+ |
IRAK4 | up-regulates
phosphorylation
|
NCF1 |
0.39 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-152011 |
Ser288 |
QKSGQDVsQAQRQIK |
Homo sapiens |
Neutrophil |
pmid |
sentence |
17217339 |
Phosphorylation of the cytosolic factor p47phox is essential for activation of the nadph oxidase.We found that thr133, ser288 and thr356, targets for irak-4 phosphorylation in vitro, are also phosphorylated in endogenous p47phox after lps stimulation. We conclude that irak-4 phosphorylates p47phox and regulates nadph oxidase activation after lps stimulation. |
|
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-152015 |
Ser320 |
QRSRKRLsQDAYRRN |
Homo sapiens |
Neutrophil |
pmid |
sentence |
17217339 |
Phosphorylation of the cytosolic factor p47phox is essential for activation of the nadph oxidase.These results strongly support the observation that irak-4 is a kinase for p47phox in vivo. We also detected the signature of phosphorylation at ser320 and ser345 |
|
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-152019 |
Ser345 |
QARPGPQsPGSPLEE |
Homo sapiens |
Neutrophil |
pmid |
sentence |
17217339 |
Phosphorylation of the cytosolic factor p47phox is essential for activation of the nadph oxidase.These results strongly support the observation that irak-4 is a kinase for p47phox in vivo. We also detected the signature of phosphorylation at ser320 and ser345 |
|
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-152023 |
Thr133 |
KLPTDNQtKKPETYL |
Homo sapiens |
Neutrophil |
pmid |
sentence |
17217339 |
Phosphorylation of the cytosolic factor p47phox is essential for activation of the nadph oxidase.We found that thr133, ser288 and thr356, targets for irak-4 phosphorylation in vitro, are also phosphorylated in endogenous p47phox after lps stimulation. We conclude that irak-4 phosphorylates p47phox and regulates nadph oxidase activation after lps stimulation. |
|
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-152027 |
Thr356 |
PLEEERQtQRSKPQP |
Homo sapiens |
Neutrophil |
pmid |
sentence |
17217339 |
Phosphorylation of the cytosolic factor p47phox is essential for activation of the nadph oxidase.We found that thr133, ser288 and thr356, targets for irak-4 phosphorylation in vitro, are also phosphorylated in endogenous p47phox after lps stimulation. We conclude that irak-4 phosphorylates p47phox and regulates nadph oxidase activation after lps stimulation. |
|
Publications: |
5 |
Organism: |
Homo Sapiens |
+ |
PRKCB | up-regulates
phosphorylation
|
NCF1 |
0.549 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-89182 |
Ser303 |
RGAPPRRsSIRNAHS |
Homo sapiens |
Neutrophil |
pmid |
sentence |
12056906 |
Phosphopeptide mapping of p47(phox) showed that, as opposed to pkc zeta, pkc alpha, beta ii, and delta are able to phosphorylate all the major pkc sites. The use of p47(phox) mutants identified serines 303, 304, 315, 320, 328, 359, 370, and 379 as targets of pkc alpha, beta ii, and delta.Taken together, these results suggest that pkc alpha, beta ii, delta, and zeta expressed in human neutrophils can individually phosphorylate p47(phox) and induce both its translocation and nadph oxidase activation. |
|
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-89186 |
Ser304 |
GAPPRRSsIRNAHSI |
Homo sapiens |
Neutrophil |
pmid |
sentence |
12056906 |
Phosphopeptide mapping of p47(phox) showed that, as opposed to pkc zeta, pkc alpha, beta ii, and delta are able to phosphorylate all the major pkc sites. The use of p47(phox) mutants identified serines 303, 304, 315, 320, 328, 359, 370, and 379 as targets of pkc alpha, beta ii, and delta.Taken together, these results suggest that pkc alpha, beta ii, delta, and zeta expressed in human neutrophils can individually phosphorylate p47(phox) and induce both its translocation and nadph oxidase activation. |
|
