node1 | node2 | node1 accession | node2 accession | node1 annotation | node2 annotation | score |
Dshi_0068 | Dshi_0069 | Dshi_0068 | Dshi_0069 | Lipoprotein; KEGG: sil:SPO3414 lipoprotein, putative; Lytic Transglycosylase (LT) and Goose Egg White Lysozyme (GEWL) domain. LTs catalyze the cleavage of the beta-1,4-glycosidic bond between N-acetylmuramic acid (MurNAc) and N-acetyl-D-glucosamine (GlcNAc), as do goose-type lysozymes. However, in addition to this, they also make a new glycosidic bond with the C6 hydroxyl group of the same muramic acid residue. | PFAM: Auxin Efflux Carrier; COG0679 Predicted permeases, good Ref ZP hit to auxin efflux carrier family protein fromSulfitobacter sp. EE-36, swissprot hit to Uncharacterized transporter MTH_1382 from Methanothermobacter thermautotrophicus str. Delta H. | 0.674 |
Dshi_0068 | yccV | Dshi_0068 | Dshi_0070 | Lipoprotein; KEGG: sil:SPO3414 lipoprotein, putative; Lytic Transglycosylase (LT) and Goose Egg White Lysozyme (GEWL) domain. LTs catalyze the cleavage of the beta-1,4-glycosidic bond between N-acetylmuramic acid (MurNAc) and N-acetyl-D-glucosamine (GlcNAc), as do goose-type lysozymes. However, in addition to this, they also make a new glycosidic bond with the C6 hydroxyl group of the same muramic acid residue. | TIGRFAM: hemimethylated DNA binding protein PFAM: Hemimethylated DNA-binding region KEGG: sil:SPO3412 hypothetical protein, no swissprot. | 0.638 |
Dshi_0069 | Dshi_0068 | Dshi_0069 | Dshi_0068 | PFAM: Auxin Efflux Carrier; COG0679 Predicted permeases, good Ref ZP hit to auxin efflux carrier family protein fromSulfitobacter sp. EE-36, swissprot hit to Uncharacterized transporter MTH_1382 from Methanothermobacter thermautotrophicus str. Delta H. | Lipoprotein; KEGG: sil:SPO3414 lipoprotein, putative; Lytic Transglycosylase (LT) and Goose Egg White Lysozyme (GEWL) domain. LTs catalyze the cleavage of the beta-1,4-glycosidic bond between N-acetylmuramic acid (MurNAc) and N-acetyl-D-glucosamine (GlcNAc), as do goose-type lysozymes. However, in addition to this, they also make a new glycosidic bond with the C6 hydroxyl group of the same muramic acid residue. | 0.674 |
Dshi_0069 | yccV | Dshi_0069 | Dshi_0070 | PFAM: Auxin Efflux Carrier; COG0679 Predicted permeases, good Ref ZP hit to auxin efflux carrier family protein fromSulfitobacter sp. EE-36, swissprot hit to Uncharacterized transporter MTH_1382 from Methanothermobacter thermautotrophicus str. Delta H. | TIGRFAM: hemimethylated DNA binding protein PFAM: Hemimethylated DNA-binding region KEGG: sil:SPO3412 hypothetical protein, no swissprot. | 0.664 |
Dshi_1516 | Dshi_2616 | Dshi_1516 | Dshi_2616 | Conserved hypothetical protein; PFAM: PF01592, COG: COG0822 - NifU homolog involved in Fe-S cluster formation; related to NIFU. | PFAM: GcrA cell cycle regulator KEGG: jan:Jann_1020 GcrA cell cycle regulator. | 0.615 |
Dshi_1516 | Dshi_3232 | Dshi_1516 | Dshi_3232 | Conserved hypothetical protein; PFAM: PF01592, COG: COG0822 - NifU homolog involved in Fe-S cluster formation; related to NIFU. | KEGG: sil:SPO3807 hypothetical protein. | 0.750 |
Dshi_1516 | atpE2 | Dshi_1516 | Dshi_3029 | Conserved hypothetical protein; PFAM: PF01592, COG: COG0822 - NifU homolog involved in Fe-S cluster formation; related to NIFU. | ATP synthase F0; 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. | 0.675 |
