Id: | acc0890 |
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: | Testicular Cancer |
Disease Subtype: | testicular germ cell tumors |
Disease Cellline: | SuSa |
Disease Info: | |
Drug: | Cisplatin |
Drug Info: | "Cisplatin is a platinum-based chemotherapeutic agent widely used in the treatment of various malignancies, including ovarian, bladder, testicular, and non-small cell lung cancers, by forming DNA cross-links to interfere with replication and repair, thereby inhibiting cancer cell growth and proliferation." |
Effect: | modulate |
Effect Info: | "Cisplatin causes the persistent phosphorylation of Chk2, which in turn leads to the activation of the cell apoptosis pathway." |
Note: | |
Score: | 4.0 |
Pubmed(PMID): | 20846399 |
Sentence Index: | 20846399_7-8 |
Sentence: | "We observed that repair of intrastrand crosslinks is similar in cisplatin sensitive TTC and resistant bladder cancer cells, whereas repair of ICLs was significantly reduced in TTC. gammaH2AX formation, which serves as a marker of DNA breaks formed in response to ICLs, persisted in cisplatin-treated TTC and correlated with sustained phosphorylation of Chk2 and enhanced PARP-1 cleavage." |
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.