Functional analysis of substrate and cofactor complex structures of a thymidylate synthase-complementing protein

Structure. 2003 Jun;11(6):677-90. doi: 10.1016/s0969-2126(03)00097-2.


Like thymidylate synthase (TS) in eukaryotes, the thymidylate synthase-complementing proteins (TSCPs) are mandatory for cell survival of many prokaryotes in the absence of external sources of thymidylate. Details of the mechanism of this novel family of enzymes are unknown. Here, we report the structural and functional analysis of a TSCP from Thermotoga maritima and its complexes with substrate, analogs, and cofactor. The structures presented here provide a basis for rationalizing the TSCP catalysis and reveal the possibility of the design of an inhibitor. We have identified a new helix-loop-strand FAD binding motif characteristic of the enzymes in the TSCP family. The presence of a hydrophobic core with residues conserved among the TSCP family suggests a common overall fold.

Publication types

  • Research Support, U.S. Gov't, Non-P.H.S.
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Amino Acid Sequence
  • Anti-Bacterial Agents / chemistry
  • Bacterial Infections / epidemiology
  • Bacterial Proteins / chemistry*
  • Bacterial Proteins / metabolism
  • Binding Sites
  • Crystallography, X-Ray
  • Deoxyuracil Nucleotides / metabolism
  • Flavin-Adenine Dinucleotide / metabolism
  • Macromolecular Substances
  • Models, Molecular
  • Molecular Sequence Data
  • Molecular Structure
  • Protein Folding
  • Protein Structure, Tertiary*
  • Thermotoga maritima / enzymology*
  • Thymidylate Synthase / chemistry*
  • Thymidylate Synthase / metabolism*


  • Anti-Bacterial Agents
  • Bacterial Proteins
  • Deoxyuracil Nucleotides
  • Macromolecular Substances
  • Flavin-Adenine Dinucleotide
  • 2'-deoxyuridylic acid
  • Thymidylate Synthase

Associated data

  • PDB/1O24
  • PDB/1O25
  • PDB/1O26
  • PDB/1O27
  • PDB/1O28
  • PDB/1O29
  • PDB/1O2A
  • PDB/1O2B