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. 2022 Jul 22;13:4239. doi: 10.1038/s41467-022-31837-9

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

Variant calling was performed using the Snippy software (https://github.com/tseemann/snippy) after annotation of the reference genome of morphotype n°1 (Prokka software).