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. 2020 Nov 19;18(9):1324–1338. doi: 10.1080/15476286.2020.1846388

Table 1.

Top 10 predicted targets of Ec-rnTrpL, based on the CopraRNA p-value. For each gene, 200 nt upstream and 100 nt downstream of the first nucleotide of the coding region are extracted as 5ʹUTR for target prediction. The interaction site coordinates are given relative to the first nucleotide of the coding region. Positive coordinates indicate interaction in the coding regions. In case of operons, negative numbers might indicate an interaction within the predecessor gene in the operon. 1The upstream gene sanA was tested, in which the interaction site is located; 2mhpC was tested, although the interaction site is located in the upstream gene mhpB (see Fig. 4); NA, not applicable

p-value Locustag Gene Interaction site borders in mRNA Experimentally tested Regulation Annotation
6,55E-09 b3702 dnaA +12 to + 87 yes negative chromosomal replication initiator protein DnaA
2,58E-05 b0905 ycaO +70 to +89 yes no effect ribosomal protein S12 methylthiotransferase accessory factor YcaO
5,32E-05 b2145 sanA/yeiS −180 to −142 yes negative1 DUF2542 domain-containing protein YeiS
7,95E-05 b0349 mhpB/mhpC −200 to −177 yes positive2 2-hydroxy-6-ketonona-2 4-dienedioate hydrolase
0,000186 b2182 bcr −74 to −20 no NA multidrug efflux pump Bcr
0,000189 b0661 miaB −200 to −185 no NA isopentenyl-adenosine A37 tRNA methylthiolase
0,000368 b3052 rfaE −95 to −87 no NA fused heptose 7-phosphate kinase/heptose 1-phosphate adenyltransferase
0,000433 b2465 tktB −178 to −169 no NA transketolase 2
0,000488 b1888 cheA −1 to +6 no NA chemotaxis protein CheA
0,000766 b2808 gcvA −142 to −118 no NA DNA-binding transcriptional dual regulator GcvA