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4DF8

Crystal structure of the large fragment of DNA Polymerase I from Thermus aquaticus in a closed ternary complex with aminopentinyl-7-deaza-2-dATP

Summary for 4DF8
Entry DOI10.2210/pdb4df8/pdb
Related3KTQ 3LWL 3LWM 3M8S 3OJS 3OJU
DescriptorDNA polymerase I, thermostable, DNA (5'-D(*GP*AP*CP*CP*AP*CP*GP*GP*CP*GP*CP*(DOC))-3'), DNA (5'-D(*AP*AP*AP*TP*GP*GP*CP*GP*CP*CP*GP*TP*GP*GP*TP*C)-3'), ... (9 entities in total)
Functional Keywordsdna polymerase, transferase-dna complex, transferase/dna
Biological sourceThermus aquaticus
More
Total number of polymer chains3
Total formula weight70641.04
Authors
Bergen, K.,Steck, A.,Struett, S.,Baccaro, A.,Welte, W.,Diederichs, K.,Marx, A. (deposition date: 2012-01-23, release date: 2012-05-16, Last modification date: 2023-09-13)
Primary citationBergen, K.,Steck, A.L.,Strutt, S.,Baccaro, A.,Welte, W.,Diederichs, K.,Marx, A.
Structures of KlenTaq DNA Polymerase Caught While Incorporating C5-Modified Pyrimidine and C7-Modified 7-Deazapurine Nucleoside Triphosphates.
J.Am.Chem.Soc., 134:11840-11843, 2012
Cited by
PubMed Abstract: The capability of DNA polymerases to accept chemically modified nucleotides is of paramount importance for many biotechnological applications. Although these analogues are widely used, the structural basis for the acceptance of the unnatural nucleotide surrogates has been only sparsely explored. Here we present in total six crystal structures of modified 2'-deoxynucleoside-5'-O-triphosphates (dNTPs) carrying modifications at the C5 positions of pyrimidines or C7 positions of 7-deazapurines in complex with a DNA polymerase and a primer/template complex. The modified dNTPs are in positions poised for catalysis leading to incorporation. These structural data provide insight into the mechanism of incorporation and acceptance of modified dNTPs. Our results open the door for rational design of modified nucleotides, which should offer great opportunities for future applications.
PubMed: 22475415
DOI: 10.1021/ja3017889
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2 Å)
Structure validation

227561

数据于2024-11-20公开中

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