Id: | acc0679 |
Group: | 1sens |
Protein: | HMGB1 |
Gene Symbol: | HMGB1 |
Protein Id: | P09429 |
Protein Name: | HMGB1_HUMAN |
PTM: | phosphorylation |
Site: | unclear |
Site Sequence: | |
Disease Category: | Cancer |
Disease: | Gastric Cancer |
Disease Subtype: | |
Disease Cellline: | HGC-27 |
Disease Info: | |
Drug: | Lactate |
Drug Info: | "Lactate (Lactic Acid) is a hydroxycarboxylic acid receptor 1 (HCAR1) activator, an epigenetic modulator inducing lysine residue lactylation, and a glycolytic end-product involved in antitumor immunity. " |
Effect: | modulate |
Effect Info: | "Lactic acid enhances the phosphorylation of HMGB1 via the Akt signaling pathway, promotes the nuclear translocation and release of HMGB1, and induces the proliferation and migration of gastric cancer cells." |
Note: | |
Score: | 4.0 |
Pubmed(PMID): | 37968076 |
Sentence Index: | 37968076_0 |
Sentence: | [Lactate promotes HMGB1 phosphorylation and release via Akt signaling pathway in gastric cancer cells HGC-27]. |
Sequence & Structure:
MGKGDPKKPRGKMSSYAFFVQTCREEHKKKHPDASVNFSEFSKKCSERWKTMSAKEKGKFEDMAKADKARYEREMKTYIPPKGETKKKFKDPNAPKRPPSAFFLFCSEYRPKIKGEHPGLSIGDVAKKLGEMWNNTAADDKQPYEKKAAKLKEKYEKDIAAYRAKGKPDAAKKGVVKAEKSKKKKEEEEDEEDEEDEEEEEDEEDEDEEEDDDDE
Select PDB:
Target | Drug name | MOA | Phase | Status | Disease | Source |
---|---|---|---|---|---|---|
HMGB1 | CD24FC | High mobility group protein B1 inhibitor | 3 | Completed | COVID-19 | ClinicalTrials |
HMGB1 | CD24FC | High mobility group protein B1 inhibitor | 1 | Terminated | neoplasm | ClinicalTrials |
HMGB1 | CD24FC | High mobility group protein B1 inhibitor | 1 | Withdrawn | metastatic melanoma | ClinicalTrials |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!
HMGB1-Ser100 | |||||
---|---|---|---|---|---|
Cancer | Intensity | ||||
BRCA | 0.624 | ||||
COAD | 0.3 | ||||
HGSC | |||||
ccRCC | 0.175 | ||||
GBM | 0.87 | ||||
HNSC | -0.067 | ||||
LUAD | -0.054 | ||||
LUSC | 0.075 | ||||
non_ccRCC | -0.653 | ||||
PDAC | 1.165 | ||||
UCEC | -2.436 |
HMGB1-Ser121 | |||||
---|---|---|---|---|---|
Cancer | Intensity | ||||
BRCA | |||||
COAD | |||||
HGSC | |||||
ccRCC | -0.521 | ||||
GBM | 0.487 | ||||
HNSC | |||||
LUAD | -1.312 | ||||
LUSC | -0.281 | ||||
non_ccRCC | |||||
PDAC | -0.013 | ||||
UCEC | 1.64 |
HMGB1-Ser35 | |
---|---|
Cancer | Intensity |
BRCA | 1.728 |
COAD | 0.903 |
HGSC | -1.88 |
ccRCC | 0.698 |
GBM | -0.638 |
HNSC | 0.595 |
LUAD | -0.308 |
LUSC | 0.172 |
non_ccRCC | 0.179 |
PDAC | -0.403 |
UCEC | -1.047 |
PTM-Disease Association:
source: PTMDResidue | Position | State | Disease | Class | PMID |
---|---|---|---|---|---|
- | - | D | Ovarian cancer | Acetylation | 30058682 |
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.