node1 | node2 | node1 accession | node2 accession | node1 annotation | node2 annotation | score |
DR97_2650 | DR97_2652 | DR97_2650 | DR97_2652 | Uncharacterized protein; DUF484 domain-containing protein | Fmn hydrolase / 5-amino-6-(5-phospho-d-ribitylamino)uracil phosphatase; HAD-SF-IA-v1: HAD hydrolase, IA, variant 1 family protein | 0.836 |
DR97_2650 | dapF | DR97_2650 | DR97_2649 | Uncharacterized protein; DUF484 domain-containing protein | Diaminopimelate epimerase; Catalyzes the stereoinversion of LL-2,6-diaminoheptanedioate (L,L-DAP) to meso-diaminoheptanedioate (meso-DAP), a precursor of L- lysine and an essential component of the bacterial peptidoglycan | 0.859 |
DR97_2650 | xerC | DR97_2650 | DR97_2651 | Uncharacterized protein; DUF484 domain-containing protein | Site-specific tyrosine recombinase, which acts by catalyzing the cutting and rejoining of the recombining DNA molecules. The XerC- XerD complex is essential to convert dimers of the bacterial chromosome into monomers to permit their segregation at cell division. It also contributes to the segregational stability of plasmids (By similarity) | 0.868 |
DR97_2652 | DR97_2650 | DR97_2652 | DR97_2650 | Fmn hydrolase / 5-amino-6-(5-phospho-d-ribitylamino)uracil phosphatase; HAD-SF-IA-v1: HAD hydrolase, IA, variant 1 family protein | Uncharacterized protein; DUF484 domain-containing protein | 0.836 |
DR97_2652 | dapF | DR97_2652 | DR97_2649 | Fmn hydrolase / 5-amino-6-(5-phospho-d-ribitylamino)uracil phosphatase; HAD-SF-IA-v1: HAD hydrolase, IA, variant 1 family protein | Diaminopimelate epimerase; Catalyzes the stereoinversion of LL-2,6-diaminoheptanedioate (L,L-DAP) to meso-diaminoheptanedioate (meso-DAP), a precursor of L- lysine and an essential component of the bacterial peptidoglycan | 0.794 |
DR97_2652 | xerC | DR97_2652 | DR97_2651 | Fmn hydrolase / 5-amino-6-(5-phospho-d-ribitylamino)uracil phosphatase; HAD-SF-IA-v1: HAD hydrolase, IA, variant 1 family protein | Site-specific tyrosine recombinase, which acts by catalyzing the cutting and rejoining of the recombining DNA molecules. The XerC- XerD complex is essential to convert dimers of the bacterial chromosome into monomers to permit their segregation at cell division. It also contributes to the segregational stability of plasmids (By similarity) | 0.930 |
DR97_311 | DR97_4687 | DR97_311 | DR97_4687 | annotation not available | annotation not available | 0.854 |
DR97_311 | xerC | DR97_311 | DR97_2651 | annotation not available | Site-specific tyrosine recombinase, which acts by catalyzing the cutting and rejoining of the recombining DNA molecules. The XerC- XerD complex is essential to convert dimers of the bacterial chromosome into monomers to permit their segregation at cell division. It also contributes to the segregational stability of plasmids (By similarity) | 0.851 |
DR97_311 | xerD | DR97_311 | DR97_4138 | annotation not available | Site-specific tyrosine recombinase, which acts by catalyzing the cutting and rejoining of the recombining DNA molecules. The XerC- XerD complex is essential to convert dimers of the bacterial chromosome into monomers to permit their segregation at cell division. It also contributes to the segregational stability of plasmids | 0.850 |
DR97_4687 | DR97_311 | DR97_4687 | DR97_311 | annotation not available | annotation not available | 0.854 |
DR97_4687 | xerC | DR97_4687 | DR97_2651 | annotation not available | Site-specific tyrosine recombinase, which acts by catalyzing the cutting and rejoining of the recombining DNA molecules. The XerC- XerD complex is essential to convert dimers of the bacterial chromosome into monomers to permit their segregation at cell division. It also contributes to the segregational stability of plasmids (By similarity) | 0.852 |
DR97_4687 | xerD | DR97_4687 | DR97_4138 | annotation not available | Site-specific tyrosine recombinase, which acts by catalyzing the cutting and rejoining of the recombining DNA molecules. The XerC- XerD complex is essential to convert dimers of the bacterial chromosome into monomers to permit their segregation at cell division. It also contributes to the segregational stability of plasmids | 0.858 |
dapF | DR97_2650 | DR97_2649 | DR97_2650 | Diaminopimelate epimerase; Catalyzes the stereoinversion of LL-2,6-diaminoheptanedioate (L,L-DAP) to meso-diaminoheptanedioate (meso-DAP), a precursor of L- lysine and an essential component of the bacterial peptidoglycan | Uncharacterized protein; DUF484 domain-containing protein | 0.859 |
dapF | DR97_2652 | DR97_2649 | DR97_2652 | Diaminopimelate epimerase; Catalyzes the stereoinversion of LL-2,6-diaminoheptanedioate (L,L-DAP) to meso-diaminoheptanedioate (meso-DAP), a precursor of L- lysine and an essential component of the bacterial peptidoglycan | Fmn hydrolase / 5-amino-6-(5-phospho-d-ribitylamino)uracil phosphatase; HAD-SF-IA-v1: HAD hydrolase, IA, variant 1 family protein | 0.794 |
dapF | xerC | DR97_2649 | DR97_2651 | Diaminopimelate epimerase; Catalyzes the stereoinversion of LL-2,6-diaminoheptanedioate (L,L-DAP) to meso-diaminoheptanedioate (meso-DAP), a precursor of L- lysine and an essential component of the bacterial peptidoglycan | Site-specific tyrosine recombinase, which acts by catalyzing the cutting and rejoining of the recombining DNA molecules. The XerC- XerD complex is essential to convert dimers of the bacterial chromosome into monomers to permit their segregation at cell division. It also contributes to the segregational stability of plasmids (By similarity) | 0.947 |
