Id: | acc1570 |
Group: | 2sens |
Protein: | Jak2 |
Gene Symbol: | JAK2 |
Protein Id: | O60674 |
Protein Name: | JAK2_HUMAN |
PTM: | phosphorylation |
Site: | Tyr1007 |
Site Sequence: | TKVLPQDKEYYKVKEPGESPI |
Disease Category: | Cancer |
Disease: | Breast Cancer |
Disease Subtype: | basal |
Disease Cellline: | MDA-MB-231 |
Disease Info: | |
Drug: | paclitaxel |
Drug Info: | "Paclitaxel is a plant-derived alkaloid and potent antineoplastic agent that stabilizes microtubules to inhibit cancer cell division, primarily used in the treatment of ovarian, breast, and lung cancers. " |
Effect: | decrease |
Effect Info: | Silencing B7-H3 enhances the sensitivity of multiple human breast cancer cell lines to paclitaxel and induces drug-related apoptosis by reducing Jak2/Stat3 phosphorylation. |
Note: | |
Score: | 5.0 |
Pubmed(PMID): | 21518725 |
Sentence Index: | 21518725_4-5 |
Sentence: | "Overexpression of B7-H3 made the cancer cells more resistant to the drug. Next, we investigated the mechanisms behind B7-H3-mediated paclitaxel resistance and found that the level of Stat3 Tyr705 phosphorylation was decreased in B7-H3 knockdown cells along with the expression of its direct downstream targets Mcl-1 and survivin." |
Sequence & Structure:
MGMACLTMTEMEGTSTSSIYQNGDISGNANSMKQIDPVLQVYLYHSLGKSEADYLTFPSGEYVAEEICIAASKACGITPVYHNMFALMSETERIWYPPNHVFHIDESTRHNVLYRIRFYFPRWYCSGSNRAYRHGISRGAEAPLLDDFVMSYLFAQWRHDFVHGWIKVPVTHETQEECLGMAVLDMMRIAKENDQTPLAIYNSISYKTFLPKCIRAKIQDYHILTRKRIRYRFRRFIQQFSQCKATARNLKLKYLINLETLQSAFYTEKFEVKEPGSGPSGEEIFATIIITGNGGIQWSRGKHKESETLTEQDLQLYCDFPNIIDVSIKQANQEGSNESRVVTIHKQDGKNLEIELSSLREALSFVSLIDGYYRLTADAHHYLCKEVAPPAVLENIQSNCHGPISMDFAISKLKKAGNQTGLYVLRCSPKDFNKYFLTFAVERENVIEYKHCLITKNENEEYNLSGTKKNFSSLKDLLNCYQMETVRSDNIIFQFTKCCPPKPKDKSNLLVFRTNGVSDVPTSPTLQRPTHMNQMVFHKIRNEDLIFNESLGQGTFTKIFKGVRREVGDYGQLHETEVLLKVLDKAHRNYSESFFEAASMMSKLSHKHLVLNYGVCVCGDENILVQEFVKFGSLDTYLKKNKNCINILWKLEVAKQLAWAMHFLEENTLIHGNVCAKNILLIREEDRKTGNPPFIKLSDPGISITVLPKDILQERIPWVPPECIENPKNLNLATDKWSFGTTLWEICSGGDKPLSALDSQRKLQFYEDRHQLPAPKWAELANLINNCMDYEPDFRPSFRAIIRDLNSLFTPDYELLTENDMLPNMRIGALGFSGAFEDRDPTQFEERHLKFLQQLGKGNFGSVEMCRYDPLQDNTGEVVAVKKLQHSTEEHLRDFEREIEILKSLQHDNIVKYKGVCYSAGRRNLKLIMEYLPYGSLRDYLQKHKERIDHIKLLQYTSQICKGMEYLGTKRYIHRDLATRNILVENENRVKIGDFGLTKVLPQDKEYYKVKEPGESPIFWYAPESLTESKFSVASDVWSFGVVLYELFTYIEKSKSPPAEFMRMIGNDKQGQMIVFHLIELLKNNGRLPRPDGCPDEIYMIMTECWNNNVNQRPSFRDLALRVDQIRDNMAG
Select PDB:
Target | Drug name | MOA | Phase | Status | Disease | Source |
---|---|---|---|---|---|---|
JAK2 | BARICITINIB | Tyrosine-protein kinase JAK2 inhibitor | 4 | - | immune system disease | ATC |
JAK2 | FILGOTINIB | Tyrosine-protein kinase JAK2 inhibitor | 4 | - | immune system disease | ATC |
JAK2 | RUXOLITINIB | Tyrosine-protein kinase JAK2 inhibitor | 4 | - | neoplasm | ATC |
JAK2 | PACRITINIB | Tyrosine-protein kinase JAK2 inhibitor | 4 | - | neoplasm | ATC |
JAK2 | FEDRATINIB | Tyrosine-protein kinase JAK2 inhibitor | 4 | - | neoplasm | ATC |
