Id: | acc1508 |
Group: | 2sens |
Protein: | erbB3 |
Gene Symbol: | ERBB3 |
Protein Id: | P21860 |
Protein Name: | ERBB3_HUMAN |
PTM: | phosphorylation |
Site: | unclear |
Site Sequence: | |
Disease Category: | Cancer |
Disease: | Breast Cancer |
Disease Subtype: | |
Disease Cellline: | BT474? |
Disease Info: | |
Drug: | SNDX-275 + trastuzumab |
Drug Info: | "SNDX-275: A histone deacetylase (HDAC) inhibitor investigated for its potential in treating herpes virus-related conditions and cancers by inducing viral gene expression in infected cells. Trastuzumab: A monoclonal antibody targeting HER2/neu receptors, widely used in the treatment of HER2-positive breast cancer and gastric cancers. " |
Effect: | modulate |
Effect Info: | "The combination of SNDX - 275 and trastuzumab can significantly reduce the levels of erbB3 and its phosphorylation, inhibit the Akt signaling pathway, and enhance apoptosis." |
Note: | |
Score: | 4.0 |
Pubmed(PMID): | 21497990 |
Sentence Index: | 21497990_6-7 |
Sentence: | "SNDX-275 in combination with trastuzumab resulted in a dramatic reduction of erbB3 and its phosphorylation (P-erbB3), and inhibition of Akt signaling. Apoptotic-ELISA and western blot analyses confirmed that the combinations of SNDX-275 and trastuzumab as compared to SNDX-275 alone significantly enhanced DNA fragmentation and induced more PARP cleavage and caspase-3 activation in both trastuzumab-sensitive and -resistant breast cancer cells." |
Sequence & Structure:
MRANDALQVLGLLFSLARGSEVGNSQAVCPGTLNGLSVTGDAENQYQTLYKLYERCEVVMGNLEIVLTGHNADLSFLQWIREVTGYVLVAMNEFSTLPLPNLRVVRGTQVYDGKFAIFVMLNYNTNSSHALRQLRLTQLTEILSGGVYIEKNDKLCHMDTIDWRDIVRDRDAEIVVKDNGRSCPPCHEVCKGRCWGPGSEDCQTLTKTICAPQCNGHCFGPNPNQCCHDECAGGCSGPQDTDCFACRHFNDSGACVPRCPQPLVYNKLTFQLEPNPHTKYQYGGVCVASCPHNFVVDQTSCVRACPPDKMEVDKNGLKMCEPCGGLCPKACEGTGSGSRFQTVDSSNIDGFVNCTKILGNLDFLITGLNGDPWHKIPALDPEKLNVFRTVREITGYLNIQSWPPHMHNFSVFSNLTTIGGRSLYNRGFSLLIMKNLNVTSLGFRSLKEISAGRIYISANRQLCYHHSLNWTKVLRGPTEERLDIKHNRPRRDCVAEGKVCDPLCSSGGCWGPGPGQCLSCRNYSRGGVCVTHCNFLNGEPREFAHEAECFSCHPECQPMEGTATCNGSGSDTCAQCAHFRDGPHCVSSCPHGVLGAKGPIYKYPDVQNECRPCHENCTQGCKGPELQDCLGQTLVLIGKTHLTMALTVIAGLVVIFMMLGGTFLYWRGRRIQNKRAMRRYLERGESIEPLDPSEKANKVLARIFKETELRKLKVLGSGVFGTVHKGVWIPEGESIKIPVCIKVIEDKSGRQSFQAVTDHMLAIGSLDHAHIVRLLGLCPGSSLQLVTQYLPLGSLLDHVRQHRGALGPQLLLNWGVQIAKGMYYLEEHGMVHRNLAARNVLLKSPSQVQVADFGVADLLPPDDKQLLYSEAKTPIKWMALESIHFGKYTHQSDVWSYGVTVWELMTFGAEPYAGLRLAEVPDLLEKGERLAQPQICTIDVYMVMVKCWMIDENIRPTFKELANEFTRMARDPPRYLVIKRESGPGIAPGPEPHGLTNKKLEEVELEPELDLDLDLEAEEDNLATTTLGSALSLPVGTLNRPRGSQSLLSPSSGYMPMNQGNLGESCQESAVSGSSERCPRPVSLHPMPRGCLASESSEGHVTGSEAELQEKVSMCRSRSRSRSPRPRGDSAYHSQRHSLLTPVTPLSPPGLEEEDVNGYVMPDTHLKGTPSSREGTLSSVGLSSVLGTEEEDEDEEYEYMNRRRRHSPPHPPRPSSLEELGYEYMDVGSDLSASLGSTQSCPLHPVPIMPTAGTTPDEDYEYMNRQRDGGGPGGDYAAMGACPASEQGYEEMRAFQGPGHQAPHVHYARLKTLRSLEATDSAFDNPDYWHSRLFPKANAQRT
Select PDB:
Target | Drug name | MOA | Phase | Status | Disease | Source |
---|---|---|---|---|---|---|
ERBB3 | VANDETANIB | Epidermal growth factor receptor inhibitor | 4 | - | neoplasm | ATC |
ERBB3 | VANDETANIB | Epidermal growth factor receptor inhibitor | 4 | - | thyroid carcinoma | DailyMed |
