Biology:NUFIP2

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A representation of the 3D structure of the protein myoglobin showing turquoise α-helices.
Generic protein structure example

Nuclear fragile X mental retardation-interacting protein 2 is a protein that in humans is encoded by the NUFIP2 gene.[1][2][3]


Interactions

NUFIP2 has been shown to interact with FMR1 and Roquin-1.[4][1]

References

  1. 1.0 1.1 "82-FIP, a novel FMRP (fragile X mental retardation protein) interacting protein, shows a cell cycle-dependent intracellular localization". Hum Mol Genet 12 (14): 1689–98. Jul 2003. doi:10.1093/hmg/ddg181. PMID 12837692. 
  2. "The structure of the N-terminal domain of the fragile X mental retardation protein: a platform for protein-protein interaction". Structure 14 (1): 21–31. Jan 2006. doi:10.1016/j.str.2005.09.018. PMID 16407062. 
  3. "Entrez Gene: NUFIP2 nuclear fragile X mental retardation protein interacting protein 2". https://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=57532. 
  4. Rehage, Nina (2018). "Binding of NUFIP2 to Roquin promotes recognition and regulation of ICOS mRNA". Nature Communications 9 (1): 299. doi:10.1038/s41467-017-02582-1. PMID 29352114. Bibcode2018NatCo...9..299R. 

Further reading