Id: | acc1778 |
Group: | 2sens |
Protein: | GPNMB |
Gene Symbol: | GPNMB |
Protein Id: | Q14956 |
Protein Name: | GPNMB_HUMAN |
PTM: | glycosylation |
Site: | Asn134 |
Site Sequence: | GLSADPYVYNWTAWSEDSDGE |
Disease Category: | Cancer |
Disease: | Lung Cancer |
Disease Subtype: | NSCLC |
Disease Cellline: | H1299 |
Disease Info: | |
Drug: | - |
Drug Info: | - |
Effect: | resist |
Effect Info: | "Glycosylation at the N134 site of GPNMB plays a crucial role in this regulation. Removal of N134 glycosylation can significantly inhibit the binding of GPNMB to mutant EGFR and its downstream signaling, ultimately suppressing the metastasis of NSCLC." |
Note: | no drug |
Score: | 3.0 |
Pubmed(PMID): | 33706413 |
Sentence Index: | 33706413_8-9 |
Sentence: | "Further examination showed that GPNMB could activate mutated EGFR without ligand stimulation and could bind to the C-terminus of EGFR, assist phosphorylation at Y845, turn on downstream STAT3 signaling, and promote cancer metastasis. Moreover, we also found that Asn134 (N134) glycosylation of GPNMB played a crucial role in this ligand-independent regulation." |
Sequence & Structure:
MECLYYFLGFLLLAARLPLDAAKRFHDVLGNERPSAYMREHNQLNGWSSDENDWNEKLYPVWKRGDMRWKNSWKGGRVQAVLTSDSPALVGSNITFAVNLIFPRCQKEDANGNIVYEKNCRNEAGLSADPYVYNWTAWSEDSDGENGTGQSHHNVFPDGKPFPHHPGWRRWNFIYVFHTLGQYFQKLGRCSVRVSVNTANVTLGPQLMEVTVYRRHGRAYVPIAQVKDVYVVTDQIPVFVTMFQKNDRNSSDETFLKDLPIMFDVLIHDPSHFLNYSTINYKWSFGDNTGLFVSTNHTVNHTYVLNGTFSLNLTVKAAAPGPCPPPPPPPRPSKPTPSLATTLKSYDSNTPGPAGDNPLELSRIPDENCQINRYGHFQATITIVEGILEVNIIQMTDVLMPVPWPESSLIDFVVTCQGSIPTEVCTIISDPTCEITQNTVCSPVDVDEMCLLTVRRTFNGSGTYCVNLTLGDDTSLALTSTLISVPDRDPASPLRMANSALISVGCLAIFVTVISLLVYKKHKEYNPIENSPGNVVRSKGLSVFLNRAKAVFFPGNQEKDPLLKNQEFKGVS
No data.
Target | Drug name | MOA | Phase | Status | Disease | Source |
---|---|---|---|---|---|---|
GPNMB | GLEMBATUMUMAB VEDOTIN | Transmembrane glycoprotein NMB binding agent | 2 | Completed | osteosarcoma | ClinicalTrials |
GPNMB | GLEMBATUMUMAB VEDOTIN | Transmembrane glycoprotein NMB binding agent | 2 | Terminated | melanoma | ClinicalTrials |
GPNMB | GLEMBATUMUMAB VEDOTIN | Transmembrane glycoprotein NMB binding agent | 2 | Completed | Uveal Melanoma | ClinicalTrials |
GPNMB | GLEMBATUMUMAB VEDOTIN | Transmembrane glycoprotein NMB binding agent | 2 | Completed | breast cancer | ClinicalTrials ClinicalTrials |
GPNMB | GLEMBATUMUMAB VEDOTIN | Transmembrane glycoprotein NMB binding agent | 1 | Terminated | squamous cell lung carcinoma | ClinicalTrials |
GPNMB | GLEMBATUMUMAB | Transmembrane glycoprotein NMB binding agent | 1 | Completed | melanoma | ClinicalTrials |
GPNMB | GLEMBATUMUMAB | Transmembrane glycoprotein NMB binding agent | 1 | Completed | breast cancer | ClinicalTrials |
GPNMB | GLEMBATUMUMAB VEDOTIN | Transmembrane glycoprotein NMB binding agent | 0.5 | Withdrawn | breast cancer | 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 |
---|---|---|---|---|---|
N | 134 | U | Non-small cell lung cancer | Glycosylation | 33706413 |
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.