| node1 | node2 | node1 accession | node2 accession | node1 annotation | node2 annotation | score |
| Rcas_0051 | Rcas_3209 | Rcas_0051 | Rcas_3209 | KEGG: rrs:RoseRS_3313 hypothetical protein. | KEGG: rrs:RoseRS_3908 hypothetical protein. | 0.895 |
| Rcas_0063 | Rcas_3209 | Rcas_0063 | Rcas_3209 | PFAM: Peptidoglycan-binding LysM; KEGG: rrs:RoseRS_4013 peptidoglycan-binding LysM. | KEGG: rrs:RoseRS_3908 hypothetical protein. | 0.930 |
| Rcas_1069 | Rcas_3209 | Rcas_1069 | Rcas_3209 | PFAM: Peptidoglycan-binding LysM; KEGG: rrs:RoseRS_0425 peptidoglycan-binding LysM. | KEGG: rrs:RoseRS_3908 hypothetical protein. | 0.918 |
| Rcas_1258 | Rcas_3209 | Rcas_1258 | Rcas_3209 | PFAM: Peptidoglycan-binding LysM; polysaccharide deacetylase; KEGG: rrs:RoseRS_0503 polysaccharide deacetylase. | KEGG: rrs:RoseRS_3908 hypothetical protein. | 0.924 |
| Rcas_1395 | Rcas_3209 | Rcas_1395 | Rcas_3209 | KEGG: rrs:RoseRS_2211 type IV secretory pathway VirB4 components-like protein. | KEGG: rrs:RoseRS_3908 hypothetical protein. | 0.916 |
| Rcas_2807 | Rcas_3209 | Rcas_2807 | Rcas_3209 | FHA domain containing protein; PFAM: Forkhead-associated protein; KEGG: rrs:RoseRS_1673 FHA domain containing protein. | KEGG: rrs:RoseRS_3908 hypothetical protein. | 0.912 |
| Rcas_3116 | Rcas_3209 | Rcas_3116 | Rcas_3209 | KEGG: rrs:RoseRS_2363 hypothetical protein. | KEGG: rrs:RoseRS_3908 hypothetical protein. | 0.786 |
| Rcas_3209 | Rcas_0051 | Rcas_3209 | Rcas_0051 | KEGG: rrs:RoseRS_3908 hypothetical protein. | KEGG: rrs:RoseRS_3313 hypothetical protein. | 0.895 |
| Rcas_3209 | Rcas_0063 | Rcas_3209 | Rcas_0063 | KEGG: rrs:RoseRS_3908 hypothetical protein. | PFAM: Peptidoglycan-binding LysM; KEGG: rrs:RoseRS_4013 peptidoglycan-binding LysM. | 0.930 |
| Rcas_3209 | Rcas_1069 | Rcas_3209 | Rcas_1069 | KEGG: rrs:RoseRS_3908 hypothetical protein. | PFAM: Peptidoglycan-binding LysM; KEGG: rrs:RoseRS_0425 peptidoglycan-binding LysM. | 0.918 |
| Rcas_3209 | Rcas_1258 | Rcas_3209 | Rcas_1258 | KEGG: rrs:RoseRS_3908 hypothetical protein. | PFAM: Peptidoglycan-binding LysM; polysaccharide deacetylase; KEGG: rrs:RoseRS_0503 polysaccharide deacetylase. | 0.924 |
| Rcas_3209 | Rcas_1395 | Rcas_3209 | Rcas_1395 | KEGG: rrs:RoseRS_3908 hypothetical protein. | KEGG: rrs:RoseRS_2211 type IV secretory pathway VirB4 components-like protein. | 0.916 |
| Rcas_3209 | Rcas_2807 | Rcas_3209 | Rcas_2807 | KEGG: rrs:RoseRS_3908 hypothetical protein. | FHA domain containing protein; PFAM: Forkhead-associated protein; KEGG: rrs:RoseRS_1673 FHA domain containing protein. | 0.912 |
| Rcas_3209 | Rcas_3116 | Rcas_3209 | Rcas_3116 | KEGG: rrs:RoseRS_3908 hypothetical protein. | KEGG: rrs:RoseRS_2363 hypothetical protein. | 0.786 |
| Rcas_3209 | Rcas_3351 | Rcas_3209 | Rcas_3351 | KEGG: rrs:RoseRS_3908 hypothetical protein. | KEGG: rrs:RoseRS_4063 hypothetical protein. | 0.895 |
| Rcas_3209 | Rcas_3601 | Rcas_3209 | Rcas_3601 | KEGG: rrs:RoseRS_3908 hypothetical protein. | KEGG: mlo:mll3244 hypothetical protein. | 0.912 |
| Rcas_3209 | gyrB | Rcas_3209 | Rcas_4195 | KEGG: rrs:RoseRS_3908 hypothetical protein. | DNA gyrase, B subunit; A type II topoisomerase that negatively supercoils closed circular double-stranded (ds) DNA in an ATP-dependent manner to modulate DNA topology and maintain chromosomes in an underwound state. Negative supercoiling favors strand separation, and DNA replication, transcription, recombination and repair, all of which involve strand separation. Also able to catalyze the interconversion of other topological isomers of dsDNA rings, including catenanes and knotted rings. Type II topoisomerases break and join 2 DNA strands simultaneously in an ATP-dependent manner. | 0.885 |
| Rcas_3351 | Rcas_3209 | Rcas_3351 | Rcas_3209 | KEGG: rrs:RoseRS_4063 hypothetical protein. | KEGG: rrs:RoseRS_3908 hypothetical protein. | 0.895 |
| Rcas_3601 | Rcas_3209 | Rcas_3601 | Rcas_3209 | KEGG: mlo:mll3244 hypothetical protein. | KEGG: rrs:RoseRS_3908 hypothetical protein. | 0.912 |
| gyrB | Rcas_3209 | Rcas_4195 | Rcas_3209 | DNA gyrase, B subunit; A type II topoisomerase that negatively supercoils closed circular double-stranded (ds) DNA in an ATP-dependent manner to modulate DNA topology and maintain chromosomes in an underwound state. Negative supercoiling favors strand separation, and DNA replication, transcription, recombination and repair, all of which involve strand separation. Also able to catalyze the interconversion of other topological isomers of dsDNA rings, including catenanes and knotted rings. Type II topoisomerases break and join 2 DNA strands simultaneously in an ATP-dependent manner. | KEGG: rrs:RoseRS_3908 hypothetical protein. | 0.885 |