JAK2 | TOFACITINIB CITRATE | Janus Kinase (JAK) inhibitor | 4 | - | rheumatoid arthritis | DailyMed DailyMed |
JAK2 | BARICITINIB | Tyrosine-protein kinase JAK2 inhibitor | 4 | - | rheumatoid arthritis | FDA DailyMed EMA |
JAK2 | TOFACITINIB CITRATE | Janus Kinase (JAK) inhibitor | 4 | Recruiting | rheumatoid arthritis | ClinicalTrials |
JAK2 | BARICITINIB | Tyrosine-protein kinase JAK2 inhibitor | 4 | Recruiting | rheumatoid arthritis | ClinicalTrials ClinicalTrials ClinicalTrials |
JAK2 | BARICITINIB | Tyrosine-protein kinase JAK2 inhibitor | 4 | Terminated | rheumatoid arthritis | ClinicalTrials |
JAK2 | BARICITINIB | Tyrosine-protein kinase JAK2 inhibitor | 4 | Active, not recruiting | rheumatoid arthritis | ClinicalTrials |
JAK2 | BARICITINIB | Tyrosine-protein kinase JAK2 inhibitor | 4 | Completed | rheumatoid arthritis | ClinicalTrials |
JAK2 | FILGOTINIB MALEATE | Tyrosine-protein kinase JAK2 inhibitor | 4 | - | rheumatoid arthritis | EMA |
JAK2 | UPADACITINIB HEMIHYDRATE | Tyrosine-protein kinase JAK2 inhibitor | 4 | - | rheumatoid arthritis | FDA DailyMed |
JAK2 | PACRITINIB CITRATE | Tyrosine-protein kinase JAK2 inhibitor | 4 | - | primary myelofibrosis | FDA |
JAK2 | RUXOLITINIB PHOSPHATE | Tyrosine-protein kinase JAK2 inhibitor | 4 | - | polycythemia vera | EMA DailyMed |
JAK2 | PACRITINIB CITRATE | Tyrosine-protein kinase JAK2 inhibitor | 4 | - | polycythemia vera | FDA |
JAK2 | RUXOLITINIB PHOSPHATE | Tyrosine-protein kinase JAK2 inhibitor | 4 | - | primary myelofibrosis | DailyMed |
JAK2 | FEDRATINIB HYDROCHLORIDE | Tyrosine-protein kinase JAK2 inhibitor | 4 | - | primary myelofibrosis | FDA EMA |
JAK2 | TOFACITINIB CITRATE | Janus Kinase (JAK) inhibitor | 4 | - | psoriatic arthritis | DailyMed |
JAK2 | RUXOLITINIB PHOSPHATE | Tyrosine-protein kinase JAK2 inhibitor | 4 | - | myeloproliferative disorder | EMA |
JAK2 | FEDRATINIB HYDROCHLORIDE | Tyrosine-protein kinase JAK2 inhibitor | 4 | - | myeloproliferative disorder | EMA |
JAK2 | RUXOLITINIB | Tyrosine-protein kinase JAK2 inhibitor | 4 | - | Eczematoid dermatitis | ATC |
JAK2 | FEDRATINIB HYDROCHLORIDE | Tyrosine-protein kinase JAK2 inhibitor | 4 | - | Myelofibrosis | DailyMed |
JAK2 | RUXOLITINIB PHOSPHATE | Tyrosine-protein kinase JAK2 inhibitor | 4 | - | Myelofibrosis | DailyMed |
Note: Only show clinically investigational or approved drugs with protein targets.
Protein Tractability:
source: Open TargetsPTM Intensity:
source: CPTACJAK2-Tyr570 | |
---|---|
Cancer | Intensity |
BRCA | |
COAD | |
HGSC | |
ccRCC | |
GBM | -0.417 |
HNSC | -0.724 |
LUAD | |
LUSC | 1.141 |
non_ccRCC | |
PDAC | |
UCEC |
PTM-Disease Association:
source: PTMDResidue | Position | State | Disease | Class | PMID |
---|---|---|---|---|---|
Y | 1007 | U | Prostate cancer/carcinoma/adenocarcinoma | Phosphorylation | 22307624 |
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.