STK17B and RPS24

Number of citations of the paper that reports this interaction (PubMedID 21988832)
75

Data Source:
BioGRID (two hybrid)

		STK17B	RPS24
Description		serine/threonine kinase 17b	ribosomal protein S24
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GO Annotations	Cellular Component	Nucleus Endoplasmic Reticulum-Golgi Intermediate Compartment Plasma Membrane Actin Cytoskeleton	Nucleus Nucleoplasm Cytosol Small Ribosomal Subunit Membrane Cytosolic Small Ribosomal Subunit
	Molecular Function	Protein Kinase Activity Protein Serine/threonine Kinase Activity ATP Binding	RNA Binding Structural Constituent Of Ribosome Translation Initiation Factor Binding
	Biological Process	Protein Phosphorylation Apoptotic Process Intracellular Signal Transduction Protein Autophosphorylation Positive Regulation Of Fibroblast Apoptotic Process	Nuclear-transcribed MRNA Catabolic Process, Nonsense-mediated Decay RRNA Processing Translation Translational Initiation SRP-dependent Cotranslational Protein Targeting To Membrane Viral Transcription Erythrocyte Homeostasis Ribosomal Small Subunit Biogenesis
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		Quercetin
Diseases			Diamond-Blackfan anemia (DBA)
GWAS			California verbal learning test score ( 31596458) Diverticular disease ( 30177863) Metabolite levels ( 23823483)
Interacting Genes		3 interacting genes: APP CHP1 RPS24	5 interacting genes: PAH PCBD1 PNISR STK17B TAF9
Entrez ID		9262	6229
HPRD ID		05289	03877
Ensembl ID		ENSG00000081320	ENSG00000138326
Uniprot IDs		O94768 Q53QE7	A0A2R8Y849 P62847
PDB IDs		3LM0 3LM5 6QF4	4UG0 4V6X 5A2Q 5AJ0 5FLX 5LKS 5OA3 5T2C 5VYC 6EK0 6FEC 6G18 6G4S 6G4W 6G51 6G53 6G5H 6G5I 6IP5 6IP6 6IP8 6OLE 6OLF 6OLG 6OLI 6OLZ 6OM0 6OM7 6QZP
Enriched GO Terms of Interacting Partners?
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