Dshi_1516 | yccV | Dshi_1516 | Dshi_0070 | Conserved hypothetical protein; PFAM: PF01592, COG: COG0822 - NifU homolog involved in Fe-S cluster formation; related to NIFU. | TIGRFAM: hemimethylated DNA binding protein PFAM: Hemimethylated DNA-binding region KEGG: sil:SPO3412 hypothetical protein, no swissprot. | 0.585 |
Dshi_1558 | asnC | Dshi_1558 | Dshi_0245 | Hypothetical protein. | PFAM: regulatory protein AsnC/Lrp family KEGG: jan:Jann_0459 transcriptional regulator, AsnC family; AsnC family. | 0.426 |
Dshi_1558 | yccV | Dshi_1558 | Dshi_0070 | Hypothetical protein. | TIGRFAM: hemimethylated DNA binding protein PFAM: Hemimethylated DNA-binding region KEGG: sil:SPO3412 hypothetical protein, no swissprot. | 0.483 |
Dshi_1703 | asnC | Dshi_1703 | Dshi_0245 | SWISSPROT P0AC51: Zinc uptake regulation protein; PRODOM: PD002003; PFAM: pfam01475; zur; Belongs to the Fur family. | PFAM: regulatory protein AsnC/Lrp family KEGG: jan:Jann_0459 transcriptional regulator, AsnC family; AsnC family. | 0.618 |
Dshi_1703 | yccV | Dshi_1703 | Dshi_0070 | SWISSPROT P0AC51: Zinc uptake regulation protein; PRODOM: PD002003; PFAM: pfam01475; zur; Belongs to the Fur family. | TIGRFAM: hemimethylated DNA binding protein PFAM: Hemimethylated DNA-binding region KEGG: sil:SPO3412 hypothetical protein, no swissprot. | 0.546 |
Dshi_1703 | znuC | Dshi_1703 | Dshi_1702 | SWISSPROT P0AC51: Zinc uptake regulation protein; PRODOM: PD002003; PFAM: pfam01475; zur; Belongs to the Fur family. | Zinc import ATP-binding protein; Part of the ABC transporter complex ZnuABC involved in zinc import. Responsible for energy coupling to the transport system. Belongs to the ABC transporter superfamily. Zinc importer (TC 3.A.1.15.5) family. | 0.990 |
Dshi_2616 | Dshi_1516 | Dshi_2616 | Dshi_1516 | PFAM: GcrA cell cycle regulator KEGG: jan:Jann_1020 GcrA cell cycle regulator. | Conserved hypothetical protein; PFAM: PF01592, COG: COG0822 - NifU homolog involved in Fe-S cluster formation; related to NIFU. | 0.615 |
Dshi_2616 | Dshi_3232 | Dshi_2616 | Dshi_3232 | PFAM: GcrA cell cycle regulator KEGG: jan:Jann_1020 GcrA cell cycle regulator. | KEGG: sil:SPO3807 hypothetical protein. | 0.741 |
Dshi_2616 | atpE2 | Dshi_2616 | Dshi_3029 | PFAM: GcrA cell cycle regulator KEGG: jan:Jann_1020 GcrA cell cycle regulator. | ATP synthase F0; 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 |
Dshi_2616 | yccV | Dshi_2616 | Dshi_0070 | PFAM: GcrA cell cycle regulator KEGG: jan:Jann_1020 GcrA cell cycle regulator. | TIGRFAM: hemimethylated DNA binding protein PFAM: Hemimethylated DNA-binding region KEGG: sil:SPO3412 hypothetical protein, no swissprot. | 0.472 |
Dshi_3232 | Dshi_1516 | Dshi_3232 | Dshi_1516 | KEGG: sil:SPO3807 hypothetical protein. | Conserved hypothetical protein; PFAM: PF01592, COG: COG0822 - NifU homolog involved in Fe-S cluster formation; related to NIFU. | 0.750 |
Dshi_3232 | Dshi_2616 | Dshi_3232 | Dshi_2616 | KEGG: sil:SPO3807 hypothetical protein. | PFAM: GcrA cell cycle regulator KEGG: jan:Jann_1020 GcrA cell cycle regulator. | 0.741 |
Dshi_3232 | atpE2 | Dshi_3232 | Dshi_3029 | KEGG: sil:SPO3807 hypothetical protein. | ATP synthase F0; 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. | 0.762 |