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CD2BP2  -  CD2 (cytoplasmic tail) binding protein 2

Homo sapiens

Synonyms: CD2 antigen cytoplasmic tail-binding protein 2, CD2 cytoplasmic domain-binding protein 2, CD2 tail-binding protein 2, FWP010, KIAA1178, ...
 
 
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Disease relevance of CD2BP2

  • Histological diagnoses were subdivided into keratosis without dysplasia (KWD), with mild dysplasia (LIN 1), with moderate dysplasia (LIN 2), and with severe dysplasia or carcinoma in situ (LIN 3) [1].
  • The frequency of associated invasive carcinomas (ductal and lobular) increased from 14% in LIN 1 to 23% in LIN 3 [2].
  • Remarkably, while the frequency of invasive lobular carcinoma increased dramatically from 11% in LIN 1 to 86% in LIN 3, the frequency of invasive ductal carcinoma markedly decreased with advancing grade of LIN from 89% in LIN 1 to 14% in LIN 3 [2].
 

High impact information on CD2BP2

  • NMR analysis shows that the Fyn but not the Lck tyrosine kinase SH3 domain competes with CD2BP2 GYF-domain binding to the same CD2 proline-rich sequence in vitro [3].
  • An intracellular protein termed CD2 binding protein 2 (CD2BP2), which binds to a site containing two PPPGHR segments within the cytoplasmic region of CD2, was identified [4].
  • Mutagenesis and NMR analysis demonstrated that the CD2 binding region of CD2BP2 includes a 17-aa motif (GPY[orF]xxxxM[orV]xxWxxx GYF), also found in several yeast and Caenorhabditis elegans proteins of unknown function [4].
  • The GYF domain of CD2BP2 serves as an adapter that recognizes proline-rich sequences in intracellular proteins [5].
  • The colocalization of CD2BP2 and SmB proteins in the nucleus of Jurkat T cells and HeLa cells suggests a function of the GYF domain of CD2BP2 in mediating protein-protein interactions within the spliceosome [6].
 

Biological context of CD2BP2

  • Identical LOH patterns were determined in 100% of the LIN3 peritumoral cells, 60% of LIN2, 50% of LIN 1 and 25% of KWD [1].
 

Anatomical context of CD2BP2

  • Protein sequencing revealed that U5-52K is identical to the CD2BP2, which interacts with the cytoplasmic portion of the human T-cell surface protein CD2 [7].
  • CONCLUSIONS: KWD and LIN 1 can be successfully treated by stripping the mucous membrane, close follow-up, and a change in smoking habits [8].
 

Associations of CD2BP2 with chemical compounds

  • The latter subfamily comprises most GYF domains and is characterized by a shorter beta(1)-beta(2) loop and an aspartate instead of the tryptophan found at position 8 in CD2BP2-type GYF domains [9].
  • In this study, two bacterial isolates (LIN-1 and LIN-3) that can grow on gamma-HCH as a sole source of carbon and energy were isolated from an enrichment culture [10].
 

Other interactions of CD2BP2

  • Among the cases of LIN unassociated with invasive carcinoma, DIN was present in 75% of LIN 1, 75% of LIN 2, and 66% of LIN 3 cases [2].

References

  1. 3p21, 5q21, 9p21 and 17p13 allelic deletions accumulate in the dysplastic spectrum of laryngeal carcinogenesis and precede malignant transformation. Sanz-Ortega, J., Valor, C., Saez, M.C., Ortega, L., Sierra, E., Poch, J., Hernández, S., Sanz-Esponera, J. Histol. Histopathol. (2003) [Pubmed]
  2. Lobular intraepithelial neoplasia: previously unexplored aspects assessed in 775 cases and their clinical implications. Bratthauer, G.L., Tavassoli, F.A. Virchows Arch. (2002) [Pubmed]
  3. Dynamic interaction of CD2 with the GYF and the SH3 domain of compartmentalized effector molecules. Freund, C., Kühne, R., Yang, H., Park, S., Reinherz, E.L., Wagner, G. EMBO J. (2002) [Pubmed]
  4. Identification of a proline-binding motif regulating CD2-triggered T lymphocyte activation. Nishizawa, K., Freund, C., Li, J., Wagner, G., Reinherz, E.L. Proc. Natl. Acad. Sci. U.S.A. (1998) [Pubmed]
  5. Novel interaction partners of the CD2BP2-GYF domain. Kofler, M., Motzny, K., Beyermann, M., Freund, C. J. Biol. Chem. (2005) [Pubmed]
  6. Recognition sequences for the GYF domain reveal a possible spliceosomal function of CD2BP2. Kofler, M., Heuer, K., Zech, T., Freund, C. J. Biol. Chem. (2004) [Pubmed]
  7. The human U5 snRNP 52K protein (CD2BP2) interacts with U5-102K (hPrp6), a U4/U6.U5 tri-snRNP bridging protein, but dissociates upon tri-snRNP formation. Laggerbauer, B., Liu, S., Makarov, E., Vornlocher, H.P., Makarova, O., Ingelfinger, D., Achsel, T., Lührmann, R. RNA (2005) [Pubmed]
  8. Evolution of precancerous laryngeal lesions: a clinicopathologic study with long-term follow-up on 259 patients. Gallo, A., de Vincentiis, M., Della Rocca, C., Moi, R., Simonelli, M., Minni, A., Shaha, A.R. Head & neck. (2001) [Pubmed]
  9. The GYF domain. Kofler, M.M., Freund, C. FEBS J. (2006) [Pubmed]
  10. Biodegradation of gamma-hexachlorocyclohexane (lindane) and alpha-hexachlorocyclohexane in water and a soil slurry by a Pandoraea species. Okeke, B.C., Siddique, T., Arbestain, M.C., Frankenberger, W.T. J. Agric. Food Chem. (2002) [Pubmed]
 
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