Identification of residues critical for the polymerase activity of the Klenow fragment of DNA polymerase I from Escherichia coli.
Open Access
- 1 August 1990
- journal article
- research article
- Published by Elsevier in Journal of Biological Chemistry
- Vol. 265 (24) , 14579-14591
- https://doi.org/10.1016/s0021-9258(18)77342-0
Abstract
No abstract availableThis publication has 53 references indexed in Scilit:
- Primary structure of bacteriophage M2 DNA polymerase: conserved segments within protein-priming DNA polymerases and DNA polymerase I of Escherichia coliGene, 1989
- Pyridoxal 5'-phosphate mediated inactivation of Escherichia coli DNA polymerase I: identification of lysine-635 as an essential residue for the processive mode of DNA synthesisBiochemistry, 1988
- Electrostatic field of the large fragment of Escherichia coli DNA polymerase IJournal of Molecular Biology, 1985
- Genetic mapping and DNA sequence analysis of mutations in the polA gene of Escherichia coliJournal of Molecular Biology, 1985
- Rate-limiting steps in the DNA polymerase I reaction pathwayBiochemistry, 1985
- Domain of E. coli DNA polymerase I showing sequence homology to T7 DNA polymeraseNature, 1985
- Improved M13 phage cloning vectors and host strains: nucleotide sequences of the M13mpl8 and pUC19 vectorsGene, 1985
- Elementary steps in the DNA polymerase I reaction pathwayBiochemistry, 1983
- A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye bindingAnalytical Biochemistry, 1976
- An active fragment of DNA polymerase produced by proteolytic cleavageBiochemical and Biophysical Research Communications, 1969