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-89193 |
Ser315 |
AHSIHQRsRKRLSQD |
Homo sapiens |
Neutrophil |
pmid |
sentence |
12056906 |
Phosphopeptide mapping of p47(phox) showed that, as opposed to pkc zeta, pkc alpha, beta ii, and delta are able to phosphorylate all the major pkc sites. The use of p47(phox) mutants identified serines 303, 304, 315, 320, 328, 359, 370, and 379 as targets of pkc alpha, beta ii, and delta.Taken together, these results suggest that pkc alpha, beta ii, delta, and zeta expressed in human neutrophils can individually phosphorylate p47(phox) and induce both its translocation and nadph oxidase activation. |
|
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-89197 |
Ser320 |
QRSRKRLsQDAYRRN |
Homo sapiens |
Neutrophil |
pmid |
sentence |
12056906 |
Phosphopeptide mapping of p47(phox) showed that, as opposed to pkc zeta, pkc alpha, beta ii, and delta are able to phosphorylate all the major pkc sites. The use of p47(phox) mutants identified serines 303, 304, 315, 320, 328, 359, 370, and 379 as targets of pkc alpha, beta ii, and delta.Taken together, these results suggest that pkc alpha, beta ii, delta, and zeta expressed in human neutrophils can individually phosphorylate p47(phox) and induce both its translocation and nadph oxidase activation. |
|
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-89201 |
Ser328 |
QDAYRRNsVRFLQQR |
Homo sapiens |
Neutrophil |
pmid |
sentence |
12056906 |
Phosphopeptide mapping of p47(phox) showed that, as opposed to pkc zeta, pkc alpha, beta ii, and delta are able to phosphorylate all the major pkc sites. The use of p47(phox) mutants identified serines 303, 304, 315, 320, 328, 359, 370, and 379 as targets of pkc alpha, beta ii, and delta.Taken together, these results suggest that pkc alpha, beta ii, delta, and zeta expressed in human neutrophils can individually phosphorylate p47(phox) and induce both its translocation and nadph oxidase activation. |
|
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-89205 |
Ser359 |
EERQTQRsKPQPAVP |
Homo sapiens |
|
pmid |
sentence |
12056906 |
Phosphopeptide mapping of p47(phox) showed that, as opposed to pkc zeta, pkc alpha, beta ii, and delta are able to phosphorylate all the major pkc sites. The use of p47(phox) mutants identified serines 303, 304, 315, 320, 328, 359, 370, and 379 as targets of pkc alpha, beta ii, and delta.Taken together, these results suggest that pkc alpha, beta ii, delta, and zeta expressed in human neutrophils can individually phosphorylate p47(phox) and induce both its translocation and nadph oxidase activation. |
|
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-89209 |
Ser370 |
PAVPPRPsADLILNR |
Homo sapiens |
|
pmid |
sentence |
12056906 |
Phosphopeptide mapping of p47(phox) showed that, as opposed to pkc zeta, pkc alpha, beta ii, and delta are able to phosphorylate all the major pkc sites. The use of p47(phox) mutants identified serines 303, 304, 315, 320, 328, 359, 370, and 379 as targets of pkc alpha, beta ii, and delta.Taken together, these results suggest that pkc alpha, beta ii, delta, and zeta expressed in human neutrophils can individually phosphorylate p47(phox) and induce both its translocation and nadph oxidase activation. |
|
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-89213 |
Ser379 |
DLILNRCsESTKRKL |
Homo sapiens |
Neutrophil |
pmid |
sentence |
12056906 |
Phosphopeptide mapping of p47(phox) showed that, as opposed to pkc zeta, pkc alpha, beta ii, and delta are able to phosphorylate all the major pkc sites. The use of p47(phox) mutants identified serines 303, 304, 315, 320, 328, 359, 370, and 379 as targets of pkc alpha, beta ii, and delta.Taken together, these results suggest that pkc alpha, beta ii, delta, and zeta expressed in human neutrophils can individually phosphorylate p47(phox) and induce both its translocation and nadph oxidase activation. |
