Copyright © Philip M. Parker, INSEAD. Terms of Use.

| Domain | Definition |
Health | An enzyme of the oxidoreductase class that catalyzes the formation of L-tyrosine, dihydrobiopterin, and water from L-phenylalanine, tetrahydrobiopterin, and oxygen. Deficiency of this enzyme may cause phenylketonurias and phenylketonuria, maternal. EC 1.14.16.1. (references) |
Source: compiled by the editor from various references; see credits. | |
(From Wikipedia, the free Encyclopedia)
Source: adapted by the editor from Wikipedia, the free encyclopedia under a copyleft GNU Free Documentation License (GFDL) from the article "Phenylalanine hydroxylase."
| Subject | Topic | Quote |
Health | Classical phenylketonuria (PKU) is a rare metabolic disorder (and orphan disease) that usually results from a deficiency of a liver enzyme known as phenylalanine hydroxylase (PAH). (references) | |
Source: compiled by the editor from ICON Group International, Inc.; see credits. | ||
Hexadecimal (or equivalents, 770AD-1900s) (references)50 48 45 4E 59 4C 41 4C 41 4E 49 4E 45      48 59 44 52 4F 58 59 4C 41 53 45 |
| Leonardo da Vinci (1452-1519; backwards) (references)
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Binary Code (1918-1938, probably earlier) (references)01010000 01001000 01000101 01001110 01011001 01001100 01000001 01001100 01000001 01001110 01001001 01001110 01000101 00100000 01001000 01011001 01000100 01010010 01001111 01011000 01011001 01001100 01000001 01010011 01000101 |
HTML Code (1990) (references)P H E N Y L A L A N I N E   H Y D R O X Y L A S E |
ISO 10646 (1991-1993) (references)0050 0048 0045 004E 0059 004C 0041 004C 0041 004E 0049 004E 0045      0048 0059 0044 0052 004F 0058 0059 004C 0041 0053 0045 |
Encryption (beginner's substitution cypher): (references)5042394859463546354843483924259385249585946355339 |
Copyright © Philip M. Parker, INSEAD. Terms of Use.