VAPA
VAPA (VAMP associated protein A) هوَ بروتين يُشَفر بواسطة جين VAPA في الإنسان.[1][2][3]
الوظيفة
المراجع
- Weir ML، Klip A، Trimble WS (سبتمبر 1998). "Identification of a human homologue of the vesicle-associated membrane protein (VAMP)-associated protein of 33 kDa (VAP-33): a broadly expressed protein that binds to VAMP". Biochem J. ج. 333 ع. 2: 247–51. DOI:10.1042/bj3330247. PMC:1219579. PMID:9657962.
- "Entrez Gene: VAPA VAMP (vesicle-associated membrane protein)-associated protein A, 33kDa". مؤرشف من الأصل في 2010-12-05.
- Nishimura Y، Hayashi M، Inada H، Tanaka T (فبراير 1999). "Molecular cloning and characterization of mammalian homologues of vesicle-associated membrane protein-associated (VAMP-associated) proteins". Biochem Biophys Res Commun. ج. 254 ع. 1: 21–6. DOI:10.1006/bbrc.1998.9876. PMID:9920726.
قراءة متعمقة
- Lapierre LA، Tuma PL، Navarre J، وآخرون (1999). "VAP-33 localizes to both an intracellular vesicle population and with occludin at the tight junction". J. Cell Sci. ج. 112 ع. 21: 3723–32. PMID:10523508.
- Tu H، Gao L، Shi ST، وآخرون (1999). "Hepatitis C virus RNA polymerase and NS5A complex with a SNARE-like protein". Virology. ج. 263 ع. 1: 30–41. DOI:10.1006/viro.1999.9893. PMID:10544080.
- Weir ML، Xie H، Klip A، Trimble WS (2001). "VAP-A binds promiscuously to both v- and tSNAREs". Biochem. Biophys. Res. Commun. ج. 286 ع. 3: 616–21. DOI:10.1006/bbrc.2001.5437. PMID:11511104.
- Wyles JP، McMaster CR، Ridgway ND (2002). "Vesicle-associated membrane protein-associated protein-A (VAP-A) interacts with the oxysterol-binding protein to modify export from the endoplasmic reticulum". J. Biol. Chem. ج. 277 ع. 33: 29908–18. DOI:10.1074/jbc.M201191200. PMID:12023275.
- 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. Bibcode:2002PNAS...9916899M. DOI:10.1073/pnas.242603899. PMC:139241. PMID:12477932.
- Matsuda A، Suzuki Y، Honda G، وآخرون (2003). "Large-scale identification and characterization of human genes that activate NF-kappaB and MAPK signaling pathways". Oncogene. ج. 22 ع. 21: 3307–18. DOI:10.1038/sj.onc.1206406. PMID:12761501.
- Ota T، Suzuki Y، Nishikawa T، وآخرون (2004). "Complete sequencing and characterization of 21,243 full-length human cDNAs". Nat. Genet. ج. 36 ع. 1: 40–5. DOI:10.1038/ng1285. PMID:14702039.
- Gao L، Aizaki H، He JW، Lai MM (2004). "Interactions between viral nonstructural proteins and host protein hVAP-33 mediate the formation of hepatitis C virus RNA replication complex on lipid raft". J. Virol. ج. 78 ع. 7: 3480–8. DOI:10.1128/JVI.78.7.3480-3488.2004. PMC:371042. PMID:15016871.
- Evans MJ، Rice CM، Goff SP (2004). "Phosphorylation of hepatitis C virus nonstructural protein 5A modulates its protein interactions and viral RNA replication". Proc. Natl. Acad. Sci. U.S.A. ج. 101 ع. 35: 13038–43. Bibcode:2004PNAS..10113038E. DOI:10.1073/pnas.0405152101. PMC:516513. PMID:15326295.
- Suzuki Y، Yamashita R، Shirota M، وآخرون (2004). "Sequence comparison of human and mouse genes reveals a homologous block structure in the promoter regions". Genome Res. ج. 14 ع. 9: 1711–8. DOI:10.1101/gr.2435604. PMC:515316. PMID:15342556.
- 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. Bibcode:2005Natur.437.1173R. DOI:10.1038/nature04209. PMID:16189514.
- Hamamoto I، Nishimura Y، Okamoto T، وآخرون (2005). "Human VAP-B is involved in hepatitis C virus replication through interaction with NS5A and NS5B". J. Virol. ج. 79 ع. 21: 13473–82. DOI:10.1128/JVI.79.21.13473-13482.2005. PMC:1262604. PMID:16227268.
- Kawano M، Kumagai K، Nishijima M، Hanada K (2006). "Efficient trafficking of ceramide from the endoplasmic reticulum to the Golgi apparatus requires a VAMP-associated protein-interacting FFAT motif of CERT". J. Biol. Chem. ج. 281 ع. 40: 30279–88. DOI:10.1074/jbc.M605032200. PMID:16895911.
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- بوابة الكيمياء الحيوية
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