Single stranded binding protein

From Proteopedia

Revision as of 15:00, 1 November 2013

Sandbox Single Stranded DNA-Binding Protein (SSB)

spinqualitylabelsall models Structure of Single Stranded DNA-Binding Protein bound to ssDNA (PDB entry 1eyg) Show:Asymmetric Unit Biological Assembly Drag the structure with the mouse to rotate   Export Animated Image Introduction The single stranded DNA binding protein (SSB) of E. coli plays an important role in three aspects of DNA metabolism – namely in replication, repair and recombination. During DNA replication, SSB molecules bind to the newly separated DNA strands, keeping the strands separated by holding them in place so that each strand can serve as a template. Structure SSB consists is a homotetramer that has a DNA binding domain which binds to a single strand of DNA. The tetramers consist of α-helices, β-sheets, and random coils.

Binding Interactions in the Active Site

Phe-60 is an important DNA binding site. It has been shown to be the site for cross-linking. Tryptophan and Lysine residues are important in binding as well. “Treatments resulting in modification of arginine, cysteine, or tyrosine residues had no effect on binding of SSB to DNA, whereas modification of either lysine residues (with acetic anhydride) or tryptophan residues (with N-bromosuccinimide) led to complete loss of binding activity” ( Meyer, 348). The two tryptophan residues involved in DNA binding are Try-40 and Try-54, which was determined by mutagenesis. One more binding site was determined by site-specific mutagenesis. When His-55 is substituted with Leu it decreases binding affinity. All of these residues are found in a hydrophobic region, which is suitable for nucleotide base interactions.

spinqualitylabelsall models Structure of Single Stranded DNA-Binding Protein bound to ssDNA (PDB entry 2vw9) Show:Asymmetric Unit Biological Assembly Drag the structure with the mouse to rotate   Export Animated Image SSB-Protein Interactions It is believed that Gly-15 may play an important role in binding the RecA protein. Mutations in Gly-15 have extreme effects on recombinational repair. SSB has also been thought to bind with exonuclease I, DNA polymerase II, and a protein n, which is used to help synthesize RNA primers for the lagging strand.

See Also

References

PMID: 2087220