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1 to 11 of 11  Show
  1. 1
    "Gathering STYX: phosphatase-like form predicts functions for unique protein-interaction domains."
    Wishart M.J., Dixon J.E.
    Trends Biochem. Sci. 23:301-306(1998) [PubMed] [Europe PMC] [Abstract]
    Cited for: NUCLEOTIDE SEQUENCE [MRNA] (ISOFORM 1).
    Category: Sequences.
    Source: UniProtKB/Swiss-Prot (reviewed).

    This publication is cited by 1 and mapped to 1 other entries.

  2. 2
    Category: Sequences.
    Source: UniProtKB/Swiss-Prot (reviewed).

    This publication is cited by 3287 other entries.

  3. 3
    "The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)."
    The MGC Project Team
    Genome Res. 14:2121-2127(2004) [PubMed] [Europe PMC] [Abstract]
    Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA] (ISOFORM 1).
    Category: Sequences.
    Tissue: Skin.
    Source: UniProtKB/Swiss-Prot (reviewed).

    This publication is cited by 50481 other entries.

  4. 4
    Walker L.C., Morris C.M.
    Submitted (SEP-1999) to the EMBL/GenBank/DDBJ databases
    Cited for: NUCLEOTIDE SEQUENCE [MRNA] OF 46-313 (ISOFORMS 3; 4 AND 5).
    Category: Sequences.
    Source: UniProtKB/Swiss-Prot (reviewed).
  5. 5
    "Differential expression of PTPase RNAs resulting from K562 differentiation induced by PMA."
    Dayton M.A., Blanchard K.L.
    Submitted (JUL-1999) to the EMBL/GenBank/DDBJ databases
    Cited for: NUCLEOTIDE SEQUENCE [MRNA] OF 149-313 (ISOFORMS 2 AND 3).
    Category: Sequences.
    Source: UniProtKB/Swiss-Prot (reviewed).
  6. 6
    "The pseudophosphatase MK-STYX interacts with G3BP and decreases stress granule formation."
    Hinton S.D., Myers M.P., Roggero V.R., Allison L.A., Tonks N.K.
    Biochem. J. 427:349-357(2010) [PubMed] [Europe PMC] [Abstract]
    Cited for: FUNCTION, LACK OF CATALYTIC ACTIVITY, INTERACTION WITH G3BP1, MUTAGENESIS OF 245-PHE-SER-246.
    Category: Function, Pathology & Biotech, Interaction.
    Source: UniProtKB/Swiss-Prot (reviewed).

    This publication is cited by 1 and mapped to 8 other entries.

  7. 7
    "MK-STYX, a catalytically inactive phosphatase regulating mitochondrially dependent apoptosis."
    Niemi N.M., Lanning N.J., Klomp J.A., Tait S.W., Xu Y., Dykema K.J., Murphy L.O., Gaither L.A., Xu H.E., Furge K.A., Green D.R., MacKeigan J.P.
    Mol. Cell. Biol. 31:1357-1368(2011) [PubMed] [Europe PMC] [Abstract]
    Cited for: FUNCTION, SUBCELLULAR LOCATION.
    Category: Function, Subcellular Location.
    Source: UniProtKB/Swiss-Prot (reviewed).

    This publication is mapped to 2 other entries.

  8. 8
    "The pseudophosphatase MK-STYX inhibits stress granule assembly independently of Ser149 phosphorylation of G3BP-1."
    Barr J.E., Munyikwa M.R., Frazier E.A., Hinton S.D.
    FEBS J. 280:273-284(2013) [PubMed] [Europe PMC] [Abstract]
    Cited for: FUNCTION, LACK OF CATALYTIC ACTIVITY, MUTAGENESIS OF 245-PHE-SER-246.
    Category: Function, Pathology & Biotech.
    Source: UniProtKB/Swiss-Prot (reviewed).

    This publication is mapped to 9 other entries.

  9. 9
    "The pseudophosphatase MK-STYX physically and genetically interacts with the mitochondrial phosphatase PTPMT1."
    Niemi N.M., Sacoman J.L., Westrate L.M., Gaither L.A., Lanning N.J., Martin K.R., MacKeigan J.P.
    PLoS ONE 9:E93896-E93896(2014) [PubMed] [Europe PMC] [Abstract]
    Cited for: FUNCTION, INTERACTION WITH PTPMT1.
    Category: Function, Interaction.
    Source: UniProtKB/Swiss-Prot (reviewed).

    This publication is cited by 1 and mapped to 3 other entries.

  10. 10
    "MK-STYX Alters the Morphology of Primary Neurons, and Outgrowths in MK-STYX Overexpressing PC-12 Cells Develop a Neuronal Phenotype."
    Banks D.A., Dahal A., McFarland A.G., Flowers B.M., Stephens C.A., Swack B., Gugssa A., Anderson W.A., Hinton S.D.
    Front. Mol. Biosci. 4:76-76(2017) [PubMed] [Europe PMC] [Abstract]
    Cited for: FUNCTION.
    Category: Function.
    Source: UniProtKB/Swiss-Prot (reviewed).
  11. 11
    "Homozygous missense mutation in STYXL1 associated with moderate intellectual disability, epilepsy and behavioural complexities."
    Isrie M., Zamani Esteki M., Peeters H., Voet T., Van Houdt J., Van Paesschen W., Van Esch H.
    Eur J Med Genet 58:205-210(2015) [PubMed] [Europe PMC] [Abstract]
    Annotation: this study revealed STYXL1 as a novel candidate gene for moderate intellectual disability seizures and behavioral complexities.Imported.
    Source: GeneRIF:51657.

    This publication is mapped to 3 other entries.

1 to 11 of 11  Show

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