From Wikipedia, the free encyclopedia
Protein-coding gene in the species Homo sapiens
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 .