WDFY1 and BCS1L

Data Source:
BioGRID (biochemical)

		WDFY1	BCS1L
Description		WD repeat and FYVE domain containing 1	BCS1 homolog, ubiquinol-cytochrome c reductase complex chaperone
Image		No pdb structure	No pdb structure
GO Annotations	Cellular Component	Nucleus Early Endosome Cytosol	Mitochondrion Mitochondrial Inner Membrane Mitochondrial Respiratory Chain Complex III Integral Component Of Membrane
	Molecular Function	Protein Binding 1-phosphatidylinositol Binding Zinc Ion Binding	Protein Binding ATP Binding ATPase Activity
	Biological Process	Positive Regulation Of Toll-like Receptor 3 Signaling Pathway Positive Regulation Of Toll-like Receptor 4 Signaling Pathway	Mitochondrion Organization Protein Insertion Into Mitochondrial Inner Membrane From Matrix Mitochondrial Respiratory Chain Complex I Assembly Mitochondrial Cytochrome C Oxidase Assembly Mitochondrial Respiratory Chain Complex III Assembly
Pathways			Mitochondrial protein import
Drugs
Diseases			Bjornstad syndrome Mitochondrial respiratory chain deficiencies (MRCD), including: Mitochondrial complex I deficiency (MT-C1D); Complex II deficiency (MT-C2D); Complex III deficiency (MT-C3D); Complex IV deficiency (MT-C4D); Complex V deficiency (MT-ATPSD); Leigh syndrome (LS); Kearns-Sayre Syndrome (KSS); LCHD deficiency (LCHD); Leber Hereditary Optic Neuropathy (LHON); Myoclonic Epilepsy and Ragged-Red Fiber Disease (MERRF); NARP; MELAS; ACAD9 deficiency; HADH deficiency; HIBCH deficiency; GRACILE syndrome
GWAS		Night sleep phenotypes ( 27126917)	Male-pattern baldness ( 28196072)
Interacting Genes			3 interacting genes: DDX24 DNAJA1 MTDH
Entrez ID		57590	617
HPRD ID		15663	04708
Ensembl ID		ENSG00000085449	ENSG00000074582
Uniprot IDs		A0A024R488 Q8IWB7 Q9H8N9	A0A024R445 A8JZZ8 Q9Y276
PDB IDs
Enriched GO Terms of Interacting Partners?
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