Gene Id | COG Id | Definition | Comment |
PG0229 | K | N utilization substance protein A (NusA) (transcription termination-antitermination factor) (transcriptional terminator) | |
PG0230 | J | translation initiation factor IF-2 | |
PG0232 | R | ABC transporter subunit | PG0234 does not exist. |
PG0233 | R | ABC transporter ATPase | |
PG0235 | R | conserved hypothetical protein (possible ABC transporter related membrane protein) | |
PG0288 | J | 50S ribosomal protein L21 | |
PG0289 | J | 50S ribosomal protein L27 | |
PG0342 | J | 50S ribosomal protein L13 | |
PG0343 | J | 30S ribosomal protein S9 | |
PG0344 | J | 30S ribosomal protein S2 | |
PG0345 | J | elongation factor TS (EF-TS) | |
PG0353 | "J,E" | elongation factor Tu | |
PG0354 | N | hypothetical protein(possible translocase secE subunit) | |
PG0355 | K | transcription antiterminator | |
PG0356 | J | 50S ribosomal protein L11 | |
PG0357 | J | 50S ribosomal protein L1 | |
PG0358 | J | 50S ribosomal protein L10 | |
PG0359 | J | 50S ribosomal protein L7/L12 | |
PG0360 | K | DNA-directed RNA polymerase subunit beta | |
PG0361 | K | DNA-directed RNA polymerase subunit beta' | |
PG0382 | O | ATP-dependent ClpX-related protease | PG0383 does not exist. |
PG0384 | O | ATP-dependent clp protease proteolytic subunit (endopeptidase CLP) | |
PG0474 | O | 60 kD chaperonin (protein cpn60) (GroEL protein) (heat shock protein 60) | |
PG0475 | O | 10 kDa chaperonin/heat shock protein (protein cpn10) (protein GroES) | |
PG0482 | E F | carbamoyl-phosphate synthase small subunit | PG 0483 does not exist. |
PG0484 | E F | glutamine-hydrolyzing carbamoyl-phosphate synthase (CPSase) | |
PG0519 | M | phospho-N-acetylmuramoyl pentapeptide transferase | |
PG0520 | M | N-acetylymuramoyl-L-alanine-D-glutamate ligase | |
PG0522 | M | GLCNAC transferase (UDP-N-acetylglucosamine-N-acetylmuramyl-(pentapeptide)-pyrophosphoryl-undecaprenol Nacetylglucosamine transferase) | |
PG0523 | M | UDP-N-acetylmuramate--alanine ligase | |
PG0525 | D | cell division protein ftsA | |
PG0526 | D | cell division protein ftsZ | |
PG0537 | J | 30S ribosomal protein S6 | PG0539 does not exist. |
PG0538 | J | 30S ribsomal protein S18 | |
PG0540 | J | 50S ribosomal protein L9 | |
PG0802 | C | cytochrome d oxidase subunit II | |
PG0803 | C | cytochrome d oxidase subunit I | |
PG0886 | J | 50S ribosomal protein L20 | |
PG0887 | J | translation initiation factor 3 (IF-3) | |
PG0888 | J | threonyl-tRNA synthetase | |
PG0959 | C | electron transfer flavoprotein beta-subunit | |
PG0960 | C | electron-transfer flavoprotein alpha-subunit | |
PG1044 | C | conserved hypothetical protein | |
PG1045 | C | conserved hypothetical protein (containing ferredoxin-like domain) | |
PG1168 | C | NAD(P)+ transhydrogenase subunit alpha | |
PG1169 | C | probable NAD(P) transhydrogenase subunit alpha (pyridine nucleotide transhydrogenase subunit alpha) (nicotinamide nucleotide transhydrogenase subunit alpha) | |
PG1170 | C | NAD(P) transhydrogenase subunit beta | |
PG1223 | D | rod shape-determining protein | |
PG1224 | M | penicillin binding protein 2 | |
PG1367 | M | dTDP-4-dehydrorhamnose 3,5-epimerase rfbD | |
PG1368 | M | glucose-1-phosphate thymidyltransferase rfbA | |
PG1532 | P | ABC transporter (SBP domain); adhesin | |
