breseq  version 0.33.1  revision 8505477f25b3
mutation predictions | marginal predictions | summary statistics | genome diff | command line log

Predicted mutations
evidence position mutation annotation gene description
RA 101,810 G→A V202M (GTG→ATG)  ftsW → integral membrane protein involved in stabilizing FstZ ring during cell division
MC JC 475,062 Δ4 bp coding (241‑244/1677 nt) ybaL ← predicted transporter with NAD(P)‑binding Rossmann‑fold domain
JC 990,173 +CGT coding (321/780 nt) ycbC ← conserved inner membrane protein
JC JC 1,305,487 IS150 (–) +3 bp coding (751‑753/1461 nt) cls ← cardiolipin synthetase
RA 1,329,516 C→T H33Y (CAC→TAC)  topA → DNA topoisomerase I
RA 1,345,210 (T)8→7 intergenic (‑98/+137) yciR ← / ← rnb modulator of Rnase II stability/exoribonuclease II
JC 1,733,297 (CGTATGAA)1→2 coding (333/1413 nt) pykF → pyruvate kinase
RA 2,193,779 G→T L143I (CTT→ATT)  yeiB ← conserved inner membrane protein
RA 2,295,476 A→C *85C (TGA→TGC yfaE → predicted 2Fe‑2S cluster‑containing protein
RA 3,145,984 A→T I41F (ATC→TTC)  rpoD → RNA polymerase sigma factor
RA 3,762,741 A→T K662I (AAA→ATA)  spoT → bifunctional (p)ppGpp synthetase II/ guanosine‑3',5'‑bis pyrophosphate 3'‑pyrophosphohydrolase
RA 3,875,632 (T)7→8 intergenic (‑66/+287) glmU ← / ← atpC bifunctional N‑acetylglucosamine‑1‑phosphate uridyltransferase/glucosamine‑1‑phosphate acetyltransferase/F0F1 ATP synthase subunit epsilon
MC JC 3,894,997 Δ6,991 bp IS150‑mediated rbsD[yieO] rbsD, rbsA, rbsC, rbsB, rbsK, rbsR, [yieO]
RA 3,911,997 (A)6→5 intergenic (‑198/‑125) yifB ← / → ilvL predicted bifunctional enzyme and transcriptional regulator/ilvG operon leader peptide
RA 4,096,926 A→G L216P (CTG→CCG)  glpF ← glycerol facilitator
RA 4,166,437 C→T P493S (CCG→TCG)  rpoC → DNA‑directed RNA polymerase subunit beta'
RA 4,273,299 A→T intergenic (+227/‑115) nrfG → / → gltP heme lyase (NrfEFG) for insertion of heme into c552, subunit NrfG/glutamate/aspartate:proton symporter
JC JC 4,524,522 IS186 (+) +6 bp coding (494‑499/549 nt) fimA → major type 1 subunit fimbrin (pilin)

Unassigned missing coverage evidence
   seq id start end size ←reads reads→ gene description
* * ÷ REL606 546985–547700 593372 45673–46388 11 [9] [10] 11 [insB‑6]–[fepA] [insB‑6],insA‑6,nmpC,ybcR,ybcS,ybcT,ybcU,ECB_00510,nohB,ECB_00512,ECB_00513,ECB_00514,ECB_00515,ECB_00516,ECB_00517,appY,ompT,envY,ybcH,nfrA,nfrB,nfrB,ECB_00524,yhhI,ECB_00526,ECB_00527,ECB_00528,ECB_00529,ECB_00530,cusS,cusR,cusC,ylcC,cusB,cusA,pheP,ybdG,nfnB,ybdF,ybdJ,ybdK,insJ‑1,insK‑1,insB‑7,insA‑7,insK‑1,hokE,insL‑3,entD,[fepA]
* * ÷ REL606 593565 619839–619116 25552–26275 11 [10] [9] 11 [fepA]–insA‑8 [fepA],fes,ybdZ,entF,fepE,fepC,fepG,fepD,ybdA,fepB,entC,entE,entB,entA,ybdB,cstA,cstA,ybdD,ybdH,ybdL,ybdM,ybdN,insB‑8,insA‑8
* * ÷ REL606 2842143–2842194 2842242–2842211 18–100 11 [10] [10] 11 [metW]–[metV] [metW],[metV]