5KFG image
Deposition Date 2016-06-12
Release Date 2016-06-29
Last Version Date 2023-09-27
Entry Detail
PDB ID:
5KFG
Title:
Human DNA polymerase eta-DNA ternary complex: reaction with 10 mM Mn2+ for 30s
Biological Source:
Source Organism(s):
Homo sapiens (Taxon ID: 9606)
Expression System(s):
Method Details:
Experimental Method:
Resolution:
1.55 Å
R-Value Free:
0.20
R-Value Work:
0.17
R-Value Observed:
0.17
Space Group:
P 61
Macromolecular Entities
Structures with similar UniProt ID
Protein Blast
Polymer Type:polypeptide(L)
Molecule:DNA polymerase eta
Gene (Uniprot):POLH
Mutagens:R61A
Chain IDs:A
Chain Length:435
Number of Molecules:1
Biological Source:Homo sapiens
Polymer Type:polydeoxyribonucleotide
Molecule:DNA (5'-D(*AP*GP*CP*GP*TP*CP*
Chain IDs:C (auth: P)
Chain Length:8
Number of Molecules:1
Biological Source:Homo sapiens
Polymer Type:polydeoxyribonucleotide
Molecule:DNA (5'-D(*CP*AP*TP*TP*AP*TP*
Chain IDs:B (auth: T)
Chain Length:12
Number of Molecules:1
Biological Source:Homo sapiens
Primary Citation
Capture of a third Mg2+ is essential for catalyzing DNA synthesis.
Science 352 1334 1337 (2016)
PMID: 27284197 DOI: 10.1126/science.aad9633

Abstact

It is generally assumed that an enzyme-substrate (ES) complex contains all components necessary for catalysis and that conversion to products occurs by rearrangement of atoms, protons, and electrons. However, we find that DNA synthesis does not occur in a fully assembled DNA polymerase-DNA-deoxynucleoside triphosphate complex with two canonical metal ions bound. Using time-resolved x-ray crystallography, we show that the phosphoryltransfer reaction takes place only after the ES complex captures a third divalent cation that is not coordinated by the enzyme. Binding of the third cation is incompatible with the basal ES complex and requires thermal activation of the ES for entry. It is likely that the third cation provides the ultimate boost over the energy barrier to catalysis of DNA synthesis.

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Primary Citation of related structures
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