PLS3

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

Plastin-3 is a highly conserved protein that in humans is encoded by the PLS3 gene on the X chromosome.[5][6]

PDBOrtholog search: PDBe RCSB
AliasesPLS3, BMND18, T-plastin, plastin 3
Quick facts Available structures, PDB ...
PLS3
Available structures
PDBOrtholog search: PDBe RCSB
Identifiers
AliasesPLS3, BMND18, T-plastin, plastin 3
External IDsOMIM: 300131; MGI: 104807; HomoloGene: 128200; GeneCards: PLS3; OMA:PLS3 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_001136025
NM_001172335
NM_001282337
NM_001282338
NM_005032

NM_001166453
NM_001166454
NM_145629
NM_001346519
NM_001346520

RefSeq (protein)

NP_001129497
NP_001165806
NP_001269266
NP_001269267
NP_005023

NP_001159925
NP_001159926
NP_001333448
NP_001333449
NP_663604

Location (UCSC)Chr X: 115.56 – 115.65 MbChr X: 74.83 – 74.92 Mb
PubMed search[3][4]
Wikidata
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Function

Plastins are a family of actin-binding proteins that are conserved throughout eukaryote evolution and expressed in most tissues of higher eukaryotes. In humans, two ubiquitous plastin isoforms (L and T) have been identified. Plastin 1 (otherwise known as Fimbrin) is a third distinct plastin isoform which is specifically expressed at high levels in the small intestine. The L isoform is expressed only in hemopoietic cell lineages, while the T isoform has been found in all other normal cells of solid tissues that have replicative potential (fibroblasts, endothelial cells, epithelial cells, melanocytes, etc.). The C-terminal 570 amino acids of the T-plastin and L-plastin proteins are 83% identical. It contains a potential calcium-binding site near the N-terminus.[6]

Clinical significance

Defects in PLS3 are associated with osteoporosis and bone fracture in humans and in knockout zebrafish.[7]

References

Further reading

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