| node1 | node2 | node1 accession | node2 accession | node1 annotation | node2 annotation | score |
| CAZ94621.1 | CAZ94658.1 | ZOBELLIA_550 | ZOBELLIA_587 | Cytochrome c-containing protein; Protein containing a N-terminal beta-propeller fold domain, three central PBS lyase HEAT-like repeats and a C-terminal cytochrome c domain. Cytochromes c typically function in electron transfer, but c-type cytochrome centers are also found in the active sites of many enzymes. Contains a prokaryotic lipoprotein signal peptide cleaved between the residues 22 and 23; Localized in the outer membrane; Function unclear. | Gluconolactonases hydrolyze the gluconolactone formed by glucose oxidoreductase. The proximity of the galactonate dehydratase gene dgoD suggests that this lactonase would be specific for D-galactono-1,4-lactone instead of gluconolactone; Signal peptide cleaved between the residues 19 and 20; Localized in the periplasm; Specificity unclear. | 0.935 |
| CAZ94621.1 | CAZ95740.1 | ZOBELLIA_550 | ZOBELLIA_1686 | Cytochrome c-containing protein; Protein containing a N-terminal beta-propeller fold domain, three central PBS lyase HEAT-like repeats and a C-terminal cytochrome c domain. Cytochromes c typically function in electron transfer, but c-type cytochrome centers are also found in the active sites of many enzymes. Contains a prokaryotic lipoprotein signal peptide cleaved between the residues 22 and 23; Localized in the outer membrane; Function unclear. | Pyrroloquinoline quinone-dependent dehydrogenase; Dehydrogenase with a N-terminal domain that adopts a beta-propeller fold and binds the pyrroloquinoline quinone (PQQ) as prosthetic group. Contains also a C-type cytochrome domain with a heme group covalently bound by thioether bonds to two conserved cysteine residues; Belongs to the Quinoprotein alcohol dehydrogenase family; Putative lipoprotein signal peptide cleaved between the residues 21 and 22; Possibly localized in the outer membrane; Specificity unclear. | 0.948 |
| CAZ94621.1 | gnlA | ZOBELLIA_550 | ZOBELLIA_2920 | Cytochrome c-containing protein; Protein containing a N-terminal beta-propeller fold domain, three central PBS lyase HEAT-like repeats and a C-terminal cytochrome c domain. Cytochromes c typically function in electron transfer, but c-type cytochrome centers are also found in the active sites of many enzymes. Contains a prokaryotic lipoprotein signal peptide cleaved between the residues 22 and 23; Localized in the outer membrane; Function unclear. | Gluconolactonases hydrolyze the gluconolactone, formed either by the glucose oxidoreductase or by the glucose dehydrogenase in aerobic conditions, to gluconate; Contains a putative lipoprotein signal peptide cleaved between the residues 20 and 21; Possibly localized in the outer membrane; High confidence in function and specificity. | 0.925 |
| CAZ94658.1 | CAZ94621.1 | ZOBELLIA_587 | ZOBELLIA_550 | Gluconolactonases hydrolyze the gluconolactone formed by glucose oxidoreductase. The proximity of the galactonate dehydratase gene dgoD suggests that this lactonase would be specific for D-galactono-1,4-lactone instead of gluconolactone; Signal peptide cleaved between the residues 19 and 20; Localized in the periplasm; Specificity unclear. | Cytochrome c-containing protein; Protein containing a N-terminal beta-propeller fold domain, three central PBS lyase HEAT-like repeats and a C-terminal cytochrome c domain. Cytochromes c typically function in electron transfer, but c-type cytochrome centers are also found in the active sites of many enzymes. Contains a prokaryotic lipoprotein signal peptide cleaved between the residues 22 and 23; Localized in the outer membrane; Function unclear. | 0.935 |
