PDIA2
PDIA2 (Protein disulfide isomerase family A member 2) هوَ بروتين يُشَفر بواسطة جين PDIA2 في الإنسان.[1]
الوظيفة
المراجع
- "Entrez Gene: Protein disulfide isomerase family A member 2". مؤرشف من الأصل في 2014-10-10. اطلع عليه بتاريخ 2017-12-20.
قراءة متعمقة
- VanderWaal RP، Spitz DR، Griffith CL، Higashikubo R، Roti Roti JL (2002). "Evidence that protein disulfide isomerase (PDI) is involved in DNA-nuclear matrix anchoring". J. Cell. Biochem. ج. 85 ع. 4: 689–702. DOI:10.1002/jcb.10169. PMID:11968009.
- Ko HS، Uehara T، Nomura Y (2002). "Role of ubiquilin associated with protein-disulfide isomerase in the endoplasmic reticulum in stress-induced apoptotic cell death". J. Biol. Chem. ج. 277 ع. 38: 35386–92. DOI:10.1074/jbc.M203412200. PMID:12095988.
- Lumb RA، Bulleid NJ (2002). "Is protein disulfide isomerase a redox-dependent molecular chaperone?". EMBO J. ج. 21 ع. 24: 6763–70. PMC:139105. PMID:12485997.
- Clissold PM، Bicknell R (2003). "The thioredoxin-like fold: hidden domains in protein disulfide isomerases and other chaperone proteins". BioEssays. ج. 25 ع. 6: 603–11. DOI:10.1002/bies.10287. PMID:12766950.
- Pirneskoski A، Klappa P، Lobell M، Williamson RA، Byrne L، Alanen HI، Salo KE، Kivirikko KI، Freedman RB، Ruddock LW (2004). "Molecular characterization of the principal substrate binding site of the ubiquitous folding catalyst protein disulfide isomerase". J. Biol. Chem. ج. 279 ع. 11: 10374–81. DOI:10.1074/jbc.M312193200. PMID:14684740.
- Spooner RA، Watson PD، Marsden CJ، Smith DC، Moore KA، Cook JP، Lord JM، Roberts LM (2004). "Protein disulphide-isomerase reduces ricin to its A and B chains in the endoplasmic reticulum". Biochem. J. ج. 383 ع. Pt 2: 285–93. DOI:10.1042/BJ20040742. PMC:1134069. PMID:15225124.
- Li SJ، Hong XG، Shi YY، Li H، Wang CC (2006). "Annular arrangement and collaborative actions of four domains of protein-disulfide isomerase: a small angle X-ray scattering study in solution". J. Biol. Chem. ج. 281 ع. 10: 6581–8. DOI:10.1074/jbc.M508422200. PMID:16407203.
- Otsu M، Bertoli G، Fagioli C، Guerini-Rocco E، Nerini-Molteni S، Ruffato E، Sitia R (2006). "Dynamic retention of Ero1alpha and Ero1beta in the endoplasmic reticulum by interactions with PDI and ERp44". Antioxid. Redox Signal. ج. 8 ع. 3–4: 274–82. DOI:10.1089/ars.2006.8.274. PMID:16677073.
- Park B، Lee S، Kim E، Cho K، Riddell SR، Cho S، Ahn K (2006). "Redox regulation facilitates optimal peptide selection by MHC class I during antigen processing". Cell. ج. 127 ع. 2: 369–82. DOI:10.1016/j.cell.2006.08.041. PMID:17055437.
- بوابة علم الأحياء الخلوي والجزيئي
- بوابة طب
- بوابة الكيمياء الحيوية
This article is issued from Wikipedia. The text is licensed under Creative Commons - Attribution - Sharealike. Additional terms may apply for the media files.