Entity Details

Primary name ENTP1_HUMAN
Entity type UniProt
Source Source Link

Details

AccessionP49961
EntryNameENTP1_HUMAN
FullNameEctonucleoside triphosphate diphosphohydrolase 1
TaxID9606
Evidenceevidence at protein level
Length510
SequenceStatuscomplete
DateCreated1996-10-01
DateModified2021-06-02

Ontological Relatives

GenesENTPD1

GO terms

Show/Hide Table
GOName
GO:0004382 guanosine-diphosphatase activity
GO:0005524 ATP binding
GO:0005886 plasma membrane
GO:0005887 integral component of plasma membrane
GO:0007155 cell adhesion
GO:0007596 blood coagulation
GO:0009134 nucleoside diphosphate catabolic process
GO:0016020 membrane
GO:0017110 nucleoside-diphosphatase activity
GO:0034656 nucleobase-containing small molecule catabolic process
GO:0035590 purinergic nucleotide receptor signaling pathway
GO:0045134 uridine-diphosphatase activity
GO:0070062 extracellular exosome
GO:0102485 dATP phosphohydrolase activity
GO:0102486 dCTP phosphohydrolase activity
GO:0102487 dUTP phosphohydrolase activity
GO:0102488 dTTP phosphohydrolase activity
GO:0102489 GTP phosphohydrolase activity
GO:0102490 8-oxo-dGTP phosphohydrolase activity
GO:0102491 dGTP phosphohydrolase activity

Subcellular Location

Show/Hide Table
Subcellular Location
Membrane

Domains

Show/Hide Table
DomainNameCategoryType
IPR000407 Nucleoside phosphatase GDA1/CD39FamilyFamily

Diseases

Show/Hide Table
Disease IDSourceNameDescription
615683 OMIMSpastic paraplegia 64, autosomal recessive (SPG64)A form of spastic paraplegia, a neurodegenerative disorder characterized by a slow, gradual, progressive weakness and spasticity of the lower limbs. Rate of progression and the severity of symptoms are quite variable. Initial symptoms may include difficulty with balance, weakness and stiffness in the legs, muscle spasms, and dragging the toes when walking. In some forms of the disorder, bladder symptoms (such as incontinence) may appear, or the weakness and stiffness may spread to other parts of the body. The disease is caused by variants affecting the gene represented in this entry.

Interactions

1 interaction

InteractorPartnerSourcesPublicationsLink
ENTP1_HUMANRANB9_HUMANBioGRID, HPRD, MINT16478441 details