SH3BP1
SH3 domain-binding protein 1 is a protein that in humans is encoded by the SH3BP1 gene.[1][2][3]
References
References
- ↑ Dunham I, Shimizu N, Roe BA, Chissoe S, Hunt AR, Collins JE, Bruskiewich R, Beare DM, Clamp M, Smink LJ, Ainscough R, Almeida JP, Babbage A, Bagguley C, Bailey J, Barlow K, Bates KN, Beasley O, Bird CP, Blakey S, Bridgeman AM, Buck D, Burgess J, Burrill WD, O’Brien KP, et al. (Dec 1999). “The DNA sequence of human chromosome 22”. Nature. 402 (6761): 489–95. doi:10.1038/990031. PMID 10591208.
- ↑ Scott MP, Zappacosta F, Kim EY, Annan RS, Miller WT (Jul 2002). “Identification of novel SH3 domain ligands for the Src family kinase Hck. Wiskott-Aldrich syndrome protein (WASP), WASP-interacting protein (WIP), and ELMO1”. J Biol Chem. 277 (31): 28238–46. doi:10.1074/jbc.M202783200. PMID 12029088.
- ↑ “Entrez Gene: SH3BP1 SH3-domain binding protein 1”.
Further reading
Further reading
- Cicchetti P, Mayer BJ, Thiel G, Baltimore D (1992). “Identification of a protein that binds to the SH3 region of Abl and is similar to Bcr and GAP-rho”. Science. 257 (5071): 803–6. doi:10.1126/science.1379745. PMID 1379745.
- Zhang B, Zheng Y (1998). “Regulation of RhoA GTP hydrolysis by the GTPase-activating proteins p190, p50RhoGAP, Bcr, and 3BP-1”. Biochemistry. 37 (15): 5249–57. doi:10.1021/bi9718447. PMID 9548756.
- Västrik I, Eickholt BJ, Walsh FS, et al. (2000). “Sema3A-induced growth-cone collapse is mediated by Rac1 amino acids 17-32”. Curr. Biol. 9 (18): 991–8. doi:10.1016/S0960-9822(99)80447-3. PMID 10508610.
- So CW, So CK, Cheung N, et al. (2000). “The interaction between EEN and Abi-1, two MLL fusion partners, and synaptojanin and dynamin: implications for leukaemogenesis”. Leukemia. 14 (4): 594–601. doi:10.1038/sj.leu.2401692. PMID 10764144.
- Strausberg RL, Feingold EA, Grouse LH, et al. (2003). “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. doi:10.1073/pnas.242603899. PMC 139241. PMID 12477932.
- Ota T, Suzuki Y, Nishikawa T, et al. (2004). “Complete sequencing and characterization of 21,243 full-length human cDNAs”. Nat. Genet. 36 (1): 40–5. doi:10.1038/ng1285. PMID 14702039.
- Collins JE, Wright CL, Edwards CA, et al. (2005). “A genome annotation-driven approach to cloning the human ORFeome”. Genome Biol. 5 (10): R84. doi:10.1186/gb-2004-5-10-r84. PMC 545604. PMID 15461802.
- Gerhard DS, Wagner L, Feingold EA, et al. (2004). “The Status, Quality, and Expansion of the NIH Full-Length cDNA Project: The Mammalian Gene Collection (MGC)”. Genome Res. 14 (10B): 2121–7. doi:10.1101/gr.2596504. PMC 528928. PMID 15489334.
- Rual JF, Venkatesan K, Hao T, et al. (2005). “Towards a proteome-scale map of the human protein-protein interaction network”. Nature. 437 (7062): 1173–8. doi:10.1038/nature04209. PMID 16189514.
Looking for the patient version?
© 2026 MyEClinic – IFTM Institut für Telematik in der Medizin GmbH