https://wiki.tiffa.net/w/index.php?action=history&feed=atom&title=Translations%3AEnzyme%2F98%2FenTranslations:Enzyme/98/en - Revision history2026-07-07T10:12:24ZRevision history for this page on the wikiMediaWiki 1.43.0https://wiki.tiffa.net/w/index.php?title=Translations:Enzyme/98/en&diff=118936&oldid=prevFuzzyBot: Importing a new version from external source2024-02-21T10:18:20Z<p>Importing a new version from external source</p>
<p><b>New page</b></p><div>=== Involvement in disease ===<br />
[[File:Phenylalanine hydroxylase mutations.svg|thumb|upright=2|alt= Ribbon diagram of phenylalanine hydroxylase with bound cofactor, coenzyme and substrate|In [[phenylalanine hydroxylase]] over 300 different mutations throughout the structure cause [[phenylketonuria]]. [[Phenylalanine]] substrate and [[tetrahydrobiopterin]] coenzyme in black, and [[Iron|Fe<sup>2+</sup>]] cofactor in yellow. ({{PDB|1KW0}})]]<br />
[[File:Autosomal recessive inheritance for affected enzyme.png|thumb|upright=1.4|Hereditary defects in enzymes are generally inherited in an [[autosomal inheritance|autosomal]] fashion because there are more non-X chromosomes than X-chromosomes, and a [[recessive inheritance|recessive]] fashion because the enzymes from the unaffected genes are generally sufficient to prevent symptoms in carriers.]]<br />
{{see also|Genetic disorder}}</div>FuzzyBot