+ |
PRKCH | up-regulates
phosphorylation
|
ANXA1 |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-202792 |
Ser27 |
EYVQTVKsSKGGPGS |
Homo sapiens |
|
pmid |
sentence |
24103589 |
The authors identified several phosphorylated residues by a combination of peptide mapping and sequence analysis and showed that recombinant pp60c-src phosphorylates annexin a1 near its amino terminus, at tyrosine 21 (tyr21). Also polyoma virus middle t/pp60c-src complex, recombinant pp50v-abl, and the egf receptor/kinase phosphorylated the same tyrosine residue. It was also shown that serine 27 residue of anxa1 is the primary site phosphorylated by protein kinase c (pkc). In the same study, the threonine 41 residue has been identified as a pkc substrate as well. The adenosine cyclic 3_,5_-phosphate dependent protein kinase a (pka) phosphorylates anxa1 in its carboxyl-terminal core at the threonine 216 residue (thr216) [2].The phosphorylation of serine 27 is essential for annexin a1 membrane localization. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
PRKCB | up-regulates
phosphorylation
|
ANXA1 |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-202784 |
Ser27 |
EYVQTVKsSKGGPGS |
Homo sapiens |
|
pmid |
sentence |
24103589 |
The authors identified several phosphorylated residues by a combination of peptide mapping and sequence analysis and showed that recombinant pp60c-src phosphorylates annexin a1 near its amino terminus, at tyrosine 21 (tyr21). Also polyoma virus middle t/pp60c-src complex, recombinant pp50v-abl, and the egf receptor/kinase phosphorylated the same tyrosine residue. It was also shown that serine 27 residue of anxa1 is the primary site phosphorylated by protein kinase c (pkc). In the same study, the threonine 41 residue has been identified as a pkc substrate as well. The adenosine cyclic 3_,5_-phosphate dependent protein kinase a (pka) phosphorylates anxa1 in its carboxyl-terminal core at the threonine 216 residue (thr216) [2].The phosphorylation of serine 27 is essential for annexin a1 membrane localization. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
PRKCG | up-regulates
phosphorylation
|
ANXA1 |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-202788 |
Ser27 |
EYVQTVKsSKGGPGS |
Homo sapiens |
|
pmid |
sentence |
24103589 |
The authors identified several phosphorylated residues by a combination of peptide mapping and sequence analysis and showed that recombinant pp60c-src phosphorylates annexin a1 near its amino terminus, at tyrosine 21 (tyr21). Also polyoma virus middle t/pp60c-src complex, recombinant pp50v-abl, and the egf receptor/kinase phosphorylated the same tyrosine residue. It was also shown that serine 27 residue of anxa1 is the primary site phosphorylated by protein kinase c (pkc). In the same study, the threonine 41 residue has been identified as a pkc substrate as well. The adenosine cyclic 3_,5_-phosphate dependent protein kinase a (pka) phosphorylates anxa1 in its carboxyl-terminal core at the threonine 216 residue (thr216) [2].The phosphorylation of serine 27 is essential for annexin a1 membrane localization. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
PRKCA | up-regulates
phosphorylation
|
ANXA1 |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-202780 |
Ser27 |
EYVQTVKsSKGGPGS |
Homo sapiens |
|
pmid |
sentence |
24103589 |
The authors identified several phosphorylated residues by a combination of peptide mapping and sequence analysis and showed that recombinant pp60c-src phosphorylates annexin a1 near its amino terminus, at tyrosine 21 (tyr21). Also polyoma virus middle t/pp60c-src complex, recombinant pp50v-abl, and the egf receptor/kinase phosphorylated the same tyrosine residue. It was also shown that serine 27 residue of anxa1 is the primary site phosphorylated by protein kinase c (pkc). In the same study, the threonine 41 residue has been identified as a pkc substrate as well. The adenosine cyclic 3_,5_-phosphate dependent protein kinase a (pka) phosphorylates anxa1 in its carboxyl-terminal core at the threonine 216 residue (thr216) [2].The phosphorylation of serine 27 is essential for annexin a1 membrane localization. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
TRPM7 | up-regulates
phosphorylation
|
ANXA1 |
0.561 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-202804 |
Ser5 |
sEFLKQAW |
Homo sapiens |
|
pmid |
sentence |
24103589 |
