EEA1
Early endosome antigen 1
Also known as: EEA1_HUMAN, ZFYVE2
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q15075
- Gene
- EEA1
- Ensembl
- ENSG00000102189
- Chromosome
- 12
- Canonical length
- 1411 aa
- Protein class
- Plasma proteins, Predicted intracellular proteins
- Subcellular location
- Vesicles
- Quaternary structure
- Homodimer
OverviewNCBI Gene
Enables 1-phosphatidylinositol binding activity; GTP-dependent protein binding activity; and protein homodimerization activity. Involved in endocytosis and vesicle fusion. Located in cytosol and early endosome membrane. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
1411 residues, UniProt reviewed canonical sequence.
>Q15075|EEA1
1 MLRRILQRTP GRVGSQGSDL DSSATPINTV DVNNESSSEG FICPQCMKSL GSADELFKHY
61 EAVHDAGNDS GHGGESNLAL KRDDVTLLRQ EVQDLQASLK EEKWYSEELK KELEKYQGLQ
121 QQEAKPDGLV TDSSAELQSL EQQLEEAQTE NFNIKQMKDL FEQKAAQLAT EIADIKSKYD
181 EERSLREAAE QKVTRLTEEL NKEATVIQDL KTELLQRPGI EDVAVLKKEL VQVQTLMDNM
241 TLERERESEK LKDECKKLQS QYASSEATIS QLRSELAKGP QEVAVYVQEL QKLKSSVNEL
301 TQKNQTLTEN LLKKEQDYTK LEEKHNEESV SKKNIQATLH QKDLDCQQLQ SRLSASETSL
361 HRIHVELSEK GEATQKLKEE LSEVETKYQH LKAEFKQLQQ QREEKEQHGL QLQSEINQLH
421 SKLLETERQL GEAHGRLKEQ RQLSSEKLMD KEQQVADLQL KLSRLEEQLK EKVTNSTELQ
481 HQLDKTKQQH QEQQALQQST TAKLREAQND LEQVLRQIGD KDQKIQNLEA LLQKSKENIS
541 LLEKEREDLY AKIQAGEGET AVLNQLQEKN HTLQEQVTQL TEKLKNQSES HKQAQENLHD
601 QVQEQKAHLR AAQDRVLSLE TSVNELNSQL NESKEKVSQL DIQIKAKTEL LLSAEAAKTA
661 QRADLQNHLD TAQNALQDKQ QELNKITTQL DQVTAKLQDK QEHCSQLESH LKEYKEKYLS
721 LEQKTEELEG QIKKLEADSL EVKASKEQAL QDLQQQRQLN TDLELRATEL SKQLEMEKEI
781 VSSTRLDLQK KSEALESIKQ KLTKQEEEKK ILKQDFETLS QETKIQHEEL NNRIQTTVTE
841 LQKVKMEKEA LMTELSTVKD KLSKVSDSLK NSKSEFEKEN QKGKAAILDL EKTCKELKHQ
901 LQVQMENTLK EQKELKKSLE KEKEASHQLK LELNSMQEQL IQAQNTLKQN EKEEQQLQGN
961 INELKQSSEQ KKKQIEALQG ELKIAVLQKT ELENKLQQQL TQAAQELAAE KEKISVLQNN
1021 YEKSQETFKQ LQSDFYGRES ELLATRQDLK SVEEKLSLAQ EDLISNRNQI GNQNKLIQEL
1081 KTAKATLEQD SAKKEQQLQE RCKALQDIQK EKSLKEKELV NEKSKLAEIE EIKCRQEKEI
1141 TKLNEELKSH KLESIKEITN LKDAKQLLIQ QKLELQGKAD SLKAAVEQEK RNQQILKDQV
1201 KKEEEELKKE FIEKEAKLHS EIKEKEVGMK KHEENEAKLT MQITALNENL GTVKKEWQSS
1261 QRRVSELEKQ TDDLRGEIAV LEATVQNNQD ERRALLERCL KGEGEIEKLQ TKVLELQRKL
1321 DNTTAAVQEL GRENQSLQIK HTQALNRKWA EDNEVQNCMA CGKGFSVTVR RHHCRQCGNI
1381 FCAECSAKNA LTPSSKKPVR VCDACFNDLQ GLocalizationUniProt · AlphaFold · HPA
Whether an antibody against EEA1 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
- Other membrane
- Secreted
- No
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.5
- Highest tissue expression
- 13 nTPM
Expression across tissuesHPA
Tissue
- retina: 13 nTPM
- esophagus: 12 nTPM
- adipose tissue: 11 nTPM
- tongue: 9.7 nTPM
- skin: 9.6 nTPM
- skeletal muscle: 9 nTPM
Single-cell type
- syncytiotrophoblasts: 307 nCPM
- prostatic hillock cells: 304 nCPM
- ocular epithelial cells: 291 nCPM
- esophageal apical cells: 288 nCPM
- esophageal suprabasal cells: 287 nCPM
- urothelial cells: 284 nCPM
Immune cell
- non-classical monocyte: 0.9 nTPM
- naive CD4 T-cell: 0.8 nTPM
- classical monocyte: 0.6 nTPM
- memory B-cell: 0.5 nTPM
- myeloid DC: 0.5 nTPM
- naive CD8 T-cell: 0.5 nTPM
Brain region
- cerebellum: 24 nTPM
- pons: 21 nTPM
- cerebral cortex: 21 nTPM
- medulla oblongata: 21 nTPM
- white matter: 19 nTPM
- hypothalamus: 18 nTPM
ReferencesPubMed · IEDB
Publications for EEA1 from three distinct lines of evidence, kept separate because they answer different questions: whether antibodies are directed at the protein, whether a B-cell epitope has been mapped on it, and whether a T-cell epitope has. Each is labelled with its source.
