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. 2017 Dec 21;62(1):e01235-17. doi: 10.1128/AAC.01235-17

TABLE 3.

Mutations identified by whole-genome sequencing in the DAP-resistant mutants

Mutant Gene description Nucleotide variation (frequency [%])a Amino acid changeb E. faecalis V583 ortholog
DAP-A1 Eftg_02287 ABC transporter C67008T (98.47) Ala290Val EF2226
Eftg_01724 RelA/SpoT (relA) CTAGGATTTAC30479Del (98.19) Leu505fs EF1974
Eftg_01135 alpha/beta hydrolase G137748A (55.64) Trp150* EF1505
Eftg_00577 cytidylate kinase (cmk) promoter A618699IS1251 IS1251 insertion EF1547
DAP-A2 Eftg_02287 ABC transporter C67008T (99.77) Ala290Val EF2226
Eftg_01724 RelA/SpoT (relA) CA29139AG (95.74) Ala58Glu EF1974
Eftg_01135 alpha/beta hydrolase 137847G insertion (88.17) Ile184fs EF1505
Eftg_00577 cytidylate kinase (cmk) promoter A618699IS1251 IS1251 insertion EF1547
DAP-B1 Eftg_02287 ABC transporter C67008T (98.962) Ala290Val EF2226
Eftg_01175 PhoU regulator G173845A (99.61) Glu61Lys EF1754
Eftg_02534 transposase C71844A (99.47) Lys206Asn
DAP-B2 Eftg_02287 ABC transporter C67008T (99.36) Ala290Val EF2226
Eftg_02162 glycosyltransferase (bgsB) C50223T (67.09) Val57Met EF2890
a

The mutation frequency in the read assembly was determined by variant detection in CLC Genomics Workbench where applicable. The precise location of insertion for variation A618699IS1251 was mapped by Sanger sequencing.

b

Asterisk indicates stop codon.