Trpm7 was responsible for phosphorylation of the serine 5 (ser5) residue [29]. In 2009, the study focused on an association between anxa1 and trpm7 confirmed the presence of a trpm7/annexin a1/mg2_+ complex, suggesting a novel pathway in bradykinin signaling, dependent on pkc and c-src [30]. Even though that pathway is not fully characterized, the same team that discovered the ser5 phosphorylation of anxa1 also reported crucial relevance of this modification for anxa1 membrane binding and especially for the interaction between annexin a1 and its known partner, the calcium binding protein s100a11 |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
SRC |
phosphorylation
|
ANXA1 |
0.398 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-202800 |
Thr216 |
AGERRKGtDVNVFNT |
Homo sapiens |
|
pmid |
sentence |
24103589 |
Location of sites in human lipocortin i that are phosphorylated by protein tyrosine kinases and protein kinases a and cthe primary site of phosphorylation by protein kinase c was also near the amino terminus at ser-27. The major site of phosphorylation by adenosine cyclic 3',5'-phosphate dependent protein kinase was on the carboxy-terminal half of the molecule at thr-216 |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
EGFR | up-regulates
phosphorylation
|
ANXA1 |
0.523 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-202776 |
Tyr21 |
IENEEQEyVQTVKSS |
Homo sapiens |
|
pmid |
sentence |
24103589 |
The authors identified several phosphorylated residues by a combination of peptide mapping and sequence analysis and showed that recombinant pp60c-src phosphorylates annexin a1 near its amino terminus, at tyrosine 21 (tyr21). Also polyoma virus middle t/pp60c-src complex, recombinant pp50v-abl, and the egf receptor/kinase phosphorylated the same tyrosine residue. It was also shown that serine 27 residue of anxa1 is the primary site phosphorylated by protein kinase c (pkc). In the same study, the threonine 41 residue has been identified as a pkc substrate as well. The adenosine cyclic 3_,5_-phosphate dependent protein kinase a (pka) phosphorylates anxa1 in its carboxyl-terminal core at the threonine 216 residue (thr216) [2].Finally in 2013 caron et al. showed the relevance of y21 phosphorylation for the anxa1 stability. In fact the authors demonstrated that the tyrosine 21 phosphorylation is crucial for anxa1 sumoylation induced by egf |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
SRC | up-regulates
phosphorylation
|
ANXA1 |
0.398 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-202796 |
Tyr21 |
IENEEQEyVQTVKSS |
Homo sapiens |
|
pmid |
sentence |
24103589 |
The authors identified several phosphorylated residues by a combination of peptide mapping and sequence analysis and showed that recombinant pp60c-src phosphorylates annexin a1 near its amino terminus, at tyrosine 21 (tyr21). Also polyoma virus middle t/pp60c-src complex, recombinant pp50v-abl, and the egf receptor/kinase phosphorylated the same tyrosine residue. It was also shown that serine 27 residue of anxa1 is the primary site phosphorylated by protein kinase c (pkc). In the same study, the threonine 41 residue has been identified as a pkc substrate as well. The adenosine cyclic 3_,5_-phosphate dependent protein kinase a (pka) phosphorylates anxa1 in its carboxyl-terminal core at the threonine 216 residue (thr216) [2].Finally in 2013 caron et al. showed the relevance of y21 phosphorylation for the anxa1 stability. In fact the authors demonstrated that the tyrosine 21 phosphorylation is crucial for anxa1 sumoylation induced by egf |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
ANXA1 | up-regulates
|
Apoptosis |
0.7 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-261689 |
|
|
Homo sapiens |
Kasumi-1 Cell |
pmid |
sentence |
17464329 |
We next focused on the pro-apoptotic function of ANXA1 in AML1-ETO-expressing AML cells. In this regard, FK228 was found to increase the protein levels of both the full-length and 33 kDa N-terminal cleavage products of ANXA1, which led to the localization of ANXA1 on the plasma membrane. Conversely, the inhibition of ANXA1 function (by ANXA1 neutralizing antibody, which blocked ANXA1 localization on the plasma membrane) or expression (by siRNA) significantly reduced FK228-induced apoptosis, indicating that ANXA1 is involved in apoptosis induction in response to FK228. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
ANXA1 | up-regulates quantity by expression
transcriptional regulation
|
TNF |
0.34 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-261941 |
|
|
Mus musculus |
|
pmid |
sentence |
27426034 |
Our study demonstrates that ANXA1 can be phosphorylated by PKC and is subsequently translocated to the nucleus of BV-2 microglial cells after OGD/R, resulting in the induction of pro-inflammatory cytokines. we set out to examine the relationship between the different subcellular distributions of ANXA1 and the upregulation of inflammatory cytokines. When BV-2 microglial cells were transfected with ANXA1-S27A constructs following by OGD/R treatment, the pro-inflammatory cytokines, IL-1β, IL-6, and TNF-α, were found to be expressed at lower levels than those of control groups |
|
Publications: |
1 |
Organism: |
Mus Musculus |
+ |
ANXA1 | up-regulates activity
binding
|
FPR2 |
0.63 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-259437 |
|
|
Homo sapiens |
HEK-293 Cell |
pmid |
sentence |
15187149 |
We show that the mimetic N-terminal annexin 1 peptide Ac1-25 is able to activate and desensitize not only FPR but also FPRL1 and FPRL2. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
ANXA1 | up-regulates activity
binding
|
FPR3 |
0.604 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-259438 |
|
|
Homo sapiens |
HEK-293 Cell |
pmid |
sentence |
15187149 |
We show that the mimetic N-terminal annexin 1 peptide Ac1-25 is able to activate and desensitize not only FPR but also FPRL1 and FPRL2. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
ANXA1 | up-regulates quantity by expression
transcriptional regulation
|
IL6 |
0.412 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-261939 |
|
|
Mus musculus |
|
pmid |
sentence |
27426034 |
Our study demonstrates that ANXA1 can be phosphorylated by PKC and is subsequently translocated to the nucleus of BV-2 microglial cells after OGD/R, resulting in the induction of pro-inflammatory cytokines. we set out to examine the relationship between the different subcellular distributions of ANXA1 and the upregulation of inflammatory cytokines. When BV-2 microglial cells were transfected with ANXA1-S27A constructs following by OGD/R treatment, the pro-inflammatory cytokines, IL-1β, IL-6, and TNF-α, were found to be expressed at lower levels than those of control groups |
|
Publications: |
1 |
Organism: |
Mus Musculus |
+ |
ANXA1 | up-regulates activity
binding
|
FPR1 |
0.734 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-259439 |
|
|
Homo sapiens |
HEK-293 Cell |
pmid |
sentence |
15187149 |
We show that the mimetic N-terminal annexin 1 peptide Ac1-25 is able to activate and desensitize not only FPR but also FPRL1 and FPRL2. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
SPI1 | down-regulates quantity by repression
transcriptional regulation
|
ANXA1 |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-261688 |
|
|
Homo sapiens |
|
pmid |
sentence |
19428102 |
Identification of annexin 1 as a PU.1 target gene in leukemia cells. PU.1 is a master regulator, and critical for the developmen tof a common progenitor for lymphoid-myeloid cell lineages in the hematopoietic system. From microarray analysis, we found that several genes including annexin 1 were markedly induced in K562PU.1KD cells. Annexin 1 is a calcium- and phospholipid-binding protein and increased expression leads to the constitutive activation of extracellular signal-regulated kinase (ERK) |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
ANXA1 | up-regulates quantity by expression
transcriptional regulation
|
IL1B |
0.386 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-261940 |
|
|
Mus musculus |
|
pmid |
sentence |
27426034 |
Our study demonstrates that ANXA1 can be phosphorylated by PKC and is subsequently translocated to the nucleus of BV-2 microglial cells after OGD/R, resulting in the induction of pro-inflammatory cytokines. we set out to examine the relationship between the different subcellular distributions of ANXA1 and the upregulation of inflammatory cytokines. When BV-2 microglial cells were transfected with ANXA1-S27A constructs following by OGD/R treatment, the pro-inflammatory cytokines, IL-1β, IL-6, and TNF-α, were found to be expressed at lower levels than those of control groups |
|
Publications: |
1 |
Organism: |
Mus Musculus |