Autodigestion and RecA-dependent cleavage of Ind- mutant LexA proteins.
暂无分享,去创建一个
J. W. Little | J W Little | L L Lin | L. Lin | L. L. Lin
[1] D. Mount,et al. The SOS regulatory system of Escherichia coli , 1982, Cell.
[2] W. Rutter,et al. The catalytic role of the active site aspartic acid in serine proteases. , 1987, Science.
[3] D. Mount,et al. Preferential cleavage of phage λ repressor monomers by recA protease , 1981, Nature.
[4] R. Sauer,et al. Lambda repressor inactivation: properties of purified ind- proteins in the autodigestion and RecA-mediated cleavage reactions. , 1986, Journal of molecular biology.
[5] R. Sauer,et al. Lambda repressor mutants that are better substrates for RecA-mediated cleavage. , 1989, Journal of molecular biology.
[6] Jeffrey W. Roberts,et al. Kinetics of recA protein-directed inactivation of repressors of phage λ and phage P22☆ , 1980 .
[7] J. A. Rupley,et al. Intramolecular cleavage of LexA and phage lambda repressors: dependence of kinetics on repressor concentration, pH, temperature, and solvent. , 1986, Biochemistry.
[8] Jeffrey W. Roberts,et al. Two mutations that alter the regulatory activity of E. coli recA protein , 1981, Nature.
[9] J. W. Little,et al. Isolation and characterization of noncleavable (Ind-) mutants of the LexA repressor of Escherichia coli K-12 , 1988, Journal of bacteriology.
[10] F. Galibert,et al. New recA mutations that dissociate the various RecA protein activities in Escherichia coli provide evidence for an additional role for RecA protein in UV mutagenesis , 1989, Journal of bacteriology.
[11] T. Ogawa,et al. Cleavage of bacteriophage φ80 CI repressor by RecA protein , 1988 .
[12] M. Daune,et al. Large-scale purification, oligomerization equilibria, and specific interaction of the LexA repressor of Escherichia coli. , 1985, Biochemistry.
[13] Jeffrey W. Roberts,et al. E. coli recA protein-directed cleavage of phage λ repressor requires polynucleotide , 1980, Nature.
[14] J. Kraut. Serine proteases: structure and mechanism of catalysis. , 1977, Annual review of biochemistry.
[15] A. Fersht,et al. Rational modification of enzyme catalysis by engineering surface charge , 1987, Nature.
[16] Alan R. Fersht,et al. Prediction of electrostatic effects of engineering of protein charges , 1987, Nature.
[17] I. Lehman,et al. Enzymes of general recombination. , 1987, Annual review of biochemistry.
[18] I. Lehman,et al. A simple and rapid procedure for the large scale purification of the recA protein of Escherichia coli. , 1981, The Journal of biological chemistry.
[19] F. Westheimer,et al. A reporter group at the active site of acetoacetate decarboxylase. II. Ionization constant of the amino group. , 1971, Journal of the American Chemical Society.
[20] J. W. Little,et al. The SOS regulatory system: control of its state by the level of RecA protease. , 1983, Journal of molecular biology.
[21] D. Mount,et al. Differential repression of SOS genes by unstable lexA41 (tsl-1) protein causes a "split-phenotype" in Escherichia coli K-12. , 1987, Journal of molecular biology.
[22] D. Wallach,et al. Electrophoretic analysis of the major polypeptides of the human erythrocyte membrane. , 1971, Biochemistry.
[23] W. N. Burnette,et al. "Western blotting": electrophoretic transfer of proteins from sodium dodecyl sulfate--polyacrylamide gels to unmodified nitrocellulose and radiographic detection with antibody and radioiodinated protein A. , 1981, Analytical biochemistry.
[24] H. Echols,et al. Repressor cleavage as a prophage induction mechanism: hypersensitivity of a mutant lambda cI protein to recA-mediated proteolysis. , 1981, Journal of molecular biology.
[25] M. L. Bender,et al. Conformation of delta-chymotrypsin during catalysis. Chemical reactivity of the isoleucine 16 amino group in the acyl-enzyme intermediate. , 1971, Biochimica et biophysica acta.
[26] U. K. Laemmli,et al. Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4 , 1970, Nature.
[27] A. Fersht,et al. Electrostatic effects on modification of charged groups in the active site cleft of subtilisin by protein engineering. , 1987, Journal of molecular biology.
[28] J. Sportsman,et al. Improved technique utilizing nonfat dry milk for analysis of proteins and nucleic acids transferred to nitrocellulose , 1984 .
[29] Schmidt De,et al. PK of the lysine amino group at the active site of acetoacetate decarboxylase. , 1971 .
[30] Alan R. Fersht,et al. Tailoring the pH dependence of enzyme catalysis using protein engineering , 1985, Nature.
[31] J. Shafer,et al. Determination of a low pK for histidine-159 in the S-methylthio derivative of papain by proton nuclear magnetic resonance spectroscopy. , 1981, Biochemistry.