MANEA
Glycoprotein endo-alpha-1,2-mannosidase
Also known as: FLJ12838, mandaselin, MANEA_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q5SRI9
- Gene
- MANEA
- Ensembl
- ENSG00000172469
- Chromosome
- 6
- Canonical length
- 462 aa
- Protein class
- Enzymes, Predicted intracellular proteins, Predicted membrane proteins
- Subcellular location
- Golgi apparatus
OverviewNCBI Gene
N-glycosylation of proteins is initiated in the endoplasmic reticulum (ER) by the transfer of the preassembled oligosaccharide glucose-3-mannose-9-N-acetylglucosamine-2 from dolichyl pyrophosphate to acceptor sites on the target protein by an oligosaccharyltransferase complex. This core oligosaccharide is sequentially processed by several ER glycosidases and by an endomannosidase (E.C. 3.2.1.130), such as MANEA, in the Golgi. MANEA catalyzes the release of mono-, di-, and triglucosylmannose oligosaccharides by cleaving the alpha-1,2-mannosidic bond that links them to high-mannose glycans (Hamilton et al., 2005 [PubMed 15677381]).[supplied by OMIM, Sep 2008]
Canonical amino-acid sequenceUniProt
462 residues, UniProt reviewed canonical sequence.
>Q5SRI9|MANEA
1 MAKFRRRTCI ILALFILFIF SLMMGLKMLR PNTATFGAPF GLDLLPELHQ RTIHLGKNFD
61 FQKSDRINSE TNTKNLKSVE ITMKPSKASE LNLDELPPLN NYLHVFYYSW YGNPQFDGKY
121 IHWNHPVLEH WDPRIAKNYP QGRHNPPDDI GSSFYPELGS YSSRDPSVIE THMRQMRSAS
181 IGVLALSWYP PDVNDENGEP TDNLVPTILD KAHKYNLKVT FHIEPYSNRD DQNMYKNVKY
241 IIDKYGNHPA FYRYKTKTGN ALPMFYVYDS YITKPEKWAN LLTTSGSRSI RNSPYDGLFI
301 ALLVEEKHKY DILQSGFDGI YTYFATNGFT YGSSHQNWAS LKLFCDKYNL IFIPSVGPGY
361 IDTSIRPWNT QNTRNRINGK YYEIGLSAAL QTRPSLISIT SFNEWHEGTQ IEKAVPKRTS
421 NTVYLDYRPH KPGLYLELTR KWSEKYSKER ATYALDRQLP VSLocalizationUniProt · AlphaFold · HPA
Whether an antibody against MANEA 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
- 1
- Mean surface accessibility (rSASA)
- 0.31
- Highest tissue expression
- 21 nTPM
Expression across tissuesHPA
Tissue
- liver: 21 nTPM
- kidney: 11 nTPM
- adipose tissue: 10 nTPM
- parathyroid gland: 10 nTPM
- stomach: 10 nTPM
- thyroid gland: 9.8 nTPM
Single-cell type
- plasma cells: 130 nCPM
- hepatocytes: 69 nCPM
- corticotrophs: 42 nCPM
- gastric chief cells: 36 nCPM
- podocytes: 34 nCPM
- mucous neck cells: 29 nCPM
Immune cell
- basophil: 5.9 nTPM
- T-reg: 3.6 nTPM
- intermediate monocyte: 2.9 nTPM
- MAIT T-cell: 2.7 nTPM
- non-classical monocyte: 2.6 nTPM
- memory B-cell: 2.5 nTPM
Brain region
- white matter: 10 nTPM
- medulla oblongata: 8.7 nTPM
- spinal cord: 7.7 nTPM
- hypothalamus: 7.6 nTPM
- cerebellum: 7.1 nTPM
- thalamus: 6.9 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)
- 0.87
- gnomAD pLI
- 0
- gnomAD missense Z
- -0.01
- DepMap mean gene effect
- 0.08
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 4% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Molecular functions
- alpha-mannosidase activity
- glycoprotein endo-alpha-1,2-mannosidase activity
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads MANEA as an antibody target. Whether an autoantibody or antibody against MANEA could matter depends on whether native MANEA is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
MANEA 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 MANEA as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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