Rank |
Title |
Journal |
Year |
PubWeight™‹?› |
1
|
Synthesis and characterization of an octanucleotide containing the EcoRI recognition sequence with a phosphorothioate group at the cleavage site.
|
Biochemistry
|
1984
|
3.03
|
2
|
Horizontal gene transfer contributes to the wide distribution and evolution of type II restriction-modification systems.
|
J Mol Evol
|
1996
|
1.82
|
3
|
The interaction of the EcoRI restriction endonuclease with its substrate. A physico-chemical study employing natural and synthetic oligonucleotides and polynucleotides.
|
Eur J Biochem
|
1980
|
1.75
|
4
|
Influence of DNA target melting behavior on real-time PCR quantification.
|
Clin Chem
|
2000
|
1.66
|
5
|
A site-directed mutagenesis study to identify amino acid residues involved in the catalytic function of the restriction endonuclease EcoRV.
|
Biochemistry
|
1992
|
1.62
|
6
|
Linear diffusion of restriction endonucleases on DNA.
|
J Biol Chem
|
1985
|
1.54
|
7
|
Ternary complex formation between elongation factor Tu, GTP and aminoacyl-tRNA: an equilibrium study.
|
Eur J Biochem
|
1977
|
1.50
|
8
|
Pausing of the restriction endonuclease EcoRI during linear diffusion on DNA.
|
Biochemistry
|
1994
|
1.46
|
9
|
Kinetic characterization of linear diffusion of the restriction endonuclease EcoRV on DNA.
|
Biochemistry
|
1998
|
1.39
|
10
|
Role of thymidine residues in DNA recognition by the EcoRI and EcoRV restriction endonucleases.
|
Nucleic Acids Res
|
1986
|
1.34
|
11
|
Linear diffusion of the restriction endonuclease EcoRV on DNA is essential for the in vivo function of the enzyme.
|
EMBO J
|
1996
|
1.34
|
12
|
The stereochemical course of the restriction endonuclease EcoRI-catalyzed reaction.
|
J Biol Chem
|
1984
|
1.33
|
13
|
Site-directed mutagenesis studies with EcoRV restriction endonuclease to identify regions involved in recognition and catalysis.
|
Biochemistry
|
1991
|
1.32
|
14
|
Substrate-assisted catalysis in the cleavage of DNA by the EcoRI and EcoRV restriction enzymes.
|
Proc Natl Acad Sci U S A
|
1993
|
1.31
|
15
|
Accuracy of the EcoRI restriction endonuclease: binding and cleavage studies with oligodeoxynucleotide substrates containing degenerate recognition sequences.
|
Biochemistry
|
1990
|
1.31
|
16
|
The influence of sequences adjacent to the recognition site on the cleavage of oligodeoxynucleotides by the EcoRI endonuclease.
|
Eur J Biochem
|
1984
|
1.30
|
17
|
Equivalent and non-equivalent binding sites for tRNA on aminoacyl-tRNA synthetases.
|
Eur J Biochem
|
1975
|
1.29
|
18
|
Mg2+ confers DNA binding specificity to the EcoRV restriction endonuclease.
|
Biochemistry
|
1992
|
1.27
|
19
|
Inhibition of Eco RI action by polynucleotides. A characterization of the non-specific binding of the enzyme to DNA.
|
Nucleic Acids Res
|
1980
|
1.25
|
20
|
Direct analysis of polymerase chain reaction products using enzyme-linked immunosorbent assay techniques.
|
Anal Biochem
|
1991
|
1.20
|
21
|
Evidence for an evolutionary relationship among type-II restriction endonucleases.
|
Gene
|
1995
|
1.19
|
22
|
Sau3AI, a monomeric type II restriction endonuclease that dimerizes on the DNA and thereby induces DNA loops.
|
J Biol Chem
|
2001
|
1.18
|
23
|
Cross-linking of bromodeoxyuridine-substituted oligonucleotides to the EcoRI and EcoRV restriction endonucleases.
