Nucleic Acids Research · 2010 · 68 citations · 22 references
Life SciencesBiochemistryBioinformaticsEnzyme MechanismEnzymologyStructural BioinformaticsEnzyme ClassificationEnzyme StructureEnzyme-substrate RecognitionFatty Acid BiosynthesisPolyketide BiosynthesisStructural EnzymologyAcyl-coa DehydrogenasesCatalytic Reaction MechanismsEnzyme Structure-function RelationshipsEnzymesFatty Acid Biosynthetic EnzymesFatty Acyl-coa ThioestersThioester ChemistryThioesterase Activity
The ThYme (Thioester-active enzYme; http://www.enzyme.cbirc.iastate.edu) database has been constructed to bring together amino acid sequences and 3D (tertiary) structures of all the enzymes constituting the fatty acid synthesis and polyketide synthesis cycles. These enzymes are active on thioester-containing substrates, specifically those that are parts of the acyl-CoA synthase, acyl-CoA carboxylase, acyl transferase, ketoacyl synthase, ketoacyl reductase, hydroxyacyl dehydratase, enoyl reductase and thioesterase enzyme groups. These groups have been classified into families, members of which are similar in sequences, tertiary structures and catalytic mechanisms, implying common protein ancestry. ThYme is continually updated as sequences and tertiary structures become available.
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Helen M. Berman · Nucleic Acids Research · 2000 · 39.8K citations
The Pfam Protein Families Database
Alex Bateman · Nucleic Acids Research · 2002 · 14.2K citations · Full text