| node1 | node2 | node1 accession | node2 accession | node1 annotation | node2 annotation | score |
| STM1254 | STM1328 | STM1254 | STM1328 | Putative outer membrane lipoprotein. | Putative outer membrane protein. | 0.833 |
| STM1328 | STM1254 | STM1328 | STM1254 | Putative outer membrane protein. | Putative outer membrane lipoprotein. | 0.833 |
| STM1328 | invG | STM1328 | STM2898 | Putative outer membrane protein. | Outer membrane invasion protein; Component of the type III secretion system (T3SS), also called injectisome, which is used to inject bacterial effector proteins into eukaryotic host cells. Forms a ring-shaped multimeric structure with an apparent central pore in the outer membrane. | 0.711 |
| STM1328 | lpxO | STM1328 | STM4286 | Putative outer membrane protein. | Putative dioxygenase for synthesis of lipid; Putative dioxygenase; LpxO (gi|9454389). | 0.900 |
| STM1328 | msbB | STM1328 | STM1889 | Putative outer membrane protein. | Myristoyl transferase in lipid A biosynthesis; Catalyzes the transfer of myristate from myristoyl-acyl carrier protein (ACP) to Kdo(2)-(lauroyl)-lipid IV(A) to form Kdo(2)- lipid A. | 0.921 |
| STM1328 | pagP | STM1328 | STM0628 | Putative outer membrane protein. | PhoPQ-activated gene; Transfers a palmitate residue from the sn-1 position of a phospholipid to the N-linked hydroxymyristate on the proximal unit of lipid A or its precursors. Required for resistance to cationic antimicrobial peptides (CAMPs). Modifications of lipid A with a palmitate chain allow to evade host immune defenses by resisting antimicrobial peptides and attenuating the inflammatory response to infection triggered by lipopolysaccharide through the Toll-like receptor 4 (TLR4) signal transduction pathway. | 0.975 |
| STM1328 | pqaB | STM1328 | STM2301 | Putative outer membrane protein. | Putative melittin resistance protein; Catalyzes the transfer of the L-Ara4N moiety of the glycolipid undecaprenyl phosphate-alpha-L-Ara4N to lipid A. The modified arabinose is attached to lipid A and is required for resistance to polymyxin and cationic antimicrobial peptides. Belongs to the glycosyltransferase 83 family. | 0.900 |
| STM1328 | sopB | STM1328 | STM1091 | Putative outer membrane protein. | Pathogenicity island encoded protein: SPI5; Converts phosphatidylinositol 3,4,5-trisphosphate (PtdIns 3,4,5-P3) to PtdIns 3-P and prevents the transition of PtdIns 3-P to PtdIns 3,5-P2. It is one of the known effectors injected by Salmonella into the host cell and is required for invasion and for an efficient generation and maintenance of Salmonella-containing vacuole (SVC). Alteration of the phosphoinositide composition of the plasma membrane causes membrane ruffling and actin cytoskeleton rearrangements. The persistence of PtdIns 3-P diverts the SCV from the endocytic pathway resulti [...] | 0.750 |
| STM1328 | yeiU | STM1328 | STM2213 | Putative outer membrane protein. | Putative permease; Involved in the modification of the lipid A domain of lipopolysaccharides (LPS). Transfers a phosphate group from undecaprenyl pyrophosphate (C55-PP) to lipid A to form lipid A 1- diphosphate. Contributes to the recycling of undecaprenyl phosphate (C55-P); Belongs to the LpxT phosphotransferase family. | 0.915 |
| STM1328 | yhjW | STM1328 | STM3635 | Putative outer membrane protein. | Putative membrane-associated metal-dependent hydrolase; Catalyzes the addition of a phosphoethanolamine (pEtN) moiety to the outer 3-deoxy-D-manno-octulosonic acid (Kdo) residue of a Kdo(2)-lipid A. Phosphatidylethanolamines with one unsaturated acyl group functions as pEtN donors and the reaction releases diacylglycerol. | 0.900 |
| STM1328 | yjdB | STM1328 | STM4293 | Putative outer membrane protein. | Putative integral membrane protein; Catalyzes the addition of a phosphoethanolamine moiety to the lipid A. The phosphoethanolamine modification is required for resistance to polymyxin; Belongs to the phosphoethanolamine transferase family. EptA subfamily. | 0.900 |
