Figure 1

Structure of Fe and MnSOD. Structures are visualized using WebLab ViewerLite 4.2 software. Catalytically essential aspartate or histidine residues are represented in ball and stick mode binding the active metal (yellow) is shown to identify the location of the active site. Protein database codes are given in parentheses: (i) FeSOD (PDB 1gv3); (ii) MnSOD (PDB 1my6). (A) FeSOD of T.elongatus BP-1 dimers are distinguished by colour (violet and slate), and structures are represented with the active site (yellow) of subunit. (B) Monomeric subunit of FeSOD represents an N terminal (green) and a C- terminal (red). Similarly (C) represents dimer structure of Anabaena sp. MnSOD in pink and green with active site highlighted in yellow. (D) Monomeric MnSOD showing the N-terminal residues in blue and C-terminal in pink with metal binding ligands. The transmembrane hydrophobic pocket specific for MnSOD is highlighted in red (D).