2,4-dienoyl-CoA reductase 1 is a protein that in humans is encoded by the DECR1 gene .
[5]
Function [ ]
This gene encodes an accessory enzyme which participates in the beta-oxidation and metabolism of unsaturated fatty enoyl-CoA esters .
See also [ ]
References [ ]
Further reading [ ]
Alphey MS, Yu W, Byres E, Li D, Hunter WN (2005). "Structure and reactivity of human mitochondrial 2,4-dienoyl-CoA reductase: enzyme-ligand interactions in a distinctive short-chain reductase active site" . J. Biol. Chem . 280 (4): 3068–77. doi :10.1074/jbc.M411069200 . PMID 15531764 .
Yu W, Chu X, Chen G, Li D (2005). "Studies of human mitochondrial 2,4-dienoyl-CoA reductase". Arch. Biochem. Biophys . 434 (1): 195–200. doi :10.1016/j.abb.2004.10.018 . PMID 15629123 .
Rosenzweig SD (2008). "Inflammatory manifestations in chronic granulomatous disease (CGD)". J. Clin. Immunol . 28 Suppl 1: S67–72. doi :10.1007/s10875-007-9160-5 . PMID 18193341 . S2CID 5965278 .
Kardon T, Senesi S, Marcolongo P, Legeza B, Bánhegyi G, Mandl J, Fulceri R, Benedetti A (2008). "Maintenance of luminal NADPH in the endoplasmic reticulum promotes the survival of human neutrophil granulocytes" . FEBS Lett . 582 (13): 1809–15. doi :10.1016/j.febslet.2008.04.045 . PMID 18472006 . S2CID 41166916 .
Mizuta I, Tsunoda T, Satake W, Nakabayashi Y, Watanabe M, Takeda A, Hasegawa K, Nakashima K, Yamamoto M, Hattori N, Murata M, Toda T (2008). "Calbindin 1, fibroblast growth factor 20, and alpha-synuclein in sporadic Parkinson's disease". Hum. Genet . 124 (1): 89–94. doi :10.1007/s00439-008-0525-5 . PMID 18568448 . S2CID 20604147 .
Moe KT, Woon FP, De Silva DA, Wong P, Koh TH, Kingwell B, Chin-Dusting J, Wong MC (2008). "Association of acute ischemic stroke with the MTHFR C677T polymorphism but not with NOS3 gene polymorphisms in a Singapore population". Eur. J. Neurol . 15 (12): 1309–14. doi :10.1111/j.1468-1331.2008.02308.x . PMID 19049547 . S2CID 10457617 .
Hosgood HD, Zhang L, Shen M, Berndt SI, Vermeulen R, Li G, Yin S, Yeager M, Yuenger J, Rothman N, Chanock S, Smith M, Lan Q (2009). "Association between genetic variants in VEGF, ERCC3 and occupational benzene haematotoxicity" . Occup Environ Med . 66 (12): 848–53. doi :10.1136/oem.2008.044024 . PMC 2928224 . PMID 19773279 .
Rose JE, Behm FM, Drgon T, Johnson C, Uhl GR (2010). "Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype score" . Mol. Med . 16 (7–8): 247–53. doi :10.2119/molmed.2009.00159 . PMC 2896464 . PMID 20379614 .
Hendrickson SL, Lautenberger JA, Chinn LW, Malasky M, Sezgin E, Kingsley LA, Goedert JJ, Kirk GD, Gomperts ED, Buchbinder SP, Troyer JL, O'Brien SJ (2010). "Genetic variants in nuclear-encoded mitochondrial genes influence AIDS progression" . PLOS ONE . 5 (9): e12862. Bibcode :2010PLoSO...512862H . doi :10.1371/journal.pone.0012862 . PMC 2943476 . PMID 20877624 .
This article incorporates text from the United States National Library of Medicine , which is in the public domain .