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5K03

Crystal Structure of COMT in complex with 2,6-dimethyl-3-(1H-pyrazol-3-yl)imidazo[1,2-a]pyridine

Summary for 5K03
Entry DOI10.2210/pdb5k03/pdb
DescriptorCatechol O-methyltransferase, 2,6-dimethyl-3-(1H-pyrazol-5-yl)imidazo[1,2-a]pyridine, POTASSIUM ION, ... (4 entities in total)
Functional Keywordsmethyltransferase, neurotransmitter degradation, catechol, transferase
Biological sourceRattus norvegicus (Norway Rat)
Total number of polymer chains1
Total formula weight24241.89
Authors
Ehler, A.,Rodriguez-Sarmiento, R.M.,Rudolph, M.G. (deposition date: 2016-05-17, release date: 2016-09-07, Last modification date: 2019-06-12)
Primary citationLerner, C.,Jakob-Roetne, R.,Buettelmann, B.,Ehler, A.,Rudolph, M.,Rodriguez Sarmiento, R.M.
Design of Potent and Druglike Nonphenolic Inhibitors for Catechol O-Methyltransferase Derived from a Fragment Screening Approach Targeting the S-Adenosyl-l-methionine Pocket.
J. Med. Chem., 59:10163-10175, 2016
Cited by
PubMed: 27685665
DOI: 10.1021/acs.jmedchem.6b00927
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (1.81 Å)
Structure validation

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