b2120 |
43 |
58 |
48 |
54 |
10.52 |
RyhB |
71 |
86 |
75 |
81 |
11.6 |
-12.11 |
-34.23 |
-1.27334 |
GCCUGCGCCCGGCUGG&CCAGCCGGGUGCUGGC |
(((.((((((((((((&)))))))))))).))) |
GUGUCGCCACACAUAAAGAAGCUCACUGGCAGGCUUAUUAUCAAGCCCGCCACCGCCUGCCGUGAGGAAAGAUGCAUGAGCGAGCCGUUAAUUGUCGGCAUCCGGCAUCAUAGUCCGGCCUGCGCCCGGCUGGUGAAAUCGUUAAUCGAA |
GCGAUCAGGAAGACCCUCGCGGAGAACCUGAAAGCACGACAUUGCUCACAUUGCUUCCAGUAUUACUUAGCCAGCCGGGUGCUGGCUUUU |
0.0155581 |
0.9496255 |
yehM |
946651 |
uncharacterized protein |
b0968 |
-11 |
6 |
-2 |
5 |
3.42 |
RyhB |
37 |
58 |
38 |
44 |
3.22 |
-13.79 |
-20.43 |
-1.44998 |
GGAGAGCAGCAAUGUCG&CGACAUUGCUCACAUUGCUUCC |
(((.(((((((((((((&)))))))))......))))))) |
GCAAAGAAAUGGGCGUCAUUGUCCGGAGUUUUCCAUGGAUUUGCAACGCGUCCAUUAAGGAUAAGGAGAGCAGCAAUGUCGAAAGUCUGCAUAAUUGCCUGGGUUUACGGGCGAGUUCAGGGCGUAGGAUUUCGCUACACCACACAGUAC |
GCGAUCAGGAAGACCCUCGCGGAGAACCUGAAAGCACGACAUUGCUCACAUUGCUUCCAGUAUUACUUAGCCAGCCGGGUGCUGGCUUUU |
0.0061458 |
0.9291058 |
yccX |
945304 |
weak acylphosphatase |
b3573 |
47 |
75 |
68 |
74 |
7.83 |
RyhB |
37 |
66 |
38 |
44 |
3.3 |
-11.77 |
-22.9 |
-1.23759 |
GUACCUGUGAAGUGGCUUGCGCAGUGUCG&CGACAUUGCUCACAUUGCUUCCAGUAUUAC |
(((.(((.((((.....((.(((((((((&))))))))).)).....)))))))...))) |
ACAUUUCCUUCGUUGGAUCAAAGCAGUAGGGACGCGCUCUCUGGCACUCUGCUGUUUUAGUGCAAAGGAGUGAUCAUGAACCGGUUUAUUAUUGCGGAUGCGACGAAAUGUAUCGGUUGCCGUACCUGUGAAGUGGCUUGCGCAGUGUCG |
GCGAUCAGGAAGACCCUCGCGGAGAACCUGAAAGCACGACAUUGCUCACAUUGCUUCCAGUAUUACUUAGCCAGCCGGGUGCUGGCUUUU |
0.0186683 |
0.9496255 |
ysaA |
948085 |
putative hydrogenase 4Fe-4S ferredoxin-type component |
b4551 |
57 |
73 |
67 |
73 |
3.25 |
RyhB |
39 |
58 |
39 |
45 |
3.21 |
-10.85 |
-17.31 |
-1.14085 |
GGAUUCAAUGGCGAUGU&ACAUUGCUCACAUUGCUUCC |
(((..((((((((((((&)))))))...)))))..))) |
GAGAUUUUCCAGCGUGAAAUGCAACAAGAACGACGCCAGCUGGACGGCUGGGAUGAAUUUGAGUAGAGGGUAAAGAUGGCAAUCCGAAAACGUUUUAUUGCGGGCGCAAAAUGCCCGGCCUGUCAGGCGCAGGAUUCAAUGGCGAUGUGG |
GCGAUCAGGAAGACCCUCGCGGAGAACCUGAAAGCACGACAUUGCUCACAUUGCUUCCAGUAUUACUUAGCCAGCCGGGUGCUGGCUUUU |
0.0302697 |
0.9496255 |
yheV |
1450290 |
DUF2387 family putative metal-binding protein |
b3311 |
-68 |
-41 |
-49 |
-43 |
11.36 |
RyhB |
37 |
60 |
39 |
45 |
3.3 |
-11.34 |
-26 |
-1.19237 |
CUGUUGAAGCAAGUGCGUCGCGAUGUCG&CGACAUUGCUCACAUUGCUUCCAG |
(((..((((((((((....(((((((((&))))))))).))).)))))))))) |
GUCUCACCUGUUGAAGCAAGUGCGUCGCGAUGUCGCACGCGUUAAGACUUUACUGAACGAGAAGGCGGGUGCGUAAUGACCGAUAAAAUCCGUACUCUGCAAGGUCGCGUUGUUAGCGACAAAAUGGAGAAAUCCAUUGUUGUUGCUAUC |
GCGAUCAGGAAGACCCUCGCGGAGAACCUGAAAGCACGACAUUGCUCACAUUGCUUCCAGUAUUACUUAGCCAGCCGGGUGCUGGCUUUU |
0.0234421 |
0.9496255 |
rpsQ |
947808 |
30S ribosomal subunit protein S17 |
b3391 |
-11 |
13 |
5 |
11 |
0.42 |
RyhB |
46 |
68 |
49 |
55 |
3.24 |
-11.42 |
-15.08 |
-1.20079 |