| CAZ94658.1 | CAZ95740.1 | ZOBELLIA_587 | ZOBELLIA_1686 | Gluconolactonases hydrolyze the gluconolactone formed by glucose oxidoreductase. The proximity of the galactonate dehydratase gene dgoD suggests that this lactonase would be specific for D-galactono-1,4-lactone instead of gluconolactone; Signal peptide cleaved between the residues 19 and 20; Localized in the periplasm; Specificity unclear. | Pyrroloquinoline quinone-dependent dehydrogenase; Dehydrogenase with a N-terminal domain that adopts a beta-propeller fold and binds the pyrroloquinoline quinone (PQQ) as prosthetic group. Contains also a C-type cytochrome domain with a heme group covalently bound by thioether bonds to two conserved cysteine residues; Belongs to the Quinoprotein alcohol dehydrogenase family; Putative lipoprotein signal peptide cleaved between the residues 21 and 22; Possibly localized in the outer membrane; Specificity unclear. | 0.937 |
| CAZ94658.1 | CAZ96473.1 | ZOBELLIA_587 | ZOBELLIA_2318 | Gluconolactonases hydrolyze the gluconolactone formed by glucose oxidoreductase. The proximity of the galactonate dehydratase gene dgoD suggests that this lactonase would be specific for D-galactono-1,4-lactone instead of gluconolactone; Signal peptide cleaved between the residues 19 and 20; Localized in the periplasm; Specificity unclear. | Fumarylacetoacetate hydrolase (FAH), or fumarylacetoacetase (FAA) is the last enzyme in the tyrosine catabolic pathway, it hydrolyses fumarylacetoacetate into fumarate and acetoacetate which then join the citric acid cycle; Localized in the cytoplasm; High confidence in function and specificity. | 0.651 |
| CAZ94658.1 | gdhA | ZOBELLIA_587 | ZOBELLIA_1102 | Gluconolactonases hydrolyze the gluconolactone formed by glucose oxidoreductase. The proximity of the galactonate dehydratase gene dgoD suggests that this lactonase would be specific for D-galactono-1,4-lactone instead of gluconolactone; Signal peptide cleaved between the residues 19 and 20; Localized in the periplasm; Specificity unclear. | Glucose dehydrogenase catalyses the oxidation of D-glucose without prior phosphorylation to D-beta-gluconolactone using NAD or NADP as a coenzyme; Belongs to the short-chain dehydrogenases/reductases family, Glucose/ribitol dehydrogenase subfamily; Localized in the cytoplasm; High confidence in function and specificity. | 0.902 |
| CAZ94658.1 | gdhB2 | ZOBELLIA_587 | ZOBELLIA_3786 | Gluconolactonases hydrolyze the gluconolactone formed by glucose oxidoreductase. The proximity of the galactonate dehydratase gene dgoD suggests that this lactonase would be specific for D-galactono-1,4-lactone instead of gluconolactone; Signal peptide cleaved between the residues 19 and 20; Localized in the periplasm; Specificity unclear. | Quinoprotein glucose dehydrogenase; The mature protein is a multidomain protein: The first 430 residues would be The signal peptide is cleaved between the residues 26 and 27; Protein probably localized in the outer membrane; Hypothetical protein. | 0.515 |
| CAZ94658.1 | gdhB3 | ZOBELLIA_587 | ZOBELLIA_3726 | Gluconolactonases hydrolyze the gluconolactone formed by glucose oxidoreductase. The proximity of the galactonate dehydratase gene dgoD suggests that this lactonase would be specific for D-galactono-1,4-lactone instead of gluconolactone; Signal peptide cleaved between the residues 19 and 20; Localized in the periplasm; Specificity unclear. | Quinoprotein glucose dehydrogenase; Lipoprotein putatively localized in the outer membrane is a soluble glucose dehydrogenase (s-GDH) that oxidizes glucose to gluconolactone using a quinone as cofactor; Signale peptide cleaved between the residues 18 and 19; Family membership. | 0.535 |
| CAZ94658.1 | gnlA | ZOBELLIA_587 | ZOBELLIA_2920 | Gluconolactonases hydrolyze the gluconolactone formed by glucose oxidoreductase. The proximity of the galactonate dehydratase gene dgoD suggests that this lactonase would be specific for D-galactono-1,4-lactone instead of gluconolactone; Signal peptide cleaved between the residues 19 and 20; Localized in the periplasm; Specificity unclear. | Gluconolactonases hydrolyze the gluconolactone, formed either by the glucose oxidoreductase or by the glucose dehydrogenase in aerobic conditions, to gluconate; Contains a putative lipoprotein signal peptide cleaved between the residues 20 and 21; Possibly localized in the outer membrane; High confidence in function and specificity. | 0.924 |
