Pub. Date : 1999 Aug 13
PMID : 10438531
6 Functional Relationships(s)Download |
Sentence | Compound Name | Protein Name | Organism |
| 1 | Influence of flavin analogue structure on the catalytic activities and flavinylation reactions of recombinant human liver monoamine oxidases A and B. | 4,6-dinitro-o-cresol | monoamine oxidase A | Homo sapiens |
| 2 | The selectivities of MAO A and MAO B for flavin analogue incorporation are found to be similar, although 8alpha-methylation of the flavin resulted in a higher level of catalytic activity for MAO B than for MAO A. | 4,6-dinitro-o-cresol | monoamine oxidase A | Homo sapiens |
| 3 | The selectivities of MAO A and MAO B for flavin analogue incorporation are found to be similar, although 8alpha-methylation of the flavin resulted in a higher level of catalytic activity for MAO B than for MAO A. | 4,6-dinitro-o-cresol | monoamine oxidase A | Homo sapiens |
| 4 | The selectivities of MAO A and MAO B for flavin analogue incorporation are found to be similar, although 8alpha-methylation of the flavin resulted in a higher level of catalytic activity for MAO B than for MAO A. | 4,6-dinitro-o-cresol | monoamine oxidase A | Homo sapiens |
| 5 | MAO A partially purified from yeast grown on 8-nor-8-chlororiboflavin exhibited an absorption spectrum indicating the covalent flavin is an 8-nor-8-S-thioflavin, suggesting a nucleophilic displacement mechanism that supports the quinone-methide mechanism previously suggested as a general mechanism for covalent flavin attachment. | 4,6-dinitro-o-cresol | monoamine oxidase A | Homo sapiens |
| 6 | MAO A partially purified from yeast grown on 8-nor-8-chlororiboflavin exhibited an absorption spectrum indicating the covalent flavin is an 8-nor-8-S-thioflavin, suggesting a nucleophilic displacement mechanism that supports the quinone-methide mechanism previously suggested as a general mechanism for covalent flavin attachment. | 4,6-dinitro-o-cresol | monoamine oxidase A | Homo sapiens |