| + |
CDK13 | up-regulates activity 
phosphorylation
|
POLR2A |
0.559 |
| Identifier |
Residue |
Sequence |
Organism |
Cell Line |
| SIGNOR-273054 |
Ser1616 |
TPQSPSYsPTSPSYS |
Homo sapiens |
MV-4-11 Cell |
| pmid |
sentence |
| 32917631 |
Together, these studies demonstrate the important, yet largely redundant, role for CDK12 and CDK13 for the regulation of POLII CTD phosphorylation at multiple residues, as well as the global role for both of these kinases in regulating POLII occupancy across the genome.|CDK12 and CDK13 are thus evolutionarily related and structurally similar kinases, and biochemical assays have demonstrated that both have POLII C-terminal domain (CTD) kinase activity and the ability to phosphorylate the Ser2 residue of the repetitive CTD heptad sequence |
|
| Identifier |
Residue |
Sequence |
Organism |
Cell Line |
| SIGNOR-273047 |
Ser1623 |
SPTSPSYsPTSPSYS |
Homo sapiens |
MV-4-11 Cell |
| pmid |
sentence |
| 32917631 |
Together, these studies demonstrate the important, yet largely redundant, role for CDK12 and CDK13 for the regulation of POLII CTD phosphorylation at multiple residues, as well as the global role for both of these kinases in regulating POLII occupancy across the genome.|CDK12 and CDK13 are thus evolutionarily related and structurally similar kinases, and biochemical assays have demonstrated that both have POLII C-terminal domain (CTD) kinase activity and the ability to phosphorylate the Ser2 residue of the repetitive CTD heptad sequence |
|
| Identifier |
Residue |
Sequence |
Organism |
Cell Line |
| SIGNOR-273042 |
Ser1644 |
SPTSPSYsPTSPSYS |
Homo sapiens |
MV-4-11 Cell |
| pmid |
sentence |
| 32917631 |
Together, these studies demonstrate the important, yet largely redundant, role for CDK12 and CDK13 for the regulation of POLII CTD phosphorylation at multiple residues, as well as the global role for both of these kinases in regulating POLII occupancy across the genome.|CDK12 and CDK13 are thus evolutionarily related and structurally similar kinases, and biochemical assays have demonstrated that both have POLII C-terminal domain (CTD) kinase activity and the ability to phosphorylate the Ser2 residue of the repetitive CTD heptad sequence |
|
| Identifier |
Residue |
Sequence |
Organism |
Cell Line |
| SIGNOR-273040 |
Ser1651 |
SPTSPSYsPTSPSYS |
Homo sapiens |
MV-4-11 Cell |
| pmid |
sentence |
| 32917631 |
Together, these studies demonstrate the important, yet largely redundant, role for CDK12 and CDK13 for the regulation of POLII CTD phosphorylation at multiple residues, as well as the global role for both of these kinases in regulating POLII occupancy across the genome.|CDK12 and CDK13 are thus evolutionarily related and structurally similar kinases, and biochemical assays have demonstrated that both have POLII C-terminal domain (CTD) kinase activity and the ability to phosphorylate the Ser2 residue of the repetitive CTD heptad sequence |
|
| Identifier |
Residue |
Sequence |
Organism |
Cell Line |
| SIGNOR-273041 |
Ser1665 |
SPTSPSYsPTSPSYS |
Homo sapiens |
MV-4-11 Cell |
| pmid |
sentence |
| 32917631 |
Together, these studies demonstrate the important, yet largely redundant, role for CDK12 and CDK13 for the regulation of POLII CTD phosphorylation at multiple residues, as well as the global role for both of these kinases in regulating POLII occupancy across the genome.|CDK12 and CDK13 are thus evolutionarily related and structurally similar kinases, and biochemical assays have demonstrated that both have POLII C-terminal domain (CTD) kinase activity and the ability to phosphorylate the Ser2 residue of the repetitive CTD heptad sequence |
|
| Identifier |
Residue |
Sequence |
Organism |
Cell Line |
| SIGNOR-273046 |
Ser1672 |
SPTSPSYsPTSPSYS |
Homo sapiens |
MV-4-11 Cell |
| pmid |
sentence |
| 32917631 |
