ANKRD29 and HLCS

Number of citations of the paper that reports this interaction (PubMedID 32296183)
50

		ANKRD29	HLCS
Description		ankyrin repeat domain 29	holocarboxylase synthetase
Image		No pdb structure	No pdb structure
GO Annotations	Cellular Component		Chromatin Nuclear Lamina Cytoplasm Mitochondrion Cytosol Nuclear Matrix
	Molecular Function	Protein Binding	Nucleotide Binding Catalytic Activity Biotin--[biotin Carboxyl-carrier Protein] Ligase Activity Protein Binding ATP Binding Biotin Binding Ligase Activity Enzyme Binding Identical Protein Binding
	Biological Process		Biotin Metabolic Process Post-translational Protein Modification Response To Biotin
Pathways			Biotin transport and metabolism Defective HLCS causes multiple carboxylase deficiency
Drugs			Biotin
Diseases			Holocarboxylase synthetase deficiency
GWAS		Amyotrophic lateral sclerosis (sporadic) ( 24256812)	Developmental language disorder ( 27016271) Developmental language disorder (linguistic errors) ( 27016271) Hematocrit ( 32888494) Hemoglobin ( 32888494) Intracranial aneurysm ( 29531279) Night sleep phenotypes ( 27126917) Red blood cell count ( 32888494) Seasonality and depression ( 30217971)
Interacting Genes		10 interacting genes: CABP2 CRACR2A FAM90A1 FERMT3 GTF2H5 GYPA HLCS MRPL53 RABGEF1 USP32	10 interacting genes: ACACB ANKRD29 DDX52 KRTAP5-9 MED19 POT1 QKI SARS2 SNX27 TXNDC15
Entrez ID		147463	3141
HPRD ID		12464	08360
Ensembl ID		ENSG00000154065	ENSG00000159267
Uniprot IDs		Q8N6D5	A0A8C8QSB1 P50747
PDB IDs
Enriched GO Terms of Interacting Partners?
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