KPNA4
Importin subunit alpha-3
Also known as: IMA3_HUMAN, IPOA3, MGC12217, MGC26703, QIP1, SRP3
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- O00629
- Gene
- KPNA4
- Ensembl
- ENSG00000186432
- Chromosome
- 3
- Canonical length
- 521 aa
- Protein class
- Predicted intracellular proteins, Transporters
- Subcellular location
- Nucleoplasm,Nuclear membrane
OverviewNCBI Gene
The nuclear import of karyophilic proteins is directed by short amino acid sequences termed nuclear localization signals (NLSs). Karyopherins, or importins, are cytoplasmic proteins that recognize NLSs and dock NLS-containing proteins to the nuclear pore complex. The protein encoded by this gene shares the sequence similarity with Xenopus importin-alpha and Saccharomyces cerevisiae Srp1. This protein is found to interact with the NLSs of DNA helicase Q1 and SV40 T antigen. [provided by RefSeq, Jul 2008]
Canonical amino-acid sequenceUniProt
521 residues, UniProt reviewed canonical sequence.
>O00629|KPNA4
1 MADNEKLDNQ RLKNFKNKGR DLETMRRQRN EVVVELRKNK RDEHLLKRRN VPHEDICEDS
61 DIDGDYRVQN TSLEAIVQNA SSDNQGIQLS AVQAARKLLS SDRNPPIDDL IKSGILPILV
121 HCLERDDNPS LQFEAAWALT NIASGTSEQT QAVVQSNAVP LFLRLLHSPH QNVCEQAVWA
181 LGNIIGDGPQ CRDYVISLGV VKPLLSFISP SIPITFLRNV TWVMVNLCRH KDPPPPMETI
241 QEILPALCVL IHHTDVNILV DTVWALSYLT DAGNEQIQMV IDSGIVPHLV PLLSHQEVKV
301 QTAALRAVGN IVTGTDEQTQ VVLNCDALSH FPALLTHPKE KINKEAVWFL SNITAGNQQQ
361 VQAVIDANLV PMIIHLLDKG DFGTQKEAAW AISNLTISGR KDQVAYLIQQ NVIPPFCNLL
421 TVKDAQVVQV VLDGLSNILK MAEDEAETIG NLIEECGGLE KIEQLQNHEN EDIYKLAYEI
481 IDQFFSSDDI DEDPSLVPEA IQGGTFGFNS SANVPTEGFQ FLocalizationUniProt · AlphaFold · HPA
Whether an antibody against KPNA4 can act on the native protein depends on physical access: surface and secreted proteins are reachable by circulating antibodies, intracellular proteins usually are not.
- Antibody reachability
- Intracellular
- Secreted
- No
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.28
- Highest tissue expression
- 117 nTPM
Expression across tissuesHPA
Tissue
- skeletal muscle: 117 nTPM
- tongue: 56 nTPM
- heart muscle: 21 nTPM
- adipose tissue: 19 nTPM
- esophagus: 16 nTPM
- bone marrow: 14 nTPM
Single-cell type
- neutrophils: 433 nCPM
- neutrophil progenitors: 285 nCPM
- urothelial cells: 263 nCPM
- endometrial secretory cells: 250 nCPM
- salivary basal cells: 240 nCPM
- salivary myoepithelial cells: 216 nCPM
Immune cell
- basophil: 7.6 nTPM
- non-classical monocyte: 5.7 nTPM
- neutrophil: 4.2 nTPM
- NK-cell: 4 nTPM
- intermediate monocyte: 3.5 nTPM
- eosinophil: 2.9 nTPM
Brain region
- hypothalamus: 36 nTPM
- cerebellum: 35 nTPM
- white matter: 35 nTPM
- medulla oblongata: 34 nTPM
- pons: 33 nTPM
- spinal cord: 33 nTPM
Genetic constraint and essentialitygnomAD · DepMap
Does the body need this protein intact? Low LOEUF or a strong DepMap dependency means loss or blockade of the protein is likely to be felt.
- gnomAD LOEUF (loss-of-function intolerance)
- 0.16
- gnomAD pLI
- 1
- gnomAD missense Z
- 3.23
- DepMap mean gene effect
- -0.26
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 15% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of KPNA4 in the human serome: UniProt-annotated complex subunits plus reported interactors. Each links to its own Seroatlas record.
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads KPNA4 as an antibody target. Whether an autoantibody or antibody against KPNA4 could matter depends on whether native KPNA4 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
KPNA4 is annotated as predominantly intracellular. Intracellular proteins are common autoantibody markers, becoming visible to the immune system after cell injury or altered processing, but are usually markers of disease rather than direct drivers.
Annotation status
The present source text does not explicitly label KPNA4 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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