Id: | acc2189 |
Group: | 2sens |
Protein: | JAK-1 |
Gene Symbol: | JAK1 |
Protein Id: | P23458 |
Protein Name: | JAK1_HUMAN |
PTM: | phosphorylation |
Site: | Tyr1023 |
Site Sequence: | EHQVKIGDFGLTKAIETDKEY |
Disease Category: | Cancer |
Disease: | Oral Cancer |
Disease Subtype: | SCC |
Disease Cellline: | HSC-3 |
Disease Info: | |
Drug: | EGCG |
Drug Info: | "EGCG (Epigallocatechin gallate) is a polyphenolic compound primarily found in green tea, recognized for its potent antioxidant and anti-inflammatory properties, and approved by the FDA as the main ingredient in the prescription drug Veregen? (sinecatechins) for topical treatment of genital warts caused by human papillomavirus. " |
Effect: | modulate |
Effect Info: | "EGCG blocks the IFNgamma-induced JAK-PKC-delta-STAT1 signaling pathway, inhibits IDO expression, and reduces IDO-mediated tumor immune escape." |
Note: | |
Score: | 4.0 |
Pubmed(PMID): | 19928918 |
Sentence Index: | 19928918_10-11 |
Sentence: | "Moreover, phosphorylation of PKC-delta, JAK-1, and JAK-2, which are the upstream event for the activation of STAT1, are also inhibited by EGCG in IFN-gamma-stimulated human oral cancer cells. These data show that EGCG inhibited IDO expression by blocking the IFN-gamma-induced JAK-PKC-delta-STAT1 signaling pathway." |
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.