipoate-bearing dihydrolipoyl transacylase (E2) subunits, associated with the branched
61 to the 24-meric transacylase (dihydrolipoyl transacylase; E2b) core of BCKDC results in a 3-fold inc
62 The malonyl-coenzyme A:acyl carrier protein transacylase (FabD) of P. syringae was overproduced and
63 ins, malonyl coenzyme A-acyl carrier protein transacylase (fabD), 3-ketoacyl-acyl carrier protein red
64 -coenzyme A [CoA]:acyl carrier protein [ACP] transacylase), fabG (encoding beta-ketoacyl-ACP reductas
65 BCKD kinase depends on a fully lipoylated transacylase for maximal activity, but the interaction b
66 ination, a nonpolar mutation within the lktC transacylase gene of the leukotoxin operon was created.
67 n intronic nucleotide substitution in the E2 transacylase gene of type II MSUD, in which the E2 subun
69 anched chain alpha-ketoacid dihydrolipoamide transacylase in these parasite stages was confirmed by W
70 ow that knockdown of Tafazzin (TAZ kd), a CL transacylase, in mice results in protection against the
71 nct inhibitors of the enzyme CoA-independent transacylase, including the antiproliferative alkyllysop
72 gene encodes a phospholipid-lysophospholipid transacylase involved in cardiolipin metabolism, but it
73 dular polyketide synthase by malonyl-CoA:ACP transacylase is an effective strategy for the engineered
74 t the interaction between the kinase and the transacylase is impeded in the presence of high salt con
75 dition, the level of tafazzin, a cardiolipin transacylase, is drastically reduced and the composition
78 cyl carrier protein (ACP), a malonyl-CoA:ACP transacylase (MAT), an acyl-ACP thioesterase, a ketoredu
79 e fatty acid synthase (fabD) malonyl CoA:ACP transacylase (MAT), recruited from primary metabolism.
82 he presence of S. coelicolor malonyl CoA:ACP transacylase (MCAT), the rate of loading increases and t
85 transferase of Taxol biosynthesis, a set of transacylases obtained from an enriched cDNA library (co
86 sing consensus sequences from an assembly of transacylases of plant origin and from many deduced prot
87 plain these results is to postulate that the transacylase reaction occurs in two successive steps: a
88 EC and may occur through the CoA-independent transacylase remodeling pathway rather than as a direct
90 the N-terminal domain is a starter unit:ACP transacylase (SAT domain) that selects a C(6) fatty acid
92 In yeast, this process is completed by the transacylase tafazzin, which associates with intermembra
93 The maturation of cardiolipin requires the transacylase tafazzin, which is mutated in the human dis
94 ations in the mitochondrial cardiolipin (CL) transacylase, tafazzin (Taz1p), result in the X-linked c
95 tis membranes contain a coenzyme A-dependent transacylase that can catalyze the preferential transfer
97 an acyl-acyl carrier protein (ACP):phosphate transacylase that interconverts the two acyl donors in G
99 dentify three novel TAG lipases/acylglycerol transacylases that likely participate in TAG hydrolysis
100 two other enzymes, DGAT2 and diacylglycerol transacylase, that catalyze triacylglycerol synthesis an
103 CoA-independent, acyl-specific phospholipid transacylase with substrate preference for cardiolipin a
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