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. 2015 Dec 11;5(1):152–173. doi: 10.1002/mbo3.320

Table 2.

KEGG enrichment for acetylated proteinsa in glutamate‐producing and nonproducing conditions

Termb KEGG pathway Countc %d Detected proteome backgrounde Entire proteome backgroundf
P‐value Fold enrichment P‐value Fold enrichment Bonferroni
In nonproducing condition (325 DAVID IDs in the 1396 detected proteome)
cgl00020 Citrate cycle (TCA cycle) 15 4.6 4.98E‐06 2.9 2.59E‐12 9.3 4.02E‐10
cgl00970 Aminoacyl‐tRNA biosynthesis 15 4.6 0.00 579 1.9 1.03E‐09 7.0 1.59E‐07
cgl03010 Ribosome 26 8.0 0.00 582 1.6 1.98E‐10 4.2 3.07E‐08
In glutamate‐producing condition (213 DAVID IDs in the 1181 detected proteome)
cgl03010 Ribosome 24 12.1 0.00 101 1.8 1.18E‐11 5.2 1.48E‐09
cgl00020 Citrate cycle (TCA cycle) 11 4.7 0.00 191 2.6 2.84E‐08 9.3 3.58E‐06
cgl00970 Aminoacyl‐tRNA biosynthesis 13 6.1 0.00 541 2.2 5.11E‐09 8.2 6.44E‐07
209 proteins that contain reproducible and more than 2‐fold changed acetylation sites
cgl00020 Citrate cycle (TCA cycle) 11 5.3 1.09E‐04 3.6 3.65E‐09 11.4 4.63E‐07
a

Proteins that contain reproducible acetylation sites were used.

b

Kyoto Encyclopedia of Genes and Genome pathway (KEGG) pathway term.

c

Number of genes matching a given KEGG pathway term.

d

Percentage of genes matching a given term divided by the total number of input genes.

e

The detected proteome in each condition was used as background (P‐value < 0.01).

f

The entire proteome of Corynebacterium glutamicum was used as background. The Database for Annotation, Visualization, and Integrated Discovery.DAVID