Your browser version may not work well with NCBI's Web applications. More information here...
1: Nature. 1994 Mar 24;368(6469):354-8.Click here to read Links

Crystal structure of catechol O-methyltransferase.

Orion Corporation, Espoo, Finland.

Catechol O-methyltransferase (COMT, EC 2.1.1.6) is important in the central nervous system because it metabolizes catecholamine neurotransmitters such as dopamine. The enzyme catalyses the transfer of the methyl group from S-adenosyl-L-methionine (AdoMet) to one hydroxyl group of catechols. COMT also inactivates catechol-type compounds such as L-DOPA. With selective inhibitors of COMT in combination with L-DOPA, a new principle has been realized in the therapy of Parkinson's disease. Here we solve the atomic structure of COMT to 2.0 A resolution, which provides new insights into the mechanism of the methyl transfer reaction. The co-enzyme-binding domain is strikingly similar to that of an AdoMet-dependent DNA methylase, indicating that all AdoMet methylases may have a common structure.

PMID: 8127373 [PubMed - indexed for MEDLINE]

Structures reported by this article