Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Pivot Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Target Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Query: EC:2.7.12.2 (
MEK
)
18,161
document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)
Death-associated protein kinase 1
(
DAPK-1
) is a multidomain protein kinase with diverse roles in autophagic, apoptotic and survival pathways. Bioinformatic screens were used to identify a small internal mRNA from the
DAPK-1
locus (named s-
DAPK-1
). This encodes a 295 amino acid polypeptide encompassing part of the ankyrin-repeat domain, the P-loop motifs, part of the cytoskeletal binding domain of
DAPK-1
, and a unique C-terminal 'tail' extension not present in
DAPK-1
. Expression of s-
DAPK-1
mRNA was detected in a panel of normal human tissues as well as primary colorectal cancers, indicating that its expression occurs in vivo. s-
DAPK-1
gene transfection into cells produces two protein products: one with a denatured mass of 44 kDa, and a smaller product of 40 kDa. Double alanine mutation of the C-terminal tail extension of s-
DAPK-1
(Gly296/Arg297) prevented production of the 40 kDa fragment, suggesting that the smaller product is generated by in vivo proteolytic processing. The s-
DAPK-1
gene cannot substitute for full-length
DAPK-1
in an
mitogen-activated protein kinase kinase
/extracellular signal-regulated kinase-dependent apoptotic transfection assay. However, the transfection of s-
DAPK-1
was able to mimic full-length
DAPK-1
in the induction of membrane blebbing. The 44 kDa protease-resistant mutant s-DAPK-1G296A/R297A had very low activity in membrane blebbing, whereas the 40 kDa s-DAPK-1Deltatail protein exhibited the highest levels of membrane blebbing. Deletion of the tail extension of s-
DAPK-1
increased its half-life, shifted the equilibrium of the protein from cytoskeletal to soluble cytosolic pools, and altered green fluorescent protein-tagged s-
DAPK-1
protein localization as observed by confocal microscopy. These data highlight the existence of an alternative product of the
DAPK-1
locus, and suggest that proteolytic removal of the C-terminal tail of s-
DAPK-1
is required to stimulate maximally its membrane-blebbing function.
...
PMID:An alternative transcript from the death-associated protein kinase 1 locus encoding a small protein selectively mediates membrane blebbing. 1842 56