TABLE 4.
Human | Drosophila | Function | Function | Loc |
ACAA1 | CG9149 | β-Oxidation | β-Ketoacyl-CoA thiolase | (−)B |
ACAD11 | CG4860 | β-Oxidation | Short-chain acyl-CoA dehydrogenase | (−)B |
ACOX2 | CG17544 | β-Oxidation | Acyl-CoA oxidase | (+)B |
ACSL1 | CG3961 | β-Oxidation | Long-chain-fatty-acid–CoA ligase | (−)B |
ACSL3/4 | Acsl | β-Oxidation | Acyl-CoA synthetase long-chain | (−)B (+)H |
DECR2 | CG3699 | β-Oxidation | 17-Beta-estradiol 17-dehydrogenase | (−)B |
DRS7B | CG31548 | β-Oxidation | 17-Beta-estradiol 17-dehydrogenase | (−)B |
EPHX2 | Pummelig | ROS metabolism | Carboxylesterase | (−)B (+)HT |
HMGCL | Hmgcl | Amino acid metabolism | Hydroxymethylglutaryl-CoA lyase | (+)B |
HMGCR | Hmgcr | Isoprenoid synthesis | HMG coenzyme A reductase | (+)B |
IDI1/2 | Idi | Isoprenoid synthesis | Isopentenyl-diphosphate delta-isomerase | (−)B |
IDH1 | Idh | α-Oxidation | Isocitrate dehydrogenase | (−)B |
LONP | Lon | Protease | Lon protease | (+)B |
MARF1 | Marf1 | mRNA stability | Meiosis regulator and mRNA stability | (−)B |
NUDT7 | CG11095 | Coenzyme A diphosphatase | (−)B | |
PAOX | CG8032 | Spermine/spermidine oxidase | (−)B | |
PHYH | CG14688 | α-Oxidation | Phytanoyl-CoA dioxygenase | (−)B |
PMVK | CG10268 | Isoprenoid synthesis | Phosphomevalonate kinase | (+)B |
PRDX1 | Jafrac | ROS metabolism | Peroxiredoxin | (−)B |
PRDX5/PMP20 | Prx5 | ROS metabolism | Peroxiredoxin | (−)B |
XDH | Ry | Purine metabolism | Xanthine dehydrogenase | (+)B |
ACSF3 | CG18155 | β-Oxidation | Long-chain-fatty-acid–CoA ligase Malonate–CoA ligase | (+)B |
NUDT19 | CG10194 | Coenzyme A diphosphatase | (+)B | |
MUL1 | Mul1 | Mitochondrial E3 ubiquitin protein ligase | (+)B | |
MVK | CG33671 | Isoprenoid synthesis | Mevalonate kinase | (−)B |
NOS2 | Nos | ROS metabolism | Nitric oxide synthase | (+)B |
SERHL/SEHL2 | Kraken | Protease | Serine hydrolase-like | (−)B |
SOD2 | Sod2 | ROS metabolism | Superoxide dismutase | (−)B |
“Loc”: (+) experimentally validated localization to peroxisomes, (−) did not localize to peroxisomes in B-(Baron et al., 2016), F-(Faust et al., 2012), H-(Huang et al., 2016) or HT-(Hehlert et al., 2019).