| node1 | node2 | node1 accession | node2 accession | node1 annotation | node2 annotation | score |
| SFV73859.1 | SFV73860.1 | DESPIGER_2035 | DESPIGER_2036 | Inner membrane protein translocase component YidC, long form. | Putative bifunctional polymerase. | 0.774 |
| SFV73859.1 | SFV73861.1 | DESPIGER_2035 | DESPIGER_2037 | Inner membrane protein translocase component YidC, long form. | Cholinephosphate cytidylyltransferase. | 0.759 |
| SFV73859.1 | atpE | DESPIGER_2035 | DESPIGER_2044 | Inner membrane protein translocase component YidC, long form. | ATP synthase F0 sector subunit c; F(1)F(0) ATP synthase produces ATP from ADP in the presence of a proton or sodium gradient. F-type ATPases consist of two structural domains, F(1) containing the extramembraneous catalytic core and F(0) containing the membrane proton channel, linked together by a central stalk and a peripheral stalk. During catalysis, ATP synthesis in the catalytic domain of F(1) is coupled via a rotary mechanism of the central stalk subunits to proton translocation. | 0.708 |
| SFV73859.1 | rho | DESPIGER_2035 | DESPIGER_0580 | Inner membrane protein translocase component YidC, long form. | Transcription termination factor Rho; Facilitates transcription termination by a mechanism that involves Rho binding to the nascent RNA, activation of Rho's RNA- dependent ATPase activity, and release of the mRNA from the DNA template. | 0.728 |
| SFV73859.1 | rnpA | DESPIGER_2035 | DESPIGER_2304 | Inner membrane protein translocase component YidC, long form. | Ribonuclease P protein component; RNaseP catalyzes the removal of the 5'-leader sequence from pre-tRNA to produce the mature 5'-terminus. It can also cleave other RNA substrates such as 4.5S RNA. The protein component plays an auxiliary but essential role in vivo by binding to the 5'-leader sequence and broadening the substrate specificity of the ribozyme. | 0.752 |
| SFV73859.1 | rpsE | DESPIGER_2035 | DESPIGER_2559 | Inner membrane protein translocase component YidC, long form. | SSU ribosomal protein S5p (S2e); Located at the back of the 30S subunit body where it stabilizes the conformation of the head with respect to the body. Belongs to the universal ribosomal protein uS5 family. | 0.673 |
| SFV73859.1 | secD | DESPIGER_2035 | DESPIGER_0205 | Inner membrane protein translocase component YidC, long form. | Protein-export membrane protein SecD (TC 3.A.5.1.1); Part of the Sec protein translocase complex. Interacts with the SecYEG preprotein conducting channel. SecDF uses the proton motive force (PMF) to complete protein translocation after the ATP-dependent function of SecA. | 0.798 |
| SFV73859.1 | secF | DESPIGER_2035 | DESPIGER_0206 | Inner membrane protein translocase component YidC, long form. | Protein-export membrane protein SecF (TC 3.A.5.1.1); Part of the Sec protein translocase complex. Interacts with the SecYEG preprotein conducting channel. SecDF uses the proton motive force (PMF) to complete protein translocation after the ATP-dependent function of SecA. | 0.695 |
| SFV73859.1 | secG | DESPIGER_2035 | DESPIGER_0244 | Inner membrane protein translocase component YidC, long form. | Preprotein translocase subunit SecG (TC 3.A.5.1.1); Involved in protein export. Participates in an early event of protein translocation; Belongs to the SecG family. | 0.726 |
| SFV73859.1 | secY | DESPIGER_2035 | DESPIGER_2562 | Inner membrane protein translocase component YidC, long form. | Preprotein translocase secY subunit (TC 3.A.5.1.1); The central subunit of the protein translocation channel SecYEG. Consists of two halves formed by TMs 1-5 and 6-10. These two domains form a lateral gate at the front which open onto the bilayer between TMs 2 and 7, and are clamped together by SecE at the back. The channel is closed by both a pore ring composed of hydrophobic SecY resides and a short helix (helix 2A) on the extracellular side of the membrane which forms a plug. The plug probably moves laterally to allow the channel to open. The ring and the pore may move independently. | 0.709 |
| SFV73860.1 | SFV73859.1 | DESPIGER_2036 | DESPIGER_2035 | Putative bifunctional polymerase. | Inner membrane protein translocase component YidC, long form. | 0.774 |
| SFV73860.1 | SFV73861.1 | DESPIGER_2036 | DESPIGER_2037 | Putative bifunctional polymerase. | Cholinephosphate cytidylyltransferase. | 0.837 |
