NSFL1C

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

NSFL1 cofactor p47 is a protein that in humans is encoded by the NSFL1C gene.[5][6]

PDBOrtholog search: PDBe RCSB
AliasesNSFL1C, P47, UBX1, UBXD10, UBXN2C, dJ776F14.1, NSFL1 cofactor
Quick facts Available structures, PDB ...
NSFL1C
Available structures
PDBOrtholog search: PDBe RCSB
Identifiers
AliasesNSFL1C, P47, UBX1, UBXD10, UBXN2C, dJ776F14.1, NSFL1 cofactor
External IDsOMIM: 606610; MGI: 3042273; HomoloGene: 41114; GeneCards: NSFL1C; OMA:NSFL1C - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_001206736
NM_016143
NM_018839
NM_182483

NM_001291074
NM_198326

RefSeq (protein)

NP_001193665
NP_057227
NP_061327

NP_001278003
NP_938085

Location (UCSC)Chr 20: 1.44 – 1.47 MbChr 2: 151.34 – 151.35 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse
Close

N-ethylmaleimide-sensitive factor (NSF) and valosin-containing protein (p97) are two ATPases known to be involved in transport vesicle/target membrane fusion and fusions between membrane compartments. A trimer of the protein encoded by this gene binds a hexamer of cytosolic p97 and is required for p97-mediated regrowth of Golgi cisternae from mitotic Golgi fragments. Multiple transcript variants encoding several different isoforms have been found for this gene.[6]

Interactions

NSFL1C has been shown to interact with Valosin-containing protein.[7]

References

Further reading

Related Articles

Wikiwand AI