See separate file for EC 2.1.1.101 to EC 2.1.1.150, EC 2.1.1.151 to EC 2.1.1.200 and EC 2.1.1.201 to EC 2.1.1.268.
See the following file:
EC 2.1.1.101 to EC 2.1.1.150
EC 2.1.1.151 to EC 2.1.1.200
EC 2.1.1.201 to EC 2.1.1.250
EC 2.1.1.251 to EC 2.1.1.268
[EC 2.1.1.52 Transferred entry: rRNA (guanine-N2)-methyltransferase. Now covered by EC 2.1.1.171 [16S rRNA (guanine966-N2)-methyltransferase], EC 2.1.1.172 [16S rRNA (guanine1207-N2)-methyltransferase], EC 2.1.1.173 [23S rRNA (guanine2445-N2)-methyltransferase] and EC 2.1.1.174 [23S rRNA (guanine1835-N2)-methyltransferase] (EC 2.1.1.52 created 1976, deleted 2010)]
Accepted name: putrescine N-methyltransferase
Reaction: S-adenosyl-L-methionine + putrescine = S-adenosyl-L-homocysteine + N-methylputrescine
For diagram of reaction, click here.
Other name(s): putrescine methyltransferase
Systematic name: S-adenosyl-L-methionine:putrescine N-methyltransferase
Links to other databases: BRENDA, EXPASY, KEGG, Metacyc, CAS registry number: 9075-39-2
References:
1. Mizusaki, S., Tanabe, Y., Noguchi, M. and Tamaki, E. Phytochemical studies on tobacco alkaloids. XIV. The occurence and properties of putrescine N-methyltransferase in tobacco roots. Plant Cell Physiol. 12 (1971) 633-640.
Accepted name: deoxycytidylate C-methyltransferase
Reaction: 5,10-methylenetetrahydrofolate + dCMP = dihydrofolate + deoxy-5-methylcytidylate
Other name(s): deoxycytidylate methyltransferase; dCMP methyltransferase
Systematic name: 5,10-methylenetetrahydrofolate:dCMP C-methyltransferase
Comments: dCMP is methylated by formaldehyde in the presence of tetrahydrofolate. CMP, dCTP and CTP can act as acceptors, but more slowly.
Links to other databases: BRENDA, EXPASY, KEGG, Metacyc, CAS registry number: 61970-01-2
References:
1. Kuo, T.-T. and Tu, J. Enzymatic synthesis of deoxy-5-methyl-cytidylic acid replacing deoxycytidylic acid in Xanthomonas oryzae phage Xp12DNA. Nature 263 (1976) 615. [PMID: 980110]
Accepted name: tRNA (adenine-N6-)-methyltransferase
Reaction: S-adenosyl-L-methionine + tRNA = S-adenosyl-L-homocysteine + tRNA containing N6-methyladenine
Systematic name: S-adenosyl-L-methionine:tRNA (adenine-N6-)-methyltransferase
Links to other databases: BRENDA, EXPASY, KEGG, Metacyc, CAS registry number: 9014-53-3
References:
1. Mandel, R., Hacker, B. and Maag, T.A. Altered transfer RNA methylase patterns in Marek's disease tumors. Cancer Res. 31 (1971) 613-616. [PMID: 4996578]
2. Mittelman, A., Hall, R.H., Yohn, D.S. and Grace, J.T. The in vitro soluble RNA methylase activity of SV40-induced hamster tumors. Cancer Res. 27 (1967) 1409-1414. [PMID: 4292682]
3. Sharma, O.K. Differences in the transfer RNA methyltransferases from normal rat liver and Novikoff hepatoma. Biochim. Biophys. Acta 299 (1973) 415-427. [PMID: 4349332]
Accepted name: mRNA (guanine-N7-)-methyltransferase
Reaction: S-adenosyl-L-methionine + G5'ppp5'R-mRNA = S-adenosyl-L-homocysteine + m7G5'ppp5'R-mRNA
Other name(s): messenger ribonucleate guanine 7-methyltransferase; guanine-7-methyltransferase; messenger RNA guanine 7-methyltransferase
Systematic name: S-adenosyl-L-methionine:mRNA (guanine-N7-)-methyltransferase
Comments: The nucleoside next to the terminal guanosine may be either guanosine or adenosine.
Links to other databases: BRENDA, EXPASY, KEGG, Metacyc, PDB, CAS registry number: 56941-25-4
References:
1. Ensinger, M.J., Martin, S.A., Paoletti, E. and Moss, B. Modification of the 5'-terminus of mRNA by soluble guanylyl and methyl transferases from vaccinia virus. Proc. Natl. Acad. Sci. USA 72 (1975) 2525-2529. [PMID: 1058472]
2. Groner, Y., Gilbao, E. and Aviv, H. Methylation and capping of RNA polymerase II primary transcripts by HeLa nuclear homogenates. Biochemistry 17 (1978) 977-982. [PMID: 629955]
3. Martin, S.A. and Moss, B. Modification of RNA by mRNA guanylyltransferase and mRNA (guanine-7)methyltransferase from vaccinia virions. J. Biol. Chem. 250 (1975) 9330-9335. [PMID: 1194287]
4. Martin, S.A., Paoletti, E. and Moss, B. Purification of mRNA guanylyltransferase and mRNA (guanine-7-) methyltransferase from vaccinia virions. J. Biol. Chem. 250 (1975) 9322-9329. [PMID: 1194286]
Accepted name: mRNA (nucleoside-2'-O-)-methyltransferase
Reaction: S-adenosyl-L-methionine + m7G5'ppp5'R-mRNA = S-adenosyl-L-homocysteine + m7G5'ppp5'Rm-mRNA
Other name(s): messenger ribonucleate nucleoside 2'-methyltransferase; messenger RNA (nucleoside-2'-)-methyltransferase
Systematic name: S-adenosyl-L-methionine:mRNA (nucleoside-2'-O-)-methyltransferase
Comments: The nucleoside next to the terminal guanosine may be either guanosine or adenosine. The formation of a 2'-O-methyladenosine cap was formerly listed as EC 2.1.1.58.
Links to other databases: BRENDA, EXPASY, KEGG, Metacyc, PDB, CAS registry number: 61970-02-3
References:
1. Barbosa, E. and Moss, B. mRNA(nucleoside-2'-)-methyltransferase from vaccinia virus. Purification and physical properties. J. Biol. Chem. 253 (1978) 7692-7697. [PMID: 701281]
2. Barbosa, E. and Moss, B. mRNA(nucleoside-2'-)-methyltransferase from vaccinia virus. Characteristics and substrate specificity. J. Biol. Chem. 253 (1978) 7698-7702. [PMID: 701282]
3. Boone, R.F., Ensinger, M.J. and Moss, B. Synthesis of mRNA guanylyltransferase and mRNA methyltransferases in cells infected with vaccinia virus. J. Virol. 21 (1977) 475-483. [PMID: 833934]
4. Ensinger, M.J., Martin, S.A., Paoletti, E. and Moss, B. Modification of the 5'-terminus of mRNA by soluble guanylyl and methyl transferases from vaccinia virus. Proc. Natl. Acad. Sci. USA 72 (1975) 2525-2529. [PMID: 1058472]
5. Groner, Y., Gilbao, E. and Aviv, H. Methylation and capping of RNA polymerase II primary transcripts by HeLa nuclear homogenates. Biochemistry 17 (1978) 977-982. [PMID: 629955]
[EC 2.1.1.58 Deleted entry: mRNA (adenosine-2'-O-)-methyltransferase. Now included with EC 2.1.1.57 mRNA (nucleoside-2'-O-)-methyltransferase. (EC 2.1.1.58 created 1981, deleted 1984)]
Accepted name: [cytochrome c]-lysine N-methyltransferase
Reaction: S-adenosyl-L-methionine + [cytochrome c]-L-lysine = S-adenosyl-L-homocysteine + [cytochrome c]-N6-methyl-L-lysine
Other name(s): cytochrome c (lysine) methyltransferase; cytochrome c methyltransferase; cytochrome c-specific protein methylase III; cytochrome c-specific protein-lysine methyltransferase
Systematic name: S-adenosyl-L-methionine:[cytochrome c]-L-lysine N6-methyltransferase
Comments: One of a group of enzymes methylating proteins; see also EC 2.1.1.43 histone-lysine N-methyltransferase and EC 2.1.1.60 calmodulin-lysine N-methyltransferase.
