Table 3.
Non-synonymous mutations in genes related to nutrient acquisition and local environment.
| Pair ID | Gene | Position* | Amino acid Substitution |
|---|---|---|---|
| 1 | GTPase | 524:gCa-gAa | Ala-175-Glu |
| 1 | L-xylulose/3-keto-L-gulonate kinase | 65:cAc-cGc | His-22-Arg |
| 2 | taurine-binding periplasmic protein | 523:Gtc-Atc | Val-175-Ile |
| 5 | protein CsiD | 718:Gtg-Atg | Val-240-Met |
| 11 | cold shock-like protein CspE | 179:gGc-gAc | Gly-60-Asp |
| 11 | periplasmic AppA protein | 125:cGt-cAt | Arg-42-His |
| 11 | D-tagatose-1,6-bisphosphate aldolase subunit kbaZ | 169:Ggc-Agc | Gly-57-Ser |
| 11 | PTS system protein | 761:tAt-tGt | Tyr-254-Cys |
| 11 | protein ydeP | 2239:Tga-Cga | STP-747-Arg |
| 20 | dihydrolipoyl dehydrogenase | 1124:gAa-gCa | Glu-375-Ala |
| 22 | carboxysome structural protein, ethanolamine utilization | 271:Aaa-Taa | Lys-91-STP |
| 23 | carbamate kinase | 328:Cag-Gag | Gln-110-Glu |
| 23 | inner membrane protein | 1894:Tca-Cca | Ser-632-Pro |
| 27 | maltodextrin phosphorylase | 791:gTc-gCc | Val-264-Ala |
| 28 | Phosphomannomutase | 661:Att-Gtt | Ile-221-Val |
| 31 | maltose regulon periplasmic protein | 653:tCg-tTg | Ser-218-Leu |
| 32 | tautomerase ppt | 176:gAa-gCa | Glu-59-Ala |
| 33 | GTPase | 784:Gtt-Att | Val-262-Ile |
| 33 | oxygen-insensitive NADPH nitroreductase | 214:Taa-Caa | STP-72-Gln |
| 34 | Phosphomannomutase | 880:Gtt-Att | Val-294-Ile |
| 37 | phospho-2-dehydro-3-deoxyheptonate aldolase, Tyr-sensitive | 198:gaA-gaT | Glu-66-Asp |
| 37 | carbon storage regulator | 34:Ttc-Ctc | Phe-12-Leu |
| 37 | carbon storage regulator | 32:aCc-aTc | Thr-11-Ile |
| 37 | undecaprenyl-phosphate galactose phosphotransferase WbaP | 238:Gaa-Taa | Glu-80-STP |
| 40 | Ecotin | 56:tTg-tGg | Leu-19-Trp |
| 42 | serine/threonine-protein phosphatase 1 | 126:gaT-gaA | Asp-42-Glu |
| 42 | inorganic phosphate transporter 1 | 1265:cAg-cCg | Gln-422-Pro |
| 43 | ribosomal RNA large subunit methyltransferase L | 664:Tgt-Cgt | Cys-222-Arg |
Capital letters indicate the codon position of the mutation
STP: Stop codon