PLSCR3

Phospholipid scramblase 3 is an enzyme that in humans is encoded by the PLSCR3 gene (abbreviated to PLS3 in this section). Like the other phospholipid scramblase family members (PLS1, PLS2, PLS4), PLS3 is a type II plasma membrane protein that is rich in proline and integral in apoptosis, or programmed cell death. The regulation of apoptosis is critical for both cell development and tissue homeostasis

PLSCR3
Identifiers
AliasesPLSCR3, phospholipid scramblase 3
External IDsOMIM: 607611 MGI: 1917560 HomoloGene: 23219 GeneCards: PLSCR3
Orthologs
SpeciesHumanMouse
Entrez

57048

70310

Ensembl

ENSG00000187838
ENSG00000284009

ENSMUSG00000019461

UniProt

Q9NRY6

Q9JIZ9

RefSeq (mRNA)

NM_020360
NM_001201576

NM_001168497
NM_023564

RefSeq (protein)

NP_001161969
NP_076053

Location (UCSC)Chr 17: 7.39 – 7.39 MbChr 11: 69.74 – 69.74 Mb
PubMed search
Wikidata
View/Edit HumanView/Edit Mouse

Although phospholipid scramblase is thought to exist in all eukaryotic cells, PLS3 is a protein that is novel to the mitochondria. This is very important because mitochondria are central in the apoptotic cell pathway. This newly found member of the scramblase family is "responsible for phospholipid translocation between two lipid compartments," the inner mitochondrial membrane and the outer membrane. Further experimental evidence suggests that the mechanism and effectors of PLS3's enzymatic activity are rather nuanced.

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