+ |
PRKD3 |
phosphorylation
|
GIT1 |
0.37 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-191839 |
Ser46 |
RSLGRHIsIVKHLRH |
Homo sapiens |
|
pmid |
sentence |
22893698 |
We propose that phosphorylation of git1 on serine 46 by pkd3 represents a molecular switch by which git1 localization, paxillin trafficking, and cellular protrusive activity are regulated. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
SRC | up-regulates activity
phosphorylation
|
GIT1 |
0.559 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-276626 |
Tyr246 |
PDHKNGHyIIPQMAD |
Chlorocebus aethiops |
COS-7 Cell |
pmid |
sentence |
24699139 |
Tyrosines 246 and 293 are required to hold GIT1 in a closed conformation.Hyperphosphorylation of GIT1-N by Src and pervanadate does not affect its binding in vitro to full length GIT1 proteins. Mutations Y246E and Y293E of GIT1 enhance binding to paxillin. |
|
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-276627 |
Tyr284 |
EELAMDVyDEVDRRE |
Chlorocebus aethiops |
COS-7 Cell |
pmid |
sentence |
24699139 |
Tyrosines 246 and 293 are required to hold GIT1 in a closed conformation.Hyperphosphorylation of GIT1-N by Src and pervanadate does not affect its binding in vitro to full length GIT1 proteins. Mutations Y246E and Y293E of GIT1 enhance binding to paxillin. |
|
Publications: |
2 |
Organism: |
Chlorocebus Aethiops |
+ |
GIT1 | up-regulates activity
binding
|
ARHGEF6 |
0.846 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-272165 |
|
|
Homo sapiens |
Blood Platelet |
pmid |
sentence |
26507661 |
Screening for potential mediators of this effect resulted in the identification of the Rac1-specific GTPase-activating protein ARHGAP17 and the guanine nucleotide exchange factor ARHGEF6 as new PKA and PKG substrates in platelets. We mapped the PKA/PKG phosphorylation sites to serine 702 on ARHGAP17 using Phos-tag gels and to serine 684 on ARHGEF6. |we show that ARHGEF6 is constitutively linked to GIT1, a GAP of Arf family small G proteins, and that ARHGEF6 phosphorylation enables binding of the 14-3-3 adaptor protein to the ARHGEF6/GIT1 complex. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
GIT1 | up-regulates activity
binding
|
MAP2K1 |
0.401 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-261245 |
|
|
Homo sapiens |
Hep-G2 Cell |
pmid |
sentence |
23325602 |
We found both MAT2B variants interact with GIT1. MAT2B directly promoted binding of GIT1 and ERK2 to MEK1. MAT2B and GIT1 interact and are overexpressed in most human liver and colon cancer specimens. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
GIT1 | up-regulates
binding
|
PLCG1 |
0.537 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-118454 |
|
|
Homo sapiens |
|
pmid |
sentence |
14523024 |
Git1 interaction with plcgamma is required for plcgamma activation based on inhibition of tyrosine phosphorylation |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
Tissue: |
Muscle, Smooth Muscle |
+ |
MAT2B | up-regulates activity
binding
|
GIT1 |
0.409 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-261244 |
|
|
Homo sapiens |
Hep-G2 Cell |
pmid |
sentence |
23325601 |
We found both MAT2B variants interact with GIT1. MAT2B directly promoted binding of GIT1 and ERK2 to MEK1. MAT2B and GIT1 interact and are overexpressed in most human liver and colon cancer specimens. MAT2B and GIT1 require each other to activate MEK1/ERK and increase growth. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |