node1 | node2 | node1 accession | node2 accession | node1 annotation | node2 annotation | score |
Oant_0393 | Oant_0914 | Oant_0393 | Oant_0914 | PFAM: GcrA cell cycle regulator; KEGG: bmb:BruAb1_0325 hypothetical protein. | TIGRFAM: cobalt chelatase, pCobS small subunit; PFAM: ATPase associated with various cellular activities AAA_5; KEGG: bmb:BruAb1_1997 cobalamin biosynthesis protein, hypothetical. | 0.480 |
Oant_0393 | Oant_0915 | Oant_0393 | Oant_0915 | PFAM: GcrA cell cycle regulator; KEGG: bmb:BruAb1_0325 hypothetical protein. | KEGG: bme:BMEI0050 CobT protein; TIGRFAM: cobalt chelatase, pCobT subunit; PFAM: Cobalt chelatase CobT subunit; SMART: von Willebrand factor type A. | 0.642 |
Oant_0393 | atpF2 | Oant_0393 | Oant_0503 | PFAM: GcrA cell cycle regulator; KEGG: bmb:BruAb1_0325 hypothetical protein. | ATP synthase F0, B subunit; 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. | 0.568 |
Oant_0393 | ccrM | Oant_0393 | Oant_0605 | PFAM: GcrA cell cycle regulator; KEGG: bmb:BruAb1_0325 hypothetical protein. | DNA methylase N-4/N-6 domain protein; This methylase recognizes the double-stranded sequence GANTC and causes specific methylation on A-2 on both strands. CcrM-mediated methylation has important cellular functions. Appears to contribute to the accurate cell-cycle control of DNA replication and cellular morphology. Essential for viability; Belongs to the N(4)/N(6)-methyltransferase family. | 0.651 |
Oant_0393 | secE | Oant_0393 | Oant_1941 | PFAM: GcrA cell cycle regulator; KEGG: bmb:BruAb1_0325 hypothetical protein. | Preprotein translocase, SecE subunit; Essential subunit of the Sec protein translocation channel SecYEG. Clamps together the 2 halves of SecY. May contact the channel plug during translocation. | 0.436 |
Oant_0914 | Oant_0393 | Oant_0914 | Oant_0393 | TIGRFAM: cobalt chelatase, pCobS small subunit; PFAM: ATPase associated with various cellular activities AAA_5; KEGG: bmb:BruAb1_1997 cobalamin biosynthesis protein, hypothetical. | PFAM: GcrA cell cycle regulator; KEGG: bmb:BruAb1_0325 hypothetical protein. | 0.480 |
Oant_0914 | Oant_0915 | Oant_0914 | Oant_0915 | TIGRFAM: cobalt chelatase, pCobS small subunit; PFAM: ATPase associated with various cellular activities AAA_5; KEGG: bmb:BruAb1_1997 cobalamin biosynthesis protein, hypothetical. | KEGG: bme:BMEI0050 CobT protein; TIGRFAM: cobalt chelatase, pCobT subunit; PFAM: Cobalt chelatase CobT subunit; SMART: von Willebrand factor type A. | 0.991 |
Oant_0914 | atpF2 | Oant_0914 | Oant_0503 | TIGRFAM: cobalt chelatase, pCobS small subunit; PFAM: ATPase associated with various cellular activities AAA_5; KEGG: bmb:BruAb1_1997 cobalamin biosynthesis protein, hypothetical. | ATP synthase F0, B subunit; 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. | 0.460 |
Oant_0914 | ccrM | Oant_0914 | Oant_0605 | TIGRFAM: cobalt chelatase, pCobS small subunit; PFAM: ATPase associated with various cellular activities AAA_5; KEGG: bmb:BruAb1_1997 cobalamin biosynthesis protein, hypothetical. | DNA methylase N-4/N-6 domain protein; This methylase recognizes the double-stranded sequence GANTC and causes specific methylation on A-2 on both strands. CcrM-mediated methylation has important cellular functions. Appears to contribute to the accurate cell-cycle control of DNA replication and cellular morphology. Essential for viability; Belongs to the N(4)/N(6)-methyltransferase family. | 0.440 |
Oant_0914 | secE | Oant_0914 | Oant_1941 | TIGRFAM: cobalt chelatase, pCobS small subunit; PFAM: ATPase associated with various cellular activities AAA_5; KEGG: bmb:BruAb1_1997 cobalamin biosynthesis protein, hypothetical. | Preprotein translocase, SecE subunit; Essential subunit of the Sec protein translocation channel SecYEG. Clamps together the 2 halves of SecY. May contact the channel plug during translocation. | 0.545 |