Links to other databases: BRENDA, EXPASY, KEGG, Metacyc, CAS registry number: 82047-78-7
References:
1. Durban, E., Nochumson, S., Kim, S. and Paik, W.K. Cytochrome c-specific protein-lysine methyltransferase from Neurospora crassa. Purification, characterization, and substrate requirements. J. Biol. Chem. 253 (1978) 1427-1435. [PMID: 203592]
2. Nochumson, S., Durban, E., Sangduk, K. and Paik, W.K. Cytochrome c-specific protein methylase III from Neurospora crassa. Biochem. J. 165 (1977) 11-18. [PMID: 196592]
3. Valentine, J. and Pettigrew, G.W. A cytochrome c methyltransferase from Crithidia oncopelti. Biochem. J. 201 (1982) 329-338. [PMID: 6282265]
Accepted name: calmodulin-lysine N-methyltransferase
Reaction: S-adenosyl-L-methionine + calmodulin L-lysine = S-adenosyl-L-homocysteine + calmodulin N6-methyl-L-lysine
Other name(s): S-adenosylmethionine:calmodulin (lysine) N-methyltransferase
Systematic name: S-adenosyl-L-methionine:calmodulin-L-lysine N6-methyltransferase
Comments: One of a group of enzymes methylating proteins; see also EC 2.1.1.43 histone-lysine N-methyltransferase and EC 2.1.1.59 [cytochrome-c]-lysine N-methyltransferase.
Links to other databases: BRENDA, EXPASY, KEGG, Metacyc, CAS registry number: 75603-20-2
References:
1. Sitaramayya, A., Wright, L.S. and Siegel, F.L. Enzymatic methylation of calmodulin in rat brain cytosol. J. Biol. Chem. 255 (1980) 8894-8900. [PMID: 6773954]
Accepted name: tRNA (5-methylaminomethyl-2-thiouridylate)-methyltransferase
Reaction: S-adenosyl-L-methionine + tRNA containing 5-aminomethyl-2-thiouridine = S-adenosyl-L-homocysteine + tRNA containing 5-methylaminomethyl-2-thiouridylate
Other name(s): transfer ribonucleate 5-methylaminomethyl-2-thiouridylate 5-methyltransferase; tRNA 5-methylaminomethyl-2-thiouridylate 5'-methyltransferase
Systematic name: S-adenosyl-L-methionine:tRNA (5-methylaminomethyl-2-thio-uridylate)-methyltransferase
Comments: This enzyme is specific for the terminal methyl group of 5-methylaminomethyl-2-thiouridylate.
Links to other databases: BRENDA, EXPASY, KEGG, Metacyc, PDB, CAS registry number: 39391-17-8
References:
1. Taya, Y. and Nishimura, S. Biosynthesis of 5-methylaminomethyl-2-thiouridylate. I. Isolation of a new tRNA-methylase specific for 5-methylaminomethyl-2-thiouridylate. Biochem. Biophys. Res. Commun. 51 (1973) 1062-1068. [PMID: 4703553]
2. Taya, Y. and Nishimura, S. In: Salvatore, F., Borek, E., Zappia, V., Williams-Ashman, H.G. and Schlenk, F. (Eds), The Biochemistry of Adenosylmethionine, Columbia University Press, New York, 1977, p. 251.
Accepted name: mRNA (2'-O-methyladenosine-N6-)-methyltransferase
Reaction: S-adenosyl-L-methionine + m7G(5')pppAm = S-adenosyl-L-homocysteine + m7G(5')pppm6Am (mRNA containing an N6,2'-O-dimethyladenosine cap)
Other name(s): messenger ribonucleate 2'-O-methyladenosine NG-methyltransferase
Systematic name: S-adenosyl-L-methionine:mRNA (2'-O-methyladenosine-N6-)-methyltransferase
Links to other databases: BRENDA, EXPASY, KEGG, Metacyc, CAS registry number: 68009-87-0
References:
1. Keith, J.M., Ensinger, M.J. and Moss, B. HeLa cell RNA (2'-O-methyladenosine-N6-)-methyltransferase specific for the capped 5'-end of messenger RNA. J. Biol. Chem. 253 (1978) 5033-5039. [PMID: 670176]
Accepted name: methylated-DNA—[protein]-cysteine S-methyltransferase
Reaction: DNA (containing 6-O-methylguanine) + protein L-cysteine = DNA (without 6-O-methylguanine) + protein S-methyl-L-cysteine
Systematic name: DNA-6-O-methylguanine:[protein]-L-cysteine S-methyltransferase
Comments: This protein is involved in the repair of alkylated DNA. It acts only on the alkylated DNA (cf. EC 3.2.2.20, DNA-3-methyladenine glycosidase I and EC 3.2.2.21, DNA-3-methyladenine glycosidase II). This enzyme catalyses only one turnover and therefore is not strictly catalytic.
Links to other databases: BRENDA, EXPASY, KEGG, Metacyc, PDB, CAS registry number: 77271-19-3
References:
1. Foote, R.S., Mitra, S. and Pal, B.C. Demethylation of O6-methylguanine in a synthetic DNA polymer by an inducible activity in Escherichia coli. Biochem. Biophys. Res. Commun. 97 (1980) 654-659. [PMID: 81133635]
2. Olsson, M. and Lindehl, T. Repair of alkylated DNA in Escherichia coli. Methyl group transfer from O6-methylguanine to a protein cysteine residue. J. Biol. Chem. 255 (1980) 10569-10571. [PMID: 81046903]
3. Pegg, A.E. and Byers, T.L. Repair of DNA containing O6-alkylguanine. FASEB J. 6 (1992) 2302-2310. [PMID: 92184065]
Accepted name: 3-demethylubiquinol 3-O-methyltransferase
Reaction: S-adenosyl-L-methionine + 3-demethylubiquinol-n = S-adenosyl-L-homocysteine + ubiquinol-n
For diagram of reaction click here.
Glossary: 3-demethylubiquinol-n = 3-hydroxy-2-methoxy-5-methyl-6-(all-trans-polyprenyl)-1,4-benzoquinol
Other name(s): 5-demethylubiquinone-9 methyltransferase; OMHMB-methyltransferase; 2-octaprenyl-3-methyl-5-hydroxy-6-methoxy-1,4-benzoquinone methyltransferase; S-adenosyl-L-methionine:2-octaprenyl-3-methyl-5-hydroxy-6-methoxy-1,4-benzoquinone-O-methyltransferase; COQ3 (gene name); Coq3 O-methyltransferase; ubiG (gene name, ambiguous)
Systematic name: S-adenosyl-L-methionine:3-hydroxy-2-methoxy-5-methyl-6-(all-trans-polyprenyl)-1,4-benzoquinol 3-O-methyltransferase
Comments: This enzyme is involved in ubiquinone biosynthesis. Ubiquinones from different organisms have a different number of prenyl units (for example, ubiquinone-6 in Saccharomyces, ubiquinone-9 in rat and ubiquinone-10 in human), and thus the natural substrate for the enzymes from different organisms has a different number of prenyl units. However, the enzyme usually shows a low degree of specificity regarding the number of prenyl units. For example, the human COQ3 enzyme can restore biosynthesis of ubiquinone-6 in coq3 deletion mutants of yeast [3]. The enzymes from yeast, Escherichia coli and rat also catalyse the methylation of 3,4-dihydroxy-5-all-trans-polyprenylbenzoate [3] (a reaction that is classified as EC 2.1.1.114, polyprenyldihydroxybenzoate methyltransferase).
