node1 | node2 | node1 accession | node2 accession | node1 annotation | node2 annotation | score |
SCM57690.1 | SCM57692.1 | ING2E5A_1463 | ING2E5A_1464 | Putative protein {ECO:0000313|EMBL:CEA16360,1}; tr|A0A098C0E9|A0A098C0E9_9PORP;evalue=2e-097; PctID=77.63; score=361. | UPF0145 protein; sp|Q5LIM4|Y226_BACFN, sp|Q64ZQ7|Y270_BACFR;evalue=4e-040; PctID=74.53; score=162; Belongs to the UPF0145 family. | 0.487 |
SCM57690.1 | nfo | ING2E5A_1463 | ING2E5A_1466 | Putative protein {ECO:0000313|EMBL:CEA16360,1}; tr|A0A098C0E9|A0A098C0E9_9PORP;evalue=2e-097; PctID=77.63; score=361. | Putative endonuclease 4 {ECO:0000255|HAMAP-Rule:MF_00152}; Endonuclease IV plays a role in DNA repair. It cleaves phosphodiester bonds at apurinic or apyrimidinic sites (AP sites) to produce new 5'-ends that are base-free deoxyribose 5-phosphate residues. It preferentially attacks modified AP sites created by bleomycin and neocarzinostatin. | 0.431 |
SCM57692.1 | SCM57690.1 | ING2E5A_1464 | ING2E5A_1463 | UPF0145 protein; sp|Q5LIM4|Y226_BACFN, sp|Q64ZQ7|Y270_BACFR;evalue=4e-040; PctID=74.53; score=162; Belongs to the UPF0145 family. | Putative protein {ECO:0000313|EMBL:CEA16360,1}; tr|A0A098C0E9|A0A098C0E9_9PORP;evalue=2e-097; PctID=77.63; score=361. | 0.487 |
SCM57692.1 | SCM57694.1 | ING2E5A_1464 | ING2E5A_1465 | UPF0145 protein; sp|Q5LIM4|Y226_BACFN, sp|Q64ZQ7|Y270_BACFR;evalue=4e-040; PctID=74.53; score=162; Belongs to the UPF0145 family. | Hypothetical protein. | 0.570 |
SCM57692.1 | nfo | ING2E5A_1464 | ING2E5A_1466 | UPF0145 protein; sp|Q5LIM4|Y226_BACFN, sp|Q64ZQ7|Y270_BACFR;evalue=4e-040; PctID=74.53; score=162; Belongs to the UPF0145 family. | Putative endonuclease 4 {ECO:0000255|HAMAP-Rule:MF_00152}; Endonuclease IV plays a role in DNA repair. It cleaves phosphodiester bonds at apurinic or apyrimidinic sites (AP sites) to produce new 5'-ends that are base-free deoxyribose 5-phosphate residues. It preferentially attacks modified AP sites created by bleomycin and neocarzinostatin. | 0.570 |
SCM57692.1 | nhaD3 | ING2E5A_1464 | ING2E5A_1467 | UPF0145 protein; sp|Q5LIM4|Y226_BACFN, sp|Q64ZQ7|Y270_BACFR;evalue=4e-040; PctID=74.53; score=162; Belongs to the UPF0145 family. | Na(+)/H(+) antiporter that extrudes sodium in exchange for external protons. Can also transport lithium. pH dependence: Optimum pH is 8.0. Totally inactive at pH 9.0; Multi-pass membrane protein family; sp|A5F120|NHAD_VIBC3;evalue=1e-007; PctID=40.86; score=58.5. | 0.545 |
SCM57694.1 | SCM57692.1 | ING2E5A_1465 | ING2E5A_1464 | Hypothetical protein. | UPF0145 protein; sp|Q5LIM4|Y226_BACFN, sp|Q64ZQ7|Y270_BACFR;evalue=4e-040; PctID=74.53; score=162; Belongs to the UPF0145 family. | 0.570 |
SCM57694.1 | nfo | ING2E5A_1465 | ING2E5A_1466 | Hypothetical protein. | Putative endonuclease 4 {ECO:0000255|HAMAP-Rule:MF_00152}; Endonuclease IV plays a role in DNA repair. It cleaves phosphodiester bonds at apurinic or apyrimidinic sites (AP sites) to produce new 5'-ends that are base-free deoxyribose 5-phosphate residues. It preferentially attacks modified AP sites created by bleomycin and neocarzinostatin. | 0.773 |
SCM57694.1 | nhaD3 | ING2E5A_1465 | ING2E5A_1467 | Hypothetical protein. | Na(+)/H(+) antiporter that extrudes sodium in exchange for external protons. Can also transport lithium. pH dependence: Optimum pH is 8.0. Totally inactive at pH 9.0; Multi-pass membrane protein family; sp|A5F120|NHAD_VIBC3;evalue=1e-007; PctID=40.86; score=58.5. | 0.737 |
