Cofactor chemogenomics
- PMID: 19727612
- DOI: 10.1007/978-1-60761-274-2_4
Cofactor chemogenomics
Abstract
Cofactors are organic molecules, most of them originating from vitamins, that bind to enzymes making them able to catalyze defined reactions. A cofactor-based chemogenomics approach exploits the presence of a cofactor-binding domain to develop compound scaffolds tailored to mimic the cofactor and to replace it within target enzyme classes. As a result, a loss of function is observed. An expansion of the cofactor scaffold to include structural/chemical features derived from the substrate, that usually binds at cofactor adjacent sites, increases the specificity of the enzyme fishing. This approach has been so far applied only to NAD(P)(+)-dependent enzymes. However, it is suitable for all other cofactors, with difficulties, for some of them, originated by very tight binding. In the case of cofactors covalently bound to the enzyme, the competition between the natural cofactor and the cofactor scaffold mimic can only occur during enzyme folding.
Similar articles
-
Comparative kinetics of cofactor association and dissociation for the human and trypanosomal S-adenosylhomocysteine hydrolases. 1. Basic features of the association and dissociation processes.Biochemistry. 2007 May 15;46(19):5798-809. doi: 10.1021/bi700170m. Epub 2007 Apr 21. Biochemistry. 2007. PMID: 17447732
-
Molecular and structural basis of drift in the functions of closely-related homologous enzyme domains: implications for function annotation based on homology searches and structural genomics.In Silico Biol. 2009;9(1-2):S41-55. In Silico Biol. 2009. PMID: 19537164
-
Targeting the purinome.Methods Mol Biol. 2009;575:47-92. doi: 10.1007/978-1-60761-274-2_3. Methods Mol Biol. 2009. PMID: 19727611 Review.
-
Compound library design for target families.Methods Mol Biol. 2009;575:21-46. doi: 10.1007/978-1-60761-274-2_2. Methods Mol Biol. 2009. PMID: 19727610 Review.
-
The CoFactor database: organic cofactors in enzyme catalysis.Bioinformatics. 2010 Oct 1;26(19):2496-7. doi: 10.1093/bioinformatics/btq442. Epub 2010 Aug 2. Bioinformatics. 2010. PMID: 20679331 Free PMC article.
Cited by
-
Affinity-based profiling of dehydrogenase subproteomes.Methods Mol Biol. 2012;803:157-65. doi: 10.1007/978-1-61779-364-6_11. Methods Mol Biol. 2012. PMID: 22065224 Free PMC article.
-
Structure and mechanism of human UDP-glucose 6-dehydrogenase.J Biol Chem. 2011 Jul 8;286(27):23877-87. doi: 10.1074/jbc.M111.234682. Epub 2011 Apr 18. J Biol Chem. 2011. PMID: 21502315 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Research Materials