HLCS and ANKRD29

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

		HLCS	ANKRD29
Description		holocarboxylase synthetase	ankyrin repeat domain 29
Image		No pdb structure	No pdb structure
GO Annotations	Cellular Component	Chromatin Nuclear Lamina Cytoplasm Mitochondrion Cytosol Nuclear Matrix
	Molecular Function	Nucleotide Binding Catalytic Activity Biotin--[biotin Carboxyl-carrier Protein] Ligase Activity Protein Binding ATP Binding Biotin Binding Ligase Activity Enzyme Binding Identical Protein Binding	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		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)	Amyotrophic lateral sclerosis (sporadic) ( 24256812)
Interacting Genes		10 interacting genes: ACACB ANKRD29 DDX52 KRTAP5-9 MED19 POT1 QKI SARS2 SNX27 TXNDC15	10 interacting genes: CABP2 CRACR2A FAM90A1 FERMT3 GTF2H5 GYPA HLCS MRPL53 RABGEF1 USP32
Entrez ID		3141	147463
HPRD ID		08360	12464
Ensembl ID		ENSG00000159267	ENSG00000154065
Uniprot IDs		A0A8C8QSB1 P50747	Q8N6D5
PDB IDs
Enriched GO Terms of Interacting Partners?
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