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(3Z)-enoyl CoA
(2Z)-enoyl CoA
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a (3E)-alk-3-enoyl-CoA
a (2E)-alk-2-enoyl-CoA
a (3Z)-alk-3-enoyl-CoA
a (2E)-alk-2-enoyl-CoA
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a (3E)-alk-3-enoyl-CoA
a (2E)-alk-2-enoyl-CoA
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a (3E)-alk-3-enoyl-CoA
a (2E)-alk-2-enoyl-CoA
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a (3Z)-alk-3-enoyl-CoA
a (2E)-alk-2-enoyl-CoA
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a (3Z)-alk-3-enoyl-CoA
a (2E)-alk-2-enoyl-CoA
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enzyme participates in the degradation of unsaturated fatty acids through beta-oxidation
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oleate is mostly (about 90%) degraded via beta-oxidation in Escherichia coli. A small amount of 2-trans,5-cis-tetradecadienoyl-CoA is diverted from the pathway via conversion to 3,5-cis-tetradecadienoyl-CoA by DELTA3,DELTA2-enoyl-CoA isomerase. The CoA-bound intermediate, which would strongly inhibit beta-oxidation if allowed to accumulate, is hydrolyzed and the resultant 3,5-tetradecadienoate is excreted into the growth medium.
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oleate is mostly (about 90%) degraded via beta-oxidation in Escherichia coli. A small amount of 2-trans,5-cis-tetradecadienoyl-CoA is diverted from the pathway via conversion to 3,5-cis-tetradecadienoyl-CoA by DELTA3,DELTA2-enoyl-CoA isomerase. The CoA-bound intermediate, which would strongly inhibit beta-oxidation if allowed to accumulate, is hydrolyzed and the resultant 3,5-tetradecadienoate is excreted into the growth medium.
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the enzyme is essential for unsaturated fatty acid metabolism
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involved in mitochondrial beta-oxidation of unsaturated fatty acids. Decreased levels of this enzyme in metastatic breast cancer cells might have impact on the aberrant behavior of cancer cells
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involved in mitochondrial beta-oxidation of unsaturated fatty acids. Decreased levels of this enzyme in metastatic breast cancer cells might have impact on the aberrant behavior of cancer cells
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catalyzes the transformation of 3-cis- and 3-trans-enoyl-CoA esters arising during the stepwise degradation of cis-, mono-, and polyunsaturated fatty acids to the 2-trans-enoyl-CoA intermediates
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catalyzes the transformation of 3-cis- and 3-trans-enoyl-CoA esters arising during the stepwise degradation of cis-, mono-, and polyunsaturated fatty acids to the 2-trans-enoyl-CoA intermediates
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enzyme is important for the degradation of unsaturated fatty acids in the beta-oxidation system
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the enzyme is essential for unsaturated fatty acid metabolism
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key enzyme in mitochondrial beta-oxidation of unsaturated fatty acids
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enzyme is responsible for the positional and geometric isomerization of beta,gamma-unsaturated fatty acyl-CoA intermediates arising during beta-oxidation of unsaturated long-chain fatty acids
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mitochondrial enzyme is markedly induced by peroxisome proliferators, di-(2-ethylhexyl)phthalate and clofibrate
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enzyme is important for the degradation of unsaturated fatty acids in the beta-oxidation system
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enzyme is important for the degradation of unsaturated fatty acids in the beta-oxidation system
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key enzyme in the degradation of unsaturated fatty acids
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involved in the enzymatic degradation of the cis-olefinic system of monounsaturated and polyunsaturated fatty acids
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auxiliary enzyme that is essential for the operation of the major pathway of oleate beta-oxidation
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key enzyme for the beta-oxidation of unsaturated fatty acids
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the enzyme is involved in beta-oxidation of unsaturated fatty acids
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one of the key enzymes involved in fatty acid oxidation
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one of the key enzymes involved in fatty acid oxidation
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auxiliary enzyme required for beta-oxidation of unsaturated fatty acids
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the enzyme is essential for the beta-oxidation of unsaturated fatty acids
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the enzyme is essential for the beta-oxidation of unsaturated fatty acids
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main pathway for 9-cis,11-trans-octadecadienoic acid degradation requires the participation of DELTA3,DELTA2-enoyl-CoA isomerase
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the synthesis of polyhydroxyalkanoate in cells grown in media containing 10-cis-heptadecenoic acid is dependent on the presence of DELTA3,DELTA2-enoyl-CoA isomerase activity. Degradation of 10-trans-heptadecenoic acid through beta-oxidation is severly reduced in mutants devoid of DELTA3,DELTA2-enoyl-CoA isomerase. The synthesis of the intermediate 3-trans-enoyl-CoA in the absence of the DELTA3,DELTA2-enoyl-CoA isomerase leads to the blockage of the direct multifunctional enzyme dependent pathway in vivo
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the synthesis of polyhydroxyalkanoate in cells grown in media containing 10-cis-heptadecenoic acid is dependent on the presence of DELTA3,DELTA2-enoyl-CoA isomerase activity. Degradation of 10-trans-heptadecenoic acid through beta-oxidation is severly reduced in mutants devoid of DELTA3,DELTA2-enoyl-CoA isomerase. The synthesis of the intermediate 3-trans-enoyl-CoA in the absence of the DELTA3,DELTA2-enoyl-CoA isomerase leads to the blockage of the direct multifunctional enzyme dependent pathway in vivo
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main pathway for 9-cis,11-trans-octadecadienoic acid degradation requires the participation of DELTA3,DELTA2-enoyl-CoA isomerase
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