B

BiohacksAI

Evidence-Based Biohacking

Patent Pending

AMPK-induced ERAD and lysosome mediated degradation of PD-L1(CD274)

REACTOME PATHWAY
Reactome: R-HSA-993126940 genes32 compounds

The AMPK-induced ERAD and lysosome mediated degradation of PD-L1(CD274) pathway (Reactome ID: R-HSA-9931269) involves 40 genes and is affected by 32 compounds in the BiohacksAI evidence corpus. Compound-pathway associations are derived from target overlap: a compound is linked to this pathway if it targets ≥2 genes within the pathway.

Genes in this Pathway

ADRM1PRKAA1PRKAA2PRKAB1PRKAB2PRKAG1PRKAG2PRKAG3PSMA1PSMA2PSMA3PSMA4PSMA5PSMA6PSMA7PSMB1PSMB2PSMB3PSMB4PSMB5PSMB6PSMB7PSMC1PSMC2PSMC3PSMC4PSMC5PSMC6PSMD1PSMD11+10 more

Compounds Affecting AMPK-induced ERAD and lysosome mediated degradation of PD-L1(CD274)

#CompoundTargets HitStudies
1Bortezomib300
2Reserpine297
3Adenosine Monophosphate Adenine nucleotide containing300
4Proguanil299
5Carbonyl Cyanide p-Trifluoromethoxyphenylhydrazone76
6Niclosamide299
7Berberine300
8Ursolic Acid300
9Antimycin300
10Oleanolic Acid300
11Rotenone300
12Metformin1,000
13Quercetin300
14egcg300
15Emodin Purgative anthraquinone found in several plants, especially RHAMNUS PURSHIANA. It was formerly used as300
16Kaempferols300
17Rutin300
18Disulfiram297
194-Hydroxybenzoate-3-Monooxygenase300
20Apigenin 5,7,4'-trihydroxy-flavone,300
21chrysin300
22Luteolin 5,7,3',4'-tetrahydroxy-flavone,150
23Genistein300
24myricetin-3-O-galactopyranoside [Supplementary Concept]300
25Crizotinib298
26Hexachlorophene300
27Oxytetracycline300
28Clotrimazole296
29Demeclocycline5
30Edaravone298
31Pioglitazone297
32Harmaline300

About the AMPK-induced ERAD and lysosome mediated degradation of PD-L1(CD274) Pathway

The AMPK-induced ERAD and lysosome mediated degradation of PD-L1(CD274) pathway is catalogued in Reactome (ID: R-HSA-9931269) and involves 40 genes. In the BiohacksAI corpus, 32 compounds have documented interactions with at least 2 genes in this pathway, establishing mechanistic relevance. Key pathway genes include ADRM1, PRKAA1, PRKAA2, PRKAB1, PRKAB2.