Functional evolution of PLP-dependent enzymes based on active-site structural similarities

Proteins. 2014 Oct;82(10):2597-608. doi: 10.1002/prot.24624. Epub 2014 Jun 20.

Abstract

Families of distantly related proteins typically have very low sequence identity, which hinders evolutionary analysis and functional annotation. Slowly evolving features of proteins, such as an active site, are therefore valuable for annotating putative and distantly related proteins. To date, a complete evolutionary analysis of the functional relationship of an entire enzyme family based on active-site structural similarities has not yet been undertaken. Pyridoxal-5'-phosphate (PLP) dependent enzymes are primordial enzymes that diversified in the last universal ancestor. Using the comparison of protein active site structures (CPASS) software and database, we show that the active site structures of PLP-dependent enzymes can be used to infer evolutionary relationships based on functional similarity. The enzymes successfully clustered together based on substrate specificity, function, and three-dimensional-fold. This study demonstrates the value of using active site structures for functional evolutionary analysis and the effectiveness of CPASS.

Keywords: CPASS; PLP-dependent enzymes; functional evolution; ligand binding sites.

Publication types

  • Comparative Study
  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Binding Sites
  • Catalytic Domain
  • Coenzymes / chemistry
  • Coenzymes / metabolism*
  • Databases, Protein
  • Evolution, Molecular
  • Humans
  • Ligands
  • Models, Molecular*
  • Molecular Sequence Data
  • Phylogeny
  • Protein Conformation
  • Pyridoxal Phosphate / chemistry
  • Pyridoxal Phosphate / metabolism*
  • Sequence Alignment
  • Sequence Homology, Amino Acid
  • Software
  • Substrate Specificity
  • Transaminases / chemistry*
  • Transaminases / classification
  • Transaminases / genetics
  • Transaminases / metabolism

Substances

  • Coenzymes
  • Ligands
  • Pyridoxal Phosphate
  • Transaminases