homocysteine has been researched along with s-ribosyl-l-homocysteine in 17 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 1 (5.88) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 10 (58.82) | 29.6817 |
2010's | 5 (29.41) | 24.3611 |
2020's | 1 (5.88) | 2.80 |
Authors | Studies |
---|---|
DUERRE, JA | 1 |
Alfaro, JF; Bassler, BL; Cornell, KA; Mansouri, S; Wan, W; Zhao, G; Zhou, ZS | 1 |
Patel, R; Pei, D; Zhu, J | 1 |
Alfaro, JF; Karschner, EL; Wynn, DP; Zhang, T; Zhou, ZS | 1 |
Pei, D; Zhu, J | 1 |
Challan Belval, S; Gal, L; Garmyn, D; Guzzo, J; Margiewes, S; Piveteau, P | 1 |
Bell, CE; Pei, D; Rajan, R; Shen, G; Zhu, J | 1 |
Garmendia, CA; Lalama, J; Robert, J; Wnuk, SF | 1 |
Garmendia, CA; Lalama, J; Pei, D; Robert, J; Wnuk, SF; Zhu, J | 1 |
Han, X; Lu, C | 1 |
Gopishetty, B; Malladi, VL; Meyers, BP; Pei, D; Robert, J; Sobczak, AJ; Wnuk, SF; Zhu, J | 1 |
Malladi, VL; Meyer, TM; Pei, D; Sobczak, AJ; Wnuk, SF | 1 |
Bai, H; Chen, W; Ding, C; Han, X; Hu, Q; Liu, L; Qi, K; Yu, S | 1 |
Bolitho, ME; Corcoran, BJ; Showell-Rouse, EI; Wang, KQ | 1 |
Chbib, C; Sobczak, AJ; Wnuk, SF | 1 |
Chbib, C; Mina, G | 1 |
Chbib, C | 1 |
2 review(s) available for homocysteine and s-ribosyl-l-homocysteine
Article | Year |
---|---|
Mechanism of action of S-ribosylhomocysteinase (LuxS).
Topics: Anti-Bacterial Agents; Bacterial Proteins; Binding Sites; Carbon-Sulfur Lyases; Catalysis; Ferrous Compounds; Homocysteine; Hydrolases; Models, Molecular; Oxidation-Reduction; Pentanes; Substrate Specificity; Sulfides | 2004 |
Recent progresses on synthesized LuxS inhibitors: A mini-review.
Topics: Anti-Bacterial Agents; Bacterial Proteins; Carbon-Sulfur Lyases; Enzyme Inhibitors; Homocysteine; Quorum Sensing | 2019 |
15 other study(ies) available for homocysteine and s-ribosyl-l-homocysteine
Article | Year |
---|---|
Preparation and properties of S-adenosyl-L-homocysteine, S-adenosyl-L-homocysteine sulfoxide and S-ribosyl-L-homocysteine.
Topics: Cysteine; Homocysteine; Nucleosides; Nucleotides; Safrole; Sulfoxides | 1962 |
Chemical synthesis of S-ribosyl-L-homocysteine and activity assay as a LuxS substrate.
Topics: Bacillus subtilis; Bacterial Proteins; Carbon-Sulfur Lyases; Homocysteine; Kinetics; Substrate Specificity | 2003 |
Catalytic mechanism of S-ribosylhomocysteinase (LuxS): stereochemical course and kinetic isotope effect of proton transfer reactions.
Topics: Bacillus subtilis; Bacterial Proteins; Binding Sites; Carbon-Sulfur Lyases; Catalysis; Deuterium Exchange Measurement; Homocysteine; Kinetics; N-Glycosyl Hydrolases; Nuclear Magnetic Resonance, Biomolecular; Protein Conformation; Protons; Substrate Specificity; Vibrio | 2004 |
Synthesis of LuxS inhibitors targeting bacterial cell-cell communication.
Topics: Bacteria; Bacterial Proteins; Carbon-Sulfur Lyases; Homocysteine; Stereoisomerism; Substrate Specificity | 2004 |
Assessment of the roles of LuxS, S-ribosyl homocysteine, and autoinducer 2 in cell attachment during biofilm formation by Listeria monocytogenes EGD-e.
