Entity Details

Primary name PLST_HUMAN
Entity type UniProt
Source Source Link

Details

AccessionP13797
EntryNamePLST_HUMAN
FullNamePlastin-3
TaxID9606
Evidenceevidence at protein level
Length630
SequenceStatuscomplete
DateCreated1990-01-01
DateModified2021-06-02

Ontological Relatives

GenesPLS3

GO terms

Show/Hide Table
GOName
GO:0005509 calcium ion binding
GO:0005737 cytoplasm
GO:0005829 cytosol
GO:0005884 actin filament
GO:0005886 plasma membrane
GO:0032432 actin filament bundle
GO:0051015 actin filament binding
GO:0051017 actin filament bundle assembly
GO:0051639 actin filament network formation
GO:0060348 bone development

Subcellular Location

Show/Hide Table
Subcellular Location
Cytoplasm

Domains

Show/Hide Table
DomainNameCategoryType
IPR001589 Actinin-type actin-binding domain, conserved siteSiteConserved site
IPR001715 Calponin homology domainDomainDomain
IPR002048 EF-hand domainDomainDomain
IPR011992 EF-hand domain pairFamilyHomologous superfamily
IPR018247 EF-Hand 1, calcium-binding siteSiteBinding site
IPR036872 CH domain superfamilyFamilyHomologous superfamily
IPR039956 Plastin-2/3FamilyFamily
IPR039959 Fimbrin/PlastinFamilyFamily

Diseases

Show/Hide Table
Disease IDSourceNameDescription
166710 OMIMOsteoporosis (OSTEOP)A systemic skeletal disorder characterized by decreased bone mass and deterioration of bone microarchitecture without alteration in the composition of bone. The result is fragile bones and an increased risk of fractures, even after minimal trauma. Osteoporosis is a chronic condition of multifactorial etiology and is usually clinically silent until a fracture occurs. Disease susceptibility is associated with variants affecting the gene represented in this entry.