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3r6t
From Proteopedia
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| - | + | [[Image:3r6t.png|left|200px]] | |
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| + | {{STRUCTURE_3r6t| PDB=3r6t | SCENE= }} | ||
| - | + | ===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=== | |
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| + | The line below this paragraph, {{ABSTRACT_PUBMED_21538606}}, adds the Publication Abstract to the page | ||
| + | (as it appears on PubMed at http://www.pubmed.gov), where 21538606 is the PubMed ID number. | ||
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| + | {{ABSTRACT_PUBMED_21538606}} | ||
| + | |||
| + | ==About this Structure== | ||
| + | [[3r6t]] is a 1 chain structure with sequence from [http://en.wikipedia.org/wiki/Rattus_norvegicus Rattus norvegicus]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=3R6T OCA]. | ||
| + | |||
| + | ==Reference== | ||
| + | <ref group="xtra">PMID:021538606</ref><references group="xtra"/> | ||
| + | [[Category: Catechol O-methyltransferase]] | ||
| + | [[Category: Rattus norvegicus]] | ||
| + | [[Category: Benz, J.]] | ||
| + | [[Category: Ehler, A.]] | ||
| + | [[Category: Rudolph, M G.]] | ||
| + | [[Category: Schlatter, D.]] | ||
| + | [[Category: Stihle, M.]] | ||
| + | [[Category: Alternative initiation]] | ||
| + | [[Category: Catecholamine metabolism]] | ||
| + | [[Category: Metal-binding]] | ||
| + | [[Category: Methyltransferase]] | ||
| + | [[Category: Neurotransmitter degradation]] | ||
| + | [[Category: S-adenosyl-l-methionine]] | ||
| + | [[Category: Transferase-transferase inhibitor complex]] | ||
| + | [[Category: Transmembrane]] | ||
Revision as of 05:38, 8 February 2012
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