Together, these studies demonstrate the important, yet largely redundant, role for CDK12 and CDK13 for the regulation of POLII CTD phosphorylation at multiple residues, as well as the global role for both of these kinases in regulating POLII occupancy across the genome.|CDK12 and CDK13 are thus evolutionarily related and structurally similar kinases, and biochemical assays have demonstrated that both have POLII C-terminal domain (CTD) kinase activity and the ability to phosphorylate the Ser2 residue of the repetitive CTD heptad sequence |
|
| Identifier |
Residue |
Sequence |
Organism |
Cell Line |
| SIGNOR-273045 |
Ser1693 |
SPTSPSYsPTSPSYS |
Homo sapiens |
MV-4-11 Cell |
| pmid |
sentence |
| 32917631 |
Together, these studies demonstrate the important, yet largely redundant, role for CDK12 and CDK13 for the regulation of POLII CTD phosphorylation at multiple residues, as well as the global role for both of these kinases in regulating POLII occupancy across the genome.|CDK12 and CDK13 are thus evolutionarily related and structurally similar kinases, and biochemical assays have demonstrated that both have POLII C-terminal domain (CTD) kinase activity and the ability to phosphorylate the Ser2 residue of the repetitive CTD heptad sequence |
|
| Identifier |
Residue |
Sequence |
Organism |
Cell Line |
| SIGNOR-273044 |
Ser1714 |
SPTSPSYsPTSPSYS |
Homo sapiens |
MV-4-11 Cell |
| pmid |
sentence |
| 32917631 |
Together, these studies demonstrate the important, yet largely redundant, role for CDK12 and CDK13 for the regulation of POLII CTD phosphorylation at multiple residues, as well as the global role for both of these kinases in regulating POLII occupancy across the genome.|CDK12 and CDK13 are thus evolutionarily related and structurally similar kinases, and biochemical assays have demonstrated that both have POLII C-terminal domain (CTD) kinase activity and the ability to phosphorylate the Ser2 residue of the repetitive CTD heptad sequence |
|
| Identifier |
Residue |
Sequence |
Organism |
Cell Line |
| SIGNOR-273048 |
Ser1721 |
SPTSPSYsPTSPSYS |
Homo sapiens |
MV-4-11 Cell |
| pmid |
sentence |
| 32917631 |
Together, these studies demonstrate the important, yet largely redundant, role for CDK12 and CDK13 for the regulation of POLII CTD phosphorylation at multiple residues, as well as the global role for both of these kinases in regulating POLII occupancy across the genome.|CDK12 and CDK13 are thus evolutionarily related and structurally similar kinases, and biochemical assays have demonstrated that both have POLII C-terminal domain (CTD) kinase activity and the ability to phosphorylate the Ser2 residue of the repetitive CTD heptad sequence |
|
| Identifier |
Residue |
Sequence |
Organism |
Cell Line |
| SIGNOR-273043 |
Ser1735 |
SPTSPSYsPTSPSYS |
Homo sapiens |
MV-4-11 Cell |
| pmid |
sentence |
| 32917631 |
Together, these studies demonstrate the important, yet largely redundant, role for CDK12 and CDK13 for the regulation of POLII CTD phosphorylation at multiple residues, as well as the global role for both of these kinases in regulating POLII occupancy across the genome.|CDK12 and CDK13 are thus evolutionarily related and structurally similar kinases, and biochemical assays have demonstrated that both have POLII C-terminal domain (CTD) kinase activity and the ability to phosphorylate the Ser2 residue of the repetitive CTD heptad sequence |
|
| Identifier |
Residue |
Sequence |
Organism |
Cell Line |
| SIGNOR-273058 |
Ser1763 |
TPTSPSYsPTSPSYS |
Homo sapiens |
MV-4-11 Cell |
| pmid |
sentence |
| 32917631 |
Together, these studies demonstrate the important, yet largely redundant, role for CDK12 and CDK13 for the regulation of POLII CTD phosphorylation at multiple residues, as well as the global role for both of these kinases in regulating POLII occupancy across the genome.|CDK12 and CDK13 are thus evolutionarily related and structurally similar kinases, and biochemical assays have demonstrated that both have POLII C-terminal domain (CTD) kinase activity and the ability to phosphorylate the Ser2 residue of the repetitive CTD heptad sequence |
