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 AZPAE14352 | NQ48_RS15615 |
phenylhydantoinase
|
2 same-strain members: NQ48_RS14355 NQ48_RS15615 |
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Pseudomonas aeruginosa AZPAE14359 | NQ50_RS01155 |
D-hydantoinase/dihydropyrimidinase
|
2 same-strain members: NQ50_RS01155 NQ50_RS09205 |
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|
Pseudomonas aeruginosa AZPAE14359 | NQ50_RS09205 |
dihydroorotase
|
2 same-strain members: NQ50_RS01155 NQ50_RS09205 |
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|
Pseudomonas aeruginosa AZPAE14372 | NQ51_RS22945 |
D-hydantoinase/dihydropyrimidinase
|
2 same-strain members: NQ51_RS22945 NQ51_RS25225 |
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|
Pseudomonas aeruginosa AZPAE14372 | NQ51_RS25225 |
dihydroorotase
|
2 same-strain members: NQ51_RS22945 NQ51_RS25225 |
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|
Pseudomonas aeruginosa AZPAE14373 | NQ52_RS09510 |
dihydroorotase
|
2 same-strain members: NQ52_RS16945 NQ52_RS09510 |
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|
Pseudomonas aeruginosa AZPAE14373 | NQ52_RS16945 |
phenylhydantoinase
|
2 same-strain members: NQ52_RS16945 NQ52_RS09510 |
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|
Pseudomonas aeruginosa AZPAE14379 | NQ53_RS15515 |
D-hydantoinase/dihydropyrimidinase
|
2 same-strain members: NQ53_RS15515 NQ53_RS13765 |
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|
Pseudomonas aeruginosa AZPAE14379 | NQ53_RS13765 |
dihydroorotase
|
2 same-strain members: NQ53_RS15515 NQ53_RS13765 |
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|
Pseudomonas aeruginosa AZPAE14395 | NQ58_RS14580 |
phenylhydantoinase
|
2 same-strain members: NQ58_RS02245 NQ58_RS14580 |
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|
Pseudomonas aeruginosa AZPAE14395 | NQ58_RS02245 |
dihydroorotase
|
2 same-strain members: NQ58_RS02245 NQ58_RS14580 |
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|
Pseudomonas aeruginosa AZPAE14402 | NQ60_RS19385 |
dihydroorotase
|
2 same-strain members: NQ60_RS19385 NQ60_RS27490 |
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Pseudomonas aeruginosa AZPAE14402 | NQ60_RS27490 |
phenylhydantoinase
|
2 same-strain members: NQ60_RS19385 NQ60_RS27490 |
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|
Pseudomonas aeruginosa AZPAE14403 | NQ61_RS12760 |
phenylhydantoinase
|
2 same-strain members: NQ61_RS12760 NQ61_RS14675 |
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Pseudomonas aeruginosa AZPAE14403 | NQ61_RS14675 |
dihydroorotase
|
2 same-strain members: NQ61_RS12760 NQ61_RS14675 |
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|
Pseudomonas aeruginosa AZPAE14404 | NQ62_RS06965 |
dihydroorotase
|
2 same-strain members: NQ62_RS06965 NQ62_RS09355 |
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Pseudomonas aeruginosa AZPAE14404 | NQ62_RS09355 |
phenylhydantoinase
|
2 same-strain members: NQ62_RS06965 NQ62_RS09355 |
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|
Pseudomonas aeruginosa AZPAE14410 | NQ63_RS20715 |
dihydroorotase
|
2 same-strain members: NQ63_RS12740 NQ63_RS20715 |
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Pseudomonas aeruginosa AZPAE14410 | NQ63_RS12740 |
phenylhydantoinase
|
2 same-strain members: NQ63_RS12740 NQ63_RS20715 |
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|
Pseudomonas aeruginosa AZPAE14443 | NQ69_RS17515 |
phenylhydantoinase
|
2 same-strain members: NQ69_RS17515 NQ69_RS25910 |
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