AGGAGAUACAAAUGAAGCAAUGGA&UCACAUUGCUUCCAGUAUUACUU |
(((..((((....(((((((((((&)).)))))))))..))))..))) |
CAGACGUACUAACGCUGGGUACCGGGACAAACUGCGAACCGCCACAAUGGUUGUGGCAACGGCAAGGAGAUACAAAUGAAGCAAUGGAUAGCCGCACUACUGUUGAUGCUGAUACCCGGCGUACAGGCGGCAAAGCCGCAAAAAGUGACG |
GCGAUCAGGAAGACCCUCGCGGAGAACCUGAAAGCACGACAUUGCUCACAUUGCUUCCAGUAUUACUUAGCCAGCCGGGUGCUGGCUUUU |
0.0224751 |
0.9496255 |
hofQ |
947901 |
DNA catabolic putative fimbrial transporter |
b3835 |
-35 |
-4 |
-23 |
-17 |
9.16 |
RyhB |
53 |
86 |
71 |
77 |
14.49 |
-11.36 |
-35.01 |
-1.19448 |
GCCCUGACCAAACGGCUGGAAAAACUGGAGGC&GCUUCCAGUAUUACUUAGCCAGCCGGGUGCUGGC |
(((...(((...(((((((..(((((((((((&))))))))).....))..))))))))))...))) |
GUUUGCGGAAGAGACGGCUGCCGUCGAGCGUGCUGUUGAUGCCCUGACCAAACGGCUGGAAAAACUGGAGGCUAAAUGACGCCAGGUGAAGUACGGCGCCUAUAUUUCAUCAUUCGCACUUUUUUAAGCUACGGACUUGAUGAACUGAUC |
GCGAUCAGGAAGACCCUCGCGGAGAACCUGAAAGCACGACAUUGCUCACAUUGCUUCCAGUAUUACUUAGCCAGCCGGGUGCUGGCUUUU |
0.0231967 |
0.9496255 |
ubiB |
948322 |
regulator of octaprenylphenol hydroxylation ubiquinone synthesis regulator of 2'-N-acetyltransferase putative ABC1 family protein kinase |
b4633 |
-42 |
-17 |
-32 |
-26 |
9.35 |
RyhB |
37 |
66 |
49 |
55 |
3.3 |
-12.21 |
-24.86 |
-1.28385 |
GUAUUUGGGGAGCAAUGGCGAUGACG&CGACAUUGCUCACAUUGCUUCCAGUAUUAC |
(((....((((((((((((((((.((&)).))))))...)))))))))).....))) |
AAAAUGGACGAGGCACUGGCUGAAAUUGGUUUUGUAUUUGGGGAGCAAUGGCGAUGACGCAUCCUCACGAUAAUAUCCGGGUACCUCACAACACGGCAAGCCUGCAUUGCGGCGCUUCAGUCUCCGCUGCAUACUGUCCAGGUGAGCGCG |
GCGAUCAGGAAGACCCUCGCGGAGAACCUGAAAGCACGACAUUGCUCACAUUGCUUCCAGUAUUACUUAGCCAGCCGGGUGCUGGCUUUU |
0.0147406 |
0.9496255 |
xisD |
5625559 |
pseudogene exisionase in defective prophage DLP12Phage or Prophage Related |
b1279 |
-12 |
4 |
-9 |
-3 |
7.4 |
RyhB |
46 |
61 |
52 |
58 |
3.24 |
-10.81 |
-21.45 |
-1.13665 |
ACGGGAAGUAAUGUGA&UCACAUUGCUUCCAGU |
((.(((((((((((((&))))))))))))).)) |
AAAAUGGUACUUUAAAGGGCUAUUGCGGUAAGUUGACCAUAAUUUAUUCGCUCUAACCACAUAACGGGAAGUAAUGUGAAAUAUUUACUCAUUUUCUUACUGGUGUUAGCGAUCUUCGUGAUUUCGGUCACGUUGGGUGCGCAGAACGAU |
GCGAUCAGGAAGACCCUCGCGGAGAACCUGAAAGCACGACAUUGCUCACAUUGCUUCCAGUAUUACUUAGCCAGCCGGGUGCUGGCUUUU |
0.0309022 |
0.9496255 |
yciS |
944936 |
DUF1049 family inner membrane protein function unknown |
b1189 |
10 |
30 |
13 |
19 |
8.06 |
RyhB |
47 |
66 |
57 |
63 |
3.09 |
-11.54 |
-22.69 |
-1.2134 |
GUCAUACUGGGAAGUGGUGUG&CACAUUGCUUCCAGUAUUAC |
((.(((((((.((((((((((&))))))))))))))))).)) |
AAUAUUUUCAACUGAGUUAUCAAGAUGUGAUUAGAUUAUUAUUCUUUUACUGUAUCUACCGUUAUCGGAGUGGCUAUGCGAGUUGUCAUACUGGGAAGUGGUGUGGUAGGCGUUGCCAGCGCCUGGUACUUAAAUCAGGCAGGACAUGAG |
GCGAUCAGGAAGACCCUCGCGGAGAACCUGAAAGCACGACAUUGCUCACAUUGCUUCCAGUAUUACUUAGCCAGCCGGGUGCUGGCUUUU |
0.0210945 |
0.9496255 |
dadA |
945752 |
D-amino acid dehydrogenase |