|
| Identifier |
Residue |
Sequence |
Organism |
Cell Line |
| SIGNOR-273057 |
Ser1784 |
TPTSPNYsPTSPSYS |
Homo sapiens |
MV-4-11 Cell |
| pmid |
sentence |
| 32917631 |
Together, these studies demonstrate the important, yet largely redundant, role for CDK12 and CDK13 for the regulation of POLII CTD phosphorylation at multiple residues, as well as the global role for both of these kinases in regulating POLII occupancy across the genome.|CDK12 and CDK13 are thus evolutionarily related and structurally similar kinases, and biochemical assays have demonstrated that both have POLII C-terminal domain (CTD) kinase activity and the ability to phosphorylate the Ser2 residue of the repetitive CTD heptad sequence |
|
| Identifier |
Residue |
Sequence |
Organism |
Cell Line |
| SIGNOR-273055 |
Ser1861 |
TPTSPKYsPTSPKYS |
Homo sapiens |
MV-4-11 Cell |
| pmid |
sentence |
| 32917631 |
Together, these studies demonstrate the important, yet largely redundant, role for CDK12 and CDK13 for the regulation of POLII CTD phosphorylation at multiple residues, as well as the global role for both of these kinases in regulating POLII occupancy across the genome.|CDK12 and CDK13 are thus evolutionarily related and structurally similar kinases, and biochemical assays have demonstrated that both have POLII C-terminal domain (CTD) kinase activity and the ability to phosphorylate the Ser2 residue of the repetitive CTD heptad sequence |
|
| Identifier |
Residue |
Sequence |
Organism |
Cell Line |
| SIGNOR-273037 |
Ser1868 |
SPTSPKYsPTSPKYS |
Homo sapiens |
MV-4-11 Cell |
| pmid |
sentence |
| 32917631 |
Together, these studies demonstrate the important, yet largely redundant, role for CDK12 and CDK13 for the regulation of POLII CTD phosphorylation at multiple residues, as well as the global role for both of these kinases in regulating POLII occupancy across the genome.|CDK12 and CDK13 are thus evolutionarily related and structurally similar kinases, and biochemical assays have demonstrated that both have POLII C-terminal domain (CTD) kinase activity and the ability to phosphorylate the Ser2 residue of the repetitive CTD heptad sequence |
|
| Identifier |
Residue |
Sequence |
Organism |
Cell Line |
| SIGNOR-273039 |
Ser1875 |
SPTSPKYsPTSPTYS |
Homo sapiens |
MV-4-11 Cell |
| pmid |
sentence |
| 32917631 |
Together, these studies demonstrate the important, yet largely redundant, role for CDK12 and CDK13 for the regulation of POLII CTD phosphorylation at multiple residues, as well as the global role for both of these kinases in regulating POLII occupancy across the genome.|CDK12 and CDK13 are thus evolutionarily related and structurally similar kinases, and biochemical assays have demonstrated that both have POLII C-terminal domain (CTD) kinase activity and the ability to phosphorylate the Ser2 residue of the repetitive CTD heptad sequence |
|
| Identifier |
Residue |
Sequence |
Organism |
Cell Line |
| SIGNOR-273035 |
Ser1878 |
SPKYSPTsPTYSPTT |
Homo sapiens |
MV-4-11 Cell |
| pmid |
sentence |
| 32917631 |
Together, these studies demonstrate the important, yet largely redundant, role for CDK12 and CDK13 for the regulation of POLII CTD phosphorylation at multiple residues, as well as the global role for both of these kinases in regulating POLII occupancy across the genome.|CDK12 and CDK13 are thus evolutionarily related and structurally similar kinases, and biochemical assays have demonstrated that both have POLII C-terminal domain (CTD) kinase activity and the ability to phosphorylate the Ser2 residue of the repetitive CTD heptad sequence |
|
| Identifier |
Residue |
Sequence |
Organism |
Cell Line |
| SIGNOR-273052 |
Ser1882 |
SPTSPTYsPTTPKYS |
Homo sapiens |
MV-4-11 Cell |
| pmid |
sentence |
| 32917631 |
