Target Interacting Protein Information
Target General Information | Top | ||||
---|---|---|---|---|---|
Target ID | T28713 | Target Info | |||
Target Name | Serine/threonine-protein kinase Chk2 (RAD53) | ||||
Synonyms | hCds1; Hucds1; Checkpoint kinase 2; Cds1 homolog; Cds1; CHK2 checkpoint homolog; CHK2 | ||||
Target Type | Clinical trial Target | ||||
Gene Name | CHEK2 | ||||
Biochemical Class | Kinase | ||||
UniProt ID |
Target Interacting Proteins | Top | ||||
---|---|---|---|---|---|
Acyltransferases | [+] 1 Acyltransferases | + | |||
Interacting Protein Name | Breast cancer type 1 susceptibility protein (BRCA1) | Interacting Protein | Interacting Protein Info | ||
UniProt ID | |||||
Synonyms | BRCAI; BRCC1; BROVCA1; FANCS; IRIS; PNCA4; PPP1R53; PSCP; RNF53 | ||||
Evidence Score (E-score) | 5 Experimental Evidences | + | |||
1 | Affinity Capture-Western | [1] | |||
2 | Biochemical Activity | [2] | |||
3 | Biochemical Activity | [3] | |||
4 | Biochemical Activity | [4] | |||
5 | Reconstituted Complex | [1] | |||
Ester hydrolases | [+] 1 Ester hydrolases | + | |||
Interacting Target Name | M-phase inducer phosphatase 1 (MPIP1) | Literature-reported Target | Interacting Protein Info | ||
UniProt ID | |||||
Synonyms | Dual specificity phosphatase Cdc25A; Cdc25A phosphatase | ||||
Evidence Score (E-score) | 5 Experimental Evidences | + | |||
1 | Biochemical Activity | [5] | |||
2 | Biochemical Activity | [6] | |||
3 | Biochemical Activity | [7] | |||
4 | Biochemical Activity | [8] | |||
5 | Reconstituted Complex | [8] | |||
Kinases | [+] 2 Kinases | + | |||
Interacting Target Name | Polo-like kinase 1 (PLK1) | Clinical trial Target | Interacting Protein Info | ||
UniProt ID | |||||
Synonyms | STPK13; Serine-threonine protein kinase 13; Serine/threonine-protein kinase PLK1; Serine/threonine-protein kinase 13; PLK-1; Plk1; PLK; Mitoticserine-threonine kinase polo-like kinase 1 | ||||
Evidence Score (E-score) | 2 Experimental Evidences | + | |||
1 | Affinity Capture-Western | [9] | |||
2 | Biochemical Activity | [9] | |||
Interacting Target Name | ATM serine/threonine kinase (ATM) | Clinical trial Target | Interacting Protein Info | ||
UniProt ID | |||||
Synonyms | Serine-protein kinase ATM; Ataxia telangiectasia mutated; A-T mutated | ||||
Evidence Score (E-score) | 2 Experimental Evidences | + | |||
1 | Biochemical Activity | [10] | |||
2 | Reconstituted Complex | [10] | |||
Pore-forming toxins | [+] 1 Pore-forming toxins | + | |||
Interacting Target Name | Cellular tumor antigen p53 (TP53) | Clinical trial Target | Interacting Protein Info | ||
UniProt ID | |||||
Synonyms | Tumor suppressor p53; Phosphoprotein p53; P53; Antigen NY-CO-13 | ||||
Evidence Score (E-score) | 5 Experimental Evidences | + | |||
1 | Affinity Capture-Western | [11] | |||
2 | Biochemical Activity | [12] | |||
3 | Biochemical Activity | [13] | |||
4 | Biochemical Activity | [14] | |||
5 | Biochemical Activity | [15] | |||
Ubiquitin related proteins | [+] 1 Ubiquitin related proteins | + | |||
Interacting Target Name | Ubiquitin-protein ligase E3 Mdm2 (MDM2) | Clinical trial Target | Interacting Protein Info | ||
UniProt ID | |||||
Synonyms | RING-type E3 ubiquitin transferase Mdm2; P53-binding protein Mdm2; Oncoprotein Mdm2; MDM2 protein; Hdm2; E3 ubiquitin-protein ligase Mdm2; Double minute 2 protein | ||||
Evidence Score (E-score) | 4 Experimental Evidences | + | |||
1 | Affinity Capture-Western | [16] | |||
2 | Biochemical Activity | [17] | |||
3 | Biochemical Activity | [13] | |||
4 | Reconstituted Complex | [13] | |||
Other proteins | [+] 2 Other proteins | + | |||
Interacting Target Name | Breast cancer type 2 susceptibility protein (BRCA2) | Literature-reported Target | Interacting Protein Info | ||
