S Wikipedije, slobodne enciklopedije
Protein 8 Ras pridruženosti sa domenom je protein koji je kod ljudi kodiran genom RASSF8 .[ 5]
Dužina polipeptidnog lanca je 419 aminokiselina , a molekulska težina 48.327 Da .[ 6]
Simboli
10 20 30 40 50 MELKVWVDGV QRIVCGVTEV TTCQEVVIAL AQAIGRTGRY TLIEKWRDTE RHLAPHENPI ISLNKWGQYA SDVQLILRRT GPSLSERPTS DSVARIPERT LYRQSLPPLA KLRPQIDKSI KRREPKRKSL TFTGGAKGLM DIFGKGKETE FKQKVLNNCK TTADELKKLI RLQTEKLQSI EKQLESNEIE IRFWEQKYNS NLEEEIVRLE QKIKRNDVEI EEEEFWENEL QIEQENEKQL KDQLQEIRQK ITECENKLKD YLAQIRTMES GLEAEKLQRE VQEAQVNEEE VKGKIGKVKG EIDIQGQQSL RLENGIKAVE RSLGQATKRL QDKEQELEQL TKELRQVNLQ QFIQQTGTKV TVLPAEPIEI EASHADIERE APFQSGSLKR PGSSRQLPSN LRILQNPISS GFNPEGIYV
Falvella FS, Spinola M, Manenti G, et al. (2007). "Common polymorphisms in D12S1034 flanking genes RASSF8 and BHLHB3 are not associated with lung adenocarcinoma risk". Lung Cancer . 56 (1): 1–7. doi :10.1016/j.lungcan.2006.11.008 . PMID 17194498 . Falvella FS, Manenti G, Spinola M, et al. (2006). "Identification of RASSF8 as a candidate lung tumor suppressor gene" . Oncogene . 25 (28): 3934–3938. doi :10.1038/sj.onc.1209422 PMID 16462760 . Rual JF, Venkatesan K, Hao T, et al. (2005). "Towards a proteome-scale map of the human protein-protein interaction network". Nature . 437 (7062): 1173–1178. doi :10.1038/nature04209 . PMID 16189514 . S2CID 4427026 . 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): 2121–2127. doi :10.1101/gr.2596504 . PMC 528928 PMID 15489334 . Jin J, Smith FD, Stark C, et al. (2004). "Proteomic, functional, and domain-based analysis of in vivo 14-3-3 binding proteins involved in cytoskeletal regulation and cellular organization" . Curr. Biol . 14 (16): 1436–1450. doi :10.1016/j.cub.2004.07.051 PMID 15324660 . 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): 16899–16903. doi :10.1073/pnas.242603899 . PMC 139241 PMID 12477932 . Debeer P, Schoenmakers EF, Twal WO, et al. (2002). "The fibulin-1 gene (FBLN1) is disrupted in a t(12;22) associated with a complex type of synpolydactyly" . J. Med. Genet . 39 (2): 98–104. doi :10.1136/jmg.39.2.98 . PMC 1735038 PMID 11836357 . Debeer P, Schoenmakers EF, Thoelen R, et al. (2000). "Physical map of a 1.5 mb region on 12p11.2 harbouring a synpolydactyly associated chromosomal breakpoint" . Eur. J. Hum. Genet . 8 (8): 561–570. doi :10.1038/sj.ejhg.5200497 PMID 10951517 .
