| NC_009484 |
Acry_0371 |
hypothetical protein |
100 |
|
|
213 aa |
435 |
1e-121 |
Acidiphilium cryptum JF-5 |
Bacteria |
normal |
1 |
n/a |
|
|
|
- |
| NC_011365 |
Gdia_2115 |
hypothetical protein |
65.05 |
|
|
215 aa |
285 |
2.9999999999999996e-76 |
Gluconacetobacter diazotrophicus PAl 5 |
Bacteria |
normal |
1 |
normal |
1 |
|
|
- |
| NC_009484 |
Acry_1264 |
hypothetical protein |
43.9 |
|
|
228 aa |
172 |
2.9999999999999996e-42 |
Acidiphilium cryptum JF-5 |
Bacteria |
normal |
1 |
n/a |
|
|
|
- |
| NC_013422 |
Hneap_2128 |
hypothetical protein |
40 |
|
|
212 aa |
163 |
2.0000000000000002e-39 |
Halothiobacillus neapolitanus c2 |
Bacteria |
normal |
1 |
n/a |
|
|
|
- |
| NC_009719 |
Plav_2309 |
hypothetical protein |
38.83 |
|
|
259 aa |
160 |
2e-38 |
Parvibaculum lavamentivorans DS-1 |
Bacteria |
normal |
0.496757 |
hitchhiker |
0.00288669 |
|
|
- |
| NC_008347 |
Mmar10_1758 |
hypothetical protein |
31.07 |
|
|
227 aa |
126 |
3e-28 |
Maricaulis maris MCS10 |
Bacteria |
normal |
0.348328 |
normal |
0.303504 |
|
|
- |
| NC_011894 |
Mnod_0668 |
Prolyl 4-hydroxylase alpha subunit |
30.95 |
|
|
210 aa |
124 |
2e-27 |
Methylobacterium nodulans ORS 2060 |
Bacteria |
normal |
1 |
n/a |
|
|
|
- |
| NC_010511 |
M446_1851 |
hypothetical protein |
30.48 |
|
|
210 aa |
120 |
9.999999999999999e-27 |
Methylobacterium sp. 4-46 |
Bacteria |
normal |
0.1503 |
normal |
1 |
|
|
- |
| NC_010505 |
Mrad2831_3432 |
hypothetical protein |
29.52 |
|
|
210 aa |
116 |
1.9999999999999998e-25 |
Methylobacterium radiotolerans JCM 2831 |
Bacteria |
normal |
0.30695 |
normal |
0.242236 |
|
|
- |
| NC_009469 |
Acry_3549 |
hypothetical protein |
30.37 |
|
|
229 aa |
95.9 |
4e-19 |
Acidiphilium cryptum JF-5 |
Bacteria |
normal |
1 |
n/a |
|
|
|
- |
| NC_013422 |
Hneap_2131 |
hypothetical protein |
25.32 |
|
|
223 aa |
51.2 |
0.00001 |
Halothiobacillus neapolitanus c2 |
Bacteria |
normal |
1 |
n/a |
|
|
|
- |
| NC_009484 |
Acry_1265 |
hypothetical protein |
25 |
|
|
215 aa |
48.9 |
0.00005 |
Acidiphilium cryptum JF-5 |
Bacteria |
normal |
1 |
n/a |
|
|
|
- |