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VPS4B
An Error has occured retrieving Wikidata item for infobox VPS4B (Vacuolar protein sorting 4 homolog B) هوَ بروتين يُشَفر بواسطة جين VPS4B في الإنسان.[1][2]
الوظيفة
![[أيقونة]](/%D9%85%D9%84%D9%81:Crystal_xedit.svg){kind=small} | هذا القسم فارغ أو غير مكتمل. ساهم في توسيعه. (يوليو 2018) |
الأهمية السريرية
| هذا القسم فارغ أو غير مكتمل. ساهم في توسيعه. (يوليو 2018) |
المراجع
- ^ Scheuring S، Rohricht RA، Schoning-Burkhardt B، Beyer A، Muller S، Abts HF، Kohrer K (سبتمبر 2001). "Mammalian cells express two VPS4 proteins both of which are involved in intracellular protein trafficking". J Mol Biol. ج. 312 ع. 3: 469–80. DOI:10.1006/jmbi.2001.4917. PMID:11563910.
- ^ "Entrez Gene: VPS4B vacuolar protein sorting 4 homolog B (S. cerevisiae)". مؤرشف من الأصل في 2010-12-05.
قراءة متعمقة
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- Mao M، Fu G، Wu JS، وآخرون (1998). "Identification of genes expressed in human CD34+ hematopoietic stem/progenitor cells by expressed sequence tags and efficient full-length cDNA cloning". Proc. Natl. Acad. Sci. U.S.A. ج. 95 ع. 14: 8175–80. DOI:10.1073/pnas.95.14.8175. PMC:20949. PMID:9653160.
- Scheuring S، Bodor O، Röhricht RA، وآخرون (1999). "Cloning, characterisation, and functional expression of the Mus musculus SKD1 gene in yeast demonstrates that the mouse SKD1 and the yeast VPS4 genes are orthologues and involved in intracellular protein trafficking". Gene. ج. 234 ع. 1: 149–59. DOI:10.1016/S0378-1119(99)00163-8. PMID:10393249.
- Bishop N، Woodman P (2000). "ATPase-defective Mammalian VPS4 Localizes to Aberrant Endosomes and Impairs Cholesterol Trafficking". Mol. Biol. Cell. ج. 11 ع. 1: 227–39. DOI:10.1091/mbc.11.1.227. PMC:14770. PMID:10637304.
- Zhang QH، Ye M، Wu XY، وآخرون (2001). "Cloning and Functional Analysis of cDNAs with Open Reading Frames for 300 Previously Undefined Genes Expressed in CD34+ Hematopoietic Stem/Progenitor Cells". Genome Res. ج. 10 ع. 10: 1546–60. DOI:10.1101/gr.140200. PMC:310934. PMID:11042152.
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- 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.
- Beyer A، Scheuring S، Müller S، وآخرون (2003). "Comparative sequence and expression analyses of four mammalian VPS4 genes". Gene. ج. 305 ع. 1: 47–59. DOI:10.1016/S0378-1119(02)01205-2. PMID:12594041.
- Strack B، Calistri A، Craig S، وآخرون (2003). "AIP1/ALIX is a binding partner for HIV-1 p6 and EIAV p9 functioning in virus budding". Cell. ج. 114 ع. 6: 689–99. DOI:10.1016/S0092-8674(03)00653-6. PMID:14505569.
- von Schwedler UK، Stuchell M، Müller B، وآخرون (2003). "The protein network of HIV budding". Cell. ج. 114 ع. 6: 701–13. DOI:10.1016/S0092-8674(03)00714-1. PMID:14505570.
- Fujita H، Umezuki Y، Imamura K، وآخرون (2005). "Mammalian class E Vps proteins, SBP1 and mVps2/CHMP2A, interact with and regulate the function of an AAA-ATPase SKD1/Vps4B". J. Cell Sci. ج. 117 ع. Pt 14: 2997–3009. DOI:10.1242/jcs.01170. PMID:15173323.
- 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.
- Katoh K، Suzuki H، Terasawa Y، وآخرون (2006). "The penta-EF-hand protein ALG-2 interacts directly with the ESCRT-I component TSG101, and Ca2+-dependently co-localizes to aberrant endosomes with dominant-negative AAA ATPase SKD1/Vps4B". Biochem. J. ج. 391 ع. Pt 3: 677–85. DOI:10.1042/BJ20050398. PMC:1276969. PMID:16004603.
- Takasu H، Jee JG، Ohno A، وآخرون (2005). "Structural characterization of the MIT domain from human Vps4b". Biochem. Biophys. Res. Commun. ج. 334 ع. 2: 460–5. DOI:10.1016/j.bbrc.2005.06.110. PMID:16018968.
- Scott A، Chung HY، Gonciarz-Swiatek M، وآخرون (2005). "Structural and mechanistic studies of VPS4 proteins". EMBO J. ج. 24 ع. 20: 3658–69. DOI:10.1038/sj.emboj.7600818. PMC:1276703. PMID:16193069.
- Kimura K، Wakamatsu A، Suzuki Y، وآخرون (2006). "Diversification of transcriptional modulation: Large-scale identification and characterization of putative alternative promoters of human genes". Genome Res. ج. 16 ع. 1: 55–65. DOI:10.1101/gr.4039406. PMC:1356129. PMID:16344560.
- Welsch S، Habermann A، Jäger S، وآخرون (2007). "Ultrastructural analysis of ESCRT proteins suggests a role for endosome-associated tubular-vesicular membranes in ESCRT function". Traffic. ج. 7 ع. 11: 1551–66. DOI:10.1111/j.1600-0854.2006.00489.x. PMID:17014699.
- Olsen JV، Blagoev B، Gnad F، وآخرون (2006). "Global, in vivo, and site-specific phosphorylation dynamics in signaling networks". Cell. ج. 127 ع. 3: 635–48. DOI:10.1016/j.cell.2006.09.026. PMID:17081983.
- Lambert C، Döring T، Prange R (2007). "Hepatitis B Virus Maturation Is Sensitive to Functional Inhibition of ESCRT-III, Vps4, and γ2-Adaptin". J. Virol. ج. 81 ع. 17: 9050–60. DOI:10.1128/JVI.00479-07. PMC:1951427. PMID:17553870.
