node1 | node2 | node1 accession | node2 accession | node1 annotation | node2 annotation | score |
HIST1H4A | HIST2H2AA3 | ENSP00000352980 | ENSP00000358158 | histone cluster 1, H4a | histone cluster 2, H2aa3 | 0.849 |
HIST1H4A | HIST2H2AC | ENSP00000352980 | ENSP00000332194 | histone cluster 1, H4a | histone cluster 2, H2ac; Core component of nucleosome. Nucleosomes wrap and compact DNA into chromatin, limiting DNA accessibility to the cellular machineries which require DNA as a template. Histones thereby play a central role in transcription regulation, DNA repair, DNA replication and chromosomal stability. DNA accessibility is regulated via a complex set of post-translational modifications of histones, also called histone code, and nucleosome remodeling | 0.968 |
HIST1H4A | KAT8 | ENSP00000352980 | ENSP00000406037 | histone cluster 1, H4a | K(lysine) acetyltransferase 8 | 0.891 |
HIST1H4A | MSL2 | ENSP00000352980 | ENSP00000311827 | histone cluster 1, H4a | male-specific lethal 2 homolog (Drosophila); Component of histone acetyltransferase complex responsible for the majority of histone H4 acetylation at lysine 16 which is implicated in the formation of higher-order chromatin structure. Acts as an E3 ubiquitin ligase that promotes monoubiquitination of histone H2B at ’Lys-35’ (H2BK34Ub), but not that of H2A. This activity is greatly enhanced by heterodimerization with MSL1. H2B ubiquitination in turn stimulates histine H3 methylation at ’Lys-4’ (H3K4me) and ’Lys-79’ (H3K79me) and leads to gene activation, including that of HOXA9 and MEIS1 | 0.570 |
HIST1H4A | MSL3 | ENSP00000352980 | ENSP00000312244 | histone cluster 1, H4a | male-specific lethal 3 homolog (Drosophila); May be involved in chromatin remodeling and transcriptional regulation. May have a role in X inactivation. Component of the MSL complex which is responsible for the majority of histone H4 acetylation at ’Lys-16’ which is implicated in the formation of higher-order chromatin structure. Specifically recognizes histone H4 monomethylated at ’Lys-20’ (H4K20Me1) in a DNA-dependent manner and is proposed to be involved in chromosomal targeting of the MSL complex | 0.628 |
HIST2H2AA3 | HIST1H4A | ENSP00000358158 | ENSP00000352980 | histone cluster 2, H2aa3 | histone cluster 1, H4a | 0.849 |
HIST2H2AA3 | MSL2 | ENSP00000358158 | ENSP00000311827 | histone cluster 2, H2aa3 | male-specific lethal 2 homolog (Drosophila); Component of histone acetyltransferase complex responsible for the majority of histone H4 acetylation at lysine 16 which is implicated in the formation of higher-order chromatin structure. Acts as an E3 ubiquitin ligase that promotes monoubiquitination of histone H2B at ’Lys-35’ (H2BK34Ub), but not that of H2A. This activity is greatly enhanced by heterodimerization with MSL1. H2B ubiquitination in turn stimulates histine H3 methylation at ’Lys-4’ (H3K4me) and ’Lys-79’ (H3K79me) and leads to gene activation, including that of HOXA9 and MEIS1 | 0.570 |
HIST2H2AC | HIST1H4A | ENSP00000332194 | ENSP00000352980 | histone cluster 2, H2ac; Core component of nucleosome. Nucleosomes wrap and compact DNA into chromatin, limiting DNA accessibility to the cellular machineries which require DNA as a template. Histones thereby play a central role in transcription regulation, DNA repair, DNA replication and chromosomal stability. DNA accessibility is regulated via a complex set of post-translational modifications of histones, also called histone code, and nucleosome remodeling | histone cluster 1, H4a | 0.968 |
HIST2H2AC | KAT8 | ENSP00000332194 | ENSP00000406037 | histone cluster 2, H2ac; Core component of nucleosome. Nucleosomes wrap and compact DNA into chromatin, limiting DNA accessibility to the cellular machineries which require DNA as a template. Histones thereby play a central role in transcription regulation, DNA repair, DNA replication and chromosomal stability. DNA accessibility is regulated via a complex set of post-translational modifications of histones, also called histone code, and nucleosome remodeling | K(lysine) acetyltransferase 8 | 0.497 |