|
Eur J Biochem
|
1986
|
1.16
|
24
|
A fast and accurate enzyme-linked immunosorbent assay for the determination of the DNA cleavage activity of restriction endonucleases.
|
Anal Biochem
|
1993
|
1.16
|
25
|
The monomeric homing endonuclease PI-SceI has two catalytic centres for cleavage of the two strands of its DNA substrate.
|
EMBO J
|
1999
|
1.15
|
26
|
A similar active site for non-specific and specific endonucleases.
|
Nat Struct Biol
|
1999
|
1.15
|
27
|
A comparison of the structural requirements for DNA cleavage by the isoschizomers HaeIII, BspRI and BsuRI.
|
Eur J Biochem
|
1985
|
1.14
|
28
|
On the catalytic mechanism of EcoRI and EcoRV. A detailed proposal based on biochemical results, structural data and molecular modelling.
|
FEBS Lett
|
1992
|
1.14
|
29
|
Analysis of the mechanism of the Serratia nuclease using site-directed mutagenesis.
|
Nucleic Acids Res
|
1996
|
1.13
|
30
|
Distinct steps in the specific binding of tRNA to aminoacyl-tRNA synthetase. Temperature-jump studies on the serine-specific system from yeast and the tyrosine-specific system from Escherichia coli.
|
Eur J Biochem
|
1976
|
1.11
|
31
|
Introduction of asymmetry in the naturally symmetric restriction endonuclease EcoRV to investigate intersubunit communication in the homodimeric protein.
|
Proc Natl Acad Sci U S A
|
1996
|
1.10
|
32
|
Site directed mutagenesis experiments suggest that Glu 111, Glu 144 and Arg 145 are essential for endonucleolytic activity of EcoRI.
|
Nucleic Acids Res
|
1986
|
1.10
|
33
|
The elongation factor Tu binds aminoacyl-tRNA in the presence of GDP.
|
J Biol Chem
|
1982
|
1.09
|
34
|
Transient cleavage kinetics of the Eco RI restriction endonuclease measured in a pulsed quench-flow apparatus: enzyme concentration-dependent activity change.
|
Nucleic Acids Res
|
1981
|
1.09
|
35
|
Analysis of the recognition mechanism involved in the EcoRV catalyzed cleavage of DNA using modified oligodeoxynucleotides.
|
Nucleic Acids Res
|
1988
|
1.08
|
36
|
On the possibilities and limitations of rational protein design to expand the specificity of restriction enzymes: a case study employing EcoRV as the target.
|
Protein Eng
|
2000
|
1.06
|
37
|
The effect of several nucleic acid binding drugs on the cleavage of d(GGAATTCC) and pBR 322 by the Eco RI restriction endonuclease.
|
Nucleic Acids Res
|
1981
|
1.05
|
38
|
Binding, bending and cleavage of DNA substrates by the homing endonuclease Pl-SceI.
|
Nucleic Acids Res
|
1996
|
1.03
|
39
|
Probing the indirect readout of the restriction enzyme EcoRV. Mutational analysis of contacts to the DNA backbone.
|
J Biol Chem
|
1996
|
1.03
|
40
|
DNA binding specificity of the EcoRV restriction endonuclease is increased by Mg2+ binding to a metal ion binding site distinct from the catalytic center of the enzyme.
|
Biochemistry
|
1995
|
1.03
|
41
|
The inhibition of the GTPase activating protein-Ha-ras interaction by acidic lipids is due to physical association of the C-terminal domain of the GTPase activating protein with micellar structures.
|
EMBO J
|
1991
|
1.02
|
42
|
Quantitative analysis of polymerase chain reaction (PCR) products using primers labeled with biotin and a fluorescent dye.
|
Anal Biochem
|
1991
|
1.01
|
43
|
Effect of polyamines and basic proteins on cleavage of DNA by restriction endonucleases.
|
Biochemistry
|
1984
|
1.00
|
44
|
Identification of catalytically relevant amino acids of the extracellular Serratia marcescens endonuclease by alignment-guided mutagenesis.
