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PLSCR3

PLSCR3
Identifiers
Aliases PLSCR3, phospholipid scramblase 3
External IDs MGI: 1917560 HomoloGene: 23219 GeneCards: PLSCR3
Gene location (Human)
Chromosome 17 (human)
Chr. Chromosome 17 (human)
Chromosome 17 (human)
Genomic location for PLSCR3
Genomic location for PLSCR3
Band n/a Start 7,389,727 bp
End 7,394,843 bp
RNA expression pattern
PBB GE PLSCR3 218828 at fs.png

PBB GE PLSCR3 56197 at fs.png
More reference expression data
Orthologs
Species Human Mouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_020360
NM_001201576

NM_001168497
NM_023564

RefSeq (protein)

NP_001188505
NP_065093

NP_001161969
NP_076053

Location (UCSC) Chr 17: 7.39 – 7.39 Mb Chr 17: 69.85 – 69.85 Mb
PubMed search

NM_020360
NM_001201576

NM_001168497
NM_023564

NP_001188505
NP_065093

NP_001161969
NP_076053

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

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 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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