Oant_0915 | Oant_0393 | Oant_0915 | Oant_0393 | KEGG: bme:BMEI0050 CobT protein; TIGRFAM: cobalt chelatase, pCobT subunit; PFAM: Cobalt chelatase CobT subunit; SMART: von Willebrand factor type A. | PFAM: GcrA cell cycle regulator; KEGG: bmb:BruAb1_0325 hypothetical protein. | 0.642 |
Oant_0915 | Oant_0914 | Oant_0915 | Oant_0914 | KEGG: bme:BMEI0050 CobT protein; TIGRFAM: cobalt chelatase, pCobT subunit; PFAM: Cobalt chelatase CobT subunit; SMART: von Willebrand factor type A. | TIGRFAM: cobalt chelatase, pCobS small subunit; PFAM: ATPase associated with various cellular activities AAA_5; KEGG: bmb:BruAb1_1997 cobalamin biosynthesis protein, hypothetical. | 0.991 |
Oant_0915 | atpF2 | Oant_0915 | Oant_0503 | KEGG: bme:BMEI0050 CobT protein; TIGRFAM: cobalt chelatase, pCobT subunit; PFAM: Cobalt chelatase CobT subunit; SMART: von Willebrand factor type A. | ATP synthase F0, B subunit; 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. | 0.564 |
Oant_0915 | ccrM | Oant_0915 | Oant_0605 | KEGG: bme:BMEI0050 CobT protein; TIGRFAM: cobalt chelatase, pCobT subunit; PFAM: Cobalt chelatase CobT subunit; SMART: von Willebrand factor type A. | DNA methylase N-4/N-6 domain protein; This methylase recognizes the double-stranded sequence GANTC and causes specific methylation on A-2 on both strands. CcrM-mediated methylation has important cellular functions. Appears to contribute to the accurate cell-cycle control of DNA replication and cellular morphology. Essential for viability; Belongs to the N(4)/N(6)-methyltransferase family. | 0.524 |
Oant_0915 | secE | Oant_0915 | Oant_1941 | KEGG: bme:BMEI0050 CobT protein; TIGRFAM: cobalt chelatase, pCobT subunit; PFAM: Cobalt chelatase CobT subunit; SMART: von Willebrand factor type A. | Preprotein translocase, SecE subunit; Essential subunit of the Sec protein translocation channel SecYEG. Clamps together the 2 halves of SecY. May contact the channel plug during translocation. | 0.641 |
Oant_1272 | ccrM | Oant_1272 | Oant_0605 | PFAM: HNH endonuclease; SMART: HNH nuclease; KEGG: bms:BR1643 HNH endonuclease family protein. | DNA methylase N-4/N-6 domain protein; This methylase recognizes the double-stranded sequence GANTC and causes specific methylation on A-2 on both strands. CcrM-mediated methylation has important cellular functions. Appears to contribute to the accurate cell-cycle control of DNA replication and cellular morphology. Essential for viability; Belongs to the N(4)/N(6)-methyltransferase family. | 0.446 |
atpF2 | Oant_0393 | Oant_0503 | Oant_0393 | ATP synthase F0, B subunit; 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. | PFAM: GcrA cell cycle regulator; KEGG: bmb:BruAb1_0325 hypothetical protein. | 0.568 |
atpF2 | Oant_0914 | Oant_0503 | Oant_0914 | ATP synthase F0, B subunit; 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. | TIGRFAM: cobalt chelatase, pCobS small subunit; PFAM: ATPase associated with various cellular activities AAA_5; KEGG: bmb:BruAb1_1997 cobalamin biosynthesis protein, hypothetical. | 0.460 |
atpF2 | Oant_0915 | Oant_0503 | Oant_0915 | ATP synthase F0, B subunit; 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. | KEGG: bme:BMEI0050 CobT protein; TIGRFAM: cobalt chelatase, pCobT subunit; PFAM: Cobalt chelatase CobT subunit; SMART: von Willebrand factor type A. | 0.564 |
atpF2 | ccrM | Oant_0503 | Oant_0605 | ATP synthase F0, B subunit; 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. | DNA methylase N-4/N-6 domain protein; This methylase recognizes the double-stranded sequence GANTC and causes specific methylation on A-2 on both strands. CcrM-mediated methylation has important cellular functions. Appears to contribute to the accurate cell-cycle control of DNA replication and cellular morphology. Essential for viability; Belongs to the N(4)/N(6)-methyltransferase family. | 0.472 |