RNF20 and PA2G4

Number of citations of the paper that reports this interaction (PMID 19037095)
8

Data Source:
BioGRID (enzymatic study, affinity chromatography technology, imaging technique)

		RNF20	PA2G4
Gene Name		ring finger protein 20, E3 ubiquitin protein ligase	proliferation-associated 2G4, 38kDa
Image		No pdb structure
Gene Ontology Annotations	Cellular Component	Ubiquitin Ligase Complex Nucleus Nucleoplasm Nucleolus HULC Complex	Nucleus Nucleoplasm Nucleolus Cytoplasm Membrane Ribonucleoprotein Complex Extracellular Vesicular Exosome
	Molecular Function	P53 Binding Chromatin Binding Transcription Coactivator Activity Ubiquitin-protein Transferase Activity Protein Binding Zinc Ion Binding Ligase Activity Ubiquitin Protein Ligase Binding Histone Binding	DNA Binding Sequence-specific DNA Binding Transcription Factor Activity Protein Binding Ubiquitin Protein Ligase Binding Poly(A) RNA Binding
	Biological Process	Protein Polyubiquitination Regulation Of Transcription, DNA-templated Ubiquitin-dependent Protein Catabolic Process Histone Monoubiquitination Negative Regulation Of Cell Migration Positive Regulation Of Histone Methylation Histone H2B Ubiquitination Positive Regulation Of Transcription, DNA-templated	Transcription, DNA-templated RRNA Processing Regulation Of Translation Cell Cycle Arrest Cell Proliferation Negative Regulation Of Apoptotic Process Positive Regulation Of Cell Differentiation Negative Regulation Of Transcription, DNA-templated
Pathways
Drugs
Diseases
GWAS			Vitiligo ( 22951725)
Protein-Protein Interactions		22 interactors: AMOTL2 ATM CDC73 HIST1H2BB HIST2H2AA3 HIST2H2AC HIST2H2BE HIST2H3C HIST2H4A HTT ITSN2 MSL1 PA2G4 PAF1 SMURF2 UBC UBE2A UBE2B UBE2E1 USHBP1 WAC ZDHHC17	20 interactors: AR ATR ERBB3 EXOSC5 FUS HDAC2 HMGA1 HMGA2 IKBKG LIG4 MTOR PRKCA PRKCB PRKCG RB1 RNF20 SIN3A SUMO4 TERF1 UBC
Entrez ID		56254	5036
HPRD ID		07410	03685
Ensembl ID		ENSG00000155827	ENSG00000170515
Uniprot IDs		Q5VTR2	Q9UQ80
PDB IDs			2Q8K 3J2I
Enriched GO Terms of Interacting Partners?		Histone Ubiquitination Chromatin Organization Histone Modification Histone H2B Ubiquitination Chromosome Organization Protein Monoubiquitination Chromatin Modification Histone Monoubiquitination Protein Ubiquitination Protein Modification By Small Protein Conjugation Negative Regulation Of Cellular Metabolic Process Cell Cycle Negative Regulation Of Transcription, DNA-templated Organelle Organization Negative Regulation Of Nucleic Acid-templated Transcription Negative Regulation Of RNA Biosynthetic Process Cellular Protein Modification Process Chromatin Silencing Protein K48-linked Ubiquitination Negative Regulation Of Mitotic Cell Cycle Phase Transition Negative Regulation Of Gene Expression Regulation Of Cell Cycle Negative Regulation Of Biosynthetic Process Protein Catabolic Process Protein Polyubiquitination Cell Cycle Process Negative Regulation Of Proteasomal Ubiquitin-dependent Protein Catabolic Process Negative Regulation Of Proteasomal Protein Catabolic Process G1 DNA Damage Checkpoint Negative Regulation Of Cell Cycle Regulation Of Mitotic Cell Cycle Phase Transition Negative Regulation Of Gene Expression, Epigenetic Negative Regulation Of Mitotic Cell Cycle Negative Regulation Of Cellular Protein Catabolic Process Cell Cycle Checkpoint Regulation Of Cell Cycle Phase Transition Regulation Of Cell Cycle Process DNA Methylation On Cytosine Negative