|
Publications: |
8 |
Organism: |
Homo Sapiens |
+ |
PRKCD | up-regulates
phosphorylation
|
NCF1 |
0.459 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-89217 |
Ser303 |
RGAPPRRsSIRNAHS |
Homo sapiens |
Neutrophil |
pmid |
sentence |
12056906 |
Pkc alpha, beta ii, delta, and zeta expressed in human neutrophils can individually phosphorylate p47(phox) and induce both its translocation and nadph oxidase activation. The use of p47phox mutants identified serines 303, 304, 315, 320, 328, 359, 370, and 379 as targets of pkc?, ???, And ?. |
|
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-89221 |
Ser304 |
GAPPRRSsIRNAHSI |
Homo sapiens |
|
pmid |
sentence |
12056906 |
Pkc alpha, beta ii, delta, and zeta expressed in human neutrophils can individually phosphorylate p47(phox) and induce both its translocation and nadph oxidase activation. The use of p47phox mutants identified serines 303, 304, 315, 320, 328, 359, 370, and 379 as targets of pkc?, ???, And ?. |
|
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-89225 |
Ser315 |
AHSIHQRsRKRLSQD |
Homo sapiens |
Neutrophil |
pmid |
sentence |
12056906 |
Pkc alpha, beta ii, delta, and zeta expressed in human neutrophils can individually phosphorylate p47(phox) and induce both its translocation and nadph oxidase activation. The use of p47phox mutants identified serines 303, 304, 315, 320, 328, 359, 370, and 379 as targets of pkc?, ???, And ?. |
|
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-89229 |
Ser320 |
QRSRKRLsQDAYRRN |
Homo sapiens |
Neutrophil |
pmid |
sentence |
12056906 |
Pkc alpha, beta ii, delta, and zeta expressed in human neutrophils can individually phosphorylate p47(phox) and induce both its translocation and nadph oxidase activation. The use of p47phox mutants identified serines 303, 304, 315, 320, 328, 359, 370, and 379 as targets of pkc?, ???, And ?. |
|
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-89233 |
Ser328 |
QDAYRRNsVRFLQQR |
Homo sapiens |
Neutrophil |
pmid |
sentence |
12056906 |
Pkc alpha, beta ii, delta, and zeta expressed in human neutrophils can individually phosphorylate p47(phox) and induce both its translocation and nadph oxidase activation. The use of p47phox mutants identified serines 303, 304, 315, 320, 328, 359, 370, and 379 as targets of pkc?, ???, And ?. |
|
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-89237 |
Ser359 |
EERQTQRsKPQPAVP |
Homo sapiens |
Neutrophil |
pmid |
sentence |
12056906 |
Pkc alpha, beta ii, delta, and zeta expressed in human neutrophils can individually phosphorylate p47(phox) and induce both its translocation and nadph oxidase activation. The use of p47phox mutants identified serines 303, 304, 315, 320, 328, 359, 370, and 379 as targets of pkc?, ???, And ?. |
|
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-89241 |
Ser370 |
PAVPPRPsADLILNR |
Homo sapiens |
Neutrophil |
pmid |
sentence |
12056906 |
Pkc alpha, beta ii, delta, and zeta expressed in human neutrophils can individually phosphorylate p47(phox) and induce both its translocation and nadph oxidase activation. The use of p47phox mutants identified serines 303, 304, 315, 320, 328, 359, 370, and 379 as targets of pkc?, ???, And ?. |
|
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-89248 |
Ser379 |
DLILNRCsESTKRKL |
Homo sapiens |
Neutrophil |
pmid |
sentence |
12056906 |
Pkc alpha, beta ii, delta, and zeta expressed in human neutrophils can individually phosphorylate p47(phox) and induce both its translocation and nadph oxidase activation. The use of p47phox mutants identified serines 303, 304, 315, 320, 328, 359, 370, and 379 as targets of pkc?, ???, And ?. |
|
Publications: |
8 |
Organism: |
Homo Sapiens |
+ |
PRKCZ | up-regulates
phosphorylation
|
NCF1 |
0.402 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-89252 |
Ser303 |