| SFV73861.1 | SFV73859.1 | DESPIGER_2037 | DESPIGER_2035 | Cholinephosphate cytidylyltransferase. | Inner membrane protein translocase component YidC, long form. | 0.759 |
| SFV73861.1 | SFV73860.1 | DESPIGER_2037 | DESPIGER_2036 | Cholinephosphate cytidylyltransferase. | Putative bifunctional polymerase. | 0.837 |
| atpE | SFV73859.1 | DESPIGER_2044 | DESPIGER_2035 | ATP synthase F0 sector subunit c; F(1)F(0) ATP synthase produces ATP from ADP in the presence of a proton or sodium gradient. F-type ATPases consist of two structural domains, F(1) containing the extramembraneous catalytic core and F(0) containing the membrane proton channel, linked together by a central stalk and a peripheral stalk. During catalysis, ATP synthesis in the catalytic domain of F(1) is coupled via a rotary mechanism of the central stalk subunits to proton translocation. | Inner membrane protein translocase component YidC, long form. | 0.708 |
| atpE | rpsE | DESPIGER_2044 | DESPIGER_2559 | ATP synthase F0 sector subunit c; F(1)F(0) ATP synthase produces ATP from ADP in the presence of a proton or sodium gradient. F-type ATPases consist of two structural domains, F(1) containing the extramembraneous catalytic core and F(0) containing the membrane proton channel, linked together by a central stalk and a peripheral stalk. During catalysis, ATP synthesis in the catalytic domain of F(1) is coupled via a rotary mechanism of the central stalk subunits to proton translocation. | SSU ribosomal protein S5p (S2e); Located at the back of the 30S subunit body where it stabilizes the conformation of the head with respect to the body. Belongs to the universal ribosomal protein uS5 family. | 0.759 |
| atpE | secY | DESPIGER_2044 | DESPIGER_2562 | ATP synthase F0 sector subunit c; F(1)F(0) ATP synthase produces ATP from ADP in the presence of a proton or sodium gradient. F-type ATPases consist of two structural domains, F(1) containing the extramembraneous catalytic core and F(0) containing the membrane proton channel, linked together by a central stalk and a peripheral stalk. During catalysis, ATP synthesis in the catalytic domain of F(1) is coupled via a rotary mechanism of the central stalk subunits to proton translocation. | Preprotein translocase secY subunit (TC 3.A.5.1.1); The central subunit of the protein translocation channel SecYEG. Consists of two halves formed by TMs 1-5 and 6-10. These two domains form a lateral gate at the front which open onto the bilayer between TMs 2 and 7, and are clamped together by SecE at the back. The channel is closed by both a pore ring composed of hydrophobic SecY resides and a short helix (helix 2A) on the extracellular side of the membrane which forms a plug. The plug probably moves laterally to allow the channel to open. The ring and the pore may move independently. | 0.743 |
| rho | SFV73859.1 | DESPIGER_0580 | DESPIGER_2035 | Transcription termination factor Rho; Facilitates transcription termination by a mechanism that involves Rho binding to the nascent RNA, activation of Rho's RNA- dependent ATPase activity, and release of the mRNA from the DNA template. | Inner membrane protein translocase component YidC, long form. | 0.728 |
| rho | rnpA | DESPIGER_0580 | DESPIGER_2304 | Transcription termination factor Rho; Facilitates transcription termination by a mechanism that involves Rho binding to the nascent RNA, activation of Rho's RNA- dependent ATPase activity, and release of the mRNA from the DNA template. | Ribonuclease P protein component; RNaseP catalyzes the removal of the 5'-leader sequence from pre-tRNA to produce the mature 5'-terminus. It can also cleave other RNA substrates such as 4.5S RNA. The protein component plays an auxiliary but essential role in vivo by binding to the 5'-leader sequence and broadening the substrate specificity of the ribozyme. | 0.744 |
| rnpA | SFV73859.1 | DESPIGER_2304 | DESPIGER_2035 | Ribonuclease P protein component; RNaseP catalyzes the removal of the 5'-leader sequence from pre-tRNA to produce the mature 5'-terminus. It can also cleave other RNA substrates such as 4.5S RNA. The protein component plays an auxiliary but essential role in vivo by binding to the 5'-leader sequence and broadening the substrate specificity of the ribozyme. | Inner membrane protein translocase component YidC, long form. | 0.752 |