Literature DB >> 8127373

Crystal structure of catechol O-methyltransferase.

J Vidgren1, L A Svensson, A Liljas.   

Abstract

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.

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Year:  1994        PMID: 8127373     DOI: 10.1038/368354a0

Source DB:  PubMed          Journal:  Nature        ISSN: 0028-0836            Impact factor:   49.962


  94 in total

1.  The pi-helix translates structure into function.

Authors:  T M Weaver
Journal:  Protein Sci       Date:  2000-01       Impact factor: 6.725

Review 2.  AdoMet-dependent methylation, DNA methyltransferases and base flipping.

Authors:  X Cheng; R J Roberts
Journal:  Nucleic Acids Res       Date:  2001-09-15       Impact factor: 16.971

3.  Crystal structure of a fibrillarin homologue from Methanococcus jannaschii, a hyperthermophile, at 1.6 A resolution.

Authors:  H Wang; D Boisvert; K K Kim; R Kim; S H Kim
Journal:  EMBO J       Date:  2000-02-01       Impact factor: 11.598

Review 4.  Many paths to methyltransfer: a chronicle of convergence.

Authors:  Heidi L Schubert; Robert M Blumenthal; Xiaodong Cheng
Journal:  Trends Biochem Sci       Date:  2003-06       Impact factor: 13.807

5.  Crystal complexes of a predicted S-adenosylmethionine-dependent methyltransferase reveal a typical AdoMet binding domain and a substrate recognition domain.

Authors:  Darcie J Miller; Nancy Ouellette; Elena Evdokimova; Alexei Savchenko; Aled Edwards; Wayne F Anderson
Journal:  Protein Sci       Date:  2003-07       Impact factor: 6.725

6.  Crystallization of the novel S-adenosyl-L-methionine-dependent C-methyltransferase CouO from Streptomyces rishiriensis and preliminary diffraction data analysis.

Authors:  Andrzej Lyskowski; Martin Tengg; Georg Steinkellner; Helmut Schwab; Mandana Gruber-Khadjawi; Karl Gruber
Journal:  Acta Crystallogr Sect F Struct Biol Cryst Commun       Date:  2012-05-23

7.  Sequence analysis, in silico modeling and docking studies of caffeoyl CoA-O-methyltransferase of Populus trichopora.

Authors:  Navneet Phogat; Vaibhav Vindal; Vikash Kumar; Krishna K Inampudi; Nirmal K Prasad
Journal:  J Mol Model       Date:  2010-02-19       Impact factor: 1.810

8.  Active site mapping and substrate specificity of bacterial Hen1, a manganese-dependent 3' terminal RNA ribose 2'O-methyltransferase.

Authors:  Ruchi Jain; Stewart Shuman
Journal:  RNA       Date:  2011-01-04       Impact factor: 4.942

9.  Optimization of 8-Hydroxyquinolines as Inhibitors of Catechol O-Methyltransferase.

Authors:  Ingrid Buchler; Daniel Akuma; Vinh Au; Gregory Carr; Pablo de León; Michael DePasquale; Glen Ernst; Yifang Huang; Martha Kimos; Anna Kolobova; Michael Poslusney; Huijun Wei; Dominique Swinnen; Florian Montel; Florence Moureau; Emilie Jigorel; Monika-Sarah E D Schulze; Martyn Wood; James C Barrow
Journal:  J Med Chem       Date:  2018-10-19       Impact factor: 7.446

10.  Ground- and excited-state stability of the conformers of 3,5-dinitrocatechol and its complexes with W(VI) and V(V): combined theoretical and experimental study.

Authors:  V B Delchev; K B Gavazov; I G Shterev
Journal:  J Mol Model       Date:  2014-12-10       Impact factor: 1.810

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