Seroatlas · Human Serome Atlas

SIKE1

Suppressor of IKBKE 1

Also known as: FLJ21168, SIKE, SIKE1_HUMAN

Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene

Protein identityUniProt · HPA

UniProt accession
Q9BRV8
Gene
SIKE1
Ensembl
ENSG00000052723
Chromosome
1
Canonical length
207 aa
Protein class
Predicted intracellular proteins
Subcellular location
Vesicles,Focal adhesion sites

OverviewNCBI Gene

SIKE interacts with IKK-epsilon (IKBKE; MIM 605048) and TBK1 (MIM 604834) and acts as a suppressor of TLR3 (MIM 603029) and virus-triggered interferon activation pathways (Huang et al., 2005 [PubMed 16281057]).[supplied by OMIM, Mar 2008]

Canonical amino-acid sequenceUniProt

207 residues, UniProt reviewed canonical sequence.

>Q9BRV8|SIKE1
     1  MSCTIEKILT DAKTLLERLR EHDAAAESLV DQSAALHRRV AAMREAGTAL PDQYQEDASD
    61  MKDMSKYKPH ILLSQENTQI RDLQQENREL WISLEEHQDA LELIMSKYRK QMLQLMVAKK
   121  AVDAEPVLKA HQSHSAEIES QIDRICEMGE VMRKAVQVDD DQFCKIQEKL AQLELENKEL
   181  RELLSISSES LQARKENSMD TASQAIK

LocalizationUniProt · AlphaFold · HPA

Whether an antibody against SIKE1 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)
0.51
Highest tissue expression
13 nTPM

Expression across tissuesHPA

Tissue

  • thymus: 13 nTPM
  • skin: 13 nTPM
  • liver: 11 nTPM
  • lymph node: 11 nTPM
  • tonsil: 11 nTPM
  • kidney: 10 nTPM

Single-cell type

  • esophageal apical cells: 116 nCPM
  • oocytes: 83 nCPM
  • late spermatids: 74 nCPM
  • esophageal suprabasal cells: 62 nCPM
  • parietal cells: 55 nCPM
  • hepatocytes: 50 nCPM

Immune cell

  • basophil: 6 nTPM
  • MAIT T-cell: 2.8 nTPM
  • naive CD8 T-cell: 2.8 nTPM
  • plasmacytoid DC: 2.7 nTPM
  • naive CD4 T-cell: 2.6 nTPM
  • NK-cell: 2.5 nTPM

Brain region

  • cerebellum: 18 nTPM
  • thalamus: 18 nTPM
  • hypothalamus: 17 nTPM
  • medulla oblongata: 15 nTPM
  • pons: 15 nTPM
  • white matter: 15 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)
0.7
gnomAD pLI
0.2
gnomAD missense Z
0.44
DepMap mean gene effect
-0.09
DepMap dependency class
selective

Cancer expressionTCGA

Across TCGA tumor cohorts, this protein is over-expressed in roughly 6% 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 SIKE1 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 SIKE1 as an antibody target. Whether an autoantibody or antibody against SIKE1 could matter depends on whether native SIKE1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.

SIKE1 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 SIKE1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.

Canonical record: https://seroatlas.com/gene/SIKE1. Study-independent annotations aggregated from UniProt, Human Protein Atlas, PubMed, IEDB, Pfam, InterPro, Gene Ontology, AlphaFold, gnomAD, DepMap, ClinVar, TCGA. Catalog release seroatlas-reviewed-human-uniprot-20260313.

Seroatlas is the reference for exploring autoantibody and antibody serology at the human-protein level: the autoreactome and human serome, multiplex serology (HuProt, HuScan, VirScan, PhIP-Seq).

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