HNRNPH3 and RPS4X

Number of citations of the paper that reports this interaction (PubMedID 16169070)
820

Data Source:
BioGRID (two hybrid)
HPRD (two hybrid)

		HNRNPH3	RPS4X
Description		heterogeneous nuclear ribonucleoprotein H3	ribosomal protein S4 X-linked
Image		No pdb structure
GO Annotations	Cellular Component	Nucleus Nucleoplasm Spliceosomal Complex	Nucleoplasm Cytosol Ribosome Polysome Focal Adhesion Small Ribosomal Subunit Membrane Cytosolic Small Ribosomal Subunit Cytoplasmic Ribonucleoprotein Granule Synapse Extracellular Exosome Ribonucleoprotein Complex
	Molecular Function	RNA Binding Protein Binding	RNA Binding Structural Constituent Of Ribosome Protein Binding RRNA Binding
	Biological Process	MRNA Splicing, Via Spliceosome RNA Processing RNA Splicing Epithelial Cell Differentiation	Nuclear-transcribed MRNA Catabolic Process, Nonsense-mediated Decay Translation Translational Initiation SRP-dependent Cotranslational Protein Targeting To Membrane Multicellular Organism Development Positive Regulation Of Cell Proliferation Viral Transcription Positive Regulation Of Translation
Pathways			L13a-mediated translational silencing of Ceruloplasmin expression Peptide chain elongation SRP-dependent cotranslational protein targeting to membrane SRP-dependent cotranslational protein targeting to membrane Viral mRNA Translation Selenocysteine synthesis Major pathway of rRNA processing in the nucleolus and cytosol Translation initiation complex formation Formation of a pool of free 40S subunits Formation of the ternary complex, and subsequently, the 43S complex Ribosomal scanning and start codon recognition GTP hydrolysis and joining of the 60S ribosomal subunit Eukaryotic Translation Termination Regulation of expression of SLITs and ROBOs Response of EIF2AK4 (GCN2) to amino acid deficiency Nonsense Mediated Decay (NMD) independent of the Exon Junction Complex (EJC) Nonsense Mediated Decay (NMD) enhanced by the Exon Junction Complex (EJC)
Drugs		Copper
Diseases
GWAS
Interacting Genes		26 interacting genes: ANXA11 CCL13 CHERP CRMP1 DDX17 DDX5 EEF1G ERG ERG28 HNRNPA0 HNRNPA1 HNRNPD HNRNPF HNRNPH1 HNRNPU HNRNPUL1 IL7R KAT5 MAPK6 NCBP3 PIM2 RBM4 RPS4X TTR UTP14A ZMYM2	10 interacting genes: ARPC3 CAMK2D CTBP2 HNRNPH3 MCM2 POR PTEN RPS15 RPS7 RPS8
Entrez ID		3189	6191
HPRD ID		03818	02427
Ensembl ID		ENSG00000096746	ENSG00000198034
Uniprot IDs		A0A024QZK8 A0A024QZP1 B4DHY1 P31942 Q53F48	B2R491 P62701
PDB IDs			4UG0 4V6X 5A2Q 5LKS 5OA3 5T2C 5VYC 6EK0 6FEC 6G18 6G4S 6G4W 6G51 6G53 6G5H 6G5I 6IP5 6IP6 6IP8 6OLE 6OLF 6OLI 6OM0 6OM7 6QZP
Enriched GO Terms of Interacting Partners?
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