Sandbox GGC15

DNA TOPOISOMERASE I

spinqualitylabelsall models Caption for this structure Show:Asymmetric Unit Biological Assembly Drag the structure with the mouse to rotate   Export Animated Image   Print3D Eukaryotic DNA topoisomerase I (topo I) is a protein that reduces the strain from the supercoils that are caused during transcription and translation. There are two types of topoisomerases. Type 1 topoisomerases are monomeric and break one strand of DNA. Type 2 topoisomerases are dimeric, meaning that they made up of two units and break both strands of the DNA helix. They are able to pass another part of the duplex through the cut, and close the cut using ATP. . . Structure Human topo 1 is composed of 765 amino acids . The enzyme consist of 4 regions which are the NH2-terminal, core, linker, and COOH-terminal domains. The NH2-terminal is approximately 210 residues long, it is highly charged, disordered, and contains few hydrophobic amino acids. The COOH-terminal domain is made up of residues 713 to 765 and contains the important amino aside Tyrosine 223. The location of the active site is at this amino acid. Active Site Topo 1 reduces stress in DNA by causing a transient single strand nick in the the DNA helix. This nick enables the cut to rotate around its intact complement, thus eliminating proximal supercoils. The active site of Topo 1 is catalytic and it is the location where the nicking or cutting occurs. The nicking occurs from the trans-esterification of Tyr-723 at a DNA phophodiester bond forming a 3'-phosphotyrosine covalent enzyme–DNA complex . After the DNA is relaxed, the covalent intermediate is reversed when the released 5'-OH of the broken strand reattacks the phosphotyrosine intermediate in a second transesterification reaction. Relevance Many anticancer drugs target topo 1 enzymes. This enzyme is the target of camptothecin (CPT) family of anticancer drugs. These drugs work by increasing the duration of the nicked intermediate in the topo I reaction . The stabilized intermediates prevent transcription and replication to continue in the cancer cells. This eventually leads to DNA damage and cell death. Mutations A mutation at amino acid Lysine 532 to Alanine almost abolishes enzyme activity. The location of Lys 532 to the scissile phosphate and other active site amino acids could be the reason why a mutation of this amino acid abolishes the enzyme activity.