BCS1L

Mitochondrial chaperone BCS1 (BCS1L), also known as BCS1 homolog, ubiquinol-cytochrome c reductase complex chaperone (h-BCS1), is a protein that in humans is encoded by the BCS1L gene. BCS1L is a chaperone protein involved in the assembly of Ubiquinol Cytochrome c Reductase (complex III), which is located in the inner mitochondrial membrane and is part of the electron transport chain. Mutations in this gene are associated with mitochondrial complex III deficiency (nuclear, 1), GRACILE syndrome, and Bjoernstad syndrome.

BCS1L
Identifiers
AliasesBCS1L, BCS, BCS1, BJS, FLNMS, GRACILE, Hs.6719, MC3DN1, PTD, h-BCS, h-BCS1, BCS1 homolog, ubiquinol-cytochrome c reductase complex chaperone
External IDsOMIM: 603647 MGI: 1914071 HomoloGene: 3193 GeneCards: BCS1L
Orthologs
SpeciesHumanMouse
Entrez

617

66821

Ensembl

ENSG00000074582

ENSMUSG00000026172

UniProt

Q9Y276

Q9CZP5

RefSeq (mRNA)

NM_025784
NM_001305652

RefSeq (protein)

NP_001292581
NP_080060

Location (UCSC)Chr 2: 218.66 – 218.66 MbChr 1: 74.63 – 74.63 Mb
PubMed search
Wikidata
View/Edit HumanView/Edit Mouse
BCS1 N-terminal domain
Identifiers
SymbolBCS1_N
PfamPF08740
InterProIPR014851
Available protein structures:
Pfam  structures / ECOD  
PDBRCSB PDB; PDBe; PDBj
PDBsumstructure summary
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