Id: | acc3237 |
Group: | 2sens |
Protein: | Chk2 |
Gene Symbol: | CHEK2 |
Protein Id: | O96017 |
Protein Name: | CHK2_HUMAN |
PTM: | phosphorylation |
Site: | Thr68 |
Site Sequence: | TLSSLETVSTQELYSIPEDQE |
Disease Category: | Cancer |
Disease: | Cancer |
Disease Subtype: | |
Disease Cellline: | HCT116? |
Disease Info: | |
Drug: | doxorubicin |
Drug Info: | Doxorubicin is an anthracycline antibiotic used in cancer chemotherapy to treat a wide range of cancers. |
Effect: | modulate |
Effect Info: | "Doxorubicin achieves G2/M checkpoint arrest by inducing DNA damage, activating Chk2, and inhibiting Cdc2 kinase activity. CycG2 acts as an intermediary to enhance this process." |
Note: | |
Score: | 4.0 |
Pubmed(PMID): | 22589537 |
Sentence Index: | 22589537_5-6 |
Sentence: | "Expanding our previous finding that CycG2 overexpression induces a p53-dependent G(1)/S phase cell cycle arrest in HCT116 cells, we now demonstrate that this arrest response also requires the DDR checkpoint protein kinase Chk2. In accord with this finding we establish that ectopic CycG2 expression increases phosphorylation of Chk2 on threonine 68." |
Sequence & Structure:
MSRESDVEAQQSHGSSACSQPHGSVTQSQGSSSQSQGISSSSTSTMPNSSQSSHSSSGTLSSLETVSTQELYSIPEDQEPEDQEPEEPTPAPWARLWALQDGFANLECVNDNYWFGRDKSCEYCFDEPLLKRTDKYRTYSKKHFRIFREVGPKNSYIAYIEDHSGNGTFVNTELVGKGKRRPLNNNSEIALSLSRNKVFVFFDLTVDDQSVYPKALRDEYIMSKTLGSGACGEVKLAFERKTCKKVAIKIISKRKFAIGSAREADPALNVETEIEILKKLNHPCIIKIKNFFDAEDYYIVLELMEGGELFDKVVGNKRLKEATCKLYFYQMLLAVQYLHENGIIHRDLKPENVLLSSQEEDCLIKITDFGHSKILGETSLMRTLCGTPTYLAPEVLVSVGTAGYNRAVDCWSLGVILFICLSGYPPFSEHRTQVSLKDQITSGKYNFIPEVWAEVSEKALDLVKKLLVVDPKARFTTEEALRHPWLQDEDMKRKFQDLLSEENESTALPQVLAQPSTSRKRPREGEAEGAETTKRPAVCAAVL
Select PDB:
Target | Drug name | MOA | Phase | Status | Disease | Source |
---|---|---|---|---|---|---|
CHEK2 | PREXASERTIB | Serine/threonine-protein kinase Chk2 inhibitor | 2 | Completed | small cell lung carcinoma | ClinicalTrials |
CHEK2 | PREXASERTIB | Serine/threonine-protein kinase Chk2 inhibitor | 2 | Completed | cancer | ClinicalTrials |
CHEK2 | PREXASERTIB | Serine/threonine-protein kinase Chk2 inhibitor | 2 | Terminated | breast cancer | ClinicalTrials |
CHEK2 | PREXASERTIB | Serine/threonine-protein kinase Chk2 inhibitor | 2 | Terminated | ovarian cancer | ClinicalTrials |
CHEK2 | PREXASERTIB | Serine/threonine-protein kinase Chk2 inhibitor | 2 | Completed | ovarian cancer | ClinicalTrials |
CHEK2 | XL-844 | Serine/threonine-protein kinase Chk2 inhibitor | 1 | Terminated | chronic lymphocytic leukemia | ClinicalTrials |
CHEK2 | PREXASERTIB | Serine/threonine-protein kinase Chk2 inhibitor | 1 | Completed | myelodysplastic syndrome | ClinicalTrials |
CHEK2 | PREXASERTIB | Serine/threonine-protein kinase Chk2 inhibitor | 1 | Completed | acute myeloid leukemia | ClinicalTrials |
CHEK2 | PREXASERTIB | Serine/threonine-protein kinase Chk2 inhibitor | 1 | Active, not recruiting | central nervous system cancer | ClinicalTrials |
CHEK2 | XL-844 | Serine/threonine-protein kinase Chk2 inhibitor | 1 | Terminated | lymphoma | ClinicalTrials |
CHEK2 | PREXASERTIB | Serine/threonine-protein kinase Chk2 inhibitor | 1 | Completed | neoplasm | ClinicalTrials ClinicalTrials |
CHEK2 | PREXASERTIB | Serine/threonine-protein kinase Chk2 inhibitor | 1 | Completed | squamous cell lung carcinoma | ClinicalTrials |
