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Literature summary for 3.1.3.53 extracted from

  • Hirano, M.; Niiro, N.; Hirano, K.; Nishimura, J.; Hartshorne, D.J.; Kanaide, H.
    Expression, subcellular localization, and cloning of the 130-kDa regulatory subunit of myosin phosphatase in porcine aortic endothelial cells (1999), Biochem. Biophys. Res. Commun., 254, 490-496.
    View publication on PubMed

Cloned(Commentary)

Cloned (Comment) Organism
an 89.6 kDa N-terminal fragment of MYPT1, an isoform of the 130 kDa regulatory targeting subunit of myosin phosphatase, is cloned and sequenced, MYPT is expressed by 2 genes, the two gene classes are termed MYPT1 and MYPT2 Sus scrofa

Localization

Localization Comment Organism GeneOntology No. Textmining
cell membrane subunit MYPT1, in confluent endothelial cells, at the cell membrane and cell-cell contacts Sus scrofa
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additional information subcellular localization of the subunit MYPT1 in growing and confluent endothelial cells Sus scrofa
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stress fibers subunit MYPT1, in growing endothelial cells Sus scrofa
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Organism

Organism UniProt Comment Textmining
Sus scrofa Q9TV77 89.6 kDa fragment of MYPT1, an isoform of the 130 kDa regulatory subunit of myosin phosphatase
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Source Tissue

Source Tissue Comment Organism Textmining
aorta thoracica endothelial cells, subunit MYPT1 Sus scrofa
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endothelial cell from aorta thoracica, subunit MYPT1 Sus scrofa
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