node1 | node2 | node1 accession | node2 accession | node1 annotation | node2 annotation | score |
ANKRD66 | MEP1A | ENSP00000454770 | ENSP00000230588 | Ankyrin repeat domain-containing protein 66; Ankyrin repeat domain containing | Meprin A subunit alpha; Belongs to the peptidase M12A family | 0.559 |
ANKRD66 | MEP1B | ENSP00000454770 | ENSP00000269202 | Ankyrin repeat domain-containing protein 66; Ankyrin repeat domain containing | Meprin A subunit beta; Membrane metallopeptidase that sheds many membrane-bound proteins. Exhibits a strong preference for acidic amino acids at the P1’ position. Known substrates include- FGF19, VGFA, IL1B, IL18, procollagen I and III, E-cadherin, KLK7, gastrin, ADAM10, tenascin-C. The presence of several pro-inflammatory cytokine among substrates implicate MEP1B in inflammation. It is also involved in tissue remodeling due to its capability to degrade extracellular matrix components; Astacins | 0.545 |
ANKRD66 | PLA2G7 | ENSP00000454770 | ENSP00000274793 | Ankyrin repeat domain-containing protein 66; Ankyrin repeat domain containing | Platelet-activating factor acetylhydrolase; Modulates the action of platelet-activating factor (PAF) by hydrolyzing the sn-2 ester bond to yield the biologically inactive lyso-PAF. Has a specificity for substrates with a short residue at the sn-2 position. It is inactive against long-chain phospholipids; Phospholipases | 0.447 |
ANKRD66 | RNF125 | ENSP00000454770 | ENSP00000217740 | Ankyrin repeat domain-containing protein 66; Ankyrin repeat domain containing | E3 ubiquitin-protein ligase RNF125; E3 ubiquitin-protein ligase that mediates ubiquitination and subsequent proteasomal degradation of target proteins, such as DDX58/RIG-I, MAVS/IPS1, IFIH1/MDA5, JAK1 and p53/TP53. Acts as a negative regulator of type I interferon production by mediating ubiquitination of DDX58/RIG-I at ’Lys-181’, leading to DDX58/RIG-I degradation. Mediates ubiquitination and subsequent degradation of p53/TP53. Mediates ubiquitination and subsequent degradation of JAK1. Acts as a positive regulator of T-cell activation; Ring finger proteins | 0.519 |
ANKRD66 | RNF138 | ENSP00000454770 | ENSP00000261593 | Ankyrin repeat domain-containing protein 66; Ankyrin repeat domain containing | E3 ubiquitin-protein ligase RNF138; E3 ubiquitin-protein ligase involved in DNA damage response by promoting DNA resection and homologous recombination. Recruited to sites of double- strand breaks following DNA damage and specifically promotes double-strand break repair via homologous recombination. Two different, non-exclusive, mechanisms have been proposed. According to a report, regulates the choice of double-strand break repair by favoring homologous recombination over non-homologous end joining (NHEJ)- acts by mediating ubiquitination of XRCC5/Ku80, leading to remove the Ku comple [...] | 0.559 |
ANKRD66 | TDRD6 | ENSP00000454770 | ENSP00000346065 | Ankyrin repeat domain-containing protein 66; Ankyrin repeat domain containing | Tudor domain-containing protein 6; Involved in spermiogenesis, chromatoid body formation and for proper precursor and mature miRNA expression; Tudor domain containing | 0.595 |
ANKRD66 | TRAPPC8 | ENSP00000454770 | ENSP00000283351 | Ankyrin repeat domain-containing protein 66; Ankyrin repeat domain containing | Trafficking protein particle complex subunit 8; May be involved in endoplasmic reticulum to Golgi apparatus trafficking at a very early stage; Trafficking protein particle complex | 0.587 |
MEP1A | ANKRD66 | ENSP00000230588 | ENSP00000454770 | Meprin A subunit alpha; Belongs to the peptidase M12A family | Ankyrin repeat domain-containing protein 66; Ankyrin repeat domain containing | 0.559 |
MEP1A | MEP1B | ENSP00000230588 | ENSP00000269202 | Meprin A subunit alpha; Belongs to the peptidase M12A family | Meprin A subunit beta; Membrane metallopeptidase that sheds many membrane-bound proteins. Exhibits a strong preference for acidic amino acids at the P1’ position. Known substrates include- FGF19, VGFA, IL1B, IL18, procollagen I and III, E-cadherin, KLK7, gastrin, ADAM10, tenascin-C. The presence of several pro-inflammatory cytokine among substrates implicate MEP1B in inflammation. It is also involved in tissue remodeling due to its capability to degrade extracellular matrix components; Astacins | 0.900 |
MEP1A | PLA2G7 | ENSP00000230588 | ENSP00000274793 | Meprin A subunit alpha; Belongs to the peptidase M12A family | Platelet-activating factor acetylhydrolase; Modulates the action of platelet-activating factor (PAF) by hydrolyzing the sn-2 ester bond to yield the biologically inactive lyso-PAF. Has a specificity for substrates with a short residue at the sn-2 position. It is inactive against long-chain phospholipids; Phospholipases | 0.573 |
MEP1A | RNF125 | ENSP00000230588 | ENSP00000217740 | Meprin A subunit alpha; Belongs to the peptidase M12A family | E3 ubiquitin-protein ligase RNF125; E3 ubiquitin-protein ligase that mediates ubiquitination and subsequent proteasomal degradation of target proteins, such as DDX58/RIG-I, MAVS/IPS1, IFIH1/MDA5, JAK1 and p53/TP53. Acts as a negative regulator of type I interferon production by mediating ubiquitination of DDX58/RIG-I at ’Lys-181’, leading to DDX58/RIG-I degradation. Mediates ubiquitination and subsequent degradation of p53/TP53. Mediates ubiquitination and subsequent degradation of JAK1. Acts as a positive regulator of T-cell activation; Ring finger proteins | 0.653 |
