Entity Details

Primary name NAA15_HUMAN
Entity type UniProt
Source Source Link

Details

AccessionQ9BXJ9
EntryNameNAA15_HUMAN
FullNameN-alpha-acetyltransferase 15, NatA auxiliary subunit
TaxID9606
Evidenceevidence at protein level
Length866
SequenceStatuscomplete
DateCreated2005-01-04
DateModified2021-06-02

Ontological Relatives

GenesNAA15

GO terms

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GOName
GO:0001525 angiogenesis
GO:0003723 RNA binding
GO:0005634 nucleus
GO:0005667 transcription regulator complex
GO:0005737 cytoplasm
GO:0005829 cytosol
GO:0006474 N-terminal protein amino acid acetylation
GO:0016020 membrane
GO:0016604 nuclear body
GO:0017196 N-terminal peptidyl-methionine acetylation
GO:0030154 cell differentiation
GO:0031415 NatA complex
GO:0043022 ribosome binding
GO:0043066 negative regulation of apoptotic process
GO:0043231 intracellular membrane-bounded organelle
GO:0045893 positive regulation of transcription, DNA-templated
GO:0050821 protein stabilization

Subcellular Location

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Subcellular Location
Cytoplasm
Nucleus

Domains

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DomainNameCategoryType
IPR011990 Tetratricopeptide-like helical domain superfamilyFamilyHomologous superfamily
IPR019734 Tetratricopeptide repeatRepeatRepeat
IPR021183 N-terminal acetyltransferase A, auxiliary subunitFamilyFamily

Diseases

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Disease IDSourceNameDescription
617787 OMIMMental retardation, autosomal dominant 50 (MRD50)A form of mental retardation, a disorder characterized by significantly below average general intellectual functioning associated with impairments in adaptive behavior and manifested during the developmental period. The disease is caused by variants affecting the gene represented in this entry.