TREH
Trehalase
Also known as: MGC129621, TRE, TREA, TREA_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- O43280
- Gene
- TREH
- Ensembl
- ENSG00000118094
- Chromosome
- 11
- Canonical length
- 583 aa
- Protein class
- Disease related genes, Enzymes, Human disease related genes, Metabolic proteins, Potential drug targets, Predicted intracellular proteins
- Subcellular location
- Vesicles,Cytosol
- Secretome location
- Intracellular and membrane
- Quaternary structure
- Homodimer
OverviewNCBI Gene
This gene encodes an enzyme that hydrolyses trehalose, a disaccharide formed from two glucose molecules found mainly in fungi, plants, and insects. A partial duplication of this gene is located adjacent to this locus on chromosome 11. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2014]
Canonical amino-acid sequenceUniProt
583 residues, UniProt reviewed canonical sequence.
>O43280|TREH
1 MPGRTWELCL LLLLGLGLGS QEALPPPCES EIYCHGELLN QVQMAKLYQD DKQFVDMPLS
61 IAPEQVLQTF TELSRDHNHS IPREQLQAFV HEHFQAKGQE LQPWTPADWK DSPQFLQKIS
121 DAKLRAWAGQ LHQLWKKLGK KMKPEVLSHP ERFSLIYSEH PFIVPGGRFV EFYYWDSYWV
181 MEGLLLSEMA ETVKGMLQNF LDLVKTYGHV PNGGRVYYLQ RSQPPLLTLM MDCYLTHTND
241 TAFLQENIET LALELDFWTK NRTVSVSLEG KNYLLNRYYV PYGGPRPESY SKDVELADTL
301 PEGDREALWA ELKAGAESGW DFSSRWLIGG PNPNSLSGIR TSKLVPVDLN AFLCQAEELM
361 SNFYSRLGND SQATKYRILR SQRLAALNTV LWDEQTGAWF DYDLEKKKKN REFYPSNLTP
421 LWAGCFSDPG VADKALKYLE DNRILTYQYG IPTSLQKTGQ QWDFPNAWAP LQDLVIRGLA
481 KAPLRRAQEV AFQLAQNWIR TNFDVYSQKS AMYEKYDVSN GGQPGGGGEY EVQEGFGWTN
541 GVVLMLLDRY GDRLTSGAKL AFLEPHCLAA TLLPSLLLSL LPWLocalizationUniProt · AlphaFold · HPA
Whether an antibody against TREH 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
- Cell surface
- Secreted
- No
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.23
- Highest tissue expression
- 62 nTPM
Expression across tissuesHPA
Tissue
- small intestine: 62 nTPM
- duodenum: 57 nTPM
- kidney: 13 nTPM
- liver: 5.7 nTPM
- gallbladder: 2.4 nTPM
- midbrain: 1.9 nTPM
Single-cell type
- late spermatids: 763 nCPM
- epicardial cells: 268 nCPM
- tuft cells: 185 nCPM
- enterocytes: 178 nCPM
- adipocytes: 126 nCPM
- early spermatids: 68 nCPM
Immune cell
- basophil: 0 nTPM
- classical monocyte: 0 nTPM
- eosinophil: 0 nTPM
- gdT-cell: 0 nTPM
- intermediate monocyte: 0 nTPM
- MAIT T-cell: 0 nTPM
Brain region
- white matter: 18 nTPM
- cerebral cortex: 16 nTPM
- basal ganglia: 13 nTPM
- hypothalamus: 11 nTPM
- thalamus: 10 nTPM
- medulla oblongata: 10 nTPM
DiseaseUniProt · ClinVar · IEDB · PubMed
Four sources answering four different questions about TREH.
Disease | AllUniProt
Conditions TREH is implicated in, by any mechanism.
- Trehalase deficiency (TREHD) MIM:612119
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)
- 1.02
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.44
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
- animal organ morphogenesis
- trehalose catabolic process
- trehalose metabolic process
Molecular functions
- alpha
- alpha-trehalase activity
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Six-hairpin glycosidase superfamily
- Six-hairpin glycosidase-like superfamily
- Glycoside hydrolase, family 37
- Glycoside hydrolase, family 37, conserved site
- Trehalase
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads TREH as an antibody target. Whether an autoantibody or antibody against TREH could matter depends on whether native TREH is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
TREH is annotated at the cell surface, where native TREH is exposed to circulating antibodies and is a prime autoantibody target that could block, deplete, or overstimulate it.
Annotation status
The present source text does not explicitly label TREH as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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