Links to other databases: BRENDA, EXPASY, KEGG, Metacyc, CAS registry number: 63774-48-1
References:
1. Houser, R.M. and Olson, R.E. 5-Demethylubiquinone-9-methyltransferase from rat liver mitochondria. Characterization, localization, and solubilization. J. Biol. Chem. 252 (1977) 4017-4021. [PMID: 863914]
2. Leppik, R.A., Stroobant, P., Shineberg, B., Young, I.G. and Gibson, F. Membrane-associated reactions in ubiquinone biosynthesis. 2-Octaprenyl-3-methyl-5-hydroxy-6-methoxy-1,4-benzoquinone methyltransferase. Biochim. Biophys. Acta 428 (1976) 146-156. [PMID: 769831]
3. Poon, W.W., Barkovich, R.J., Hsu, A.Y., Frankel, A., Lee, P.T., Shepherd, J.N., Myles, D.C. and Clarke, C.F. Yeast and rat Coq3 and Escherichia coli UbiG polypeptides catalyze both O-methyltransferase steps in coenzyme Q biosynthesis. J. Biol. Chem. 274 (1999) 21665-21672. [PMID: 10419476]
4. Jonassen, T. and Clarke, C.F. Isolation and functional expression of human COQ3, a gene encoding a methyltransferase required for ubiquinone biosynthesis. J. Biol. Chem. 275 (2000) 12381-12387. [PMID: 10777520]
Accepted name: licodione 2'-O-methyltransferase
Reaction: S-adenosyl-L-methionine + licodione = S-adenosyl-L-homocysteine + 2'-O-methyllicodione
For diagram click here.
Systematic name: S-adenosyl-L-methionine:licodione 2'-O-methyltransferase
Comments: As well as licodione [1-(2,4-dihydroxyphenyl)-3-(4-hydroxyphenyl)-1,3-propanedione], the 2"-hydroxy-derivative and isoliquiritigenin can act as acceptors, but more slowly.
Links to other databases: BRENDA, EXPASY, KEGG, Metacyc, PDB, CAS registry number: 77000-07-8
References:
1. Ayabe, S.-I., Yoshikawa, T., Kobayashi, M. and Furuya, T. Biosynthesis of retrochalcone, echinatin: involvement of O-methyltransferase to licodione. Phytochemistry 19 (1980) 2331-2336.
Accepted name: rRNA (adenosine-2'-O-)-methyltransferase
Reaction: S-adenosyl-L-methionine + rRNA = S-adenosyl-L-homocysteine + rRNA containing a single residue of 2'-O-methyladenosine
Other name(s): ribosomal ribonucleate adenosine 2'-methyltransferase; rRNA adenosine 2'-methylase; RNA-pentose methylase; thiostrepton-resistance methylase
Systematic name: S-adenosyl-L-methionine:rRNA (adenosine-2'-O)-methyltransferase
Links to other databases: BRENDA, EXPASY, KEGG, Metacyc, PDB, CAS registry number: 80146-87-8
References:
1. Thompson, J. and Cundliffe, E. Purification and properties of an RNA methylase produced by Streptomyces azureus and involved in resistance to thiostrepton. J. Gen. Microbiol. 124 (1981) 291-297.
Accepted name: thiopurine S-methyltransferase
Reaction: S-adenosyl-L-methionine + a thiopurine = S-adenosyl-L-homocysteine + a thiopurine S-methylether
Other name(s): mercaptopurine methyltransferase; thiopurine methyltransferase; 6-thiopurine transmethylase; TPMT
Systematic name: S-adenosyl-L-methionine:thiopurine S-methyltransferase
Comments: Also acts, more slowly, on thiopyrimidines and aromatic thiols. Not identical with EC 2.1.1.9 thiol S-methyltransferase.
Links to other databases: BRENDA, EXPASY, KEGG, Metacyc, PDB, CAS registry number: 67339-09-7
References:
1. Remy, C.N. Metabolism of thiopyrimidines and thiopurines. S-Methylation with S-adenosylmethionine transmethylase and catabolism in mammalian tissues. J. Biol. Chem. 238 (1963) 1078-1084.
2. Woodson, L.C., Ames, M.M., Selassie, C.D, Hansch, C. and Weinshilbaum, R.M. Thiopurine methyltransferase. Aromatic thiol substrates and inhibition by benzoic acid derivatives. Mol. Pharmacol. 24 (1983) 471-478. [PMID: 6633508]
3. Woodson, L.C. and Weinshilbaum, R.M. Human kidney thiopurine methyltransferase. Purification and biochemical properties. Biochem. Pharmacol. 32 (1983) 819-826. [PMID: 6838629]
Accepted name: caffeate O-methyltransferase
Reaction: S-adenosyl-L-methionine + 3,4-dihydroxy-trans-cinnamate = S-adenosyl-L-homocysteine + 3-methoxy-4-hydroxy-trans-cinnamate
Other name(s): caffeate methyltransferase; caffeate 3-O-methyltransferase; S-adenosyl-L-methionine:caffeic acid-O-methyltransferase
Systematic name: S-adenosyl-L-methionine:3,4-dihydroxy-trans-cinnamate 3-O-methyltransferase
Comments: 3,4-Dihydroxybenzaldehyde and catechol can act as acceptors, but more slowly.
Links to other databases: BRENDA, EXPASY, KEGG, Metacyc, PDB, CAS registry number: 50936-45-3
References:
1. Ebel, J., Schaller-Hekeler, B., Knobloch, K.-H., Wellman, E., Grisebach, H. and Hahlbrock, K. Coordinated changes in enzyme activities of phenylpropanoid metabolism during the growth of soybean cell suspension cultures. Biochim. Biophys. Acta 362 (1974) 417-424. [PMID: 4472044]
2. Poulton, J.E. and Butt, V.S. Purification and properties of S-adenosyl-L-methionine: caffeic acid O-methyltransferase from leaves of spinach beet (Beta vulgaris L). Biochim. Biophys. Acta 403 (1975) 301-314. [PMID: 241400]
3. Shimada, M., Kuroda, H. and Higuchi, T. Evidence for the formation of methoxyl groups of ferulic and sinapic acid in Bambusa by the same O-methyltransferase. Phytochemistry 12 (1973) 2873-2875.
Accepted name: 5-hydroxyfuranocoumarin 5-O-methyltransferase
Reaction: (1) S-adenosyl-L-methionine + a 5-hydroxyfurocoumarin = S-adenosyl-L-homocysteine + a 5- methoxyfurocoumarin (general reaction)
(2) S-adenosyl-L-methionine + bergaptol = S-adenosyl-L-homocysteine + bergapten
For diagram click here.
Glossary: bergaptol = 5-hydroxypsoralen
O-methylbergaptol = bergapten = 5-methoxypsoralen
Other name(s): furanocoumarin 5-methyltransferase; furanocoumarin 5-O-methyltransferase; bergaptol 5-O-methyltransferase; bergaptol O-methyltransferase; bergaptol methyltransferase; S-adenosyl-L-methionine:bergaptol O-methyltransferase; BMT; S-adenosyl-L-methionine:5-hydroxyfuranocoumarin 5-O-methyltransferase
Systematic name: S-adenosyl-L-methionine:5-hydroxyfurocoumarin 5-O-methyltransferase
Comments: Converts bergaptol into bergapten, which has therapeutic potential in the treatment of psoriasis as it has photosensitizing and antiproliferative activities [4]. The enzyme methylates the 5-hydroxy group of some hydroxy- and methylcoumarins, such as 5-hydroxyxanthotoxin [3], but has little activity on non-coumarin phenols [1]. Caffeate, 5-hydroxyferulate and daphnetin are not substrates [4]. Cu2+, Zn2+ and Co2+ cause enzyme inhibition [4]. (see also EC 2.1.1.70, 8-hydroxyfuranocoumarin 8-O-methyltransferase)
Links to other databases: BRENDA, EXPASY, KEGG, Metacyc, CAS registry number: 67339-12-2, 101637-31-4
References:
1. Thompson, H.J., Sharma, S.K. and Brown, S.A. O-Methyltransferases of furanocoumarin biosynthesis. Arch. Biochem. Biophys. 188 (1978) 272-281. [PMID: 28084]
2. Sharma, S.K., Garrett, J.M. and Brown, S.A. Separation of the S-adenosylmethionine: 5- and 8-hydroxyfuranocoumarin O-methyltransferases of Ruta graveolens L. by general ligand affinity chromatography. Z. Naturforsch. [C] 34C (1979) 387-391. [PMID: 156999]
3. Hauffe, K.D., Hahlbrock, K. and Scheel, D. Elicitor-stimulated furanocoumarin biosynthesis in cultured parsley cells - S-adenosyl-L-methionine-bergaptol and S-adenosyl-L-methionine-xanthotoxol O-methyltransferases. Z. Naturforsch. C: Biosci. 41 (1986) 228-239.
