Enzyme

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EC Tree
     2. Transferases
        2.1 Transferring one-carbon groups
            2.1.1 Methyltransferases
ID:2.1.1.4
Description:Acetylserotonin O-methyltransferase.
Alternative Name: Hydroxyindole O-methyltransferase.
Cath: 1.10.10.10; 3.40.630.30; 3.40.50.150;

3D structure

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References

External Links

UniProtKB Enzyme Link: UniProtKB 2.1.1.4
BRENDA Enzyme Link: BRENDA 2.1.1.4
KEGG Enzyme Link: KEGG2.1.1.4
BioCyc Enzyme Link: BioCyc 2.1.1.4
ExPASy Enzyme Link: ExPASy2.1.1.4
EC2PDB Enzyme Link: EC2PDB 2.1.1.4
ExplorEnz Enzyme Link: ExplorEnz 2.1.1.4
PRIAM enzyme-specific profiles Link: PRIAM 2.1.1.4
IntEnz Enzyme Link: IntEnz 2.1.1.4
MEDLINE Enzyme Link: MEDLINE 2.1.1.4
MSA:

2.1.1.4;

Phylogenetic Tree:

2.1.1.4;

Uniprot:
M-CSA:
RHEA:15573 N-acetylserotonin + S-adenosyl-L-methionine = H(+) + melatonin + S-adenosyl-L-homocysteine
RULE(radius=1) [*:1]-[OH;+0:2].[*:3]-[S+;H0:4](-[*:5])-[CH3;+0:6]>>[*:1]-[O;H0;+0:2]-[CH3;+0:6].[*:3]-[S;H0;+0:4]-[*:5]
Reaction
Core-to-Core No scaffolds atoms were exchanged as a result of the reaction

References

TitleAuthorsDatePubMed ID
Structural analysis of the human hydroxyindole-O-methyltransferase gene. Presence of two distinct promoters.Rodriguez IR, Mazuruk K, Schoen TJ, Chader GJ1994 Dec 167989373
Hydroxyindole-O-methyltransferase activity in the pineal gland of the muskox (Ovibos moschatus).Tedesco SC, Morton DJ, Reiter RJ1994 Apr7932034
Hydroxyindole O-methyltransferase.Sugden D, Ceña V, Klein DC19873298987
Some properties of pineal gland hydroxyindole-O-methyltransferase from black rhinoceros (Diceros bicornis).Morton DJ, Kock N19902338611
Crystal structure and functional mapping of human ASMT, the last enzyme of the melatonin synthesis pathway.Botros HG, Legrand P, Pagan C, Bondet V, Weber P, Ben-Abdallah M, Lemière N, Huguet G, Bellalou J, Maronde E, Beguin P, Haouz A, Shepard W, Bourgeron T2013 Jan22775292