|
Nucleic Acids Res
|
1994
|
0.99
|
45
|
Does the restriction endonuclease EcoRV employ a two-metal-Ion mechanism for DNA cleavage?
|
Biochemistry
|
1997
|
0.99
|
46
|
Aminoacyl transfer ribonucleic acid binding site of the bacterial elongation factor Tu.
|
Biochemistry
|
1980
|
0.98
|
47
|
Polymerase chain reaction detection of a highly polymorphic VNTR segment in intron 1 of the human p53 gene.
|
Clin Chem
|
1993
|
0.98
|
48
|
Spermidine increases the accuracy of type II restriction endonucleases. Suppression of cleavage at degenerate, non-symmetrical sites.
|
Eur J Biochem
|
1985
|
0.97
|
49
|
Sequence preferences in cleavage of dsDNA and ssDNA by the extracellular Serratia marcescens endonuclease.
|
Biochemistry
|
1995
|
0.95
|
50
|
A procedure for renaturation and purification of the extracellular Serratia marcescens nuclease from genetically engineered Escherichia coli.
|
Protein Expr Purif
|
1994
|
0.95
|
51
|
The recognition of methylated DNA by the GTP-dependent restriction endonuclease McrBC resides in the N-terminal domain of McrB.
|
Biol Chem
|
1997
|
0.95
|
52
|
Kinetic analysis of the cleavage of natural and synthetic substrates by the Serratia nuclease.
|
Eur J Biochem
|
1996
|
0.94
|
53
|
Engineering novel restriction endonucleases: principles and applications.
|
Trends Biotechnol
|
1996
|
0.94
|
54
|
Changing the hydrogen-bonding potential in the DNA binding site of EcoRI by site-directed mutagenesis drastically reduces the enzymatic activity, not, however, the preference of this restriction endonuclease for cleavage within the site-GAATTC-.
|
Biochemistry
|
1989
|
0.94
|
55
|
The role of translocation in ribosomal accuracy. Translocation rates for cognate and noncognate aminoacyl- and peptidyl-tRNAs on Escherichia coli ribosomes.
|
J Biol Chem
|
1987
|
0.94
|
56
|
Does the specific recognition of DNA by the restriction endonuclease EcoRI involve a linear diffusion step? Investigation of the processivity of the EcoRI endonuclease.
|
Nucleic Acids Res
|
1983
|
0.93
|
57
|
Fluorescence stopped-flow kinetics of the cleavage of synthetic oligodeoxynucleotides by the EcoRI restriction endonuclease.
|
Biochemistry
|
1989
|
0.93
|
58
|
Biochemical characterization of Anabaena sp. strain PCC 7120 non-specific nuclease NucA and its inhibitor NuiA.
|
Eur J Biochem
|
1998
|
0.93
|
59
|
Cleavage experiments with deoxythymidine 3',5'-bis-(p-nitrophenyl phosphate) suggest that the homing endonuclease I-PpoI follows the same mechanism of phosphodiester bond hydrolysis as the non-specific Serratia nuclease.
|
FEBS Lett
|
1999
|
0.93
|
60
|
Semiautomated quantitative detection of loss of heterozygosity in the tumor suppressor gene p53.
|
Biotechniques
|
1995
|
0.92
|
61
|
Identification of Asp218 and Asp326 as the principal Mg2+ binding ligands of the homing endonuclease PI-SceI.
|
Biochemistry
|
2000
|
0.92
|
62
|
Characterization of the interaction between the restriction endonuclease McrBC from E. coli and its cofactor GTP.
|
J Mol Biol
|
1997
|
0.92
|
63
|
Two identical subunits of the EcoRI restriction endonuclease Co-operate in the binding and cleavage of the palindromic substrate.
|
Eur J Biochem
|
1982
|
0.92
|
64
|
On the advantage of being a dimer, a case study using the dimeric Serratia nuclease and the monomeric nuclease from Anabaena sp. strain PCC 7120.
