Table 4.
Functions | Proteins involved |
---|---|
Energy or mitochondrial dysfunction | Isocitrate dehydrogenase (NAD) subunit α (IDH3A) Isoform M1 Pyruvate kinase isozymes M1/M2 (KPYM) Pyruvate dehydrogenase E1 component subunit alpha (PDHA1) Aspartate aminotransferase (AATC) ATP synthase (ATPase) Pyruvate dehydrogenase component subunit beta, mitochondrial (PDH) Prohibitin (Fragment) (PHB) Triosephosphate isomerase (protect against neuronal apoptosis) (TPI) ES1 protein homolog, mitochondrial (ES1) Alpha-enolase (ENO) |
Neuritic abnormalities | Actin-related protein 3 (Actr3) Dihydropyrimidinase-related protein 2 (CRMP-2) |
Synaptic abnormalities and LTP | N-ethylmaleimide sensitive fusion protein attachment protein beta (SNAPs) Guanine nucleotide protein G (0) subunit alpha (GNAO) |
Cell cycle; tau phosphorylation; and Abeta production | Pin-1 |
Lipid abnormalities | Isoform A of Cytosolic acyl coenzyme A thioester hydrolase (BACH) |
Lysosomal dysfunction | V-type proton ATPase (V-ATPase) |
Antioxidant defense | Protein DJ-1 (PARK7) |