Acetylserotonin O-methyltransferase

acetylserotonin O-methyltransferase
Identifiers
EC no.2.1.1.4
CAS no.9029-77-0
Databases
IntEnzIntEnz view
BRENDABRENDA entry
ExPASyNiceZyme view
KEGGKEGG entry
MetaCycmetabolic pathway
PRIAMprofile
PDB structuresRCSB PDB PDBe PDBsum
Gene OntologyAmiGO / QuickGO
Search
PMCarticles
PubMedarticles
NCBIproteins
ASMT
Available structures
PDBOrtholog search: PDBe RCSB
Identifiers
AliasesASMT, ASMTY, HIOMT, HIOMTY, acetylserotonin O-methyltransferase
External IDsOMIM: 402500, 300015; MGI: 96090; HomoloGene: 48261; GeneCards: ASMT; OMA:ASMT - orthologs
Orthologs
SpeciesHumanMouse
Entrez

438

107626

Ensembl

ENSG00000196433

ENSMUSG00000093806

UniProt

P46597

D3KU66

RefSeq (mRNA)

NM_004043
NM_001171038
NM_001171039

NM_001199212
NM_001308488

RefSeq (protein)

NP_001164509
NP_001164510
NP_004034

NP_001186141
NP_001295417

Location (UCSC)Chr X: 1.62 – 1.64 MbChr X: 169.11 – 169.11 Mb
PubMed search
Wikidata
View/Edit HumanView/Edit Mouse

N-Acetylserotonin O-methyltransferase, also known as ASMT, is an enzyme which catalyzes the final reaction in melatonin biosynthesis: converting Normelatonin to melatonin. This reaction is embedded in the more general tryptophan metabolism pathway. The enzyme also catalyzes a second reaction in tryptophan metabolism: the conversion of 5-hydroxy-indoleacetate to 5-methoxy-indoleacetate. The other enzyme which catalyzes this reaction is n-acetylserotonin-o-methyltransferase-like-protein.

In humans the ASMT enzyme is encoded by the pseudoautosomal ASMT gene. A copy exists near the endcaps of the short arms of both the X chromosome and the Y chromosome.