DNAJA1 and BCS1L

Number of citations of the paper that reports this interaction (PubMedID 21900206)
114

Data Source:
BioGRID (two hybrid)

		DNAJA1	BCS1L
Description		DnaJ heat shock protein family (Hsp40) member A1	BCS1 homolog, ubiquinol-cytochrome c reductase complex chaperone
Image			No pdb structure
GO Annotations	Cellular Component	Nucleus Mitochondrion Cytosol Microtubule Cytoskeleton Membrane Perinuclear Region Of Cytoplasm Extracellular Exosome Cytoplasmic Side Of Endoplasmic Reticulum Membrane	Mitochondrion Mitochondrial Respiratory Chain Complex III Integral Component Of Membrane
	Molecular Function	G Protein-coupled Receptor Binding ATPase Activator Activity Protein Binding ATP Binding Hsp70 Protein Binding Tat Protein Binding Ubiquitin Protein Ligase Binding Metal Ion Binding Low-density Lipoprotein Particle Receptor Binding Unfolded Protein Binding Chaperone Binding C3HC4-type RING Finger Domain Binding	Protein Binding ATP Binding
	Biological Process	Protein Folding Response To Unfolded Protein Response To Heat Negative Regulation Of Protein Ubiquitination Positive Regulation Of ATPase Activity Positive Regulation Of Apoptotic Process Negative Regulation Of Apoptotic Process Negative Regulation Of JUN Kinase Activity Regulation Of Protein Transport Protein Localization To Mitochondrion Negative Regulation Of Establishment Of Protein Localization To Mitochondrion Negative Regulation Of Nitrosative Stress-induced Intrinsic Apoptotic Signaling Pathway	Mitochondrion Organization Mitochondrial Respiratory Chain Complex I Assembly Mitochondrial Respiratory Chain Complex IV Assembly Mitochondrial Respiratory Chain Complex III Assembly
Pathways		HSP90 chaperone cycle for steroid hormone receptors (SHR)	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			Male-pattern baldness ( 28196072)
Interacting Genes		22 interacting genes: ARL4D BCS1L BRCA1 CAV2 CD58 CDC16 CFTR ERG FZR1 HIVEP1 HMGCL HSPA8 LSM2 NELFCD NUDT3 PAXIP1 PGR PTEN PTTG1 SUMO4 TM4SF1 TXN	14 interacting genes: AOX1 ARHGAP18 CD28 CLK1 CTLA4 DDX24 DNAJA1 MRPS12 MTDH ORC2 RP9 RPE SLC29A1 WDFY1
Entrez ID		3301	617
HPRD ID		04159	04708
Ensembl ID		ENSG00000086061	ENSG00000074582
Uniprot IDs		B7Z5C0 P31689	A0A024R445 A8JZZ8 Q9Y276
PDB IDs		2LO1 2M6Y 6E8M
Enriched GO Terms of Interacting Partners?
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