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TPH

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==Tryptophan hydroxylase==
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#REDIRECT [[Hydroxylase]]
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Tryptophan hydroxylase (TPH) (tryptophan 5-monooxygenase, EC 1.14.16.4) catalyses the reaction between tryptophan, 5,6,7,8-tetrahydrobiopterin (BH<sub>4</sub>) and O<sub>2</sub> to give 5-hydroxytryptophan and 4a-hydroxy-tetrahydrobiopterin (4a-hydroxy-BH<sub>4</sub>. This reaction is the first and rate limiting step in the biosynthesis of serotonin (See scheme).
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Together with phenylalanine hydroxylase (EC 1.14.16.1) and tyrosine hydroxylase (EC 1.14.16.2), TPH form the small enzyme family of aromatic amino acid hydroxylases (AAAH) []. These enzymes all contain iron and use BH<sub>4</sub> as a co-substrate in the hydroxylation of their respective aromatic amino acids [ , , ]. Additionally all mammalian AAAH form homotetramers and each monomer consists of three domains. These domains are the N-terminal regulatory domain (100-150 residues), the catalytic domain (approximately 315 residues) and the C-terminal tetramerisation domain (approximately 30-40 residues) [ , , , ].
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==The two isoforms of tryptophan hydroxylase==
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TPH exists in two isoforms called TPH isoform 1 (TPH1) and TPH isoform 2 (TPH2) [ ]. The existence of two isoforms was observed when TPH was purified and characterised from different tissues [ , , , , ]. The gene encoding for rabbit TPH1 was identified in 1987 by Grenett et al.[] and a few years later the human gene for TPH1 was identified on chromosome 11 [ , ]. The gene for isoform 2 was identified in 2003 by Walther et al. and the human gene is located on chromosome 12 [].
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The two isoforms are expressed in different tissues. TPH2 is mainly expressed in serotonergic neurons of the brain and gut [, , , , ]. TPH1 is expressed in other parts of the body such as the pineal gland [4,27], skin cells [ ], mast cells [1], intestinal mucosa and enterochromafin cells [ ] and in cancer cells [ , ]. The main difference between the two isoforms is that the N-terminal is extended by 46 residues in TPH2 [ ].
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'''Two structures are available of the catalytic domain of TPH1.'''
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<br/>
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The structure '''[[1mlw]]''' is the catalytic domain of human TPH1 with bound dihydrobiopterin.<br/>
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The structure '''[[3e2t]]''' is the catalytic domain of ckicken TPH1 with bound tryptophan
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{{STRUCTURE_1mlw | PDB=1mlw | SCENE= }}
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Current revision

  1. REDIRECT Hydroxylase

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Michael Skovbo Windahl, OCA

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