ftsK | ruvA | DR97_5347 | DR97_971 | Dna segregation atpase ftsk/spoiiie, s-dna-t family; Essential cell division protein that coordinates cell division and chromosome segregation. The N-terminus is involved in assembly of the cell-division machinery. The C-terminus functions as a DNA motor that moves dsDNA in an ATP-dependent manner towards the dif recombination site, which is located within the replication terminus region. Translocation stops specifically at Xer-dif sites, where FtsK interacts with the Xer recombinase, allowing activation of chromosome unlinking by recombination. FtsK orienting polar sequences (KOPS) gu [...] | Holliday junction dna helicase motor protein; The RuvA-RuvB complex in the presence of ATP renatures cruciform structure in supercoiled DNA with palindromic sequence, indicating that it may promote strand exchange reactions in homologous recombination. RuvAB is a helicase that mediates the Holliday junction migration by localized denaturation and reannealing. RuvA stimulates, in the presence of DNA, the weak ATPase activity of RuvB | 0.727 |
ftsK | ruvB | DR97_5347 | DR97_970 | Dna segregation atpase ftsk/spoiiie, s-dna-t family; Essential cell division protein that coordinates cell division and chromosome segregation. The N-terminus is involved in assembly of the cell-division machinery. The C-terminus functions as a DNA motor that moves dsDNA in an ATP-dependent manner towards the dif recombination site, which is located within the replication terminus region. Translocation stops specifically at Xer-dif sites, where FtsK interacts with the Xer recombinase, allowing activation of chromosome unlinking by recombination. FtsK orienting polar sequences (KOPS) gu [...] | The RuvA-RuvB complex in the presence of ATP renatures cruciform structure in supercoiled DNA with palindromic sequence, indicating that it may promote strand exchange reactions in homologous recombination. RuvAB is a helicase that mediates the Holliday junction migration by localized denaturation and reannealing | 0.594 |
ftsK | xerC | DR97_5347 | DR97_2651 | Dna segregation atpase ftsk/spoiiie, s-dna-t family; Essential cell division protein that coordinates cell division and chromosome segregation. The N-terminus is involved in assembly of the cell-division machinery. The C-terminus functions as a DNA motor that moves dsDNA in an ATP-dependent manner towards the dif recombination site, which is located within the replication terminus region. Translocation stops specifically at Xer-dif sites, where FtsK interacts with the Xer recombinase, allowing activation of chromosome unlinking by recombination. FtsK orienting polar sequences (KOPS) gu [...] | Site-specific tyrosine recombinase, which acts by catalyzing the cutting and rejoining of the recombining DNA molecules. The XerC- XerD complex is essential to convert dimers of the bacterial chromosome into monomers to permit their segregation at cell division. It also contributes to the segregational stability of plasmids (By similarity) | 0.956 |
ftsK | xerD | DR97_5347 | DR97_4138 | Dna segregation atpase ftsk/spoiiie, s-dna-t family; Essential cell division protein that coordinates cell division and chromosome segregation. The N-terminus is involved in assembly of the cell-division machinery. The C-terminus functions as a DNA motor that moves dsDNA in an ATP-dependent manner towards the dif recombination site, which is located within the replication terminus region. Translocation stops specifically at Xer-dif sites, where FtsK interacts with the Xer recombinase, allowing activation of chromosome unlinking by recombination. FtsK orienting polar sequences (KOPS) gu [...] | Site-specific tyrosine recombinase, which acts by catalyzing the cutting and rejoining of the recombining DNA molecules. The XerC- XerD complex is essential to convert dimers of the bacterial chromosome into monomers to permit their segregation at cell division. It also contributes to the segregational stability of plasmids | 0.968 |
ruvA | ftsK | DR97_971 | DR97_5347 | Holliday junction dna helicase motor protein; The RuvA-RuvB complex in the presence of ATP renatures cruciform structure in supercoiled DNA with palindromic sequence, indicating that it may promote strand exchange reactions in homologous recombination. RuvAB is a helicase that mediates the Holliday junction migration by localized denaturation and reannealing. RuvA stimulates, in the presence of DNA, the weak ATPase activity of RuvB | Dna segregation atpase ftsk/spoiiie, s-dna-t family; Essential cell division protein that coordinates cell division and chromosome segregation. The N-terminus is involved in assembly of the cell-division machinery. The C-terminus functions as a DNA motor that moves dsDNA in an ATP-dependent manner towards the dif recombination site, which is located within the replication terminus region. Translocation stops specifically at Xer-dif sites, where FtsK interacts with the Xer recombinase, allowing activation of chromosome unlinking by recombination. FtsK orienting polar sequences (KOPS) gu [...] | 0.727 |