Together, these studies demonstrate the important, yet largely redundant, role for CDK12 and CDK13 for the regulation of POLII CTD phosphorylation at multiple residues, as well as the global role for both of these kinases in regulating POLII occupancy across the genome.|CDK12 and CDK13 are thus evolutionarily related and structurally similar kinases, and biochemical assays have demonstrated that both have POLII C-terminal domain (CTD) kinase activity and the ability to phosphorylate the Ser2 residue of the repetitive CTD heptad sequence |
|
| Identifier |
Residue |
Sequence |
Organism |
Cell Line |
| SIGNOR-273053 |
Ser1889 |
SPTTPKYsPTSPTYS |
Homo sapiens |
MV-4-11 Cell |
| pmid |
sentence |
| 32917631 |
Together, these studies demonstrate the important, yet largely redundant, role for CDK12 and CDK13 for the regulation of POLII CTD phosphorylation at multiple residues, as well as the global role for both of these kinases in regulating POLII occupancy across the genome.|CDK12 and CDK13 are thus evolutionarily related and structurally similar kinases, and biochemical assays have demonstrated that both have POLII C-terminal domain (CTD) kinase activity and the ability to phosphorylate the Ser2 residue of the repetitive CTD heptad sequence |
|
| Identifier |
Residue |
Sequence |
Organism |
Cell Line |
| SIGNOR-273051 |
Ser1896 |
SPTSPTYsPTSPVYT |
Homo sapiens |
MV-4-11 Cell |
| pmid |
sentence |
| 32917631 |
Together, these studies demonstrate the important, yet largely redundant, role for CDK12 and CDK13 for the regulation of POLII CTD phosphorylation at multiple residues, as well as the global role for both of these kinases in regulating POLII occupancy across the genome.|CDK12 and CDK13 are thus evolutionarily related and structurally similar kinases, and biochemical assays have demonstrated that both have POLII C-terminal domain (CTD) kinase activity and the ability to phosphorylate the Ser2 residue of the repetitive CTD heptad sequence |
|
| Identifier |
Residue |
Sequence |
Organism |
Cell Line |
| SIGNOR-273056 |
Ser1910 |
TPTSPKYsPTSPTYS |
Homo sapiens |
MV-4-11 Cell |
| pmid |
sentence |
| 32917631 |
Together, these studies demonstrate the important, yet largely redundant, role for CDK12 and CDK13 for the regulation of POLII CTD phosphorylation at multiple residues, as well as the global role for both of these kinases in regulating POLII occupancy across the genome.|CDK12 and CDK13 are thus evolutionarily related and structurally similar kinases, and biochemical assays have demonstrated that both have POLII C-terminal domain (CTD) kinase activity and the ability to phosphorylate the Ser2 residue of the repetitive CTD heptad sequence |
|
| Identifier |
Residue |
Sequence |
Organism |
Cell Line |
| SIGNOR-273050 |
Ser1917 |
SPTSPTYsPTSPKYS |
Homo sapiens |
MV-4-11 Cell |
| pmid |
sentence |
| 32917631 |
Together, these studies demonstrate the important, yet largely redundant, role for CDK12 and CDK13 for the regulation of POLII CTD phosphorylation at multiple residues, as well as the global role for both of these kinases in regulating POLII occupancy across the genome.|CDK12 and CDK13 are thus evolutionarily related and structurally similar kinases, and biochemical assays have demonstrated that both have POLII C-terminal domain (CTD) kinase activity and the ability to phosphorylate the Ser2 residue of the repetitive CTD heptad sequence |
|
| Identifier |
Residue |
Sequence |
Organism |
Cell Line |
| SIGNOR-273038 |
Ser1924 |
SPTSPKYsPTSPTYS |
Homo sapiens |
MV-4-11 Cell |
| pmid |
sentence |
| 32917631 |
Together, these studies demonstrate the important, yet largely redundant, role for CDK12 and CDK13 for the regulation of POLII CTD phosphorylation at multiple residues, as well as the global role for both of these kinases in regulating POLII occupancy across the genome.|CDK12 and CDK13 are thus evolutionarily related and structurally similar kinases, and biochemical assays have demonstrated that both have POLII C-terminal domain (CTD) kinase activity and the ability to phosphorylate the Ser2 residue of the repetitive CTD heptad sequence |
