2.1.1.292: carminomycin 4-O-methyltransferase

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For detailed information about carminomycin 4-O-methyltransferase, go to the full flat file.

Word Map on EC 2.1.1.292

2.1.1.292

methyltransferases

sam-dependent

s-adenosyl-l-homocysteine

daunorubicin

peucetius

s-adenosyl-l-methionine-dependent

synthesis

Reaction

Synonyms

4-O-methyltransferase, anthracycline 4-O-methyltransferase, anthracycline methyltransferase, carminomycin 4-OMT, class I methyltransferase, COMT, DauK, DnrK

ECTree

2 Transferases

2.1 Transferring one-carbon groups

2.1.1 Methyltransferases

2.1.1.292 carminomycin 4-O-methyltransferase

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Results	in table
5	AA Sequence
1	Application
7	Cloned(Commentary)
4	Cofactor
2	Crystallization (Commentary)
10	General Information
3	Inhibitors
3	kcat/KM [mM/s]
6	KM Value [mM]
1	Metals/Ions
3	Molecular Weight [Da]
9	Natural Substrates/ Products (Substrates)
11	Organism
5	Pathway
57	PDB ID
3	pH Optimum
1	pH Range
6	Protein Variants
3	Purification (Commentary)
1	Reaction
11	Reference
2	Source Tissue
1	Specific Activity [micromol/min/mg]
24	Substrates and Products (Substrate)
3	Subunits
18	Synonyms
1	Systematic Name
2	Temperature Optimum [°C]
1	Temperature Range [°C]
3	Turnover Number [1/s]

Cofactor

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Cofactor on EC 2.1.1.292 - carminomycin 4-O-methyltransferase

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S-adenosyl-L-methionine

2 entries

additional information

Streptomyces peucetius

Q06528

design, synthesis, and evaluation of stable, functional AdoMet isosteres that are resistant to the primary contributors to AdoMet degradation (depurination, intramolecular cyclization, and sulfonium epimerization). The AdoMet surrogates to serve as competent enzyme cosubstrates and to bind a prototypical class I model methyltransferase (DnrK) in a manner nearly identical to AdoMet. Half-lives of AdoMet derivatives, overview. Analysis of DnrK ligand-bound structures: DnrK-S-adenosyl-(3S)-3-amino-3-(1H-tetrazol-5-yl)propane-1-thiol and DnrK-S-adenosyl-(3S)-3-amino-3-(1H-tetrazol-5-yl)propane-1-thiol-carminomycin

755675