SCM59316.1 | nfo | ING2E5A_2520 | ING2E5A_1466 | Putative protein {ECO:0000313|EMBL:CEA14912,1}; tr|A0A098BXP1|A0A098BXP1_9PORP;evalue=1e-094; PctID=67.47; score=352. | Putative endonuclease 4 {ECO:0000255|HAMAP-Rule:MF_00152}; Endonuclease IV plays a role in DNA repair. It cleaves phosphodiester bonds at apurinic or apyrimidinic sites (AP sites) to produce new 5'-ends that are base-free deoxyribose 5-phosphate residues. It preferentially attacks modified AP sites created by bleomycin and neocarzinostatin. | 0.599 |
SCM59316.1 | polA | ING2E5A_2520 | ING2E5A_0260 | Putative protein {ECO:0000313|EMBL:CEA14912,1}; tr|A0A098BXP1|A0A098BXP1_9PORP;evalue=1e-094; PctID=67.47; score=352. | DNA polymerase I; In addition to polymerase activity, this DNA polymerase exhibits 5'-3' exonuclease activity; Belongs to the DNA polymerase type-A family. | 0.573 |
SCM59466.1 | nfo | ING2E5A_2670 | ING2E5A_1466 | Trehalase; Catalyzes the hydrolysis of alpha,alpha-trehalose into two molecules of D-glucose. Does not hydrolyze maltose, isomaltose, sucrose, cellobiose, p-nitrophenyl-alpha-D-glucopyranoside, and methyl-alpha-D-glucopyranoside. Is also inactive on alpha,beta-trehalose, beta,beta-trehalose, alpha,alpha-trehalose-6,6'-dibehenate, trehalulose, nigerose, and trehalose dimycolate. + alpha-D-glucose. Name=Mg(2+); Xref=ChEBI:CHEBI:18420; Evidence=; Name=phosphate; Xref=ChEBI:CHEBI:43474; Evidence=; Note=Shows an absolute requirement for inorganic phosphate and Mg(2+) for activity. The funct [...] | Putative endonuclease 4 {ECO:0000255|HAMAP-Rule:MF_00152}; Endonuclease IV plays a role in DNA repair. It cleaves phosphodiester bonds at apurinic or apyrimidinic sites (AP sites) to produce new 5'-ends that are base-free deoxyribose 5-phosphate residues. It preferentially attacks modified AP sites created by bleomycin and neocarzinostatin. | 0.679 |
hisB | nfo | ING2E5A_1600 | ING2E5A_1466 | Histidine biosynthesis bifunctional protein HisB {ECO:0000255|HAMAP-Rule:MF_01022}; sp|Q7MLS4|HIS7_VIBVY;evalue=2e-101; PctID=51.52; score=369; In the C-terminal section; belongs to the imidazoleglycerol-phosphate dehydratase family. | Putative endonuclease 4 {ECO:0000255|HAMAP-Rule:MF_00152}; Endonuclease IV plays a role in DNA repair. It cleaves phosphodiester bonds at apurinic or apyrimidinic sites (AP sites) to produce new 5'-ends that are base-free deoxyribose 5-phosphate residues. It preferentially attacks modified AP sites created by bleomycin and neocarzinostatin. | 0.491 |
nfo | SCM57690.1 | ING2E5A_1466 | ING2E5A_1463 | Putative endonuclease 4 {ECO:0000255|HAMAP-Rule:MF_00152}; Endonuclease IV plays a role in DNA repair. It cleaves phosphodiester bonds at apurinic or apyrimidinic sites (AP sites) to produce new 5'-ends that are base-free deoxyribose 5-phosphate residues. It preferentially attacks modified AP sites created by bleomycin and neocarzinostatin. | Putative protein {ECO:0000313|EMBL:CEA16360,1}; tr|A0A098C0E9|A0A098C0E9_9PORP;evalue=2e-097; PctID=77.63; score=361. | 0.431 |
nfo | SCM57692.1 | ING2E5A_1466 | ING2E5A_1464 | Putative endonuclease 4 {ECO:0000255|HAMAP-Rule:MF_00152}; Endonuclease IV plays a role in DNA repair. It cleaves phosphodiester bonds at apurinic or apyrimidinic sites (AP sites) to produce new 5'-ends that are base-free deoxyribose 5-phosphate residues. It preferentially attacks modified AP sites created by bleomycin and neocarzinostatin. | UPF0145 protein; sp|Q5LIM4|Y226_BACFN, sp|Q64ZQ7|Y270_BACFR;evalue=4e-040; PctID=74.53; score=162; Belongs to the UPF0145 family. | 0.570 |
