PLEKHO1 – Wikipedia

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Protein-coding gene in the species Homo sapiens

Pleckstrin homology domain-containing family O member 1 is a protein that in humans is encoded by the PLEKHO1 gene.[5][6]

Interactions[edit]

PLEKHO1 has been shown to interact with Casein kinase 2, alpha 1[5] and SMURF1.[7]

References[edit]

  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000023902 – Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000015745 – Ensembl, May 2017
  3. ^ “Human PubMed Reference:”. National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. ^ “Mouse PubMed Reference:”. National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. ^ a b Bosc DG, Graham KC, Saulnier RB, Zhang C, Prober D, Gietz RD, Litchfield DW (May 2000). “Identification and characterization of CKIP-1, a novel pleckstrin homology domain-containing protein that interacts with protein kinase CK2”. The Journal of Biological Chemistry. 275 (19): 14295–306. doi:10.1074/jbc.275.19.14295. PMID 10799509.
  6. ^ “Entrez Gene: PLEKHO1 pleckstrin homology domain containing, family O member 1”.
  7. ^ Lu K, Yin X, Weng T, Xi S, Li L, Xing G, Cheng X, Yang X, Zhang L, He F (August 2008). “Targeting WW domains linker of HECT-type ubiquitin ligase Smurf1 for activation by CKIP-1”. Nature Cell Biology. 10 (8): 994–1002. doi:10.1038/ncb1760. PMID 18641638. S2CID 19216909.

Further reading[edit]