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. 2020 Jul 2;9(7):532. doi: 10.3390/pathogens9070532

Table 2.

Alignment of PorA SA Determinant Region between Sequence Types.

Sequence a,b,c cgMLST200-12
vs. MLST-8 d
Description
170- * *     * *    * *                      *     *    * * * −209 Conserved residues
NCTC11168 FMAAEQGADLLEHSNISTTS NQAPFKVDSVGNLY Reference sequence
N48272F FMAEEQGADLLGKST ISTTQKAAPFQADSLGNLY 55:53 SA clonal sequence
N43804F FMAEEQGADLLGKST ISIT QKAAPFQADSLGNLY 1:1 Substitution not in SA loci
N45191FR FMAEEQGT DLLGKST ISTTQKAAPFQADSLGNLY 1:1 Substitution not in SA loci
N46355F FMAEEQGADLLGKSTISTT QKAAPFQTNSLGNLY 1:1 Substitution in SA loci
N49694F FMEKEQ I S DLVG           SNSSTFNVDSI GNLY 16:16 Deletion and substitutions in SA loci
N44409F FMAAEQSS DLVG          ANGSAFKVDSI ENLY 1:1 Deletion and substitutions in SA loci
N45200F FMAKEQGSDLVG          ANGSAFNVDSIGNLY 1:1 Deletion and substitutions in SA loci

a * indicates conserved residue at sequence position, b Bold formatting indicates amino acid substitution associated with the SA phenotype, c Underline formatting indicates amino acid substitution not associated with the SA phenotype, d cgMLST200-12 (left) and MLST-8 (right) isolates identified with the corresponding PorA aa sequence.