| invG | STM1328 | STM2898 | STM1328 | Outer membrane invasion protein; Component of the type III secretion system (T3SS), also called injectisome, which is used to inject bacterial effector proteins into eukaryotic host cells. Forms a ring-shaped multimeric structure with an apparent central pore in the outer membrane. | Putative outer membrane protein. | 0.711 |
| invG | sopB | STM2898 | STM1091 | Outer membrane invasion protein; Component of the type III secretion system (T3SS), also called injectisome, which is used to inject bacterial effector proteins into eukaryotic host cells. Forms a ring-shaped multimeric structure with an apparent central pore in the outer membrane. | Pathogenicity island encoded protein: SPI5; Converts phosphatidylinositol 3,4,5-trisphosphate (PtdIns 3,4,5-P3) to PtdIns 3-P and prevents the transition of PtdIns 3-P to PtdIns 3,5-P2. It is one of the known effectors injected by Salmonella into the host cell and is required for invasion and for an efficient generation and maintenance of Salmonella-containing vacuole (SVC). Alteration of the phosphoinositide composition of the plasma membrane causes membrane ruffling and actin cytoskeleton rearrangements. The persistence of PtdIns 3-P diverts the SCV from the endocytic pathway resulti [...] | 0.914 |
| lpxO | STM1328 | STM4286 | STM1328 | Putative dioxygenase for synthesis of lipid; Putative dioxygenase; LpxO (gi|9454389). | Putative outer membrane protein. | 0.900 |
| lpxO | msbB | STM4286 | STM1889 | Putative dioxygenase for synthesis of lipid; Putative dioxygenase; LpxO (gi|9454389). | Myristoyl transferase in lipid A biosynthesis; Catalyzes the transfer of myristate from myristoyl-acyl carrier protein (ACP) to Kdo(2)-(lauroyl)-lipid IV(A) to form Kdo(2)- lipid A. | 0.977 |
| lpxO | pagP | STM4286 | STM0628 | Putative dioxygenase for synthesis of lipid; Putative dioxygenase; LpxO (gi|9454389). | PhoPQ-activated gene; Transfers a palmitate residue from the sn-1 position of a phospholipid to the N-linked hydroxymyristate on the proximal unit of lipid A or its precursors. Required for resistance to cationic antimicrobial peptides (CAMPs). Modifications of lipid A with a palmitate chain allow to evade host immune defenses by resisting antimicrobial peptides and attenuating the inflammatory response to infection triggered by lipopolysaccharide through the Toll-like receptor 4 (TLR4) signal transduction pathway. | 0.994 |
| lpxO | pqaB | STM4286 | STM2301 | Putative dioxygenase for synthesis of lipid; Putative dioxygenase; LpxO (gi|9454389). | Putative melittin resistance protein; Catalyzes the transfer of the L-Ara4N moiety of the glycolipid undecaprenyl phosphate-alpha-L-Ara4N to lipid A. The modified arabinose is attached to lipid A and is required for resistance to polymyxin and cationic antimicrobial peptides. Belongs to the glycosyltransferase 83 family. | 0.971 |
| lpxO | yeiU | STM4286 | STM2213 | Putative dioxygenase for synthesis of lipid; Putative dioxygenase; LpxO (gi|9454389). | Putative permease; Involved in the modification of the lipid A domain of lipopolysaccharides (LPS). Transfers a phosphate group from undecaprenyl pyrophosphate (C55-PP) to lipid A to form lipid A 1- diphosphate. Contributes to the recycling of undecaprenyl phosphate (C55-P); Belongs to the LpxT phosphotransferase family. | 0.973 |
| lpxO | yhjW | STM4286 | STM3635 | Putative dioxygenase for synthesis of lipid; Putative dioxygenase; LpxO (gi|9454389). | Putative membrane-associated metal-dependent hydrolase; Catalyzes the addition of a phosphoethanolamine (pEtN) moiety to the outer 3-deoxy-D-manno-octulosonic acid (Kdo) residue of a Kdo(2)-lipid A. Phosphatidylethanolamines with one unsaturated acyl group functions as pEtN donors and the reaction releases diacylglycerol. | 0.943 |
| lpxO | yjdB | STM4286 | STM4293 | Putative dioxygenase for synthesis of lipid; Putative dioxygenase; LpxO (gi|9454389). | Putative integral membrane protein; Catalyzes the addition of a phosphoethanolamine moiety to the lipid A. The phosphoethanolamine modification is required for resistance to polymyxin; Belongs to the phosphoethanolamine transferase family. EptA subfamily. | 0.988 |