RGAPPRRsSIRNAHS |
Homo sapiens |
Neutrophil |
pmid |
sentence |
12056906 |
Phosphopeptide mapping of p47(phox) showed that, as opposed to pkc zeta, pkc alpha, beta ii, and delta are able to phosphorylate all the major pkc sites. The use of p47(phox) mutants identified serines 303, 304, 315, 320, 328, 359, 370, and 379 as targets of pkc alpha, beta ii, and delta.Taken together, these results suggest that pkc alpha, beta ii, delta, and zeta expressed in human neutrophils can individually phosphorylate p47(phox) and induce both its translocation and nadph oxidase activation. |
|
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-89260 |
Ser304 |
GAPPRRSsIRNAHSI |
Homo sapiens |
|
pmid |
sentence |
12056906 |
Phosphopeptide mapping of p47(phox) showed that, as opposed to pkc zeta, pkc alpha, beta ii, and delta are able to phosphorylate all the major pkc sites. The use of p47(phox) mutants identified serines 303, 304, 315, 320, 328, 359, 370, and 379 as targets of pkc alpha, beta ii, and delta.Taken together, these results suggest that pkc alpha, beta ii, delta, and zeta expressed in human neutrophils can individually phosphorylate p47(phox) and induce both its translocation and nadph oxidase activation. |
|
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-89264 |
Ser315 |
AHSIHQRsRKRLSQD |
Homo sapiens |
|
pmid |
sentence |
12056906 |
Phosphopeptide mapping of p47(phox) showed that, as opposed to pkc zeta, pkc alpha, beta ii, and delta are able to phosphorylate all the major pkc sites. The use of p47(phox) mutants identified serines 303, 304, 315, 320, 328, 359, 370, and 379 as targets of pkc alpha, beta ii, and delta.Taken together, these results suggest that pkc alpha, beta ii, delta, and zeta expressed in human neutrophils can individually phosphorylate p47(phox) and induce both its translocation and nadph oxidase activation. |
|
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-89268 |
Ser320 |
QRSRKRLsQDAYRRN |
Homo sapiens |
|
pmid |
sentence |
12056906 |
Phosphopeptide mapping of p47(phox) showed that, as opposed to pkc zeta, pkc alpha, beta ii, and delta are able to phosphorylate all the major pkc sites. The use of p47(phox) mutants identified serines 303, 304, 315, 320, 328, 359, 370, and 379 as targets of pkc alpha, beta ii, and delta.Taken together, these results suggest that pkc alpha, beta ii, delta, and zeta expressed in human neutrophils can individually phosphorylate p47(phox) and induce both its translocation and nadph oxidase activation. |
|
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-89272 |
Ser328 |
QDAYRRNsVRFLQQR |
Homo sapiens |
Neutrophil |
pmid |
sentence |
12056906 |
Phosphopeptide mapping of p47(phox) showed that, as opposed to pkc zeta, pkc alpha, beta ii, and delta are able to phosphorylate all the major pkc sites. The use of p47(phox) mutants identified serines 303, 304, 315, 320, 328, 359, 370, and 379 as targets of pkc alpha, beta ii, and delta.Taken together, these results suggest that pkc alpha, beta ii, delta, and zeta expressed in human neutrophils can individually phosphorylate p47(phox) and induce both its translocation and nadph oxidase activation. |
|
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-89280 |
Ser359 |
EERQTQRsKPQPAVP |
Homo sapiens |
Neutrophil |
pmid |
sentence |
12056906 |
Phosphopeptide mapping of p47(phox) showed that, as opposed to pkc zeta, pkc alpha, beta ii, and delta are able to phosphorylate all the major pkc sites. The use of p47(phox) mutants identified serines 303, 304, 315, 320, 328, 359, 370, and 379 as targets of pkc alpha, beta ii, and delta.Taken together, these results suggest that pkc alpha, beta ii, delta, and zeta expressed in human neutrophils can individually phosphorylate p47(phox) and induce both its translocation and nadph oxidase activation. |
|