| CAZ94658.1 | gntK1 | ZOBELLIA_587 | ZOBELLIA_2637 | Gluconolactonases hydrolyze the gluconolactone formed by glucose oxidoreductase. The proximity of the galactonate dehydratase gene dgoD suggests that this lactonase would be specific for D-galactono-1,4-lactone instead of gluconolactone; Signal peptide cleaved between the residues 19 and 20; Localized in the periplasm; Specificity unclear. | Gluconokinase is involved in the gluconate catabolism pathway (Pentose phosphate pathway). It converts the D-gluconate to 6-phospho-D-gluconate; GntK adopts an alpha/beta fold, consisting of a central sheet of five parallel beta-strands flanked by alpha-helices; Belongs to the shikimate kinase family; Localized in the cytoplasm; High confidence in function and specificity. | 0.905 |
| CAZ94658.1 | gntK2 | ZOBELLIA_587 | ZOBELLIA_4757 | Gluconolactonases hydrolyze the gluconolactone formed by glucose oxidoreductase. The proximity of the galactonate dehydratase gene dgoD suggests that this lactonase would be specific for D-galactono-1,4-lactone instead of gluconolactone; Signal peptide cleaved between the residues 19 and 20; Localized in the periplasm; Specificity unclear. | Gluconokinase is involved in the gluconate catabolism pathway (Pentose phosphate pathway). It converts the D-gluconate to 6-phospho-D-gluconate; GntK adopts an alpha/beta fold, consisting of a central sheet of five parallel beta-strands flanked by alpha-helices; Belongs to the shikimate kinase family; Localized in the cytoplasm; High confidence in function and specificity. | 0.905 |
| CAZ94658.1 | gntT1 | ZOBELLIA_587 | ZOBELLIA_588 | Gluconolactonases hydrolyze the gluconolactone formed by glucose oxidoreductase. The proximity of the galactonate dehydratase gene dgoD suggests that this lactonase would be specific for D-galactono-1,4-lactone instead of gluconolactone; Signal peptide cleaved between the residues 19 and 20; Localized in the periplasm; Specificity unclear. | High-affinity gluconate transporter; GntT is part of the gluconate utilization system Gnt-I. It is a permease responsible for high-affinity intake of gluconate; Contains 13 transmembrane helices; Localized in the cytoplasmic membrane; High confidence in function and specificity. | 0.679 |
| CAZ95740.1 | CAZ94621.1 | ZOBELLIA_1686 | ZOBELLIA_550 | Pyrroloquinoline quinone-dependent dehydrogenase; Dehydrogenase with a N-terminal domain that adopts a beta-propeller fold and binds the pyrroloquinoline quinone (PQQ) as prosthetic group. Contains also a C-type cytochrome domain with a heme group covalently bound by thioether bonds to two conserved cysteine residues; Belongs to the Quinoprotein alcohol dehydrogenase family; Putative lipoprotein signal peptide cleaved between the residues 21 and 22; Possibly localized in the outer membrane; Specificity unclear. | Cytochrome c-containing protein; Protein containing a N-terminal beta-propeller fold domain, three central PBS lyase HEAT-like repeats and a C-terminal cytochrome c domain. Cytochromes c typically function in electron transfer, but c-type cytochrome centers are also found in the active sites of many enzymes. Contains a prokaryotic lipoprotein signal peptide cleaved between the residues 22 and 23; Localized in the outer membrane; Function unclear. | 0.948 |
| CAZ95740.1 | CAZ94658.1 | ZOBELLIA_1686 | ZOBELLIA_587 | Pyrroloquinoline quinone-dependent dehydrogenase; Dehydrogenase with a N-terminal domain that adopts a beta-propeller fold and binds the pyrroloquinoline quinone (PQQ) as prosthetic group. Contains also a C-type cytochrome domain with a heme group covalently bound by thioether bonds to two conserved cysteine residues; Belongs to the Quinoprotein alcohol dehydrogenase family; Putative lipoprotein signal peptide cleaved between the residues 21 and 22; Possibly localized in the outer membrane; Specificity unclear. | Gluconolactonases hydrolyze the gluconolactone formed by glucose oxidoreductase. The proximity of the galactonate dehydratase gene dgoD suggests that this lactonase would be specific for D-galactono-1,4-lactone instead of gluconolactone; Signal peptide cleaved between the residues 19 and 20; Localized in the periplasm; Specificity unclear. | 0.937 |
