ACAD8
ACAD8 | |||||||||||||||||||||||||
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Tanımlayıcılar | |||||||||||||||||||||||||
Başka adlar | ACAD8 | ||||||||||||||||||||||||
Dış kimlikler | OMIM: 604773 MGI: 1914198 HomoloGene: 8662 GeneCards: ACAD8 | ||||||||||||||||||||||||
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Ortologlar | |||||||||||||||||||||||||
Türler | İnsan | Fare | |||||||||||||||||||||||
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Ensembl | |||||||||||||||||||||||||
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RefSeq (mRNA) | |||||||||||||||||||||||||
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Yerleşim (UCSC) | Krom. 11: 134.25 – 134.27 Mb | n/a | |||||||||||||||||||||||
PubMed araması | [2] | [3] | |||||||||||||||||||||||
Vikiveri | |||||||||||||||||||||||||
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İzobütiril-CoA dehidrogenaz, mitokondriyal, insanların 11. kromozomunda yer alan ACAD8 geni tarafından kodlanan bir enzimdir.[4][5]
Kaynakça
[değiştir | kaynağı değiştir]- ^ a b c GRCh38: Ensembl release 89: ENSG00000151498 - Ensembl, May 2017
- ^ "İnsan PubMed Başvurusu:". National Center for Biotechnology Information, U.S. National Library of Medicine.
- ^ "Fare PubMed Başvurusu:". National Center for Biotechnology Information, U.S. National Library of Medicine.
- ^ Telford EA, Moynihan LM, Markham AF, Lench NJ (Sep 1999). "Isolation and characterisation of a cDNA encoding the precursor for a novel member of the acyl-CoA dehydrogenase gene family". Biochimica et Biophysica Acta (BBA) - Gene Structure and Expression. 1446 (3). ss. 371-6. doi:10.1016/s0167-4781(99)00102-5. PMID 10524212.
- ^ "Entrez Gene: ACAD8 acyl-Coenzyme A dehydrogenase family, member 8". 6 Mart 2010 tarihinde kaynağından arşivlendi. Erişim tarihi: 17 Ocak 2024.
Ek okuma
[değiştir | kaynağı değiştir]- Näär AM, Beaurang PA, Zhou S, Abraham S, Solomon W, Tjian R (Apr 1999). "Composite co-activator ARC mediates chromatin-directed transcriptional activation". Nature. 398 (6730). ss. 828-32. Bibcode:1999Natur.398..828N. doi:10.1038/19789. PMID 10235267.
- Andresen BS, Christensen E, Corydon TJ, Bross P, Pilgaard B, Wanders RJ, Ruiter JP, Simonsen H, Winter V, Knudsen I, Schroeder LD, Gregersen N, Skovby F (Nov 2000). "Isolated 2-methylbutyrylglycinuria caused by short/branched-chain acyl-CoA dehydrogenase deficiency: identification of a new enzyme defect, resolution of its molecular basis, and evidence for distinct acyl-CoA dehydrogenases in isoleucine and valine metabolism". American Journal of Human Genetics. 67 (5). ss. 1095-103. doi:10.1086/303105. PMC 1288551 $2. PMID 11013134.
- Nguyen TV, Andresen BS, Corydon TJ, Ghisla S, Abd-El Razik N, Mohsen AW, Cederbaum SD, Roe DS, Roe CR, Lench NJ, Vockley J (2003). "Identification of isobutyryl-CoA dehydrogenase and its deficiency in humans". Molecular Genetics and Metabolism. 77 (1–2). ss. 68-79. doi:10.1016/S1096-7192(02)00152-X. PMID 12359132.
- Battaile KP, Nguyen TV, Vockley J, Kim JJ (Apr 2004). "Structures of isobutyryl-CoA dehydrogenase and enzyme-product complex: comparison with isovaleryl- and short-chain acyl-CoA dehydrogenases". The Journal of Biological Chemistry. 279 (16). ss. 16526-34. doi:10.1074/jbc.M400034200 . PMID 14752098.
- Ma J, Dempsey AA, Stamatiou D, Marshall KW, Liew CC (Mar 2007). "Identifying leukocyte gene expression patterns associated with plasma lipid levels in human subjects". Atherosclerosis. 191 (1). ss. 63-72. doi:10.1016/j.atherosclerosis.2006.05.032. PMID 16806233.
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