Journal
CHEMICAL PHYSICS LETTERS
Volume 506, Issue 4-6, Pages 135-138Publisher
ELSEVIER SCIENCE BV
DOI: 10.1016/j.cplett.2011.03.048
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Funding
- National Institute of Health [R01GM080742]
- ARRA [3R01GM080742-03S1]
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Catechol O-methyltransferase (COMT) metabolizes catechol moieties by methylating a single hydroxyl group at the meta-or para-hydroxyl position. Hydrophobic amino acids near the active site of COMT influence the regioselectivity of this reaction. Our sequence analysis highlights their importance by showing that these residues are highly conserved throughout evolution. Reaction barriers calculated in the gas phase reveal a lower barrier during methylation at the meta-position, suggesting that the observed meta-regioselectivity of COMT can be attributed to the substrate itself, and that COMT has evolved residues to orient the substrate in a manner that increases the rate of catalysis. (c) 2011 Elsevier B.V. All rights reserved.
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