Methyltransferases (MTs) (EC 2.1.1.-) constitute an important class of enzymes
present in every life form. They transfer a methyl group most frequently from
S-adenosyl L-methionine (SAM or AdoMet) to a nucleophilic acceptor such as
nitrogen, oxygen, sulfur or carbon leading to S-adenosyl-L-homocysteine
(AdoHcy) and a methylated molecule. The substrates that are methylated by
these enzymes cover virtually every kind of biomolecules ranging from small
molecules, to lipids, proteins and nucleic acids. MTs are therefore involved
in many essential cellular processes including biosynthesis, signal
transduction, protein repair, chromatin regulation and gene silencing [1,2,3].
More than 230 different enzymatic reactions of MTs have been described so far,
of which more than 220 use SAM as the methyl donor [E1]. A review published in
2003  divides all MTs into 5 classes based on the structure of their
catalytic domain (fold):
- class I: Rossmann-like α/β
- class II: TIM β/α-barrel α/β
- class III: tetrapyrrole methylase α/β
- class IV: SPOUT α/β see <PDOC51604>
- class V: SET domain all β see <PDOC51565>
A more recent paper  based on a study of the Saccharomyces cerevisiae
methyltransferome argues for four more folds:
- class VI: transmembrane all α see <PDOC51598>
- class VII: DNA/RNA-binding 3-helical bundle all α
- class VIII: SSo0622-like α+β
- class IX: thymidylate synthetase α+β
The vast majority of MTs belong to the Rossmann-like fold (Class I) which
consists in a seven-stranded β sheet adjoined by α helices. The β
sheet contains a central topological switch-point resulting in a deep cleft in
which SAM binds. Class I MTs display two conserved positions, the first one is
a GxGxG motif (or at least a GxG motif) at the end of the first β strand
which is characteristic of a nucleotide-binding site and is hence used to bind
the adenosyl part of SAM, the second conserved position is an acidic residue
at the end of the second β strand that forms one hydrogen bond to each
hydroxyl of the SAM ribose part. The core of these enzymes is composed by
about 150 amino acids that show very strong spatial conservation. Catechol O-MT (EC 184.108.40.206) is the canonical Class I MT considering that it consists in
the exact consensus structural core with no extra domain (see <PDB:1VID>) .
Some enzymatic activities known to belong to the Class I superfamily:
Profiles directed against domains:
- C5-MTs (see <PDOC00089>): DNA (cytosine-5-)-MT (EC 220.127.116.11) and tRNA
(cytosine(38)-C(5))-MT (EC 18.104.22.168).
- Domains rearranged MTs (DRMs) (EC=22.214.171.124).
- Dot 1 MT (EC 126.96.36.199) (see <PDOC51569>).
- Eukaryotic and dsDNA viruses mRNA cap 0 MT (EC 188.8.131.52) (see <PDOC51562>).
- Flavivirus mRNA cap 0 and cap 1 MT (EC 184.108.40.206 and EC 220.127.116.11) [4,5,6].
- Mononegavirus L protein 2'-O-ribose MT domain, involved in the capping of
viral mRNAs (cap 1 structure) [7,8].
- Protein arginine N-MTs (PRMTs) including histone-arginine N-MT
(EC 18.104.22.168) and [Myelin basic protein]-arginine N-MT (EC 22.214.171.124).
- RMT2 MTs: arginine N-MT 2 (EC 2.1.1.-) and guanidinoacetate N-MT
(EC 126.96.36.199) [9,10].
- TRM1 tRNA (guanine(26)-N(2))-diMT (EC 188.8.131.52).
- TRM5/TYW2 tRNA (guanine(37)-N(1))-MT (EC 184.108.40.206).
- ERG6/SMT MTs: methylate sterol and triterpene.
- RsmB/NOP MTs: RNA (cytosine-5-)-MTs.
- RNA 5-methyluridine (m(5)U) MTs (EC 220.127.116.11, EC 18.104.22.168 and EC
- RrmJ mRNA (nucleoside-2'-O-)-MT (EC 22.214.171.124).
- Adrift ribose 2'-O-MT (EC 2.1.1.-).
- TrmB tRNA (guanine(46)-N(7))-MT (EC 126.96.36.199).
Profiles directed against whole-length proteins:
- Glycine and glycine/sarcosine N-methyltransferase (EC 188.8.131.52 and EC
- mRNA (2'-O-methyladenosine-N(6)-)-MT (EC 184.108.40.206) and other MT-A70-like
- Phosphoethanolamine N-MT (PEAMT) (EC 220.127.116.11).
- dsRNA viruses mRNA cap 0 MT (EC 18.104.22.168).
- Poxvirus/kinetoplastid cap ribose 2'-O-MT.
- NNT1 nicotinamide N-MT (EC 22.214.171.124).
- NNMT/PNMT/TEMT MTs (see <PDOC00844>): nicotinamide N-MT (EC 126.96.36.199),
phenylethanolamine N-MT (EC 188.8.131.52) and amine N-MT (EC 184.108.40.206).
- HNMT histamine N-MT (EC 220.127.116.11).
- Putrescine N-MT (EC 18.104.22.168).
- CLNMT calmodulin-lysine N-MT (EC 22.214.171.124).
- TRM61 tRNA (adenine(57)-N(1)/adenine(58)-N(1) or adenine(58)-N(1))-MT
(EC 126.96.36.199 or EC 188.8.131.52).
- UbiE 2-methoxy-6-polyprenyl-1,4-benzoquinol methylase (EC 184.108.40.206).
- Tocopherol O-MT (EC 220.127.116.11). The Synechocystis homologue has not a
tocopherol MT but a MPBQ/MSBQ activity (EC 18.104.22.1685) (see below) [11,12].
- 2-methyl-6-phytyl-1,4-benzoquinone/2-methyl-6-solanyl-1,4-benzoquinone MT
(MPBQ/MSBQ MT) (EC 22.214.171.1245) .
- Cation-dependent O-MT includes caffeoyl-CoA O-MT (CCoAOMT) (EC 126.96.36.199)
that is involved in plant defense, catechol O-MT (COMT) (EC 188.8.131.52) that
plays an important role in the central nervous system in the mammalian
organism, and a family of bacterial OMTs that may be involved in antibiotic
- Cation-independent O-MT includes caffeic acid OMTs that are able to
methylate the monolignol precursors caffeic acid (EC 184.108.40.206), caffeyl
aldehyde, or caffeyl alcohol, acetylserotonin OMT (EC 220.127.116.11) and
acetylserotonin OMT-like (EC 2.1.1.-).
- Magnesium protoporphyrin IX MT (EC 18.104.22.168).
- rRNA adenine N(6)-MT and adenine N(6), N(6)-diMT.
- TRM11 MTs: tRNA (guanine(10)-N2)-MT (EC 22.214.171.124) and homologs
- Methionine S-MT (EC 126.96.36.199).
- TPMT MTs: thiopurine S-MT (EC 188.8.131.52), thiol S-MT (EC 184.108.40.206) and
thiocyanate MT (EC 2.1.1.n4).
The profiles we developed cover the entire domains or families.
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