node1 | node2 | node1 accession | node2 accession | node1 annotation | node2 annotation | score |
MCM7 | Z520_06399 | A0A0D2ILH4 | A0A0D2IKS9 | 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 [...] | FACT complex subunit POB3; Component of the FACT complex, a general chromatin factor that acts to reorganize nucleosomes. The FACT complex is involved in multiple processes that require DNA as a template such as mRNA elongation, DNA replication and DNA repair. During transcription elongation the FACT complex acts as a histone chaperone that both destabilizes and restores nucleosomal structure. It facilitates the passage of RNA polymerase II and transcription by promoting the dissociation of one histone H2A-H2B dimer from the nucleosome, then subsequently promotes the reestablishment of [...] | 0.676 |
MCM7 | Z520_06802 | A0A0D2ILH4 | A0A0D2H684 | 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 helicase; Belongs to the MCM family. | 0.999 |
MCM7 | Z520_11776 | A0A0D2ILH4 | A0A0D2I5D5 | 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 [...] | Histone H2A; Belongs to the histone H2A family. | 0.564 |
MCM7 | Z520_12380 | A0A0D2ILH4 | A0A0D2JFH9 | 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 helicase; Belongs to the MCM family. | 0.999 |
Z520_00446 | Z520_01045 | A0A0D2KJV3 | A0A0D2KGJ8 | Histone-lysine N-methyltransferase, H3 lysine-79 specific; Histone methyltransferase that specifically methylates histone H3 to form H3K79me. This methylation is required for telomere silencing and for the pachytene checkpoint during the meiotic cell cycle by allowing the recruitment of RAD9 to double strand breaks. Nucleosomes are preferred as substrate compared to free histones. | Histone acetyltransferase; Belongs to the MYST (SAS/MOZ) family. | 0.588 |
Z520_00446 | Z520_03942 | A0A0D2KJV3 | A0A0D2ITF8 | Histone-lysine N-methyltransferase, H3 lysine-79 specific; Histone methyltransferase that specifically methylates histone H3 to form H3K79me. This methylation is required for telomere silencing and for the pachytene checkpoint during the meiotic cell cycle by allowing the recruitment of RAD9 to double strand breaks. Nucleosomes are preferred as substrate compared to free histones. | Deacetylase sirtuin-type domain-containing protein. | 0.493 |
Z520_00446 | Z520_07060 | A0A0D2KJV3 | A0A0D2IIX1 | Histone-lysine N-methyltransferase, H3 lysine-79 specific; Histone methyltransferase that specifically methylates histone H3 to form H3K79me. This methylation is required for telomere silencing and for the pachytene checkpoint during the meiotic cell cycle by allowing the recruitment of RAD9 to double strand breaks. Nucleosomes are preferred as substrate compared to free histones. | Uncharacterized protein. | 0.456 |
Z520_00446 | Z520_08743 | A0A0D2KJV3 | A0A0D2KG23 | Histone-lysine N-methyltransferase, H3 lysine-79 specific; Histone methyltransferase that specifically methylates histone H3 to form H3K79me. This methylation is required for telomere silencing and for the pachytene checkpoint during the meiotic cell cycle by allowing the recruitment of RAD9 to double strand breaks. Nucleosomes are preferred as substrate compared to free histones. | Deacetylase sirtuin-type domain-containing protein. | 0.493 |
Z520_00446 | Z520_11776 | A0A0D2KJV3 | A0A0D2I5D5 | Histone-lysine N-methyltransferase, H3 lysine-79 specific; Histone methyltransferase that specifically methylates histone H3 to form H3K79me. This methylation is required for telomere silencing and for the pachytene checkpoint during the meiotic cell cycle by allowing the recruitment of RAD9 to double strand breaks. Nucleosomes are preferred as substrate compared to free histones. | Histone H2A; Belongs to the histone H2A family. | 0.413 |
Z520_00547 | Z520_07578 | A0A0D2HPT1 | A0A0D2KJW5 | CULLIN_2 domain-containing protein; Belongs to the cullin family. | Uncharacterized protein. | 0.523 |
Z520_00547 | Z520_08402 | A0A0D2HPT1 | A0A0D2H1I1 | CULLIN_2 domain-containing protein; Belongs to the cullin family. | Chromo domain-containing protein. | 0.507 |
Z520_01045 | Z520_00446 | A0A0D2KGJ8 | A0A0D2KJV3 | Histone acetyltransferase; Belongs to the MYST (SAS/MOZ) family. | Histone-lysine N-methyltransferase, H3 lysine-79 specific; Histone methyltransferase that specifically methylates histone H3 to form H3K79me. This methylation is required for telomere silencing and for the pachytene checkpoint during the meiotic cell cycle by allowing the recruitment of RAD9 to double strand breaks. Nucleosomes are preferred as substrate compared to free histones. | 0.588 |
Z520_01045 | Z520_01901 | A0A0D2KGJ8 | A0A0D2K748 | Histone acetyltransferase; Belongs to the MYST (SAS/MOZ) family. | Uncharacterized protein. | 0.638 |
Z520_01045 | Z520_03942 | A0A0D2KGJ8 | A0A0D2ITF8 | Histone acetyltransferase; Belongs to the MYST (SAS/MOZ) family. | Deacetylase sirtuin-type domain-containing protein. | 0.421 |
Z520_01045 | Z520_07060 | A0A0D2KGJ8 | A0A0D2IIX1 | Histone acetyltransferase; Belongs to the MYST (SAS/MOZ) family. | Uncharacterized protein. | 0.871 |
Z520_01045 | Z520_07578 | A0A0D2KGJ8 | A0A0D2KJW5 | Histone acetyltransferase; Belongs to the MYST (SAS/MOZ) family. | Uncharacterized protein. | 0.440 |
Z520_01045 | Z520_08743 | A0A0D2KGJ8 | A0A0D2KG23 | Histone acetyltransferase; Belongs to the MYST (SAS/MOZ) family. | Deacetylase sirtuin-type domain-containing protein. | 0.421 |
Z520_01045 | Z520_11083 | A0A0D2KGJ8 | A0A0D2KA04 | Histone acetyltransferase; Belongs to the MYST (SAS/MOZ) family. | Hist_deacetyl domain-containing protein. | 0.638 |
Z520_01045 | Z520_11776 | A0A0D2KGJ8 | A0A0D2I5D5 | Histone acetyltransferase; Belongs to the MYST (SAS/MOZ) family. | Histone H2A; Belongs to the histone H2A family. | 0.759 |
Z520_01901 | Z520_01045 | A0A0D2K748 | A0A0D2KGJ8 | Uncharacterized protein. | Histone acetyltransferase; Belongs to the MYST (SAS/MOZ) family. | 0.638 |