FXYD1

An Error has occured retrieving Wikidata item for infobox FXYD1‏ (FXYD domain containing ion transport regulator 1) هوَ بروتين يُشَفر بواسطة جين FXYD1 في الإنسان.^[1]^[2]

الوظيفة

الأهمية السريرية

المراجع

^ "Entrez Gene: FXYD1 FXYD domain containing ion transport regulator 1 (phospholemman)". مؤرشف من الأصل في 2010-12-05.
^ Chen LS، Lo CF، Numann R، Cuddy M (يوليو 1997). "Characterization of the human and rat phospholemman (PLM) cDNAs and localization of the human PLM gene to chromosome 19q13.1". Genomics. ج. 41 ع. 3: 435–43. DOI:10.1006/geno.1997.4665. PMID:9169143.

قراءة متعمقة

Walaas SI، Czernik AJ، Olstad OK، وآخرون (1995). "Protein kinase C and cyclic AMP-dependent protein kinase phosphorylate phospholemman, an insulin and adrenaline-regulated membrane phosphoprotein, at specific sites in the carboxy terminal domain". Biochem. J. ج. 304 ع. 2: 635–40. PMC:1137538. PMID:7999001.
Neumann J، Maas R، Bokník P، وآخرون (1999). "Pharmacological characterization of protein phosphatase activities in preparations from failing human hearts". J. Pharmacol. Exp. Ther. ج. 289 ع. 1: 188–93. PMID:10087003.
Mounsey JP، John JE، Helmke SM، وآخرون (2000). "Phospholemman is a substrate for myotonic dystrophy protein kinase". J. Biol. Chem. ج. 275 ع. 30: 23362–7. DOI:10.1074/jbc.M000899200. PMID:10811636.
Sweadner KJ، Rael E (2001). "The FXYD gene family of small ion transport regulators or channels: cDNA sequence, protein signature sequence, and expression". Genomics. ج. 68 ع. 1: 41–56. DOI:10.1006/geno.2000.6274. PMID:10950925.
Strausberg RL، Feingold EA، Grouse LH، وآخرون (2003). "Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences". Proc. Natl. Acad. Sci. U.S.A. ج. 99 ع. 26: 16899–903. DOI:10.1073/pnas.242603899. PMC:139241. PMID:12477932.
Crowell KJ، Franzin CM، Koltay A، وآخرون (2003). "Expression and characterization of the FXYD ion transport regulators for NMR structural studies in lipid micelles and lipid bilayers". Biochim. Biophys. Acta. ج. 1645 ع. 1: 15–21. DOI:10.1016/S1570-9639(02)00473-9. PMC:2917601. PMID:12535606.
Fuller W، Eaton P، Bell JR، Shattock MJ (2004). "Ischemia-induced phosphorylation of phospholemman directly activates rat cardiac Na/K-ATPase". FASEB J. ج. 18 ع. 1: 197–9. DOI:10.1096/fj.03-0213fje. PMID:14597563.
Gerhard DS، Wagner L، Feingold EA، وآخرون (2004). "The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)". Genome Res. ج. 14 ع. 10B: 2121–7. DOI:10.1101/gr.2596504. PMC:528928. PMID:15489334.
Rual JF، Venkatesan K، Hao T، وآخرون (2005). "Towards a proteome-scale map of the human protein-protein interaction network". Nature. ج. 437 ع. 7062: 1173–8. DOI:10.1038/nature04209. PMID:16189514.
Franzin CM، Yu J، Thai K، وآخرون (2006). "Correlation of gene and protein structures in the FXYD family proteins". J. Mol. Biol. ج. 354 ع. 4: 743–50. DOI:10.1016/j.jmb.2005.10.018. PMC:2907130. PMID:16288923.
Wang J، Zhang XQ، Ahlers BA، وآخرون (2006). "Cytoplasmic tail of phospholemman interacts with the intracellular loop of the cardiac Na+/Ca2+ exchanger". J. Biol. Chem. ج. 281 ع. 42: 32004–14. DOI:10.1074/jbc.M606876200. PMC:1613256. PMID:16921169.
Deng V، Matagne V، Banine F، وآخرون (2007). "FXYD1 is an MeCP2 target gene overexpressed in the brains of Rett syndrome patients and Mecp2-null mice". Hum. Mol. Genet. ج. 16 ع. 6: 640–50. DOI:10.1093/hmg/ddm007. PMID:17309881.

هذه بذرة مقالة عن بروتين بحاجة للتوسيع. فضلًا شارك في تحريرها.

[1] "Entrez Gene: FXYD1 FXYD domain containing ion transport regulator 1 (phospholemman)". مؤرشف من الأصل في 2010-12-05.

[2] Chen LS، Lo CF، Numann R، Cuddy M (يوليو 1997). "Characterization of the human and rat phospholemman (PLM) cDNAs and localization of the human PLM gene to chromosome 19q13.1". Genomics. ج. 41 ع. 3: 435–43. DOI:10.1006/geno.1997.4665. PMID:9169143.

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