+ |
LCK | up-regulates activity
phosphorylation
|
CD3E |
0.679 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-251368 |
Tyr188 |
PPVPNPDyEPIRKGQ |
Chlorocebus aethiops |
COS Cell |
pmid |
sentence |
11855827 |
Tyrosine Phosphorylation of CD8- Chimeras by Lck and ZAP-70 in COS Cells. both Y170F and Y181F chimeric proteins could be efficiently phosphorylated by Lck in vivo. phosphorylation of Y170 and Y181 within CD3- –ITAM provides to CD3- the potential to interact with multiple downstream effectors and signaling pathways. |
|
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-251369 |
Tyr199 |
RKGQRDLySGLNQRR |
Chlorocebus aethiops |
|
pmid |
sentence |
11855827 |
Tyrosine Phosphorylation of CD8- Chimeras by Lck and ZAP-70 in COS Cells. both Y170F and Y181F chimeric proteins could be efficiently phosphorylated by Lck in vivo. phosphorylation of Y170 and Y181 within CD3- –ITAM provides to CD3- the potential to interact with multiple downstream effectors and signaling pathways. |
|
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-259930 |
|
|
Mus musculus |
|
pmid |
sentence |
2470098 |
Last, we demonstrate directly that members of the CD3 complex, including the gamma, delta, and epsilon chains, as well as a putative zeta subunit, can be phosphorylated at tyrosine residues by the CD4/CD8.p56lck complex. |
|
Publications: |
3 |
Organism: |
Chlorocebus Aethiops, Mus Musculus |
Pathways: | T cell activation |
+ |
STOML2 | up-regulates activity
binding
|
CD3E |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-260375 |
|
|
Homo sapiens |
JURKAT Cell |
pmid |
sentence |
18641330 |
We observed that SLP-2 steadily associated with the CD3-epsilon chain of the TCR complex under resting conditions and during the 60 min of stimulation|The SLP-2-associated pool of these molecules became phosphorylated/activated in a sequential manner, a profile compatible with their temporal involvement in early TCR signalling. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
CD3E | form complex
binding
|
CD3 |
0.8 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-255294 |
|
|
Homo sapiens |
|
pmid |
sentence |
12507424 |
The T cell receptor-CD3 complex (TCR-CD3) serves a critical role in the differentiation, survival, and function of T cells, and receptor triggering elicits a complex set of biological responses that serve to protect the organism from infectious agents. The receptor is composed of six different chains that form the TCR heterodimer responsible for ligand recognition, as well as the CD3γε, CD3δε, and ζζ signaling modules. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
Pathways: | T cell activation |
+ |
CD3E | up-regulates activity
relocalization
|
NCK1 |
0.379 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-259934 |
|
|
Homo sapiens |
JURKAT Cell |
pmid |
sentence |
12110186 |
We present strong evidence that ligand engagement of TCR-CD3 induces a conformational change that exposes a proline-rich sequence in CD3ϵ and results in recruitment of the adaptor protein Nck. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
Pathways: | T cell activation |