In order to generate a more inclusive dataset of Pseudomonas genes mapped to putative in-paralogs and putative orthologs in other Pseudomonas species/strains, we developed a Pseudomonas Orthologous Groups classification system.
To generate ortholog groups, pair-wise DIAMOND searches were run on all genomes in the database to find reciprocal best hits (RBHs) for each gene. These analyses often resulted in multiple candidate genes for RBH status, which were narrowed down by examining the similarity between the query's flanking genes and the hit's flanking genes. If two candidate genes were directly adjacent, they where both accepted as RBHs that involve putative in-parology.
Pairwise intra-genome DIAMOND searches were also performed to acquire in-paralog information (i.e. gene duplications occurring after species divergence). If two genes in one genome were reciprocally more similar to each other than to any gene in the other genomes, the two genes were designated putative in-paralogs. Ortholog groups are built by starting with a seed gene and then adding all genes to which there is a RBH or in-paralog relationship.
Every new gene added to an ortholog group was then treated as a seed gene and the addition process was repeated until all qualifying genes had been added. The result was the development of orthologous groups, specifically generated for Pseudomonas species genomes, which can be used to sort search results.
Strain | Locus Tag | Description | Same-Strain Members | Fragment ? | |
---|---|---|---|---|---|
Pseudomonas aeruginosa AZPAE14443 | NQ69_RS25910 |
dihydroorotase
|
2 same-strain members: NQ69_RS17515 NQ69_RS25910 |
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Pseudomonas aeruginosa AZPAE14453 | NQ70_RS16150 |
phenylhydantoinase
|
2 same-strain members: NQ70_RS16150 NQ70_RS23720 |
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|
Pseudomonas aeruginosa AZPAE14453 | NQ70_RS23720 |
dihydroorotase
|
2 same-strain members: NQ70_RS16150 NQ70_RS23720 |
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|
Pseudomonas aeruginosa AZPAE14509 | NQ74_RS02205 |
dihydroorotase
|
2 same-strain members: NQ74_RS10390 NQ74_RS02205 |
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Pseudomonas aeruginosa AZPAE14509 | NQ74_RS10390 |
phenylhydantoinase
|
2 same-strain members: NQ74_RS10390 NQ74_RS02205 |
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Pseudomonas aeruginosa AZPAE14526 | NQ75_RS20800 |
phenylhydantoinase
|
2 same-strain members: NQ75_RS20800 NQ75_RS25260 |
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Pseudomonas aeruginosa AZPAE14526 | NQ75_RS25260 |
dihydroorotase
|
2 same-strain members: NQ75_RS20800 NQ75_RS25260 |
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|
Pseudomonas aeruginosa AZPAE14538 | NQ78_RS22550 |
dihydroorotase
|
2 same-strain members: NQ78_RS22550 NQ78_RS14230 |
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Pseudomonas aeruginosa AZPAE14538 | NQ78_RS14230 |
phenylhydantoinase
|
2 same-strain members: NQ78_RS22550 NQ78_RS14230 |
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Pseudomonas aeruginosa AZPAE14550 | NQ79_RS21055 |
dihydroorotase
|
2 same-strain members: NQ79_RS21055 NQ79_RS25780 |
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Pseudomonas aeruginosa AZPAE14550 | NQ79_RS25780 |
phenylhydantoinase
|
2 same-strain members: NQ79_RS21055 NQ79_RS25780 |
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|
Pseudomonas aeruginosa AZPAE14557 | NQ81_RS10935 |
phenylhydantoinase
|
2 same-strain members: NQ81_RS10935 NQ81_RS00785 |
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Pseudomonas aeruginosa AZPAE14557 | NQ81_RS00785 |
dihydroorotase
|
2 same-strain members: NQ81_RS10935 NQ81_RS00785 |
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Pseudomonas aeruginosa AZPAE14693 | NQ90_RS06670 |
dihydroorotase
|
2 same-strain members: NQ90_RS05905 NQ90_RS06670 |
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Pseudomonas aeruginosa AZPAE14693 | NQ90_RS05905 |
phenylhydantoinase
|
2 same-strain members: NQ90_RS05905 NQ90_RS06670 |
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Pseudomonas aeruginosa AZPAE14809 | NR28_RS02670 |
dihydroorotase
|
2 same-strain members: NR28_RS02670 NR28_RS05005 |
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Pseudomonas aeruginosa AZPAE14809 | NR28_RS05005 |
phenylhydantoinase
|
2 same-strain members: NR28_RS02670 NR28_RS05005 |
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Pseudomonas aeruginosa AZPAE14817 | NR36_RS18370 |
dihydroorotase
|
2 same-strain members: NR36_RS18370 NR36_RS24770 |
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Pseudomonas aeruginosa AZPAE14817 | NR36_RS24770 |
phenylhydantoinase
|
2 same-strain members: NR36_RS18370 NR36_RS24770 |
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Pseudomonas aeruginosa AZPAE14825 | NR43_RS16840 |
phenylhydantoinase
|
2 same-strain members: NR43_RS16840 NR43_RS06140 |
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