TABLE 3

Analysis of smvR mutations arising in chlorhexidine-adapted populations

TABLE 3
  • a NT, nucleotide position in smvR.

  • b Mutations, NT substitution (e.g., C > T); duplication (e.g., [ATGATCAC] 1 > 2); deletion (e.g., Δ14 bp).

  • c Frequency, predicted frequency of sequences containing the mutation.

  • d Amino acid change, reference aa; aa position; new aa. Substitutions highlighted in bold indicate those where mutations lead to formation of a stop codon (*), predicted to truncate the translated protein at the indicated position.