UBR5

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Template:Short description Template:Cs1 config An Error has occurred retrieving Wikidata item for infobox E3 ubiquitin-protein ligase UBR5 is an enzyme that in humans is encoded by the UBR5 gene.[1][2][3]

Function

This gene encodes a progestin-induced protein, which belongs to the HECT (homology to E6-AP carboxyl terminus) family. The HECT family proteins function as E3 ubiquitin-protein ligases, targeting specific proteins for ubiquitin-mediated proteolysis. This gene is localized to chromosome 8q22 which is disrupted in a variety of cancers. This gene potentially has a role in regulation of cell proliferation or differentiation.[3]

Mutations in UBR5 have been associated with autism spectrum disorder.[4][5]

Interactions

UBR5 has been shown to interact with:

References

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  1. ^ Page Module:Citation/CS1/styles.css has no content.Callaghan MJ, Russell AJ, Woollatt E, Sutherland GR, Sutherland RL, Watts CK (December 1998). "Identification of a human HECT family protein with homology to the Drosophila tumor suppressor gene hyperplastic discs". Oncogene. 17 (26): 3479–3491. doi:10.1038/sj.onc.1202249. PMID 10030672. S2CID 19850921.
  2. ^ Page Module:Citation/CS1/styles.css has no content.Tasaki T, Mulder LC, Iwamatsu A, Lee MJ, Davydov IV, Varshavsky A, et al. (August 2005). "A family of mammalian E3 ubiquitin ligases that contain the UBR box motif and recognize N-degrons". Molecular and Cellular Biology. 25 (16): 7120–7136. doi:10.1128/MCB.25.16.7120-7136.2005. PMC 1190250. PMID 16055722.
  3. ^ a b Page Module:Citation/CS1/styles.css has no content."Entrez Gene: EDD1 E3 ubiquitin protein ligase, HECT domain containing, 1".
  4. ^ Page Module:Citation/CS1/styles.css has no content.Sabeh P, Dumas SA, Maios C, Daghar H, Korzeniowski M, Rousseau J, et al. (January 2025). "Heterozygous UBR5 variants result in a neurodevelopmental syndrome with developmental delay, autism, and intellectual disability". American Journal of Human Genetics. 112 (1): 75–86. doi:10.1016/j.ajhg.2024.11.009. PMC 11739880. PMID 39721588.
  5. ^ Page Module:Citation/CS1/styles.css has no content.Reuter MS, Salazar NB, Howe JL, Hoang N, Sarikaya E, Selvanayagam T, et al. (November 2025). "UBR5 loss-of-function variants in autism spectrum disorder and intellectual disability: case series and review of the literature". Npj Genomic Medicine. doi:10.1038/s41525-025-00536-x. hdl:10400.18/10782. PMID 41318701.
  6. ^ a b Page Module:Citation/CS1/styles.css has no content.Henderson MJ, Russell AJ, Hird S, Muñoz M, Clancy JL, Lehrbach GM, et al. (July 2002). "EDD, the human hyperplastic discs protein, has a role in progesterone receptor coactivation and potential involvement in DNA damage response". The Journal of Biological Chemistry. 277 (29): 26468–26478. doi:10.1074/jbc.M203527200. hdl:1885/64590. PMID 12011095.
  7. ^ Page Module:Citation/CS1/styles.css has no content.Eblen ST, Kumar NV, Shah K, Henderson MJ, Watts CK, Shokat KM, et al. (April 2003). "Identification of novel ERK2 substrates through use of an engineered kinase and ATP analogs". The Journal of Biological Chemistry. 278 (17): 14926–14935. doi:10.1074/jbc.M300485200. PMID 12594221.
  8. ^ Page Module:Citation/CS1/styles.css has no content.Honda Y, Tojo M, Matsuzaki K, Anan T, Matsumoto M, Ando M, et al. (February 2002). "Cooperation of HECT-domain ubiquitin ligase hHYD and DNA topoisomerase II-binding protein for DNA damage response". The Journal of Biological Chemistry. 277 (5): 3599–3605. doi:10.1074/jbc.M104347200. PMID 11714696.

Further reading

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