+ |
ATR |
phosphorylation
|
MCM2 |
0.697 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-126363 |
Ser108 |
DVEELTAsQREAAER |
Homo sapiens |
|
pmid |
sentence |
15210935 |
Atm phosphorylates mcm3 on s535 in response to ionizing radiation. Second, atr phosphorylates mcm2 on s108 in response to multiple forms of dna damage and stalling of replication forksthe functional consequences of mcm2 s108 and mcm3 s535 phosphorylation are not clear |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
CDC7 | up-regulates
phosphorylation
|
MCM2 |
0.961 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-187388 |
Ser108 |
DVEELTAsQREAAER |
Homo sapiens |
|
pmid |
sentence |
19647517 |
Phosphorylation of mcm2 by cdc7 promotes pre-replication complex assembly during cell-cycle re-entry |
|
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-143984 |
Ser13 |
ESFTMASsPAQRRRG |
Homo sapiens |
|
pmid |
sentence |
16446360 |
In this work, by in vitro kinase reactions and mass spectrometry analysis of the products, we have mapped phosphorylation sites in the n terminus of mcm2 by cdc7, cdk2, cdk1, and ck2 |
|
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-143988 |
Ser139 |
RRGLLYDsDEEDEER |
Homo sapiens |
|
pmid |
sentence |
16446360 |
In the present study, we report the identification of cdc7/dbf4 phosphorylation sites on mcm2 and determine the functional role of cdc7/dbf4 phosphorylation of mcm2 in the initiation of dna replication in human cells. |
|
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-148709 |
Ser139 |
RRGLLYDsDEEDEER |
Homo sapiens |
HeLa Cell |
pmid |
sentence |
16899510 |
In the present study, we report the identification of cdc7/dbf4 phosphorylation sites on mcm2 and determine the functional role of cdc7/dbf4 phosphorylation of mcm2 in the initiation of dna replication in human cells. |
|
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-143992 |
Ser27 |
GNDPLTSsPGRSSRR |
Homo sapiens |
|
pmid |
sentence |
16446360 |
In the present study, we report the identification of cdc7/dbf4 phosphorylation sites on mcm2 and determine the functional role of cdc7/dbf4 phosphorylation of mcm2 in the initiation of dna replication in human cells. |
|
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-148713 |
Ser27 |
GNDPLTSsPGRSSRR |
Homo sapiens |
HeLa Cell |
pmid |
sentence |
16899510 |
In the present study, we report the identification of cdc7/dbf4 phosphorylation sites on mcm2 and determine the functional role of cdc7/dbf4 phosphorylation of mcm2 in the initiation of dna replication in human cells. |
|
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-187392 |
Ser40 |
RRTDALTsSPGRDLP |
Homo sapiens |
|
pmid |
sentence |
19647517 |
Phosphorylation of mcm2 by cdc7 promotes pre-replication complex assembly during cell-cycle re-entry |
|
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-148717 |
Ser41 |
RTDALTSsPGRDLPP |
Homo sapiens |
|
pmid |
sentence |
16899510 |
In the present study, we report the identification of cdc7/dbf4 phosphorylation sites on mcm2 and determine the functional role of cdc7/dbf4 phosphorylation of mcm2 in the initiation of dna replication in human cells. |
|
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-143996 |
Ser41 |
RTDALTSsPGRDLPP |
Homo sapiens |
|
pmid |
sentence |
16446360 |
In the present study, we report the identification of cdc7/dbf4 phosphorylation sites on mcm2 and determine the functional role of cdc7/dbf4 phosphorylation of mcm2 in the initiation of dna replication in human cells. |
|
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-187396 |
Ser5 |
sESFTMAS |
Homo sapiens |
|
pmid |
sentence |
19647517 |
Phosphorylation of mcm2 by cdc7 promotes pre-replication complex assembly during cell-cycle re-entry |
|
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-187400 |
Ser53 |
LPPFEDEsEGLLGTE |
Homo sapiens |
|
pmid |
sentence |
19647517 |
Phosphorylation of mcm2 by cdc7 promotes pre-replication complex assembly during cell-cycle re-entry |
|
Publications: |
11 |
Organism: |
Homo Sapiens |
+ |
CSNK2A1 | up-regulates
phosphorylation
|
MCM2 |
0.262 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-144004 |
Ser13 |
ESFTMASsPAQRRRG |
Homo sapiens |
|
pmid |
sentence |
16446360 |
In this work, by in vitro kinase reactions and mass spectrometry analysis of the products, we have mapped phosphorylation sites in the n terminus of mcm2 by cdc7, cdk2, cdk1, and ck2 |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
CDK2 | up-regulates
phosphorylation
|
MCM2 |
0.724 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-144000 |
Ser13 |
ESFTMASsPAQRRRG |
Homo sapiens |
|
pmid |
sentence |
16446360 |
In this work, by in vitro kinase reactions and mass spectrometry analysis of the products, we have mapped phosphorylation sites in the n terminus of mcm2 by cdc7, cdk2, cdk1, and ck2 |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
CDK7 | up-regulates activity
phosphorylation
|
MCM2 |
0.304 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-259850 |
Ser139 |
RRGLLYDsDEEDEER |
Homo sapiens |
|
pmid |
sentence |
16899510 |
Taken together, these results indicate that Cdc7/Dbf4 phosphorylation of MCM2 is essential for the initiation of DNA replication in mammalian cells. | Because MCM2 was phosphorylated in vivo at Ser27, Ser41, and Ser139, which were phosphorylated by Cdc7/Dbf4 in vitro, the results suggested that Ser27, Ser41, and Ser139 are in vivo Cdc7/Dbf4 phosphorylation sites in MCM2. |
|
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-259848 |
Ser27 |
GNDPLTSsPGRSSRR |
Homo sapiens |
|
pmid |
sentence |
16899510 |
Taken together, these results indicate that Cdc7/Dbf4 phosphorylation of MCM2 is essential for the initiation of DNA replication in mammalian cells. | Because MCM2 was phosphorylated in vivo at Ser27, Ser41, and Ser139, which were phosphorylated by Cdc7/Dbf4 in vitro, the results suggested that Ser27, Ser41, and Ser139 are in vivo Cdc7/Dbf4 phosphorylation sites in MCM2. |
|
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-259849 |
Ser41 |
RTDALTSsPGRDLPP |
Homo sapiens |
|
pmid |
sentence |
16899510 |
Taken together, these results indicate that Cdc7/Dbf4 phosphorylation of MCM2 is essential for the initiation of DNA replication in mammalian cells. | Because MCM2 was phosphorylated in vivo at Ser27, Ser41, and Ser139, which were phosphorylated by Cdc7/Dbf4 in vitro, the results suggested that Ser27, Ser41, and Ser139 are in vivo Cdc7/Dbf4 phosphorylation sites in MCM2. |
|
Publications: |
3 |
Organism: |
Homo Sapiens |
+ |
CDT1 | up-regulates activity
binding
|
MCM2 |
0.806 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-261681 |
|
|
Homo sapiens |
HEK-293 Cell |
pmid |
sentence |
14672932 |
Chromosomal DNA replication requires the recruitment of the six-subunit minichromosome maintenance (Mcm) complex to chromatin through the action of Cdc6 and Cdt1. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
MCM2 | form complex
binding
|
MCM |
0.766 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-198428 |
|
|
Homo sapiens |
|
pmid |
sentence |
19946136 |
The Mcm2-7 complex serves as the eukaryotic replicative helicase, the molecular motor that both unwinds duplex DNA and powers fork progression during DNA replication. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |