b4602 |
-44 |
-10 |
-16 |
-10 |
7.78 |
FnrS |
53 |
92 |
53 |
59 |
4.83 |
-10.3 |
-22.91 |
-1.04945 |
CGUAAUAUCACUUUUUGUGUGGUAAUAAAAAAGGA&UCCUUUUUUGAAUUACUGCAUAGCACAAUUGAUUCGUACG |
((((..((((.....((((((((((((((((((((&)))))))))..))))))))))).......))))...)))) |
GGAGAUUUUUUCAUCACAGUGUGUAAAAAUGCGUAAUAUCACUUUUUGUGUGGUAAUAAAAAAGGAGAAAACUUGAUGAGCACCGACCUUAAAUUUUCACUGGUAACAACGAUUAUCGUCCUCGGUUUGAUCGUAGCCGUGGGUUUGACU |
GCAGGUGAAUGCAACGUCAAGCGAUGGGCGUUGCGCUCCAUAUUGUCUUACUUCCUUUUUUGAAUUACUGCAUAGCACAAUUGAUUCGUACGACGCCGACUUUGAUGAGUCGGCUUUUUUUU |
0.0212222 |
0.9422174 |
ynhF |
5061505 |
stress response membrane |
b2513 |
-21 |
5 |
-18 |
-12 |
4.32 |
FnrS |
37 |
63 |
54 |
60 |
5.31 |
-12.12 |
-21.75 |
-1.23489 |
UUAAGGAAGGAGAAGGACAGCGUGGA&UCCAUAUUGUCUUACUUCCUUUUUUGA |
((((((((((((.((((((...((((&))))...)))))).)).)))))))))) |
GCAAACGGCAGUUGCGCAGGAUAGCGUAGCCGCGCAUUUGCGCACGUUACUGGGUUAAGGAAGGAGAAGGACAGCGUGGAAAUUUACGAGAACGAAAACGACCAGGUAGAAGCGGUUAAACGCUUUUUUGCUGAAAAUGGCAAAGCACUG |
GCAGGUGAAUGCAACGUCAAGCGAUGGGCGUUGCGCUCCAUAUUGUCUUACUUCCUUUUUUGAAUUACUGCAUAGCACAAUUGAUUCGUACGACGCCGACUUUGAUGAGUCGGCUUUUUUUU |
0.0060206 |
0.9422174 |
yfgM |
946981 |
ancillary SecYEG translocon subunit putative anti-RcsB factor |
b4552 |
21 |
44 |
22 |
28 |
3.19 |
FnrS |
38 |
61 |
54 |
60 |
3.96 |
-11.14 |
-18.29 |
-1.13504 |
AAGAAAGGCAAGUAAAGAGUAUGG&CCAUAUUGUCUUACUUCCUUUUUU |
((((((((.((((((..(((((((&)))))))...)))))))))))))) |
GCUGAUGGCAGAGUAGGUGGAGGACUCCAGACAGUCAAACGAUAGAAAAAGAUAGCCUUUAUGGAGGUUCCUGCAAUGUCAAAUACAUACCAGAAAAGAAAGGCAAGUAAAGAGUAUGGUUUAUAUAAUAAAUGUAAGAAACUAAAUGAU |
GCAGGUGAAUGCAACGUCAAGCGAUGGGCGUUGCGCUCCAUAUUGUCUUACUUCCUUUUUUGAAUUACUGCAUAGCACAAUUGAUUCGUACGACGCCGACUUUGAUGAGUCGGCUUUUUUUU |
0.0120834 |
0.9422174 |
yrhC |
1450291 |
pseudogene fragment |
b3928 |
-21 |
10 |
-9 |
-3 |
10.1 |
FnrS |
40 |
76 |
55 |
61 |
5.75 |
-11.36 |
-27.21 |
-1.15745 |
GCCUUGCAAUUCAGGAGAGGUAUGACAAUGU&AUAUUGUCUUACUUCCUUUUUUGAAUUACUGCAUAGC |
((..((((((((((((((((...((((((((&))))))))......))))))))))))...))))..)) |