4. Hehmann, M., Lukacin, R., Ekiert, H. and Matern, U. Furanocoumarin biosynthesis in Ammi majus L. Cloning of bergaptol O-methyltransferase. Eur. J. Biochem. 271 (2004) 932-940. [PMID: 15009205]
Accepted name: 8-hydroxyfuranocoumarin 8-O-methyltransferase
Reaction: (1) S-adenosyl-L-methionine + an 8-hydroxyfurocoumarin = S-adenosyl-L-homocysteine + an 8-methoxyfurocoumarin (general reaction)
(2) S-adenosyl-L-methionine + xanthotoxol = S-adenosyl-L-homocysteine + xanthotoxin
For diagram of reaction, click here
Glossary: xanthotoxin = O-methylxanthotoxol = 8-methoxypsoralen
xanthotoxol = 8-hydroxypsoralen
Other name(s): furanocoumarin 8-methyltransferase; furanocoumarin 8-O-methyl-transferase; xanthotoxol 8-O-methyltransferase; XMT; 8-hydroxyfuranocoumarin 8-O-methyltransferase; SAM:xanthotoxol O-methyltransferase; S-adenosyl-L-methionine:8-hydroxyfuranocoumarin 8-O-methyltransferase; xanthotoxol methyltransferase; xanthotoxol O-methyltransferase; S-adenosyl-L-methionine:xanthotoxol O-methyltransferase; S-adenosyl-L-methionine-xanthotoxol O-methyltransferase
Systematic name: S-adenosyl-L-methionine:8-hydroxyfurocoumarin 8-O-methyltransferase
Comments: Converts xanthotoxol into xanthotoxin, which has therapeutic potential in the treatment of psoriasis as it has photosensitizing and antiproliferative activities [4]. Methylates the 8-hydroxy group of some hydroxy- and methylcoumarins, but has little activity on non-coumarin phenols (see also EC 2.1.1.69, 5-hydroxyfuranocoumarin 5-O-methyltransferase).
Links to other databases: BRENDA, EXPASY, KEGG, Metacyc, CAS registry number: 67339-13-3
References:
1. Thompson, H.J., Sharma, S.K. and Brown, S.A. O-Methyltransferases of furanocoumarin biosynthesis. Arch. Biochem. Biophys. 188 (1978) 272-281. [PMID: 28084]
2. Hauffe, K.D., Hahlbrock, K. and Scheel, D. Elicitor-stimulated furanocoumarin biosynthesis in cultured parsley cells - S-adenosyl-L-methionine-bergaptol and S-adenosyl-L-methionine-xanthotoxol O-methyltransferases. Z. Naturforsch. C: Biosci. 41 (1986) 228-239.
3. Sharma, S.K., Garrett, J.M. and Brown, S.A. Separation of the S-adenosylmethionine: 5- and 8-hydroxyfuranocoumarin O-methyltransferases of Ruta graveolens L. by general ligand affinity chromatography. Z. Naturforsch. [C] 34C (1979) 387-391. [PMID: 156999]
4. Hehmann, M., Lukačin, R., Ekiert, H. and Matern, U. Furanocoumarin biosynthesis in Ammi majus L. Cloning of bergaptol O-methyltransferase. Eur. J. Biochem. 271 (2004) 932-940. [PMID: 15009205]
Note For reference 4 an accent may not be seen. č is c-hacek.
Accepted name: phosphatidyl-N-methylethanolamine N-methyltransferase
Reaction: S-adenosyl-L-methionine + phosphatidyl-N-methylethanolamine = S-adenosyl-L-homocysteine + phosphatidyl-N-dimethylethanolamine
Other name(s): phosphatidylmonomethylethanolamine methyltransferase; methyltransferase II; phospholipid methyltransferase; PLMT; phosphatidyl-N-methylethanolamine methyltransferase; phosphatidyl-N-monomethylethanolamine methyltransferase; phosphatidylethanolamine methyltransferase I; phosphatidylmonomethylethanolamine methyltransferase
Systematic name: S-adenosyl-L-methionine:phosphatidyl-N-methylethanolamine N-methyltransferase
Comments: The enzyme also catalyses the transfer of a further methyl group, producing phosphatidylcholine.
Links to other databases: BRENDA, EXPASY, KEGG, Metacyc, CAS registry number: 67167-73-1
References:
1. Hirata, F., Viveros, O.H., Diliberto, E.J., Jr. and Axelrod, J. Identification and properties of two methyltransferases in conversion of phosphatidylethanolamine to phosphatidylcholine. Proc. Natl. Acad. Sci. USA 75 (1978) 1718-1721. [PMID: 25437]
2. Schneider, W.J. and Vance, D.E. Conversion of phosphatidylethanolamine to phosphatidylcholine in rat liver. Partial purification and characterization of the enzymatic activities. J. Biol. Chem. 254 (1979) 3886-3891. [PMID: 438165]
Accepted name: site-specific DNA-methyltransferase (adenine-specific)
Reaction: S-adenosyl-L-methionine + DNA adenine = S-adenosyl-L-homocysteine + DNA 6-methylaminopurine
Other name(s): modification methylase; restriction-modification system
Comments: This is a large group of enzymes, most of which, with enzymes of similar site specificity listed as EC 3.1.21.3 type 1 site-specific deoxyribonuclease, EC 3.1.21.4 type II site-specific deoxyribonuclease or EC 3.1.21.5 type III site-specific deoxyribonuclease, form so-called 'restriction-modification systems'. A complete listing of all of these enzymes has been produced by R.J. Roberts and is available on-line at http://rebase.neb.com/rebase/rebase.html.
Links to other databases: BRENDA, EXPASY, KEGG, Metacyc, PDB, CAS registry number: 69553-52-2
References:
1. Kessler, C. and Manta, V. Specificity of restriction endonucleases and DNA modification methyltransferases: a review (Edition 3). Gene 92 (1990) 1-248. [PMID: 2172084]
2. Roberts, R.J. Restriction enzymes and their isoschizomers. Nucleic Acids Res. 18 (1990) 2331-2365. [PMID: 2159140]
3. Yuan, R. Structure and mechanism of multifunctional restriction endonucleases. Annu. Rev. Biochem. 50 (1981) 285-319. [PMID: 6267988]
[EC 2.1.1.73 Deleted entry: site-specific DNA-methyltransferase (cytosine-specific). Reaction is that of EC 2.1.1.37, DNA (cytosine-5-)-methyltransferase. (EC 2.1.1.73 created 1984, deleted 2003)]
Accepted name: methylenetetrahydrofolate—tRNA-(uracil54-C5)-methyltransferase (FADH2-oxidizing)
Reaction: 5,10-methylenetetrahydrofolate + uridine54 in tRNA + FADH2 = tetrahydrofolate + 5-methyluridine54 in tRNA + FAD
Glossary: Ψ = pseudouridine
T = ribothymidine = 5-methyluridine
Other name(s): folate-dependent ribothymidyl synthase; methylenetetrahydrofolate-transfer ribonucleate uracil 5-methyltransferase; 5,10-methylenetetrahydrofolate:tRNA-UPsiC (uracil-5-)-methyl-transferase; 5,10-methylenetetrahydrofolate:tRNA (uracil-5-)-methyl-transferase; TrmFO; folate/FAD-dependent tRNA T54 methyltransferase
Systematic name: 5,10-methylenetetrahydrofolate:tRNA (uracil54-C5)-methyltransferase
Comments: Up to 25% of the bases in mature tRNA are post-translationally modified or hypermodified. One almost universal post-translational modification is the conversion of U54 into ribothymidine in the TPsiC loop, and this modification is found in most species studied to date [2]. Unlike this enzyme, which uses 5,10-methylenetetrahydrofolate and FADH2 to supply the atoms for methylation of U54, EC 2.1.1.35, tRNA (uracil54-C5)-methyltransferase, uses S-adenosyl-L-methionine.
