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. 2003 Aug;71(8):4674–4683. doi: 10.1128/IAI.71.8.4674-4683.2003

TABLE 3.

Regions of the K-12 chromosomal backbone with more than 10 consecutive genes absent from at least two strainsa

Start End Strains which lack this region
b0245 b0254 (perR) E139229; E140065; E33167; EC1388; EC172; EC1722; EC1725; EC1727; EC1840; EC225; EC335; EC370; EC459; EC622; EDL933; SO29; SO55
b0245 b0255 (yi91a) EC38; EC720; SO111; EC157; EC681∗; EC558∗
b0264 (insB_2) b0280 (yagN) E140065; EC720; EC157∗; EC370∗
b0274 (insB_3) b0286 (yagT) EC370; EC558
b0504 (ybbS) b0521 (arcC) EC370; EC558
b0557 (ybcU) b0566 (envY) EC1388; EC622
b0933 (ycbE) b0942 EC370; EC558
b1021 (ycdP) b1031 (ycdV) EC370; EC558
b1136 (icdA) b1146 EC720; EC172*; SO111; EC370∗; EC38
b1137 (ymfD) b1157 E139229; E140065∗; EC157; EC1727∗; EC558∗; EC622*; EDL933∗
b1149 (ymfN) b1161 (ycgX) EC183; EC681; EC172∗; EC1722∗; EC720∗; SO126∗; SO29
b1159 (mcrA) b1172 E139229; E140065; EC370∗; EC558∗; EC157∗
b1305 (pspB) b1321 (ycjX) EC558; EC370∗
b1345 b1360 EC720; O126; SO29∗; EC622
b1382 (ynbE) b1401 (ydbA_1) E139229; E140065; EC558; EC720; EC157; EC370∗; EDL933∗; SO111∗
b2030 (trs5_7) b2039 (rfbA) EC38; EC622
b2030 (trs5_7) b2041 (rfbB) E139229; E140065; EDL933; EC157; SO55; SO126; SO29∗; EC720∗; SO111∗; EC1727∗
b2043 (wcaM) b2062 (wza) EC370; EC558; SO111∗
b2347 (yfdC) b2363 EC370; EC558; EC1727∗; EC622∗; EC720∗
b2355 (yfdL) b2365 (dsdX) E139229; EDL933
b2622 (intA) b2644 (yfjY) EC1388; EC1727; EC183; EC1840; EC370; EC537; EC558; EC157; EC720∗; EC622∗; EC459
b2622 (intA) b2646 (ypjF) E139229; E140065; E33167; EC172; EC1722; EC1725; EC225; EC335; EC38; EC681; EDL933; SO111; SO126; SO29; SO55
b2648 b2659 EC558; SO29; EC335
b2968 (yghD) b2986 (yghT) E139229; E140065; EDL933; EC157
b3318 (rplW) b3338 (yheB) EC335; EC558; EC681; SO126
b3320 (rplC) b3338 (yheB) SO111; EC157
b3321 (rpsJ) b3338 (yheB) EC172; EC183
b3322 (pinO) b3338 (yheB) E139229; E140065; E33167; EC1388; EC1722; EC1727; EC1840; EC225; EC370; EC38; EC459; EDL933; EC537∗; EC1725
b3574 (yiaJ) b3583 (sgbE) E139229; E140065; EDL933; EC157
b3622 (rfaL) b3632 (rfaQ) E139229; E140065; E33167; EC1388; EC172; EC1722; EC1725; EC1727; EC38; EC183; EC1840; EC225; EC335; EC459; EC537; EC681; EC720; EDL933; SO111; SO126; EC157; SO55
b3894 (fdoG) b3907 (rhaT) EC370; EC558
b4273 (yi22_6) b4282 (yjhE) EC183; EC681; EC1722∗; EC622
b4274 (yjgW) b4283 (yi91b) EC1388; EC38; SO111; SO126; EC157; EC370∗; EC558
b4285 b4308 (yjhR) EC157; EC720∗; EC558∗; EC370∗
b4294 (insA_7) b4308 (yjhR) EC183; EC335; EC622; SO111; SO126
b4295 (yjhU) b4308 (yjhR) E139229; E140065; E33167; EC1388; EC172; EC1722; EC1725; EC1727; EC1840; EC225; EC459; EC537; EC681; EDL933; SO29; SO55; EC38
b4338 (yjiP) b4351 (mrr) SO111; SO126; SO29
b4341 (yjiS) b4351 (mrr) EC1388; EC1725; EC459
b4342 (yjiT) b4351 (mrr) EC1727; EC38; SO55
a

The start and end positions of regions that are absent from the K-12 chromosomal backbone are given by the gene identifier and gene name (in parentheses), where applicable. Strains belonging to the O26 serotype are shown in bold. The names of some clinical isolates have been shortened by omitting the suffix. ∗, strain in which the missing region has a significant overlap but starts before or extends beyond or is not as large as the positions given but is still missing at least 10 consecutive genes.