2.1.1.303: 2,7-dihydroxy-5-methyl-1-naphthoate 7-O-methyltransferase

This is an abbreviated version!
For detailed information about 2,7-dihydroxy-5-methyl-1-naphthoate 7-O-methyltransferase, go to the full flat file.

Reaction

2-hydroxy-7-methoxy-5-methyl-1-naphthoate

Synonyms

NcsB1

ECTree

2 Transferases

2.1 Transferring one-carbon groups

2.1.1 Methyltransferases

2.1.1.303 2,7-dihydroxy-5-methyl-1-naphthoate 7-O-methyltransferase

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Results	in table
1	Activating Compound
4	AA Sequence
2	Cloned(Commentary)
1	Crystallization (Commentary)
2	General Information
3	Inhibitors
9	kcat/KM [mM/s]
9	KM Value [mM]
2	Metals/Ions
1	Molecular Weight [Da]
2	Natural Substrates/ Products (Substrates)
2	Organism
3	Pathway
2	pH Optimum
1	pH Range
4	Protein Variants
2	Purification (Commentary)
1	Reaction
2	Reference
8	Substrates and Products (Substrate)
1	Subunits
2	Synonyms
1	Systematic Name
2	Temperature Optimum [°C]
9	Turnover Number [1/s]

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Reference on EC 2.1.1.303 - 2,7-dihydroxy-5-methyl-1-naphthoate 7-O-methyltransferase

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724276

Cooke, H.A.; Guenther, E.L.; Luo, Y.; Shen, B.; Bruner, S.D.

Molecular basis of substrate promiscuity for the SAM-dependent O-methyltransferase NcsB1, involved in the biosynthesis of the enediyne antitumor antibiotic neocarzinostatin

Biochemistry

9590-9598

2009

Streptomyces carzinostaticus (Q84HC8)

19702337

725380

Luo, Y.; Lin, S.; Zhang, J.; Cooke, H.A.; Bruner. S.D.; Shen, B.

Regiospecific O-methylation of naphthoic acids catalyzed by NcsB1, an O-methyltransferase involved in the biosynthesis of the enediyne antitumor antibiotic neocarzinostatin

J. Biol. Chem.

283

14694-14702

2008

Streptomyces carzinostaticus (Q84HC8)

18387946