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. 2019 Jun 13;9:8592. doi: 10.1038/s41598-019-45023-3

Table 1.

Differentially abundant proteins for the main effect oxygen, where p < 0.05 and log2FC > |0.2|.

Gene Description Function log2FC p
Up-regulated
COPS2 COP9 signalosome complex subunit 2 regulates protein degradation 0.274 0.016
COX2 Cytochrome oxidase subunit II oxidative phosphorylation 0.240 0.024
ARHGDIA Rho GDP-dissociation inhibitor 1 regulates GTPase signalling 0.226 0.017
PSMD4 Proteasome 26S subunit 4 degradation of ubiquitinated proteins 0.217 0.035
MAIP1/C2orf47 Matrix AAA peptidase interacting protein 1 mitochondrial protease 0.209 0.031
MRPS29/DAP3 Mitochondrial 28S ribosomal protein translation; apoptosis 0.203 0.030
YWHAB 14-3-3 alpha intracellular signalling 0.200 0.020
Down-regulated
FIS1 Mitochondrial fission protein 1 regulates mitochondrial morphology −0.396 0.015
(KYO27548.1) No human ortholog unknown −0.377 0.026
CRK Adapter molecule crk intracellular signalling −0.365 0.021
PPM1E Protein phosphatase 1E protein dephosphorylation, including CAMK −0.340 0.032
DYNC1LI2 Dynein cytoplasmic 1 intermediate light chain 2 microtubule-associated motor protein −0.324 0.045
SMS Spermine synthase catalyzes spermine production −0.304 0.045
STX12 Syntaxin-12 regulates protein transport −0.265 0.034
RTN1 Reticulon-1 membrane trafficking −0.243 0.028
CDK5RAP3 CDK5 regulatory subunit-associated protein 3 transcriptional regulation, cell cycle progression −0.242 0.020
GPD1L Glycerol-3-phosphate dehydrogenase 1-like regulates cardiac sodium current −0.232 0.031
TPMT Thiopurine S-methyltransferase thiopurine metabolism; endogenous function unknown −0.211 0.011
NRAP Nebulin related anchoring protein myofibrilar organization in cardiomyocytes −0.210 0.033
COA3 Cytochrome c oxidase assembly factor 3 mitochondrial assembly −0.207 0.034
SAMHD1 Deoxynucleoside triphosphate triphosphohydrolase regulates dNTP pool −0.204 0.001
ADHFE1 Hydroxyacid-oxoacid transhydrogenase, mitochondrial oxidoreductase activity −0.202 0.003

Up-regulated and down-regulated proteins are presented separately, ordered by magnitude of log2FC. Where no human homolog was found and function was unknown, protein is listed by Accession number in place of gene symbol. FC = fold change.