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Literature summary for 3.4.22.62 extracted from

  • Martin, M.C.; Allan, L.A.; Mancini, E.J.; Clarke, P.R.
    The docking interaction of caspase-9 with ERK2 provides a mechanism for the selective inhibitory phosphorylation of caspase-9 at threonine 125 (2008), J. Biol. Chem., 283, 3854-3865.
    View publication on PubMed

Cloned(Commentary)

Cloned (Comment) Organism
human caspase-9 (wild type or mutant R10A) are subcloned into the pIND expression plasmid before cotransfection of recombinant pIND and pVgRXR into U2OS cells Homo sapiens

Organism

Organism UniProt Comment Textmining
Homo sapiens
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Posttranslational Modification

Posttranslational Modification Comment Organism
phosphoprotein caspase-9 is phosphorylated at Thr125 in cells by ERK1/2 but not by c-Jun N-terminal kinases or p38 MAPKs Homo sapiens