b2095 |
-73 |
-39 |
-73 |
-67 |
12.38 |
RyhB |
14 |
49 |
43 |
49 |
10.32 |
-11.15 |
-33.85 |
-1.1724 |
GUGAGCAAAGUGAUUGCCGAUUGUGGCUGCGAGGG&CCCUCGCGGAGAACCUGAAAGCACGACAUUGCUCAC |
((((((((.((...(((.....((..(((((((((&)))))))))...))......)))..)).)))))))) |
UGGUGAGCAAAGUGAUUGCCGAUUGUGGCUGCGAGGGCAGGGCAUAACGCACCUGCCAUUUAACAAGGAAAAAACAUGAAAACGUUAAUUGCCCGGCAUAAAGCUGGUGAACAUAUCGGCAUAUGUUCAGUCUGUUCUGCCCAUCCGUUG |
GCGAUCAGGAAGACCCUCGCGGAGAACCUGAAAGCACGACAUUGCUCACAUUGCUUCCAGUAUUACUUAGCCAGCCGGGUGCUGGCUUUU |
0.0258974 |
0.9496255 |
gatZ |
946641 |
D-tagatose 16-bisphosphate aldolase 2 subunit |
b3991 |
-75 |
-66 |
-75 |
-69 |
2.89 |
RyhB |
40 |
49 |
43 |
49 |
1.15 |
-13.4 |
-17.44 |
-1.40898 |
GUGAGCAGUG&CAUUGCUCAC |
((((((((((&)))))))))) |
GUGAGCAGUGGGCGCAACAUAUCGUGCAGGAUGGCGACCAGAUCCUGCUUUUUCAGGUUAUUGCAGGGGGUUGAAAUGUUACGUAUUGCGGACAAAACGUUUGAUUCACAUCUGUUUACCGGCACAGGGAAAUUCGCUUCUUCACAACUG |
GCGAUCAGGAAGACCCUCGCGGAGAACCUGAAAGCACGACAUUGCUCACAUUGCUUCCAGUAUUACUUAGCCAGCCGGGUGCUGGCUUUU |
0.0076567 |
0.9291058 |
thiG |
948493 |
thiamine biosynthesis ThiGH complex subunit |
b2727 |
-7 |
4 |
-6 |
1 |
4.77 |
RyhB |
39 |
49 |
42 |
48 |
1.15 |
-12.05 |
-17.97 |
-1.26703 |
GUGAGCGAUGU&ACAUUGCUCAC |
(((((((((((&))))))))))) |
CAUGGUGACAUGCUGCAGAUUGUGGCAGACGACGGUUUACAGAUUCGGCGGAUAGAAAUAGACCAGGAGUGAGCGAUGUGUACAACAUGCGGUUGCGGUGAAGGCAACCUGUAUAUCGAGGGUGAUGAACAUAACCCUCAUUCCGCGUUU |
GCGAUCAGGAAGACCCUCGCGGAGAACCUGAAAGCACGACAUUGCUCACAUUGCUUCCAGUAUUACUUAGCCAGCCGGGUGCUGGCUUUU |
0.0160688 |
0.9496255 |
hypB |
947194 |
GTP hydrolase involved in nickel liganding into hydrogenases |
b2550 |
-75 |
-66 |
-72 |
-66 |
1.49 |
RyhB |
39 |
49 |
39 |
45 |
1.15 |
-11.07 |
-13.71 |
-1.16398 |
GUGGCAGUGU&ACAUUGCUCAC |
((((((((((&))))))).))) |
GUGGCAGUGUAUUGAACAAUCUGGCAAUGUUUUCGCGGAAUAAUCACGCAAUUAACUAAACAAGGUUUAGUGAAGAUGAGAGCCUGCAUUAAUAAUCAACAGAUUCGCCACCAUAACAAAUGCGUGAUUCUGGAACUGCUGUACCGGCAA |
GCGAUCAGGAAGACCCUCGCGGAGAACCUGAAAGCACGACAUUGCUCACAUUGCUUCCAGUAUUACUUAGCCAGCCGGGUGCUGGCUUUU |
0.0270016 |
0.9496255 |
yphH |
947023 |
putative DNA-binding transcriptional regulator |
b3645 |
-7 |
3 |
-7 |
-1 |
3.42 |
RyhB |
40 |
49 |
43 |
49 |
1.15 |
-11.31 |
-15.88 |
-1.18922 |
GUGGGCAAUG&CAUUGCUCAC |
((((((((((&)))))))))) |
UGAGAUACUCACAACUGUAUAUAAAUACAGUUACAGAUUUACUUUCUUUGCAAUUGAUAUCACAUGGAGUGGGCAAUGAACGAACAUCAUCAACCUUUUGAAGAGAUAAAACUGAUUAAUGCAAACGGAGCAGAACAAUGGUCAGCAAGA |
GCGAUCAGGAAGACCCUCGCGGAGAACCUGAAAGCACGACAUUGCUCACAUUGCUUCCAGUAUUACUUAGCCAGCCGGGUGCUGGCUUUU |
0.0238147 |
0.9496255 |
dinD |
948153 |
DNA damage-inducible protein |
b0624 |
35 |
48 |
35 |
41 |
3.25 |
RyhB |
53 |
66 |
