Results 251 to 260 of about 464,765 (299)
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Supported proline and proline-derivatives as recyclable organocatalysts

Chemical Society Reviews, 2008
In the last eight years, L-proline and L-proline derivatives, such as substituted prolinamides or pyrrolidines, have been successfully used as organocatalysts in several reactions. In this critical review we summarize the immobilization procedures of such organocatalysts highlighting their application, recoverability and reusability (86 references).
Michelangelo Gruttadauria   +2 more
exaly   +4 more sources

DL-Proline

Acta Crystallographica Section C Crystal Structure Communications, 2005
In the structure of DL-proline, C5H9NO2, the molecules are connected via classical intermolecular N-H...O hydrogen bonds involving the amine and carboxyl groups [N...O = 2.7129 (15) and 2.8392 (16) A], and form chains along the b-axis direction and parallel to (-101). The chains are linked into sheets via weak non-classical hydrogen bonds.
Sunnie, Myung   +3 more
openaire   +4 more sources

Proline-Glutamate/Proline-Proline-Glutamate (PE/PPE) proteins of Mycobacterium tuberculosis: The multifaceted immune-modulators

Acta Tropica, 2021
The PE/PPE proteins encoded by seven percent (7%) of Mycobacterium tuberculosis (Mtb) genome are the chief constituents to pathogen's virulence reservoir. The fact that these genes have evolved along ESX secretory system in pathogenic Mtb strains make their investigation very intriguing.
null Medha, Sadhna Sharma, Monika Sharma
openaire   +2 more sources

Proline specific peptidases

Biochimica et Biophysica Acta (BBA) - Protein Structure and Molecular Enzymology, 1997
Proline is unique among the 20 amino acids due to its cyclic structure. This specific conformation imposes many restrictions on the structural aspects of peptides and proteins and confers particular biological properties upon a wide range of physiologically important biomolecules.
D F, Cunningham, B, O'Connor
openaire   +2 more sources

Conformations of proline

Journal of the American Chemical Society, 1977
The present study concerns the energies of the conformations of proline. We present results of an improved molecular mechanics calculation for ring conformations of Ac-Pro-OCH/sub 3/ and for the s-cis and s-trans conformations. Internal coordinates including all torsions have been calculated from crystal coordinates for more than 40 x-ray ...
D F, De Tar, N P, Luthra
openaire   +2 more sources

Proline-Specific Endopeptidases

Russian Journal of Bioorganic Chemistry, 2003
Prolyl endopeptidases, or post-proline-cleaving enzymes, are the specific endopeptidases that hydrolyze peptide substrates at the carbonyl of the internal Pro residue. All the currently known prolyl endopeptidases from animals, microorganisms, fungi, and plants as well as the post-proline-cleaving enzymes that do not exhibit the strict specificity to ...
D V, Besedin, G N, Rudenskaia
openaire   +2 more sources

Biosynthesis of Proline

EcoSal Plus, 2007
Proline was among the last biosynthetic precursors to have its biosynthetic pathway unraveled. This review recapitulates the findings on the biosynthesis and transport of proline. Glutamyl kinase (GK) catalyzes the ATP-dependent phosphorylation of L-glutamic acid.
Laszlo N, Csonka, Thomas, Leisinger
openaire   +2 more sources

Fasciolicidal potential of proline analogues and proline biosynthesis inhibitors

International Journal for Parasitology, 1982
Abstract Sheers Marion , Campbell Anne J. , Beames D. J. , Edwards S. R. , Moore R. J. and Montague P. E. 1982. Fasciolicidal potential of proline analogues and proline biosynthesis inhibitors. International Journal for Parasitology 12 : 47–52.
M, Sheers   +5 more
openaire   +2 more sources

Mechanism-based inhibition of proline dehydrogenase by proline analogues

Biochimica et Biophysica Acta (BBA) - Protein Structure and Molecular Enzymology, 1993
The inactivation of proline dehydrogenase by several L-Pro analogues was investigated with the aim to block the essential metabolic pathway of tsetse flies allowing the degradation of L-Pro to L-Glu. In vitro studies on rat liver mitochondria showed that only 4-methylene-L-proline was able to inactivate proline dehydrogenase.
D, Tritsch, H, Mawlawi, J F, Biellmann
openaire   +2 more sources

Proline metabolism in cartilage: The importance of proline biosynthesis

Metabolism, 1978
Abstract Mammalian cells have the capacity to synthesize proline from ornithine or glutamic acid, although preformed proline usually is available from extracellular sources. We have measured the rate of proline formation from ornithine in the presence of physiologic concentrations of proline. In rat xiphoid cartilage organ cultures with ornithine and
R J, Smith, J M, Phang
openaire   +2 more sources

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