|
J Biol Chem
|
1999
|
0.91
|
65
|
Protein engineering of the restriction endonuclease EcoRV: replacement of an amino acid residue in the DNA binding site leads to an altered selectivity towards unmodified and modified substrates.
|
Biochim Biophys Acta
|
1994
|
0.91
|
66
|
The protein splicing domain of the homing endonuclease PI-sceI is responsible for specific DNA binding.
|
Nucleic Acids Res
|
1998
|
0.91
|
67
|
The production and characterization of artificial heterodimers of the restriction endonuclease EcoRV.
|
Biol Chem
|
1996
|
0.91
|
68
|
Fluoresceinylthiocarbamyl-tRNATyr: a useful derivative of tRNATyr (E.coli) for physicochemical studies.
|
Nucleic Acids Res
|
1977
|
0.90
|
69
|
Adenylate kinases from thermosensitive Escherichia coli strains.
|
J Mol Biol
|
1989
|
0.90
|
70
|
Identification of functionally relevant histidine residues in the apoptotic nuclease CAD.
|
Nucleic Acids Res
|
2001
|
0.90
|
71
|
Protein engineering of the restriction endonuclease EcoRV--structure-guided design of enzyme variants that recognize the base pairs flanking the recognition site.
|
Eur J Biochem
|
1998
|
0.90
|
72
|
Plasmid DNA cleavage by MunI restriction enzyme: single-turnover and steady-state kinetic analysis.
|
Biochemistry
|
1999
|
0.90
|
73
|
Crosslinking the EcoRV restriction endonuclease across the DNA-binding site reveals transient intermediates and conformational changes of the enzyme during DNA binding and catalytic turnover.
|
EMBO J
|
1998
|
0.89
|
74
|
The pharmacokinetics, bioequivalence and bioavailability of different formulations of metoclopramide in man.
|
Arzneimittelforschung
|
1981
|
0.89
|
75
|
Determination of the DNA bend angle induced by the restriction endonuclease EcoRV in the presence of Mg2+.
|
J Biol Chem
|
1993
|
0.89
|
76
|
How many EF-Tu molecules participate in aminoacyl-tRNA binding?
|
Biochimie
|
1992
|
0.88
|
77
|
Influence of fluorophor dye labels on the migration behavior of polymerase chain reaction--amplified short tandem repeats during denaturing capillary electrophoresis.
|
Electrophoresis
|
2001
|
0.88
|
78
|
Photocross-linking of the homing endonuclease PI-SceI to its recognition sequence.
|
J Biol Chem
|
1999
|
0.88
|
79
|
The binding of kirromycin to elongation factor Tu. Structural alterations are responsible for the inhibitory action.
|
Eur J Biochem
|
1978
|
0.87
|
80
|
Towards the design of rare cutting restriction endonucleases: using directed evolution to generate variants of EcoRV differing in their substrate specificity by two orders of magnitude.
|
J Mol Biol
|
1998
|
0.87
|
81
|
Engineering of variants of the restriction endonuclease EcoRV that depend in their cleavage activity on the flexibility of sequences flanking the recognition site.
|
Biochemistry
|
1998
|
0.86
|
82
|
Mechanism of DNA cleavage by the DNA/RNA-non-specific Anabaena sp. PCC 7120 endonuclease NucA and its inhibition by NuiA.
|
J Mol Biol
|
2000
|
0.86
|
83
|
The antibiotics kirromycin and pulvomycin bind to different sites on the elongation factor Tu from Escherichia coli.
|
Eur J Biochem
|
1982
|
0.86
|
84
|
Defining the location and function of domains of McrB by deletion mutagenesis.
|
Biol Chem
|
1999
|
0.85
|
85
|
Mutational analysis of the function of Gln115 in the EcoRI restriction endonuclease, a critical amino acid for recognition of the inner thymidine residue in the sequence -GAATTC- and for coupling specific DNA binding to catalysis.
|
J Mol Biol
|
1993
|
0.85
|
86
|
A quantitative microtiter plate nuclease assay based on ethidium/DNA fluorescence.