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-89284 |
Ser370 |
PAVPPRPsADLILNR |
Homo sapiens |
Neutrophil |
pmid |
sentence |
12056906 |
Phosphopeptide mapping of p47(phox) showed that, as opposed to pkc zeta, pkc alpha, beta ii, and delta are able to phosphorylate all the major pkc sites. The use of p47(phox) mutants identified serines 303, 304, 315, 320, 328, 359, 370, and 379 as targets of pkc alpha, beta ii, and delta.Taken together, these results suggest that pkc alpha, beta ii, delta, and zeta expressed in human neutrophils can individually phosphorylate p47(phox) and induce both its translocation and nadph oxidase activation. |
|
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-89288 |
Ser379 |
DLILNRCsESTKRKL |
Homo sapiens |
Neutrophil |
pmid |
sentence |
12056906 |
Phosphopeptide mapping of p47(phox) showed that, as opposed to pkc zeta, pkc alpha, beta ii, and delta are able to phosphorylate all the major pkc sites. The use of p47(phox) mutants identified serines 303, 304, 315, 320, 328, 359, 370, and 379 as targets of pkc alpha, beta ii, and delta.Taken together, these results suggest that pkc alpha, beta ii, delta, and zeta expressed in human neutrophils can individually phosphorylate p47(phox) and induce both its translocation and nadph oxidase activation. |
|
Publications: |
8 |
Organism: |
Homo Sapiens |
+ |
PRKCA | up-regulates
phosphorylation
|
NCF1 |
0.538 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-89150 |
Ser303 |
RGAPPRRsSIRNAHS |
Homo sapiens |
Neutrophil |
pmid |
sentence |
12056906 |
Phosphopeptide mapping of p47(phox) showed that, as opposed to pkc zeta, pkc alpha, beta ii, and delta are able to phosphorylate all the major pkc sites. The use of p47(phox) mutants identified serines 303, 304, 315, 320, 328, 359, 370, and 379 as targets of pkc alpha, beta ii, and delta.Taken together, these results suggest that pkc alpha, beta ii, delta, and zeta expressed in human neutrophils can individually phosphorylate p47(phox) and induce both its translocation and nadph oxidase activation. |
|
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-89154 |
Ser304 |
GAPPRRSsIRNAHSI |
Homo sapiens |
Neutrophil |
pmid |
sentence |
12056906 |
Phosphopeptide mapping of p47(phox) showed that, as opposed to pkc zeta, pkc alpha, beta ii, and delta are able to phosphorylate all the major pkc sites. The use of p47(phox) mutants identified serines 303, 304, 315, 320, 328, 359, 370, and 379 as targets of pkc alpha, beta ii, and delta.Taken together, these results suggest that pkc alpha, beta ii, delta, and zeta expressed in human neutrophils can individually phosphorylate p47(phox) and induce both its translocation and nadph oxidase activation. |
|
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-89158 |
Ser315 |
AHSIHQRsRKRLSQD |
Homo sapiens |
Neutrophil |
pmid |
sentence |
12056906 |
Phosphopeptide mapping of p47(phox) showed that, as opposed to pkc zeta, pkc alpha, beta ii, and delta are able to phosphorylate all the major pkc sites. The use of p47(phox) mutants identified serines 303, 304, 315, 320, 328, 359, 370, and 379 as targets of pkc alpha, beta ii, and delta.Taken together, these results suggest that pkc alpha, beta ii, delta, and zeta expressed in human neutrophils can individually phosphorylate p47(phox) and induce both its translocation and nadph oxidase activation. |
|
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-89162 |
Ser320 |
QRSRKRLsQDAYRRN |
Homo sapiens |
Neutrophil |
pmid |
sentence |
12056906 |
Phosphopeptide mapping of p47(phox) showed that, as opposed to pkc zeta, pkc alpha, beta ii, and delta are able to phosphorylate all the major pkc sites. The use of p47(phox) mutants identified serines 303, 304, 315, 320, 328, 359, 370, and 379 as targets of pkc alpha, beta ii, and delta.Taken together, these results suggest that pkc alpha, beta ii, delta, and zeta expressed in human neutrophils can individually phosphorylate p47(phox) and induce both its translocation and nadph oxidase activation. |