UCGUAUUUAUUAAGGCGUCACCGGUAAUCGGGACGAGGAUUUUUAUCCAUCAACGCCUUGCAAUUCAGGAGAGGUAUGACAAUGUCAUUAGAAGUGUUUGAGAAACUGGAAGCAAAAGUACAGCAGGCGAUUGAUACCAUCACUCUGUUG |
GCAGGUGAAUGCAACGUCAAGCGAUGGGCGUUGCGCUCCAUAUUGUCUUACUUCCUUUUUUGAAUUACUGCAUAGCACAAUUGAUUCGUACGACGCCGACUUUGAUGAGUCGGCUUUUUUUU |
0.0103736 |
0.9422174 |
zapB |
948420 |
FtsZ stabilizer septal ring assembly factor cell division stimulator |
b1531 |
-18 |
2 |
-18 |
-12 |
2.1 |
FnrS |
42 |
62 |
56 |
62 |
3.64 |
-11.77 |
-17.51 |
-1.19923 |
CAAAAAAGAGGUAUGACGAU&AUUGUCUUACUUCCUUUUUUG |
(((((((((((((.((((((&)))))).)))))).))))))) |
UGACGGCGGACGAAGUGGCAACACUUGAGUAUUUGCUUAAGAAAGUCCUGCCGUAAACAAAAAAGAGGUAUGACGAUGUCCAGACGCAAUACUGACGCUAUUACCAUUCAUAGCAUUUUGGACUGGAUCGAGGACAACCUGGAAUCGCCA |
GCAGGUGAAUGCAACGUCAAGCGAUGGGCGUUGCGCUCCAUAUUGUCUUACUUCCUUUUUUGAAUUACUGCAUAGCACAAUUGAUUCGUACGACGCCGACUUUGAUGAGUCGGCUUUUUUUU |
0.0077608 |
0.9422174 |
marA |
947613 |
multiple antibiotic resistance transcriptional regulator |
b3847 |
-56 |
4 |
-22 |
-16 |
10.89 |
FnrS |
38 |
89 |
56 |
62 |
7.59 |
-11.7 |
-30.18 |
-1.19209 |
AUGAACGAUGUGCUAAGAUGCGGAGACUUAAGGUCAAAAAAACAGAAGGGUAAAAAAUGG&CCAUAUUGUCUUACUUCCUUUUUUGAAUUACUGCAUAGCACAAUUGAUUCGU |
(((((((((((((((...(((((.....(((..((((((((...((((.....((.((((&)))).))......)))).)))))))).)))))))))))))).)))).))))) |
GGCAGAAAUCACGCUCUGGAUGAACGAUGUGCUAAGAUGCGGAGACUUAAGGUCAAAAAAACAGAAGGGUAAAAAAUGGAAUCACUGGCCUCGCUCUAUAAAAAUCAUAUAGCUACCUUACAAGAACGGACUCGCGAUGCGCUGGCGCGC |
GCAGGUGAAUGCAACGUCAAGCGAUGGGCGUUGCGCUCCAUAUUGUCUUACUUCCUUUUUUGAAUUACUGCAUAGCACAAUUGAUUCGUACGACGCCGACUUUGAUGAGUCGGCUUUUUUUU |
0.0081594 |
0.9422174 |
pepQ |
948335 |
proline dipeptidase |
b4638 |
-20 |
38 |
12 |
18 |
6.85 |
FnrS |
41 |
89 |
57 |
63 |
5.87 |
-10.14 |
-22.86 |
-1.03315 |
ACGAAUUGAGUCGCUUUUAAAUGUCGCAAAAUCAAGAAAUUAGUAAGAAAGAACAAUA&UAUUGUCUUACUUCCUUUUUUGAAUUACUGCAUAGCACAAUUGAUUCGU |
(((((((((...(((..........(((((.((((((((..((((((.....((((((&))))))))))))...)))))))).))..)))..)))....))))))))) |
