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PIGT
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An Error has occured retrieving Wikidata item for infobox PIGT (Phosphatidylinositol glycan anchor biosynthesis class T) هوَ بروتين يُشَفر بواسطة جين PIGT في الإنسان.[1][2][3][3]
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
- ^ Ohishi K، Inoue N، Kinoshita T (أغسطس 2001). "PIG-S and PIG-T, essential for GPI anchor attachment to proteins, form a complex with GAA1 and GPI8". EMBO J. ج. 20 ع. 15: 4088–98. DOI:10.1093/emboj/20.15.4088. PMC:149153. PMID:11483512.
- ^ Vainauskas S، Menon AK (أبريل 2005). "Endoplasmic reticulum localization of Gaa1 and PIG-T, subunits of the glycosylphosphatidylinositol transamidase complex". J Biol Chem. ج. 280 ع. 16: 16402–9. DOI:10.1074/jbc.M414253200. PMID:15713669.
- ^ أ ب "Entrez Gene: PIGT phosphatidylinositol glycan anchor biosynthesis, class T". مؤرشف من الأصل في 2010-12-05.
قراءة متعمقة
- Eisenhaber B، Maurer-Stroh S، Novatchkova M، وآخرون (2003). "Enzymes and auxiliary factors for GPI lipid anchor biosynthesis and post-translational transfer to proteins". BioEssays. ج. 25 ع. 4: 367–85. DOI:10.1002/bies.10254. PMID:12655644.
- Maruyama K، Sugano S (1994). "Oligo-capping: a simple method to replace the cap structure of eukaryotic mRNAs with oligoribonucleotides". Gene. ج. 138 ع. 1–2: 171–4. DOI:10.1016/0378-1119(94)90802-8. PMID:8125298.
- Suzuki Y، Yoshitomo-Nakagawa K، Maruyama K، وآخرون (1997). "Construction and characterization of a full length-enriched and a 5'-end-enriched cDNA library". Gene. ج. 200 ع. 1–2: 149–56. DOI:10.1016/S0378-1119(97)00411-3. PMID:9373149.
- Lai CH، Chou CY، Ch'ang LY، وآخرون (2000). "Identification of novel human genes evolutionarily conserved in Caenorhabditis elegans by comparative proteomics". Genome Res. ج. 10 ع. 5: 703–13. DOI:10.1101/gr.10.5.703. PMC:310876. PMID:10810093.
- Ohishi K، Inoue N، Kinoshita T (2001). "PIG-S and PIG-T, essential for GPI anchor attachment to proteins, form a complex with GAA1 and GPI8". EMBO J. ج. 20 ع. 15: 4088–98. DOI:10.1093/emboj/20.15.4088. PMC:149153. PMID:11483512.
- Yu Y، Zhang C، Zhou G، وآخرون (2001). "Gene expression profiling in human fetal liver and identification of tissue- and developmental-stage-specific genes through compiled expression profiles and efficient cloning of full-length cDNAs". Genome Res. ج. 11 ع. 8: 1392–403. DOI:10.1101/gr.175501. PMC:311073. PMID:11483580.
- Fossey SC، Mychaleckyj JC، Pendleton JK، وآخرون (2001). "A high-resolution 6.0-megabase transcript map of the type 2 diabetes susceptibility region on human chromosome 20". Genomics. ج. 76 ع. 1–3: 45–57. DOI:10.1006/geno.2001.6584. PMID:11549316.
- Deloukas P، Matthews LH، Ashurst J، وآخرون (2002). "The DNA sequence and comparative analysis of human chromosome 20". Nature. ج. 414 ع. 6866: 865–71. Bibcode:2001Natur.414..865D. DOI:10.1038/414865a. PMID:11780052.
- Vainauskas S، Maeda Y، Kurniawan H، وآخرون (2002). "Structural requirements for the recruitment of Gaa1 into a functional glycosylphosphatidylinositol transamidase complex". J. Biol. Chem. ج. 277 ع. 34: 30535–42. DOI:10.1074/jbc.M205402200. PMID:12052837.
- 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.
- Ohishi K، Nagamune K، Maeda Y، Kinoshita T (2003). "Two subunits of glycosylphosphatidylinositol transamidase, GPI8 and PIG-T, form a functionally important intermolecular disulfide bridge". J. Biol. Chem. ج. 278 ع. 16: 13959–67. DOI:10.1074/jbc.M300586200. PMID:12582175.
- Hong Y، Ohishi K، Kang JY، وآخرون (2004). "Human PIG-U and yeast Cdc91p are the fifth subunit of GPI transamidase that attaches GPI-anchors to proteins". Mol. Biol. Cell. ج. 14 ع. 5: 1780–9. DOI:10.1091/mbc.E02-12-0794. PMC:165076. PMID:12802054.
- Clark HF، Gurney AL، Abaya E، وآخرون (2003). "The secreted protein discovery initiative (SPDI), a large-scale effort to identify novel human secreted and transmembrane proteins: a bioinformatics assessment". Genome Res. ج. 13 ع. 10: 2265–70. DOI:10.1101/gr.1293003. PMC:403697. PMID:12975309.
- 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.
- Otsuki T، Ota T، Nishikawa T، وآخرون (2007). "Signal sequence and keyword trap in silico for selection of full-length human cDNAs encoding secretion or membrane proteins from oligo-capped cDNA libraries". DNA Res. ج. 12 ع. 2: 117–26. DOI:10.1093/dnares/12.2.117. PMID:16303743.
- 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.
- Li HL، Li Z، Qin LY، وآخرون (2006). "The novel neurotrophin-regulated neuronal development-associated protein, NDAP, mediates apoptosis". FEBS Lett. ج. 580 ع. 7: 1723–8. DOI:10.1016/j.febslet.2006.02.022. PMID:16516892.