Links to other databases: BRENDA, EXPASY, KEGG, Metacyc, CAS registry number: 56831-74-4
References:
1. Delk, A.S., Nagle, D.P., Jr. and Rabinowitz, J.C. Methylenetetrahydrofolate-dependent biosynthesis of ribothymidine in transfer RNA of Streptococcus faecalis. Evidence for reduction of the 1-carbon unit by FADH2. J. Biol. Chem. 255 (1980) 4387-4390. [PMID: 6768721]
2. Becker, H.F., Motorin, Y., Sissler, M., Florentz, C. and Grosjean, H. Major identity determinants for enzymatic formation of ribothymidine and pseudouridine in the TΨ-loop of yeast tRNAs. J. Mol. Biol. 274 (1997) 505-518. [PMID: 9417931]
3. Nishimasu, H., Ishitani, R., Yamashita, K., Iwashita, C., Hirata, A., Hori, H. and Nureki, O. Atomic structure of a folate/FAD-dependent tRNA T54 methyltransferase. Proc. Natl. Acad. Sci. USA 106 (2009) 8180-8185. [PMID: 19416846]
Accepted name: apigenin 4'-O-methyltransferase
Reaction: S-adenosyl-L-methionine + 5,7,4'-trihydroxyflavone = S-adenosyl-L-homocysteine + 4'-methoxy-5,7-dihydroxyflavone
For diagram click here.
Other name(s): flavonoid O-methyltransferase; flavonoid methyltransferase
Systematic name: S-adenosyl-L-methionine:5,7,4'-trihydroxyflavone 4'-O-methyltransferase
Comments: Converts apigenin into acacetin. Naringenin (5,7,4'-trihydroxy-flavanone) can also act as an acceptor, but more slowly.
Links to other databases: BRENDA, EXPASY, KEGG, Metacyc, CAS registry number: 118251-36-8
References:
1. Kuroki, G. and Poulton, J.E. The para-O-methylation of apigenin to acacetin by cell-free extracts of Robinia pseudoacacia L. Z. Naturforsch. C: Biosci. 36 (1981) 916-920.
Accepted name: quercetin 3-O-methyltransferase
Reaction: S-adenosyl-L-methionine + 3,5,7,3',4'-pentahydroxyflavone = S-adenosyl-L-homocysteine + 3-methoxy-5,7,3',4'-tetrahydroxyflavone
For diagram click here.
Other name(s): flavonol 3-O-methyltransferase; flavonoid 3-methyltransferase
Systematic name: S-adenosyl-L-methionine:3,5,7,3',4'-pentahydroxyflavone 3-O-methyltransferase
Comments: Specific for quercetin. Related enzymes bring about the 3-O-methylation of other flavonols, such as galangin and kaempferol.
Links to other databases: BRENDA, EXPASY, KEGG, Metacyc, PDB, CAS registry number: 81295-55-8
References:
1. De Luca, V., Brunet, G., Khouri, H., Ibrahim, R. and Hrazdina, G. Flavonol 3-O-methyltransferase in plant-tissues. Z. Naturforsch. 37 (1982) 134-135.
2. De Luca, V. and Ibrahim, R.K. Enzymatic synthesis of polymethylated flavonols in Chrysosplenium americanum. I. Partial purification and some properties of S-adenosyl-L-methionine:flavonol 3-, 6-, 7-, and 4'-O-methyltransferases. Arch. Biochem. Biophys. 238 (1985) 596-605. [PMID: 3994393]
3. De Luca, V. and Ibrahim, R.K. Enzymatic synthesis of polymethylated flavonols in Chrysosplenium americanum. II. Substrate interaction and product inhibition studies of flavonol 3-, 6-, and 4'-O-methyltransferases. Arch. Biochem. Biophys. 238 (1985) 606-618. [PMID: 3994394]
4. Ibrahim, R.K. and De Luca,V. Polymethylated flavonol synthesis is catalyzed by distinct O-methyltransferases. Naturwissenschaften 69 (1982) 41-42.
Accepted name: protein-L-isoaspartate(D-aspartate) O-methyltransferase
Reaction: S-adenosyl-L-methionine + protein L-isoaspartate = S-adenosyl-L-homocysteine + protein L-isoaspartate α-methyl ester
Other name(s): protein-L-isoaspartate O-methyltransferase; protein-β-aspartate O-methyltransferase; D-aspartyl/L-isoaspartyl methyltransferase; L-isoaspartyl/D-aspartyl protein carboxyl methyltransferase; protein (D-aspartate) methyltransferase; protein D-aspartate methyltransferase; protein L-isoaspartate methyltransferase; protein L-isoaspartyl methyltransferase; protein O-methyltransferase (L-isoaspartate); L-aspartyl/L-isoaspartyl protein methyltransferase
Systematic name: S-adenosyl-L-methionine:protein-L-isoaspartate O-methyltransferase
Comments: D-Aspartate (but not L-aspartate) residues in proteins can also act as acceptors. Previously also listed as EC 2.1.1.24.
Links to other databases: BRENDA, EXPASY, KEGG, Metacyc, PDB, CAS registry number: 105638-50-4
References:
1. Aswad, D.W. and Johnson, B.A. The unusual substrate-specificity of eukaryotic protein carboxyl methyltransferases. Trends Biochem. Sci. 12 (1987) 155-158.
2. Clarke, S. Protein carboxyl methyltransferases: two distinct classes of enzymes. Annu. Rev. Biochem. 54 (1985) 479-506. [PMID: 3896126]
3. Kim, S. and Paik, W.K. Purification and properties of protein methylase II. J. Biol. Chem. 245 (1970) 1806-1813. [PMID: 5438363]
4. Ota, I.M., Ding, L. and Clarke, S. Methylation at specific altered aspartyl and asparaginyl residues in glucagon by the erythrocyte protein carboxyl methyltransferase. J. Biol. Chem. 262 (1987) 8522-8531. [PMID: 3597386]
Accepted name: isoorientin 3'-O-methyltransferase
Reaction: S-adenosyl-L-methionine + isoorientin = S-adenosyl-L-homocysteine + isoscoparin
Other name(s): isoorientin 3'-methyltransferase
Systematic name: S-adenosyl-L-methionine:isoorientin 3'-O-methyltransferase
Comments: Also acts on isoorientin 2"-O-rhamnoside. Involved in the biosynthesis of flavones.
Links to other databases: BRENDA, EXPASY, KEGG, Metacyc, CAS registry number: 83061-51-2
References:
1. van Brederode, J., Kamps-Heinsbroek, R. and Mastenbroek, O. Biochemical and ontogenetic evidence that the ferulic acid and isoscoparin formation in silene are catalyzed by different enzymes. Z. Pflanzenphysiol. 106 (1982) 43-53.
Accepted name: cyclopropane-fatty-acyl-phospholipid synthase
Reaction: S-adenosyl-L-methionine + phospholipid olefinic fatty acid = S-adenosyl-L-homocysteine + phospholipid cyclopropane fatty acid
Other name(s): cyclopropane synthetase; unsaturated-phospholipid methyltransferase; cyclopropane synthase; cyclopropane fatty acid synthase; cyclopropane fatty acid synthetase; CFA synthase
Systematic name: S-adenosyl-L-methionine:unsaturated-phospholipid methyltransferase (cyclizing)
Comments: The enzyme adds a methylene group across the 9,10 position of a δ9-olefinic acyl chain in phosphatidylethanolamine or, more slowly, phosphatidylglycerol or phosphatidylinositol, forming a cyclopropane derivative (cf. EC 2.1.1.16 methylene-fatty-acyl-phospholipid synthase).
Links to other databases: BRENDA, EXPASY, KEGG, Metacyc, PDB, CAS registry number: 51845-48-8
References:
1. Chung, A.E. and Law, J.H. Cyclopropane fatty acid synthetase: Partial purification and properties. Biochemistry 3 (1964) 967-974.
2. Zalkin, H., Law, J.H. and Goldfine, H. Enzymatic synthesis of cyclopropane fatty acids catalyzed by bacterial extracts. J. Biol. Chem. 238 (1963) 1242-1248.
