| scholarly article | Q13442814 |
| P2093 | author name string | Benkovic SJ | |
| Gottschall DW | |||
| Dietrich RF | |||
| Shiman R | |||
| P433 | issue | 2 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 845-849 | |
| P577 | publication date | 1982-01-01 | |
| P1433 | published in | Journal of Biological Chemistry | Q867727 |
| P1476 | title | Phenylalanine hydroxylase. Correlation of the iron content with activity and the preparation and reconstitution of the apoenzyme | |
| P478 | volume | 257 |
| Q37023585 | A delicate balance: Iron metabolism and diseases of the brain. |
| Q43227635 | Kinetic isotope effects on aromatic and benzylic hydroxylation by Chromobacterium violaceum phenylalanine hydroxylase as probes of chemical mechanism and reactivity |
| Q41817640 | Kinetic mechanism of phenylalanine hydroxylase: intrinsic binding and rate constants from single-turnover experiments |
| Q24673681 | Mechanism of aromatic amino acid hydroxylation |
| Q42177277 | Modulation by pterins of the phosphorylation and phenylalanine activation of phenylalanine 4-mono-oxygenase |
| Q24537314 | Purification and characterization of carbazole 1,9a-dioxygenase, a three-component dioxygenase system of Pseudomonas resinovorans strain CA10 |
| Q42797292 | Purification and characterization of the blue-green rat phaeochromocytoma (PC12) tyrosine hydroxylase with a dopamine-Fe(III) complex. Reversal of the endogenous feedback inhibition by phosphorylation of serine-40 |
| Q36157496 | Purification and properties of NADH-ferredoxinNAP reductase, a component of naphthalene dioxygenase from Pseudomonas sp. strain NCIB 9816. |
| Q28578299 | Reduction and oxidation of the active site iron in tyrosine hydroxylase: kinetics and specificity |
| Q40375232 | Structure and function of the aromatic amino acid hydroxylases. |
| Q43665230 | Studies on the partially uncoupled oxidation of tetrahydropterins by phenylalanine hydroxylase |
| Q36246601 | The possibility that the spectrum of intermediate two, seen in the course of reaction of flavoenzyme phenol hydroxylases, may be attributable to iminol isomers of a flavin-derived 6-arylamino-5-oxo(3H,5H)uracil |
Search more.