| node1 | node2 | node1 accession | node2 accession | node1 annotation | node2 annotation | score |
| Ping_0115 | mgsA | Ping_0115 | Ping_0116 | PFAM: ferredoxin; MOSC domain containing protein; MOSC domain protein beta barrel domain protein; KEGG: vfi:VFA0264 oxidoreductase (iron-sulfur cluster biosynthesis). | Methylglyoxal synthase; Catalyzes the formation of methylglyoxal from dihydroxyacetone phosphate. | 0.708 |
| Ping_1645 | Ping_2513 | Ping_1645 | Ping_2513 | PFAM: iron-containing alcohol dehydrogenase; KEGG: ppr:PBPRA2759 putative iron-containing alcohol dehydrogenase. | PFAM: iron-containing alcohol dehydrogenase; KEGG: sfx:S3258 putative oxidoreductase. | 0.903 |
| Ping_1645 | Ping_3349 | Ping_1645 | Ping_3349 | PFAM: iron-containing alcohol dehydrogenase; KEGG: ppr:PBPRA2759 putative iron-containing alcohol dehydrogenase. | PFAM: iron-containing alcohol dehydrogenase; KEGG: cps:CPS_3111 alcohol dehydrogenase, iron-containing. | 0.901 |
| Ping_1645 | mgsA | Ping_1645 | Ping_0116 | PFAM: iron-containing alcohol dehydrogenase; KEGG: ppr:PBPRA2759 putative iron-containing alcohol dehydrogenase. | Methylglyoxal synthase; Catalyzes the formation of methylglyoxal from dihydroxyacetone phosphate. | 0.904 |
| Ping_2513 | Ping_1645 | Ping_2513 | Ping_1645 | PFAM: iron-containing alcohol dehydrogenase; KEGG: sfx:S3258 putative oxidoreductase. | PFAM: iron-containing alcohol dehydrogenase; KEGG: ppr:PBPRA2759 putative iron-containing alcohol dehydrogenase. | 0.903 |
| Ping_2513 | Ping_3349 | Ping_2513 | Ping_3349 | PFAM: iron-containing alcohol dehydrogenase; KEGG: sfx:S3258 putative oxidoreductase. | PFAM: iron-containing alcohol dehydrogenase; KEGG: cps:CPS_3111 alcohol dehydrogenase, iron-containing. | 0.903 |
| Ping_2513 | mgsA | Ping_2513 | Ping_0116 | PFAM: iron-containing alcohol dehydrogenase; KEGG: sfx:S3258 putative oxidoreductase. | Methylglyoxal synthase; Catalyzes the formation of methylglyoxal from dihydroxyacetone phosphate. | 0.904 |
| Ping_3349 | Ping_1645 | Ping_3349 | Ping_1645 | PFAM: iron-containing alcohol dehydrogenase; KEGG: cps:CPS_3111 alcohol dehydrogenase, iron-containing. | PFAM: iron-containing alcohol dehydrogenase; KEGG: ppr:PBPRA2759 putative iron-containing alcohol dehydrogenase. | 0.901 |
| Ping_3349 | Ping_2513 | Ping_3349 | Ping_2513 | PFAM: iron-containing alcohol dehydrogenase; KEGG: cps:CPS_3111 alcohol dehydrogenase, iron-containing. | PFAM: iron-containing alcohol dehydrogenase; KEGG: sfx:S3258 putative oxidoreductase. | 0.903 |
| Ping_3349 | mgsA | Ping_3349 | Ping_0116 | PFAM: iron-containing alcohol dehydrogenase; KEGG: cps:CPS_3111 alcohol dehydrogenase, iron-containing. | Methylglyoxal synthase; Catalyzes the formation of methylglyoxal from dihydroxyacetone phosphate. | 0.904 |
| birA | cca | Ping_0219 | Ping_0176 | biotin--acetyl-CoA-carboxylase ligase; Acts both as a biotin--[acetyl-CoA-carboxylase] ligase and a biotin-operon repressor. In the presence of ATP, BirA activates biotin to form the BirA-biotinyl-5'-adenylate (BirA-bio-5'-AMP or holoBirA) complex. HoloBirA can either transfer the biotinyl moiety to the biotin carboxyl carrier protein (BCCP) subunit of acetyl-CoA carboxylase, or bind to the biotin operator site and inhibit transcription of the operon. | Metal dependent phosphohydrolase; Catalyzes the addition and repair of the essential 3'- terminal CCA sequence in tRNAs without using a nucleic acid template. Adds these three nucleotides in the order of C, C, and A to the tRNA nucleotide-73, using CTP and ATP as substrates and producing inorganic pyrophosphate. Also shows phosphatase, 2'-nucleotidase and 2',3'-cyclic phosphodiesterase activities. These phosphohydrolase activities are probably involved in the repair of the tRNA 3'-CCA terminus degraded by intracellular RNases. | 0.721 |
