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PDBsum entry 2bcq

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Top Page protein dna_rna ligands metals links
Transferase, lyase/DNA PDB id
2bcq
Contents
Protein chain
324 a.a.
DNA/RNA
Ligands
PPV
EDO
Metals
_NA ×3
_MG
Waters ×570

References listed in PDB file
Key reference
Title Structural analysis of strand misalignment during DNA synthesis by a human DNA polymerase.
Authors M.Garcia-Diaz, K.Bebenek, J.M.Krahn, L.C.Pedersen, T.A.Kunkel.
Ref. Cell, 2006, 124, 331-342. [DOI no: 10.1016/j.cell.2005.10.039]
PubMed id 16439207
Abstract
Insertions and deletions in coding sequences can alter the reading frame of genes and have profound biological consequences. In 1966, Streisinger proposed that these mutations result from strand slippage, which in repetitive sequences generates misaligned intermediates stabilized by correct base pairing that support polymerization. We report here crystal structures of human DNA polymerase lambda, which frequently generates deletion mutations, bound to such intermediates. Each contains an extrahelical template nucleotide upstream of the active site. Surprisingly, the extra nucleotide, even when combined with an adjacent mismatch, does not perturb polymerase active site geometry, which is indistinguishable from that for correctly aligned strands. These structures reveal how pol lambda can polymerize on substrates with minimal homology during repair of double-strand breaks and represent strand-slippage intermediates consistent with Streisinger's classical hypothesis. They are thus relevant to the origin of single-base deletions, a class of mutations that can confer strong biological phenotypes.
Figure 3.
Figure 3. The Extrahelical Adenine Is in Close Proximity to β strand 8
Figure 4.
Figure 4. Pol λ Can Tolerate Distortion upstream of the Primer Terminus
The above figures are reprinted by permission from Cell Press: Cell (2006, 124, 331-342) copyright 2006.
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