ABL2

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Template:Short description Template:Cs1 config An Error has occurred retrieving Wikidata item for infobox Tyrosine-protein kinase ABL2 also known as Abelson-related gene (Arg) is an enzyme that in humans is encoded by the ABL2 gene.[1][2]

Function

ABL2 is a cytoplasmic tyrosine kinase which is closely related to but distinct from ABL1. The similarity of the proteins includes the tyrosine kinase domains and extends amino-terminal to include the SH2 and SH3 domains. ABL2 is expressed in both normal and tumor cells. The expression of ABL2 gene is higher in KRAS mutant non-small cell lung cancer.[3] The ABL2 gene product is expressed as two variants bearing different amino termini, both approximately 12-kb in length.[2]

Interactions

ABL2 has been shown to interact with three proteins: Abl gene,[4] catalase,[5] and SORBS2.[6] The protein Abl gene is also known as abelson murine leukemia viral oncogene homolog 1 and is a protein that is encoded by the human ABL1 gene.[7] Catalase is a common enzyme that catalyzes the decomposition of hydrogen peroxide to water and oxygen.[8] SORBS2 is also known as Sorbin and SH3 domain-containing protein 2 and is a protein encoded by the SORBS2 gene in humans.[2][6][9]

References

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  1. ^ Page Module:Citation/CS1/styles.css has no content.Kruh GD, King CR, Kraus MH, Popescu NC, Amsbaugh SC, McBride WO, et al. (December 1986). "A novel human gene closely related to the abl proto-oncogene". Science. 234 (4783): 1545–1548. Bibcode:1986Sci...234.1545K. doi:10.1126/science.3787260. PMID 3787260.
  2. ^ a b c Page Module:Citation/CS1/styles.css has no content."Entrez Gene: ABL2 v-abl Abelson murine leukemia viral oncogene homolog 2 (arg, Abelson-related gene)".
  3. ^ Page Module:Citation/CS1/styles.css has no content.Nagy Á, Pongor LS, Szabó A, Santarpia M, Győrffy B (February 2017). "KRAS driven expression signature has prognostic power superior to mutation status in non-small cell lung cancer". International Journal of Cancer. 140 (4): 930–937. doi:10.1002/ijc.30509. PMC 5299512. PMID 27859136.
  4. ^ Page Module:Citation/CS1/styles.css has no content.Cao C, Leng Y, Li C, Kufe D (April 2003). "Functional interaction between the c-Abl and Arg protein-tyrosine kinases in the oxidative stress response". The Journal of Biological Chemistry. 278 (15): 12961–12967. doi:10.1074/jbc.M300058200. PMID 12569093.
  5. ^ Page Module:Citation/CS1/styles.css has no content.Cao C, Leng Y, Kufe D (August 2003). "Catalase activity is regulated by c-Abl and Arg in the oxidative stress response". The Journal of Biological Chemistry. 278 (32): 29667–29675. doi:10.1074/jbc.M301292200. PMID 12777400.
  6. ^ a b Page Module:Citation/CS1/styles.css has no content.Wang B, Golemis EA, Kruh GD (July 1997). "ArgBP2, a multiple Src homology 3 domain-containing, Arg/Abl-interacting protein, is phosphorylated in v-Abl-transformed cells and localized in stress fibers and cardiocyte Z-disks". The Journal of Biological Chemistry. 272 (28): 17542–17550. doi:10.1074/jbc.272.28.17542. hdl:20.500.12613/9174. PMID 9211900.
  7. ^ Page Module:Citation/CS1/styles.css has no content.Szczylik C, Skorski T, Nicolaides NC, Manzella L, Malaguarnera L, Venturelli D, et al. (August 1991). "Selective inhibition of leukemia cell proliferation by BCR-ABL antisense oligodeoxynucleotides". Science. 253 (5019): 562–565. Bibcode:1991Sci...253..562S. doi:10.1126/science.1857987. hdl:11380/745303. PMID 1857987.
  8. ^ Page Module:Citation/CS1/styles.css has no content.Chelikani P, Fita I, Loewen PC (January 2004). "Diversity of structures and properties among catalases". Cellular and Molecular Life Sciences. 61 (2): 192–208. doi:10.1007/s00018-003-3206-5. hdl:10261/111097. PMC 11138816. PMID 14745498. S2CID 4411482.
  9. ^ Page Module:Citation/CS1/styles.css has no content.Nagase T, Ishikawa K, Suyama M, Kikuno R, Miyajima N, Tanaka A, et al. (October 1998). "Prediction of the coding sequences of unidentified human genes. XI. The complete sequences of 100 new cDNA clones from brain which code for large proteins in vitro". DNA Research. 5 (5): 277–286. doi:10.1093/dnares/5.5.277. PMID 9872452.

Further reading

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