نتایج جستجو برای: l proline

تعداد نتایج: 631454  

Journal: :Journal of bacteriology 1966
L Unger R D DeMoss

Unger, Leon (University of Illinois, Urbana), and R. D. DeMoss. Action of a proline analogue, l-thiazolidine-4-carboxylic acid, in Escherichia coli. J. Bacteriol. 91:1556-1563. 1966.-The effect of the proline analogue, l-thiazolidine-4-carboxylic acid (thioproline), on growth, and its relation to the metabolic function of proline in protein synthesis in Escherichia coli K-12, has been studied. ...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 1973
P Van der Werf R A Stephani M Orlowski A Meister

L-2-Imidazolidone-4-carboxylic acid is an effective competitive inhibitor of the reaction catalyzed by 5-oxoprolinase, in which 5-oxo-L-proline (L-pyroglutamic acid, L-2-pyrrolidone-5-carboxylic acid, L-5-oxopyrrolidine-2-carboxylic acid) is converted to L-glutamate, with concomitant cleavage of ATP to ADP and orthophosphate. L-2-Imidazolidone-4-carboxylate decreased the rate of metabolism of 5...

Journal: :Applied and environmental microbiology 1998
T Kosuge T Hoshino

Growth of Thermus thermophilus HB27 was inhibited by a proline analog, 3,4-dehydroproline (DHP). This result suggested that the gamma-glutamyl kinase (the product of the proB gene) was inhibited by feedback inhibition in T. thermophilus. DHP-resistant mutants were reported previously for Escherichia coli (A. M. Dandekar and S. L. Uratsu, J. Bacteriol. 170:5943-5945, 1988) and Serratia marcescen...

Journal: :Journal of bacteriology 1965
J D PUNCH J C OLSON J V SCALETTI

Punch, J. D. (University of Minnesota, St. Paul), J. C. Olson, Jr., and J. V. Scaletti. Amino acid utilization by Alcaligenes viscolactis for growth and slime production. J. Bacteriol. 89:1521-1525. 1965.-The ability of Alcaligenes viscolactis to utilize amino acids in a basal salts solution (K(2)HPO(4), KH(2)PO(4), MgSO(4), MnSO(4), FeSO(4), NaCl) was studied. Of 27 amino acids, only l-asparag...

Journal: :Agricultural and biological chemistry 1991
T Yoshimoto D Tsuru N Yamamoto R Ikezawa S Furukawa

Structural requirements of N-blocked L-proline derivatives as specific inhibitors for prolyl endopeptidase were investigated using a series of substrate analogs. Replacement of L-proline by its D-isomer remarkably reduced the inhibition. Introduction of a sulfur atom in proline and/or in the penultimate pyrrolidine rings significantly increased the inhibition, but the introduction of oxygen rat...

Journal: :Journal of the American Chemical Society 1996
Eric S Eberhardt Nicholas Panisik Ronald T Raines

The hydroxylation of proline residues in collagen enhances the stability of the collagen triple helix. Previous X-ray diffraction analyses had demonstrated that the presence of an electron-withdrawing substituent on the pyrrolidine ring of proline residues has significant structural consequences [Panasik, N., Jr.; Eberhardt, E. S.; Edison, A. S.; Powell, D. R.; Raines, R. T. Int. J. Pept. Prote...

Journal: :The Journal of biological chemistry 1951
R E NEUMAN E L SMITH

Two types of peptidases are known to hydrolyze peptides containing proline and hydroxyproline. The first of these, prolidase (l-3), attacks peptide bonds involving t,he nitrogen of the imino acids in the typical substrates, glycyl-L-proline and glycylhydroxy+proline. The individuality of this enzyme has already been demonstrated by purification and by specificity studies. The second enzyme, nam...

The purpose of this study was to isolate and characterize Proline Dehydrogenase (ProDH) enzyme frommicroorganisms isolated from soil in Iran. Isolation and screening of L-proline degradative enzymes from soilsamples was carried out. The isolate was characterized by biochemical markers and 16S rRNA geneanalysis. The target ProDH was purified and the effects of pH and temperatur...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 1965
L A Salzman H Weissbach E Katz

26 Gerhart, J. C., and A. B. Pardee, in Synthesis and Structure of Macromolecules, Cold Spring Harbor Symposia on Quantitative Biology, vol. 28 (1963), p. 491. 27 Changeux, J. P., in Subunit Structure of Proteins, Brookhaven Symposia in Biology, no. 17 (1964), p. 232. 28 Antonini, E., J. Wyman, M. Brunori, J. F. Taylor, A. Rossi-Fanelli, and A. Caputo, J. Biol. Chem., 239, 907 (1964). 29 Gibson...

2017
Aaron M Chesna Jordan M Cox Sanjukta Basso Jason B Benedict

The title compound [systematic name: benzoic acid-pyrrolidin-1-ium-2-carboxyl-ate (1/1)], C7H6O2·C5H9NO2, is an example of the application of non-centrosymmetric co-crystallization for the growth of a crystal containing a typically centrosymmetric component in a chiral space group. It co-crystallizes in the space group P212121 and contains benzoic acid and l-proline in equal proportions. The cr...

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