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Literature summary for 3.1.3.36 extracted from

  • Artemenko, Y.; Gagnon, A.; Sorisky, A.
    Catalytically inactive SHIP2 inhibits proliferation by attenuating PDGF signaling in 3T3-L1 preadipocytes (2009), J. Cell. Physiol., 218, 228-236.
    View publication on PubMed

Application

Application Comment Organism
molecular biology catalytically inactive SHIP2 mutant P686A/D690A/R691A reduces preadipocyte proliferation by attenuating PDGFR signaling Homo sapiens

Cloned(Commentary)

Cloned (Comment) Organism
expressed in murine 3T3-L1 preadipocytes Homo sapiens

Protein Variants

Protein Variants Comment Organism
P686A/D690A/R691A catalytically inactive dominant-negative mutant inhibits proliferation of preadipocytes more potently than wild-type SHIP2. Phospho-Akt, phospho-ERK1/2, and PDGF receptor (PDGFR) levels are reduced in mutant-expressing preadipocytes. The inhibition of PDGF-activated mitogenic pathways by SHIP2 mutant is consistent with a decrease in PDGFR phosphorylation caused by a drop in receptor levels in SHIP2 mutant-expressing cells. SHIP2 mutant promotes ubiquitination of the PDGFR and its degradation via the lysosomal pathway independently of the association between the E3 ubiquitin ligase c-Cbl and PDGFR Homo sapiens

Organism

Organism UniProt Comment Textmining
Homo sapiens
-
-
-

Synonyms

Synonyms Comment Organism
SHIP2
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Homo sapiens