Topics: Animals; Bacterial Adhesion; Bacterial Proteins; Biofilms; Carbon-Sulfur Lyases; Gene Expression Regulation, Bacterial; Genetic Complementation Test; Homocysteine; Homoserine; Lactones; Listeria monocytogenes; Rabbits | 2006 |
Design and synthesis of substrate and intermediate analogue inhibitors of S-ribosylhomocysteinase.
Topics: Amides; Anti-Bacterial Agents; Bacillus subtilis; Bacterial Proteins; Binding Sites; Butyrates; Caproates; Carbamates; Carbon-Sulfur Lyases; Crystallography, X-Ray; Dioxolanes; Drug Design; Homocysteine; Models, Molecular; Stereoisomerism; Structure-Activity Relationship | 2006 |
Novel S-ribosylhomocysteine analogues as potential inhibitors of LuxS enzyme.
Topics: Bacterial Proteins; Carbon-Sulfur Lyases; Drug Design; Enzyme Inhibitors; Homocysteine | 2007 |
S-Ribosylhomocysteine analogues with the carbon-5 and sulfur atoms replaced by a vinyl or (fluoro)vinyl unit.
Topics: Bacillus subtilis; Bacterial Proteins; Carbon; Carbon-Sulfur Lyases; Dose-Response Relationship, Drug; Enzyme Inhibitors; Homocysteine; Molecular Structure; Stereoisomerism; Structure-Activity Relationship; Sulfones; Sulfur; Vinyl Compounds | 2008 |
Biological activity and identification of a peptide inhibitor of LuxS from Streptococcus suis serotype 2.
Topics: Amino Acid Sequence; Bacterial Proteins; Biological Assay; Carbon-Sulfur Lyases; Enzyme Inhibitors; Gene Expression Profiling; Homocysteine; Homoserine; Humans; Lactones; Molecular Sequence Data; Peptide Library; Peptides; Quorum Sensing; Reverse Transcriptase Polymerase Chain Reaction; Streptococcus suis; Vibrio; Virulence Factors | 2009 |
Inhibition of S-ribosylhomocysteinase (LuxS) by substrate analogues modified at the ribosyl C-3 position.
Topics: Anti-Bacterial Agents; Bacillus subtilis; Bacterial Proteins; Carbon-Sulfur Lyases; Homocysteine; Ribose; Structure-Activity Relationship | 2009 |
Inhibition of LuxS by S-ribosylhomocysteine analogues containing a [4-aza]ribose ring.
Topics: Bacillus subtilis; Bacterial Proteins; Carbon-Sulfur Lyases; Dose-Response Relationship, Drug; Homocysteine; Molecular Structure; Ribose; Stereoisomerism; Structure-Activity Relationship | 2011 |
[Cloning and expression of luxS and pfs and in vitro biosynthesis autoinducer 2 of avian pathogenic Escherichia coli from Anhui Province].
Topics: Animals; Animals, Wild; Bacterial Proteins; Bird Diseases; Carbon-Sulfur Lyases; Chickens; China; Cloning, Molecular; Ducks; Escherichia coli; Escherichia coli Infections; Gene Expression Regulation, Bacterial; Homocysteine; Homoserine; Lactones; N-Glycosyl Hydrolases | 2012 |
Revisiting synthetic preparation of the quorum sensing substrate S-D-ribosyl-L-homocysteine (SRH).
Topics: Bacterial Proteins; Carbon-Sulfur Lyases; Chemistry Techniques, Synthetic; Homocysteine; Quorum Sensing | 2014 |
S-Ribosylhomocysteine analogs containing a [4-thio]ribose ring.
Topics: Carbon; Homocysteine; Homocystine; Sulfur; Trifluoroacetic Acid | 2015 |
Unexpected furanose-pyranose isomerization of 4-C-alkylribofuranose.
Topics: Carbohydrate Conformation; Homocysteine; Monosaccharides; Stereoisomerism | 2020 |