| birA | dapB | Ping_0219 | Ping_3648 | biotin--acetyl-CoA-carboxylase ligase; Acts both as a biotin--[acetyl-CoA-carboxylase] ligase and a biotin-operon repressor. In the presence of ATP, BirA activates biotin to form the BirA-biotinyl-5'-adenylate (BirA-bio-5'-AMP or holoBirA) complex. HoloBirA can either transfer the biotinyl moiety to the biotin carboxyl carrier protein (BCCP) subunit of acetyl-CoA carboxylase, or bind to the biotin operator site and inhibit transcription of the operon. | Dihydrodipicolinate reductase; Catalyzes the conversion of 4-hydroxy-tetrahydrodipicolinate (HTPA) to tetrahydrodipicolinate; Belongs to the DapB family. | 0.654 |
| birA | mgsA | Ping_0219 | Ping_0116 | biotin--acetyl-CoA-carboxylase ligase; Acts both as a biotin--[acetyl-CoA-carboxylase] ligase and a biotin-operon repressor. In the presence of ATP, BirA activates biotin to form the BirA-biotinyl-5'-adenylate (BirA-bio-5'-AMP or holoBirA) complex. HoloBirA can either transfer the biotinyl moiety to the biotin carboxyl carrier protein (BCCP) subunit of acetyl-CoA carboxylase, or bind to the biotin operator site and inhibit transcription of the operon. | Methylglyoxal synthase; Catalyzes the formation of methylglyoxal from dihydroxyacetone phosphate. | 0.764 |
| birA | pcnB | Ping_0219 | Ping_0582 | biotin--acetyl-CoA-carboxylase ligase; Acts both as a biotin--[acetyl-CoA-carboxylase] ligase and a biotin-operon repressor. In the presence of ATP, BirA activates biotin to form the BirA-biotinyl-5'-adenylate (BirA-bio-5'-AMP or holoBirA) complex. HoloBirA can either transfer the biotinyl moiety to the biotin carboxyl carrier protein (BCCP) subunit of acetyl-CoA carboxylase, or bind to the biotin operator site and inhibit transcription of the operon. | poly(A) polymerase; Adds poly(A) tail to the 3' end of many RNAs, which usually targets these RNAs for decay. Plays a significant role in the global control of gene expression, through influencing the rate of transcript degradation, and in the general RNA quality control. Belongs to the tRNA nucleotidyltransferase/poly(A) polymerase family. | 0.755 |
| cca | birA | Ping_0176 | Ping_0219 | Metal dependent phosphohydrolase; Catalyzes the addition and repair of the essential 3'- terminal CCA sequence in tRNAs without using a nucleic acid template. Adds these three nucleotides in the order of C, C, and A to the tRNA nucleotide-73, using CTP and ATP as substrates and producing inorganic pyrophosphate. Also shows phosphatase, 2'-nucleotidase and 2',3'-cyclic phosphodiesterase activities. These phosphohydrolase activities are probably involved in the repair of the tRNA 3'-CCA terminus degraded by intracellular RNases. | biotin--acetyl-CoA-carboxylase ligase; Acts both as a biotin--[acetyl-CoA-carboxylase] ligase and a biotin-operon repressor. In the presence of ATP, BirA activates biotin to form the BirA-biotinyl-5'-adenylate (BirA-bio-5'-AMP or holoBirA) complex. HoloBirA can either transfer the biotinyl moiety to the biotin carboxyl carrier protein (BCCP) subunit of acetyl-CoA carboxylase, or bind to the biotin operator site and inhibit transcription of the operon. | 0.721 |
