TIMM10B

Protein-coding gene in the species Homo sapiens From Wikipedia, the free encyclopedia

Mitochondrial import inner membrane translocase subunit Tim9 B is an enzyme that in humans is encoded by the FXC1 gene.[5][6]

PDBOrtholog search: PDBe RCSB
AliasesTIMM10B, FXC1, TIM10B, Tim9b, translocase of inner mitochondrial membrane 10 homolog B (yeast), translocase of inner mitochondrial membrane 10B
Quick facts Available structures, PDB ...
TIMM10B
Available structures
PDBOrtholog search: PDBe RCSB
Identifiers
AliasesTIMM10B, FXC1, TIM10B, Tim9b, translocase of inner mitochondrial membrane 10 homolog B (yeast), translocase of inner mitochondrial membrane 10B
External IDsOMIM: 607388; MGI: 1315196; HomoloGene: 8142; GeneCards: TIMM10B; OMA:TIMM10B - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_012192

NM_019502

RefSeq (protein)

NP_036324

Location (UCSC)Chr 11: 6.48 – 6.48 MbChr 7: 105.64 – 105.64 Mb
PubMed search[3][4]
Wikidata
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FXC1, or TIMM10B, belongs to a family of evolutionarily conserved proteins that are organized in heterooligomeric complexes in the mitochondrial intermembrane space. These proteins mediate the import and insertion of hydrophobic membrane proteins into the mitochondrial inner membrane.[supplied by OMIM][6]

References

Further reading

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