Id: | acc0212 |
Group: | 2sens |
Protein: | JAK1 |
Gene Symbol: | JAK1 |
Protein Id: | P23458 |
Protein Name: | JAK1_HUMAN |
PTM: | phosphorylation |
Site: | Tyr701 |
Site Sequence: | FKVAKQLASALSYLEDKDLVH |
Disease Category: | Cancer |
Disease: | Medulloblastoma |
Disease Subtype: | |
Disease Cellline: | TE671 |
Disease Info: | |
Drug: | ISG15 OV |
Drug Info: | "Pembrolizumab is a humanized monoclonal antibody that targets the programmed cell death protein 1 (PD-1) receptor, used in the treatment of various cancers including melanoma, non-small cell lung cancer, and classical Hodgkin lymphoma. Olaparib is a poly (ADP-ribose) polymerase (PARP) inhibitor used for the treatment of ovarian, breast, pancreatic, and prostate cancers with specific genetic mutations, such as BRCA1/2." |
Effect: | modulate |
Effect Info: | "Overexpression of ISG15 reduces the phosphorylation levels of JAK1 (Tyr701), Tyk2 (Tyr1054/1055), STAT2 (Tyr690), and STAT5 (Tyr694) in JEV-infected cells." |
Note: | Non-conventional drugs |
Score: | 3.0 |
Pubmed(PMID): | 20035788 |
Sentence Index: | 20035788_4-5 |
Sentence: | "ISG15 over-expression in human medulloblastoma cells significantly reduced the JEV-induced cytopathic effect and inhibited JEV replication by reducing the viral titers and genomes (p<0.05, Student's t-test); it also increased activation of the interferon stimulatory response element (ISRE)-luciferase cis-acting reporter in JEV-infected cells (p<0.05, Chi-square test). Furthermore, Western blotting revealed that ISG15 over-expression increased phosphorylation of IRF-3 (Ser396), JAK2 (Tyr1007/1008) and STAT1 (Tyr701 and Ser727) in JEV-infected cells (P<0.05, Chi-square test)." |
Sequence & Structure:
MQYLNIKEDCNAMAFCAKMRSSKKTEVNLEAPEPGVEVIFYLSDREPLRLGSGEYTAEELCIRAAQACRISPLCHNLFALYDENTKLWYAPNRTITVDDKMSLRLHYRMRFYFTNWHGTNDNEQSVWRHSPKKQKNGYEKKKIPDATPLLDASSLEYLFAQGQYDLVKCLAPIRDPKTEQDGHDIENECLGMAVLAISHYAMMKKMQLPELPKDISYKRYIPETLNKSIRQRNLLTRMRINNVFKDFLKEFNNKTICDSSVSTHDLKVKYLATLETLTKHYGAEIFETSMLLISSENEMNWFHSNDGGNVLYYEVMVTGNLGIQWRHKPNVVSVEKEKNKLKRKKLENKHKKDEEKNKIREEWNNFSYFPEITHIVIKESVVSINKQDNKKMELKLSSHEEALSFVSLVDGYFRLTADAHHYLCTDVAPPLIVHNIQNGCHGPICTEYAINKLRQEGSEEGMYVLRWSCTDFDNILMTVTCFEKSEQVQGAQKQFKNFQIEVQKGRYSLHGSDRSFPSLGDLMSHLKKQILRTDNISFMLKRCCQPKPREISNLLVATKKAQEWQPVYPMSQLSFDRILKKDLVQGEHLGRGTRTHIYSGTLMDYKDDEGTSEEKKIKVILKVLDPSHRDISLAFFEAASMMRQVSHKHIVYLYGVCVRDVENIMVEEFVEGGPLDLFMHRKSDVLTTPWKFKVAKQLASALSYLEDKDLVHGNVCTKNLLLAREGIDSECGPFIKLSDPGIPITVLSRQECIERIPWIAPECVEDSKNLSVAADKWSFGTTLWEICYNGEIPLKDKTLIEKERFYESRCRPVTPSCKELADLMTRCMNYDPNQRPFFRAIMRDINKLEEQNPDIVSEKKPATEVDPTHFEKRFLKRIRDLGEGHFGKVELCRYDPEGDNTGEQVAVKSLKPESGGNHIADLKKEIEILRNLYHENIVKYKGICTEDGGNGIKLIMEFLPSGSLKEYLPKNKNKINLKQQLKYAVQICKGMDYLGSRQYVHRDLAARNVLVESEHQVKIGDFGLTKAIETDKEYYTVKDDRDSPVFWYAPECLMQSKFYIASDVWSFGVTLHELLTYCDSDSSPMALFLKMIGPTHGQMTVTRLVNTLKEGKRLPCPPNCPDEVYQLMRKCWEFQPSNRTSFQNLIEGFEALLK
Select PDB:
Target | Drug name | MOA | Phase | Status | Disease | Source |
---|---|---|---|---|---|---|
JAK1 | ABROCITINIB | Tyrosine-protein kinase JAK1 inhibitor | 4 | - | atopic eczema | FDA EMA |
JAK1 | ABROCITINIB | Tyrosine-protein kinase JAK1 inhibitor | 4 | Recruiting | atopic eczema | ClinicalTrials |
