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Literature summary for 1.3.1.93 extracted from

  • Wakashima, T.; Abe, K.; Kihara, A.
    Dual functions of the trans-2-enoyl-CoA reductase TER in the sphingosine 1-phosphate metabolic pathway and in fatty acid elongation (2014), J. Biol. Chem., 289, 24736-24748 .
    View publication on PubMedView publication on EuropePMC

Cloned(Commentary)

Cloned (Comment) Organism
gene TECR Rattus norvegicus
gene TECR, cloning from liver cDNA, Ectopic expression of human trans-2-enoyl-CoA reductase TER in Saccharomyces cerevisiae TER homologue Tsc13-lowered cells Homo sapiens
gene TSC13, recombinant expression as N-terminal FLAG3-tagged enzyme from pAKNF313 and pAKNF315, or as N-terminal HA2-tagged enzyme Saccharomyces cerevisiae

Protein Variants

Protein Variants Comment Organism
additional information HeLa cells are transfected with control siRNA or TER si RNA, siRNA-generated enzyme knockout mutant. Knockdown of TER in HeLa cells causes decreased sphingosine 1-phosphate metabolism in vitro and a reduction in the dihydrosphingosine metabolism Homo sapiens
additional information YRF50 cells (BY4741,pTSC13::KanMX4-tTA-ptetO7) are constructed by replacing the promoter of the TSC13 gene (pTSC13) with tetO7 promoter (ptetO7) using the KanMX4-tTA-ptetO7 cassette from the pCM225 plasmid. Strains ABY83 and ABY80 cells are constructed by deletion of the TSC13 gene in BY4741 cells bearing the pTW6 or pAB119 plasmid, respectively, using a tsc13DELTA::LEU2 fragment by homologous recombination. Generation of Saccharomyces cerevisiae Tsc13-lowered cells Saccharomyces cerevisiae

Localization

Localization Comment Organism GeneOntology No. Textmining
endoplasmic reticulum
-
Saccharomyces cerevisiae 5783
-
endoplasmic reticulum
-
Homo sapiens 5783
-
endoplasmic reticulum
-
Rattus norvegicus 5783
-

Natural Substrates/ Products (Substrates)

Natural Substrates Organism Comment (Nat. Sub.) Natural Products Comment (Nat. Pro.) Rev. Reac.
a very-long-chain trans-2,3-dehydroacyl-CoA + NADPH + H+ Saccharomyces cerevisiae
-
a very-long-chain acyl-CoA + NADP+
-
?
a very-long-chain trans-2,3-dehydroacyl-CoA + NADPH + H+ Homo sapiens
-
a very-long-chain acyl-CoA + NADP+
-
?
a very-long-chain trans-2,3-dehydroacyl-CoA + NADPH + H+ Rattus norvegicus
-
a very-long-chain acyl-CoA + NADP+
-
?
a very-long-chain trans-2,3-dehydroacyl-CoA + NADPH + H+ Saccharomyces cerevisiae BY4741
-
a very-long-chain acyl-CoA + NADP+
-
?
trans-2-hexadecenoyl-CoA + NADPH + H+ Saccharomyces cerevisiae
-
palmitoyl-CoA + NADP+
-
?
trans-2-hexadecenoyl-CoA + NADPH + H+ Homo sapiens
-
palmitoyl-CoA + NADP+
-
?
trans-2-hexadecenoyl-CoA + NADPH + H+ Rattus norvegicus
-
palmitoyl-CoA + NADP+
-
?
trans-2-hexadecenoyl-CoA + NADPH + H+ Saccharomyces cerevisiae BY4741
-
palmitoyl-CoA + NADP+
-
?

Organism

Organism UniProt Comment Textmining
Homo sapiens Q9NZ01
-
-
Rattus norvegicus Q64232
-
-
Saccharomyces cerevisiae
-
-
-
Saccharomyces cerevisiae BY4741
-
-
-

Source Tissue

Source Tissue Comment Organism Textmining
HeLa cell
-
Homo sapiens
-
Hep-G2 cell
-
Homo sapiens
-
hepatocyte
-
Homo sapiens
-
IEC-6 cell
-
Rattus norvegicus
-
intestinal epithelial cell
-
Rattus norvegicus
-
neuronal cell
-
Rattus norvegicus
-
PC-12 cell
-
Rattus norvegicus
-

Substrates and Products (Substrate)

Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
a very-long-chain trans-2,3-dehydroacyl-CoA + NADPH + H+
-
Saccharomyces cerevisiae a very-long-chain acyl-CoA + NADP+
-
?
a very-long-chain trans-2,3-dehydroacyl-CoA + NADPH + H+
-
Homo sapiens a very-long-chain acyl-CoA + NADP+
-
?
a very-long-chain trans-2,3-dehydroacyl-CoA + NADPH + H+
-
Rattus norvegicus a very-long-chain acyl-CoA + NADP+
-
?
a very-long-chain trans-2,3-dehydroacyl-CoA + NADPH + H+
-
Saccharomyces cerevisiae BY4741 a very-long-chain acyl-CoA + NADP+
-
?
trans-2-hexadecenoyl-CoA + NADPH + H+
-
Saccharomyces cerevisiae palmitoyl-CoA + NADP+
-
?
trans-2-hexadecenoyl-CoA + NADPH + H+
-
Homo sapiens palmitoyl-CoA + NADP+
-
?
trans-2-hexadecenoyl-CoA + NADPH + H+
-
Rattus norvegicus palmitoyl-CoA + NADP+
-
?
trans-2-hexadecenoyl-CoA + NADPH + H+
-
Saccharomyces cerevisiae BY4741 palmitoyl-CoA + NADP+
-
?

Synonyms

Synonyms Comment Organism
TER
-
Saccharomyces cerevisiae
TER
-
Homo sapiens
TER
-
Rattus norvegicus
trans-2-enoyl-CoA reductase
-
Saccharomyces cerevisiae
trans-2-enoyl-CoA reductase
-
Homo sapiens
trans-2-enoyl-CoA reductase
-
Rattus norvegicus
TSC13
-
Saccharomyces cerevisiae

Cofactor

Cofactor Comment Organism Structure
NADPH
-
Saccharomyces cerevisiae
NADPH
-
Homo sapiens
NADPH
-
Rattus norvegicus

General Information

General Information Comment Organism
malfunction ectopic expression of human trans-2-enoyl-CoA reductase TER in Saccharomyces cerevisiae TER homologue Tsc13-lowered cells causes recovery in the deficient sphingosine 1-phosphate metabolic pathway, lethality of VLCFA-deficient mutations Saccharomyces cerevisiae
malfunction in membrane fractions prepared from TER siRNA-treated HeLa cells, the conversion of trans-2-hexadecenoyl-CoA to palmitoyl-CoA is largely impaired, and only a small amount of palmitoyl-CoA is produced. Instead, trans-2-hexadecenoyl-CoA is the main product, and C14:0-CoA is also detected Homo sapiens
metabolism TER is involved sphingosine degradation within sphingolipids in the S1P metabolic pathway. trans-2-enoyl-CoA reductase TER catalyzes the saturation step of the sphingosine 1-phosphate (S1P) metabolic pathway. The pathways of sphingolipid degradation and synthesis, overview Saccharomyces cerevisiae
metabolism TER is involved sphingosine degradation within sphingolipids in the S1P metabolic pathway. trans-2-enoyl-CoA reductase TER catalyzes the saturation step of the sphingosine 1-phosphate (S1P) metabolic pathway. The pathways of sphingolipid degradation and synthesis, overview Rattus norvegicus
metabolism TER is involved sphingosine degradation within sphingolipids in the S1P metabolic pathway. trans-2-enoyl-CoA reductase TER catalyzes the saturation step of the sphingosine 1-phosphate (S1P) metabolic pathway. The pathways of sphingolipid degradation and synthesis, overview. Ectopic expression of human trans-2-enoyl-CoA reductase TER in Saccharomyces cerevisiae TER homologue Tsc13-lowered cells causes recovery in the deficient sphingosine 1-phosphate metabolic pathway Homo sapiens
physiological function the trans-2-enoyl-CoA reductase, TER, functions in very long-chain fatty acid (VLCFA) synthesis and is involved in the fatty acid elongation cycle, where palmitic acid synthesized by fatty acid synthase or fatty acids taken from foods are elongated to very long-chain fatty acids (VLCFAs) with carbon chain lengths greater than 20 Saccharomyces cerevisiae
physiological function the trans-2-enoyl-CoA reductase, TER, functions in very long-chain fatty acid (VLCFA) synthesis and is involved in the fatty acid elongation cycle, where palmitic acid synthesized by fatty acid synthase or fatty acids taken from foods are elongated to very long-chain fatty acids (VLCFAs) with carbon chain lengths greater than 20 Homo sapiens
physiological function the trans-2-enoyl-CoA reductase, TER, functions in very long-chain fatty acid (VLCFA) synthesis and is involved in the fatty acid elongation cycle, where palmitic acid synthesized by fatty acid synthase or fatty acids taken from foods are elongated to very long-chain fatty acids (VLCFAs) with carbon chain lengths greater than 20 Rattus norvegicus