|
Anal Biochem
|
1996
|
0.85
|
87
|
Intra- vs intersubunit communication in the homodimeric restriction enzyme EcoRV: Thr 37 and Lys 38 involved in indirect readout are only important for the catalytic activity of their own subunit.
|
Biochemistry
|
1998
|
0.84
|
88
|
Evidence for substrate-assisted catalysis in the DNA cleavage of several restriction endonucleases.
|
Gene
|
1995
|
0.83
|
89
|
The GTP-binding domain of McrB: more than just a variation on a common theme?
|
J Mol Biol
|
1999
|
0.83
|
90
|
Comparison between Taq DNA polymerase and its Stoffel fragment for quantitative real-time PCR with hybridization probes.
|
Biotechniques
|
2001
|
0.82
|
91
|
Binding of the H-ras p21 GTPase activating protein by the activated epidermal growth factor receptor leads to inhibition of the p21 GTPase activity in vitro.
|
Biochemistry
|
1992
|
0.82
|
92
|
A model for the PI-SceIxDNA complex based on multiple base and phosphate backbone-specific photocross-links.
|
J Mol Biol
|
2000
|
0.82
|
93
|
The elongation factor Tu from Escherichia coli, aminoacyl-tRNA, and guanosine tetraphosphate form a ternary complex which is bound by programmed ribosomes.
|
J Biol Chem
|
1983
|
0.82
|
94
|
The mechanism of DNA cleavage by the type II restriction enzyme EcoRV: Asp36 is not directly involved in DNA cleavage but serves to couple indirect readout to catalysis.
|
Biol Chem
|
1998
|
0.82
|
95
|
Genetic engineering of EcoRI mutants with altered amino acid residues in the DNA binding site: physicochemical investigations give evidence for an altered monomer/dimer equilibrium for the Gln144Lys145 and Gln144Lys145Lys200 mutants.
|
Biochemistry
|
1989
|
0.82
|
96
|
Identification of a base-specific contact between the restriction endonuclease SsoII and its recognition sequence by photocross-linking.
|
Nucleic Acids Res
|
2000
|
0.81
|
97
|
Polymorphism of the pentanucleotide repeat d(AAAAT) within intron 1 of the human tumor suppressor gene p53 (17p13.1).
|
Hum Genet
|
1995
|
0.81
|
98
|
Numerical analysis of binding studies: a direct procedure avoiding the pitfalls of a Scatchard analysis of equilibrium data for unknown binding models.
|
Int J Biomed Comput
|
1979
|
0.81
|
99
|
Structural and functional analysis of the homing endonuclease PI-sceI by limited proteolytic cleavage and molecular cloning of partial digestion products.
|
Biochemistry
|
1998
|
0.80
|
100
|
Analysis of the reaction mechanism of the non-specific endonuclease of Serratia marcescens using an artificial minimal substrate.
|
FEBS Lett
|
1996
|
0.80
|
101
|
Genetic engineering of Escherichia coli to produce a 1:1 complex of the anabaena sp. PCC 7120 nuclease NucA and its inhibitor NuiA.
|
Gene
|
2000
|
0.80
|
102
|
The determination of binding parameters from protection experiments. A quantitative assay for ternary complex formation of elongation factor Tu, GTP, and aminoacyl-tRNA.
|
Anal Biochem
|
1979
|
0.79
|
103
|
Automated purification of His6-tagged proteins allows exhaustive screening of libraries generated by random mutagenesis.
|
Biotechniques
|
2000
|
0.79
|
104
|
Genetic engineering, isolation and characterization of a truncated Escherichia coli elongation factor Tu comprising domains 2 and 3.
|
Biochim Biophys Acta
|
1990
|
0.79
|
105
|
EcoRV-T94V: a mutant restriction endonuclease with an altered substrate specificity towards modified oligodeoxynucleotides.
|
Protein Eng
|
1996
|
0.79
|
106
|
Probing the function of individual amino acid residues in the DNA binding site of the EcoRI restriction endonuclease by analysing the toxicity of genetically engineered mutants.
