3-amino-5-hydroxybenzoic acid has been researched along with rifamycins in 10 studies
| Studies (3-amino-5-hydroxybenzoic acid) | Trials (3-amino-5-hydroxybenzoic acid) | Recent Studies (post-2010) (3-amino-5-hydroxybenzoic acid) | Studies (rifamycins) | Trials (rifamycins) | Recent Studies (post-2010) (rifamycins) |
|---|---|---|---|---|---|
| 38 | 0 | 11 | 2,351 | 203 | 626 |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 1 (10.00) | 18.7374 |
| 1990's | 2 (20.00) | 18.2507 |
| 2000's | 5 (50.00) | 29.6817 |
| 2010's | 2 (20.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Ghisalba, O; Nüesch, J | 1 |
| Floss, HG; Fryhle, CB; Handa, S; Kim, CG; Yu, TW | 1 |
| August, PR; Floss, HG; Hoffmann, D; Hutchinson, CR; Kim, CG; Müller, R; Ning, S; Tang, L; Taylor, M; Yoon, YJ; Yu, TW; Zhang, X | 1 |
| Draeger, G; Floss, HG; Kim, CG; Leistner, E; Muller, M; Muller, R; Yu, TW; Zhang, X | 1 |
| Admiraal, SJ; Khosla, C; Walsh, CT | 2 |
| Arakawa, K; Floss, HG; Mahmud, T; Müller, R; Yu, TW | 1 |
| Hartung, IV; Hunziker, D; Khosla, C; Rude, MA; Schnarr, NA | 1 |
| Bai, L; Kang, Q; Shen, Y | 1 |
| Biggins, JB; Brady, SF; Braffman, N; Calle, PY; Campbell, EA; Danziger, M; Darst, SA; Fay, A; Glickman, MS; Lilic, M; Milshteyn, A; Montiel, D; Peek, J; Saito, K; Ternei, MA; Warrier, T; Woodworth, I | 1 |
1 review(s) available for 3-amino-5-hydroxybenzoic acid and rifamycins
| Article | Year |
|---|---|
Biosynthesis of 3,5-AHBA-derived natural products.
Topics: Actinomycetales; Aminobenzoates; Biological Products; Biosynthetic Pathways; Bridged Bicyclo Compounds, Heterocyclic; Hydroxybenzoates; Maytansine; Mitomycin; Molecular Structure; Naphthoquinones; Rifamycins | 2012 |
9 other study(ies) available for 3-amino-5-hydroxybenzoic acid and rifamycins
| Article | Year |
|---|---|
A genetic approach to the biosynthesis of the rifamycin-chromophore in Nocardia mediterranei. IV. Identification of 3-amino-5-hydroxybenzoic acid as a direct precursor of the seven-carbon amino starter-unit.
Topics: Aminobenzoates; Benzoates; Hydroxybenzoates; Mutation; Nocardia; Rifamycins | 1981 |
3-Amino-5-hydroxybenzoic acid synthase, the terminal enzyme in the formation of the precursor of mC7N units in rifamycin and related antibiotics.
Topics: Actinobacteria; Actinomycetales; Amino Acid Sequence; Aminobenzoates; Base Sequence; Cloning, Molecular; Cyclohexanecarboxylic Acids; Escherichia coli; Evolution, Molecular; Hydro-Lyases; Hydroxybenzoates; Molecular Sequence Data; Phylogeny; Pyridoxal Phosphate; Pyridoxamine; Recombinant Proteins; Restriction Mapping; Rifamycins; Sequence Analysis, DNA; Sequence Homology, Amino Acid; Shikimic Acid; Stereoisomerism; Substrate Specificity; Transaminases | 1998 |
Biosynthesis of the ansamycin antibiotic rifamycin: deductions from the molecular analysis of the rif biosynthetic gene cluster of Amycolatopsis mediterranei S699.
Topics: Actinobacteria; Amino Acid Sequence; Aminobenzoates; Anti-Bacterial Agents; Gene Expression Regulation, Bacterial; Genes, Bacterial; Hydro-Lyases; Hydroxybenzoates; Lactams, Macrocyclic; Molecular Sequence Data; Molecular Structure; Multienzyme Complexes; Open Reading Frames; Rifamycins; Sequence Analysis, DNA; Sequence Homology, Amino Acid | 1998 |
Mutational analysis and reconstituted expression of the biosynthetic genes involved in the formation of 3-amino-5-hydroxybenzoic acid, the starter unit of rifamycin biosynthesis in amycolatopsis Mediterranei S699.
Topics: Actinomycetales; Amino Acid Sequence; Aminobenzoates; Base Sequence; DNA Mutational Analysis; DNA Primers; Genes, Bacterial; Genes, Regulator; Hydroxybenzoates; Molecular Sequence Data; Multigene Family; Open Reading Frames; Plasmids; Promoter Regions, Genetic; Restriction Mapping; Rifabutin; Rifamycins | 2001 |
The loading module of rifamycin synthetase is an adenylation-thiolation didomain with substrate tolerance for substituted benzoates.
Topics: Actinomycetales; Adenosine Monophosphate; Amino Acid Motifs; Aminobenzoates; Benzoates; Coenzyme A Ligases; Genetic Vectors; Holoenzymes; Hydroxybenzoates; Kinetics; Multienzyme Complexes; Peptide Synthases; Protein Structure, Tertiary; Rifamycins; Substrate Specificity | 2001 |
The loading and initial elongation modules of rifamycin synthetase collaborate to produce mixed aryl ketide products.
Topics: Acylation; Aminobenzoates; Anti-Bacterial Agents; Hydroxybenzoates; Kinetics; Multienzyme Complexes; Peptide Chain Elongation, Translational; Peptide Synthases; Phenylpropionates; Recombinant Fusion Proteins; Rifamycins; Substrate Specificity | 2002 |
Characterization of the early stage aminoshikimate pathway in the formation of 3-amino-5-hydroxybenzoic acid: the RifN protein specifically converts kanosamine into kanosamine 6-phosphate.
Topics: Actinomycetales; Aminobenzoates; Escherichia coli; Glucosamine; Hydroxybenzoates; Organophosphates; Recombinant Proteins; Rifamycins; Shikimic Acid; Sugar Acids | 2002 |
Stereochemical assignment of intermediates in the rifamycin biosynthetic pathway by precursor-directed biosynthesis.
Topics: Actinomycetales; Aminobenzoates; Hydro-Lyases; Hydroxybenzoates; Molecular Structure; Polyketide Synthases; Rifamycins | 2005 |
Rifamycin congeners kanglemycins are active against rifampicin-resistant bacteria via a distinct mechanism.
Topics: Aminobenzoates; Antibiotics, Antitubercular; Bacteria; Bacterial Proteins; DNA-Directed RNA Polymerases; Drug Resistance, Bacterial; Humans; Hydroxybenzoates; Metagenomics; Molecular Structure; Mutation; Mycobacterium tuberculosis; Rifampin; Rifamycins; Soil Microbiology; Tuberculosis | 2018 |