ERBB3 | VANDETANIB | Epidermal growth factor receptor inhibitor | 4 | - | thyroid neoplasm | EMA |
ERBB3 | VANDETANIB | Epidermal growth factor receptor inhibitor | 4 | Active, not recruiting | thyroid cancer | ClinicalTrials |
ERBB3 | VANDETANIB | Epidermal growth factor receptor inhibitor | 4 | - | medullary thyroid gland carcinoma | DailyMed |
ERBB3 | VANDETANIB | Epidermal growth factor receptor inhibitor | 3 | Completed | non-small cell lung carcinoma | ClinicalTrials ClinicalTrials ClinicalTrials ClinicalTrials |
ERBB3 | PATRITUMAB | Receptor tyrosine-protein kinase erbB-3 inhibitor | 3 | Terminated | non-small cell lung carcinoma | ClinicalTrials |
ERBB3 | POZIOTINIB | Epidermal growth factor receptor inhibitor | 3 | Suspended | non-small cell lung carcinoma | ClinicalTrials |
ERBB3 | VANDETANIB | Epidermal growth factor receptor inhibitor | 3 | Active, not recruiting | thyroid cancer | ClinicalTrials |
ERBB3 | VANDETANIB | Epidermal growth factor receptor inhibitor | 3 | Completed | thyroid cancer | ClinicalTrials |
ERBB3 | PATRITUMAB | Receptor tyrosine-protein kinase erbB-3 inhibitor | 3 | Terminated | lung cancer | ClinicalTrials |
ERBB3 | VANDETANIB | Epidermal growth factor receptor inhibitor | 3 | Completed | lung cancer | ClinicalTrials |
ERBB3 | VANDETANIB | Epidermal growth factor receptor inhibitor | 3 | Active, not recruiting | medullary thyroid gland carcinoma | ClinicalTrials ClinicalTrials |
ERBB3 | VANDETANIB | Epidermal growth factor receptor inhibitor | 3 | Withdrawn | medullary thyroid gland carcinoma | ClinicalTrials |
ERBB3 | VANDETANIB | Epidermal growth factor receptor inhibitor | 2 | Completed | hepatocellular carcinoma | ClinicalTrials |
ERBB3 | VANDETANIB | Epidermal growth factor receptor inhibitor | 2 | Completed | head and neck squamous cell carcinoma | ClinicalTrials |
ERBB3 | TARLOXOTINIB | Epidermal growth factor receptor inhibitor | 2 | Terminated | head and neck squamous cell carcinoma | ClinicalTrials |
ERBB3 | CDX-3379 | Receptor tyrosine-protein kinase erbB-3 inhibitor | 2 | Terminated | head and neck squamous cell carcinoma | ClinicalTrials |
ERBB3 | VANDETANIB | Epidermal growth factor receptor inhibitor | 2 | Unknown status | acute myeloid leukemia | ClinicalTrials |
ERBB3 | VANDETANIB | Epidermal growth factor receptor inhibitor | 2 | Terminated | clear cell renal carcinoma | ClinicalTrials |
ERBB3 | SAPITINIB | Receptor tyrosine-protein kinase erbB-3 inhibitor | 2 | Completed | colorectal adenocarcinoma | ClinicalTrials |
ERBB3 | VANDETANIB | Epidermal growth factor receptor inhibitor | 2 | Completed | glioblastoma multiforme | ClinicalTrials |
ERBB3 | POZIOTINIB | Epidermal growth factor receptor inhibitor | 2 | Terminated | lung adenocarcinoma | ClinicalTrials |
ERBB3 | VANDETANIB | Epidermal growth factor receptor inhibitor | 2 | Terminated | follicular thyroid carcinoma | ClinicalTrials |
ERBB3 | VANDETANIB | Epidermal growth factor receptor inhibitor | 2 | Terminated | mesothelioma | 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!
