210 related articles for article (PubMed ID: 19883660)
1. phi29 DNA polymerase active site: role of residue Val250 as metal-dNTP complex ligand and in protein-primed initiation.
Pérez-Arnaiz P; Lázaro JM; Salas M; de Vega M
J Mol Biol; 2010 Jan; 395(2):223-33. PubMed ID: 19883660
[TBL] [Abstract][Full Text] [Related]
2. ø29 DNA polymerase residue Lys383, invariant at motif B of DNA-dependent polymerases, is involved in dNTP binding.
Saturno J; Lázaro JM; Esteban FJ; Blanco L; Salas M
J Mol Biol; 1997 Jun; 269(3):313-25. PubMed ID: 9199402
[TBL] [Abstract][Full Text] [Related]
3. Functional importance of bacteriophage phi29 DNA polymerase residue Tyr148 in primer-terminus stabilisation at the 3'-5' exonuclease active site.
Pérez-Arnaiz P; Lázaro JM; Salas M; de Vega M
J Mol Biol; 2009 Sep; 391(5):797-807. PubMed ID: 19576228
[TBL] [Abstract][Full Text] [Related]
4. A highly conserved lysine residue in phi29 DNA polymerase is important for correct binding of the templating nucleotide during initiation of phi29 DNA replication.
Truniger V; Lázaro JM; Blanco L; Salas M
J Mol Biol; 2002 Apr; 318(1):83-96. PubMed ID: 12054770
[TBL] [Abstract][Full Text] [Related]
5. phi29 DNA polymerase-terminal protein interaction. Involvement of residues specifically conserved among protein-primed DNA polymerases.
Rodríguez I; Lázaro JM; Salas M; De Vega M
J Mol Biol; 2004 Apr; 337(4):829-41. PubMed ID: 15033354
[TBL] [Abstract][Full Text] [Related]
6. 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
J Mol Biol; 1997 Jul; 270(1):65-78. PubMed ID: 9231901
[TBL] [Abstract][Full Text] [Related]
7. 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
J Mol Biol; 2000 Dec; 304(3):289-300. PubMed ID: 11090274
[TBL] [Abstract][Full Text] [Related]
8. Two positively charged residues of phi29 DNA polymerase, conserved in protein-primed DNA polymerases, are involved in stabilisation of the incoming nucleotide.
Truniger V; Lázaro JM; Salas M
J Mol Biol; 2004 Jan; 335(2):481-94. PubMed ID: 14672657
[TBL] [Abstract][Full Text] [Related]
9. 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
J Mol Biol; 2000 Nov; 304(1):1-9. PubMed ID: 11071805
[TBL] [Abstract][Full Text] [Related]
10. phi29 DNA polymerase residue Phe128 of the highly conserved (S/T)Lx(2)h motif is required for a stable and functional interaction with the terminal protein.
Rodríguez I; Lázaro JM; Salas M; de Vega M
J Mol Biol; 2003 Jan; 325(1):85-97. PubMed ID: 12473453
[TBL] [Abstract][Full Text] [Related]
11. Loss of polymerase activity due to Tyr to Phe substitution in the YMDD motif of human immunodeficiency virus type-1 reverse transcriptase is compensated by Met to Val substitution within the same motif.
Harris D; Yadav PN; Pandey VN
Biochemistry; 1998 Jul; 37(27):9630-40. PubMed ID: 9657675
[TBL] [Abstract][Full Text] [Related]
12. Functional characterization of the genes coding for the terminal protein and DNA polymerase from bacteriophage GA-1. Evidence for a sliding-back mechanism during protein-primed GA-1 DNA replication.
Illana B; Blanco L; Salas M
J Mol Biol; 1996 Dec; 264(3):453-64. PubMed ID: 8969297
[TBL] [Abstract][Full Text] [Related]
13. Involvement of phi29 DNA polymerase thumb subdomain in the proper coordination of synthesis and degradation during DNA replication.
Pérez-Arnaiz P; Lázaro JM; Salas M; de Vega M
Nucleic Acids Res; 2006; 34(10):3107-15. PubMed ID: 16757576
[TBL] [Abstract][Full Text] [Related]
14. Crystal structure of a pol alpha family DNA polymerase from the hyperthermophilic archaeon Thermococcus sp. 9 degrees N-7.
Rodriguez AC; Park HW; Mao C; Beese LS
J Mol Biol; 2000 Jun; 299(2):447-62. PubMed ID: 10860752
[TBL] [Abstract][Full Text] [Related]
15. Functional consequences and exonuclease kinetic parameters of point mutations in bacteriophage T4 DNA polymerase.
Abdus Sattar AK; Lin TC; Jones C; Konigsberg WH
Biochemistry; 1996 Dec; 35(51):16621-9. PubMed ID: 8987997
[TBL] [Abstract][Full Text] [Related]
16. Crystal structures of human DNA polymerase beta complexed with DNA: implications for catalytic mechanism, processivity, and fidelity.
Pelletier H; Sawaya MR; Wolfle W; Wilson SH; Kraut J
Biochemistry; 1996 Oct; 35(39):12742-61. PubMed ID: 8841118
[TBL] [Abstract][Full Text] [Related]
17. Structure of a bifunctional DNA primase-polymerase.
Lipps G; Weinzierl AO; von Scheven G; Buchen C; Cramer P
Nat Struct Mol Biol; 2004 Feb; 11(2):157-62. PubMed ID: 14730355
[TBL] [Abstract][Full Text] [Related]
18. Role of the LEXE motif of protein-primed DNA polymerases in the interaction with the incoming nucleotide.
Santos E; Lázaro JM; Pérez-Arnaiz P; Salas M; de Vega M
J Biol Chem; 2014 Jan; 289(5):2888-98. PubMed ID: 24324256
[TBL] [Abstract][Full Text] [Related]
19. A single tyrosine prevents insertion of ribonucleotides in the eukaryotic-type phi29 DNA polymerase.
Bonnin A; Lázaro JM; Blanco L; Salas M
J Mol Biol; 1999 Jul; 290(1):241-51. PubMed ID: 10388570
[TBL] [Abstract][Full Text] [Related]
20. 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
EMBO J; 1996 Mar; 15(5):1182-92. PubMed ID: 8605889
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]