+ |
EPHA4 | up-regulates activity
phosphorylation
|
EPHA4 |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-251118 |
Tyr596 |
LNQGVRTyVDPFTYE |
in vitro |
|
pmid |
sentence |
8622893 |
Two dimensional phosphopeptide mapping and site-directed mutagenesis defined juxtamembrane residue Y602 as a major site of in vitro autophosphorylation in Sek, whilst Y596 was phosphorylated to a lower stoichiometry. |
|
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-251119 |
Tyr602 |
TYVDPFTyEDPNQAV |
in vitro |
|
pmid |
sentence |
8622893 |
Two dimensional phosphopeptide mapping and site-directed mutagenesis defined juxtamembrane residue Y602 as a major site of in vitro autophosphorylation in Sek, whilst Y596 was phosphorylated to a lower stoichiometry. Complimentary approaches of in vitro binding assays and BIAcore analysis revealed a high affinity association between the Y602 Sek autophosphorylation site and the cytoplasmic tyrosine kinase p59fyn, an interaction mediated through the SH2 domain of this intracellular signalling molecule. |
|
Publications: |
2 |
Organism: |
In Vitro |
+ |
EFNB3 | up-regulates
binding
|
EPHA4 |
0.832 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-52621 |
|
|
Homo sapiens |
|
pmid |
sentence |
9330863 |
Receptors of the epha group preferentially interact with glycosylphosphatidylinositol (gpi)-linked ligands (of the ephrin-a subclass, which comprises five ligands), while receptors of the ephb group preferentially interact with transmembrane ligands (of the ephrin-b subclass, which comprises three ligands) (table 1). In either case, binding of a ligand results in eph receptor autophosphorylation on tyrosine residues and activation of the kinase activity of the eph receptor |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
EFNA1 | up-regulates
binding
|
EPHA4 |
0.817 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-56907 |
|
|
Homo sapiens |
|
pmid |
sentence |
9576626 |
Ephrin-a1 binds and activates the tyrosine kinase activity of eph-a2, and has a dissociation constant of 20_30 nm. ephrin-a1 interacts with all the other epha subclass receptors as well, although with different affinity |
|
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-52087 |
|
|
Homo sapiens |
|
pmid |
sentence |
9330863 |
Receptors of the epha group preferentially interact with glycosylphosphatidylinositol (gpi)-linked ligands (of the ephrin-a subclass, which comprises five ligands), while receptors of the ephb group preferentially interact with transmembrane ligands (of the ephrin-b subclass, which comprises three ligands) (table 1). In either case, binding of a ligand results in eph receptor autophosphorylation on tyrosine residues and activation of the kinase activity of the eph receptor |
|
Publications: |
2 |
Organism: |
Homo Sapiens |
+ |
EFNA3 | up-regulates
binding
|
EPHA4 |
0.82 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-52315 |
|
|
Homo sapiens |
|
pmid |
sentence |
9330863 |
Eph receptors are activated by their ligands, which are membrane-anchored molecules |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
EFNA5 | up-regulates
binding
|
EPHA4 |
0.943 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-52473 |
|
|
Homo sapiens |
|
pmid |
sentence |
9330863 |
Receptors of the epha group preferentially interact with glycosylphosphatidylinositol (gpi)-linked ligands (of the ephrin-a subclass, which comprises five ligands), while receptors of the ephb group preferentially interact with transmembrane ligands (of the ephrin-b subclass, which comprises three ligands) (table 1). In either case, binding of a ligand results in eph receptor autophosphorylation on tyrosine residues and activation of the kinase activity of the eph receptor |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
NFIB | up-regulates quantity
transcriptional regulation
|
EPHA4 |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-268901 |
|
|
Mus musculus |
|
pmid |
sentence |
31838646 |
For example, within the NFI targetome, we identified 6 collagen genes, 13 genes encoding potassium channel or glutamate receptor subunits and a range of factors related to axon guidance (e.g. Slit1, Robo1, Epha4, Epha5, Epha8) |
|
Publications: |
1 |
Organism: |
Mus Musculus |
+ |
NFIA | up-regulates quantity
transcriptional regulation
|
EPHA4 |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-268894 |
|
|
Mus musculus |
|
pmid |
sentence |
31838646 |
For example, within the NFI targetome, we identified 6 collagen genes, 13 genes encoding potassium channel or glutamate receptor subunits and a range of factors related to axon guidance (e.g. Slit1, Robo1, Epha4, Epha5, Epha8) |
|
Publications: |
1 |
Organism: |
Mus Musculus |
+ |
EFNA2 | up-regulates
binding
|
EPHA4 |
0.921 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-52203 |
|
|
Homo sapiens |
|
pmid |
sentence |
9330863 |
Receptors of the epha group preferentially interact with glycosylphosphatidylinositol (gpi)-linked ligands (of the ephrin-a subclass, which comprises five ligands), while receptors of the ephb group preferentially interact with transmembrane ligands (of the ephrin-b subclass, which comprises three ligands) (table 1). In either case, binding of a ligand results in eph receptor autophosphorylation on tyrosine residues and activation of the kinase activity of the eph receptor |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
NFIX | up-regulates quantity
transcriptional regulation
|
EPHA4 |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-268908 |
|
|
Mus musculus |
|
pmid |
sentence |
31838646 |
For example, within the NFI targetome, we identified 6 collagen genes, 13 genes encoding potassium channel or glutamate receptor subunits and a range of factors related to axon guidance (e.g. Slit1, Robo1, Epha4, Epha5, Epha8) |
|
Publications: |
1 |
Organism: |
Mus Musculus |