ASMT
Acetylserotonin O-methyltransferase
Also known as: ASMT_HUMAN, ASMTY, HIOMT, HIOMTY
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- P46597
- Gene
- ASMT
- Ensembl
- ENSG00000196433
- Chromosome
- X
- Canonical length
- 345 aa
- Protein class
- Enzymes, Metabolic proteins, Predicted intracellular proteins
- Quaternary structure
- Homodimer
OverviewNCBI Gene
This gene belongs to the methyltransferase superfamily, and is located in the pseudoautosomal region (PAR) at the end of the short arms of the X and Y chromosomes. The encoded enzyme catalyzes the final reaction in the synthesis of melatonin, and is abundant in the pineal gland. Alternatively spliced transcript variants have been noted for this gene. [provided by RefSeq, Jan 2010]
Canonical amino-acid sequenceUniProt
345 residues, UniProt reviewed canonical sequence.
>P46597|ASMT
1 MGSSEDQAYR LLNDYANGFM VSQVLFAACE LGVFDLLAEA PGPLDVAAVA AGVRASAHGT
61 ELLLDICVSL KLLKVETRGG KAFYRNTELS SDYLTTVSPT SQCSMLKYMG RTSYRCWGHL
121 ADAVREGRNQ YLETFGVPAE ELFTAIYRSE GERLQFMQAL QEVWSVNGRS VLTAFDLSVF
181 PLMCDLGGGA GALAKECMSL YPGCKITVFD IPEVVWTAKQ HFSFQEEEQI DFQEGDFFKD
241 PLPEADLYIL ARVLHDWADG KCSHLLERIY HTCKPGGGIL VIESLLDEDR RGPLLTQLYS
301 LNMLVQTEGQ ERTPTHYHML LSSAGFRDFQ FKKTGAIYDA ILARKLocalizationUniProt · AlphaFold · HPA
Whether an antibody against ASMT 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)
- 0.26
- Highest tissue expression
- 7.2 nTPM
Expression across tissuesHPA
Tissue
- choroid plexus: 7.2 nTPM
- epididymis: 1.7 nTPM
- pituitary gland: 1.4 nTPM
- adrenal gland: 0.7 nTPM
- bone marrow: 0.7 nTPM
- cervix: 0.7 nTPM
Single-cell type
- oocytes: 4.6 nCPM
- epididymal clear cells: 4.1 nCPM
- extravillous trophoblasts: 2.7 nCPM
- thymocytes: 2.5 nCPM
- epicardial cells: 2.3 nCPM
- epididymal principal cells: 2.2 nCPM
Immune cell
- naive B-cell: 2.1 nTPM
- memory B-cell: 0.6 nTPM
- memory CD8 T-cell: 0.6 nTPM
- NK-cell: 0.4 nTPM
- memory CD4 T-cell: 0.1 nTPM
- neutrophil: 0.1 nTPM
Brain region
- choroid plexus: 3.1 nTPM
- hypothalamus: 2.5 nTPM
- cerebellum: 1.4 nTPM
- cerebral cortex: 1.3 nTPM
- white matter: 1.2 nTPM
- basal ganglia: 1.1 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)
- 1.93
- gnomAD pLI
- 0
- gnomAD missense Z
- -1.7
OntologyGO
Biological processes
- indolalkylamine biosynthetic process
- lipid metabolic process
- melatonin biosynthetic process
- methylation
- translation
Molecular functions
- identical protein binding
- O-methyltransferase activity
- protein homodimerization activity
- acetylserotonin O-methyltransferase activity
- S-methyltransferase activity
Cellular components
Protein domainsUniProt · Pfam · InterPro
- O-methyltransferase, C-terminal domain
- Caffeic acid 3-O-methyltransferase-like, dimerisation domain
- O-methyltransferase-like
- S-adenosyl-L-methionine-dependent methyltransferase superfamily
- Winged helix-like DNA-binding domain superfamily
- Winged helix DNA-binding domain superfamily
- O-methyltransferase domain
- O-methyltransferase dimerisation domain
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads ASMT as an antibody target. Whether an autoantibody or antibody against ASMT could matter depends on whether native ASMT is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
ASMT 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 ASMT as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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