UniProt ID | |||||
Synonyms | Fanconi anemia group D1 protein; FANCD1; FACD | ||||
Evidence Score (E-score) | 2 Experimental Evidences | + | |||
1 | Affinity Capture-Western | [18] | |||
2 | Protein-peptide | [19] | |||
Interacting Protein Name | Proteasome activator complex subunit 3 (PSME3) | Interacting Protein | Interacting Protein Info | ||
UniProt ID | |||||
Synonyms | HEL.S.283; Ki; PA28.gamma; PA28G; PA28gamma; REG.GAMMA | ||||
Evidence Score (E-score) | 2 Experimental Evidences | + | |||
1 | Affinity Capture-Western | [20] | |||
2 | Biochemical Activity | [21] |
References | Top | ||||
---|---|---|---|---|---|
REF 1 | hCds1-mediated phosphorylation of BRCA1 regulates the DNA damage response. Nature. 2000 Mar 9;404(6774):201-4. | ||||
REF 2 | BRCA1 is regulated by Chk2 in response to spindle damage. Biochim Biophys Acta. 2008 Dec;1783(12):2223-33. | ||||
REF 3 | Phosphorylation of pRB at Ser612 by Chk1/2 leads to a complex between pRB and E2F-1 after DNA damage. EMBO J. 2007 Apr 18;26(8):2083-93. | ||||
REF 4 | Regulation of BRCA1 phosphorylation by interaction with protein phosphatase 1alpha. Cancer Res. 2002 Nov 15;62(22):6357-61. | ||||
REF 5 | Differential roles for checkpoint kinases in DNA damage-dependent degradation of the Cdc25A protein phosphatase. J Biol Chem. 2008 Jul 11;283(28):19322-8. | ||||
REF 6 | Chk1 regulates the S phase checkpoint by coupling the physiological turnover and ionizing radiation-induced accelerated proteolysis of Cdc25A. Cancer Cell. 2003 Mar;3(3):247-58. | ||||
REF 7 | Phosphorylation at serine 75 is required for UV-mediated degradation of human Cdc25A phosphatase at the S-phase checkpoint. J Biol Chem. 2003 Aug 8;278(32):29824-9. | ||||
REF 8 | The ATM-Chk2-Cdc25A checkpoint pathway guards against radioresistant DNA synthesis. Nature. 2001 Apr 12;410(6830):842-7. | ||||
REF 9 | Polo-like kinase 1 and Chk2 interact and co-localize to centrosomes and the midbody. J Biol Chem. 2003 Mar 7;278(10):8468-75. | ||||
REF 10 | Direct activation of the ATM protein kinase by the Mre11/Rad50/Nbs1 complex. Science. 2004 Apr 2;304(5667):93-6. | ||||
REF 11 | The promyelocytic leukemia protein protects p53 from Mdm2-mediated inhibition and degradation. J Biol Chem. 2003 Aug 29;278(35):33134-41. | ||||
REF 12 | The human homologs of checkpoint kinases Chk1 and Cds1 (Chk2) phosphorylate p53 at multiple DNA damage-inducible sites. Genes Dev. 2000 Feb 1;14(3):289-300. | ||||
REF 13 | HDM2 negatively affects the Chk2-mediated phosphorylation of p53. FEBS Lett. 2005 May 9;579(12):2604-8. | ||||
REF 14 | DNA damage-induced activation of p53 by the checkpoint kinase Chk2. Science. 2000 Mar 10;287(5459):1824-7. | ||||
REF 15 | ATM and Chk2 kinase target the p53 cofactor Strap. EMBO Rep. 2008 Dec;9(12):1222-9. | ||||
REF 16 | Mdm2 and PCAF increase Chk2 ubiquitination and degradation independently of their intrinsic E3 ligase activities. Cell Cycle. 2009 Feb 1;8(3):430-7. | ||||
REF 17 | Differential roles of ATM- and Chk2-mediated phosphorylations of Hdmx in response to DNA damage. Mol Cell Biol. 2006 Sep;26(18):6819-31. | ||||
REF 18 | ATM and ATR substrate analysis reveals extensive protein networks responsive to DNA damage. Science. 2007 May 25;316(5828):1160-6. | ||||
REF 19 | Identification of potential binding sites for the FHA domain of human Chk2 by in vitro binding studies. Biochem Biophys Res Commun. 2003 Nov 28;311(4):803-8. | ||||
REF 20 | REGgamma/PA28gamma proteasome activator interacts with PML and Chk2 and affects PML nuclear bodies number. Cell Cycle. 2009 Aug;8(15):2399-407. | ||||
REF 21 | Chk2 and REG-dependent DBC1 regulation in DNA damage induced apoptosis. Nucleic Acids Res. 2014 Dec 1;42(21):13150-60. |
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