CHEK2 | PREXASERTIB | Serine/threonine-protein kinase Chk2 inhibitor | 1 | Completed | squamous cell carcinoma | ClinicalTrials |
CHEK2 | PREXASERTIB | Serine/threonine-protein kinase Chk2 inhibitor | 1 | Active, not recruiting | medulloblastoma | ClinicalTrials |
CHEK2 | PREXASERTIB | Serine/threonine-protein kinase Chk2 inhibitor | 1 | Completed | non-small cell lung carcinoma | ClinicalTrials |
CHEK2 | PREXASERTIB | Serine/threonine-protein kinase Chk2 inhibitor | 1 | Completed | colorectal neoplasm | ClinicalTrials |
CHEK2 | PREXASERTIB | Serine/threonine-protein kinase Chk2 inhibitor | 1 | Completed | upper aerodigestive tract neoplasm | ClinicalTrials |
CHEK2 | PREXASERTIB | Serine/threonine-protein kinase Chk2 inhibitor | 1 | Completed | metastasis | ClinicalTrials |
CHEK2 | PREXASERTIB | Serine/threonine-protein kinase Chk2 inhibitor | 1 | Completed | Central Nervous System Neoplasm | ClinicalTrials |
CHEK2 | PREXASERTIB | Serine/threonine-protein kinase Chk2 inhibitor | 1 | Completed | chronic myelomonocytic leukemia | ClinicalTrials |
CHEK2 | PREXASERTIB | Serine/threonine-protein kinase Chk2 inhibitor | 1 | Active, not recruiting | brain cancer | ClinicalTrials |
CHEK2 | PREXASERTIB | Serine/threonine-protein kinase Chk2 inhibitor | 1 | Completed | cancer | ClinicalTrials ClinicalTrials ClinicalTrials |
CHEK2 | XL-844 | Serine/threonine-protein kinase Chk2 inhibitor | 1 | Terminated | cancer | ClinicalTrials |
Note: Only show clinically investigational or approved drugs with protein targets.
Protein Tractability:
source: Open TargetsPTM Intensity:
source: CPTACNo intensity data of this site,
show all other sites!
CHEK2-Ser163 | |||||
---|---|---|---|---|---|
Cancer | Intensity | ||||
BRCA | |||||
COAD | |||||
HGSC | |||||
ccRCC | |||||
GBM | |||||
HNSC | 0.165 | ||||
LUAD | 0.907 | ||||
LUSC | -1.072 | ||||
non_ccRCC | |||||
PDAC | |||||
UCEC |
CHEK2-Thr430 | |||||
---|---|---|---|---|---|
Cancer | Intensity | ||||
BRCA | |||||
COAD | |||||
HGSC | -0.707 | ||||
ccRCC | |||||
GBM | |||||
HNSC | |||||
LUAD | 0.707 | ||||
LUSC | |||||
non_ccRCC | |||||
PDAC | |||||
UCEC |
CHEK2-Thr432 | |
---|---|
Cancer | Intensity |
BRCA | |
COAD | |
HGSC | -1.151 |
ccRCC | |
GBM | |
HNSC | 0.655 |
LUAD | 0.496 |
LUSC | |
non_ccRCC | |
PDAC | |
UCEC |
PTM-Disease Association:
source: PTMDResidue | Position | State | Disease | Class | PMID |
---|---|---|---|---|---|
T | 68 | D | Colorectal cancer | Phosphorylation | 33500399 |
T | 68 | U | Colorectal carcinoma | Phosphorylation | 35999268 |
T | 68 | U | Gastric cancer | Phosphorylation | 33747205 |
T | 68 | U | Bladder cancer | Phosphorylation | 15361851 |
T | 68 | U | Bloom syndrome | Phosphorylation | 17634426 |
T | 68 | U | Non-small cell lung cancer/carcinoma | Phosphorylation | 16705183 |
State Note: Based on the distinct PTM states in diseases, PTMD classified all disease-associated PTMs into six classes, including whether the up-regulation (U) or down-regulation (D) of PTM levels, the absence (A) or presence (P) of PTMs, and the creation (C) or disruption (N) of PTM sites are associated with diseases.
PTM-Drug Perturbation Response:
source: DecryptMNo data.
Function score:
source: funscoRNo data.