Entity Details

Primary name APRV1_HUMAN
Entity type UniProt
Source Source Link

Details

AccessionQ53RT3
EntryNameAPRV1_HUMAN
FullNameRetroviral-like aspartic protease 1
TaxID9606
Evidenceevidence at protein level
Length343
SequenceStatuscomplete
DateCreated2007-01-09
DateModified2021-06-02

Ontological Relatives

GenesASPRV1

GO terms

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GOName
GO:0004190 aspartic-type endopeptidase activity
GO:0016021 integral component of membrane
GO:0016485 protein processing
GO:0043588 skin development

Subcellular Location

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Subcellular Location
Membrane

Domains

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DomainNameCategoryType
IPR001969 Aspartic peptidase, active siteSiteActive site
IPR001995 Peptidase A2A, retrovirus, catalyticDomainDomain
IPR021109 Aspartic peptidase domain superfamilyFamilyHomologous superfamily
IPR033539 Retroviral-like aspartic protease 1FamilyFamily

Diseases

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Disease IDSourceNameDescription
146750 OMIMIchthyosis, lamellar, autosomal dominant (ADLI)An autosomal dominant form of ichthyosis, a disorder of keratinization with abnormal differentiation and desquamation of the epidermis, resulting in abnormal skin scaling. ADLI is characterized by onset at birth or within the first months of life, skin scaling on the entire body with relative sparing of face, anterior chest, and abdomen, and palmoplantar keratoderma. Patients may manifest mild erythema and moderate pruritus. The disease is caused by variants affecting the gene represented in this entry.

Interactions

3 interactions