60 |
66 |
2.88 |
-11.71 |
-17.84 |
-1.23128 |
GUGGUACGGGAAGC&GCUUCCAGUAUUAC |
(((((((.((((((&)))))).))))))) |
GUCGUAAAAUUCGCCAACGACGAUUAUUCGGCGUUACACUUAUCACUCAUACAAAUCAAAUAGCAGGAUUUUGCAGUGUUACAACUUCUUUUAGCAGUUUUUAUUGGCGGUGGUACGGGAAGCGUGGCGAGAUGGCUGUUAAGUAUGCGA |
GCGAUCAGGAAGACCCUCGCGGAGAACCUGAAAGCACGACAUUGCUCACAUUGCUUCCAGUAUUACUUAGCCAGCCGGGUGCUGGCUUUU |
0.0192746 |
0.9496255 |
flc |
945798 |
fluoride efflux channel dual topology membrane protein |
b4516 |
-39 |
-2 |
-9 |
-3 |
8.43 |
RyhB |
21 |
62 |
22 |
28 |
7.99 |
-11.31 |
-27.73 |
-1.18922 |
UACUGAUUUAGUGUAUGAUGGUGUUUUUGAGGUUCUCC&GGAGAACCUGAAAGCACGACAUUGCUCACAUUGCUUCCAGUA |
(((((....((((((((...(((((((..(((((((((&))))))))).)))))))..))).....))))).....))))) |
UUCAUCGCAUGGACAAUACGGGUGAUGCUGCCAACUUACUGAUUUAGUGUAUGAUGGUGUUUUUGAGGUUCUCCAGUGGCUUCUGUUUCUAUCAGCUGUCCCUCCUGUUCAGCUACUGACGGGGUGGUGCGUAACGGCAAAAGCACUGCC |
GCGAUCAGGAAGACCCUCGCGGAGAACCUGAAAGCACGACAUUGCUCACAUUGCUUCCAGUAUUACUUAGCCAGCCGGGUGCUGGCUUUU |
0.0238147 |
0.9496255 |
insA |
1450250 |
IS1 repressor TnpA |
b2819 |
20 |
33 |
23 |
29 |
4.07 |
RyhB |
47 |
62 |
53 |
59 |
3.09 |
-12.43 |
-19.59 |
-1.30698 |
UACUGGAAGCUGUG&CACAUUGCUUCCAGUA |
((((((((((((((&))))..)))))))))) |
CACAACCCGACCCAACGCCGGGUUGAUUGCCCUGAUGGAUGAGAUGUUUGCCGGUAUGACCCUGGAGGAGGCGUAAUGAAAUUGCAAAAGCAAUUACUGGAAGCUGUGGAGCACAAACAGCUACGCCCGCUGGAUGUGCAAUUUGCCCUG |
GCGAUCAGGAAGACCCUCGCGGAGAACCUGAAAGCACGACAUUGCUCACAUUGCUUCCAGUAUUACUUAGCCAGCCGGGUGCUGGCUUUU |
0.0130826 |
0.9496255 |
recD |
947287 |
exonuclease V (RecBCD complex) alpha chain |
b0894 |
-38 |
-18 |
-24 |
-18 |
3.25 |
RyhB |
43 |
62 |
43 |
49 |
3.3 |
-19.93 |
-26.48 |
-2.09559 |
UACUGGAAUCAAUCGUGAGCA&UGCUCACAUUGCUUCCAGUA |
((((((((.((((.(((((((&))))))))))).)))))))) |
CGAACUGCUAUAGAAAUAAUUACACAAUACGGUUUGUUACUGGAAUCAAUCGUGAGCAAGCUUGAGUGAGCCAUUAUGAAAACGAAAAUCCCUGAUGCGGUAUUGGCUGCUGAGGUGAGUCGCCGUGGUUUGGUAAAAACGACAGCGAUC |
GCGAUCAGGAAGACCCUCGCGGAGAACCUGAAAGCACGACAUUGCUCACAUUGCUUCCAGUAUUACUUAGCCAGCCGGGUGCUGGCUUUU |
0.0001337 |
0.1837117 |
dmsA |
945508 |
dimethyl sulfoxide reductase anaerobic subunit A |
b2789 |
55 |
75 |
55 |
61 |
3.43 |
RyhB |
37 |
62 |
56 |
62 |
3.3 |
-13.26 |
-19.99 |
-1.39426 |
UACUGGAUAGUGGUGAUGUUG&CGACAUUGCUCACAUUGCUUCCAGUA |
(((((((..((((((((((((&))))))))).)))......))))))) |
ACGUCACCUCUGAUUUCCUGGCGAUGUCGCAGUCCAGAGUGAGCGUGGCUAACGCGAAUUUUCAGGAGUGCAACAAUGAGUUCUUUAAGUCAGGCUGCGAGCAGUGUGGAAAAACGCACAAAUGCUCGUUACUGGAUAGUGGUGAUGUUG |
GCGAUCAGGAAGACCCUCGCGGAGAACCUGAAAGCACGACAUUGCUCACAUUGCUUCCAGUAUUACUUAGCCAGCCGGGUGCUGGCUUUU |
0.0082802 |
0.9291058 |
gudP |
947265 |
putative D-glucarate transporter |