node1 | node2 | node1 accession | node2 accession | node1 annotation | node2 annotation | score |
LOC107900946 | LOC107912324 | A0A1U8IVY2 | A0A1U8K0A3 | Protein SDE2 homolog. | DNA replication licensing factor MCM7; Acts as component of the mcm2-7 complex (mcm complex) which is the putative replicative helicase essential for 'once per cell cycle' DNA replication initiation and elongation in eukaryotic cells. The active ATPase sites in the mcm2-7 ring are formed through the interaction surfaces of two neighboring subunits such that a critical structure of a conserved arginine finger motif is provided in trans relative to the ATP-binding site of the Walker A box of the adjacent subunit. The six ATPase active sites, however, are likely to contribute differential [...] | 0.693 |
LOC107900946 | LOC107913425 | A0A1U8IVY2 | A0A1U8KA19 | Protein SDE2 homolog. | Ubiquitin-like modifier-activating enzyme 5. | 0.671 |
LOC107900946 | LOC107923086 | A0A1U8IVY2 | A0A1U8L291 | Protein SDE2 homolog. | E3 ubiquitin-protein ligase TRAIP-like isoform X1. | 0.408 |
LOC107900946 | LOC107924650 | A0A1U8IVY2 | A0A1U8LBB4 | Protein SDE2 homolog. | DNA replication licensing factor MCM7; Acts as component of the mcm2-7 complex (mcm complex) which is the putative replicative helicase essential for 'once per cell cycle' DNA replication initiation and elongation in eukaryotic cells. The active ATPase sites in the mcm2-7 ring are formed through the interaction surfaces of two neighboring subunits such that a critical structure of a conserved arginine finger motif is provided in trans relative to the ATP-binding site of the Walker A box of the adjacent subunit. The six ATPase active sites, however, are likely to contribute differential [...] | 0.693 |
LOC107912324 | LOC107900946 | A0A1U8K0A3 | A0A1U8IVY2 | DNA replication licensing factor MCM7; Acts as component of the mcm2-7 complex (mcm complex) which is the putative replicative helicase essential for 'once per cell cycle' DNA replication initiation and elongation in eukaryotic cells. The active ATPase sites in the mcm2-7 ring are formed through the interaction surfaces of two neighboring subunits such that a critical structure of a conserved arginine finger motif is provided in trans relative to the ATP-binding site of the Walker A box of the adjacent subunit. The six ATPase active sites, however, are likely to contribute differential [...] | Protein SDE2 homolog. | 0.693 |
LOC107912324 | LOC107923086 | A0A1U8K0A3 | A0A1U8L291 | DNA replication licensing factor MCM7; Acts as component of the mcm2-7 complex (mcm complex) which is the putative replicative helicase essential for 'once per cell cycle' DNA replication initiation and elongation in eukaryotic cells. The active ATPase sites in the mcm2-7 ring are formed through the interaction surfaces of two neighboring subunits such that a critical structure of a conserved arginine finger motif is provided in trans relative to the ATP-binding site of the Walker A box of the adjacent subunit. The six ATPase active sites, however, are likely to contribute differential [...] | E3 ubiquitin-protein ligase TRAIP-like isoform X1. | 0.411 |
LOC107912324 | LOC107924650 | A0A1U8K0A3 | A0A1U8LBB4 | DNA replication licensing factor MCM7; Acts as component of the mcm2-7 complex (mcm complex) which is the putative replicative helicase essential for 'once per cell cycle' DNA replication initiation and elongation in eukaryotic cells. The active ATPase sites in the mcm2-7 ring are formed through the interaction surfaces of two neighboring subunits such that a critical structure of a conserved arginine finger motif is provided in trans relative to the ATP-binding site of the Walker A box of the adjacent subunit. The six ATPase active sites, however, are likely to contribute differential [...] | DNA replication licensing factor MCM7; Acts as component of the mcm2-7 complex (mcm complex) which is the putative replicative helicase essential for 'once per cell cycle' DNA replication initiation and elongation in eukaryotic cells. The active ATPase sites in the mcm2-7 ring are formed through the interaction surfaces of two neighboring subunits such that a critical structure of a conserved arginine finger motif is provided in trans relative to the ATP-binding site of the Walker A box of the adjacent subunit. The six ATPase active sites, however, are likely to contribute differential [...] | 0.900 |