MEP1A | RNF138 | ENSP00000230588 | ENSP00000261593 | Meprin A subunit alpha; Belongs to the peptidase M12A family | E3 ubiquitin-protein ligase RNF138; E3 ubiquitin-protein ligase involved in DNA damage response by promoting DNA resection and homologous recombination. Recruited to sites of double- strand breaks following DNA damage and specifically promotes double-strand break repair via homologous recombination. Two different, non-exclusive, mechanisms have been proposed. According to a report, regulates the choice of double-strand break repair by favoring homologous recombination over non-homologous end joining (NHEJ)- acts by mediating ubiquitination of XRCC5/Ku80, leading to remove the Ku comple [...] | 0.668 |
MEP1A | TDRD6 | ENSP00000230588 | ENSP00000346065 | Meprin A subunit alpha; Belongs to the peptidase M12A family | Tudor domain-containing protein 6; Involved in spermiogenesis, chromatoid body formation and for proper precursor and mature miRNA expression; Tudor domain containing | 0.521 |
MEP1A | TRAPPC8 | ENSP00000230588 | ENSP00000283351 | Meprin A subunit alpha; Belongs to the peptidase M12A family | Trafficking protein particle complex subunit 8; May be involved in endoplasmic reticulum to Golgi apparatus trafficking at a very early stage; Trafficking protein particle complex | 0.667 |
MEP1B | ANKRD66 | ENSP00000269202 | ENSP00000454770 | Meprin A subunit beta; Membrane metallopeptidase that sheds many membrane-bound proteins. Exhibits a strong preference for acidic amino acids at the P1’ position. Known substrates include- FGF19, VGFA, IL1B, IL18, procollagen I and III, E-cadherin, KLK7, gastrin, ADAM10, tenascin-C. The presence of several pro-inflammatory cytokine among substrates implicate MEP1B in inflammation. It is also involved in tissue remodeling due to its capability to degrade extracellular matrix components; Astacins | Ankyrin repeat domain-containing protein 66; Ankyrin repeat domain containing | 0.545 |
MEP1B | MEP1A | ENSP00000269202 | ENSP00000230588 | Meprin A subunit beta; Membrane metallopeptidase that sheds many membrane-bound proteins. Exhibits a strong preference for acidic amino acids at the P1’ position. Known substrates include- FGF19, VGFA, IL1B, IL18, procollagen I and III, E-cadherin, KLK7, gastrin, ADAM10, tenascin-C. The presence of several pro-inflammatory cytokine among substrates implicate MEP1B in inflammation. It is also involved in tissue remodeling due to its capability to degrade extracellular matrix components; Astacins | Meprin A subunit alpha; Belongs to the peptidase M12A family | 0.900 |
MEP1B | TRAPPC8 | ENSP00000269202 | ENSP00000283351 | Meprin A subunit beta; Membrane metallopeptidase that sheds many membrane-bound proteins. Exhibits a strong preference for acidic amino acids at the P1’ position. Known substrates include- FGF19, VGFA, IL1B, IL18, procollagen I and III, E-cadherin, KLK7, gastrin, ADAM10, tenascin-C. The presence of several pro-inflammatory cytokine among substrates implicate MEP1B in inflammation. It is also involved in tissue remodeling due to its capability to degrade extracellular matrix components; Astacins | Trafficking protein particle complex subunit 8; May be involved in endoplasmic reticulum to Golgi apparatus trafficking at a very early stage; Trafficking protein particle complex | 0.520 |
PLA2G7 | ANKRD66 | ENSP00000274793 | ENSP00000454770 | Platelet-activating factor acetylhydrolase; Modulates the action of platelet-activating factor (PAF) by hydrolyzing the sn-2 ester bond to yield the biologically inactive lyso-PAF. Has a specificity for substrates with a short residue at the sn-2 position. It is inactive against long-chain phospholipids; Phospholipases | Ankyrin repeat domain-containing protein 66; Ankyrin repeat domain containing | 0.447 |
PLA2G7 | MEP1A | ENSP00000274793 | ENSP00000230588 | Platelet-activating factor acetylhydrolase; Modulates the action of platelet-activating factor (PAF) by hydrolyzing the sn-2 ester bond to yield the biologically inactive lyso-PAF. Has a specificity for substrates with a short residue at the sn-2 position. It is inactive against long-chain phospholipids; Phospholipases | Meprin A subunit alpha; Belongs to the peptidase M12A family | 0.573 |
PLA2G7 | RNF125 | ENSP00000274793 | ENSP00000217740 | Platelet-activating factor acetylhydrolase; Modulates the action of platelet-activating factor (PAF) by hydrolyzing the sn-2 ester bond to yield the biologically inactive lyso-PAF. Has a specificity for substrates with a short residue at the sn-2 position. It is inactive against long-chain phospholipids; Phospholipases | E3 ubiquitin-protein ligase RNF125; E3 ubiquitin-protein ligase that mediates ubiquitination and subsequent proteasomal degradation of target proteins, such as DDX58/RIG-I, MAVS/IPS1, IFIH1/MDA5, JAK1 and p53/TP53. Acts as a negative regulator of type I interferon production by mediating ubiquitination of DDX58/RIG-I at ’Lys-181’, leading to DDX58/RIG-I degradation. Mediates ubiquitination and subsequent degradation of p53/TP53. Mediates ubiquitination and subsequent degradation of JAK1. Acts as a positive regulator of T-cell activation; Ring finger proteins | 0.518 |