+ |
PRKCD | down-regulates activity
phosphorylation
|
CXCR4 |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-260898 |
Ser324 |
LTSVSRGsSLKILSK |
Homo sapiens |
|
pmid |
sentence |
10521508 |
Therefore, internalization of CXCR4 in response to PMA appears to be mediated by activation of protein kinase C | However, mutation of the dileucine motif or the serines at positions 324, 325, 338, and 339 profoundly decreased internalization. |
|
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-260899 |
Ser325 |
LTSVSRGsSLKILSK |
Homo sapiens |
|
pmid |
sentence |
10521508 |
Therefore, internalization of CXCR4 in response to PMA appears to be mediated by activation of protein kinase C | However, mutation of the dileucine motif or the serines at positions 324, 325, 338, and 339 profoundly decreased internalization. |
|
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-260900 |
Ser338 |
KGKRGGHsSVSTESE |
Homo sapiens |
|
pmid |
sentence |
10521508 |
Therefore, internalization of CXCR4 in response to PMA appears to be mediated by activation of protein kinase C | However, mutation of the dileucine motif or the serines at positions 324, 325, 338, and 339 profoundly decreased internalization. |
|
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-260901 |
Ser339 |
GKRGGHSsVSTESES |
Homo sapiens |
|
pmid |
sentence |
10521508 |
Therefore, internalization of CXCR4 in response to PMA appears to be mediated by activation of protein kinase C | However, mutation of the dileucine motif or the serines at positions 324, 325, 338, and 339 profoundly decreased internalization. |
|
Publications: |
4 |
Organism: |
Homo Sapiens |
+ |
SNAI2 | up-regulates quantity by expression
transcriptional regulation
|
CXCR4 |
0.414 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-255171 |
|
|
Homo sapiens |
Prostate Cancer Cell Line |
pmid |
sentence |
22074556 |
We demonstrated that forced expression of SLUG elevated CXCR4 and CXCL12 expression in human prostate cancer cell lines PC3, DU145, 22RV1, and LNCaP; conversely, reduced expression of SLUG by shRNA downregulated CXCR4 and CXCL12 expression at RNA and protein levels in prostate cancer cells. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
ERG | up-regulates quantity by expression
transcriptional regulation
|
CXCR4 |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-253911 |
|
|
Homo sapiens |
|
pmid |
sentence |
19396168 |
ADAMTS1 and CXCR4, two candidate genes strongly associated with cell migration, were upregulated in the presence of ERG overexpression. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
CD74 | up-regulates
binding
|
CXCR4 |
0.547 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-187461 |
|
|
Homo sapiens |
HEK-293 Cell, Monocyte |
pmid |
sentence |
19665027 |
Cd74 forms functional complexes with cxcr4 that mediate mif-specific signaling. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
Pathways: | Toll like receptors |
+ |
USP14 | up-regulates quantity by stabilization
deubiquitination
|
CXCR4 |
0.459 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-265057 |
|
|
Homo sapiens |
HEK-293 Cell |
pmid |
sentence |
26523394 |
The physical interaction of CXCR4 and USP14 is paralleled by USP14-catalyzed deubiquitination of the receptor|We also observed that ubiquitination of CXCR4 facilitated receptor degradation, whereas overexpression of USP14 or RNAi-induced knockdown of USP14 blocked CXCL12-mediated CXCR4 degradation |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
1-[[4-(1,4,8,11-tetrazacyclotetradec-1-ylmethyl)phenyl]methyl]-1,4,8,11-tetrazacyclotetradecane | down-regulates
chemical inhibition
|
CXCR4 |
0.8 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-206268 |
|
|
Homo sapiens |
|
pmid |
sentence |
Other |
|
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
CXCL12 | up-regulates
binding
|
CXCR4 |
0.803 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-115029 |
|
|
Homo sapiens |
|
pmid |
sentence |
11859124 |
To study the role of the sdf-1/cxcr4-chemokine/receptor system as a regulator of vertebrate development, we isolated and characterized a cdna encoding sdf-1 of the lower vertebrate xenopus laevis (xsdf-1). Recombinant xsdf-1 was produced in insect cells, purified, and functionally characterized. Although xsdf-1 is only 64-66% identical with its mammalian counterparts, it is indistinguishable from human (h)sdf-1alpha in terms of activating both x. laevis cxcr4 and hcxcr4. Thus, both xsdf-1 and hsdf-1alpha promoted cxcr4-mediated activation of heterotrimeric g(i2) in a cell-free system and induced release of intracellular calcium ions in and chemotaxis of intact lymphoblastic cells. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
YBX1 | up-regulates quantity by expression
transcriptional regulation
|
CXCR4 |
0.272 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-255611 |
|
|
Homo sapiens |
|
pmid |
sentence |
17072343 |
YB-1 knockdown by siRNA upregulated 344 genes, including MDR1, thymidylate synthetase, S100 calcium binding protein and cyclin B, and downregulated 534 genes, including CXCR4, N-myc downstream regulated gene 1, E-cadherin and phospholipase C. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
CXCR4 | up-regulates
|
Angiogenesis |
0.7 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-252266 |
|
|
Homo sapiens |
SUM-102 Cell |
pmid |
sentence |
19584257 |
However, we show that soluble factors secreted by SUM102 breast cancer cells stimulated the expression of MMP-1 and CXCR4 in HMFs. As a result, these stromal cells acquired an invasive and migratory phenotype |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
miR-146a | up-regulates quantity by expression
post transcriptional regulation
|
CXCR4 |
0.4 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-268952 |
|
|
Homo sapiens |
|
pmid |
sentence |
20516212 |
MiR-221 strongly upregulated GAX.ZEB2 is upregulated by serum and downregulates GAX, while the expression of miR-221 upregulates GAX and downregulates ZEB2. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
MIF | up-regulates activity
binding
|
CXCR4 |
0.38 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-252062 |
|
|
Mus musculus |
Monocyte |
pmid |
sentence |
17435771 |
We identify the chemokine receptors CXCR2 and CXCR4 as functional receptors for MIF [] By activating both CXCR2 and CXCR4, MIF displays chemokine-like functions and acts as a major regulator of inflammatory cell recruitment and atherogenesis. |
|
Publications: |
1 |
Organism: |
Mus Musculus |
Pathways: | Toll like receptors |