Entity Details

Primary name PADI3_HUMAN
Entity type UniProt
Source Source Link

Details

AccessionQ9ULW8
EntryNamePADI3_HUMAN
FullNameProtein-arginine deiminase type-3
TaxID9606
Evidenceevidence at protein level
Length664
SequenceStatuscomplete
DateCreated2001-01-11
DateModified2021-06-02

Ontological Relatives

GenesPADI3

GO terms

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GOName
GO:0004668 protein-arginine deiminase activity
GO:0005509 calcium ion binding
GO:0005634 nucleus
GO:0005737 cytoplasm
GO:0005829 cytosol
GO:0006325 chromatin organization
GO:0018101 protein citrullination
GO:0036414 histone citrullination
GO:0042802 identical protein binding

Subcellular Location

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Subcellular Location
Cytoplasm

Domains

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DomainNameCategoryType
IPR004303 Protein-arginine deiminaseFamilyFamily
IPR008972 CupredoxinFamilyHomologous superfamily
IPR013530 Protein-arginine deiminase, C-terminalDomainDomain
IPR013732 Protein-arginine deiminase (PAD), N-terminalDomainDomain
IPR013733 Protein-arginine deiminase (PAD), central domainDomainDomain
IPR036556 Protein-arginine deiminase, central domain superfamilyFamilyHomologous superfamily
IPR038685 PAD, N-terminal domain superfamilyFamilyHomologous superfamily

Diseases

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Disease IDSourceNameDescription
191480 OMIMUncombable hair syndrome 1 (UHS1)A form of uncombable hair syndrome, a condition characterized by scalp hair that is impossible to comb due to the haphazard arrangement of the hair bundles. A characteristic morphologic feature is a triangular to reniform to heart shape on cross-sections, and a groove, canal or flattening along the entire length of the hair. Most individuals are affected early in childhood and the hair takes on a spun-glass appearance with the hair becoming dry, curly, glossy, lighter in color, and progressively uncombable. The hair growth rate can range from slow to normal, and the condition improves with age. UHS1 inheritance is autosomal dominant. The disease is caused by variants affecting the gene represented in this entry.

Drugs

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DrugNameSourceType
DB00155 CitrullineDrugbanksmall molecule