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FYVE, RhoGEF i PH domen sadržavajući‎ 3
	; PDB prikaz baziran na 2coc.
Dostupne strukture
	2COC
Identifikatori
Simboli	FGD3; ZFYVE5
Vanjski ID	MGI: 1353657 HomoloGene: 22925 GeneCards: FGD3 Gene
Ontologija gena
Molekulska funkcija	• aktivnost guanil-nukleotidnog faktora razmene; • aktivnost Rho guanil-nukleotidnog faktora razmene; • vezivanje male GTPaze;
Ćelijska komponenta	• citoplazma; • Goldžijev aparat; • citozol;
Biološki proces	• organizacija citoskeletona; • malom GTPazom posredovana transdukcija signala; • regulacija ćelijskog oblika;
Ortolozi

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FYVE, RhoGEF i PH domen sadržavajući‎ 3 je protein koji je kod čoveka kodiran FGD3 genom.^[1]^[2]

Reference

↑ Hattori A, Okumura K, Nagase T, Kikuno R, Hirosawa M, Ohara O (Feb 2001). „Characterization of long cDNA clones from human adult spleen”. DNA Res 7 (6): 357–66. DOI:10.1093/dnares/7.6.357. PMID 11214971.
↑ „Entrez Gene: FGD3 FYVE, RhoGEF and PH domain containing 3”.

Literatura

Maruyama K, Sugano S (1994). „Oligo-capping: a simple method to replace the cap structure of eukaryotic mRNAs with oligoribonucleotides”. Gene 138 (1–2): 171–4. DOI:10.1016/0378-1119(94)90802-8. PMID 8125298.
Suzuki Y, Yoshitomo-Nakagawa K, Maruyama K, et al. (1997). „Construction and characterization of a full length-enriched and a 5'-end-enriched cDNA library”. Gene 200 (1–2): 149–56. DOI:10.1016/S0378-1119(97)00411-3. PMID 9373149.
Pasteris NG, Nagata K, Hall A, Gorski JL (2000). „Isolation, characterization, and mapping of the mouse Fgd3 gene, a new Faciogenital Dysplasia (FGD1; Aarskog Syndrome) gene homologue”. Gene 242 (1–2): 237–47. DOI:10.1016/S0378-1119(99)00518-1. PMID 10721717.
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. DOI:10.1073/pnas.242603899. PMC 139241. PMID 12477932.
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.
Humphray SJ, Oliver K, Hunt AR, et al. (2004). „DNA sequence and analysis of human chromosome 9”. Nature 429 (6990): 369–74. DOI:10.1038/nature02465. PMC 2734081. PMID 15164053.
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.
Kimura K, Wakamatsu A, Suzuki Y, et al. (2006). „Diversification of transcriptional modulation: large-scale identification and characterization of putative alternative promoters of human genes”. Genome Res. 16 (1): 55–65. DOI:10.1101/gr.4039406. PMC 1356129. PMID 16344560.
Delague V, Jacquier A, Hamadouche T, et al. (2007). „Mutations in FGD4 encoding the Rho GDP/GTP exchange factor FRABIN cause autosomal recessive Charcot-Marie-Tooth type 4H”. Am. J. Hum. Genet. 81 (1): 1–16. DOI:10.1086/518428. PMC 1950914. PMID 17564959.

[pmid11214971-1] Hattori A, Okumura K, Nagase T, Kikuno R, Hirosawa M, Ohara O (Feb 2001). „Characterization of long cDNA clones from human adult spleen”. DNA Res 7 (6): 357–66. DOI:10.1093/dnares/7.6.357. PMID 11214971.

[entrez-2] „Entrez Gene: FGD3 FYVE, RhoGEF and PH domain containing 3”.

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