Regulation Of Myeloid Cell Differentiation Ubiquitin-dependent Protein Catabolic Process Proteasome-mediated Ubiquitin-dependent Protein Catabolic Process Modification-dependent Protein Catabolic Process Negative Regulation Of Chromosome Organization Positive Regulation Of Signal Transduction Cellular Macromolecule Catabolic Process Proteasomal Protein Catabolic Process Cellular Protein Metabolic Process Histone H2A Ubiquitination Positive Regulation Of MRNA 3'-end Processing Chromatin Silencing At RDNA	Chromatin Modification Negative Regulation Of Apoptotic Process Negative Regulation Of Programmed Cell Death Negative Regulation Of Cell Death Chromatin Organization Chromosome Organization Regulation Of Apoptotic Process Regulation Of Sequence-specific DNA Binding Transcription Factor Activity Regulation Of Cellular Protein Metabolic Process Regulation Of Cell Death Positive Regulation Of Cellular Metabolic Process Positive Regulation Of Cellular Biosynthetic Process Positive Regulation Of Sequence-specific DNA Binding Transcription Factor Activity Neurotrophin TRK Receptor Signaling Pathway Regulation Of Protein Metabolic Process Neurotrophin Signaling Pathway Regulation Of Nitrogen Compound Metabolic Process Response To Stress Positive Regulation Of Transcription, DNA-templated Negative Regulation Of Biosynthetic Process Cellular Metabolic Process DNA Metabolic Process Negative Regulation Of Signal Transduction Positive Regulation Of Cell Cycle Positive Regulation Of Macromolecule Biosynthetic Process Nucleobase-containing Compound Metabolic Process Positive Regulation Of Gene Expression Negative Regulation Of Signaling Negative Regulation Of Cellular Metabolic Process Heterocycle Metabolic Process Cellular Aromatic Compound Metabolic Process Epidermal Growth Factor Receptor Signaling Pathway Fibroblast Growth Factor Receptor Signaling Pathway ERBB Signaling Pathway Immune System Process Positive Regulation Of Metabolic Process Cellular Nitrogen Compound Metabolic Process Cell Aging Cellular Response To Fibroblast Growth Factor Stimulus Response To Fibroblast Growth Factor Histone Modification Histone H3-T6 Phosphorylation Oncogene-induced Cell Senescence Regulation Of Mitotic Cell Cycle Transmembrane Receptor Protein Tyrosine Kinase Signaling Pathway Positive Regulation Of Cell Cycle Process Cell Cycle Checkpoint Regulation Of Cell Proliferation Nitrogen Compound Metabolic Process Cellular Response To Stress
Tagcloud ?		abundance coincide contributions di dot1l drives dynamic e3 employ evolutionarily exhibit garnered h2b h2bub1 h3k4me2 h3k79me2 implicate lysines mitosis mitotic normally overlooked patterning ptm reaches requisite rnai stability virtually	a8 acidic acting afgf agnwtpi ap8 arrested biopanning clone competed contained display erk1 fgfr1 fgfrs fibroblast g0 gtpnptl heptapeptide homology identical library named pcna peptide phage rounds suppressing tp
Tagcloud (Difference) ?		abundance coincide contributions di dot1l drives dynamic e3 employ evolutionarily exhibit garnered h2b h2bub1 h3k4me2 h3k79me2 implicate lysines mitosis mitotic normally overlooked patterning ptm reaches requisite rnai stability virtually	a8 acidic acting afgf agnwtpi ap8 arrested biopanning clone competed contained display erk1 fgfr1 fgfrs fibroblast g0 gtpnptl heptapeptide homology identical library named pcna peptide phage rounds suppressing tp
Tagcloud (Intersection) ?