|
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-89166 |
Ser328 |
QDAYRRNsVRFLQQR |
Homo sapiens |
|
pmid |
sentence |
12056906 |
Phosphopeptide mapping of p47(phox) showed that, as opposed to pkc zeta, pkc alpha, beta ii, and delta are able to phosphorylate all the major pkc sites. The use of p47(phox) mutants identified serines 303, 304, 315, 320, 328, 359, 370, and 379 as targets of pkc alpha, beta ii, and delta.Taken together, these results suggest that pkc alpha, beta ii, delta, and zeta expressed in human neutrophils can individually phosphorylate p47(phox) and induce both its translocation and nadph oxidase activation. |
|
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-89170 |
Ser359 |
EERQTQRsKPQPAVP |
Homo sapiens |
Neutrophil |
pmid |
sentence |
12056906 |
Phosphopeptide mapping of p47(phox) showed that, as opposed to pkc zeta, pkc alpha, beta ii, and delta are able to phosphorylate all the major pkc sites. The use of p47(phox) mutants identified serines 303, 304, 315, 320, 328, 359, 370, and 379 as targets of pkc alpha, beta ii, and delta.Taken together, these results suggest that pkc alpha, beta ii, delta, and zeta expressed in human neutrophils can individually phosphorylate p47(phox) and induce both its translocation and nadph oxidase activation. |
|
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-89174 |
Ser370 |
PAVPPRPsADLILNR |
Homo sapiens |
Neutrophil |
pmid |
sentence |
12056906 |
Phosphopeptide mapping of p47(phox) showed that, as opposed to pkc zeta, pkc alpha, beta ii, and delta are able to phosphorylate all the major pkc sites. The use of p47(phox) mutants identified serines 303, 304, 315, 320, 328, 359, 370, and 379 as targets of pkc alpha, beta ii, and delta.Taken together, these results suggest that pkc alpha, beta ii, delta, and zeta expressed in human neutrophils can individually phosphorylate p47(phox) and induce both its translocation and nadph oxidase activation. |
|
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-89178 |
Ser379 |
DLILNRCsESTKRKL |
Homo sapiens |
Neutrophil |
pmid |
sentence |
12056906 |
Phosphopeptide mapping of p47(phox) showed that, as opposed to pkc zeta, pkc alpha, beta ii, and delta are able to phosphorylate all the major pkc sites. The use of p47(phox) mutants identified serines 303, 304, 315, 320, 328, 359, 370, and 379 as targets of pkc alpha, beta ii, and delta.Taken together, these results suggest that pkc alpha, beta ii, delta, and zeta expressed in human neutrophils can individually phosphorylate p47(phox) and induce both its translocation and nadph oxidase activation. |
|
Publications: |
8 |
Organism: |
Homo Sapiens |
+ |
AKT1 | up-regulates
phosphorylation
|
NCF1 |
0.577 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-252586 |
Ser304 |
GAPPRRSsIRNAHSI |
Homo sapiens |
Neutrophil |
pmid |
sentence |
10559253 |
Akt phosphorylates p47phox and mediates respiratory burst activity in human neutrophils. A direct interaction between p47(phox) and akt was shown. Active recombinant akt phosphorylated recombinant p47(phox) in vitro. Mutation analysis indicated that 2 aa residues, ser(304) and ser(328), were phosphorylated by akt. Inhibition of akt activity also inhibited fmlp-stimulated neutrophil chemotaxis. |
|
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-252587 |
Ser328 |
QDAYRRNsVRFLQQR |
Homo sapiens |
Neutrophil |
pmid |
sentence |
10559253 |
Akt phosphorylates p47phox and mediates respiratory burst activity in human neutrophils. A direct interaction between p47(phox) and akt was shown. Active recombinant akt phosphorylated recombinant p47(phox) in vitro. Mutation analysis indicated that 2 aa residues, ser(304) and ser(328), were phosphorylated by akt. Inhibition of akt activity also inhibited fmlp-stimulated neutrophil chemotaxis. |
