"Case 67: Phenylalanine hydroxylase: An investigation of its structure leads to the development of PKU new therapies" by Kathleen Cornely

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Case 67: Phenylalanine hydroxylase: An investigation of its structure leads to the development of PKU new therapies

Biochemistry (2019)

Kathleen Cornely, Providence College

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Description

The characteristics of phenylalanine hydroxylase, the enzyme missing in persons afflicted with the genetic disorder phenylketonuria (PKU), are examined. Understanding how the enzyme works will allow the development of drugs to treat this condition.

Disciplines

Biochemistry, Biophysics, and Structural Biology

Publication Date

November 20, 2019

Citation Information

Kathleen Cornely. "Case 67: Phenylalanine hydroxylase: An investigation of its structure leads to the development of PKU new therapies" Biochemistry (2019)
Available at: http://works.bepress.com/kathleen-cornely/20/