| node1 | node2 | node1 accession | node2 accession | node1 annotation | node2 annotation | score |
| Slit_0277 | Slit_0372 | Slit_0277 | Slit_0372 | KEGG: mei:Msip34_2513 glutamine amidotransferase of anthranilate synthase; TIGRFAM: glutamine amidotransferase of anthranilate synthase; PFAM: glutamine amidotransferase class-I. | KEGG: tbd:Tbd_2762 hypothetical protein. | 0.900 |
| Slit_0277 | Slit_2065 | Slit_0277 | Slit_2065 | KEGG: mei:Msip34_2513 glutamine amidotransferase of anthranilate synthase; TIGRFAM: glutamine amidotransferase of anthranilate synthase; PFAM: glutamine amidotransferase class-I. | TIGRFAM: chorismate mutase; PFAM: prephenate dehydratase; amino acid-binding ACT domain protein; Chorismate mutase, type II; KEGG: nmu:Nmul_A2192 chorismate mutase; SMART: Chorismate mutase. | 0.958 |
| Slit_0277 | aroC | Slit_0277 | Slit_0339 | KEGG: mei:Msip34_2513 glutamine amidotransferase of anthranilate synthase; TIGRFAM: glutamine amidotransferase of anthranilate synthase; PFAM: glutamine amidotransferase class-I. | Chorismate synthase; Catalyzes the anti-1,4-elimination of the C-3 phosphate and the C-6 proR hydrogen from 5-enolpyruvylshikimate-3-phosphate (EPSP) to yield chorismate, which is the branch point compound that serves as the starting substrate for the three terminal pathways of aromatic amino acid biosynthesis. This reaction introduces a second double bond into the aromatic ring system. | 0.959 |
| Slit_0277 | trpE | Slit_0277 | Slit_0278 | KEGG: mei:Msip34_2513 glutamine amidotransferase of anthranilate synthase; TIGRFAM: glutamine amidotransferase of anthranilate synthase; PFAM: glutamine amidotransferase class-I. | Anthranilate synthase component I; Part of a heterotetrameric complex that catalyzes the two- step biosynthesis of anthranilate, an intermediate in the biosynthesis of L-tryptophan. In the first step, the glutamine-binding beta subunit (TrpG) of anthranilate synthase (AS) provides the glutamine amidotransferase activity which generates ammonia as a substrate that, along with chorismate, is used in the second step, catalyzed by the large alpha subunit of AS (TrpE) to produce anthranilate. In the absence of TrpG, TrpE can synthesize anthranilate directly from chorismate and high concentr [...] | 0.999 |
| Slit_0363 | Slit_0364 | Slit_0363 | Slit_0364 | KEGG: rso:RSc0433 hypothetical protein. | PFAM: AMP-dependent synthetase and ligase; KEGG: dar:Daro_4173 AMP-dependent synthetase and ligase. | 0.948 |
| Slit_0363 | Slit_0365 | Slit_0363 | Slit_0365 | KEGG: rso:RSc0433 hypothetical protein. | KEGG: rso:RSc0432 hypothetical protein. | 0.947 |
| Slit_0363 | Slit_0367 | Slit_0363 | Slit_0367 | KEGG: rso:RSc0433 hypothetical protein. | Putative transmembrane protein; Participates in the translocation of lipoproteins from the inner membrane to the outer membrane. Only forms a complex with a lipoprotein if the residue after the N-terminal Cys is not an aspartate (The Asp acts as a targeting signal to indicate that the lipoprotein should stay in the inner membrane). | 0.950 |
| Slit_0363 | Slit_0368 | Slit_0363 | Slit_0368 | KEGG: rso:RSc0433 hypothetical protein. | KEGG: pna:Pnap_1374 hypothetical protein. | 0.948 |
| Slit_0363 | Slit_0372 | Slit_0363 | Slit_0372 | KEGG: rso:RSc0433 hypothetical protein. | KEGG: tbd:Tbd_2762 hypothetical protein. | 0.830 |
| Slit_0364 | Slit_0363 | Slit_0364 | Slit_0363 | PFAM: AMP-dependent synthetase and ligase; KEGG: dar:Daro_4173 AMP-dependent synthetase and ligase. | KEGG: rso:RSc0433 hypothetical protein. | 0.948 |
| Slit_0364 | Slit_0365 | Slit_0364 | Slit_0365 | PFAM: AMP-dependent synthetase and ligase; KEGG: dar:Daro_4173 AMP-dependent synthetase and ligase. | KEGG: rso:RSc0432 hypothetical protein. | 0.954 |
| Slit_0364 | Slit_0367 | Slit_0364 | Slit_0367 | PFAM: AMP-dependent synthetase and ligase; KEGG: dar:Daro_4173 AMP-dependent synthetase and ligase. | Putative transmembrane protein; Participates in the translocation of lipoproteins from the inner membrane to the outer membrane. Only forms a complex with a lipoprotein if the residue after the N-terminal Cys is not an aspartate (The Asp acts as a targeting signal to indicate that the lipoprotein should stay in the inner membrane). | 0.954 |
| Slit_0364 | Slit_0368 | Slit_0364 | Slit_0368 | PFAM: AMP-dependent synthetase and ligase; KEGG: dar:Daro_4173 AMP-dependent synthetase and ligase. | KEGG: pna:Pnap_1374 hypothetical protein. | 0.954 |
| Slit_0364 | Slit_0372 | Slit_0364 | Slit_0372 | PFAM: AMP-dependent synthetase and ligase; KEGG: dar:Daro_4173 AMP-dependent synthetase and ligase. | KEGG: tbd:Tbd_2762 hypothetical protein. | 0.818 |
| Slit_0365 | Slit_0363 | Slit_0365 | Slit_0363 | KEGG: rso:RSc0432 hypothetical protein. | KEGG: rso:RSc0433 hypothetical protein. | 0.947 |
| Slit_0365 | Slit_0364 | Slit_0365 | Slit_0364 | KEGG: rso:RSc0432 hypothetical protein. | PFAM: AMP-dependent synthetase and ligase; KEGG: dar:Daro_4173 AMP-dependent synthetase and ligase. | 0.954 |
| Slit_0365 | Slit_0367 | Slit_0365 | Slit_0367 | KEGG: rso:RSc0432 hypothetical protein. | Putative transmembrane protein; Participates in the translocation of lipoproteins from the inner membrane to the outer membrane. Only forms a complex with a lipoprotein if the residue after the N-terminal Cys is not an aspartate (The Asp acts as a targeting signal to indicate that the lipoprotein should stay in the inner membrane). | 0.953 |
| Slit_0365 | Slit_0368 | Slit_0365 | Slit_0368 | KEGG: rso:RSc0432 hypothetical protein. | KEGG: pna:Pnap_1374 hypothetical protein. | 0.953 |
| Slit_0365 | Slit_0372 | Slit_0365 | Slit_0372 | KEGG: rso:RSc0432 hypothetical protein. | KEGG: tbd:Tbd_2762 hypothetical protein. | 0.820 |
| Slit_0367 | Slit_0363 | Slit_0367 | Slit_0363 | Putative transmembrane protein; Participates in the translocation of lipoproteins from the inner membrane to the outer membrane. Only forms a complex with a lipoprotein if the residue after the N-terminal Cys is not an aspartate (The Asp acts as a targeting signal to indicate that the lipoprotein should stay in the inner membrane). | KEGG: rso:RSc0433 hypothetical protein. | 0.950 |