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Literature summary extracted from

  • Rasmussen, A.L.; Diamond, D.L.; McDermott, J.E.; Gao, X.; Metz, T.O.; Matzke, M.M.; Carter, V.S.; Belisle, S.E.; Korth, M.J.; Waters, K.M.; Smith, R.D.; Katze, M.G.
    Systems virology identifies a mitochondrial fatty acid oxidation enzyme, dodecenoyl coenzyme A delta isomerase, required for hepatitis C virus replication and likely pathogenesis (2011), J. Virol., 85, 11646-11654.
    View publication on PubMedView publication on EuropePMC

Application

EC Number Application Comment Organism
5.3.3.8 medicine enzyme is involved in controlling host metabolic reprogramming during hepatitis C virus infection. Hepatitis C virus growth and RNA replication in hepatoma cell lines stably expressing dodecenoyl coenzyme A delta isomerase-targeting short hairpin RNA (shRNA) are abrogated, indicating that dodecenoyl coenzyme A delta isomerase is required for productive infection. Pharmacologic inhibition of fatty acid oxidation also blocks hepatitis C virus replication. Production of infectious hepatitis C virus is restored by overexpression of an shRNA-resistant dodecenoyl coenzyme A delta isomerase allele Homo sapiens

Cloned(Commentary)

EC Number Cloned (Comment) Organism
5.3.3.8 expressed in Escherichia coli DH5alpha cells Hepacivirus C

Localization

EC Number Localization Comment Organism GeneOntology No. Textmining
5.3.3.8 mitochondrion
-
Homo sapiens 5739
-

Organism

EC Number Organism UniProt Comment Textmining
5.3.3.8 Hepacivirus C
-
-
-
5.3.3.8 Homo sapiens P42126
-
-

Synonyms

EC Number Synonyms Comment Organism
5.3.3.8 DCI
-
Hepacivirus C
5.3.3.8 dodecenoyl coenzyme A DELTA isomerase
-
Hepacivirus C
5.3.3.8 dodecenoyl coenzyme A DELTA isomerase
-
Homo sapiens
5.3.3.8 ECI1
-
Homo sapiens

General Information

EC Number General Information Comment Organism
5.3.3.8 malfunction enzyme knockdown of inhibits hepatitis C virus RNA replication in cultured hepatoma cells. Enzyme deficiency causes alterations in the cellular metabolome Hepacivirus C
5.3.3.8 physiological function the enzyme is required for hepatitis C virus replication and likely pathogenesis Hepacivirus C