de Vega M - Search Results

1

DNA polymerase from temperate phage Bam35 is endowed with processive polymerization and abasic sites translesion synthesis capacity.

Berjón-Otero M, Villar L, de Vega M, Salas M, Redrejo-Rodríguez M. Berjón-Otero M, et al. Among authors: de vega m. Proc Natl Acad Sci U S A. 2015 Jul 7;112(27):E3476-84. doi: 10.1073/pnas.1510280112. Epub 2015 Jun 22. Proc Natl Acad Sci U S A. 2015. PMID: 26100910 Free PMC article.

2

Terminal protein-primed DNA amplification.

Blanco L, Lázaro JM, de Vega M, Bonnin A, Salas M. Blanco L, et al. Among authors: de vega m. Proc Natl Acad Sci U S A. 1994 Dec 6;91(25):12198-202. doi: 10.1073/pnas.91.25.12198. Proc Natl Acad Sci U S A. 1994. PMID: 7991606 Free PMC article.

3

Primer-terminus stabilization at the 3'-5' exonuclease active site of phi29 DNA polymerase. Involvement of two amino acid residues highly conserved in proofreading DNA polymerases.

de Vega M, Lazaro JM, Salas M, Blanco L. de Vega M, et al. EMBO J. 1996 Mar 1;15(5):1182-92. EMBO J. 1996. PMID: 8605889 Free PMC article.

4

An invariant lysine residue is involved in catalysis at the 3'-5' exonuclease active site of eukaryotic-type DNA polymerases.

de Vega M, Ilyina T, Lázaro JM, Salas M, Blanco L. de Vega M, et al. J Mol Biol. 1997 Jul 4;270(1):65-78. doi: 10.1006/jmbi.1997.1093. J Mol Biol. 1997. PMID: 9231901

5

Mutational analysis of phi29 DNA polymerase residues acting as ssDNA ligands for 3'-5' exonucleolysis.

de Vega M, Lázaro JM, Salas M, Blanco L. de Vega M, et al. J Mol Biol. 1998 Jun 19;279(4):807-22. doi: 10.1006/jmbi.1998.1805. J Mol Biol. 1998. PMID: 9642062

6

phi29 DNA polymerase residue Ser122, a single-stranded DNA ligand for 3'-5' exonucleolysis, is required to interact with the terminal protein.

de Vega M, Blanco L, Salas M. de Vega M, et al. J Biol Chem. 1998 Oct 30;273(44):28966-77. doi: 10.1074/jbc.273.44.28966. J Biol Chem. 1998. PMID: 9786901 Free article.

Three amino acid residues highly conserved in most proofreading DNA polymerases, a phenylalanine contained in the Exo II motif and a serine and a leucine belonging to the S/TLx2h motif, were recently shown to be critical for 3'-5' exonucleolysis by acting as single-stranded DNA l …

Three amino acid residues highly conserved in most proofreading DNA polymerases, a phenylalanine contained in the Exo II motif and a serine …

7

Processive proofreading and the spatial relationship between polymerase and exonuclease active sites of bacteriophage phi29 DNA polymerase.

de Vega M, Blanco L, Salas M. de Vega M, et al. J Mol Biol. 1999 Sep 10;292(1):39-51. doi: 10.1006/jmbi.1999.3052. J Mol Biol. 1999. PMID: 10493855

8

Phage phi 29 DNA polymerase residues involved in the proper stabilisation of the primer-terminus at the 3'-5' exonuclease active site.

de Vega M, Lázaro JM, Salas M. de Vega M, et al. J Mol Biol. 2000 Nov 17;304(1):1-9. doi: 10.1006/jmbi.2000.4178. J Mol Biol. 2000. PMID: 11071805

9

An aspartic acid residue in TPR-1, a specific region of protein-priming DNA polymerases, is required for the functional interaction with primer terminal protein.

Dufour E, Méndez J, Lázaro JM, de Vega M, Blanco L, Salas M. Dufour E, et al. Among authors: de vega m. J Mol Biol. 2000 Dec 1;304(3):289-300. doi: 10.1006/jmbi.2000.4216. J Mol Biol. 2000. PMID: 11090274

10

Phi29 DNA polymerase residues Tyr59, His61 and Phe69 of the highly conserved ExoII motif are essential for interaction with the terminal protein.

Eisenbrandt R, Lázaro JM, Salas M, de Vega M. Eisenbrandt R, et al. Among authors: de vega m. Nucleic Acids Res. 2002 Mar 15;30(6):1379-86. doi: 10.1093/nar/30.6.1379. Nucleic Acids Res. 2002. PMID: 11884636 Free PMC article.

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