Gene interactions and pathways from curated databases and text-mining

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KDR — SHC1

Pathways - manually collected, often from reviews:

  • BioCarta vegf hypoxia and angiogenesis: VEGF/VEGF R complex (VEGF-FLT4_KDR_FLT1) → SHC/GRB2/SOS-1 complex (SOS1-GRB2-SHC1) (modification, activates)
  • KEGG Focal adhesion: EGFR/ERBB2/FLT1/FLT4/IGF1R/KDR/MET/PDGFRA/PDGFRB → SHC1/SHC2/SHC3/SHC4 (protein-protein, activation)
  • WikiPathways Focal Adhesion: BLK/EGFR/ERBB2/FGR/FLT1/HCK/IGF1R/KDR/MET/PDGFRA/PDGFRB/PTK6/SRMS/TXK/TESK2/STYK1/TNK2/TNK1 → SHC1/SHC3 (activation)

Protein-Protein interactions - manually collected from original source literature:

Studies that report less than 10 interactions are marked with *

Text-mined interactions from Literome

Ratcliffe et al., Oncogene 2002 : The Sck and Shc SH2 domains, and not the PTB domain, mediates its interactions with KDR , as recombinant Sck SH2 domain binds to a tyrosine phosphorylated KDR 1175 derived synthetic peptide, but not to a peptide synthesized without tyrosine phosphate
Oshikawa et al., Am J Physiol Heart Circ Physiol 2012 (MAP Kinase Signaling System) : Fractionation of caveolin enriched lipid raft demonstrates that p66Shc plays a critical role in VEGFR2 phosphorylation in caveolae/lipid rafts as well as downstream p38MAP kinase activation