PG1533 | P | ABC transporter/NBD protein for possibly Zn/Mn | |
PG1575 | C | ATP synthase subunit A (V-type ATPase subunit A) | |
PG1576 | C | ATP synthase subunit B (V-type ATPase subunit B) | |
PG1577 | C | H+-transporting ATP synthase subunit D | |
PG1578 | C | vacuolar ATPase subunit I | |
PG1579 | C | putative H+-transporting ATP synthase subunit K | |
PG1657 | J | ribosome recycling factor (ribosome releasing factor) | |
PG1658 | F | uridylate kinase (uridine monophosphate kinase) (UMP kinase) | |
PG1666 | J | 50S ribosomal protein L17 | |
PG1667 | K | RNA polymerase alpha subunit (DNA-directed RNA polymerase alpha subunit) (transcriptase alpha chain) | |
PG1668 | J | 30S ribosomal protein S4 | |
PG1669 | J | 30S ribosomal protein S11 | |
PG1670 | J | 30S ribosomal protein S13 | |
PG1673 | N | preprotein translocase SecY | |
PG1673.1 | J | 50S ribosomal protein L15 | |
PG1674 | J | 30S ribosomal protein S5 | |
PG1675 | J | 50S ribosomal protein L18 | |
PG1676 | J | 50S ribosomal protein L6 | |
PG1677 | J | 30S ribosomal protein S8 | |
PG1678 | J | 30S ribosomal protein S14 | |
PG1679 | J | 50S ribosomal protein L5 | |
PG1680 | J | 50S ribosomal protein L24 | |
PG1681 | J | 50S ribosomal protein L14 | |
PG1682 | J | 30S ribosomal protein S17 | |
PG1683 | J | 50S ribosomal protein L16 | |
PG1684 | J | 30S ribosomal protein S3 | |
PG1685 | J | 50S ribosomal protein L22 | |
PG1686 | J | 30S ribosomal protein S19 | |
PG1687 | J | 50S ribosomal protein L2 | |
PG1688 | J | 50S ribosomal protein L23 | |
PG1689 | J | 50S ribosomal protein L4 | |
PG1690 | J | 50S ribosomal protein L3 | |
PG1691 | J | 30S ribosomal protein S10 | |
PG1692 | J | elongation factor G protein | |
PG1693 | J | 30S ribosomal protein S7 | |
PG1694 | J | 30S ribosomal protein S12 | |
PG1906 | H, C | Na+-translocating NADH-quinone reductase nqr6 | |
PG1907 | C | Na+-translocating NADH-quinone reductase subunit Nqr5 (sodium-translocating NADH dehydrogenase) | |
PG1908 | C | Na+-translocating NADH-quinone reductase subunit Nqr4 (sodium-translocating NADH dehydrogenase) | |
PG1909 | Na+-translocating NADH-quinone reductase gamma subunit (sodium-translocating NADH dehydrogenase subunit nqr3) | ||
PG1910 | S | NADH dehydrogenase (ubiquinone) | |
PG1911 | I | Na+-translocating NADH-ubiquinone oxidoreductase alpha subunit nqrA |
Not only is it useful to find which orthologous clusters are shared between multiple bacteria, but also to determine which orthologous clusters in Porphyromonas gingivalis are shared by bacteria capable of being sexually transmitted (since P. gingivalis is most closely related to this group of sequenced bacteria) but not found in bacteria such as Escherichia coli, Haemophilus ducreyi, or Streptococcus pyogenes. This analysis helps to identify the gene clusters responsible for the pathogens' unique characteristics, e.g. genes unique to mucosal obligate anaerobes. Note that only genes found in clusters are included in this comparison.
It is also useful to determine which genes in Porphyromonas gingivalis are shared by Chlamydia tracomatis, a bacterium capable of being sexually transmitted, but not shared by Escherichia coli. This analysis helps to identify the genes responsible for the pathogens' unique characteristics, e.g. genes unique to mucosal obligate anaerobes.