|
| Identifier |
Residue |
Sequence |
Organism |
Cell Line |
| SIGNOR-273049 |
Ser1931 |
SPTSPTYsPTSPKGS |
Homo sapiens |
MV-4-11 Cell |
| pmid |
sentence |
| 32917631 |
Together, these studies demonstrate the important, yet largely redundant, role for CDK12 and CDK13 for the regulation of POLII CTD phosphorylation at multiple residues, as well as the global role for both of these kinases in regulating POLII occupancy across the genome.|CDK12 and CDK13 are thus evolutionarily related and structurally similar kinases, and biochemical assays have demonstrated that both have POLII C-terminal domain (CTD) kinase activity and the ability to phosphorylate the Ser2 residue of the repetitive CTD heptad sequence |
|
| Identifier |
Residue |
Sequence |
Organism |
Cell Line |
| SIGNOR-273034 |
Ser1941 |
SPKGSTYsPTSPGYS |
Homo sapiens |
MV-4-11 Cell |
| pmid |
sentence |
| 32917631 |
Together, these studies demonstrate the important, yet largely redundant, role for CDK12 and CDK13 for the regulation of POLII CTD phosphorylation at multiple residues, as well as the global role for both of these kinases in regulating POLII occupancy across the genome.|CDK12 and CDK13 are thus evolutionarily related and structurally similar kinases, and biochemical assays have demonstrated that both have POLII C-terminal domain (CTD) kinase activity and the ability to phosphorylate the Ser2 residue of the repetitive CTD heptad sequence |
|
| Identifier |
Residue |
Sequence |
Organism |
Cell Line |
| SIGNOR-273036 |
Ser1948 |
SPTSPGYsPTSPTYS |
Homo sapiens |
MV-4-11 Cell |
| pmid |
sentence |
| 32917631 |
Together, these studies demonstrate the important, yet largely redundant, role for CDK12 and CDK13 for the regulation of POLII CTD phosphorylation at multiple residues, as well as the global role for both of these kinases in regulating POLII occupancy across the genome.|CDK12 and CDK13 are thus evolutionarily related and structurally similar kinases, and biochemical assays have demonstrated that both have POLII C-terminal domain (CTD) kinase activity and the ability to phosphorylate the Ser2 residue of the repetitive CTD heptad sequence |
|
| Publications: |
25 |
Organism: |
Homo Sapiens |
| + |
CDK13 | up-regulates activity
phosphorylation
|
EIF4B |
0.254 |
| Identifier |
Residue |
Sequence |
Organism |
Cell Line |
| SIGNOR-273115 |
Ser422 |
RERSRTGsESSQTGT |
Homo sapiens |
HCT-116 Cell |
| pmid |
sentence |
| 36882522 |
CDK13 directly phosphorylates 4E-BP1 at Thr46 and eIF4B at Ser422; genetically or pharmacologically inhibiting CDK13 disrupts mRNA translation. |
|
| Publications: |
1 |
Organism: |
Homo Sapiens |
| + |
CDK13 | up-regulates activity
phosphorylation
|
EIF4EBP1 |
0.2 |
| Identifier |
Residue |
Sequence |
Organism |
Cell Line |
| SIGNOR-273113 |
Thr46 |
GGTLFSTtPGGTRII |
Homo sapiens |
HCT-116 Cell |
| pmid |
sentence |
| 36882522 |
CDK13 directly phosphorylates 4E-BP1 at Thr46 and eIF4B at Ser422; genetically or pharmacologically inhibiting CDK13 disrupts mRNA translation. |
|
| Publications: |
1 |
Organism: |
Homo Sapiens |
| + |
CDK13 | form complex 
binding
|
CyclinK/CDK13 |
0.913 |
| Identifier |
Residue |
Sequence |
Organism |
Cell Line |
| SIGNOR-176844 |
|
|
Homo sapiens |
|
| pmid |
sentence |
| 22012619 |
We identified a 70-kda cyclin k (cyck) that binds cdk12 and cdk13 to form two different complexes (cyck/cdk12 or cyck/cdk13) in human cells |
|
| Publications: |
1 |
Organism: |
Homo Sapiens |
| + |
CCNO | up-regulates activity
binding
|
CDK13 |
0.275 |
| Identifier |
Residue |
Sequence |
Organism |
Cell Line |
| SIGNOR-275618 |
|
|
|
|
| pmid |
sentence |
| 37197505 |
Cyclin O promotes lung cancer progression and cetuximab resistance via cell cycle regulation and CDK13 interaction|CCNO promoted tumor cell proliferation and survival in vivo via CDK13| |
|
| Publications: |
1 |
3.0
CDK13
- 
- 