ERBB3-Ser1083 | |||||
---|---|---|---|---|---|
Cancer | Intensity | ||||
BRCA | |||||
COAD | |||||
HGSC | |||||
ccRCC | |||||
GBM | |||||
HNSC | -0.707 | ||||
LUAD | |||||
LUSC | |||||
non_ccRCC | |||||
PDAC | 0.707 | ||||
UCEC |
ERBB3-Ser1130 | |||||
---|---|---|---|---|---|
Cancer | Intensity | ||||
BRCA | |||||
COAD | |||||
HGSC | 1.99 | ||||
ccRCC | -0.465 | ||||
GBM | 0.291 | ||||
HNSC | 0.168 | ||||
LUAD | -1.063 | ||||
LUSC | -0.18 | ||||
non_ccRCC | -0.741 | ||||
PDAC | |||||
UCEC |
ERBB3-Ser1315 | |||||
---|---|---|---|---|---|
Cancer | Intensity | ||||
BRCA | |||||
COAD | 0.707 | ||||
HGSC | -0.707 | ||||
ccRCC | |||||
GBM | |||||
HNSC | |||||
LUAD | |||||
LUSC | |||||
non_ccRCC | |||||
PDAC | |||||
UCEC |
ERBB3-Ser686 | |||||
---|---|---|---|---|---|
Cancer | Intensity | ||||
BRCA | -2.071 | ||||
COAD | 0.3 | ||||
HGSC | -0.053 | ||||
ccRCC | 0.176 | ||||
GBM | 0.849 | ||||
HNSC | 0.074 | ||||
LUAD | 0.314 | ||||
LUSC | 0.955 | ||||
non_ccRCC | -1.734 | ||||
PDAC | 0.855 | ||||
UCEC | 0.334 |
ERBB3-Ser693 | |||||
---|---|---|---|---|---|
Cancer | Intensity | ||||
BRCA | |||||
COAD | 0.707 | ||||
HGSC | -0.707 | ||||
ccRCC | |||||
GBM | |||||
HNSC | |||||
LUAD | |||||
LUSC | |||||
non_ccRCC | |||||
PDAC | |||||
UCEC |
ERBB3-Ser717 | |||||
---|---|---|---|---|---|
Cancer | Intensity | ||||
BRCA | -1.767 | ||||
COAD | 1.86 | ||||
HGSC | |||||
ccRCC | 0.331 | ||||
GBM | |||||
HNSC | |||||
LUAD | 0.353 | ||||
LUSC | -0.059 | ||||
non_ccRCC | -0.311 | ||||
PDAC | -0.176 | ||||
UCEC | -0.231 |
ERBB3-Ser982 | |||||
---|---|---|---|---|---|
Cancer | Intensity | ||||
BRCA | -1.796 | ||||
COAD | 0.398 | ||||
HGSC | 2.013 | ||||
ccRCC | -0.413 | ||||
GBM | 0.808 | ||||
HNSC | 0.277 | ||||
LUAD | -0.37 | ||||
LUSC | -0.474 | ||||
non_ccRCC | -0.906 | ||||
PDAC | -0.2 | ||||
UCEC | 0.664 |
ERBB3-Tyr1132 | |||||
---|---|---|---|---|---|
Cancer | Intensity | ||||
BRCA | |||||
COAD | |||||
HGSC | 0.707 | ||||
ccRCC | |||||
GBM | |||||
HNSC | |||||
LUAD | -0.707 | ||||
LUSC | |||||
non_ccRCC | |||||
PDAC | |||||
UCEC |
ERBB3-Tyr1307 | |||||
---|---|---|---|---|---|
Cancer | Intensity | ||||
BRCA | |||||
COAD | |||||
HGSC | |||||
ccRCC | |||||
GBM | |||||
HNSC | 0.707 | ||||
LUAD | -0.707 | ||||
LUSC | |||||
non_ccRCC | |||||
PDAC | |||||
UCEC |
ERBB3-Tyr1328 | |
---|---|
Cancer | Intensity |
BRCA | -0.4 |
COAD | |
HGSC | |
ccRCC | |
GBM | |
HNSC | 1.138 |
LUAD | -0.738 |
LUSC | |
non_ccRCC | |
PDAC | |
UCEC |
PTM-Disease Association:
source: PTMDResidue | Position | State | Disease | Class | PMID |
---|---|---|---|---|---|
- | - | P | Breast cancer/tumor/carcinoma | Phosphorylation | 11389077 |
- | - | P | Hepatocellular carcinoma/hepatocarcinoma/hepatoma | Phosphorylation | 21246584 |
- | - | U | Ovarian cancer/carcinoma | Phosphorylation | 22841590 |
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.