HIST2H2AC | MSL2 | ENSP00000332194 | ENSP00000311827 | histone cluster 2, H2ac; Core component of nucleosome. Nucleosomes wrap and compact DNA into chromatin, limiting DNA accessibility to the cellular machineries which require DNA as a template. Histones thereby play a central role in transcription regulation, DNA repair, DNA replication and chromosomal stability. DNA accessibility is regulated via a complex set of post-translational modifications of histones, also called histone code, and nucleosome remodeling | male-specific lethal 2 homolog (Drosophila); Component of histone acetyltransferase complex responsible for the majority of histone H4 acetylation at lysine 16 which is implicated in the formation of higher-order chromatin structure. Acts as an E3 ubiquitin ligase that promotes monoubiquitination of histone H2B at ’Lys-35’ (H2BK34Ub), but not that of H2A. This activity is greatly enhanced by heterodimerization with MSL1. H2B ubiquitination in turn stimulates histine H3 methylation at ’Lys-4’ (H3K4me) and ’Lys-79’ (H3K79me) and leads to gene activation, including that of HOXA9 and MEIS1 | 0.570 |
HIST2H2AC | MSL3 | ENSP00000332194 | ENSP00000312244 | histone cluster 2, H2ac; Core component of nucleosome. Nucleosomes wrap and compact DNA into chromatin, limiting DNA accessibility to the cellular machineries which require DNA as a template. Histones thereby play a central role in transcription regulation, DNA repair, DNA replication and chromosomal stability. DNA accessibility is regulated via a complex set of post-translational modifications of histones, also called histone code, and nucleosome remodeling | male-specific lethal 3 homolog (Drosophila); May be involved in chromatin remodeling and transcriptional regulation. May have a role in X inactivation. Component of the MSL complex which is responsible for the majority of histone H4 acetylation at ’Lys-16’ which is implicated in the formation of higher-order chromatin structure. Specifically recognizes histone H4 monomethylated at ’Lys-20’ (H4K20Me1) in a DNA-dependent manner and is proposed to be involved in chromosomal targeting of the MSL complex | 0.460 |
HIST2H2AC | TP53 | ENSP00000332194 | ENSP00000269305 | histone cluster 2, H2ac; Core component of nucleosome. Nucleosomes wrap and compact DNA into chromatin, limiting DNA accessibility to the cellular machineries which require DNA as a template. Histones thereby play a central role in transcription regulation, DNA repair, DNA replication and chromosomal stability. DNA accessibility is regulated via a complex set of post-translational modifications of histones, also called histone code, and nucleosome remodeling | tumor protein p53; Acts as a tumor suppressor in many tumor types; induces growth arrest or apoptosis depending on the physiological circumstances and cell type. Involved in cell cycle regulation as a trans-activator that acts to negatively regulate cell division by controlling a set of genes required for this process. One of the activated genes is an inhibitor of cyclin-dependent kinases. Apoptosis induction seems to be mediated either by stimulation of BAX and FAS antigen expression, or by repression of Bcl-2 expression (By similarity) | 0.581 |
HIST2H2AC | UBE2D3 | ENSP00000332194 | ENSP00000349722 | histone cluster 2, H2ac; Core component of nucleosome. Nucleosomes wrap and compact DNA into chromatin, limiting DNA accessibility to the cellular machineries which require DNA as a template. Histones thereby play a central role in transcription regulation, DNA repair, DNA replication and chromosomal stability. DNA accessibility is regulated via a complex set of post-translational modifications of histones, also called histone code, and nucleosome remodeling | ubiquitin-conjugating enzyme E2D 3; Accepts ubiquitin from the E1 complex and catalyzes its covalent attachment to other proteins. In vitro catalyzes ’Lys- 11’-, as well as ’Lys-48’-linked polyubiquitination. Cooperates with the E2 CDC34 and the SCF(FBXW11) E3 ligase complex for the polyubiquitination of NFKBIA leading to its subsequent proteasomal degradation. Acts as an initiator E2, priming the phosphorylated NFKBIA target at positions ’Lys-21’ and/or ’Lys-22’ with a monoubiquitin. Ubiquitin chain elongation is then performed by CDC34, building ubiquitin chains from the UBE2D3-prime [...] | 0.718 |
