GABARAP
Gamma-aminobutyric acid receptor-associated protein
Also known as: ATG8A, GBRAP_HUMAN, MM46
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- O95166
- Gene
- GABARAP
- Ensembl
- ENSG00000170296
- Chromosome
- 17
- Canonical length
- 117 aa
- Protein class
- Predicted intracellular proteins, Transporters
- Subcellular location
- Vesicles
OverviewNCBI Gene
Gamma-aminobutyric acid A receptors [GABA(A) receptors] are ligand-gated chloride channels that mediate inhibitory neurotransmission. This gene encodes GABA(A) receptor-associated protein, which is highly positively charged in its N-terminus and shares sequence similarity with light chain-3 of microtubule-associated proteins 1A and 1B. This protein clusters neurotransmitter receptors by mediating interaction with the cytoskeleton. [provided by RefSeq, Jul 2008]
Canonical amino-acid sequenceUniProt
117 residues, UniProt reviewed canonical sequence.
>O95166|GABARAP
1 MKFVYKEEHP FEKRRSEGEK IRKKYPDRVP VIVEKAPKAR IGDLDKKKYL VPSDLTVGQF
61 YFLIRKRIHL RAEDALFFFV NNVIPPTSAT MGQLYQEHHE EDFFLYIAYS DESVYGLLocalizationUniProt · AlphaFold · HPA
Whether an antibody against GABARAP 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)
- 0.29
- Highest tissue expression
- 1,113 nTPM
Expression across tissuesHPA
Tissue
- choroid plexus: 1,113 nTPM
- skeletal muscle: 935 nTPM
- spinal cord: 872 nTPM
- tongue: 854 nTPM
- pituitary gland: 815 nTPM
- adrenal gland: 802 nTPM
Single-cell type
- parietal cells: 371 nCPM
- gastric chief cells: 341 nCPM
- enterocytes: 335 nCPM
- colonocytes: 268 nCPM
- neuroendocrine cells: 253 nCPM
- goblet cells: 247 nCPM
Immune cell
- neutrophil: 7,142 nTPM
- total PBMC: 4,751 nTPM
- classical monocyte: 4,105 nTPM
- eosinophil: 3,759 nTPM
- intermediate monocyte: 3,673 nTPM
- non-classical monocyte: 3,231 nTPM
Brain region
- white matter: 553 nTPM
- medulla oblongata: 485 nTPM
- cerebellum: 484 nTPM
- spinal cord: 469 nTPM
- hypothalamus: 451 nTPM
- thalamus: 444 nTPM
DiseaseUniProt · ClinVar · IEDB · PubMed
Four sources answering four different questions about GABARAP.
Disease | AutoantibodyPubMed
Conditions in which antibodies against GABARAP are reported. Each links to that disease's full target list.
ReferencesPubMed · IEDB
Publications for GABARAP 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
3 publications
- Autoimmunity to GABAA-receptor-associated protein in stiff-person syndrome.
2006 · Brain · RCR 2.6 · 95 citations - A critical update on the immunopathogenesis of Stiff Person Syndrome.
2010 · Eur J Clin Invest · RCR 1.4 · 46 citations - Advances in the pathogenesis and treatment of patients with stiff person syndrome.
2008 · Curr Neurol Neurosci Rep · RCR 1.2 · 45 citations
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)
- 0.82
- gnomAD pLI
- 0.26
- gnomAD missense Z
- 1.55
- DepMap mean gene effect
- -0.23
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 3% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- autophagosome assembly
- autophagosome maturation
- cellular response to nitrogen starvation
- chemical synaptic transmission
- extrinsic apoptotic signaling pathway via death domain receptors
- microtubule cytoskeleton organization
- mitophagy
- positive regulation of proteasomal ubiquitin-dependent protein catabolic process
- positive regulation of protein K48-linked ubiquitination
- protein targeting
- protein transport
- regulation of neurotransmitter receptor localization to postsynaptic specialization membrane
- regulation of Rac protein signal transduction
Molecular functions
- beta-tubulin binding
- GABA receptor binding
- microtubule binding
- phosphatidylethanolamine binding
- ubiquitin protein ligase binding
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of GABARAP 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 GABARAP as an antibody target. Whether an autoantibody or antibody against GABARAP could matter depends on whether native GABARAP is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
GABARAP 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 GABARAP as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
Loading the interactive Seroatlas protein explorer...