// Workers AI · dad joke modeWhat did Fatty acyl-CoA reductase 1 say? "I'm reducing stress.
| FAR1 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||
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| Identifiers | ||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Aliases | FAR1, MLSTD2, SDR10E1, PFCRD, fatty acyl-CoA reductase 1, CSPSD | |||||||||||||||||||||||||||||||||||||||||||||||||||||
| External IDs | OMIM: 616107; MGI: 1914670; GeneCards: FAR1 | |||||||||||||||||||||||||||||||||||||||||||||||||||||
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Fatty acyl-CoA reductase 1 is an enzyme that in humans is encoded by the FAR1 gene.[5][6][7][8] This enzyme produces fatty alcohols from 16 or 18 carbon fatty acyl-CoA and 2 copies of NADPH.[9] These fatty alcohols are needed for the production of ether lipids and wax esters.[9] Unlike its paralog FAR2, FAR1 is able to not only act on unsaturated fatty acids, but also saturated fatty acids.[9][10] FAR1 is part of the alcohol-forming fatty acyl-CoA reductase class of enzymes.[9]
References
[edit]- 1 2 3 GRCh38: Ensembl release 89: ENSG00000197601 – Ensembl, May 2017
- 1 2 3 GRCm38: Ensembl release 89: ENSMUSG00000030759 – Ensembl, May 2017
- ↑ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
- ↑ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
- ↑ Cheng JB, Russell DW (Aug 2004). "Mammalian wax biosynthesis. I. Identification of two fatty acyl-Coenzyme A reductases with different substrate specificities and tissue distributions". J Biol Chem. 279 (36): 37789–97. doi:10.1074/jbc.M406225200. PMC 2757098. PMID 15220348.
- ↑ Cheng JB, Russell DW (Aug 2004). "Mammalian wax biosynthesis. II. Expression cloning of wax synthase cDNAs encoding a member of the acyltransferase enzyme family". J Biol Chem. 279 (36): 37798–807. doi:10.1074/jbc.M406226200. PMC 2743083. PMID 15220349.
- ↑ Persson B, Kallberg Y, Bray JE, Bruford E, Dellaporta SL, Favia AD, Duarte RG, Jornvall H, Kavanagh KL, Kedishvili N, Kisiela M, Maser E, Mindnich R, Orchard S, Penning TM, Thornton JM, Adamski J, Oppermann U (Feb 2009). "The SDR (short-chain dehydrogenase/reductase and related enzymes) nomenclature initiative". Chem Biol Interact. 178 (1–3): 94–8. Bibcode:2009CBI...178...94P. doi:10.1016/j.cbi.2008.10.040. PMC 2896744. PMID 19027726.
- ↑ "Entrez Gene: MLSTD2 male sterility domain containing 2".
- 1 2 3 4 "Q8WVX9 · FACR1_HUMAN". uniprot.org. UniProt consortium. Retrieved 2026-09-07.
- ↑ "Q96K12 · FACR2_HUMAN". uniprot.org. UniProt consortium. Retrieved 2026-09-07.
Further reading
[edit]- Ewing RM, Chu P, Elisma F, et al. (2007). "Large-scale mapping of human protein-protein interactions by mass spectrometry". Mol. Syst. Biol. 3 (1): 89. doi:10.1038/msb4100134. PMC 1847948. PMID 17353931.
- Foster LJ, Rudich A, Talior I, et al. (2006). "Insulin-dependent interactions of proteins with GLUT4 revealed through stable isotope labeling by amino acids in cell culture (SILAC)". J. Proteome Res. 5 (1): 64–75. doi:10.1021/pr0502626. PMID 16396496.
- Gerhard DS, Wagner L, Feingold EA, et al. (2004). "The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)". Genome Res. 14 (10B): 2121–7. doi:10.1101/gr.2596504. PMC 528928. PMID 15489334.
- Ota T, Suzuki Y, Nishikawa T, et al. (2004). "Complete sequencing and characterization of 21,243 full-length human cDNAs". Nat. Genet. 36 (1): 40–5. doi:10.1038/ng1285. PMID 14702039.
- Clark HF, Gurney AL, Abaya E, et al. (2003). "The secreted protein discovery initiative (SPDI), a large-scale effort to identify novel human secreted and transmembrane proteins: a bioinformatics assessment". Genome Res. 13 (10): 2265–70. doi:10.1101/gr.1293003. PMC 403697. PMID 12975309.
- Strausberg RL, Feingold EA, Grouse LH, et al. (2003). "Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences". Proc. Natl. Acad. Sci. U.S.A. 99 (26): 16899–903. Bibcode:2002PNAS...9916899M. doi:10.1073/pnas.242603899. PMC 139241. PMID 12477932.