Accepted name: protein-glutamate O-methyltransferase
Reaction: S-adenosyl-L-methionine + protein L-glutamate = S-adenosyl-L-homocysteine + protein L-glutamate methyl ester
Other name(s): methyl-accepting chemotaxis protein O-methyltransferase; S-adenosylmethionine-glutamyl methyltransferase; methyl-accepting chemotaxis protein methyltransferase II; S-adenosylmethionine:protein-carboxyl O-methyltransferase; protein methylase II; MCP methyltransferase I; MCP methyltransferase II; protein O-methyltransferase; protein(aspartate)methyltransferase; protein(carboxyl)methyltransferase; protein carboxyl-methylase; protein carboxyl-O-methyltransferase; protein carboxylmethyltransferase II; protein carboxymethylase; protein carboxymethyltransferase; protein methyltransferase II
Systematic name: S-adenosyl-L-methionine:protein-L-glutamate O-methyltransferase
Comments: Forms ester groups with L-glutamate residues in a number of membrane proteins.
Links to other databases: BRENDA, EXPASY, KEGG, Metacyc, PDB, CAS registry number: 9055-09-8
References:
1. Burgess-Cassler, A., Ulla, A.H.J. and Ordal, G.W. Purification and characterization of Bacillus subtilis methyl-accepting chemotaxis protein methyltransferase II. J. Biol. Chem. 257 (1982) 8412-8417. [PMID: 6806296]
2. Kleene, S.J., Toews, M.L. and Adler, J. Isolation of glutamic acid methyl ester from an Escherichia coli membrane protein involved in chemotaxis. J. Biol. Chem. 252 (1977) 3214-3218. [PMID: 16888]
3. Simms, S.A., Stock, A.M. and Stock, J.B. Purification and characterization of the S-adenosylmethionine:glutamyl methyltransferase that modifies membrane chemoreceptor proteins in bacteria. J. Biol. Chem. 262 (1987) 8537-8543. [PMID: 3298235]
4. Springer, W.R. and Koshland, D.E., Jr. Identification of a protein methyltransferase as the cheR gene product in the bacterial sensing system. Proc. Natl. Acad. Sci. USA 74 (1977) 533-537. [PMID: 322131]
[EC 2.1.1.81 Deleted entry: nicotine N-methyltransferase. Now included with EC 2.1.1.49 amine N-methyltransferase. (EC 2.1.1.81 created 1989, deleted 1990)]
Accepted name: 3-methylquercetin 7-O-methyltransferase
Reaction: S-adenosyl-L-methionine + 5,7,3',4'-tetrahydroxy-3-methoxyflavone = S-adenosyl-L-homocysteine + 5,3',4'-trihydroxy-3,7-dimethoxyflavone
For diagram click here.
Other name(s): flavonol 7-O-methyltransferase; flavonol 7-methyltransferase; 7-OMT; S-adenosyl-L-methionine:3',4',5,7-tetrahydroxy-3-methoxyflavone 7-O-methyltransferase; 3-methylquercitin 7-O-methyltransferase [mis-spelt]
Systematic name: S-adenosyl-L-methionine:5,7,3',4'-tetrahydroxy-3-methoxyflavone 7-O-methyltransferase
Comments: Involved with EC 2.1.1.76 quercetin 3-O-methyltransferase and EC 2.1.1.83 3,7-dimethylquercetin 4'-O-methyltransferase in the methylation of quercetin to 3,7,4'-trimethylquercetin in Chrysosplenium americanum. Does not act on flavones, dihydroflavonols, or their glucosides.
Links to other databases: BRENDA, EXPASY, KEGG, Metacyc, CAS registry number: 97089-67-3
References:
1. De Luca, V. and Ibrahim, R.K. Enzymatic synthesis of polymethylated flavonols in Chrysosplenium americanum. I. Partial purification and some properties of S-adenosyl-L-methionine:flavonol 3-, 6-, 7-, and 4'-O-methyltransferases. Arch. Biochem. Biophys. 238 (1985) 596-605. [PMID: 3994393]
Accepted name: 3,7-dimethylquercetin 4'-O-methyltransferase
Reaction: S-adenosyl-L-methionine + 5,3',4'-trihydroxy-3,7-dimethoxyflavone = S-adenosyl-L-homocysteine + 5,3'-dihydroxy-3,7,4'-trimethoxyflavone
For diagram click here.
Other name(s): flavonol 4'-O-methyltransferase; flavonol 4'-methyltransferase; 4'-OMT; S-adenosyl-L-methionine:3',4',5-trihydroxy-3,7-dimethoxyflavone 4'-O-methyltransferase; 3,7-dimethylquercitin 4'-O-methyltransferase [mis-spelt]
Systematic name: S-adenosyl-L-methionine:5,3',4'-trihydroxy-3,7-dimethoxyflavone 4'-O-methyltransferase
Comments: 3,7-Dimethylquercetagetin can also act as acceptor. Involved with EC 2.1.1.76 quercetin 3-O-methyltransferase and EC 2.1.1.82 3-methylquercetin 7-O-methyltransferase in the methylation of quercetin to 3,7,4'-trimethylquercetin in Chrysosplenium americanum. Does not act on flavones, dihydroflavonols, or their glucosides.
Links to other databases: BRENDA, EXPASY, KEGG, Metacyc, CAS registry number: 96477-60-0
References:
1. De Luca, V. and Ibrahim, R.K. Enzymatic synthesis of polymethylated flavonols in Chrysosplenium americanum. I. Partial purification and some properties of S-adenosyl-L-methionine:flavonol 3-, 6-, 7-, and 4'-O-methyltransferases. Arch. Biochem. Biophys. 238 (1985) 596-605. [PMID: 3994393]
2. De Luca, V. and Ibrahim, R.K. Enzymatic synthesis of polymethylated flavonols in Chrysosplenium americanum. II. Substrate interaction and product inhibition studies of flavonol 3-, 6-, and 4'-O-methyltransferases. Arch. Biochem. Biophys. 238 (1985) 606-618. [PMID: 3994394]
Accepted name: methylquercetagetin 6-O-methyltransferase
Reaction: S-adenosyl-L-methionine + 5,6,3',4'-tetrahydroxy-3,7-dimethoxyflavone = S-adenosyl-L-homocysteine + 5,3',4'-trihydroxy-3,6,7-trimethoxyflavone
Other name(s): flavonol 6-O-methyltransferase; flavonol 6-methyltransferase; 6-OMT; S-adenosyl-L-methionine:3',4',5,6-tetrahydroxy-3,7-dimethoxyflavone 6-O-methyltransferase
Systematic name: S-adenosyl-L-methionine:3',4',5,6-tetrahydroxy-3,7-dimethoxyflavone 6-O-methyltransferase
Comments: The enzymes from Chrysosplenium americanum also methylates 3,7,3'-trimethylquercetagetin at the 6-position. Does not act on flavones, dihydroflavonols, or their glucosides.
Links to other databases: BRENDA, EXPASY, KEGG, Metacyc, CAS registry number: 97089-68-4
References:
1. De Luca, V. and Ibrahim, R.K. Enzymatic synthesis of polymethylated flavonols in Chrysosplenium americanum. I. Partial purification and some properties of S-adenosyl-L-methionine:flavonol 3-, 6-, 7-, and 4'-O-methyltransferases. Arch. Biochem. Biophys. 238 (1985) 596-605. [PMID: 3994393]
2. De Luca, V. and Ibrahim, R.K. Enzymatic synthesis of polymethylated flavonols in Chrysosplenium americanum. II. Substrate interaction and product inhibition studies of flavonol 3-, 6-, and 4'-O-methyltransferases. Arch. Biochem. Biophys. 238 (1985) 606-618. [PMID: 3994394]
Accepted name: protein-histidine N-methyltransferase
Reaction: S-adenosyl-L-methionine + protein L-histidine = S-adenosyl-L-homocysteine + protein Nτ-methyl-L-histidine
Other name(s): protein methylase IV; protein (histidine) methyltransferase; actin-specific histidine methyltransferase; S-adenosyl methionine:protein-histidine N-methyltransferase
Systematic name: S-adenosyl-L-methionine:protein-L-histidine N-tele-methyltransferase
Comments: Highly specific for histidine residues, for example, in actin.
Links to other databases: BRENDA, EXPASY, KEGG, Metacyc, CAS registry number: 108022-17-9
References:
1. Vijayasarathy, C. and Narasinga Rao, B.S. Partial purification and characterisation of S-adenosylmethionine:protein-histidine N-methyltransferase from rabbit skeletal muscle. Biochim. Biophys. Acta 923 (1987) 156-165. [PMID: 3801515]
Accepted name: tetrahydromethanopterin S-methyltransferase
Reaction: 5-methyl-5,6,7,8-tetrahydromethanopterin + 2-mercaptoethanesulfonate = 5,6,7,8-tetrahydromethanopterin + 2-(methylthio)ethanesulfonate
For diagram of reaction click here
Glossary:
coenzyme M (CoM) = 2-mercaptoethanesulfonate
tetrahydromethanopterin
Other name(s): tetrahydromethanopterin methyltransferase
Systematic name: 5-methyl-5,6,7,8-tetrahydromethanopterin:2-mercaptoethanesulfonate 2-methyltransferase
Comments: Involved in the formation of methane from CO in Methanobacterium thermoautotrophicum. Methanopterin is a pterin analogue. The reaction involves the export of one or two sodium ions in Archaea.
Links to other databases: BRENDA, EXPASY, KEGG, Metacyc, UM-BBD, CAS registry number: 103406-60-6
References:
1. Sauer, F.D. Tetrahydromethanopterin methyltransferase, a component of the methane synthesizing complex of Methanobacterium thermoautotrophicum. Biochem. Biophys. Res. Commun. 136 (1986) 542-547. [PMID: 3085670]
Accepted name: pyridine N-methyltransferase
Reaction: S-adenosyl-L-methionine + pyridine = S-adenosyl-L-homocysteine + N-methylpyridinium
Other name(s): pyridine methyltransferase
Systematic name: S-adenosyl-L-methionine:pyridine N-methyltransferase
Links to other databases: BRENDA, EXPASY, KEGG, Metacyc, CAS registry number: 104327-10-8
References:
1. Damani, L.A., Shaker, M.S., Crooks, P.A., Godin, C.S. and Nwosu, C. N-Methylation and quaternization of pyridine in vitro by rabbit lung, liver and kidney N-methyltransferases: an S-adenosyl-L-methionine-dependent reaction. Xenobiotica 16 (1986) 645-650. [PMID: 3751119]
Accepted name: 8-hydroxyquercetin 8-O-methyltransferase
Reaction: S-adenosyl-L-methionine + 3,5,7,8,3',4'-hexahydroxyflavone = S-adenosyl-L-homocysteine + 3,5,7,3',4'-pentahydroxy-8-methoxyflavone
Other name(s): flavonol 8-O-methyltransferase; flavonol 8-methyltransferase; S-adenosyl-L-methionine:3,3',4',5,7,8-hexahydroxyflavone 8-O-methyltransferase; 8-hydroxyquercitin 8-O-methyltransferase [mis-spelt]
Systematic name: S-adenosyl-L-methionine:3,5,7,8,3',4'-hexahydroxyflavone 8-O-methyltransferase
Comments: Also acts on 8-hydroxykaempferol, but not on the glycosides of 8-hydroxyflavonols. An enzyme from the flower buds of Lotus corniculatus.
Links to other databases: BRENDA, EXPASY, KEGG, Metacyc, CAS registry number: 99775-17-4
References:
1. Jay, M., De Luca, V. and Ibrahim, R.K. Purification, properties and kinetic mechanism of flavonol 8-O-methyltransferase from Lotus corniculatus L. Eur. J. Biochem. 153 (1985) 321-325. [PMID: 4076180]
Accepted name: tetrahydrocolumbamine 2-O-methyltransferase
Reaction: S-adenosyl-L-methionine + 5,8,13,13a-tetrahydrocolumbamine = S-adenosyl-L-homocysteine + tetrahydropalmatine
Other name(s): tetrahydrocolumbamine methyltransferase
Systematic name: S-adenosyl-L-methionine:5,8,13,13a-tetrahydrocolumbamine 2-O-methyltransferase
Comments: Involved in the biosynthesis of the berberine alkaloids.
Links to other databases: BRENDA, EXPASY, KEGG, Metacyc, CAS registry number: 93792-09-7
References:
1. Beecher, C.W.W. and Kelleher, W.J. Enzymatic study of the late stages of protoberberine alkaloid biosynthesis. Tetrahedron Lett. 25 (1984) 4595-4598.
Accepted name: methanol—corrinoid protein Co-methyltransferase
Reaction: methanol + a [Co(I) methanol-specific corrinoid protein] = a [methyl-Co(III) methanol-specific corrinoid protein] + H2O
Other name(s): methanol cobalamin methyltransferase; methanol:5-hydroxybenzimidazolylcobamide methyltransferase; MT 1 (ambiguous); methanol—5-hydroxybenzimidazolylcobamide Co-methyltransferase; mtaB (gene name)
Systematic name: methanol:5-hydroxybenzimidazolylcobamide Co-methyltransferase
Comments: The enzyme, which catalyses the transfer of methyl groups from methanol to a methanol-specific corrinoid protein (MtaC), is involved in methanogenesis from methanol. Methylation of the corrinoid protein requires the central cobalt to be in the Co(I) state. During methylation the cobalt is oxidized to the Co(III) state. Free cob(I)alamin can substitute for the corrinoid protein in vitro [2]. Inactivated by oxygen and other oxidizing agents, and reactivated by catalytic amounts of ATP and hydrogen.
Links to other databases: BRENDA, EXPASY, KEGG, Metacyc, PDB, CAS registry number: 86611-98-5
References:
1. van der Meijden, P., te Brömmelstroet, B.W., Poirot, C.M., van der Drift, C. and Vogels, G.D. Purification and properties of methanol:5-hydroxybenzimidazolylcobamide methyltransferase from Methanosarcina barkeri. J. Bacteriol. 160 (1984) 629-635. [PMID: 6438059]
2. Sauer, K. and Thauer, R.K. Methanol:coenzyme M methyltransferase from Methanosarcina barkeri – substitution of the corrinoid harbouring subunit MtaC by free cob(I)alamin. Eur. J. Biochem. 261 (1999) 674-681. [PMID: 10215883]
Accepted name: isobutyraldoxime O-methyltransferase
Reaction: S-adenosyl-L-methionine + 2-methylpropanal oxime = S-adenosyl-L-homocysteine + 2-methylpropanal O-methyloxime
Other name(s): aldoxime methyltransferase; S-adenosylmethionine:aldoxime O-methyltransferase; aldoxime O-methyltransferase
Systematic name: S-adenosyl-L-methionine:2-methylpropanal-oxime O-methyltransferase
Comments: Oximes of C4 to C6 aldehydes can act as acceptors; the most active substrate is 2-methylbutyroaldoxime.
Links to other databases: BRENDA, EXPASY, KEGG, Metacyc, CAS registry number: 95471-32-2
References:
1. Harper, D.B. and Kennedy, J.T. Purification and properties of S-adenosylmethionine: aldoxime O-methyltransferase from Pseudomonas sp. N.C.I.B. 11652. Biochem. J. 226 (1985) 147-153. [PMID: 3977861]
[EC 2.1.1.92 Deleted entry: bergaptol O-methyltransferase. Now included with EC 2.1.1.69, 5-hydroxyfuranocoumarin 5-O-methyltransferase. The reaction with bergaptol is a specific example of the general reaction associated with EC 2.1.1.69. (EC 2.1.1.92 created 1989, deleted 2006)]
[EC 2.1.1.93 Deleted entry: xanthotoxol O-methyltransferase. Enzyme is identical to EC 2.1.1.70, 8-hydroxyfuranocoumarin 8-O-methyltransferase. (EC 2.1.1.93 created 1989, deleted 2008)]
Accepted name: tabersonine 16-O-methyltransferase
Reaction: S-adenosyl-L-methionine + 16-hydroxytabersonine = S-adenosyl-L-homocysteine + 16-methoxytabersonine
For diagram click here.
Other name(s): 11-demethyl-17-deacetylvindoline 11-methyltransferase; 11-O-demethyl-17-O-deacetylvindoline O-methyltransferase; S-adenosyl-L-methionine:11-O-demethyl-17-O-deacetylvindoline 11-O-methyltransferase
Systematic name: S-adenosyl-L-methionine:16-hydroxytabersonine 16-O-methyltransferase
Comments: Involved in the biosynthesis of vindoline from tabersonine in the Madagascar periwinkle, Catharanthus roseus.