| CAZ95740.1 | gnlA | ZOBELLIA_1686 | ZOBELLIA_2920 | Pyrroloquinoline quinone-dependent dehydrogenase; Dehydrogenase with a N-terminal domain that adopts a beta-propeller fold and binds the pyrroloquinoline quinone (PQQ) as prosthetic group. Contains also a C-type cytochrome domain with a heme group covalently bound by thioether bonds to two conserved cysteine residues; Belongs to the Quinoprotein alcohol dehydrogenase family; Putative lipoprotein signal peptide cleaved between the residues 21 and 22; Possibly localized in the outer membrane; Specificity unclear. | Gluconolactonases hydrolyze the gluconolactone, formed either by the glucose oxidoreductase or by the glucose dehydrogenase in aerobic conditions, to gluconate; Contains a putative lipoprotein signal peptide cleaved between the residues 20 and 21; Possibly localized in the outer membrane; High confidence in function and specificity. | 0.935 |
| CAZ96473.1 | CAZ94658.1 | ZOBELLIA_2318 | ZOBELLIA_587 | Fumarylacetoacetate hydrolase (FAH), or fumarylacetoacetase (FAA) is the last enzyme in the tyrosine catabolic pathway, it hydrolyses fumarylacetoacetate into fumarate and acetoacetate which then join the citric acid cycle; Localized in the cytoplasm; High confidence in function and specificity. | Gluconolactonases hydrolyze the gluconolactone formed by glucose oxidoreductase. The proximity of the galactonate dehydratase gene dgoD suggests that this lactonase would be specific for D-galactono-1,4-lactone instead of gluconolactone; Signal peptide cleaved between the residues 19 and 20; Localized in the periplasm; Specificity unclear. | 0.651 |
| CAZ96473.1 | gnlA | ZOBELLIA_2318 | ZOBELLIA_2920 | Fumarylacetoacetate hydrolase (FAH), or fumarylacetoacetase (FAA) is the last enzyme in the tyrosine catabolic pathway, it hydrolyses fumarylacetoacetate into fumarate and acetoacetate which then join the citric acid cycle; Localized in the cytoplasm; High confidence in function and specificity. | Gluconolactonases hydrolyze the gluconolactone, formed either by the glucose oxidoreductase or by the glucose dehydrogenase in aerobic conditions, to gluconate; Contains a putative lipoprotein signal peptide cleaved between the residues 20 and 21; Possibly localized in the outer membrane; High confidence in function and specificity. | 0.429 |
| gdhA | CAZ94658.1 | ZOBELLIA_1102 | ZOBELLIA_587 | Glucose dehydrogenase catalyses the oxidation of D-glucose without prior phosphorylation to D-beta-gluconolactone using NAD or NADP as a coenzyme; Belongs to the short-chain dehydrogenases/reductases family, Glucose/ribitol dehydrogenase subfamily; Localized in the cytoplasm; High confidence in function and specificity. | Gluconolactonases hydrolyze the gluconolactone formed by glucose oxidoreductase. The proximity of the galactonate dehydratase gene dgoD suggests that this lactonase would be specific for D-galactono-1,4-lactone instead of gluconolactone; Signal peptide cleaved between the residues 19 and 20; Localized in the periplasm; Specificity unclear. | 0.902 |
| gdhA | gnlA | ZOBELLIA_1102 | ZOBELLIA_2920 | Glucose dehydrogenase catalyses the oxidation of D-glucose without prior phosphorylation to D-beta-gluconolactone using NAD or NADP as a coenzyme; Belongs to the short-chain dehydrogenases/reductases family, Glucose/ribitol dehydrogenase subfamily; Localized in the cytoplasm; High confidence in function and specificity. | Gluconolactonases hydrolyze the gluconolactone, formed either by the glucose oxidoreductase or by the glucose dehydrogenase in aerobic conditions, to gluconate; Contains a putative lipoprotein signal peptide cleaved between the residues 20 and 21; Possibly localized in the outer membrane; High confidence in function and specificity. | 0.902 |