JAK1 | FILGOTINIB | Tyrosine-protein kinase JAK1 inhibitor | 4 | - | immune system disease | ATC |
JAK1 | BARICITINIB | Tyrosine-protein kinase JAK1 inhibitor | 4 | - | immune system disease | ATC |
JAK1 | RUXOLITINIB | Tyrosine-protein kinase JAK1 inhibitor | 4 | - | neoplasm | ATC |
JAK1 | TOFACITINIB CITRATE | Janus Kinase (JAK) inhibitor | 4 | Recruiting | rheumatoid arthritis | ClinicalTrials |
JAK1 | TOFACITINIB CITRATE | Janus Kinase (JAK) inhibitor | 4 | - | rheumatoid arthritis | DailyMed DailyMed |
JAK1 | BARICITINIB | Tyrosine-protein kinase JAK1 inhibitor | 4 | - | rheumatoid arthritis | EMA DailyMed FDA |
JAK1 | BARICITINIB | Tyrosine-protein kinase JAK1 inhibitor | 4 | Active, not recruiting | rheumatoid arthritis | ClinicalTrials |
JAK1 | BARICITINIB | Tyrosine-protein kinase JAK1 inhibitor | 4 | Completed | rheumatoid arthritis | ClinicalTrials |
JAK1 | BARICITINIB | Tyrosine-protein kinase JAK1 inhibitor | 4 | Recruiting | rheumatoid arthritis | ClinicalTrials ClinicalTrials ClinicalTrials |
JAK1 | BARICITINIB | Tyrosine-protein kinase JAK1 inhibitor | 4 | Terminated | rheumatoid arthritis | ClinicalTrials |
JAK1 | FILGOTINIB MALEATE | Tyrosine-protein kinase JAK1 inhibitor | 4 | - | rheumatoid arthritis | EMA |
JAK1 | UPADACITINIB HEMIHYDRATE | Tyrosine-protein kinase JAK1 inhibitor | 4 | - | rheumatoid arthritis | DailyMed FDA |
JAK1 | RUXOLITINIB PHOSPHATE | Tyrosine-protein kinase JAK1 inhibitor | 4 | - | polycythemia vera | EMA DailyMed |
JAK1 | RUXOLITINIB PHOSPHATE | Tyrosine-protein kinase JAK1 inhibitor | 4 | - | primary myelofibrosis | DailyMed |
JAK1 | TOFACITINIB CITRATE | Janus Kinase (JAK) inhibitor | 4 | - | psoriatic arthritis | DailyMed |
JAK1 | RUXOLITINIB PHOSPHATE | Tyrosine-protein kinase JAK1 inhibitor | 4 | - | myeloproliferative disorder | EMA |
JAK1 | RUXOLITINIB | Tyrosine-protein kinase JAK1 inhibitor | 4 | - | Eczematoid dermatitis | ATC |
JAK1 | ABROCITINIB | Tyrosine-protein kinase JAK1 inhibitor | 4 | - | Eczematoid dermatitis | ATC |
JAK1 | RUXOLITINIB PHOSPHATE | Tyrosine-protein kinase JAK1 inhibitor | 4 | - | Myelofibrosis | DailyMed |
JAK1 | RUXOLITINIB PHOSPHATE | Tyrosine-protein kinase JAK1 inhibitor | 4 | - | graft versus host disease | EMA |
JAK1 | RUXOLITINIB | Tyrosine-protein kinase JAK1 inhibitor | 3 | Active, not recruiting | atopic eczema | ClinicalTrials |
JAK1 | RUXOLITINIB | Tyrosine-protein kinase JAK1 inhibitor | 3 | Recruiting | atopic eczema | ClinicalTrials |
JAK1 | BARICITINIB | Tyrosine-protein kinase JAK1 inhibitor | 3 | Active, not recruiting | atopic eczema | ClinicalTrials |
Note: Only show clinically investigational or approved drugs with protein targets.
Protein Tractability:
source: Open TargetsPTM Intensity:
source: CPTACNo data.
PTM-Disease Association:
source: PTMDResidue | Position | State | Disease | Class | PMID |
---|---|---|---|---|---|
- | - | P | Myeloma | Phosphorylation | 11986233 |
- | - | P | Colon cancer/carcinoma | Phosphorylation | 24050550 |
- | - | U | Non-small cell lung cancer/carcinoma | Phosphorylation | 21861134 |
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.