| cca | dapB | Ping_0176 | Ping_3648 | Metal dependent phosphohydrolase; Catalyzes the addition and repair of the essential 3'- terminal CCA sequence in tRNAs without using a nucleic acid template. Adds these three nucleotides in the order of C, C, and A to the tRNA nucleotide-73, using CTP and ATP as substrates and producing inorganic pyrophosphate. Also shows phosphatase, 2'-nucleotidase and 2',3'-cyclic phosphodiesterase activities. These phosphohydrolase activities are probably involved in the repair of the tRNA 3'-CCA terminus degraded by intracellular RNases. | Dihydrodipicolinate reductase; Catalyzes the conversion of 4-hydroxy-tetrahydrodipicolinate (HTPA) to tetrahydrodipicolinate; Belongs to the DapB family. | 0.719 |
| cca | mgsA | Ping_0176 | Ping_0116 | Metal dependent phosphohydrolase; Catalyzes the addition and repair of the essential 3'- terminal CCA sequence in tRNAs without using a nucleic acid template. Adds these three nucleotides in the order of C, C, and A to the tRNA nucleotide-73, using CTP and ATP as substrates and producing inorganic pyrophosphate. Also shows phosphatase, 2'-nucleotidase and 2',3'-cyclic phosphodiesterase activities. These phosphohydrolase activities are probably involved in the repair of the tRNA 3'-CCA terminus degraded by intracellular RNases. | Methylglyoxal synthase; Catalyzes the formation of methylglyoxal from dihydroxyacetone phosphate. | 0.739 |
| coaE | mgsA | Ping_1159 | Ping_0116 | dephospho-CoA kinase; Catalyzes the phosphorylation of the 3'-hydroxyl group of dephosphocoenzyme A to form coenzyme A; Belongs to the CoaE family. | Methylglyoxal synthase; Catalyzes the formation of methylglyoxal from dihydroxyacetone phosphate. | 0.913 |
| dapB | birA | Ping_3648 | Ping_0219 | Dihydrodipicolinate reductase; Catalyzes the conversion of 4-hydroxy-tetrahydrodipicolinate (HTPA) to tetrahydrodipicolinate; Belongs to the DapB family. | biotin--acetyl-CoA-carboxylase ligase; Acts both as a biotin--[acetyl-CoA-carboxylase] ligase and a biotin-operon repressor. In the presence of ATP, BirA activates biotin to form the BirA-biotinyl-5'-adenylate (BirA-bio-5'-AMP or holoBirA) complex. HoloBirA can either transfer the biotinyl moiety to the biotin carboxyl carrier protein (BCCP) subunit of acetyl-CoA carboxylase, or bind to the biotin operator site and inhibit transcription of the operon. | 0.654 |
| dapB | cca | Ping_3648 | Ping_0176 | Dihydrodipicolinate reductase; Catalyzes the conversion of 4-hydroxy-tetrahydrodipicolinate (HTPA) to tetrahydrodipicolinate; Belongs to the DapB family. | Metal dependent phosphohydrolase; Catalyzes the addition and repair of the essential 3'- terminal CCA sequence in tRNAs without using a nucleic acid template. Adds these three nucleotides in the order of C, C, and A to the tRNA nucleotide-73, using CTP and ATP as substrates and producing inorganic pyrophosphate. Also shows phosphatase, 2'-nucleotidase and 2',3'-cyclic phosphodiesterase activities. These phosphohydrolase activities are probably involved in the repair of the tRNA 3'-CCA terminus degraded by intracellular RNases. | 0.719 |