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. 2020 Aug 5;32:106121. doi: 10.1016/j.dib.2020.106121

Table 2.

Reactome pathway overrepresented in positive samples.

Reactome pathway
Homo sapiens (REF) Input (proteins overrepresented in positive samples)
#* #⁎⁎ Expected⁎⁎⁎ Fold enrichment +/- Raw
p-value
SRP-dependent cotranslational protein targeting to membrane 112 17 0.53 31.97 + 6.62E-17
Viral mRNA Translation 89 15 0.42 35.50 + 3.04E-15
Peptide chain elongation 89 15 0.42 35.50 + 3.04E-15
Nonsense Mediated Decay (NMD) enhanced by the Exon Junction Complex (EJC) 115 16 0.55 29.30 + 3.21E-15
Selenocysteine synthesis 93 15 0.44 33.97 + 5.94E-15
Eukaryotic Translation Termination 93 15 0.44 33.97 + 5.94E-15
Nonsense Mediated Decay (NMD) independent of the Exon Junction Complex (EJC) 95 15 0.45 33.97 + 7.31E-15
Formation of a pool of free 40S subunits 101 15 0.48 31.28 + 1.67E-14
Response of EIF2AK4 (GCN2) to amino acid deficiency 101 15 0.48 31.28 + 1.67E-14
Regulation of expression of SLITs and ROBOs 169 17 0.80 21.19 + 3.82E-14
L13a-mediated translational silencing of Ceruloplasmin expression 111 15 0.53 28.46 + 6.03E-14
GTP hydrolysis and joining of the 60S ribosomal subunit 112 15 0.53 28.21 + 6.81E-14
Major pathway of rRNA processing in the nucleolus and cytosol 182 15 0.86 17.36 + 5.18E-11
Formation of the ternary complex, and subsequently, the 43S complex 51 7 0.24 28.91 + 2.17E-05
Ribosomal scanning and start codon recognition 58 7 0.28 25.42 + 4.88E-05
Translation initiation complex formation 58 7 0.28 25.42 + 4.88E-05
Mitochondrialproteinimport 65 6 0.31 19.44 + 2.21E-03
Interferon gamma signaling 91 6 0.43 13.89 + 1.38E-02
Downstream TCR signaling 102 6 0.48 12.39 + 2.56E-02

All genes from H. sapiens were used as comparative dataset.

⁎⁎

The number of proteins found in the input dataset that were assigned to the corresponding biological process.

⁎⁎⁎

This column represents the expected number of H. sapiens genes according to the size of dataset used as an input. The input dataset was all proteins incremented in positive samples when compared to negative samples. Fisher exact was used as statistical analysis with Bonferroni correction for multiple testing. Biological processes are ordered according to the p-value. Pathways with less than 5 proteins found in the input dataset were not considered.