PIGT
من أرابيكا، الموسوعة العربية الحرة
المزيد من اللغات
المزيد من الإجراءات
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.