nfo | SCM57694.1 | ING2E5A_1466 | ING2E5A_1465 | Putative endonuclease 4 {ECO:0000255|HAMAP-Rule:MF_00152}; Endonuclease IV plays a role in DNA repair. It cleaves phosphodiester bonds at apurinic or apyrimidinic sites (AP sites) to produce new 5'-ends that are base-free deoxyribose 5-phosphate residues. It preferentially attacks modified AP sites created by bleomycin and neocarzinostatin. | Hypothetical protein. | 0.773 |
nfo | SCM59316.1 | ING2E5A_1466 | ING2E5A_2520 | Putative endonuclease 4 {ECO:0000255|HAMAP-Rule:MF_00152}; Endonuclease IV plays a role in DNA repair. It cleaves phosphodiester bonds at apurinic or apyrimidinic sites (AP sites) to produce new 5'-ends that are base-free deoxyribose 5-phosphate residues. It preferentially attacks modified AP sites created by bleomycin and neocarzinostatin. | Putative protein {ECO:0000313|EMBL:CEA14912,1}; tr|A0A098BXP1|A0A098BXP1_9PORP;evalue=1e-094; PctID=67.47; score=352. | 0.599 |
nfo | SCM59466.1 | ING2E5A_1466 | ING2E5A_2670 | Putative endonuclease 4 {ECO:0000255|HAMAP-Rule:MF_00152}; Endonuclease IV plays a role in DNA repair. It cleaves phosphodiester bonds at apurinic or apyrimidinic sites (AP sites) to produce new 5'-ends that are base-free deoxyribose 5-phosphate residues. It preferentially attacks modified AP sites created by bleomycin and neocarzinostatin. | Trehalase; Catalyzes the hydrolysis of alpha,alpha-trehalose into two molecules of D-glucose. Does not hydrolyze maltose, isomaltose, sucrose, cellobiose, p-nitrophenyl-alpha-D-glucopyranoside, and methyl-alpha-D-glucopyranoside. Is also inactive on alpha,beta-trehalose, beta,beta-trehalose, alpha,alpha-trehalose-6,6'-dibehenate, trehalulose, nigerose, and trehalose dimycolate. + alpha-D-glucose. Name=Mg(2+); Xref=ChEBI:CHEBI:18420; Evidence=; Name=phosphate; Xref=ChEBI:CHEBI:43474; Evidence=; Note=Shows an absolute requirement for inorganic phosphate and Mg(2+) for activity. The funct [...] | 0.679 |
nfo | hisB | ING2E5A_1466 | ING2E5A_1600 | Putative endonuclease 4 {ECO:0000255|HAMAP-Rule:MF_00152}; Endonuclease IV plays a role in DNA repair. It cleaves phosphodiester bonds at apurinic or apyrimidinic sites (AP sites) to produce new 5'-ends that are base-free deoxyribose 5-phosphate residues. It preferentially attacks modified AP sites created by bleomycin and neocarzinostatin. | Histidine biosynthesis bifunctional protein HisB {ECO:0000255|HAMAP-Rule:MF_01022}; sp|Q7MLS4|HIS7_VIBVY;evalue=2e-101; PctID=51.52; score=369; In the C-terminal section; belongs to the imidazoleglycerol-phosphate dehydratase family. | 0.491 |
nfo | nhaD3 | ING2E5A_1466 | ING2E5A_1467 | Putative endonuclease 4 {ECO:0000255|HAMAP-Rule:MF_00152}; Endonuclease IV plays a role in DNA repair. It cleaves phosphodiester bonds at apurinic or apyrimidinic sites (AP sites) to produce new 5'-ends that are base-free deoxyribose 5-phosphate residues. It preferentially attacks modified AP sites created by bleomycin and neocarzinostatin. | Na(+)/H(+) antiporter that extrudes sodium in exchange for external protons. Can also transport lithium. pH dependence: Optimum pH is 8.0. Totally inactive at pH 9.0; Multi-pass membrane protein family; sp|A5F120|NHAD_VIBC3;evalue=1e-007; PctID=40.86; score=58.5. | 0.737 |