Tryptophan side chain oxidase from Pseudomonas. Oxidation of skatole to indole-3-carboxaldehyde via indole-3-methanol. 1978

H Ushiro, and K Takai, and Y Noda, and S Narumiya, and T Tokuyama, and O Hayaishi

UI MeSH Term Description Entries
D007211 Indoles Benzopyrroles with the nitrogen at the number one carbon adjacent to the benzyl portion, in contrast to ISOINDOLES which have the nitrogen away from the six-membered ring.
D007700 Kinetics The rate dynamics in chemical or physical systems.
D011549 Pseudomonas A genus of gram-negative, aerobic, rod-shaped bacteria widely distributed in nature. Some species are pathogenic for humans, animals, and plants. Chryseomonas,Pseudomona,Flavimonas
D006899 Mixed Function Oxygenases Widely distributed enzymes that carry out oxidation-reduction reactions in which one atom of the oxygen molecule is incorporated into the organic substrate; the other oxygen atom is reduced and combined with hydrogen ions to form water. They are also known as monooxygenases or hydroxylases. These reactions require two substrates as reductants for each of the two oxygen atoms. There are different classes of monooxygenases depending on the type of hydrogen-providing cosubstrate (COENZYMES) required in the mixed-function oxidation. Hydroxylase,Hydroxylases,Mixed Function Oxidase,Mixed Function Oxygenase,Monooxygenase,Monooxygenases,Mixed Function Oxidases,Function Oxidase, Mixed,Function Oxygenase, Mixed,Oxidase, Mixed Function,Oxidases, Mixed Function,Oxygenase, Mixed Function,Oxygenases, Mixed Function
D012862 Skatole 3-Methylindole,3 Methylindole
D013055 Spectrophotometry, Infrared Spectrophotometry in the infrared region, usually for the purpose of chemical analysis through measurement of absorption spectra associated with rotational and vibrational energy levels of molecules. (McGraw-Hill Dictionary of Scientific and Technical Terms, 4th ed) IR Spectra,Infrared Spectrophotometry,IR Spectras,Spectra, IR
D013056 Spectrophotometry, Ultraviolet Determination of the spectra of ultraviolet absorption by specific molecules in gases or liquids, for example Cl2, SO2, NO2, CS2, ozone, mercury vapor, and various unsaturated compounds. (McGraw-Hill Dictionary of Scientific and Technical Terms, 4th ed) Ultraviolet Spectrophotometry
D013379 Substrate Specificity A characteristic feature of enzyme activity in relation to the kind of substrate on which the enzyme or catalytic molecule reacts. Specificities, Substrate,Specificity, Substrate,Substrate Specificities
D014364 Tryptophan An essential amino acid that is necessary for normal growth in infants and for NITROGEN balance in adults. It is a precursor of INDOLE ALKALOIDS in plants. It is a precursor of SEROTONIN (hence its use as an antidepressant and sleep aid). It can be a precursor to NIACIN, albeit inefficiently, in mammals. Ardeydorm,Ardeytropin,L-Tryptophan,L-Tryptophan-ratiopharm,Levotryptophan,Lyphan,Naturruhe,Optimax,PMS-Tryptophan,Trofan,Tryptacin,Tryptan,Tryptophan Metabolism Alterations,ratio-Tryptophan,L Tryptophan,L Tryptophan ratiopharm,PMS Tryptophan,ratio Tryptophan

Related Publications

H Ushiro, and K Takai, and Y Noda, and S Narumiya, and T Tokuyama, and O Hayaishi
October 1991, Journal of general microbiology,
H Ushiro, and K Takai, and Y Noda, and S Narumiya, and T Tokuyama, and O Hayaishi
August 1981, The Journal of biological chemistry,
H Ushiro, and K Takai, and Y Noda, and S Narumiya, and T Tokuyama, and O Hayaishi
January 1987, Methods in enzymology,
H Ushiro, and K Takai, and Y Noda, and S Narumiya, and T Tokuyama, and O Hayaishi
May 1958, Plant physiology,
H Ushiro, and K Takai, and Y Noda, and S Narumiya, and T Tokuyama, and O Hayaishi
January 1993, Cancer investigation,
H Ushiro, and K Takai, and Y Noda, and S Narumiya, and T Tokuyama, and O Hayaishi
November 2005, The journal of peptide research : official journal of the American Peptide Society,
H Ushiro, and K Takai, and Y Noda, and S Narumiya, and T Tokuyama, and O Hayaishi
March 1974, Biochimica et biophysica acta,
H Ushiro, and K Takai, and Y Noda, and S Narumiya, and T Tokuyama, and O Hayaishi
September 2002, Journal of the American Chemical Society,
H Ushiro, and K Takai, and Y Noda, and S Narumiya, and T Tokuyama, and O Hayaishi
September 1963, Chemical & pharmaceutical bulletin,
H Ushiro, and K Takai, and Y Noda, and S Narumiya, and T Tokuyama, and O Hayaishi
November 2021, International journal of molecular sciences,
Copied contents to your clipboard!