|
Publications: |
2 |
Organism: |
Homo Sapiens |
+ |
AKT | up-regulates
phosphorylation
|
NCF1 |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-72133 |
Ser304 |
GAPPRRSsIRNAHSI |
Homo sapiens |
Neutrophil |
pmid |
sentence |
10559253 |
Akt phosphorylates p47phox and mediates respiratory burst activity in human neutrophils. A direct interaction between p47(phox) and akt was shown. Active recombinant akt phosphorylated recombinant p47(phox) in vitro. Mutation analysis indicated that 2 aa residues, ser(304) and ser(328), were phosphorylated by akt. Inhibition of akt activity also inhibited fmlp-stimulated neutrophil chemotaxis. |
|
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-72137 |
Ser328 |
QDAYRRNsVRFLQQR |
Homo sapiens |
Neutrophil |
pmid |
sentence |
10559253 |
Akt phosphorylates p47phox and mediates respiratory burst activity in human neutrophils. A direct interaction between p47(phox) and akt was shown. Active recombinant akt phosphorylated recombinant p47(phox) in vitro. Mutation analysis indicated that 2 aa residues, ser(304) and ser(328), were phosphorylated by akt. Inhibition of akt activity also inhibited fmlp-stimulated neutrophil chemotaxis. |
|
Publications: |
2 |
Organism: |
Homo Sapiens |
+ |
MAPK1 | up-regulates
phosphorylation
|
NCF1 |
0.463 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-147170 |
Ser345 |
QARPGPQsPGSPLEE |
Homo sapiens |
Neutrophil |
pmid |
sentence |
16778989 |
Erk1/2 are the kinases involved in p47phox_ phosphorylation on ser345 in gm-csfprimed human neutrophils._ Phosphorylation of ser345 is required for the priming of nadph oxidase activity in neutrophil-like cells |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
MAPK3 | up-regulates
phosphorylation
|
NCF1 |
0.432 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-40821 |
Ser345 |
QARPGPQsPGSPLEE |
Homo sapiens |
|
pmid |
sentence |
8626435 |
Upon activation, several serine residues on the cytosolic oxidase subunit p47phox become phosphorylated. Mitogen-activated protein kinase phophorylated only the peptide containing ser345/348. |
|
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-147174 |
Ser345 |
QARPGPQsPGSPLEE |
Homo sapiens |
Neutrophil |
pmid |
sentence |
16778989 |
Inhibitors of the erk1/2 pathway abrogated gm-csf-induced phosphorylation of ser345, while p38 mapk inhibitor abrogated tnf-alpha-induced phosphorylation of ser345.These results show that the ala-mutated p47phox acts as a dominant-negative inhibitor of endogenous p47phox and clearly indicate that phosphorylation of ser345 is required for the priming of nadph oxidase activity in neutrophil-like cells. |
|
Publications: |
2 |
Organism: |
Homo Sapiens |
+ |
PRKCD | up-regulates activity
phosphorylation
|
NCF1 |
0.459 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-276623 |
Ser348 |
PGPQSPGsPLEEERQ |
in vitro |
|
pmid |
sentence |
24632950 |
Of note, PKCδ, when it was activated by PDPK1, directly bound to the SH3-N domain of p47(phox) and catalyzed the phosphorylation on Ser348 and Ser473 residues of p47(phox) C-terminal in a K-Ras-dependent manner, finally leading to its membrane translocation.PKCδ phosphorylates p47phox for K-Ras-induced ROS generation. PKCδ binds to the SH3-N domain and phosphorylates Ser348 and Ser379 residues in p47phox for K-RasV12-induced ROS generation and consequent malignant transformation. |
|
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-276622 |
Ser379 |
DLILNRCsESTKRKL |
in vitro |
|
pmid |
sentence |
24632950 |
