Angiopoietin receptor

Cell-surface receptors which bind angiopoietin From Wikipedia, the free encyclopedia

The angiopoietin receptors are receptors that bind angiopoietin. TIE-1 and TIE-2 comprise the cell-surface receptors that bind and are activated by the angiopoietins, (Ang1, Ang2, Ang3, Ang4). The angiopoietins are protein growth factors required for the formation of blood vessels (angiogenesis).

Quick facts Identifiers, Symbol ...
Angiopoietin receptor
Identifiers
SymbolTIE
PfamPF10430
InterProIPR018941
Membranome1214
Available protein structures:
PDB  IPR018941 PF10430 (ECOD; PDBsum)  
AlphaFold
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SymbolTIE1
Alt. symbolsTIE, JTK14
Quick facts tyrosine kinase with immunoglobulin-like and EGF-like domains 1, Identifiers ...
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SymbolTEK
Alt. symbolsTIE2, TIE-2, VMCM1, CD202b
Quick facts TEK tyrosine kinase, endothelial, Identifiers ...
TEK tyrosine kinase, endothelial
Identifiers
SymbolTEK
Alt. symbolsTIE2, TIE-2, VMCM1, CD202b
NCBI gene7010
HGNC11724
OMIM600221
RefSeqNM_000459
UniProtQ02763
Other data
LocusChr. 9 p21
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StructuresSwiss-model
DomainsInterPro
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ANGPT1, ANGPT2, and ANGPT4 activate TIE-2. Intracellular signal transduction can proceed via DOK-R (yellow arrow) or alternatively via Akt to eNOS (orange arrow).
ANGPT1, ANGPT2, and ANGPT4 activate TIE-2. Intracellular signal transduction can proceed via DOK-R (yellow arrow) or alternatively via Akt to eNOS (orange arrow).

Angiopoietins

The angiopoietins are protein growth factors that regulate angiogenesis, the formation of blood vessels. In humans, three angiopoietins have been identified: Ang1, Ang2, and Ang4 (Ang 3 is the mouse ortholog of human Ang4).[1] Ang1 and Ang4 function as agonistic or activating ligands for Tie2, whereas Ang2 and Ang3 behave as competitive antagonists. They function by binding their physiologic receptors, Tie-1 and Tie-2. These are receptor tyrosine kinases, so named because they mediate cell signals by inducing the phosphorylation of key tyrosines, thus initiating cell signalling.

It is somewhat controversial which of the Tie receptors mediate functional signals downstream of Ang stimulation. But it is clear that at least Tie-2 is capable of physiologic activation as a result of binding the angiopoietins.[citation needed]

See also

References

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