KAT8 | HIST1H4A | ENSP00000406037 | ENSP00000352980 | K(lysine) acetyltransferase 8 | histone cluster 1, H4a | 0.891 |
KAT8 | HIST2H2AC | ENSP00000406037 | ENSP00000332194 | K(lysine) acetyltransferase 8 | histone cluster 2, H2ac; Core component of nucleosome. Nucleosomes wrap and compact DNA into chromatin, limiting DNA accessibility to the cellular machineries which require DNA as a template. Histones thereby play a central role in transcription regulation, DNA repair, DNA replication and chromosomal stability. DNA accessibility is regulated via a complex set of post-translational modifications of histones, also called histone code, and nucleosome remodeling | 0.497 |
KAT8 | MSL1 | ENSP00000406037 | ENSP00000462945 | K(lysine) acetyltransferase 8 | male-specific lethal 1 homolog (Drosophila); Component of histone acetyltransferase complex responsible for the majority of histone H4 acetylation at ’Lys-16’ (H4K16ac) which is implicated in the formation of higher-order chromatin structure. Greatly enhances MSL2 E3 ubiquitin ligase activity, promoting monoubiquitination of histone H2B at ’Lys-34’ (H2BK34Ub). This modification in turn stimulates histone H3 methylation at ’Lys-4’ (H3K4me) and ’Lys-79’ (H3K79me) and leads to gene activation, including that of HOXA9 and MEIS1 | 0.999 |
KAT8 | MSL2 | ENSP00000406037 | ENSP00000311827 | K(lysine) acetyltransferase 8 | male-specific lethal 2 homolog (Drosophila); Component of histone acetyltransferase complex responsible for the majority of histone H4 acetylation at lysine 16 which is implicated in the formation of higher-order chromatin structure. Acts as an E3 ubiquitin ligase that promotes monoubiquitination of histone H2B at ’Lys-35’ (H2BK34Ub), but not that of H2A. This activity is greatly enhanced by heterodimerization with MSL1. H2B ubiquitination in turn stimulates histine H3 methylation at ’Lys-4’ (H3K4me) and ’Lys-79’ (H3K79me) and leads to gene activation, including that of HOXA9 and MEIS1 | 0.991 |
KAT8 | MSL3 | ENSP00000406037 | ENSP00000312244 | K(lysine) acetyltransferase 8 | male-specific lethal 3 homolog (Drosophila); May be involved in chromatin remodeling and transcriptional regulation. May have a role in X inactivation. Component of the MSL complex which is responsible for the majority of histone H4 acetylation at ’Lys-16’ which is implicated in the formation of higher-order chromatin structure. Specifically recognizes histone H4 monomethylated at ’Lys-20’ (H4K20Me1) in a DNA-dependent manner and is proposed to be involved in chromosomal targeting of the MSL complex | 0.999 |
KAT8 | TP53 | ENSP00000406037 | ENSP00000269305 | K(lysine) acetyltransferase 8 | tumor protein p53; Acts as a tumor suppressor in many tumor types; induces growth arrest or apoptosis depending on the physiological circumstances and cell type. Involved in cell cycle regulation as a trans-activator that acts to negatively regulate cell division by controlling a set of genes required for this process. One of the activated genes is an inhibitor of cyclin-dependent kinases. Apoptosis induction seems to be mediated either by stimulation of BAX and FAS antigen expression, or by repression of Bcl-2 expression (By similarity) | 0.995 |
MFHAS1 | MSL2 | ENSP00000276282 | ENSP00000311827 | malignant fibrous histiocytoma amplified sequence 1 | male-specific lethal 2 homolog (Drosophila); Component of histone acetyltransferase complex responsible for the majority of histone H4 acetylation at lysine 16 which is implicated in the formation of higher-order chromatin structure. Acts as an E3 ubiquitin ligase that promotes monoubiquitination of histone H2B at ’Lys-35’ (H2BK34Ub), but not that of H2A. This activity is greatly enhanced by heterodimerization with MSL1. H2B ubiquitination in turn stimulates histine H3 methylation at ’Lys-4’ (H3K4me) and ’Lys-79’ (H3K79me) and leads to gene activation, including that of HOXA9 and MEIS1 | 0.657 |