Of note, PKCδ, when it was activated by PDPK1, directly bound to the SH3-N domain of p47(phox) and catalyzed the phosphorylation on Ser348 and Ser473 residues of p47(phox) C-terminal in a K-Ras-dependent manner, finally leading to its membrane translocation.PKCδ phosphorylates p47phox for K-Ras-induced ROS generation. PKCδ binds to the SH3-N domain and phosphorylates Ser348 and Ser379 residues in p47phox for K-RasV12-induced ROS generation and consequent malignant transformation. |
|
Publications: |
2 |
Organism: |
In Vitro |
+ |
NCF1 | form complex
binding
|
Phagocyte NADPH oxidase complex |
0.74 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-277630 |
|
|
Homo sapiens |
|
pmid |
sentence |
37263099 |
NADPH oxidase is composed of essential protein components in its active state: membranous subunits, including p22-phox and gp91-phox, and cytoplasmic subunits, including p47-phox, p67-phox, p40-phox, and RAC2 (in neutrophils), among which NCF4 encodes the cytoplasmic subunit p40-phox |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
Gbeta | up-regulates
phosphorylation
|
NCF1 |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-270091 |
|
|
Homo sapiens |
Neutrophil |
pmid |
sentence |
16778989 |
Inhibitors of the erk1/2 pathway abrogated gm-csf-induced phosphorylation of ser345, while p38 mapk inhibitor abrogated tnf-alpha-induced phosphorylation of ser345.These results show that the ala-mutated p47phox acts as a dominant-negative inhibitor of endogenous p47phox and clearly indicate that phosphorylation of ser345 is required for the priming of nadph oxidase activity in neutrophil-like cells. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
HBP1 | down-regulates quantity by repression
transcriptional regulation
|
NCF1 |
0.268 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-261614 |
|
|
Homo sapiens |
HEK-293T Cell |
pmid |
sentence |
15024088 |
Together, these results indicate that HBP1 may contribute to the regulation of NADPH oxidase-dependent superoxide production through transcriptional repression of the p47phox gene. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
NCF1 | up-regulates activity
binding
|
NOX3 |
0.612 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-276624 |
|
|
Homo sapiens |
|
pmid |
sentence |
12672956 |
Stimulus-induced phosphorylation of p47phox causes a conformational change, by which both PX and SH3 domains become accessible to their membranous targets, phosphoinositides and p22phox, respectively. Cooperation of these two interactions, each being indispensable, enables p47phox to form a stable complex with cytochrome b558 (composed of the two subunit gp91phox and p22phox), leading to activation of the phagocyte NADPH oxidase. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
NCF1 | up-regulates activity
binding
|
CYBA |
0.783 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-276625 |
|
|
Homo sapiens |
|
pmid |
sentence |
12672956 |
Stimulus-induced phosphorylation of p47phox causes a conformational change, by which both PX and SH3 domains become accessible to their membranous targets, phosphoinositides and p22phox, respectively. Cooperation of these two interactions, each being indispensable, enables p47phox to form a stable complex with cytochrome b558 (composed of the two subunit gp91phox and p22phox), leading to activation of the phagocyte NADPH oxidase. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
ERK1/2 | up-regulates
phosphorylation
|
NCF1 |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-270187 |
|
|
Homo sapiens |
Neutrophil |
pmid |
sentence |
16778989 |
Inhibitors of the erk1/2 pathway abrogated gm-csf-induced phosphorylation of ser345, while p38 mapk inhibitor abrogated tnf-alpha-induced phosphorylation of ser345.These results show that the ala-mutated p47phox acts as a dominant-negative inhibitor of endogenous p47phox and clearly indicate that phosphorylation of ser345 is required for the priming of nadph oxidase activity in neutrophil-like cells. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |