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Literature summary for 2.1.1.246 extracted from

  • LeClerc, G.M.; Grahame, D.A.
    Methylcobamide:coenzyme M methyltransferase isozymes from Methanosarcina barkeri. Physicochemical characterization, cloning, sequence analysis, and heterologous gene expression (1996), J. Biol. Chem., 271, 18725-18731.
    View publication on PubMed

Cloned(Commentary)

Cloned (Comment) Organism
genes cmtA and cmtM, DNA and amino acid sequence determination and analysis, expressionin Escherichia coli strain XL-1 Blue Methanosarcina barkeri

KM Value [mM]

KM Value [mM] KM Value Maximum [mM] Substrate Comment Organism Structure
additional information
-
additional information steady-state kinetics of isozymes MT2-A and MT2-M, overview Methanosarcina barkeri

Metals/Ions

Metals/Ions Comment Organism Structure
Zn2+
-
Methanosarcina barkeri

Molecular Weight [Da]

Molecular Weight [Da] Molecular Weight Maximum [Da] Comment Organism
34000
-
x * 34000, isozymes MT2-A and MT2-M, SDS-PAGE, x * 36700, about, isozyme MT2-A, sequence calculation Methanosarcina barkeri
36700
-
x * 34000, isozymes MT2-A and MT2-M, SDS-PAGE, x * 36700, about, isozyme MT2-A, sequence calculation Methanosarcina barkeri

Natural Substrates/ Products (Substrates)

Natural Substrates Organism Comment (Nat. Sub.) Natural Products Comment (Nat. Pro.) Rev. Reac.
a [methyl-Co(III) methanol-specific corrinoid protein] + coenzyme M Methanosarcina barkeri
-
methyl-CoM + a [Co(I) methanol-specific corrinoid protein]
-
r
additional information Methanosarcina barkeri conversions of monomethylamine and dimethylamine to CH3-SCoM are dependent upon MT2-A, and are not supported by MT2-M. In contrast, MT2-M acts specifically in metabolism of methanol, but does not substitute for MT2-A in conversion of monomethylamine or dimethylamine. Nevertheless, both isozymes are capable of supporting the conversion of trimethylamine ?
-
?

Organism

Organism UniProt Comment Textmining
Methanosarcina barkeri O30640 isozymes MT2-A and MT2-M encoded by genes cmtA and cmtM
-

Source Tissue

Source Tissue Comment Organism Textmining
cell culture the isozymes MT2-A and MT2-M are differentially expressed depending upon the substrate available for growth Methanosarcina barkeri
-

Specific Activity [micromol/min/mg]

Specific Activity Minimum [µmol/min/mg] Specific Activity Maximum [µmol/min/mg] Comment Organism
0.154
-
MT2 activity in recombinant Escherichia coli cells transfected with gene cmtM, pH 7.2, 37°C Methanosarcina barkeri
1.21
-
MT2 activity in recombinant Escherichia coli cells transfected with gene cmtA, pH 7.2, 37°C Methanosarcina barkeri
2.2
-
MT2 activity in cells grown on trimethylamine, pH 7.2, 37°C Methanosarcina barkeri
7.5
-
MT2 activity in cells grown on methanol, pH 7.2, 37°C Methanosarcina barkeri

Substrates and Products (Substrate)

Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
a [methyl-Co(III) methanol-specific corrinoid protein] + 3-mercaptopropanoic acid
-
Methanosarcina barkeri methyl-3-mercaptopropanoic acid + a [Co(I) methanol-specific corrinoid protein]
-
r
a [methyl-Co(III) methanol-specific corrinoid protein] + coenzyme M
-
Methanosarcina barkeri methyl-CoM + a [Co(I) methanol-specific corrinoid protein]
-
r
a [methyl-Co(III) methanol-specific corrinoid protein] + coenzyme M the enzyme methylcobamide:CoM methyltransferase, MT2, catalyzes the transfer of the methyl group from the MT1-bound methylcobamide prosthetic group to coenzyme M Methanosarcina barkeri methyl-CoM + a [Co(I) methanol-specific corrinoid protein]
-
r
additional information conversions of monomethylamine and dimethylamine to CH3-SCoM are dependent upon MT2-A, and are not supported by MT2-M. In contrast, MT2-M acts specifically in metabolism of methanol, but does not substitute for MT2-A in conversion of monomethylamine or dimethylamine. Nevertheless, both isozymes are capable of supporting the conversion of trimethylamine Methanosarcina barkeri ?
-
?

Subunits

Subunits Comment Organism
? x * 34000, isozymes MT2-A and MT2-M, SDS-PAGE, x * 36700, about, isozyme MT2-A, sequence calculation Methanosarcina barkeri
More the isozymes MT2-A and MT2-M differ in their overall charge Methanosarcina barkeri

Synonyms

Synonyms Comment Organism
methylcobamide:coenzyme M methyltransferase
-
Methanosarcina barkeri
methylcobamide:CoM methyltransferase
-
Methanosarcina barkeri
MT2-A
-
Methanosarcina barkeri
MT2-M
-
Methanosarcina barkeri

Temperature Optimum [°C]

Temperature Optimum [°C] Temperature Optimum Maximum [°C] Comment Organism
37
-
assay at Methanosarcina barkeri

pH Optimum

pH Optimum Minimum pH Optimum Maximum Comment Organism
7.2
-
assay at Methanosarcina barkeri