FBXO7

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

F-box only protein 7 is a protein that in humans is encoded by the FBXO7 gene.[5][6][7][8] Mutations in FBXO7 have been associated with Parkinson's disease.[9][10]

PDBOrtholog search: PDBe RCSB
AliasesFBXO7, FBX, FBX07, FBX7, PARK15, PKPS, F-box protein 7
Quick facts Available structures, PDB ...
FBXO7
Available structures
PDBOrtholog search: PDBe RCSB
Identifiers
AliasesFBXO7, FBX, FBX07, FBX7, PARK15, PKPS, F-box protein 7
External IDsOMIM: 605648; MGI: 1917004; HomoloGene: 8136; GeneCards: FBXO7; OMA:FBXO7 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_001033024
NM_001257990
NM_012179

NM_153195
NM_001310745
NM_001347151

RefSeq (protein)

NP_001028196
NP_001244919
NP_036311

NP_001297674
NP_001334080
NP_694875

Location (UCSC)Chr 22: 32.47 – 32.5 MbChr 10: 85.86 – 85.89 Mb
PubMed search[3][4]
Wikidata
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Function

This gene encodes a member of the F-box protein family which is characterized by an approximately 40 amino acid motif, the F-box. The F-box proteins constitute one of the four subunits of the ubiquitin protein ligase complex called SCFs (SKP1-cullin-F-box), which function in phosphorylation-dependent ubiquitination. The F-box proteins are divided into 3 classes: Fbws containing WD-40 domains, Fbls containing leucine-rich repeats, and Fbxs containing either different protein-protein interaction modules or no recognizable motifs. The protein encoded by this gene belongs to the Fbxs class and it may play a role in regulation of hematopoiesis. Alternatively spliced transcript variants of this gene have been identified with the full-length natures of only some variants being determined.[8]

Interactions

FBXO7 has been shown to interact with SKP1A,[11] CUL1,[5][12] CDK6,[13] p27,[13] PI31,[12] Parkin,[14] and PINK1.[14]

References

Further reading

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