Reference: AutoantibodyPubMed
13 publications
- Role of phosphatidylinositol 3-kinase and Rab5 effectors in phagosomal biogenesis and mycobacterial phagosome maturation arrest.
2001 · J Cell Biol · RCR 7.7 · 412 citations - Involvement of the endosomal autoantigen EEA1 in homotypic fusion of early endosomes.
1998 · Curr Biol · RCR 3.2 · 197 citations - Autoantibodies to protein transport and messenger RNA processing pathways: endosomes, lysosomes, Golgi complex, proteasomes, assemblyosomes, exosomes, and GW bodies.
2004 · Clin Immunol · RCR 1.4 · 66 citations - Early endosome antigen. 1: An autoantigen associated with neurological diseases.
1999 · J Investig Med · RCR 0.6 · 34 citations - Autoantibodies to a novel early endosome antigen 1.
1998 · Clin Immunol Immunopathol · RCR 0.4 · 25 citations
Show 8 more
- Identification of the B-cell epitopes of the early endosome antigen 1 (EEA1).
2003 · Clin Immunol · RCR 0.3 · 17 citations - Human autoantibodies against early endosome antigen-1 enhance excitatory synaptic transmission.
2006 · Neuroscience · RCR 0.3 · 16 citations - Altered neurological function in mice immunized with early endosome antigen 1.
2004 · BMC Neurosci · RCR 0.2 · 10 citations - Autoantibodies to early endosome antigen (EEA1) produce a staining pattern resembling cytoplasmic anti-neutrophil cytoplasmic antibodies (C-ANCA).
2000 · Clin Exp Immunol · RCR 0.2 · 13 citations - Characterization of early endosome antigen 1 in neural tissues.
2004 · Biochem Biophys Res Commun · RCR 0.1 · 6 citations - [Analysis of vesicle subpopulations carrying early endosomal autoantigen EEA1].
2014 · Tsitologiia · RCR 0.1 · 3 citations - [Detection of anti-early endosome antigen 1 antibody in sera showing cytoplasmic vesicular staining, taken from patients with connective tissue diseases].
2003 · Rinsho Byori · RCR 0 · 1 citations - Anti-early endosome antigen 1 autoantibodies were detected in a pemphigus-like patient but not in the majority of pemphigus diseases.
2016 · Exp Dermatol
Sources: PubMed — antigen-level antibody evidence from a custom retrieval. Records matching a controlled set of autoantibody terms (the MeSH descriptors Autoantibodies and Autoantigens, with title and abstract term variants) were obtained through NCBI E-utilities, and their titles and abstracts parsed for constructions that direct an antibody at a named protein rather than for co-occurrence. Captured names were resolved against UniProt nomenclature and each antigen adjudicated individually against the source text. Bibliographic records from PubMed and MeSH, U.S. National Library of Medicine; citation metrics from NIH iCite (Hutchins et al., PLoS Biology 2016). Titles link to PubMed; abstracts are not reproduced here. The NLM does not endorse this analysis.
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)
- 0.3
- gnomAD pLI
- 0.93
- gnomAD missense Z
- 1.38
- DepMap mean gene effect
- -0.05
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 5% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- chemical synaptic transmission, postsynaptic
- early endosome to late endosome transport
- endocytosis
- host-mediated perturbation of viral process
- synaptic vesicle to endosome fusion
- vesicle fusion
Molecular functions
- 1-phosphatidylinositol binding
- calmodulin binding
- GTP-dependent protein binding
- protein homodimerization activity
- zinc ion binding
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of EEA1 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 EEA1 as an antibody target. Whether an autoantibody or antibody against EEA1 could matter depends on whether native EEA1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
EEA1 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 EEA1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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