3r6t
From Proteopedia
Rat catechol o-methyltransferase in complex with the bisubstrate inhibitor 4'-fluoro-4,5-dihydroxy-biphenyl-3-carboxylic acid {(E)-3-[(2S,4R,5R)-4-hydroxy-5-(6-methyl-purin-9-yl)-tetrahydro-furan-2-yl]-allyl}-amide
Template:ABSTRACT PUBMED 21538606
About this Structure
3r6t is a 1 chain structure with sequence from Rattus norvegicus. Full crystallographic information is available from OCA.
Reference
- Ellermann M, Paulini R, Jakob-Roetne R, Lerner C, Borroni E, Roth D, Ehler A, Schweizer WB, Schlatter D, Rudolph MG, Diederich F. Molecular Recognition at the Active Site of Catechol-O-methyltransferase (COMT): Adenine Replacements in Bisubstrate Inhibitors. Chemistry. 2011 May 27;17(23):6369-81. doi: 10.1002/chem.201003648. Epub, 2011 Apr 27. PMID:21538606 doi:10.1002/chem.201003648
Categories: Catechol O-methyltransferase | Rattus norvegicus | Benz, J. | Ehler, A. | Rudolph, M G. | Schlatter, D. | Stihle, M. | Alternative initiation | Catecholamine metabolism | Metal-binding | Methyltransferase | Neurotransmitter degradation | S-adenosyl-l-methionine | Transferase-transferase inhibitor complex | Transmembrane