CAGAUUUCUUAUGCUGGGCGUUCCGGCAUGACGCAUACUCUUCUGAUGCCAUAUAACGAAUUGAGUCGCUUUUAAAUGUCGCAAAAUCAAGAAAUUAGUAAGAAAGAACAAUACAACCUGAACAAGUAAGGGCAAAAAUCACAACUCUCU |
GCAGGUGAAUGCAACGUCAAGCGAUGGGCGUUGCGCUCCAUAUUGUCUUACUUCCUUUUUUGAAUUACUGCAUAGCACAAUUGAUUCGUACGACGCCGACUUUGAUGAGUCGGCUUUUUUUU |
0.0235457 |
0.9422174 |
ttcC |
5625564 |
pseudogene prophage Rac integration site ttcA duplicationPhage or Prophage Related |
b0233 |
1 |
16 |
9 |
15 |
1.76 |
FnrS |
58 |
73 |
59 |
65 |
3.39 |
-11.29 |
-16.44 |
-1.15032 |
AUGCGGGUAUUCAAAA&UUUUGAAUUACUGCAU |
((((((..((((((((&))))))))..)))))) |
GGAAAUUACACGCCGCGCUGAACAAUAUCUUAAUGAUAUGACGGAUGAUGAUUUCAAUGACUUUAAGGAAUAAGGAUGCGGGUAUUCAAAACAAAACUUAUUCGCCUGCAACUUACAGCAGAGGAACUUGAUGCGUUAACGGCGGAUUUU |
GCAGGUGAAUGCAACGUCAAGCGAUGGGCGUUGCGCUCCAUAUUGUCUUACUUCCUUUUUUGAAUUACUGCAUAGCACAAUUGAUUCGUACGACGCCGACUUUGAUGAGUCGGCUUUUUUUU |
0.0108921 |
0.9422174 |
yafO |
944916 |
mRNA interferase toxin of the YafO-YafN toxin-antitoxin system |
b2799 |
-72 |
-54 |
-62 |
-56 |
2.19 |
FnrS |
58 |
78 |
60 |
66 |
3.57 |
-10.07 |
-15.83 |
-1.02602 |
GUGCUGGAGAAAUUCAAAA&UUUUGAAUUACUGCAUAGCAC |
((((((.((.(((((((((&))))))))).)).))..)))) |
GUAGUGCUGGAGAAAUUCAAAACCUAUGGGUUACGAAUUGAAGAGUAAUUUCGUAAAGCAACAAGGAGAAGGAUGAUGGCUAACAGAAUGAUUCUGAACGAAACGGCAUGGUUUGGUCGGGGUGCUGUUGGGGCUUUAACCGAUGAGGUG |
GCAGGUGAAUGCAACGUCAAGCGAUGGGCGUUGCGCUCCAUAUUGUCUUACUUCCUUUUUUGAAUUACUGCAUAGCACAAUUGAUUCGUACGACGCCGACUUUGAUGAGUCGGCUUUUUUUU |
0.0246323 |
0.9422174 |
fucO |
947273 |
L-12-propanediol oxidoreductase |
b1048 |
23 |
35 |
28 |
34 |
1.77 |
FnrS |
64 |
78 |
65 |
71 |
3.45 |
-10.89 |
-16.11 |
-1.10957 |
GUGCUGCAGUAAU&AUUACUGCAUAGCAC |
(((((((((((((&))))))))..))))) |
UCCAUUAAAAUAGAUCGGAUCGAUAUAAGCACACAAAGGGGGAAGUGCUUACUAAUUAUGAAACAUAAACUACAAAUGAUGAAAAUGCGUUGGUUGAGUGCUGCAGUAAUGUUAACCCUGUAUACAUCUUCAAGCUGGGCUUUCAGUAUU |
GCAGGUGAAUGCAACGUCAAGCGAUGGGCGUUGCGCUCCAUAUUGUCUUACUUCCUUUUUUGAAUUACUGCAUAGCACAAUUGAUUCGUACGACGCCGACUUUGAUGAGUCGGCUUUUUUUU |
0.0143339 |
0.9422174 |
opgG |
945005 |
OPG biosynthetic periplasmic beta-16 branching glycosyltransferase |