PIM1
Proto-oncogene with serine/threonine kinase activity involved in cell survival and cell proliferation and thus providing a selective advantage in tumorigenesis. Exerts its oncogenic activity through: the regulation of MYC transcriptional activity, the regulation of cell cycle progression and by phos...
Proto-oncogene with serine/threonine kinase activity involved in cell survival and cell proliferation and thus providing a selective advantage in tumorigenesis. Exerts its oncogenic activity through: the regulation of MYC transcriptional activity, the regulation of cell cycle progression and by phosphorylation and inhibition of proapoptotic proteins (BAD, MAP3K5, FOXO3). Phosphorylation of MYC leads to an increase of MYC protein stability and thereby an increase of transcriptional activity. The stabilization of MYC exerted by PIM1 might explain partly the strong synergism between these two oncogenes in tumorigenesis. Mediates survival signaling through phosphorylation of BAD, which induces release of the anti-apoptotic protein Bcl-X(L)/BCL2L1. Phosphorylation of MAP3K5, another proapoptotic protein, by PIM1, significantly decreases MAP3K5 kinase activity and inhibits MAP3K5-mediated phosphorylation of JNK and JNK/p38MAPK subsequently reducing caspase-3 activation and cell apoptosis. Stimulates cell cycle progression at the G1-S and G2-M transitions by phosphorylation of CDC25A and CDC25C. Phosphorylation of CDKN1A, a regulator of cell cycle progression at G1, results in the relocation of CDKN1A to the cytoplasm and enhanced CDKN1A protein stability. Promotes cell cycle progression and tumorigenesis by down-regulating expression of a regulator of cell cycle progression, CDKN1B, at both transcriptional and post-translational levels. Phosphorylation of CDKN1B, induces 14-3-3 proteins binding, nuclear export and proteasome-dependent degradation. May affect the structure or silencing of chromatin by phosphorylating HP1 gamma/CBX3. Acts also as a regulator of homing and migration of bone marrow cells involving functional interaction with the CXCL12-CXCR4 signaling axis. Also phosphorylates and activates the ATP-binding cassette transporter ABCG2, allowing resistance to drugs through their excretion from cells (PubMed:18056989). Promotes brown adipocyte differentiation (By similarity).
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GO - Biological processes (BP):
apoptotic process, cell cycle, cellular detoxification, cytokine-mediated signaling pathway, hyaluronan metabolic process, multicellular organism development, negative regulation of apoptotic process, negative regulation of DNA-binding transcription factor activity, positive regulation of brown fat ...
apoptotic process, cell cycle, cellular detoxification, cytokine-mediated signaling pathway, hyaluronan metabolic process, multicellular organism development, negative regulation of apoptotic process, negative regulation of DNA-binding transcription factor activity, positive regulation of brown fat cell differentiation, positive regulation of cardiac muscle cell proliferation, positive regulation of cardioblast proliferation, positive regulation of cyclin-dependent protein serine/threonine kinase activity, positive regulation of protein serine/threonine kinase activity, positive regulation of transcription, DNA-templated, protein autophosphorylation, protein phosphorylation, protein stabilization, regulation of hematopoietic stem cell proliferation, regulation of transmembrane transporter activity, vitamin D receptor signaling pathway
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GO - Molecular function (MF):
ATP binding, manganese ion binding, protein serine/threonine kinase activator activity, protein serine/threonine kinase activity, ribosomal small subunit binding, transcription factor binding...
ATP binding, manganese ion binding, protein serine/threonine kinase activator activity, protein serine/threonine kinase activity, ribosomal small subunit binding, transcription factor binding
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GO - Cellular component (CC):
cytosol, nucleolus, nucleoplasm, nucleus, plasma membrane, cytoplasm...
cytosol, nucleolus, nucleoplasm, nucleus, plasma membrane, cytoplasm
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