Links to other databases: BRENDA, EXPASY, KEGG, Metacyc, CAS registry number: 100984-95-0
References:
1. De Luca, V., Balsevich, J., Tyler, R.T., Eilert, U., Panchuk, B.D. and Kurz, W.G.W. Biosynthesis of indole alkaloids - developmental regulation of the biosynthetic-pathway from tabersonine to vindoline in Catharanthus roseus. J. Plant Physiol. 125 (1986) 147-156.
2. Fahn, W., Laussermair, E., Deus-Neumann, B. and Stöckigt, J. Late enzymes of vindoline biosynthesis. S-Adenosyl-L-methionine:11-O-demethyl-17-O-deacetylvindoline 11-O-methylase and unspecific acetylesterase. Plant Cell Rep. 4 (1985) 337-340.
Accepted name: tocopherol O-methyltransferase
Reaction: S-adenosyl-L-methionine + γ-tocopherol = S-adenosyl-L-homocysteine + α-tocopherol
Other name(s): γ-tocopherol methyltransferase
Systematic name: S-adenosyl-L-methionine:γ-tocopherol 5-O-methyltransferase
Links to other databases: BRENDA, EXPASY, KEGG, Metacyc, CAS registry number: 84788-82-9
References:
1. Camara, B. and D'Harlingue, A. Demonstration and solubilization of S-adenosylmethionine - γ-tocopherol methyltransferase from capsicum chromoplasts. Plant Cell Rep. 4 (1985) 31-32.
Accepted name: thioether S-methyltransferase
Reaction: S-adenosyl-L-methionine + dimethyl sulfide = S-adenosyl-L-homocysteine + trimethylsulfonium
Other name(s): S-adenosyl-L-methionine:thioether S-methyltransferase; thioether methyltransferase
Systematic name: S-adenosyl-L-methionine:dimethyl-sulfide S-methyltransferase
Comments: Also acts on dimethyl selenide, dimethyl telluride, diethyl sulfide, 1,4-dithiane and many other thioethers.
Links to other databases: BRENDA, EXPASY, KEGG, PDB, Metacyc, CAS registry number: 114797-02-3
References:
1. Mozier, N.M., McConnell, P. and Hoffman, J.L. S-Adenosyl-L-methionine:thioether S-methyltransferase, a new enzyme in sulfur and selenium metabolism. J. Biol. Chem. 263 (1988) 4527-4531. [PMID: 3350800]
Accepted name: 3-hydroxyanthranilate 4-C-methyltransferase
Reaction: S-adenosyl-L-methionine + 3-hydroxyanthranilate = S-adenosyl-L-homocysteine + 3-hydroxy-4-methylanthranilate
Other name(s): 3-hydroxyanthranilate 4-methyltransferase
Systematic name: S-adenosyl-L-methionine:3-hydroxyanthranilate 4-C-methyltransferase
Comments: Involved in the biosynthesis of the antibiotic actinomycin in Streptomyces antibioticus.
Links to other databases: BRENDA, EXPASY, KEGG, Metacyc, CAS registry number: 112445-22-4
References:
1. Fawaz, F. and Jones, G.H. Actinomycin synthesis in Streptomyces antibioticus. Purification and properties of a 3-hydroxyanthranilate 4-methyltransferase. J. Biol. Chem. 263 (1988) 4602-4606. [PMID: 2450873]
Accepted name: diphthine synthase
Reaction: S-adenosyl-L-methionine + 2-(3-carboxy-3-aminopropyl)-L-histidine = S-adenosyl-L-homocysteine + 2-[3-carboxy-3-(methylammonio)propyl]-L-histidine
Other name(s): S-adenosyl-L-methionine:elongation factor 2 methyltransferase; diphthine methyltransferase
Systematic name: S-adenosyl-L-methionine:2-(3-carboxy-3-aminopropyl)-L-histidine methyltransferase
Comments: 2-[3-Carboxy-3-(methylammonio)propyl]-L-histidine and the corresponding dimethyl compound can also act as acceptors; the trimethylated product, diphthine, is converted into diphthamide by EC 6.3.2.22 diphthine—ammonia ligase.
Links to other databases: BRENDA, EXPASY, KEGG, Metacyc, PDB, CAS registry number: 114514-25-9
References:
1. Chen, J.-Y.C. and Bodley, J.W. Biosynthesis of diphthamide in Saccharomyces cerevisiae. Partial purification and characterization of a specific S-adenosylmethionine:elongation factor 2 methyltransferase. J. Biol. Chem. 263 (1988) 11692-11696. [PMID: 3042777]
2. Moehring, J.M. and Moehring, T.J. The post-translational trimethylation of diphthamide studied in vitro. J. Biol. Chem. 263 (1988) 3840-3844. [PMID: 3346227]
Accepted name: 3-hydroxy-16-methoxy-2,3-dihydrotabersonine N-methyltransferase
Reaction: S-adenosyl-L-methionine + 3-hydroxy-16-methoxy-2,3-dihydrotabersonine = S-adenosyl-L-homocysteine + deacetoxyvindoline
For diagram click here.
Other name(s): 16-methoxy-2,3-dihydro-3-hydroxytabersonine methyltransferase; NMT; 16-methoxy-2,3-dihydro-3-hydroxytabersonine N-methyltransferase; S-adenosyl-L-methionine:16-methoxy-2,3-dihydro-3-hydroxytabersonine N-methyltransferase
Systematic name: S-adenosyl-L-methionine:3-hydroxy-16-methoxy-2,3-dihydrotabersonine N-methyltransferase
Comments: Involved in the biosynthesis of vindoline from tabersonine in the Madagascar periwinkle Catharanthus roseus.
Links to other databases: BRENDA, EXPASY, KEGG, Metacyc, CAS registry number: 113478-40-3
References:
1. De Luca, V., Balsevich, J., Tyler, R.T., Eilert, U., Panchuk, B.D. and Kurz, W.G.W. Biosynthesis of indole alkaloids - developmental regulation of the biosynthetic-pathway from tabersonine to vindoline in Catharanthus roseus. J. Plant Physiol. 125 (1986) 147-156.
2. De Luca, V. and Cutler, A.J. Subcellular localization of enzymes involved in indole alkaloid biosynthesis in Catharanthus roseus. Plant Physiol. 85 (1987) 1099-1102. [PMID: 16665811]
Accepted name: protein-S-isoprenylcysteine O-methyltransferase
Reaction: S-adenosyl-L-methionine + protein C-terminal S-farnesyl-L-cysteine = S-adenosyl-L-homocysteine + protein C-terminal S-farnesyl-L-cysteine methyl ester
Other name(s): farnesyl cysteine C-terminal methyltransferase; farnesyl-protein carboxymethyltransferase; protein C-terminal farnesylcysteine O-methyltransferase; farnesylated protein C-terminal O-methyltransferase; isoprenylated protein methyltransferase; prenylated protein methyltransferase; protein S-farnesylcysteine C-terminal methyltransferase; S-farnesylcysteine methyltransferase; prenylcysteine carboxylmethyltransferase [misleading]; prenylcysteine carboxymethyltransferase [misleading]; prenylcysteine methyltransferase
Systematic name: S-adenosyl-L-methionine:protein-C-terminal-S-farnesyl-L-cysteine O-methyltransferase
Comments: C-terminal S-geranylgeranylcysteine and S-geranylcysteine residues are also methylated, but more slowly.
Links to other databases: BRENDA, EXPASY, KEGG, Metacyc, CAS registry number: 130731-20-3
References:
1. Clarke, S., Vogel, J.P., Deschenes, R.J. and Stock, J. Posttranslational modification of the Ha-ras oncogene protein: evidence for a third class of protein carboxyl methyltransferases. Proc. Natl. Acad. Sci. USA 85 (1988) 4643-4647. [PMID: 3290900]
2. Ota, I.M. and Clarke, S. Enzymatic methylation of 23-29-kDa bovine retinal rod outer segment membrane proteins. Evidence for methyl ester formation at carboxyl-terminal cysteinyl residues. J. Biol. Chem. 264 (1989) 12879-12884. [PMID: 2753892]
3. Stephenson, R.C. and Clarke, S. Identification of a C-terminal protein carboxyl methyltransferase in rat liver membranes utilizing a synthetic farnesyl cysteine-containing peptide substrate. J. Biol. Chem. 265 (1990) 16248-16254. [PMID: 2398053]