1NKE image
Deposition Date 2003-01-02
Release Date 2004-03-30
Last Version Date 2023-08-16
Entry Detail
PDB ID:
1NKE
Keywords:
Title:
A BACILLUS DNA POLYMERASE I PRODUCT COMPLEX BOUND TO A CYTOSINE-THYMINE MISMATCH AFTER A SINGLE ROUND OF PRIMER EXTENSION, FOLLOWING INCORPORATION OF DCTP.
Biological Source:
Source Organism(s):
Expression System(s):
Method Details:
Experimental Method:
Resolution:
1.80 Å
R-Value Free:
0.24
R-Value Work:
0.21
R-Value Observed:
0.23
Space Group:
P 21 21 21
Macromolecular Entities
Structures with similar UniProt ID
Protein Blast
Polymer Type:polypeptide(L)
Molecule:DNA POLYMERASE I
Gene (Uniprot):polA
Chain IDs:C (auth: A)
Chain Length:580
Number of Molecules:1
Biological Source:Geobacillus stearothermophilus
Peptide-like Molecules
PRD_900003
Primary Citation
Structures of mismatch replication errors observed in a DNA polymerase.
Cell(Cambridge,Mass.) 116 803 816 (2004)
PMID: 15035983 DOI: 10.1016/S0092-8674(04)00252-1

Abstact

Accurate DNA replication is essential for genomic stability. One mechanism by which high-fidelity DNA polymerases maintain replication accuracy involves stalling of the polymerase in response to covalent incorporation of mismatched base pairs, thereby favoring subsequent mismatch excision. Some polymerases retain a "short-term memory" of replication errors, responding to mismatches up to four base pairs in from the primer terminus. Here we a present a structural characterization of all 12 possible mismatches captured at the growing primer terminus in the active site of a polymerase. Our observations suggest four mechanisms that lead to mismatch-induced stalling of the polymerase. Furthermore, we have observed the effects of extending a mismatch up to six base pairs from the primer terminus and find that long-range distortions in the DNA transmit the presence of the mismatch back to the enzyme active site, suggesting the structural basis for the short-term memory of replication errors.

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Primary Citation of related structures
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