|
Gene
|
1990
|
0.79
|
107
|
Comparison of N-terminal affinity fusion domains: effect on expression level and product heterogeneity of recombinant restriction endonuclease EcoRV.
|
Appl Microbiol Biotechnol
|
1994
|
0.78
|
108
|
Genetic engineering, production and characterisation of monomeric variants of the dimeric Serratia marcescens endonuclease.
|
FEBS Lett
|
1998
|
0.78
|
109
|
Polypeptide sequences involved in the cleavage of DNA by the restriction endonuclease EcoRI.
|
J Biol Chem
|
1986
|
0.78
|
110
|
[Analysis of binding and cleavage of DNA by the gene conversion PI-SCEI endonuclease using site-directed mutagenesis].
|
Mol Biol (Mosk)
|
2000
|
0.78
|
111
|
Mutant species of EF-Tu, altered at position 375, exhibit a reduced affinity for aminoacylated transfer-RNAs.
|
FEBS Lett
|
1985
|
0.78
|
112
|
The elongation factor Tu . guanosine tetraphosphate complex.
|
Eur J Biochem
|
1981
|
0.78
|
113
|
A 1H NMR study of the Escherichia coli elongation-factor Tu with guanine nucleotides and the antibiotic kirromycin.
|
FEBS Lett
|
1981
|
0.78
|
114
|
Structure prediction of the EcoRV DNA methyltransferase based on mutant profiling, secondary structure analysis, comparison with known structures of methyltransferases and isolation of catalytically inactive single mutants.
|
Protein Eng
|
1996
|
0.77
|
115
|
Affinity modification of the restriction endonuclease SsoII by 2'-aldehyde-containing double stranded DNAs.
|
Biochemistry (Mosc)
|
2005
|
0.77
|
116
|
Synthesis and biochemical characterization of obligatory dimers of the sugar non-specific nuclease from Serratia marcescens using specifically designed bismaleimidoalkanes as SH-specific crosslinking reagents.
|
J Protein Chem
|
1999
|
0.76
|
117
|
Interaction of myelin basic protein with mononuclear cells: the primary reaction for the MEM and EMT tests.
|
Br J Cancer
|
1981
|
0.75
|
118
|
Nucleic acid quantification by delta pH measurement.
|
J Biotechnol
|
2001
|
0.75
|
119
|
Product analysis of in vitro ribosomal protein synthesis for the assessment of kinetic parameters.
|
Anal Biochem
|
1985
|
0.75
|
120
|
Quantitative polymerase chain reaction with oligodeoxynucleotide ligation assay/enzyme-linked immunosorbent assay detection.
|
Anal Biochem
|
1993
|
0.75
|
121
|
The identification and analysis of nucleotides bound to the elongation factor Tu from Escherichia coli.
|
Anal Biochem
|
1981
|
0.75
|
122
|
Vectors for dual expression of target genes in bacterial and mammalian cells.
|
Biotechniques
|
2000
|
0.75
|
123
|
Immobilization of sugar-non-specific nucleases by utilizing the streptavidin--biotin interaction.
|
J Biotechnol
|
2001
|
0.75
|
124
|
A dodecapeptide comprising the extended chain-alpha 4 region of the restriction endonuclease EcoRI specifically binds to the EcoRI recognition site.
|
J Biol Chem
|
1995
|
0.75
|
125
|
Quantitative polymerase chain reaction with enzyme-linked immunosorbent assay detection of selectively digested amplified sample and control DNA.
|
Anal Biochem
|
1995
|
0.75
|
126
|
[New derivatives of azobenzene for the directed modification of proteins].
|
Bioorg Khim
|
2009
|
0.75
|
127
|
Quantitative PCR with Internal Standardization and OLA-ELISA Product Analysis for the p53 Tumor Suppressor Gene.
|
Methods Mol Med
|
1999
|
0.75
|
128
|
Application of oligonucleoside methylphosphonates in the studies on phosphodiester hydrolysis by Serratia endonuclease.
|
Nucleosides Nucleotides
|
1999
|
0.75
|