Table 3 List of chromosomal mutations identified in the genome of the SCV morphotype (n°2) when compared to the genome of morphotype n°1.
Gene | Protein | Mutation | Effect on the protein | Impact on the protein function |
|---|---|---|---|---|
Hypothetical protein | Unknown | 99T > C | synonymous variant | Unlikely |
sdhA | Succinate dehydrogenase flavoprotein subunit | 1673A > G | missense variant: His558Arg | Unlikely: same family of aminoacids |
serA | Phosphoglycerate deshydrogenase | 40T > C | missense variant: Phe14Leu | Possible: different families of aminoacids |
Hypothetical protein | Unknown | 739A > C | missense variant: Thr247Pro | Unknown |
pbuE | Purine efflux pump PbuE | 605G > AT | missence variant: insertion of Arg in 202 | Unlikely (end of protein) |
nodD2 | Nodulation protein | 303G > T | synonymous variant | Unlikely |
lgrD | non-ribosomal peptide synthetase | 2668A > T | stop gained Lys890* | Possible: truncated protein of 890 amino acids versus 991 |
