Biology:UBR1
From HandWiki
Short description: Mammalian protein found in Homo sapiens
 Generic protein structure example |
The human gene UBR1 encodes the enzyme ubiquitin-protein ligase E3 component n-recognin 1.[1][2]
The N-end rule pathway is one proteolytic pathway of the ubiquitin system. The recognition component of this pathway, encoded by this gene, binds to a destabilizing N-terminal residue of a substrate protein and participates in the formation of a substrate-linked multiubiquitin chain. This leads to the eventual degradation of the substrate protein. The protein described in this record has a RING-type zinc finger and a UBR-type zinc finger. Mutations in this gene have been associated with Johanson-Blizzard syndrome.[2]
References
- ↑ "The mouse and human genes encoding the recognition component of the N-end rule pathway". Proc Natl Acad Sci U S A 95 (14): 7898–903. Aug 1998. doi:10.1073/pnas.95.14.7898. PMID 9653112. Bibcode: 1998PNAS...95.7898K.
- ↑ 2.0 2.1 "Entrez Gene: UBR1 ubiquitin protein ligase E3 component n-recognin 1". https://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=197131.
Further reading
- Varshavsky A (1996). "The N-end rule: functions, mysteries, uses". Proc. Natl. Acad. Sci. U.S.A. 93 (22): 12142–9. doi:10.1073/pnas.93.22.12142. PMID 8901547. Bibcode: 1996PNAS...9312142V.
- "A primary expression map of the chromosome 15q15 region containing the recessive form of limb-girdle muscular dystrophy (LGMD2A) gene". Hum. Mol. Genet. 4 (4): 717–25. 1995. doi:10.1093/hmg/4.4.717. PMID 7633422.
- "Congenital Dyserythropoietic Anemia Type I Is Caused by Mutations in Codanin-1". Am. J. Hum. Genet. 71 (6): 1467–74. 2003. doi:10.1086/344781. PMID 12434312.
- "Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences". Proc. Natl. Acad. Sci. U.S.A. 99 (26): 16899–903. 2003. doi:10.1073/pnas.242603899. PMID 12477932. Bibcode: 2002PNAS...9916899M.
- "Complete sequencing and characterization of 21,243 full-length human cDNAs". Nat. Genet. 36 (1): 40–5. 2004. doi:10.1038/ng1285. PMID 14702039.
- "Large-scale characterization of HeLa cell nuclear phosphoproteins". Proc. Natl. Acad. Sci. U.S.A. 101 (33): 12130–5. 2004. doi:10.1073/pnas.0404720101. PMID 15302935. Bibcode: 2004PNAS..10112130B.
- "RECQL4, mutated in the Rothmund-Thomson and RAPADILINO syndromes, interacts with ubiquitin ligases UBR1 and UBR2 of the N-end rule pathway". Hum. Mol. Genet. 13 (20): 2421–30. 2005. doi:10.1093/hmg/ddh269. PMID 15317757.
- "The Status, Quality, and Expansion of the NIH Full-Length cDNA Project: The Mammalian Gene Collection (MGC)". Genome Res. 14 (10B): 2121–7. 2004. doi:10.1101/gr.2596504. PMID 15489334.
- "Regulation of protein catabolism by muscle-specific and cytokine-inducible ubiquitin ligase E3alpha-II during cancer cachexia". Cancer Res. 64 (22): 8193–8. 2005. doi:10.1158/0008-5472.CAN-04-2102. PMID 15548684.
- "A Family of Mammalian E3 Ubiquitin Ligases That Contain the UBR Box Motif and Recognize N-Degrons". Mol. Cell. Biol. 25 (16): 7120–36. 2005. doi:10.1128/MCB.25.16.7120-7136.2005. PMID 16055722.
- "A human protein-protein interaction network: a resource for annotating the proteome". Cell 122 (6): 957–68. 2005. doi:10.1016/j.cell.2005.08.029. PMID 16169070.
- "Deficiency of UBR1, a ubiquitin ligase of the N-end rule pathway, causes pancreatic dysfunction, malformations and mental retardation (Johanson-Blizzard syndrome)". Nat. Genet. 37 (12): 1345–50. 2006. doi:10.1038/ng1681. PMID 16311597. https://authors.library.caltech.edu/55908/2/Fig1.pdf.
- "Spatiotemporal regulation of c-Fos by ERK5 and the E3 ubiquitin ligase UBR1, and its biological role". Mol. Cell 24 (1): 63–75. 2006. doi:10.1016/j.molcel.2006.08.005. PMID 17018293.
- "Negative Regulation of ISG15 E3 ligase EFP through its autoISGylation". Biochem. Biophys. Res. Commun. 354 (1): 321–7. 2007. doi:10.1016/j.bbrc.2006.12.210. PMID 17222803.
- "Involvement of Rabring7 in EGF receptor degradation as an E3 ligase". Biochem. Biophys. Res. Commun. 357 (4): 1058–64. 2007. doi:10.1016/j.bbrc.2007.04.052. PMID 17462600.
- "Thiazolidinediones modulate the expression of beta-catenin and other cell-cycle regulatory proteins by targeting the F-box proteins of Skp1-Cul1-F-box protein E3 ubiquitin ligase independently of peroxisome proliferator-activated receptor gamma". Mol. Pharmacol. 72 (3): 725–33. 2007. doi:10.1124/mol.107.035287. PMID 17569795. http://ntur.lib.ntu.edu.tw/bitstream/246246/163063/1/23.pdf.
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