LOC107912324 | LOC107925704 | A0A1U8K0A3 | A0A1U8LFH1 | DNA replication licensing factor MCM7; Acts as component of the mcm2-7 complex (mcm complex) which is the putative replicative helicase essential for 'once per cell cycle' DNA replication initiation and elongation in eukaryotic cells. The active ATPase sites in the mcm2-7 ring are formed through the interaction surfaces of two neighboring subunits such that a critical structure of a conserved arginine finger motif is provided in trans relative to the ATP-binding site of the Walker A box of the adjacent subunit. The six ATPase active sites, however, are likely to contribute differential [...] | Cell division control protein 45 homolog. | 0.999 |
LOC107912324 | LOC107938161 | A0A1U8K0A3 | A0A1U8MMA6 | DNA replication licensing factor MCM7; Acts as component of the mcm2-7 complex (mcm complex) which is the putative replicative helicase essential for 'once per cell cycle' DNA replication initiation and elongation in eukaryotic cells. The active ATPase sites in the mcm2-7 ring are formed through the interaction surfaces of two neighboring subunits such that a critical structure of a conserved arginine finger motif is provided in trans relative to the ATP-binding site of the Walker A box of the adjacent subunit. The six ATPase active sites, however, are likely to contribute differential [...] | Protein SDE2 homolog. | 0.693 |
LOC107912324 | LOC107945861 | A0A1U8K0A3 | A0A1U8NCD5 | DNA replication licensing factor MCM7; Acts as component of the mcm2-7 complex (mcm complex) which is the putative replicative helicase essential for 'once per cell cycle' DNA replication initiation and elongation in eukaryotic cells. The active ATPase sites in the mcm2-7 ring are formed through the interaction surfaces of two neighboring subunits such that a critical structure of a conserved arginine finger motif is provided in trans relative to the ATP-binding site of the Walker A box of the adjacent subunit. The six ATPase active sites, however, are likely to contribute differential [...] | Protein SDE2 homolog. | 0.693 |
LOC107913425 | LOC107900946 | A0A1U8KA19 | A0A1U8IVY2 | Ubiquitin-like modifier-activating enzyme 5. | Protein SDE2 homolog. | 0.671 |
LOC107913425 | LOC107923086 | A0A1U8KA19 | A0A1U8L291 | Ubiquitin-like modifier-activating enzyme 5. | E3 ubiquitin-protein ligase TRAIP-like isoform X1. | 0.541 |
LOC107913425 | LOC107925704 | A0A1U8KA19 | A0A1U8LFH1 | Ubiquitin-like modifier-activating enzyme 5. | Cell division control protein 45 homolog. | 0.722 |
LOC107913425 | LOC107938161 | A0A1U8KA19 | A0A1U8MMA6 | Ubiquitin-like modifier-activating enzyme 5. | Protein SDE2 homolog. | 0.671 |
LOC107913425 | LOC107945861 | A0A1U8KA19 | A0A1U8NCD5 | Ubiquitin-like modifier-activating enzyme 5. | Protein SDE2 homolog. | 0.671 |
LOC107914186 | LOC107923086 | A0A1U8KCU6 | A0A1U8L291 | formamidopyrimidine-DNA glycosylase-like. | E3 ubiquitin-protein ligase TRAIP-like isoform X1. | 0.525 |
LOC107914186 | LOC107925704 | A0A1U8KCU6 | A0A1U8LFH1 | formamidopyrimidine-DNA glycosylase-like. | Cell division control protein 45 homolog. | 0.650 |
LOC107922455 | LOC107923086 | A0A1U8L002 | A0A1U8L291 | SWR1 complex bromodomain subunit bdf1-like. | E3 ubiquitin-protein ligase TRAIP-like isoform X1. | 0.450 |
LOC107923086 | LOC107900946 | A0A1U8L291 | A0A1U8IVY2 | E3 ubiquitin-protein ligase TRAIP-like isoform X1. | Protein SDE2 homolog. | 0.408 |
LOC107923086 | LOC107912324 | A0A1U8L291 | A0A1U8K0A3 | E3 ubiquitin-protein ligase TRAIP-like isoform X1. | DNA replication licensing factor MCM7; Acts as component of the mcm2-7 complex (mcm complex) which is the putative replicative helicase essential for 'once per cell cycle' DNA replication initiation and elongation in eukaryotic cells. The active ATPase sites in the mcm2-7 ring are formed through the interaction surfaces of two neighboring subunits such that a critical structure of a conserved arginine finger motif is provided in trans relative to the ATP-binding site of the Walker A box of the adjacent subunit. The six ATPase active sites, however, are likely to contribute differential [...] | 0.411 |