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. 2007 Sep 28;190(3):834–842. doi: 10.1128/JB.00912-07

TABLE 3.

Sequencing results and mutations in thyA in clinical normal strains and TD-SCVs

Strain Alteration(s) in nucleotide sequence Predicted results
Normal-1a
SCV-1a Δ247AAT249 3-bp deletion → deletion of Asn
Normal-2a
SCV-2a Δ247AAT249 3-bp deletion → deletion of Asn
Normal-3b T76C Point mutation Cys → Arg (amino acid 26)
SCV-3b C139T, G337A, A493G, ΔA565 Point mutations Leu → Por (amino acid 47), Gly → Ser (amino acid 113), and Asn → Asp (amino acid 165) and 1-bp deletion → stop codon (amino acid 188)
Normal-4a T730G, G835A Point mutations Ser → Ala (amino acid 244) and Gly → Ser (amino acid 279)
SCV-4a T82A, Δ592CTTCCGCCTTG601 11-bp deletion (amino acid 198 → frameshift mutation → truncated protein
Normal-5b G308A, C838T Point mutations Gly → Asp (amino acid 103) and Leu → Phe (amino acid 280)
SCV-5 ΔA51 1-bp deletion → frameshift mutation → stop codon (amino acid 19)
Normal-6b C383T, A482G, G886A Point-mutations Ser → Phe (amino acid 128), Asp → Gly (amino acid 161), and Val → Ile (amino acid 296)
SCV-6b G359A, ΔG743 Point-mutation Arg → Gln (amino acid 120) and 1-bp deletion → frameshift mutation → stop codon (amino acid 251)
SCV-7-1b T7A, C521T, G806A, ΔA893 Point-mutations Tyr → Asn (amino acid 3), Tyr → Ile (amino acid 174), and Gly → Asp (amino acid 269) and 1-bp deletion → frameshift mutation → stop codon (amino acid 311)
SCV-7-2b T7A, T616C Point-mutation Tyr → Asn (amino acid 3) and point mutation → stop codon (amino acid 206)
SCV-8-1 ΔT121 1-bp deletion → frameshift mutation → stop codon (amino acid 50)
SCV-8-2b Δ547ACATCGT553 7-bp deletion → frameshift mutation → stop codon (amino acid 212)
a

Allele 2 (C at nucleotide position 300, Asn at amino acid position 100, and same thyA sequence as S. aureus strain MW2).

b

Allele 1 (A at nucleotide position 300, Lys at amino acid position, and same thyA sequence as S. aureus strain COL).